Literature DB >> 18353404

Testosterone, androstenedione, and 5alpha-dihydrotestosterone on male sexual behavior and penile spines in the hamster.

M Arteaga-Silva1, R M Vigueras-Villaseñor, S Retana-Márquez, M Hernández-González, C Chihuahua-Serrano, H Bonilla-Jaime, J L Contreras, G Moralí.   

Abstract

The expression of masculine sexual behavior (MSB) in male hamsters is optimally stimulated by aromatizable androgens like androstenedione (AD) and testosterone (T), while the non-aromatizable androgen, 5alpha-dihydrotestosterone (DHT), exerting potent androgenic peripheral effects, only in high doses maintains MSB after castration. No data exist on the ability of these androgens to restore long intromissions after castration. In this study, AD, T, and DHT were administered to four-week gonadectomized, sexually experienced male hamsters, for three weeks, in doses of 25 microg/day or up to 1000 microg/day to compare their potency in restoring MSB, penile size, and penile spines growth. Plasma levels of these steroids and the metabolites estrone and estradiol, were determined at the end of the treatment period. Gonadectomy completely suppressed MSB and induced a regression of penile spines. AD was more potent than T in restoring MSB, ejaculatory behavior being displayed by most castrated subjects with a lower dose of AD (50 microg/day) than of T (300 microg/day), and long intromissions being shown by all AD-treated castrated hamsters but only by 20% of T-treated ones, when doses of 1000 microg/day were given. DHT did not stimulate any copulatory response. The three androgens, even at the lowest dose, partially stimulated penis and penile epithelium growth, DHT showing the highest potency. Treatment of castrated hamsters with AD (50 microg/day), restored steroid levels to similar values as those of intact animals. These results show that AD and T restored MSB even with a partial stimulation of penile spines growth, AD being more potent than T. In contrast, DHT did not restore MSB in the hamster in spite of its peripheral androgenic potency.

Entities:  

Mesh:

Substances:

Year:  2008        PMID: 18353404     DOI: 10.1016/j.physbeh.2008.02.007

Source DB:  PubMed          Journal:  Physiol Behav        ISSN: 0031-9384


  6 in total

Review 1.  Androgens are fundamental in the maintenance of male sexual health.

Authors:  Alvaro Morales
Journal:  Curr Urol Rep       Date:  2011-12       Impact factor: 3.092

Review 2.  Impact of androgen deprivation therapy on sexual function.

Authors:  Clarisse R Mazzola; John P Mulhall
Journal:  Asian J Androl       Date:  2012-01-09       Impact factor: 3.285

3.  Facilitation of male sexual behavior in Syrian hamsters by the combined action of dihydrotestosterone and testosterone.

Authors:  David J Piekarski; Ned J Place; Irving Zucker
Journal:  PLoS One       Date:  2010-09-14       Impact factor: 3.240

4.  Pubertal testosterone organizes regional volume and neuronal number within the medial amygdala of adult male Syrian hamsters.

Authors:  Kayla C De Lorme; Kalynn M Schulz; Kaliris Y Salas-Ramirez; Cheryl L Sisk
Journal:  Brain Res       Date:  2012-04-26       Impact factor: 3.252

5.  Adrenal steroids uniquely influence sexual motivation behavior in male rats.

Authors:  George T Taylor; Joshua T Dearborn; Susan E Maloney
Journal:  Behav Sci (Basel)       Date:  2012-08-31

6.  Evidence of late-summer mating readiness and early sexual maturation in migratory tree-roosting bats found dead at wind turbines.

Authors:  Paul M Cryan; Joel W Jameson; Erin F Baerwald; Craig K R Willis; Robert M R Barclay; E Apple Snider; Elizabeth G Crichton
Journal:  PLoS One       Date:  2012-10-19       Impact factor: 3.240

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.