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花生四烯酸乙醇胺对麻醉大鼠肺迷走神经C纤维的刺激作用:1型香草酸受体的作用

Stimulation of pulmonary vagal C-fibres by anandamide in anaesthetized rats: role of vanilloid type 1 receptors.

作者信息

Lin You Shuei, Lee Lu-Yuan

机构信息

Department of Physiology, University of Kentucky, 800 Rose Street, Lexington, KY 40536, USA.

出版信息

J Physiol. 2002 Mar 15;539(Pt 3):947-55. doi: 10.1113/jphysiol.2001.013290.

Abstract

This study was carried out to determine the effect of intravenous injection of anandamide on pulmonary C-fibre afferents and the cardiorespiratory reflexes. In anaesthetized, spontaneously breathing rats, intravenous bolus injection of anandamide near the right atrium immediately elicited the pulmonary chemoreflex responses, characterized by apnoea, bradycardia and hypotension. After perineural treatment of both cervical vagi with capsaicin to block the conduction of C-fibres, anandamide no longer evoked these reflex responses. In open-chest, and artificially ventilated rats, anandamide injection evoked an abrupt and intense discharge in vagal pulmonary C-fibres in a dose-dependent manner. After injection of the high dose, the fibre discharge generally started within 1 s, reached a peak in approximately 2 s, and returned to baseline within 7 s. The stimulation of C-fibres by anandamide was completely and reversibly blocked by pretreatment with capsazepine, a competitive antagonist of the vanilloid type 1 receptor. Anandamide (0.4 mg kg(-1)) stimulated approximately 93 % of pulmonary C-fibres that were activated by capsaicin at a much lower dose (0.6 microg kg(-1)); the response to anandamide showed similar intensity, but had slightly longer latency and duration than that to capsaicin. In conclusion, intravenous bolus injection of anandamide evokes a consistent and distinct stimulatory effect on pulmonary C-fibre terminals, and this effect appears to be mediated through an activation of the vanilloid type 1 receptor.

摘要

本研究旨在确定静脉注射花生四烯乙醇胺对肺C纤维传入神经及心肺反射的影响。在麻醉、自主呼吸的大鼠中,在右心房附近静脉推注花生四烯乙醇胺立即引发肺化学反射反应,其特征为呼吸暂停、心动过缓和低血压。在用辣椒素对双侧颈迷走神经进行神经周围处理以阻断C纤维传导后,花生四烯乙醇胺不再诱发这些反射反应。在开胸、人工通气的大鼠中,注射花生四烯乙醇胺以剂量依赖的方式引起迷走神经肺C纤维突然且强烈的放电。注射高剂量后,纤维放电通常在1秒内开始,约2秒达到峰值,并在7秒内恢复到基线。用辣椒素受体1型竞争性拮抗剂辣椒平预处理可完全且可逆地阻断花生四烯乙醇胺对C纤维的刺激。花生四烯乙醇胺(0.4 mg kg⁻¹)刺激了约93%的肺C纤维,这些纤维在低得多的剂量(0.6 μg kg⁻¹)下被辣椒素激活;对花生四烯乙醇胺的反应强度相似,但潜伏期和持续时间比辣椒素略长。总之,静脉推注花生四烯乙醇胺对肺C纤维终末产生一致且独特的刺激作用,且这种作用似乎是通过激活辣椒素受体1型介导的。

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