Is glandular formation of nitric oxide a prerequisite for muscarinic secretion of fructose in the guinea-pig seminal vesicle?

被引:27
作者
Ehren, I
Sjostrand, NO
Hammarstrom, M
Wiklund, NP [1 ]
机构
[1] Karolinska Hosp, Dept Urol, S-17176 Stockholm, Sweden
[2] Karolinska Inst, Dept Physiol & Pharmacol, Div Physiol 1, Stockholm, Sweden
[3] Karolinska Inst, Dept Obstet & Gynecol, S-10401 Stockholm, Sweden
来源
UROLOGICAL RESEARCH | 1997年 / 25卷 / 06期
关键词
cholinergic nerves; glandular cells; nitric oxide; secretion; seminal vesicle;
D O I
10.1007/BF01268862
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The significance of nitric oxide (NO) formation in seminal secretion was studied in guinea-pig seminal vesicles. The nitric oxide synthase (NOS) activity was estimated and reduced nicotinamide-adenine dinucleotide phosphate (NADPH)-diaphorase histochemistry was performed. Furthermore, cyclic guanosine 3,5-monophosphate (cGMP) concentration as well as fructose secretion from isolated vesicles was estimated. High Ca2+-dependent NOS activity as well as prominent glandular NADPH-diaphorase staining was found in the secretory epithelium. The NOS inhibitors N-G-nitro L-arginine methyl ester (L-NAME) and N-G-nitro L-arginine (L-NNA) inhibited carbachol-induced fructose secretion but the D-isomer to L-NAME had no effect. When L-arginine was administered together with L-NAME, no inhibitory effect on the carbachol-induced fructose secretion could be seen. Nerve-induced fructose secretion was also inhibited by L-NAME. The NO donor glyceryl trinitrate (GTN) increased the fructose secretion. Carbachol or GTN did not increase cGMP levels, nor was fructose secretion inhibited by a guanylate cyclase inhibitor (ODQ). Our results suggests that glandular NO production is a prerequisite for muscarinic fructose secretion in the seminal vesicle via a cGMP-independent pathway.
引用
收藏
页码:433 / 438
页数:6
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