Wikipedia

Steroid hormone

Asteroid hormoneis asteroidthat acts as ahormone.Steroid hormones can be grouped into two classes:corticosteroids(typically made in theadrenal cortex,hencecortico-) andsex steroids(typically made in thegonadsorplacenta). Within those two classes are five types according to thereceptorsto which they bind:glucocorticoidsandmineralocorticoids(both corticosteroids) andandrogens,estrogens,andprogestogens(sex steroids).[1][2]Vitamin Dderivatives are a sixth closely related hormone system with homologous receptors. They have some of the characteristics of true steroids asreceptor ligands.

Steroid hormone
Drug class
Estradiol,an importantestrogensteroid hormone in both women and men.
Class identifiers
SynonymsAdrenal steroid; Gonadal steroid
UseVarious
Biological targetSteroid hormone receptors
Chemical classSteroidal;Nonsteroidal
Legal status
In Wikidata

Steroid hormones help controlmetabolism,inflammation,immune functions,salt and water balance,development ofsexual characteristics,and the ability to withstand injury and illness. The termsteroiddescribes both hormones produced by the body and artificially produced medications that duplicate the action for the naturally occurring steroids.[3][4][5]

Synthesis

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Further information:Steroidogenesis
Steroidogenesiswith enzymes and intermediates.[6]

The natural steroid hormones are generally synthesized fromcholesterolin thegonadsandadrenal glands.These forms of hormones arelipids.They can pass through the cell membrane as they are fat-soluble,[7]and then bind tosteroid hormone receptors(which may be nuclear or cytosolic depending on the steroid hormone) to bring about changes within the cell. Steroid hormones are generally carried in the blood, bound to specific carrierproteinssuch assex hormone-binding globulinorcorticosteroid-binding globulin.Further conversions and catabolism occurs in the liver, in other "peripheral" tissues, and in the target tissues.

Production rates, secretion rates, clearance rates, and blood levels of major sex hormones
Sex Sex hormone Reproductive
phase 		Blood
production rate 		Gonadal
secretion rate 		Metabolic
clearance rate 		Reference range (serum levels)
SIunits Non-SIunits
Men Androstenedione
–
 2.8 mg/day 1.6 mg/day 2200 L/day 2.8–7.3 nmol/L 80–210 ng/dL
Testosterone
–
 6.5 mg/day 6.2 mg/day 950 L/day 6.9–34.7 nmol/L 200–1000 ng/dL
Estrone
–
 150 μg/day 110 μg/day 2050 L/day 37–250 pmol/L 10–70 pg/mL
Estradiol
–
 60 μg/day 50 μg/day 1600 L/day <37–210 pmol/L 10–57 pg/mL
Estrone sulfate
–
 80 μg/day Insignificant 167 L/day 600–2500 pmol/L 200–900 pg/mL
Women Androstenedione
–
 3.2 mg/day 2.8 mg/day 2000 L/day 3.1–12.2 nmol/L 89–350 ng/dL
Testosterone
–
 190 μg/day 60 μg/day 500 L/day 0.7–2.8 nmol/L 20–81 ng/dL
Estrone Follicular phase 110 μg/day 80 μg/day 2200 L/day 110–400 pmol/L 30–110 pg/mL
Luteal phase 260 μg/day 150 μg/day 2200 L/day 310–660 pmol/L 80–180 pg/mL
Postmenopause 40 μg/day Insignificant 1610 L/day 22–230 pmol/L 6–60 pg/mL
Estradiol Follicular phase 90 μg/day 80 μg/day 1200 L/day <37–360 pmol/L 10–98 pg/mL
Luteal phase 250 μg/day 240 μg/day 1200 L/day 699–1250 pmol/L 190–341 pg/mL
Postmenopause 6 μg/day Insignificant 910 L/day <37–140 pmol/L 10–38 pg/mL
Estrone sulfate Follicular phase 100 μg/day Insignificant 146 L/day 700–3600 pmol/L 250–1300 pg/mL
Luteal phase 180 μg/day Insignificant 146 L/day 1100–7300 pmol/L 400–2600 pg/mL
Progesterone Follicular phase 2 mg/day 1.7 mg/day 2100 L/day 0.3–3 nmol/L 0.1–0.9 ng/mL
Luteal phase 25 mg/day 24 mg/day 2100 L/day 19–45 nmol/L 6–14 ng/mL
Notes and sources
Notes:"Theconcentrationof a steroid in the circulation is determined by the rate at which it is secreted from glands, the rate of metabolism of precursor or prehormones into the steroid, and the rate at which it is extracted by tissues and metabolized. Thesecretion rateof a steroid refers to the total secretion of the compound from a gland per unit time. Secretion rates have been assessed by sampling the venous effluent from a gland over time and subtracting out the arterial and peripheral venous hormone concentration. Themetabolic clearance rateof a steroid is defined as the volume of blood that has been completely cleared of the hormone per unit time. Theproduction rateof a steroid hormone refers to entry into the blood of the compound from all possible sources, including secretion from glands and conversion of prohormones into the steroid of interest. At steady state, the amount of hormone entering the blood from all sources will be equal to the rate at which it is being cleared (metabolic clearance rate) multiplied by blood concentration (production rate = metabolic clearance rate × concentration). If there is little contribution of prohormone metabolism to the circulating pool of steroid, then the production rate will approximate the secretion rate. "Sources:See template.

Synthetic steroids and sterols

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A variety of synthetic steroids and sterols have also been contrived. Most are steroids, but somenonsteroidalmolecules can interact with the steroid receptors because of a similarity of shape. Some synthetic steroids are weaker or stronger than the natural steroids whose receptors they activate.[8]

Some examples of synthetic steroid hormones:

Some steroid antagonists:

Transport

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Free hormone hypothesis 2

Steroid hormones are transported through the blood by being bound to carrier proteins—serum proteins that bind them and increase the hormones' solubility in water. Some examples aresex hormone-binding globulin(SHBG),corticosteroid-binding globulin,andalbumin.[9]Most studies say that hormones can only affect cells when they are not bound by serum proteins. In order to be active, steroid hormones must free themselves from their blood-solubilizing proteins and either bind to extracellular receptors, or passively cross the cell membrane and bind tonuclear receptors.This idea is known as the free hormone hypothesis. This idea is shown in Figure 1 to the right.

This shows a possible pathway through which steroid hormones are endocytosed and proceed to affect cells via a genomic pathway.

One study has found that these steroid-carrier complexes are bound bymegalin,a membrane receptor, and are then taken into cells viaendocytosis.One possible pathway is that once inside the cell these complexes are taken to the lysosome, where the carrier protein is degraded and the steroid hormone is released into the cytoplasm of the target cell. The hormone then follows a genomic pathway of action. This process is shown in Figure 2 to the right.[10]The role of endocytosis in steroid hormone transport is not well understood and is under further investigation.

In order for steroid hormones to cross thelipid bilayerof cells, they must overcome energetic barriers that would prevent their entering or exiting the membrane.Gibbs free energyis an important concept here. These hormones, which are all derived from cholesterol, have hydrophilic functional groups at either end and hydrophobic carbon backbones. When steroid hormones are entering membranes free energy barriers exist when the functional groups are entering the hydrophobic interior of membrane, but it is energetically favorable for the hydrophobic core of these hormones to enter lipid bilayers. These energy barriers and wells are reversed for hormones exiting membranes. Steroid hormones easily enter and exit the membrane at physiologic conditions. They have been shown experimentally to cross membranes near a rate of 20 μm/s, depending on the hormone.[11]

Though it is energetically more favorable for hormones to be in the membrane than in the ECF or ICF, they do in fact leave the membrane once they have entered it. This is an important consideration because cholesterol—the precursor to all steroid hormones—does not leave the membrane once it has embedded itself inside. The difference between cholesterol and these hormones is that cholesterol is in a much larger negative Gibb's free energy well once inside the membrane, as compared to these hormones. This is because the aliphatic tail on cholesterol has a very favorable interaction with the interior of lipid bilayers.[11]

Mechanisms of action and effects

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There are many different mechanisms through which steroid hormones affect their target cells. All of these different pathways can be classified as having either a genomic effect or a non-genomic effect. Genomic pathways are slow and result in altering transcription levels of certain proteins in the cell; non-genomic pathways are much faster.

Flowchart showing the binding of a steroid hormone to a target cell

Genomic pathways

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The first identified mechanisms of steroid hormone action were the genomic effects.[12]In this pathway, the free hormones first pass through the cell membrane because they are fat soluble.[7]In the cytoplasm, the steroid may or may not undergo anenzyme-mediated alteration such as reduction, hydroxylation, or aromatization. Then the steroid binds to a specificsteroid hormone receptor,also known as anuclear receptor,which is a large metalloprotein. Upon steroid binding, many kinds of steroid receptorsdimerize:two receptor subunits join together to form one functionalDNA-binding unit that can enter the cell nucleus. Once in the nucleus, the steroid-receptor ligand complex binds to specificDNAsequences and induces transcription of its targetgenes.[4][13][14][12]

Non-genomic pathways

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Because non-genomic pathways include any mechanism that is not a genomic effect, there are various non-genomic pathways. However, all of these pathways are mediated by some type ofsteroid hormone receptorfound at the plasma membrane.[15]Ion channels, transporters,G-protein coupled receptors(GPCR), and membrane fluidity have all been shown to be affected by steroid hormones.[11]Of these, GPCR linked proteins are the most common. For more information on these proteins and pathways, visit thesteroid hormone receptorpage.

See also

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References

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  1. ^"Steroid hormones - Latest research and news | Nature".www.nature.com.Retrieved2021-12-06.
  2. ^"steroid hormone | Definition, Classification, & Function | Britannica".www.britannica.com.Retrieved2021-12-06.
  3. ^Funder JW, Krozowski Z, Myles K, Sato A, Sheppard KE, Young M (1997). "Mineralocorticoid receptors, salt, and hypertension".Recent Prog Horm Res.52:247–260.PMID9238855.
  4. ^abGupta BBP, Lalchhandama K (2002)."Molecular mechanisms of glucocorticoid action"(PDF).Current Science.83(9): 1103–1111.
  5. ^Frye CA (2009). "Steroids, reproductive endocrine function, and affect. A review".Minerva Ginecol.61(6): 541–562.PMID19942840.
  6. ^Häggström, Mikael; Richfield, David (2014)."Diagram of the pathways of human steroidogenesis".WikiJournal of Medicine.1(1).doi:10.15347/wjm/2014.005.ISSN2002-4436.
  7. ^abLinda J. Heffner; Danny J. Schust (2010).The Reproductive System at a Glance.John Wiley and Sons. pp.16–.ISBN978-1-4051-9452-5.Retrieved28 November2010.
  8. ^Nahar L, Sarker SD, Turner AB (2007). "A review on synthetic and natural steroid dimers: 1997-2006".Curr Med Chem.14(12): 1349–1370.doi:10.2174/092986707780597880.PMID17504217.
  9. ^Adams JS (2005).""Bound" to work: The free hormone hypothesis revisited ".Cell.122(5): 647–9.doi:10.1016/j.cell.2005.08.024.PMID16143095.
  10. ^Hammes A (2005)."Role of endocytosis in cellular uptake of sex steroids".Cell.122(5): 751–62.doi:10.1016/j.cell.2005.06.032.PMID16143106.
  11. ^abcOren I (2004)."Free diffusion of steroid hormones across biomembranes: A simplex search with implicit solvent model calculations".Biophysical Journal.87(2): 768–79.Bibcode:2004BpJ....87..768O.doi:10.1529/biophysj.103.035527.PMC1304487.PMID15298886.
  12. ^abRousseau G (2013). "Fifty years ago: The quest for steroid hormone receptors".Molecular and Cellular Endocrinology.375(1–2): 10–3.doi:10.1016/j.mce.2013.05.005.PMID23684885.S2CID24346074.
  13. ^Moore FL, Evans SJ (1995). "Steroid hormones use non-genomic mechanisms to control brain functions and behaviors: a review of evidence".Brain Behav Evol.54(4): 41–50.doi:10.1159/000006610.PMID10516403.S2CID1998076.
  14. ^Marcinkowska E, Wiedłocha A (2002)."Steroid signal transduction activated at the cell membrane: from plants to animals".Acta Biochim Pol.49(9): 735–745.doi:10.18388/abp.2002_3782.PMID12422243.
  15. ^Wang C, Liu Y, Cao JM (2014)."G protein-coupled receptors: Extranuclear mediators for the non-genomic actions of steroids".International Journal of Molecular Sciences.15(9): 15412–25.doi:10.3390/ijms150915412.PMC4200746.PMID25257522.

Further reading

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