Traish Abdulmaged M, Kim Soo Woong, Stankovic Miljan, Goldstein Irwin, Kim Noel N
Department of Biochemistry, Boston University School of Medicine, Boston, MA, USA;; Department of Urology, Boston University School of Medicine, Boston, MA, USA.
Department of Urology, Seoul National University College of Medicine, Seoul, South Korea.
J Sex Med. 2007 May;4(3):609-619. doi: 10.1111/j.1743-6109.2007.00491.x.
The mechanisms by which testosterone modulates female genital sexual arousal responses are poorly understood.
To investigate the effects of testosterone on vaginal blood flow and the expression of estrogen and androgen receptor proteins in the rat vagina.
Mature female Sprague-Dawley rats were sham-operated (intact) or ovariectomized. Fourteen days after ovariectomy, animals were continuously infused with vehicle or varying doses of testosterone (5.5-55 microg/day). After 2 weeks of treatment, vaginal blood flow in response to pelvic nerve stimulation was measured by laser Doppler flowmetry. Plasma levels of testosterone and estradiol were determined by radioimmunoassay and epithelial thickness was examined in fixed vaginal tissue sections. Androgen and estrogen receptor levels were assessed by equilibrium radioligand binding and by Western blot analyses.
Vaginal blood flow responses were significantly reduced in ovariectomized rats and normalized in animals infused with testosterone. Ovariectomy increased the expression of estrogen receptors and reduced the expression of androgen receptors with no change in receptor-ligand affinity. Testosterone increased the expression of both androgen and estrogen receptors in the vagina. While physiological (11 microg/day) and supraphysiological (55 microg/day) concentrations of testosterone normalized vaginal tissue weight, uterine tissue and whole body weights were not significantly different from ovariectomized rats infused with vehicle. Testosterone infusion, even at supraphysiological concentrations, did not change plasma estradiol levels when compared to vehicle-infused, ovariectomized rats. Likewise, the vaginal epithelium of testosterone-infused rats remained atrophic, similar to vehicle-infused, ovariectomized rats, indicating that testosterone is not aromatized to estrogens at significant levels in the vagina.
Our data suggest that testosterone regulates androgen and estrogen receptor protein expression in the vagina and enhances vaginal perfusion by an androgen-dependent mechanism. We conclude that testosterone plays an important role in modulating the physiology of the vagina and contributes to improvement of genital sexual arousal responses.
睾酮调节女性生殖器性唤起反应的机制尚不清楚。
研究睾酮对大鼠阴道血流以及雌激素和雄激素受体蛋白在大鼠阴道中表达的影响。
将成年雌性斯普拉格-道利大鼠进行假手术(完整)或卵巢切除。卵巢切除术后14天,给动物持续输注溶剂或不同剂量的睾酮(5.5 - 55微克/天)。治疗2周后,通过激光多普勒血流仪测量盆腔神经刺激引起的阴道血流。通过放射免疫测定法测定血浆睾酮和雌二醇水平,并在固定的阴道组织切片中检查上皮厚度。通过平衡放射性配体结合和蛋白质印迹分析评估雄激素和雌激素受体水平。
卵巢切除的大鼠阴道血流反应显著降低,而输注睾酮的动物血流反应恢复正常。卵巢切除术增加了雌激素受体的表达,降低了雄激素受体的表达,受体-配体亲和力无变化。睾酮增加了阴道中雄激素和雌激素受体的表达。虽然生理浓度(11微克/天)和超生理浓度(55微克/天)的睾酮使阴道组织重量恢复正常,但子宫组织和全身重量与输注溶剂的卵巢切除大鼠相比无显著差异。与输注溶剂的卵巢切除大鼠相比,即使在超生理浓度下输注睾酮也不会改变血浆雌二醇水平。同样,输注睾酮的大鼠阴道上皮仍处于萎缩状态,类似于输注溶剂的卵巢切除大鼠,表明睾酮在阴道中不会大量转化为雌激素。
我们的数据表明,睾酮通过雄激素依赖性机制调节阴道中雄激素和雌激素受体蛋白的表达,并增强阴道灌注。我们得出结论,睾酮在调节阴道生理方面发挥重要作用,并有助于改善生殖器性唤起反应。