Yonezawa Akihiko, Ebiko Manabu, Yoshizumi Masaru, Ise Shin-nosuke, Watanabe Chizuko, Mizoguchi Hirokazu, Iwasaki Masahiro, Kimura Yukio, Sakurada Shinobu
Department of Physiology and Anatomy, Tohoku Pharmaceutical University, Sendai, Miyagi, Japan.
Int J Urol. 2009 Feb;16(2):208-11. doi: 10.1111/j.1442-2042.2008.02214.x. Epub 2008 Dec 5.
To investigate the effects of insulin replacement on ejaculatory dysfunction in streptozotocin (STZ)-induced diabetic rats.
Rats were divided into three groups: (i) STZ-treated group; (ii) STZ-treated + insulin replacement (5 and 2 international units [IU]) group; and (iii) control group. The ejaculatory function in rats was evaluated using the spontaneous seminal emission (SSE) test. The amount of seminal vesicle fluid (SVF) stored in seminal vesicle was measured after the SSE test. Blood glucose was measured using a simplified blood glucose meter.
In the SSE test, the ejaculatory capacity in STZ-induced diabetic rats deteriorated with time after the onset of diabetes, and the incidence of SSE and the amount of ejaculated seminal material (SM) were significantly decreased from 5 weeks after STZ administration. Likewise, the amount of SVF was also significantly decreased in a time-dependent manner. One week after STZ administration when ejaculatory capacity had not yet diminished, insulin replacement (for 4 weeks) completely prevented the decrease in frequency of SSE, the amount of SM and SVF. However, insulin replacement after the dysfunction had occurred (5 or 15 weeks after STZ administration) did not allow all parameters for ejaculatory function to be restored to the levels of the control group.
This study demonstrates that at an early stage following the onset of diabetes, insulin replacement can prevent ejaculatory dysfunction in STZ-induced diabetic rats, but once the dysfunction occurs, treatment with insulin alone does not restore the ejaculatory capacity to normal levels. In addition, this study suggests that the loss of seminal emission that results from a decrease in SVF may be involved in the mechanism of ejaculatory dysfunction in diabetic rats.
研究胰岛素替代治疗对链脲佐菌素(STZ)诱导的糖尿病大鼠射精功能障碍的影响。
将大鼠分为三组:(i)STZ治疗组;(ii)STZ治疗+胰岛素替代(5和2国际单位[IU])组;(iii)对照组。采用自发性射精(SSE)试验评估大鼠的射精功能。SSE试验后测量储存在精囊中的精囊液(SVF)量。使用简易血糖仪测量血糖。
在SSE试验中,STZ诱导的糖尿病大鼠的射精能力在糖尿病发病后随时间恶化,自STZ给药后5周起,SSE的发生率和射精物质(SM)的量显著降低。同样,SVF的量也以时间依赖性方式显著降低。在STZ给药后1周,当射精能力尚未减弱时,胰岛素替代治疗(持续4周)完全阻止了SSE频率、SM量和SVF量的下降。然而,在功能障碍发生后(STZ给药后5或15周)进行胰岛素替代治疗并不能使射精功能的所有参数恢复到对照组水平。
本研究表明,在糖尿病发病后的早期阶段,胰岛素替代治疗可预防STZ诱导的糖尿病大鼠的射精功能障碍,但一旦功能障碍发生,仅用胰岛素治疗并不能使射精能力恢复到正常水平。此外,本研究表明,由SVF减少导致的射精丧失可能参与了糖尿病大鼠射精功能障碍的机制。