Dubé D, Assaf A, Pelletier G, Labrie F
MRC Group in Molecular Endocrinology, Le Centre Hospitalier de l'Université Laval, Quebec, Canada.
Acta Endocrinol (Copenh). 1987 Nov;116(3):413-7. doi: 10.1530/acta.0.1160413.
After 4 months of treatment of adult male dogs with the GnRH agonist (GnRH-A) [D-Trp6]GnRH ethylamide, the seminiferous tubules contained only type A and B spermatogonia, Sertoli cells, and rare primary spermatocytes, thus causing a 64% decrease in testis weight. At the electron microscope level, Sertoli cells showed an increase in phagosomes and lipid droplets. Leydig cells were markedly atrophied with the accumulation of lipid droplets and showed a predominance of mitochondria with lamellar instead of vesicular cristae. Four months after cessation of treatment with GnRH-A, a complete return to normal spermatogenesis and Leydig cell morphology was observed. The full reversibility of spermatogenesis in the dog after chronic GnRH-A treatment suggests that this well-tolerated peptide could be used as a reversible method of male contraception.
用促性腺激素释放激素激动剂(GnRH-A)[D-色氨酸6]GnRH乙酰胺对成年雄性犬进行4个月治疗后,曲细精管中仅含有A型和B型精原细胞、支持细胞以及罕见的初级精母细胞,睾丸重量因此下降了64%。在电子显微镜水平下,支持细胞的吞噬体和脂滴增多。间质细胞明显萎缩,脂滴积聚,线粒体以板层状嵴而非泡状嵴为主。停止GnRH-A治疗4个月后,观察到精子发生和间质细胞形态完全恢复正常。慢性GnRH-A治疗后犬精子发生的完全可逆性表明,这种耐受性良好的肽可作为一种可逆的男性避孕方法。