Happ J, Weber T, Callensee W, Ermert J A, Eshkol A, Beyer J
Fertil Steril. 1978 May;29(5):552-6. doi: 10.1016/s0015-0282(16)43284-x.
Pernasal therapy of cryptorchidism with D-Leu6-des-Gly10-gonadotropin-releasing hormone ethylamide (D-Leu6-des-Gly10-GnRH-EA), a potent, long-acting GnRH analog, was attempted. Eleven prepubertal cryptorchid boys received between 25 microgram once daily and 25 to 50 microgram twice daily for 5 to 12 weeks. Complete testicular descent was achieved in 4 of the 11 boys. GnRH tests (1.5 microgram/kg intravenously), conducted in six boys before treatment, after 4 weeks of treatment, and in 2 boys 3 months after treatment, did not reveal changes in gonadotropin secretion indicative of precocious puberty or of decreased hypophyseal sensitivity to GnRH. Antibodies to the GnRH analog or to GnRH could not be detected.
尝试采用一种强效长效促性腺激素释放激素类似物——D-亮氨酸6-去甘氨酸10-促性腺激素释放激素乙酰胺(D-Leu6-des-Gly10-GnRH-EA)经鼻治疗隐睾症。11名青春期前隐睾男孩接受了每日一次25微克至每日两次25至50微克的治疗,持续5至12周。11名男孩中有4名实现了睾丸完全下降。在6名男孩治疗前、治疗4周后以及2名男孩治疗3个月后进行了GnRH测试(静脉注射1.5微克/千克),未发现促性腺激素分泌有表明性早熟或垂体对GnRH敏感性降低的变化。未检测到针对GnRH类似物或GnRH的抗体。