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神经肽 S 抑制大鼠应激刺激的粪便排出。

Neuropeptide S inhibits stress-stimulated faecal output in the rat.

机构信息

Department of Physiology and Pharmacology "V. Erspamer", Sapienza University of Rome, Rome, Italy.

出版信息

Pharmacol Res. 2011 Nov;64(5):471-7. doi: 10.1016/j.phrs.2011.06.007. Epub 2011 Jun 17.

Abstract

Neuropeptide S (NPS) is a recently identified bioactive peptide that activates an orphan G-protein coupled receptor, called the NPS receptor (NPSR). In rats, NPS and NPSR constitute a novel neuropeptide system expressed both in the central nervous system and in peripheral tissues, controlling visceromotor, neuroendocrine, nociceptive and behavioural responses. To improve the knowledge of the role of the NPS-NPSR system in the gastrointestinal (GI) tract, we investigated: 1- the supraspinal effect of NPS on motor functions of the upper (gastric emptying and gastrointestinal transit) and lower (distal colonic transit and faecal output) GI tract under basal conditions, 2- during pathological states (restraint stress and corticotropin releasing factor (CRF)-induced defecation) in the rat, and 3- the receptor type involved in treatment with NPS using NPS, tachykinin NK(3) and opioid receptor antagonists (([D-Cys(tBu)⁵]NPS), SR142801 and naloxone, respectively). Intracerebroventricular injection of NPS failed to modify basal gastric emptying, gastrointestinal transit and distal colon propulsion, but significantly and dose-dependently reduced faecal pellet excretion and weight stimulated by restraint stress and CRF. The inhibitory effect of NPS on stress-induced defecation was unmodified by pre-treatment with either the tachykinin or opioid receptor antagonists, but was counteracted by a NPSR antagonist. The present study demonstrates, for the first time, that the supraspinal NPS system, which does not participate in the physiological control of GI motility, plays an inhibitory role on defecation stimulated by restraint stress and CRF. The combination of the ability of NPS to inhibit faecal output together with its known anxiolytic effect may be promising, especially in pathological conditions such as irritable bowel syndrome, where stress and the hyperactivity of the CRF system contribute to the co-morbidity of anxiety with colonic motor symptoms such as diarrhoea.

摘要

神经肽 S(NPS)是一种新发现的生物活性肽,能激活孤儿 G 蛋白偶联受体,即 NPS 受体(NPSR)。在大鼠中,NPS 和 NPSR 构成了一种新型的神经肽系统,在中枢神经系统和外周组织中均有表达,可控制内脏运动、神经内分泌、痛觉和行为反应。为了提高对 NPS-NPSR 系统在胃肠道(GI)中的作用的认识,我们研究了:1-NPS 对基础条件下上消化道(胃排空和胃肠道转运)和下消化道(远端结肠转运和粪便排出)运动功能的上脑效应,2-在大鼠的病理状态(束缚应激和促肾上腺皮质释放因子(CRF)诱导的排便)下,3-使用 NPS、速激肽 NK(3)和阿片受体拮抗剂(([D-Cys(tBu)⁵]NPS)、SR142801 和纳洛酮)治疗时涉及的受体类型。脑室注射 NPS 未能改变基础胃排空、胃肠道转运和远端结肠推进,但显著且剂量依赖性地减少束缚应激和 CRF 刺激的粪便颗粒排出和重量。NPS 对应激诱导排便的抑制作用不受速激肽或阿片受体拮抗剂预处理的影响,但被 NPSR 拮抗剂逆转。本研究首次证明,不参与 GI 运动生理控制的上脑 NPS 系统对束缚应激和 CRF 刺激的排便具有抑制作用。NPS 抑制粪便排出的能力与其已知的抗焦虑作用相结合可能很有前途,特别是在应激和 CRF 系统过度活跃导致焦虑与腹泻等结肠运动症状并存的病理条件下,如肠易激综合征。

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