Taste
Thegustatory systemorsense of tasteis thesensory systemthat is partially responsible for theperceptionof taste (flavor).[1]Taste is the perception stimulated when a substance in themouthreacts chemicallywithtaste receptorcells located ontaste budsin theoral cavity,mostly on thetongue.Taste, along withthe sense of smellandtrigeminal nervestimulation (registering texture, pain, and temperature), determinesflavorsoffoodand other substances.Humanshave taste receptors on taste buds and other areas, including the upper surface of thetongueand theepiglottis.[2][3]Thegustatory cortexis responsible for the perception of taste.
The tongue is covered with thousands of small bumps calledpapillae,which are visible to thenaked eye.[2]Within each papilla are hundreds of taste buds.[1][4]The exceptions to this is thefiliform papillaethat do not contain taste buds. There are between 2000 and 5000[5]taste buds that are located on the back and front of the tongue. Others are located on the roof, sides and back of the mouth, and in thethroat.Each taste bud contains 50 to 100 taste receptor cells.
Taste receptors in the mouth sense the five basic tastes:sweetness,sourness,saltiness,bitterness,andsavoriness(also known assavoryorumami).[1][2][6][7]Scientific experiments have demonstrated that these five tastes exist and are distinct from one another. Taste buds are able to tell different tastes apart when they interact with different molecules or ions. Sweetness, savoriness, and bitter tastes are triggered by the binding of molecules toG protein-coupled receptorson thecell membranesof taste buds. Saltiness and sourness are perceived whenalkali metalsorhydrogenionsmeet taste buds, respectively.[8][9]
The basic tastes contribute only partially to the sensation and flavor of food in the mouth—other factors includesmell,[1]detected by theolfactory epitheliumof the nose;[10]texture,[11]detected through a variety ofmechanoreceptors,muscle nerves, etc.;[12]temperature, detected bytemperature receptors;and "coolness" (such as ofmenthol) and "hotness" (pungency), bychemesthesis.
As the gustatory system senses both harmful and beneficial things, all basic tastes bring either caution or craving depending upon the effect the things they sense have on the body.[13]Sweetness helps to identify energy-rich foods, while bitterness warns people of poisons.[14]
Among humans, taste perception begins to fade duringageing,tongue papillae are lost, andsalivaproduction slowly decreases.[15]Humans can also have distortion of tastes (dysgeusia). Not allmammalsshare the same tastes: somerodentscan tastestarch(which humans cannot),catscannot taste sweetness, and several othercarnivores,includinghyenas,dolphins,andsea lions,have lost the ability to sense up to four of their ancestral five basic tastes.[16]
Basic tastes
[edit]This sectionneeds additional citations forverification.(September 2016) |
The gustatory system allows animals to distinguish between safe and harmful food and to gauge different foods' nutritional value.Digestive enzymesin saliva begin to dissolve food into base chemicals that are washed over the papillae and detected as tastes by the taste buds. The tongue is covered with thousands of small bumps calledpapillae,which are visible to the naked eye. Within each papilla are hundreds of taste buds.[4]The exception to this are thefiliform papillae,which do not contain taste buds. There are between 2,000 and 5,000[5]taste buds that are located on the back and front of the tongue. Others are located on the roof, sides and back of the mouth, and in the throat. Each taste bud contains 50 to 100 taste-receptor cells.
The five specific tastes received bytaste receptorsare saltiness,sweetness,bitterness, sourness, andsavoriness(often known by its Japanese nameumami,which translates to 'deliciousness').
As of the early 20th century, Western physiologists and psychologists believed that there were four basic tastes: sweetness, sourness, saltiness, and bitterness. The concept of a "savory" taste was not present in Western science at that time, but was postulated in Japanese research.[17]By the end of the 20th century, Western scholarship had begun to accept umami as a fifth basic taste.[citation needed]
One study found that salt and sour taste mechanisms both detect, in different ways, the presence ofsodium chloride(salt) in the mouth. Acids are also detected and perceived as sour.[18]The detection of salt is important to many organisms, but especially mammals, as it serves a critical role in ion and waterhomeostasisin the body. It is specifically needed in themammalian kidneyas an osmotically active compound that facilitates passive re-uptake of water into the blood.[citation needed]Because of this, salt elicits a pleasant taste in most humans.
Sour and salt tastes can be pleasant in small quantities, but in larger quantities become more and more unpleasant to taste. For sour taste, this presumably is because the sour taste can signal under-ripe fruit, rotten meat, and other spoiled foods, which can be dangerous to the body because of bacteria that grow in such media. Additionally, sour taste signalsacids,which can cause serious tissue damage.
Sweet taste signals the presence ofcarbohydratesin solution.[citation needed]Since carbohydrates have a very highcaloriecount (saccharides have many bonds, therefore much energy),[citation needed]they are desirable to the human body, which evolved to seek out the highest-calorie-intake foods.[citation needed]They are used as direct energy (sugars) and storage of energy (glycogen). Many non-carbohydrate molecules trigger a sweet response, leading to the development of many artificial sweeteners, includingsaccharin,sucralose,andaspartame.It is still unclear how these substances activate the sweet receptors and what adaptative significance this has had.
The savory taste (known in Japanese asumami), identified by Japanese chemistKikunae Ikeda,signals the presence of theamino acidL-glutamate.The amino acids in proteins are used in the body to build muscles and organs, and to transport molecules (hemoglobin),antibodies,and the organic catalysts known asenzymes.These are all critical molecules, and it is important to have a steady supply of amino acids; consequently, savory tastes trigger a pleasurable response, encouraging the intake ofpeptidesandproteins.
Pungency(piquancy or hotness) had traditionally been considered a sixth basic taste.[19]In 2015, researchers suggested a new basic taste offatty acidscalled "fat taste",[20]although "oleogustus" and "pinguis" have both been proposed as alternate terms.[21][22]
Sweetness
[edit]Sweetness, usually regarded as a pleasurable sensation, is produced by the presence ofsugarsand substances that mimic sugar. Sweetness may be connected toaldehydesandketones,which contain acarbonyl group.Sweetness is detected by a variety ofG protein coupled receptors(GPCR) coupled to theG proteingustducinfound on thetaste buds.At least two different variants of the "sweetness receptors" must be activated for the brain to register sweetness. Compounds the brain senses as sweet are compounds that can bind with varying bond strength to two different sweetness receptors. These receptors are T1R2+3 (heterodimer) and T1R3 (homodimer), which account for all sweet sensing in humans and animals.[23]
Taste detection thresholdsfor sweet substances are rated relative tosucrose,which has an index of 1.[24][25]The average human detection threshold for sucrose is 10 millimoles per liter. Forlactoseit is 30 millimoles per liter, with a sweetness index of 0.3,[24]and5-nitro-2-propoxyaniline0.002 millimoles per liter. "Natural" sweeteners such assaccharidesactivate the GPCR, which releasesgustducin.The gustducin then activates the moleculeadenylate cyclase,which catalyzes the production of the moleculecAMP,or adenosine 3', 5'-cyclic monophosphate. This molecule closes potassium ion channels, leading to depolarization and neurotransmitter release. Synthetic sweeteners such assaccharinactivate different GPCRs and induce taste receptor cell depolarization by an alternate pathway.
Sourness
[edit]Sourness is the taste that detectsacidity.The sourness of substances is rated relative to dilutehydrochloric acid,which has a sourness index of 1. By comparison,tartaric acidhas a sourness index of 0.7,citric acidan index of 0.46, andcarbonic acidan index of 0.06.[24][25]
Sour taste is detected by a small subset of cells that are distributed across all taste buds called Type III taste receptor cells. H+ ions (protons) that are abundant in sour substances can directly enter the Type III taste cells through a proton channel.[26]This channel was identified in 2018 asotopetrin 1 (OTOP1).[27]The transfer of positive charge into the cell can itself trigger an electrical response. Some weak acids such as acetic acid, can also penetrate taste cells; intracellular hydrogen ions inhibit potassium channels, which normally function to hyperpolarize the cell. By a combination of direct intake of hydrogen ions through OTOP1 ion channels (which itself depolarizes the cell) and the inhibition of the hyperpolarizing channel, sourness causes the taste cell to fire action potentials and release neurotransmitter.[28]
The most common foods with naturalsournessarefruits,such aslemon,lime,grape,orange,tamarind,and bittermelon.Fermented foods, such aswine,vinegaroryogurt,may have sour taste. Children show a greater enjoyment of sour flavors than adults,[29]andsour candycontaining citric acid ormalic acidis common.
Saltiness
[edit]Saltiness taste seems to have two components: a low-salt signal and a high-salt signal. The low-salt signal causes a sensation of deliciousness, while the high-salt signal typically causes the sensation of "too salty".[30]
The low-salt signal is understood to be caused by theepithelial sodium channel(ENaC), which is composed of three subunits. ENaC in the taste cells allow sodiumcationsto enter the cell. This on its own depolarizes the cell, and opensvoltage-dependent calcium channels,flooding the cell with positive calcium ions and leading toneurotransmitterrelease. ENaC can be blocked by the drugamiloridein many mammals, especially rats. The sensitivity of the low-salt taste to amiloride in humans is much less pronounced, leading to conjecture that there may be additional low-salt receptors besides ENaC to be discovered.[30]
A number of similar cations also trigger the low salt signal. The size oflithiumandpotassiumions most closely resemble those of sodium, and thus the saltiness is most similar. In contrast,rubidiumandcaesiumions are far larger, so their salty taste differs accordingly.[citation needed]The saltiness of substances is rated relative to sodium chloride (NaCl), which has an index of 1.[24][25]Potassium, aspotassium chloride(KCl), is the principal ingredient insalt substitutesand has a saltiness index of 0.6.[24][25]
Othermonovalentcations,e.g.ammonium(NH4+), anddivalentcations of thealkali earth metalgroup of theperiodic table,e.g. calcium (Ca2+), ions generally elicit a bitter rather than a salty taste even though they, too, can pass directly through ion channels in the tongue, generating anaction potential.But the chloride of calcium is saltier and less bitter than potassium chloride, and is commonly used in pickle brine instead of KCl.[citation needed]
The high-salt signal is still very poorly understood as of 2023. Even in rodents, this signal is not blocked by amiloride. Sour and bitter cells trigger on high chloride levels, but the specific receptor is still being identified.[30]
Bitterness
[edit]Bitterness is one of the most sensitive of the tastes, and many perceive it as unpleasant, sharp, or disagreeable, but it is sometimes desirable and intentionally added via variousbittering agents.Common bitter foods and beverages includecoffee,unsweetenedcocoa,South Americanmate,coca tea,bitter gourd,uncuredolives,citrus peel,some varieties ofcheese,many plants in the familyBrassicaceae,dandeliongreens,horehound,wildchicory,andescarole.The ethanol inalcoholic beveragestastes bitter,[31]as do the additional bitter ingredients found in some alcoholic beverages includinghopsinbeerandgentianinbitters.Quinineis also known for its bitter taste and is found intonic water.
Bitterness is of interest to those who studyevolution,as well as various health researchers[24][32]since a large number of natural bitter compounds are known to be toxic. The ability to detect bitter-tasting, toxic compounds at low thresholds is considered to provide an important protective function.[24][32][33]Plant leaves often contain toxic compounds, and amongleaf-eatingprimates there is a tendency to prefer immature leaves, which tend to be higher in protein and lower in fiber and poisons than mature leaves.[34]Amongst humans, variousfood processingtechniques are used worldwide to detoxify otherwise inedible foods and make them palatable.[35]Furthermore, the use of fire, changes in diet, and avoidance of toxins has led to neutral evolution in human bitter sensitivity. This has allowed several loss of function mutations that has led to a reduced sensory capacity towards bitterness in humans when compared to other species.[36]
The threshold for stimulation of bitter taste by quinine averages a concentration of 8 μM(8 micromolar).[24]The taste thresholds of other bitter substances are rated relative to quinine, which is thus given a reference index of 1.[24][25]For example,brucinehas an index of 11, is thus perceived as intensely more bitter than quinine, and is detected at a much lower solution threshold.[24]The most bitter natural substance isamarogentin,a compound present in the roots of the plantGentiana lutea,and the most bitter substance known is the synthetic chemicaldenatonium,which has an index of 1,000.[25]It is used as anaversive agent(abitterant) that is added to toxic substances to prevent accidental ingestion. It was discovered accidentally in 1958 during research on a local anesthetic byT. & H. SmithofEdinburgh,Scotland.[37][38]
Research has shown that TAS2Rs (taste receptors, type 2, also known as T2Rs) such asTAS2R38coupled to theG proteingustducinare responsible for the human ability to taste bitter substances.[39]They are identified not only by their ability to taste for certain "bitter"ligands,but also by the morphology of the receptor itself (surface bound, monomeric).[18]The TAS2R family in humans is thought to comprise about 25 different taste receptors, some of which can recognize a wide variety of bitter-tasting compounds.[40]Over 670 bitter-tasting compounds have been identified, on abitter database,of which over 200 have been assigned to one or more specific receptors.[41]It is speculated that the selective constraints on the TAS2R family have been weakened due to the relatively high rate of mutation and pseudogenization.[42]Researchers use two synthetic substances,phenylthiocarbamide(PTC) and6-n-propylthiouracil(PROP) to study thegeneticsof bitter perception. These two substances taste bitter to some people, but are virtually tasteless to others. Among the tasters, some are so-called "supertasters"to whom PTC and PROP are extremely bitter. The variation in sensitivity is determined by two common alleles at the TAS2R38 locus.[43]This genetic variation in the ability to taste a substance has been a source of great interest to those who study genetics.
Gustducin is made of three subunits. When it is activated by the GPCR, its subunits break apart and activatephosphodiesterase,a nearby enzyme, which in turn converts a precursor within the cell into a secondary messenger, which closes potassium ion channels.[citation needed]Also, this secondary messenger can stimulate theendoplasmic reticulumto release Ca2+ which contributes to depolarization. This leads to a build-up of potassium ions in the cell, depolarization, and neurotransmitter release. It is also possible for some bitter tastants to interact directly with the G protein, because of a structural similarity to the relevant GPCR.
Savoriness
[edit]Savoriness, or umami, is anappetitivetaste.[13][17]It can be tasted insoy sauce,meat,dashiandconsomme.Umami, aloanwordfromJapanesemeaning "good flavor" or "good taste",[44]umami(Chỉ vị)is considered fundamental to manyEast Asian cuisines,[45]such asJapanese cuisine.[46]It dates back to the use of fermentedfish sauce:garumin ancient Rome[47]andge-thcuporkoe-cheupin ancient China.[48]
Umami was first studied in 1907 byIkedaisolatingdashitaste, which he identified as the chemicalmonosodium glutamate(MSG).[17][49]MSG is a sodium salt that produces a strong savory taste, especially combined with foods rich innucleotidessuch as meats, fish, nuts, and mushrooms.[50]
Some savory taste buds respond specifically to glutamate in the same way that "sweet" ones respond to sugar. Glutamate binds to a variant ofG protein coupled glutamate receptors.[51][52]L-glutamate may bond to a type of GPCR known as a metabotropic glutamate receptor (mGluR4) which causes the G-protein complex to activate the sensation of umami.[52]
Perceptual independence from salty and sweet taste
[edit]There are doubts regarding whether umami is different from salty taste, as standalone glutamate(glutamic acid) without table salt ions(Na+), is perceived as sour, salt taste blockers reduce discrimination between monosodium glutamate and sucrose in rodents, since sweet and umami tastes share a taste receptor subunit; and part of the human population cannot tell apart umami from salty.[53]
If umami doesn't have perceptual independence, it could be classified with other tastes like fat, carbohydrate, metallic, and calcium, which can be perceived at high concentrations but may not offer a prominent taste experience.[54]
Measuring relative tastes
[edit]Measuring the degree to which a substance presents one basic taste can be achieved in a subjective way by comparing its taste to a reference substance.
Sweetness is subjectively measured by comparing the threshold values, or level at which the presence of a dilute substance can be detected by a human taster, of different sweet substances.[55]Substances are usually measured relative tosucrose,[56]which is usually given an arbitrary index of 1[57][58]or 100.[59]Rebaudioside Ais 100 times sweeter than sucrose;fructoseis about 1.4 times sweeter;glucose,a sugar found in honey and vegetables, is about three-quarters as sweet; andlactose,a milk sugar, is one-half as sweet.[b][55]
The sourness of a substance can be rated by comparing it to very dilutehydrochloric acid(HCl).[60]
Relative saltiness can be rated by comparison to a dilute salt solution.[61]
Quinine,a bitter medicinal found intonic water,can be used to subjectively rate the bitterness of a substance.[62]Units of dilute quinine hydrochloride (1 g in 2000 mL of water) can be used to measure the threshold bitterness concentration, the level at which the presence of a dilute bitter substance can be detected by a human taster, of other compounds.[62]More formal chemical analysis, while possible, is difficult.[62]
There may not be an absolute measure for pungency, though there are tests for measuring the subjective presence of a given pungent substance in food, such as theScoville scalefor capsaicine in peppers or thePyruvate scaleforpyruvatesin garlics and onions.
Functional structure
[edit]Taste is a form ofchemoreceptionwhich occurs in the specialisedtaste receptorsin the mouth. To date, there are five different types of taste these receptors can detect which are recognized: salt, sweet, sour, bitter, and umami. Each type of receptor has a different manner ofsensory transduction:that is, of detecting the presence of a certain compound and starting an action potential which alerts the brain. It is a matter of debate whether each taste cell is tuned to one specific tastant or to several; Smith and Margolskee claim that "gustatory neurons typically respond to more than one kind of stimulus, [a]lthough each neuron responds most strongly to one tastant". Researchers believe that the brain interprets complex tastes by examining patterns from a large set of neuron responses. This enables the body to make "keep or spit out" decisions when there is more than one tastant present. "No single neuron type alone is capable of discriminating among stimuli or different qualities, because a given cell can respond the same way to disparate stimuli."[63]As well,serotoninis thought to act as an intermediary hormone which communicates with taste cells within a taste bud, mediating the signals being sent to the brain. Receptor molecules are found on the top ofmicrovilliof the taste cells.
Sweetness
[edit]Sweetness is produced by the presence ofsugars,some proteins, and other substances such as alcohols likeanethol,glycerolandpropylene glycol,saponinssuch asglycyrrhizin,artificial sweeteners(organic compounds with a variety of structures), andleadcompounds such aslead acetate.[citation needed]It is often connected toaldehydesandketones,which contain acarbonyl group.[citation needed]Many foods can be perceived as sweet regardless of their actual sugar content. For example, some plants such asliquorice,aniseorsteviacan be used as sweeteners.Rebaudioside Ais asteviol glycosidecoming from stevia that is 200 times sweeter than sugar. Lead acetate and other lead compounds were used as sweeteners, mostly for wine, untillead poisoningbecame known. Romans used to deliberately boil the must inside of lead vessels to make a sweeter wine. Sweetness is detected by a variety ofG protein-coupled receptorscoupled to aG proteinthat acts as an intermediary in the communication between taste bud and brain,gustducin.[64]These receptors are T1R2+3 (heterodimer) and T1R3 (homodimer), which account for sweet sensing in humans and other animals.[65]
Saltiness
[edit]Saltiness is a taste produced best by the presence ofcations(such asNa+
,K+
orLi+
)[66]and is directly detected by cation influx into glial like cells via leak channels causing depolarisation of the cell.[66]
Othermonovalentcations, e.g.,ammonium,NH+
4,anddivalentcations of thealkali earth metalgroup of theperiodic table,e.g., calcium,Ca2+
,ions, in general, elicit a bitter rather than a salty taste even though they, too, can pass directly throughion channelsin the tongue.[citation needed]
Sourness
[edit]Sourness isacidity,[67][68]and, like salt, it is a taste sensed usingion channels.[66]Undissociated acid diffuses across the plasma membrane of a presynaptic cell, where it dissociates in accordance withLe Chatelier's principle.The protons that are released then block potassium channels, which depolarise the cell and cause calcium influx. In addition, the taste receptor PKD2L1 has been found to be involved in tasting sour.[69]
Bitterness
[edit]Research has shown that TAS2Rs (taste receptors, type 2, also known as T2Rs) such asTAS2R38are responsible for the ability to taste bitter substances in vertebrates.[70]They are identified not only by their ability to taste certain bitter ligands, but also by the morphology of the receptor itself (surface bound, monomeric).[71]
Savoriness
[edit]Theamino acidglutamic acidis responsible for savoriness,[72][73]but somenucleotides(inosinic acid[46][74]andguanylic acid[72]) can act as complements, enhancing the taste.[46][74]
Glutamic acid binds to a variant of the G protein-coupled receptor, producing asavorytaste.[51][52]
Further sensations and transmission
[edit]The tongue can also feel other sensations not generally included in the basic tastes. These are largely detected by thesomatosensorysystem. In humans, the sense of taste is conveyed via three of the twelve cranial nerves. Thefacial nerve(VII) carries taste sensations from the anterior two thirds of thetongue,theglossopharyngeal nerve(IX) carries taste sensations from the posterior one third of the tongue while a branch of thevagus nerve(X) carries some taste sensations from the back of the oral cavity.
Thetrigeminal nerve(cranial nerve V) provides information concerning the general texture of food as well as the taste-related sensations of peppery or hot (fromspices).
Pungency (also spiciness or hotness)
[edit]Substances such asethanolandcapsaicincause a burning sensation by inducing a trigeminal nerve reaction together with normal taste reception. The sensation of heat is caused by the food's activating nerves that expressTRPV1andTRPA1receptors. Some such plant-derived compounds that provide this sensation are capsaicin fromchili peppers,piperinefromblack pepper,gingerolfromginger rootandallyl isothiocyanatefromhorseradish.Thepiquant( "hot" or "spicy" ) sensation provided by such foods and spices plays an important role in a diverse range of cuisines across the world—especially in equatorial and sub-tropical climates, such asEthiopian,Peruvian,Hungarian,Indian,Korean,Indonesian,Lao,Malaysian,Mexican,New Mexican,Pakistani,Singaporean,Southwest Chinese(includingSichuan cuisine),Vietnamese,andThaicuisines.
This particular sensation, calledchemesthesis,is not a taste in the technical sense, because the sensation does not arise from taste buds, and a different set of nerve fibers carry it to the brain. Foods like chili peppers activate nerve fibers directly; the sensation interpreted as "hot" results from the stimulation of somatosensory (pain/temperature) fibers on the tongue. Many parts of the body with exposed membranes but no taste sensors (such as the nasal cavity, under the fingernails,surface of the eyeor a wound) produce a similar sensation of heat when exposed to hotness agents.
Coolness
[edit]Some substances activate coldtrigeminalreceptors even when not at low temperatures. This "fresh" or "minty" sensation can be tasted inpeppermintandspearmintand is triggered by substances such asmenthol,anethol,ethanol, andcamphor.Caused by activation of the same mechanism that signals cold,TRPM8ion channels onnerve cells,unlike the actual change in temperature described for sugar substitutes, this coolness is only a perceived phenomenon.
Numbness
[edit]Both Chinese andBatak Tobacooking include the idea of ma (máormati rasa), a tingling numbness caused by spices such asSichuan pepper.The cuisines ofSichuanprovince in China and of the Indonesian province ofNorth Sumatraoften combine this withchili pepperto produce a cay rátmálà,"numbing-and-hot", or "mati rasa" flavor.[75] Typical in northern Brazilian cuisine,jambuis an herb used in dishes liketacacá. These sensations, although not taste, fall into a category ofchemesthesis.
Astringency
[edit]Some foods, such as unripe fruits, containtanninsorcalcium oxalatethat cause an astringent or puckering sensation of the mucous membrane of the mouth. Examples includetea,red wine,orrhubarb.[citation needed]Other terms for the astringent sensation are "dry", "rough", "harsh" (especially for wine), "tart" (normally referring to sourness), "rubbery", "hard" or "styptic".[76]
Metallicness
[edit]A metallic taste may be caused by food and drink, certain medicines oramalgamdental fillings. It is generally considered an off flavor when present in food and drink. A metallic taste may be caused bygalvanicreactions in the mouth. In the case where it is caused by dental work, the dissimilar metals used may produce a measurable current.[77]Some artificial sweeteners are perceived to have a metallic taste, which is detected by theTRPV1receptors.[78]Many people considerbloodto have a metallic taste.[79][80]A metallic taste in the mouth is also a symptom of various medical conditions, in which case it may be classified under the symptomsdysgeusiaorparageusia,referring to distortions of the sense of taste,[81]and can be caused by medication, includingsaquinavir,[81]zonisamide,[82]and various kinds ofchemotherapy,[83]as well as occupational hazards, such as working withpesticides.[84]
Fat taste
[edit]Recent research reveals a potentialtaste receptorcalled theCD36 receptor.[85][86][87]CD36 was targeted as a possible lipid taste receptor because it binds tofatmolecules (more specifically, long-chainfatty acids),[88]and it has been localized totaste budcells (specifically, the circumvallate and foliatepapillae).[89]There is a debate over whether we can truly taste fats, and supporters of human ability to taste free fatty acids (FFAs) have based the argument on a few main points: there is an evolutionary advantage to oral fat detection; a potential fat receptor has been located on taste bud cells; fatty acids evoke specific responses that activategustatoryneurons, similar to other currently accepted tastes; and, there is a physiological response to the presence of oral fat.[90]Although CD36 has been studied primarily inmice,research examining human subjects' ability to taste fats found that those with high levels of CD36expressionwere more sensitive to tasting fat than were those with low levels of CD36 expression;[91]this study points to a clear association between CD36 receptor quantity and the ability to taste fat.
Other possible fat taste receptors have been identified.G protein-coupled receptorsfree fatty acid receptor 4(also termed GPR120) and to a much lesser extentFree fatty acid receptor 1(also termed GPR40)[92]have been linked to fat taste, because their absence resulted in reduced preference to two types of fatty acid (linoleic acidandoleic acid), as well as decreased neuronal response to oral fatty acids.[93]
Monovalent cation channelTRPM5has been implicated in fat taste as well,[94]but it is thought to be involved primarily in downstream processing of the taste rather than primary reception, as it is with other tastes such as bitter, sweet, and savory.[90]
Proposed alternate names to fat taste include oleogustus[95]and pinguis,[22]although these terms are not widely accepted. The main form of fat that is commonly ingested istriglycerides,which are composed of three fatty acids bound together. In this state, triglycerides are able to give fatty foods unique textures that are often described as creaminess. But this texture is not an actual taste. It is only during ingestion that the fatty acids that make up triglycerides are hydrolysed into fatty acids via lipases. The taste is commonly related to other, more negative, tastes such as bitter and sour due to how unpleasant the taste is for humans. Richard Mattes, a co-author of the study, explained that low concentrations of these fatty acids can create an overall better flavor in a food, much like how small uses of bitterness can make certain foods more rounded. A high concentration of fatty acids in certain foods is generally considered inedible.[96]To demonstrate that individuals can distinguish fat taste from other tastes, the researchers separated volunteers into groups and had them try samples that also contained the other basic tastes. Volunteers were able to separate the taste of fatty acids into their own category, with some overlap with savory samples, which the researchers hypothesized was due to poor familiarity with both. The researchers note that the usual "creaminess and viscosity we associate with fatty foods is largely due to triglycerides", unrelated to the taste; while the actual taste offatty acidsis not pleasant. Mattes described the taste as "more of a warning system" that a certain food should not be eaten.[97]
There are few regularly consumed foods rich in fat taste, due to the negative flavor that is evoked in large quantities. Foods whose flavor to which fat taste makes a small contribution include olive oil and fresh butter, along with various kinds of vegetable and nut oils.[98]
Heartiness
[edit]Kokumi(/koʊkuːmi/,Japanese:kokumi(コク vị)[99]fromkoku(こく)[99]) is translated as "heartiness", "full flavor" or "rich" and describes compounds in food that do not have their own taste, but enhance the characteristics when combined.
Alongside the five basic tastes of sweet, sour, salt, bitter and savory,kokumihas been described as something that may enhance the other five tastes by magnifying and lengthening the other tastes, or "mouthfulness".[100]: 290 [101]Garlic is a common ingredient to add flavor used to help define the characteristickokumiflavors.[101]
Calcium-sensing receptors (CaSR) are receptors forkokumisubstances which, applied around taste pores, induce an increase in the intracellular Ca concentration in a subset of cells.[100]This subset of CaSR-expressing taste cells are independent from the influenced basic taste receptor cells.[102]CaSR agonists directly activate the CaSR on the surface of taste cells and integrated in the brain via the central nervous system. A basal level of calcium, corresponding to the physiological concentration, is necessary for activation of the CaSR to develop thekokumisensation.[103]
Calcium
[edit]The distinctive taste of chalk has been identified as the calcium component of that substance.[104]In 2008, geneticists discovered acalcium receptoron the tongues ofmice.The CaSR receptor is commonly found in thegastrointestinal tract,kidneys,andbrain.Along with the "sweet" T1R3 receptor, the CaSR receptor can detect calcium as a taste. Whether the perception exists or not in humans is unknown.[105][106]
Temperature
[edit]Temperature can be an essential element of the taste experience. Heat can accentuate some flavors and decrease others by varying the density and phase equilibrium of a substance. Food and drink that—in a given culture—is traditionally served hot is often considered distasteful if cold, and vice versa. For example, alcoholic beverages, with a few exceptions, are usually thought best when served at room temperature or chilled to varying degrees, but soups—again, with exceptions—are usually only eaten hot. A cultural example aresoft drinks.In North America it is almost always preferred cold, regardless of season.
Starchiness
[edit]A 2016 study suggested that humans can tastestarch(specifically, aglucoseoligomer) independently of other tastes such as sweetness, without suggesting an associated chemical receptor.[107][108][109]
Nerve supply and neural connections
[edit]Theglossopharyngeal nerveinnervates a third of the tongue including the circumvallate papillae. Thefacial nerveinnervates the other two thirds of the tongue and thecheekvia thechorda tympani.[110]
Thepterygopalatine gangliaare ganglia (one on each side) of thesoft palate.Thegreater petrosal,lesser palatineandzygomatic nervesall synapse here. The greater petrosal carries soft palate taste signals to the facial nerve. The lesser palatine sends signals to thenasal cavity,which is why spicy foods cause nasal drip. The zygomatic sends signals to thelacrimal nervethat activate thelacrimal gland,which is the reason that spicy foods can cause tears. Both the lesser palatine and the zygomatic aremaxillary nerves(from thetrigeminal nerve).
Thespecial visceral afferentsof thevagus nervecarry taste from theepiglottalregion of the tongue.
The lingual nerve (trigeminal, not shown in diagram) is deeply interconnected with the chorda tympani in that it provides all other sensory info from the anterior ⅔ of the tongue.[111]This info is processed separately (nearby) in the rostral lateral subdivision of the nucleus of the solitary tract (NST).
The NST receives input from the amygdala (regulates oculomotor nuclei output),bed nuclei of stria terminalis,hypothalamus, and prefrontal cortex. The NST is the topographical map that processes gustatory and sensory (temp, texture, etc.) info.[112]
The reticular formation (includes Raphe nuclei responsible for serotonin production) is signaled to release serotonin during and after a meal to suppress appetite.[113]Similarly, salivary nuclei are signaled to decrease saliva secretion.
Hypoglossalandthalamicconnections aid in oral-related movements.
Hypothalamus connections hormonally regulate hunger and the digestive system.
Substantia innominataconnects the thalamus, temporal lobe, and insula.
Edinger-Westphal nucleusreacts to taste stimuli by dilating and constricting the pupils.[114]
Spinal ganglia are involved in movement.
Thefrontal operculumis speculated to be the memory and association hub for taste.[citation needed]
Theinsula cortexaids in swallowing and gastric motility.[115][116]
Taste in insects
[edit]Insects taste using small hair-like structures called taste sensilla, specialized sensory organs located on various body parts such as the mouthparts, legs, and wings. These sensilla contain gustatory receptor neurons (GRNs) sensitive to a wide range of chemical stimuli.
Insects respond to sugar, bitter, acid, and salt tastes. However, their taste spectrum extends to include water, fatty acids, metals, carbonation, RNA, ATP, and pheromones. Detecting these substances is vital for behaviors like feeding, mating, and oviposition.
Invertebrates' ability to taste these compounds is fundamental to their survival and provides insights into the evolution of sensory systems. This knowledge is crucial for understanding insect behavior and has applications in pest control and pollination biology.
Other concepts
[edit]Supertasters
[edit]A supertaster is a person whose sense of taste is significantly more sensitive than most. The cause of this heightened response is likely, at least in part, due to an increased number offungiform papillae.[117]Studies have shown that supertasters require less fat and sugar in their food to get the same satisfying effects. These people tend to consume more salt than others. This is due to their heightened sense of the taste of bitterness, and the presence of salt drowns out the taste of bitterness.[118]
Aftertaste
[edit]Aftertastes arise after food has been swallowed. An aftertaste can differ from the food it follows.Medicinesand tablets may also have a lingering aftertaste, as they can contain certain artificial flavor compounds, such asaspartame(artificial sweetener).
Acquired taste
[edit]An acquired taste often refers to an appreciation for a food or beverage that is unlikely to be enjoyed by a person who has not had substantial exposure to it, usually because of some unfamiliar aspect of the food or beverage, including bitterness, a strong or strange odor, taste, or appearance.
Clinical significance
[edit]Patients withAddison's disease,pituitary insufficiency, orcystic fibrosissometimes have a hyper-sensitivity to the five primary tastes.[119]
Disorders of taste
[edit]- ageusia(complete loss of taste)
- hypogeusia(reduced sense of taste)
- dysgeusia(distortion in sense of taste)
- hypergeusia(abnormally heightened sense of taste)
Viruses can also cause loss of taste. About 50% of patients withSARS-CoV-2(causing COVID-19) experience some type ofdisorder associated with their sense of smell or taste,includingageusiaanddysgeusia.SARS-CoV-1,MERS-CoVand even the flu (influenza virus) can also disrupt olfaction.[120][121]
History
[edit]Inthe West,Aristotlepostulated inc. 350BC[122]that the two most basic tastes were sweet and bitter.[123]He was one of the first persons to develop a list of basic tastes.[124]
Research
[edit]Thereceptorsfor the basic tastes of bitter, sweet and savory have been identified. They areG protein-coupled receptors.[125]The cells that detect sourness have been identified as a subpopulation that express the proteinPKD2L1,and The responses are mediated by an influx of protons into the cells.[125]As of 2019, molecular mechanisms for each taste appear to be different, although all taste perception relies on activation ofP2X purinoreceptorsonsensory nerves.[126]
See also
[edit]Notes
[edit]On the basis of physiologic studies, there are generally believed to be at least fourprimarysensations of taste:sour,salty,sweet,andbitter.Yet we know that a person can perceive literally hundreds of different tastes. These are all supposed to be combinations of the four primary sensations...However, there might be other less conspicuous classes or subclasses of primary sensations ",[127]
b.^Some variation in values is not uncommon between various studies. Such variations may arise from a range of methodological variables, from sampling to analysis and interpretation. In fact there is a "plethora of methods"[128]Indeed, the taste index of 1, assigned to reference substances such as sucrose (for sweetness), hydrochloric acid (for sourness), quinine (for bitterness), and sodium chloride (for saltiness), is itself arbitrary for practical purposes.[60]
Some values, such as those for maltose and glucose, vary little. Others, such as aspartame and sodium saccharin, have much larger variation. Regardless of variation, the perceived intensity of substances relative to each reference substance remains consistent for taste ranking purposes. The indices table for McLaughlin & Margolskee (1994) for example,[24][25]is essentially the same as that of Svrivastava & Rastogi (2003),[129]Guyton & Hall (2006),[60]and Joestenet al.(2007).[57]The rankings are all the same, with any differences, where they exist, being in the values assigned from the studies from which they derive.
As for the assignment of 1 or 100 to the index substances, this makes no difference to the rankings themselves, only to whether the values are displayed as whole numbers or decimal points. Glucose remains about three-quarters as sweet as sucrose whether displayed as 75 or 0.75.
References
[edit]- ^abcdTrivedi, Bijal P. (2012)."Gustatory system: The finer points of taste".Nature.486(7403): S2–S3.Bibcode:2012Natur.486S...2T.doi:10.1038/486s2a.ISSN0028-0836.PMID22717400.S2CID4325945.
- ^abcWitt, Martin (2019). "Anatomy and development of the human taste system".Smell and Taste.Handbook of Clinical Neurology. Vol. 164. pp. 147–171.doi:10.1016/b978-0-444-63855-7.00010-1.ISBN978-0-444-63855-7.ISSN0072-9752.PMID31604544.S2CID204332286.
- ^Human biology (Page 201/464)Archived26 March 2023 at theWayback MachineDaniel D. Chiras. Jones & Bartlett Learning, 2005.
- ^abSchacter, Daniel (2009).Psychology Second Edition.United States of America: Worth Publishers. p.169.ISBN978-1-4292-3719-2.
- ^abBoron, W.F., E.L. Boulpaep. 2003. Medical Physiology. 1st ed. Elsevier Science USA.
- ^Kean, Sam (Fall 2015)."The science of satisfaction".Distillations Magazine.1(3): 5.Archivedfrom the original on 17 November 2019.Retrieved20 March2018.
- ^"How does our sense of taste work?".PubMed.6 January 2012.Archivedfrom the original on 9 March 2015.Retrieved5 April2016.
- ^Human Physiology: An integrated approach 5th Edition -Silverthorn, Chapter-10, Page-354
- ^Turner, Heather N.; Liman, Emily R. (10 February 2022)."The Cellular and Molecular Basis of Sour Taste".Annual Review of Physiology.84(1): 41–58.doi:10.1146/annurev-physiol-060121-041637.ISSN0066-4278.PMC10191257.PMID34752707.S2CID243940546.
- ^Smell – The Nose KnowsArchived13 September 2017 at theWayback Machinewashington.edu, Eric H. Chudler.
- ^
- Food texture: measurement and perception (page 36/311)Andrew J. Rosenthal. Springer, 1999.
- Food texture: measurement and perception (page 3/311)Andrew J. Rosenthal. Springer, 1999.
- ^Food texture: measurement and perception (page 4/311)Archived26 March 2023 at theWayback MachineAndrew J. Rosenthal. Springer, 1999.
- ^abWhy do two great tastes sometimes not taste great together?Archived28 November 2011 at theWayback Machinescientificamerican. Dr. Tim Jacob, Cardiff University. 22 May 2009.
- ^Miller, Greg (2 September 2011). "Sweet here, salty there: Evidence of a taste map in the mammilian brain".Science.333(6047): 1213.Bibcode:2011Sci...333.1213M.doi:10.1126/science.333.6047.1213.PMID21885750.
- ^Henry M Seidel; Jane W Ball; Joyce E Dains (1 February 2010).Mosby's Guide to Physical Examination.Elsevier Health Sciences. p. 303.ISBN978-0-323-07357-8.
- ^Scully, Simone M. (9 June 2014)."The Animals That Taste Only Saltiness".Nautilus.Archived fromthe originalon 14 June 2014.Retrieved8 August2014.
- ^abcIkeda, Kikunae (2002) [1909]."New Seasonings".Chemical Senses.27(9): 847–849.doi:10.1093/chemse/27.9.847.PMID12438213.;a partial translation fromIkeda, Kikunae (1909)."New Seasonings".Journal of the Chemical Society of Tokyo(in Japanese).30(8): 820–836.doi:10.1246/nikkashi1880.30.820.PMID12438213.
- ^abLindemann, Bernd (13 September 2001). "Receptors and transduction in taste".Nature.413(6852): 219–225.Bibcode:2001Natur.413..219L.doi:10.1038/35093032.PMID11557991.S2CID4385513.
- ^Ayurvedic balancing: an integration of Western fitness with Eastern wellness (Pages 25-26/188)Joyce Bueker. Llewellyn Worldwide, 2002.
- ^Keast, Russell SJ; Costanzo, Andrew (3 February 2015)."Is fat the sixth taste primary? Evidence and implications".Flavour.4:5.doi:10.1186/2044-7248-4-5.hdl:10536/DRO/DU:30069796.ISSN2044-7248.
- ^Running, Cordelia A.; Craig, Bruce A.; Mattes, Richard D. (1 September 2015)."Oleogustus: The Unique Taste of Fat".Chemical Senses.40(7): 507–516.doi:10.1093/chemse/bjv036.ISSN0379-864X.PMID26142421.
- ^abReed, Danielle R.; Xia, Mary B. (1 May 2015)."Recent Advances in Fatty Acid Perception and Genetics".Advances in Nutrition.6(3): 353S–360S.doi:10.3945/an.114.007005.ISSN2156-5376.PMC4424773.PMID25979508.
- ^Zhao, Grace Q.; Yifeng Zhang; Mark A. Hoon; Jayaram Chandrashekar; Isolde Erlenbach; Nicholas J.P. Ryba; Charles S. Zuker (October 2003)."The Receptors for Mammalian Sweet and Savory taste".Cell.115(3): 255–266.doi:10.1016/S0092-8674(03)00844-4.PMID14636554.S2CID11773362.
- ^abcdefghijkGuyton, Arthur C. (1991)Textbook of Medical Physiology.(8th ed). Philadelphia: W.B. Saunders
- ^abcdefgMcLaughlin, Susan; Margolskee, Rorbert F. (November–December 1994). "The Sense of Taste".American Scientist.82(6): 538–545.
- ^Rui Chang, Hang Waters & Emily Liman (2010)."A proton current drives action potentials in genetically identified sour taste cells".Proc Natl Acad Sci U S A.107(51): 22320–22325.Bibcode:2010PNAS..10722320C.doi:10.1073/pnas.1013664107.PMC3009759.PMID21098668.
- ^Tu, YH (2018)."An evolutionarily conserved gene family encodes proton-selective ion channels".Science.359(6379): 1047–1050.Bibcode:2018Sci...359.1047T.doi:10.1126/science.aao3264.PMC5845439.PMID29371428.
- ^Ye W, Chang RB, Bushman JD, Tu YH, Mulhall EM, Wilson CE, Cooper AJ, Chick WS, Hill-Eubanks DC, Nelson MT, Kinnamon SC, Liman ER (2016)."The K+ channel KIR2.1 functions in tandem with proton influx to mediate sour taste transduction".Proc Natl Acad Sci U S A.113(2): E229–238.Bibcode:2016PNAS..113E.229Y.doi:10.1073/pnas.1514282112.PMC4720319.PMID26627720.
- ^Djin Gie Liem & Julie A. Mennella (February 2003)."Heightened Sour Preferences During Childhood".Chem Senses.28(2): 173–180.doi:10.1093/chemse/28.2.173.PMC2789429.PMID12588738.
- ^abcTaruno, Akiyuki; Gordon, Michael D. (10 February 2023)."Molecular and Cellular Mechanisms of Salt Taste".Annual Review of Physiology.85(1): 25–45.doi:10.1146/annurev-physiol-031522-075853.PMID36332657.
Elahi, Tasnuva (15 September 2023)."Salt Taste Is Surprisingly Mysterious".Nautilus. - ^Scinska A, Koros E, Habrat B, Kukwa A, Kostowski W, Bienkowski P (August 2000). "Bitter and sweet components of ethanol taste in humans".Drug and Alcohol Dependence.60(2): 199–206.doi:10.1016/S0376-8716(99)00149-0.PMID10940547.
- ^abLogue, Alexandra W. (1986).The Psychology of Eating and Drinking.New York: W.H. Freeman & Co.ISBN978-0-415-81708-0.[page needed]
- ^Glendinning, J. I. (1994). "Is the bitter rejection response always adaptive?".Physiol Behav.56(6): 1217–1227.doi:10.1016/0031-9384(94)90369-7.PMID7878094.S2CID22945002.
- ^Jones, S., Martin, R., & Pilbeam, D. (1994)The Cambridge Encyclopedia of Human Evolution.Cambridge: Cambridge University Press[page needed]
- ^Johns, T. (1990).With Bitter Herbs They Shall Eat It: Chemical ecology and the origins of human diet and medicine.Tucson: University of Arizona Press[page needed]
- ^Wang, X. (2004)."Relaxation Of Selective Constraint And Loss Of Function In The Evolution Of Human Bitter Taste Receptor Genes".Human Molecular Genetics.13(21): 2671–2678.doi:10.1093/hmg/ddh289.PMID15367488.
- ^"What is Bitrex?".Bitrex – Keeping children safe.21 December 2015.Archivedfrom the original on 20 May 2020.Retrieved20 May2020.
- ^"Denatonium Benzoate".Encyclopedia.Retrieved30 August2024.
- ^Maehashi, K.; Matano, M.; Wang, H.; Vo, L. A.; Yamamoto, Y.; Huang, L. (2008)."Bitter peptides activate hTAS2Rs, the human bitter receptors".Biochem Biophys Res Commun.365(4): 851–855.doi:10.1016/j.bbrc.2007.11.070.PMC2692459.PMID18037373.
- ^Meyerhof (2010)."The molecular receptive ranges of human TAS2R bitter taste receptors".Chem Senses.35(2): 157–70.doi:10.1093/chemse/bjp092.PMID20022913.
- ^Wiener (2012)."BitterDB: a database of bitter compounds".Nucleic Acids Res.40(Database issue): D413–9.doi:10.1093/nar/gkr755.PMC3245057.PMID21940398.
- ^Wang, X.; Thomas, S. D.; Zhang, J. (2004)."Relaxation of selective constraint and loss of function in the evolution of human bitter taste receptor genes".Hum Mol Genet.13(21): 2671–2678.doi:10.1093/hmg/ddh289.PMID15367488.
- ^Wooding, S.; Kim, U. K.; Bamshad, M. J.; Larsen, J.; Jorde, L. B.; Drayna, D. (2004)."Natural selection and molecular evolution in PTC, a bitter-taste receptor gene".Am J Hum Genet.74(4): 637–646.doi:10.1086/383092.PMC1181941.PMID14997422.
- ^Chỉ vị definition in EnglishArchived8 August 2011 at theWayback MachineDenshi Jisho—Online Japanese dictionary
- ^"Umami Taste Components and Their Sources in Asian Foods".researchgate.net.2015.
- ^abc"Essiential Ingredients of Japanese Food – Umami".Taste of Japan.Ministry of Agriculture, Forestry and Fisheries (Japan).Archivedfrom the original on 16 May 2021.Retrieved20 April2022.
- ^Prichep, Deena (26 October 2013)."Fish sauce: An ancient Roman condiment rises again".US National Public Radio.Archivedfrom the original on 16 June 2018.Retrieved5 April2018.
- ^Butler, Stephanie (20 July 2012)."The Surprisingly Ancient History of Ketchup".HISTORY.Archivedfrom the original on 19 April 2022.Retrieved19 April2022.
- ^Nelson G, Chandrashekar J, Hoon MA, et al. (March 2002). "An amino-acid taste receptor".Nature.416(6877): 199–202.Bibcode:2002Natur.416..199N.doi:10.1038/nature726.PMID11894099.S2CID1730089.
- ^O'Connor, Anahad (10 November 2008)."The Claim: The tongue is mapped into four areas of taste".The New York Times.Archivedfrom the original on 16 December 2017.Retrieved13 September2010.
- ^abLindemann, B (February 2000). "A taste for umami".Nature Neuroscience.3(2): 99–100.doi:10.1038/72153.PMID10649560.S2CID10885181.
- ^abcChaudhari N, Landin AM, Roper SD (February 2000). "A metabotropic glutamate receptor variant functions as a taste receptor".Nature Neuroscience.3(2): 113–9.doi:10.1038/72053.PMID10649565.S2CID16650588.
- ^Hartley, Isabella E; Liem, Djin Gie; Keast, Russell (16 January 2019)."Umami as an 'Alimentary' Taste. A New Perspective on Taste Classification".Nutrients.11(1): 182.doi:10.3390/nu11010182.ISSN2072-6643.PMC6356469.PMID30654496.
- ^Hartley, Isabella E; Liem, Djin Gie; Keast, Russell (16 January 2019)."Umami as an 'Alimentary' Taste. A New Perspective on Taste Classification".Nutrients.11(1): 182.doi:10.3390/nu11010182.ISSN2072-6643.PMC6356469.PMID30654496.
- ^abTsai, Michelle (14 May 2007),"How Sweet It Is? Measuring the intensity of sugar substitutes",Slate,The Washington Post Company,archivedfrom the original on 13 August 2010,retrieved14 September2010
- ^Walters, D. Eric (13 May 2008),"How is Sweetness Measured?",All About Sweeteners,archivedfrom the original on 24 December 2010,retrieved15 September2010
- ^abJoesten, Melvin D; Hogg, John L; Castellion, Mary E (2007),"Sweeteness Relative to Sucrose (table)",The World of Chemistry: Essentials(4th ed.), Belmont, California: Thomson Brooks/Cole, p. 359,ISBN978-0-495-01213-9,retrieved14 September2010
- ^Coultate, Tom P (2009),"Sweetness relative to sucrose as an arbitrary standard",Food: The Chemistry of its Components(5th ed.), Cambridge, UK:Royal Society of Chemistry,pp. 268–269,ISBN978-0-85404-111-4,retrieved15 September2010
- ^Mehta, Bhupinder & Mehta, Manju (2005),"Sweetness of sugars",Organic Chemistry,India: Prentice-Hall, p. 956,ISBN978-81-203-2441-1,retrieved15 September2010
- ^abcGuyton, Arthur C;Hall, John E. (2006),Guyton and Hall Textbook of Medical Physiology(11th ed.), Philadelphia: Elsevier Saunders, p. 664,ISBN978-0-7216-0240-0
- ^Food Chemistry (Page 38/1070)H. D. Belitz, Werner Grosch, Peter Schieberle. Springer, 2009.
- ^abcQuality control methods for medicinal plant materials, Pg. 38World Health Organization, 1998.
- ^David V. Smith, Robert F. Margolskee:Making Sense of TasteArchived29 October 2020 at theWayback Machine(Scientific American, September 1, 2006)
- ^How the Taste Bud Translates Between Tongue and BrainArchived5 March 2017 at theWayback Machinenytimes, 4 August 1992.
- ^Zhao GQ, Zhang Y, Hoon MA, et al. (October 2003)."The receptors for mammalian sweet and umami taste".Cell.115(3): 255–66.doi:10.1016/S0092-8674(03)00844-4.PMID14636554.S2CID11773362.
- ^abcchannels in sensory cells (Page 155/304)Stephan Frings, Jonathan Bradley. Wiley-VCH, 2004.
- ^outlines of chemistry with practical work (Page 241)Henry John Horstman Fenton. CUP Archive.
- ^Focus Ace Pmr 2009 Science (Page 242/522)Chang See Leong, Chong Kum Ying, Choo Yan Tong & Low Swee Neo. Focus Ace Pmr 2009 Science.
- ^"Biologists Discover How We Detect Sour Taste",Science Daily,24 August 2006,archivedfrom the original on 30 October 2009,retrieved12 September2010
- ^Maehashi K, Matano M, Wang H, Vo LA, Yamamoto Y, Huang L (January 2008)."Bitter peptides activate hTAS2Rs, the human bitter receptors".Biochemical and Biophysical Research Communications.365(4): 851–5.doi:10.1016/j.bbrc.2007.11.070.PMC2692459.PMID18037373.
- ^Lindemann, B (September 2001). "Receptors and transduction in taste".Nature.413(6852): 219–25.Bibcode:2001Natur.413..219L.doi:10.1038/35093032.PMID11557991.S2CID4385513.
- ^abWhat Is Umami?: What Exactly is Umami?Archived23 April 2011 at theWayback MachineUmami Information Center
- ^Chandrashekar, Jayaram; Hoon, Mark A; Ryba, Nicholas J. P. & Zuker, Charles S (16 November 2006),"The receptors and cells for mammalian taste"(PDF),Nature,444(7117): 288–294,Bibcode:2006Natur.444..288C,doi:10.1038/nature05401,PMID17108952,S2CID4431221,archived fromthe original(PDF)on 22 July 2011,retrieved13 September2010
- ^abWhat Is Umami?: The Composition of UmamiArchived27 May 2009 at theWayback MachineUmami Information Center
- ^Katzer, Gernot."Spice Pages: Sichuan Pepper (Zanthoxylum, Szechwan peppercorn, fagara, hua jiao, sansho sơn ớt, timur, andaliman, tirphal)".gernot-katzers-spice-pages.Archivedfrom the original on 19 November 2012.Retrieved16 May2013.
- ^Peleg, Hanna; Gacon, Karine; Schlich, Pascal; Noble, Ann C (June 1999). "Bitterness and astringency of flavan-3-ol monomers, dimers and trimers".Journal of the Science of Food and Agriculture.79(8): 1123–1128.doi:10.1002/(SICI)1097-0010(199906)79:8<1123::AID-JSFA336>3.0.CO;2-D.
- ^"Could your mouth charge your iPhone?".kcdentalworks. 24 April 2019.Archivedfrom the original on 3 May 2019.Retrieved3 May2019.
- ^Riera, Céline E.; Vogel, Horst; Simon, Sidney A.; le Coutre, Johannes (2007). "Artificial sweeteners and salts producing a metallic taste sensation activate TRPV1 receptors".American Journal of Physiology.293(2): R626–R634.doi:10.1152/ajpregu.00286.2007.PMID17567713.
- ^Willard, James P. (1905)."Current Events".Progress: A Monthly Journal Devoted to Medicine and Surgery.4:861–68.
- ^Monosson, Emily (2012).Evolution in a Toxic World: How Life Responds to Chemical Threats.Island Press. p. 49.ISBN9781597269766.
- ^abGoldstein, E. Bruce (2010).Encyclopedia of Perception.Vol. 2. SAGE. pp. 958–59.ISBN9781412940818.
- ^Levy, René H. (2002).Antiepileptic Drugs.Lippincott Williams & Wilkins. p. 875.ISBN9780781723213.
- ^Reith, Alastair J. M.; Spence, Charles (2020)."The mystery of" metal mouth "in chemotherapy".Chemical Senses.45(2): 73–84.doi:10.1093/chemse/bjz076.PMID32211901.Archivedfrom the original on 14 April 2021.Retrieved15 October2020.
- ^Stellman, Jeanne Mager (1998).Encyclopaedia of Occupational Health and Safety: The body, health care, management and policy, tools and approaches.International Labour Organization. p. 299.ISBN9789221098140.
- ^Biello, David."Potential Taste Receptor for Fat Identified".Scientific American.Archivedfrom the original on 9 December 2014.Retrieved20 January2015.
- ^Laugerette, F; Passilly-Degrace, P; Patris, B; Niot, I; Febbraio, M; Montmayeur, J. P.; Besnard, P (2005)."CD36 involvement in orosensory detection of dietary lipids, spontaneous fat preference, and digestive secretions".Journal of Clinical Investigation.115(11): 3177–84.doi:10.1172/JCI25299.PMC1265871.PMID16276419.
- ^Dipatrizio, N. V. (2014)."Is fat taste ready for primetime?".Physiology & Behavior.136C:145–154.doi:10.1016/j.physbeh.2014.03.002.PMC4162865.PMID24631296.
- ^Baillie, A. G.; Coburn, C. T.; Abumrad, N. A. (1996). "Reversible binding of long-chain fatty acids to purified FAT, the adipose CD36 homolog".The Journal of Membrane Biology.153(1): 75–81.doi:10.1007/s002329900111.PMID8694909.S2CID5911289.
- ^Simons, P. J.; Kummer, J. A.; Luiken, J. J.; Boon, L (2011). "Apical CD36 immunolocalization in human and porcine taste buds from circumvallate and foliate papillae".Acta Histochemica.113(8): 839–43.doi:10.1016/j.acthis.2010.08.006.PMID20950842.
- ^abMattes, R. D. (2011)."Accumulating evidence supports a taste component for free fatty acids in humans".Physiology & Behavior.104(4): 624–31.doi:10.1016/j.physbeh.2011.05.002.PMC3139746.PMID21557960.
- ^Pepino, M. Y.; Love-Gregory, L; Klein, S; Abumrad, N. A. (2012)."The fatty acid translocase gene CD36 and lingual lipase influence oral sensitivity to fat in obese subjects".The Journal of Lipid Research.53(3): 561–6.doi:10.1194/jlr.M021873.PMC3276480.PMID22210925.
- ^Kimura I, Ichimura A, Ohue-Kitano R, Igarashi M (January 2020)."Free Fatty Acid Receptors in Health and Disease".Physiological Reviews.100(1): 171–210.doi:10.1152/physrev.00041.2018.PMID31487233.
- ^Cartoni, C; Yasumatsu, K; Ohkuri, T; Shigemura, N; Yoshida, R; Godinot, N; Le Coutre, J; Ninomiya, Y; Damak, S (2010)."Taste preference for fatty acids is mediated by GPR40 and GPR120".Journal of Neuroscience.30(25): 8376–82.doi:10.1523/JNEUROSCI.0496-10.2010.PMC6634626.PMID20573884.
- ^Liu, P; Shah, B. P.; Croasdell, S; Gilbertson, T. A. (2011)."Transient receptor potential channel type M5 is essential for fat taste".Journal of Neuroscience.31(23): 8634–42.doi:10.1523/JNEUROSCI.6273-10.2011.PMC3125678.PMID21653867.
- ^Running, Cordelia A.; Craig, Bruce A.; Mattes, Richard D. (3 July 2015)."Oleogustus: The Unique Taste of Fat".Chemical Senses.40(6): 507–516.doi:10.1093/chemse/bjv036.PMID26142421.
- ^Neubert, Amy Patterson (23 July 2015)."Research confirms fat is sixth taste; names it oleogustus".Purdue News.Purdue University.Archivedfrom the original on 8 August 2015.Retrieved4 August2015.
- ^Keast, Russell (3 February 2015). "Is fat the sixth taste primary? Evidence and implications".Flavour.Vol. 4.doi:10.1186/2044-7248-4-5.
- ^Feldhausen, Teresa Shipley (31 July 2015)."The five basic tastes have sixth sibling: oleogustus".Science News.Archivedfrom the original on 16 August 2015.Retrieved4 August2015.
- ^abNishimura, Toshihide; Egusa, Ai (20 January 2016).""Koku" Involved in Food Palatability: An Overview of Pioneering Work and Outstanding Questions "Thực べ vật の “こく” を khoa học するそ の hiện trạng と triển vọng.Kagaku to Seibutsu(in Japanese). Vol. 2, no. 54. Japan Society for Bioscience, Biotechnology, and Agrochemistry (JSBBA). pp. 102–108.doi:10.1271/kagakutoseibutsu.54.102.Retrieved11 August2020.
“こく” appears in abstract. “コク vị vật chất” appears in p106 1.b
- ^abHettiarachchy, Navam S.; Sato, Kenji; Marshall, Maurice R., eds. (2010).Food proteins and peptides: chemistry, functionality interactions, and commercialization.Boca Raton, Fla.: CRC.ISBN9781420093414.Retrieved26 June2014.
- ^abUeda, Yoichi; Sakaguchi, Makoto; Hirayama, Kazuo; Miyajima, Ryuichi; Kimizuka, Akimitsu (1990). "Characteristic Flavor Constituents in Water Extract of Garlic".Agricultural and Biological Chemistry.54(1): 163–169.doi:10.1080/00021369.1990.10869909.
- ^Eto, Yuzuru; Kuroda, Motonaka; Yasuda, Reiko; Maruyama, Yutaka (12 April 2012)."Kokumi Substances, Enhancers of Basic Tastes, Induce Responses in Calcium-Sensing Receptor Expressing Taste Cells".PLOS ONE.7(4): e34489.Bibcode:2012PLoSO...734489M.doi:10.1371/journal.pone.0034489.ISSN1932-6203.PMC3325276.PMID22511946.
- ^Eto, Yuzuru; Miyamura, Naohiro; Maruyama, Yutaka; Hatanaka, Toshihiro; Takeshita, Sen; Yamanaka, Tomohiko; Nagasaki, Hiroaki; Amino, Yusuke; Ohsu, Takeaki (8 January 2010)."Involvement of the Calcium-sensing Receptor in Human Taste Perception".Journal of Biological Chemistry.285(2): 1016–1022.doi:10.1074/jbc.M109.029165.ISSN0021-9258.PMC2801228.PMID19892707.
- ^"Like the Taste of Chalk? You're in Luck—Humans May Be Able to Taste Calcium".Scientific American. 20 August 2008.Archivedfrom the original on 28 March 2014.Retrieved14 March2014.
- ^Tordorf, Michael G.(2008),"Chemosensation of Calcium",American Chemical Society National Meeting, Fall 2008, 236th,Philadelphia, PA: American Chemical Society, AGFD 207,archivedfrom the original on 25 August 2009,retrieved27 August2008
- ^"That Tastes... Sweet? Sour? No, It's Definitely Calcium!",Science Daily,21 August 2008,archivedfrom the original on 18 October 2009,retrieved14 September2010
- ^Lapis, Trina J.; Penner, Michael H.; Lim, Juyun (23 August 2016)."Humans Can Taste Glucose Oligomers Independent of the hT1R2/hT1R3 Sweet Taste Receptor"(PDF).Chemical Senses.41(9): 755–762.doi:10.1093/chemse/bjw088.ISSN0379-864X.PMID27553043.Archived(PDF)from the original on 26 September 2017.Retrieved26 September2017.
- ^Pullicin, Alexa J.; Penner, Michael H.; Lim, Juyun (29 August 2017)."Human taste detection of glucose oligomers with low degree of polymerization".PLOS ONE.12(8): e0183008.Bibcode:2017PLoSO..1283008P.doi:10.1371/journal.pone.0183008.ISSN1932-6203.PMC5574539.PMID28850567.
- ^Hamzelou, Jessica (2 September 2016)."There is now a sixth taste – and it explains why we love carbs".New Scientist.Archivedfrom the original on 16 September 2016.Retrieved14 September2016.
- ^Eliav, Eli, and Batya Kamran. "Evidence of Chorda Tympani Dysfunction in Patients with Burning Mouth Syndrome."Science Direct.May 2007. Web. 27 March 2016.
- ^Mu, Liancai, and Ira Sanders. "Human Tongue Neuroanatomy: Nerve Supply and Motor Endplates." Wiley Online Library. Oct. 2010. Web. 27 March 2016.
- ^King, Camillae T., and Susan P. Travers. "Glossopharyngeal Nerve Transection Eliminates Quinine-Stimulated Fos-Like Immunoreactivity in the Nucleus of the Solitary Tract: Implications for a Functional Topography of Gustatory Nerve Input in Rats." JNeurosci. 15 April 1999. Web. 27 March 2016.
- ^Hornung, Jean-Pierre. "The Human Raphe Nuclei and the Serotonergic System." Science Direct. Dec. 2003. Web. 27 March 2016.
- ^Reiner, Anton, and Harvey J. Karten. "Parasympathetic Ocular Control — Functional Subdivisions and Circuitry of the Avian Nucleus of Edinger-Westphal." Science Direct. 1983. Web. 27 March 2016.
- ^Wright, Christopher I., and Brain Martis. "Novelty Responses and Differential Effects of Order in the Amygdala, Substantia Innominata, and Inferior Temporal Cortex." Science Direct. Mar. 2003. Web. 27 March 2016.
- ^Menon, Vinod, and Lucina Q. Uddin. "Saliency, Switching, Attention and Control: A Network Model of Insula." Springer. 29 May 2010. Web. 28 March 2016.
- ^Bartoshuk L. M.; Duffy V. B.; et al. (1994)."PTC/PROP tasting: anatomy, psychophysics, and sex effects." 1994 ".Physiol Behav.56(6): 1165–71.doi:10.1016/0031-9384(94)90361-1.PMID7878086.S2CID40598794.
- ^Gardner, Amanda (16 June 2010)."Love salt? You might be a 'supertaster'".CNN Health.Archivedfrom the original on 9 April 2012.Retrieved9 April2012.
- ^Walker, H. Kenneth (1990)."Cranial Nerve VII: The Facial Nerve and Taste".Clinical Methods: The History, Physical, and Laboratory Examinations.Butterworths.ISBN9780409900774.Archivedfrom the original on 26 January 2016.Retrieved1 May2014.
- ^Meunier, Nicolas; Briand, Loïc; Jacquin-Piques, Agnès; Brondel, Laurent; Pénicaud, Luc (2020)."COVID 19-Induced Smell and Taste Impairments: Putative Impact on Physiology".Frontiers in Physiology.11:625110.doi:10.3389/fphys.2020.625110.ISSN1664-042X.PMC7870487.PMID33574768.
- ^Veronese, Sheila; Sbarbati, Andrea (3 March 2021)."Chemosensory Systems in COVID-19: Evolution of Scientific Research".ACS Chemical Neuroscience.12(5): 813–824.doi:10.1021/acschemneuro.0c00788.ISSN1948-7193.PMC7885804.PMID33559466.
- ^On the SoulArchived6 January 2011 at theWayback MachineAristotle. Translated by J. A. Smith. The Internet Classics Archive.
- ^Aristotle's De anima (422b10-16)Archived26 March 2023 at theWayback MachineRonald M. Polansky. Cambridge University Press, 2007.
- ^Origins of neuroscience: a history of explorations into brain function (Page 165/480)Archived26 March 2023 at theWayback MachineStanley Finger. Oxford University Press US, 2001.
- ^abBachmanov, AA.; Beauchamp, GK. (2007)."Taste receptor genes".Annu Rev Nutr.27(1): 389–414.doi:10.1146/annurev.nutr.26.061505.111329.PMC2721271.PMID17444812.
- ^Kinnamon SC, Finger TE (2019)."Recent advances in taste transduction and signaling".F1000Research.8:2117.doi:10.12688/f1000research.21099.1.PMC7059786.PMID32185015.
- ^Guyton, Arthur C.(1976),Textbook of Medical Physiology(5th ed.), Philadelphia: W.B. Saunders, p.839,ISBN978-0-7216-4393-9
- ^Macbeth, Helen M.; MacClancy, Jeremy, eds. (2004),"plethora of methods characterising human taste perception",Researching Food Habits: Methods and Problems,The anthropology of food and nutrition, vol. 5, New York: Berghahn Books, pp. 87–88,ISBN9781571815446,retrieved15 September2010
- ^Svrivastava, R. C. & Rastogi, R. P. (2003)."Relative taste indices of some substances".Transport Mediated by Electrical Interfaces.Studies in interface science 18. Amsterdam, Netherlands: Elsevier Science.ISBN978-0-444-51453-0.Retrieved12 September2010.Taste indices of table 9, p. 274 are select sample taken from table in Guyton'sTextbook of Medical Physiology(present in all editions.
Further reading
[edit]- Chandrashekar, Jayaram; Hoon, Mark A.; Ryba; Nicholas, J. P. & Zuker, Charles S. (16 November 2006)."The receptors and cells for mammalian taste"(PDF).Nature.444(7117): 288–294.Bibcode:2006Natur.444..288C.doi:10.1038/nature05401.PMID17108952.S2CID4431221.Archived fromthe original(PDF)on 22 July 2011.Retrieved13 September2010.
- Chaudhari, Nirupa & Roper, Stephen D. (2010)."The cell biology of taste".Journal of Cell Biology.190(3): 285–296.doi:10.1083/jcb.201003144.PMC2922655.PMID20696704.