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神经降压素在麻醉豚鼠中引发的血流动力学和腹部运动反射。

Haemodynamic and abdominal motor reflexes elicited by neurotensin in anaesthetized guinea-pigs.

作者信息

Rioux F, Lemieux M

机构信息

Centre de Recherche, Université Laval, Hôtel-Dieu de Québec, Canada.

出版信息

Br J Pharmacol. 1992 May;106(1):187-95. doi: 10.1111/j.1476-5381.1992.tb14313.x.

Abstract
  1. Single intraperitoneal (i.p.) injections of neurotensin (NT) (0.14- 140 nmol kg-1) in anaesthetized guinea-pigs were found to trigger transient abdominal wall contractions (TAWC) accompanied by relatively sustained increases of systemic blood pressure (BP) and heart rate (HR). The modification of the latter NT effects by various drugs and surgical manipulations was examined to obtain some insight into the nature of, and possible relationship between, these responses. 2. The abdominal motor response (i.e. TAWC) to i.p. NT (14 nmol kg-1) was inhibited by prior i.v. injection of the guinea-pigs with pancuronium (0.27 mumol kg-1), morphine (1.5 and 15 mumol kg-1), clonidine (0.34 mumol kg-1), by concomitant i.p. injection of procaine 2% w/v, or by acute spinalization. It was potentiated by naloxone (2.8 and 28 mumol kg-1), but not affected by i.v. injection of autonomic drugs (i.e. pentolinium, prazosin, yohimbine and atropine), by capsaicin desensitization, or by acute bilateral cervical vagotomy. In spinalized animals a sustained abdominal wall contraction (SAWC) was unmasked, which was resistant to i.v. morphine, clonidine or baclofen but suppressed by i.v. pancuronium or i.p. lignocaine 2% w/v. 3. Haemodynamic responses to i.p. NT were not affected by i.v. pancuronium, morphine, naloxone, atropine, or by vagotomy. They were inhibited by i.v. pentolinium or clonidine (BP, HR), i.v. prazosin (BP), i.p. procaine 2% w/v (BP, HR), capsaicin desensitization or acute spinalization (BP, HR). Yohimbine (i.v.) potentiated BP and HR increases caused by i.p. NT.4. These results suggest that: (1) the haemodynamic and TAWC responses to i.p. NT in this animal model, are two independent, neurally-mediated reflexes which are likely to originate from the abdominal cavity and require a functionally intact spinal cord for their full expression; (2) the neural pathways subserving both types of responses appear to be different from each other. The nature and time-response characteristics of the reflexes caused by i.p. NT, raise the possibility that i.p. NT is a noxious stimulus, at least in guinea-pigs.
摘要
  1. 在麻醉的豚鼠体内单次腹腔注射神经降压素(NT)(0.14 - 140 nmol·kg⁻¹),发现会引发短暂的腹壁收缩(TAWC),同时伴有全身血压(BP)和心率(HR)相对持续的升高。通过各种药物和手术操作来改变NT的后一种效应,以深入了解这些反应的性质以及它们之间可能的关系。2. 腹腔注射NT(14 nmol·kg⁻¹)引起的腹部运动反应(即TAWC),在预先静脉注射泮库溴铵(0.27 μmol·kg⁻¹)、吗啡(1.5和15 μmol·kg⁻¹)、可乐定(0.34 μmol·kg⁻¹)的豚鼠中,或通过同时腹腔注射2% w/v的普鲁卡因,或通过急性脊髓横断而受到抑制。它被纳洛酮(2.8和28 μmol·kg⁻¹)增强,但不受静脉注射自主神经药物(即潘托林铵、哌唑嗪、育亨宾和阿托品)、辣椒素脱敏或急性双侧颈迷走神经切断术的影响。在脊髓横断的动物中,一种持续的腹壁收缩(SAWC)被揭示出来,它对静脉注射吗啡、可乐定或巴氯芬有抗性,但被静脉注射泮库溴铵或腹腔注射2% w/v的利多卡因所抑制。3. 腹腔注射NT引起的血流动力学反应不受静脉注射泮库溴铵、吗啡、纳洛酮、阿托品或迷走神经切断术的影响。它们被静脉注射潘托林铵或可乐定(BP、HR)、静脉注射哌唑嗪(BP)、腹腔注射2% w/v的普鲁卡因(BP、HR)、辣椒素脱敏或急性脊髓横断(BP、HR)所抑制。育亨宾(静脉注射)增强了腹腔注射NT引起的BP和HR升高。4. 这些结果表明:(1)在这个动物模型中,腹腔注射NT引起的血流动力学和TAWC反应是两种独立的、神经介导的反射,它们可能起源于腹腔,并且需要功能完整的脊髓才能充分表现出来;(2)介导这两种反应的神经通路似乎彼此不同。腹腔注射NT引起的反射的性质和时间反应特征,增加了腹腔注射NT至少在豚鼠中是一种有害刺激的可能性。

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