Testosterone: Difference between revisions

From Citizendium
Jump to navigation Jump to search
imported>Caesar Schinas
m (Bot: Update image code)
mNo edit summary
 
(3 intermediate revisions by 2 users not shown)
Line 7: Line 7:
16,17-dodecahydrocyclopenta[a]phenanthren-3-one and its molecular formula is C<sub>19</sub>H<sub>28</sub>O<sub>2</sub>.
16,17-dodecahydrocyclopenta[a]phenanthren-3-one and its molecular formula is C<sub>19</sub>H<sub>28</sub>O<sub>2</sub>.


== brand names ==
[[Testosterone 5-alpha-reductase]] converts it to [[dehydrotestosterone]].
 
==Drug toxicity==
Testosterone administration may cause [[myocardial infarction]]s.<ref name="pmid20592293">{{cite journal| author=Basaria S, Coviello AD, Travison TG, Storer TW, Farwell WR, Jette AM et al.| title=Adverse events associated with testosterone administration. | journal=N Engl J Med | year= 2010 | volume= 363 | issue= 2 | pages= 109-22 | pmid=20592293 | doi=10.1056/NEJMoa1000485 | pmc=PMC3440621 | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=20592293 }} [http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=21173408 Review in: Ann Intern Med. 2010 Dec 21;153(12):JC6-7] </ref><ref name="pmid24193080">{{cite journal| author=Vigen R, O'Donnell CI, Barón AE, Grunwald GK, Maddox TM, Bradley SM et al.| title=Association of testosterone therapy with mortality, myocardial infarction, and stroke in men with low testosterone levels. | journal=JAMA | year= 2013 | volume= 310 | issue= 17 | pages= 1829-36 | pmid=24193080 | doi=10.1001/jama.2013.280386 | pmc= | url=http://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=24193080 }} </ref>
 
== Brand names ==
{{columns-list|4|
*Andriol  
*Andriol  
*Andro  
*Andro  
Line 94: Line 100:
*Virormone  
*Virormone  
*Virosterone
*Virosterone
}}
==References==
<references/>
[[Category:Suggestion Bot Tag]]

Latest revision as of 06:00, 26 October 2024

This article is a stub and thus not approved.
Main Article
Discussion
Related Articles  [?]
Bibliography  [?]
External Links  [?]
Citable Version  [?]
 
This editable Main Article is under development and subject to a disclaimer.
(CC) Image: David E. Volk
Structure of testosterone.

Testosterone is a steroid hormone that has been widely abused to enhance athletic performance because it is an anabolic steroid that stimulates growth. Testosterone is an androgen that controls virulization (masculinity). It is derived from another androgen, androstenedione, and is a chemical precurson to the estrogen steroid estradiol. Testosterone is mainly secreted from the testes, but some is also produced in the adrenal glands, so it is present in females as well as in males, but at much lower concentrations. Testosterone acts at specific nuclear receptors expressed in many tissues of the body, including the pituitary gland, and at some sites in the brain where it exerts effects on behaviour and regulates secretion of some hormones. In the brain, testosterone can also be metabolised (by the enzyme aromatase)to produce oestrogen. Testosterone has a negative feedback effect on the secretion of luteinising hormone and follicle stimulating hormone, which in men promote testis growth and sperm production. Accordingly, excessive levels of testosterone, while they result in muscle enhancement and increased aggression, can also result in hypogonadism (reduction in testis size) and infertility.

Its chemical IUPAC name is 8R,9S,10R,13S,14S,17S)-17-hydroxy-10,13-dimethyl-1,2,6,7,8,9,11,12,14,15, 16,17-dodecahydrocyclopenta[a]phenanthren-3-one and its molecular formula is C19H28O2.

Testosterone 5-alpha-reductase converts it to dehydrotestosterone.

Drug toxicity

Testosterone administration may cause myocardial infarctions.[1][2]

Brand names

  • Andriol
  • Andro
  • Andro 100
  • Andro L.A. 200
  • Androderm
  • Androgel
  • Android 10
  • Android 25
  • Android 5
  • Androlin
  • Andronaq
  • Andronate 100
  • Andronate 200
  • Andropatch
  • Andropository 200
  • Andrusol
  • Andryl 200
  • Beta Testosterone
  • CDB 111C
  • Cristerona T
  • Cristerone T
  • Delatest
  • Delatestryl
  • Depo-Testosterone
  • Depo-Testosterone Cypionate
  • Depotest
  • Everone 200
  • Geno-Cristaux Gremy
  • Homosteron
  • Homosterone
  • Libigel
  • Malerone
  • Malestrone
  • Malogen in Oil
  • Malogen, Aquaspension Injection
  • Mertestate
  • Metandren
  • Methyltestosterone
  • Neo-Hombreol F
  • Neo-Testis
  • Neotestis
  • Oreton
  • Oreton F
  • Oreton Methyl
  • Oreton-F
  • Orquisteron
  • Perandren
  • Percutacrine Androgenique
  • Primotest
  • Primoteston
  • Relibra
  • Scheinpharm Testone-Cyp
  • Striant
  • Sustanon
  • Sustanone
  • Sustason 250
  • Synandrol F
  • T-Cypionate
  • Teslen
  • Testamone 100
  • Testandrone
  • Testaqua
  • Testiculosterone
  • Testim
  • Testobase
  • Testoderm
  • Testoderm Tts
  • Testogel
  • Testoject-50
  • Testolin
  • Testopel Pellets
  • Testopropon
  • Testosteroid
  • Testoviron
  • Testoviron Schering
  • Testoviron T
  • Testred
  • Testred Cypionate 200
  • Testrin-P.A
  • Testro Aq
  • Testrone
  • Testryl
  • Virilon
  • Virilon IM
  • Virormone
  • Virosterone

References

  1. Basaria S, Coviello AD, Travison TG, Storer TW, Farwell WR, Jette AM et al. (2010). "Adverse events associated with testosterone administration.". N Engl J Med 363 (2): 109-22. DOI:10.1056/NEJMoa1000485. PMID 20592293. PMC PMC3440621. Research Blogging. Review in: Ann Intern Med. 2010 Dec 21;153(12):JC6-7
  2. Vigen R, O'Donnell CI, Barón AE, Grunwald GK, Maddox TM, Bradley SM et al. (2013). "Association of testosterone therapy with mortality, myocardial infarction, and stroke in men with low testosterone levels.". JAMA 310 (17): 1829-36. DOI:10.1001/jama.2013.280386. PMID 24193080. Research Blogging.