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阿片类物质在脑桥排尿中枢水平对排尿反射的调节作用。

Opioid modulation of the micturition reflex at the level of the pontine micturition center.

作者信息

Noto H, Roppolo J R, de Groat W C, Nishizawa O, Sugaya K, Tsuchida S

机构信息

Department of Urology, Akita University School of Medicine, Japan.

出版信息

Urol Int. 1991;47 Suppl 1:19-22. doi: 10.1159/000282243.

Abstract

In precollicular decerebrate cats and dogs the intravenous administration of naloxone reduced urinary bladder capacity. Successive cystometrograms revealed that naloxone in doses of 10-100 micrograms/kg i.v. reduced the volume necessary to evoke micturition by 21-67% (mean 48%) in cats and 15-81% (mean 43%) in dogs, respectively. Microinjection of fentanyl (0.4-10 nM) into the pontine micturition center (PMC) increased the bladder capacity by 4-46% (mean 18%) in cats. Naloxone injected into the same site reversed the effect of fentanyl. Microinjection of naloxone (40-120 nM) into the PMC reduced the bladder capacity by 17-57% (mean 34%) in cats. These data indicate that endogenous opioid peptides may have a role in controlling micturition in both decerebrate cat and dog, and that the enkephalinergic inhibitory mechanisms are important in modulating the micturition reflex at the level of the pontine micturition center.

摘要

在中脑前脑切断的猫和狗中,静脉注射纳洛酮可降低膀胱容量。连续的膀胱压力容积测定显示,静脉注射剂量为10 - 100微克/千克的纳洛酮,使猫引起排尿所需的尿量减少21% - 67%(平均48%),使狗减少15% - 81%(平均43%)。向猫的脑桥排尿中枢(PMC)微量注射芬太尼(0.4 - 10纳摩尔),可使膀胱容量增加4% - 46%(平均18%)。向同一部位注射纳洛酮可逆转芬太尼的作用。向猫的PMC微量注射纳洛酮(40 - 120纳摩尔),可使膀胱容量减少17% - 57%(平均34%)。这些数据表明,内源性阿片肽可能在中脑前脑切断的猫和狗的排尿控制中起作用,并且脑啡肽能抑制机制在脑桥排尿中枢水平调节排尿反射中很重要。

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