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脊髓上5-羟色胺受体在正常清醒大鼠排尿中的作用

Role of supraspinal serotonin receptors for micturition in normal conscious rats.

作者信息

Ishizuka Osamu, Gu Baojun, Igawa Yasuhiko, Nishizawa Osamu, Pehrson Rikard, Andersson Karl-Erik

机构信息

Department of Urology, Shinshu University School of Medicine, Matsumoto, Japan.

出版信息

Neurourol Urodyn. 2002;21(3):225-30. doi: 10.1002/nau.10043.

Abstract

Serotonin (5-HT) receptors are widely distributed in the central nervous system, including several areas involved in the control of micturition reflex pathways. However, the roles of the different subtypes of 5-HT receptors are not well known. We studied in normal, conscious rats, the effects on the cystometrogram of intracerebroventricular (i.c.v.) administration of 5-HT, 8-hydroxy-2-(di-N-propylaminotetralin) (8-OH-DPAT; agonist at 5-HT(1A) receptors), alpha-methyl-5-hydroxytryptamine maleate (agonist at 5-HT(2) receptors), 2-methyl-5-hydroxytryptamine hydrochloride (agonist at 5-HT(3) receptors), and 1-(4-amino-5-chloro-2methoxyphenyl)-3-(1-n-butyl-4piperidinyl)-1-propanone hydrochloride (RS67506; agonist at 5-HT(4) receptors). Female Sprague-Dawley rats, weighing approximately 230 g, were used. A polyethylene catheter was inserted into the bladder through the dome for cystometric investigations. For administration of drugs, a catheter was implanted into the right cerebral ventricle. Three days after implantation of the bladder catheter, continuous cystometry was performed. Administration of 5-HT (6 nmol/kg i.c.v.), 8-OH-DPAT (6 nmol/kg), alpha-methyl-5-hydroxytryptamine maleate (6 nmol/kg), or RS67506 hydrochloride (6 nmol/kg) significantly (P < 0.05) increased micturition pressure and decreased bladder capacity and micturition volume. The effects increased in a dose-dependent manner (18, 60 nmol/kg). Intracerebroventricular administration of 2-methyl-5-hydroxytryptamine hydrochloride (60 nmol/kg) caused no change in the cystometric parameters. The results suggest that in normal conscious rats, at the supraspinal level, 5-HT (via 5-HT(1A), 5-HT(2), and 5-HT(4) receptors) can enhance the micturition reflex induced by bladder filling. Whether this means that 5-HT(1A), 5-HT(2), and 5-HT(4) receptors can be targets for drugs meant for treatment of bladder hyperactivity, should be explored.

摘要

5-羟色胺(5-HT)受体广泛分布于中枢神经系统,包括参与控制排尿反射通路的几个区域。然而,5-HT受体不同亚型的作用尚不清楚。我们在正常清醒大鼠中研究了脑室内(i.c.v.)注射5-HT、8-羟基-2-(二-N-丙基氨基四氢萘)(8-OH-DPAT;5-HT(1A)受体激动剂)、马来酸α-甲基-5-羟色胺(5-HT(2)受体激动剂)、盐酸2-甲基-5-羟色胺(5-HT(3)受体激动剂)和盐酸1-(4-氨基-5-氯-2-甲氧基苯基)-3-(1-正丁基-4-哌啶基)-1-丙酮(RS67506;5-HT(4)受体激动剂)对膀胱内压图的影响。使用体重约230g的雌性Sprague-Dawley大鼠。通过膀胱顶部插入一根聚乙烯导管用于膀胱内压测量研究。为了给药,将一根导管植入右侧脑室。膀胱导管植入三天后,进行连续膀胱内压测量。注射5-HT(6nmol/kg i.c.v.)、8-OH-DPAT(6nmol/kg)、马来酸α-甲基-5-羟色胺(6nmol/kg)或盐酸RS67506(6nmol/kg)显著(P<0.05)增加排尿压力并降低膀胱容量和排尿量。这些作用呈剂量依赖性增加(18、60nmol/kg)。脑室内注射盐酸2-甲基-5-羟色胺(60nmol/kg)对膀胱内压测量参数无影响。结果表明,在正常清醒大鼠中,在脊髓上水平,5-HT(通过5-HT(1A)、5-HT(2)和5-HT(4)受体)可增强膀胱充盈诱导的排尿反射。这是否意味着5-HT(1A)、5-HT(2)和5-HT(4)受体可成为治疗膀胱活动亢进药物的靶点,有待探索。

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