Time-dependent alteration in cromakalim-induced relaxation of corpus cavernosum from streptozocin-induced diabetic rats
- 作者：Mehdi Ghasemi ; Hamed Sadeghipour ; Shahrzad Asadi ; Ahmad Reza Dehpour
- 关键词：Diabetes mellitus ; ATP-sensitive potassium channels ; Cromakalim ; Corpus cavernosum ; Rats
- 刊名：Life Sciences
- 出版年：2007
- 期刊代码：62_00243205
- 类别：imm
- 出版时间：1 September 2007
- 卷：81
- 期：12
- 页码：960-969
- 文件大小：1060 K
摘要
The purpose of the present study was to investigate the relaxant responses to the ATP-sensitive potassium (KATP) channel opener cromakalim in corpus cavernosum strips from 1-, 2-, 4-, 6-, and 8-week streptozocin-induced diabetic rats. Cromakalim (1 nM–0.1 mM) produced concentration-dependent relaxation in phenylephrine (7.5 μM)-precontracted isolated rat corporal strips. Compared with age-matched control animals, a significant enhancement in cromakalim-induced relaxation of corpus cavernosum was observed in 2-week diabetic animals, whereas the relaxant responses to cromakalim were decreased in 6-and 8-week diabetic animals. However, the cromakalim-induced relaxation was not altered in either 1-week or 4-week rat corporal strips in comparison with corresponding age-matched non-diabetic groups. Preincubation with the KATP channel blocker glibenclamide (10 μM) significantly inhibited the cromakalim-induced relaxation in both non-diabetic and diabetic rat corpus cavernosum, but neither the voltage-dependent K+ channel (KV) antagonist 4-aminopyridine (1 mM) nor the calcium-activated K+ channel (KCa) antagonist charybdotoxin (0.1 μM) had significant effect on cromakalim-induced relaxation in both control and diabetic rat corporal strips. Relaxation responses to the nitric oxide donor sodium nitroprusside (1 nM–0.1 mM) in diabetic rat corpus cavernosum were similar to that of age-matched controls. These data demonstrated that the relaxant responses to cromakalim were altered in diabetic cavernosal strips in a time dependent manner, suggesting that the period of diabetes mellitus may play a key role in the KATP channels function in rat corpus cavernosum.