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大鼠耳颞神经传递中突触前毒蕈碱M1和M2受体的调节作用

Presynaptic muscarinic M1 and M2 receptor modulation of auriculotemporal nerve transmission in the rat.

作者信息

Tobin G

机构信息

Department of Pharmacology, Göteborg University, Sweden.

出版信息

J Auton Nerv Syst. 1998 Aug 6;72(1):61-71. doi: 10.1016/s0165-1838(98)00088-5.

Abstract

Parotid secretory and vascular responses to electrical stimulation of the parasympathetic innervation were measured in anaesthetized rats. Stimulation was performed at 1, 10 and 40 Hz. Atropine (1.5 micromol/kg i.v.) almost abolished the secretion to stimulation of peptide depleted nerves at 40 Hz, thus confirming the existence of a pure cholinergic response. Atropine also reduced secretion by 74% during stimulation of non-depleted nerves at the same frequency. Selective blockade by the muscarinic M1 receptor antagonist pirenzepine and by the muscarinic M2 receptor antagonist methoctramine was found to occur at doses (50 nmol/kg i.v. and of 300 nmol/kg i.v., respectively) that did not inhibit the responses to exogenous acetylcholine. In the presence of methoctramine, the nerve-evoked fluid responses were increased by 200% at 1 Hz independently of the total number of impulses (10-300), suggesting that M2 receptor activation normally has an inhibitory effect on transmitter release. The magnitude of the increase was inversely related to frequency of stimulation, and changes in the secretory responses occurred at 40 Hz only when non-depleted nerves were stimulated over the longest period employed. The fluid response then increased by 35% and protein concentration by 200%. The vasodilator responses increased at 1 and 10 Hz, but not at 40 Hz. Pirenzepine reduced the secretory and vascular responses at 10 and 40 Hz but only during stimulation over short periods of time. This suggests that M1 receptor activation normally has a facilitatory effect on neurotransmitter release. During stimulation of non-depleted nerves at 10 Hz for 10 impulses, the fluid response was reduced by 29% and the protein concentration by 26%. When the peptide depleted nerves were stimulated at 10 Hz, pirenzepine also reduced the fluid response (by 43%), but not the protein concentration. It is concluded that the release of transmitter from postganglionic nerve fibres in the rat auriculotemporal nerve is modulated by presynaptic muscarinic receptors. Muscarinic M1 receptors normally facilitate cholinergic and peptidergic transmission during short, intense stimulation. On the other hand, muscarinic M2 receptors normally inhibit cholinergic transmission at low frequencies; at higher frequencies, peptidergic transmission is also inhibited, but only after some delay.

摘要

在麻醉大鼠中测量腮腺对副交感神经支配进行电刺激的分泌和血管反应。刺激频率为1、10和40赫兹。静脉注射阿托品(1.5微摩尔/千克)几乎消除了在40赫兹刺激肽耗竭神经时的分泌,从而证实了纯胆碱能反应的存在。在相同频率刺激未耗竭神经期间,阿托品也使分泌减少了74%。发现毒蕈碱M1受体拮抗剂哌仑西平和毒蕈碱M2受体拮抗剂甲溴东莨菪碱的选择性阻断分别发生在不抑制对外源性乙酰胆碱反应的剂量(静脉注射分别为50纳摩尔/千克和300纳摩尔/千克)下。在甲溴东莨菪碱存在的情况下,在1赫兹时神经诱发的液体反应增加了200%,与冲动总数(10 - 300)无关,这表明M2受体激活通常对递质释放有抑制作用。增加的幅度与刺激频率成反比,并且仅在最长刺激时间内刺激未耗竭神经时,在40赫兹时分泌反应才发生变化。此时液体反应增加了35%,蛋白质浓度增加了200%。血管舒张反应在1和10赫兹时增加,但在40赫兹时不增加。哌仑西平在10和40赫兹时降低了分泌和血管反应,但仅在短时间刺激期间。这表明M1受体激活通常对神经递质释放有促进作用。在以10赫兹刺激未耗竭神经10次冲动期间,液体反应减少了29%,蛋白质浓度减少了26%。当以10赫兹刺激肽耗竭神经时,哌仑西平也降低了液体反应(减少了43%),但不降低蛋白质浓度。得出的结论是,大鼠耳颞神经节后神经纤维的递质释放受突触前毒蕈碱受体调节。毒蕈碱M1受体通常在短时间强烈刺激期间促进胆碱能和肽能传递。另一方面,毒蕈碱M2受体通常在低频时抑制胆碱能传递;在较高频率时,肽能传递也受到抑制,但有一定延迟。

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