Chen C, Puy L A, Simard J, Li X, Singh S M, Labrie F
MRC Group in Molecular Endocrinology, CHUL Research Center, Québec, Canada.
J Invest Dermatol. 1995 Nov;105(5):678-82. doi: 10.1111/1523-1747.ep12324390.
The hamster flank organ is a widely used model of the control of sebaceous gland activity by androgens and anti-androgens. Finasteride, a 5 alpha-reductase inhibitor, was administered locally on the surface of the right flank organ and right ear twice daily for 4 weeks. The treatment caused similar 12% to 30% reductions in the size of the sebaceous glands in both flank organs. Moreover, relative mRNA levels of the androgen-regulated FAR-17a gene measured by in situ hybridization as well as [3H]-thymidine incorporation and 5 alpha-reductase activity were similarly decreased in the two flank organs after topical application. The pure anti-androgen flutamide, at the same doses, exerted a more potent effect on all the same parameters, and the effect was also comparable on both the treated and untreated sides of flank organs. Finasteride and flutamide significantly decreased ventral and dorsal prostatic weights after topical application. The present data show that the topical administration of finasteride, in analogy with flutamide, causes local inhibition of sebaceous gland growth in both the costovertebral organs and ears. However, as demonstrated by the similar inhibitory effect in the contralateral untreated side and the reduced weight of the dorsal and ventral lobes of the prostate and seminal vesicles, finasteride and flutamide both exert significant systemic effects.
仓鼠胁腹器官是一种广泛用于研究雄激素和抗雄激素对皮脂腺活动控制的模型。非那雄胺是一种5α-还原酶抑制剂,每天两次局部涂抹于右侧胁腹器官和右耳表面,持续4周。该治疗使两个胁腹器官的皮脂腺大小均出现了相似的12%至30%的减小。此外,局部应用后,通过原位杂交测量的雄激素调节的FAR-17a基因的相对mRNA水平以及[3H]-胸腺嘧啶掺入和5α-还原酶活性在两个胁腹器官中同样降低。相同剂量的纯抗雄激素氟他胺对所有相同参数产生了更强的作用,并且对胁腹器官的处理侧和未处理侧的作用也相当。局部应用非那雄胺和氟他胺后,显著降低了腹侧和背侧前列腺重量。目前的数据表明,与氟他胺类似,局部应用非那雄胺会导致肋椎器官和耳朵中的皮脂腺生长受到局部抑制。然而,正如在对侧未处理侧的类似抑制作用以及前列腺和精囊背叶和腹叶重量减轻所证明的那样,非那雄胺和氟他胺都产生了显著的全身作用。