Glezerman M, Lunenfeld E, Potashnik G, Huleihel M, Soffer Y, Segal S
Department of Obstetrics and Gynecology, Soroka Medical Center, Beer Sheba, Israel.
Fertil Steril. 1993 Dec;60(6):1052-6.
To assess the effect of kallikrein on sperm motility and sperm count in infertile oligozoospermic and asthenozoospermic men.
Double-blind placebo-controlled clinical trial.
Multicenter trial in three andrologic clinics.
Infertile men with < 20 x 10(6) total sperm count and > 3 x 10(6) sperm cells/mL and/or sperm motility of < 30%.
One hundred fourteen men received either placebo or 600 kallikrein units of kallidinogenase by mouth daily for 12 weeks. Semen analyses were performed before and at 6-week intervals during the trial. Compliance and incidence of adverse effects were assessed.
The incidence of adverse effects was similar under placebo and under kallidinogenase treatment, usually mild, transient, and did not require the cessation of treatment in any patient. Kallidinogenase was not superior to placebo in improving sperm count and sperm motility.
At the doses and for the duration given, our results were disappointing. The absence of a therapeutical effect, as evidenced in the present study may be due to the very low absorption rate of kallidinogenase after oral administration. Probably a much higher dose of kallidinogenase should be used to achieve a therapeutic affect.
评估激肽释放酶对不育少精子症和弱精子症男性精子活力及精子数量的影响。
双盲安慰剂对照临床试验。
在三家男科诊所进行的多中心试验。
总精子数<20×10⁶且精子细胞/mL>3×10⁶和/或精子活力<30%的不育男性。
114名男性每天口服安慰剂或600激肽释放酶单位的胰激肽原酶,持续12周。在试验期间,于治疗前及每间隔6周进行精液分析。评估依从性及不良反应发生率。
安慰剂组和胰激肽原酶治疗组的不良反应发生率相似,通常为轻度、短暂性,且无需任何患者停止治疗。胰激肽原酶在改善精子数量和精子活力方面并不优于安慰剂。
就所给剂量和疗程而言,我们的结果令人失望。本研究中所证明的缺乏治疗效果可能是由于口服后胰激肽原酶的吸收率极低。可能需要使用更高剂量的胰激肽原酶才能达到治疗效果。