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大鼠脑桥导水管周围灰质内 GABA 能对排尿的控制。

GABAergic control of micturition within the periaqueductal grey matter of the male rat.

机构信息

School of Clinical and Experimental Medicine, University of Birmingham, Birmingham B15 2TT, UK.

出版信息

J Physiol. 2011 Apr 15;589(Pt 8):2065-78. doi: 10.1113/jphysiol.2010.202614. Epub 2011 Feb 21.

Abstract

In urethane-anaesthetised rats continuous infusion of saline into the bladder (6 ml h⁻¹) evoked periodic sharp rises in intravesicular pressure accompanied by rhythmic bursting of external urethral sphincter (EUS) EMG and expulsion of urine from the urethral meatus. Microinjection of the GABA agonist muscimol (250 pmol) into the caudal ventrolateral periaqueductal grey (PAG), but not at other sites in the PAG, either depressed reflex voiding frequency (-60%, n = 7) and tonic EUS EMG activity (-38%, n = 6) or completely inhibited voiding (four sites). Microinjection of the GABA antagonist bicuculline (BIC; 1 nmol) into the same region, to reduce ongoing GABA tone, increased reflex voiding frequency (+467%, n = 16) and tonic activity in the EUS (+56%, n = 7) whilst bursting activity in the EUS became desynchronised. Although muscimol failed to change reflex micturition when microinjected into the dorsal caudal PAG, microinjection of BIC at these sites evoked pronounced autonomic arousal and increased reflex voiding frequency (+237%, n = 34). The results demonstrate that the functional integrity of synapses in the caudal ventrolateral PAG is essential to permit micturition. Transmission through the region is normally regulated by a tonic GABAergic inhibitory influence. In contrast, the functional integrity of the dorsal caudal PAG is not essential for reflex micturition. However, micturition may be initiated from this region via projections to the caudal ventrolateral PAG, as part of the behavioural response to psychological threat or other stressful stimuli.

摘要

在乌拉坦麻醉的大鼠中,连续向膀胱内输注盐水(6ml/h)可引起膀胱内压周期性急剧升高,同时伴有尿道外括约肌(EUS)肌电图的节律性爆发和尿道外口尿液排出。将 GABA 激动剂 muscimol(250pmol)微注射到尾侧腹外侧导水管周围灰质(PAG),但不在 PAG 的其他部位,既降低了反射性排尿频率(-60%,n=7)和紧张性 EUS 肌电图活动(-38%,n=6),也完全抑制了排尿(4 个部位)。将 GABA 拮抗剂 BIC(1nmol)微注射到同一区域,以降低持续的 GABA 张力,增加反射性排尿频率(+467%,n=16)和 EUS 中的紧张性活动(+56%,n=7),同时 EUS 中的爆发活动变得不同步。尽管 muscimol 微注射到背侧尾侧 PAG 时未能改变反射性排尿,但在这些部位微注射 BIC 会引起明显的自主觉醒和反射性排尿频率增加(+237%,n=34)。结果表明,尾侧腹外侧 PAG 中的突触功能完整性对于允许排尿是必要的。该区域的传递通常受到紧张性 GABA 能抑制影响的调节。相比之下,背侧尾侧 PAG 的功能完整性对于反射性排尿不是必需的。然而,排尿可能从该区域通过投射到尾侧腹外侧 PAG 开始,作为对心理威胁或其他应激刺激的行为反应的一部分。

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