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毒蕈碱激动剂他索氯铵对麻醉豚鼠包括肾上腺在内的交感神经系统的中枢激活作用。

Central activation of the sympathetic nervous system including the adrenals in anaesthetized guinea pigs by the muscarinic agonist talsaclidine.

作者信息

Walland A, Pieper M P

机构信息

Boehringer Ingelheim KG, Dept. of Biol. Research, General Pharmacology, Ingelheim, Germany.

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1998 Apr;357(4):426-30. doi: 10.1007/pl00005189.

Abstract

Talsaclidine, a novel M1-receptor selective muscarinic agonist for cholinergic substitution therapy of Alzheimer's disease, activates the sympathetic nervous system in guinea pigs and dogs at the orthosympathic ganglia and the paraganglionic adrenals. Results from guinea pigs provide indirect evidence for an additional central site of action. The present investigation in anaesthetized and vagotomized guinea pigs intended to demonstrate central activation of the sympathetic nervous system directly by comparing the blood pressure effects of intracerebroventricular and intravenous injections of small doses of talsaclidine. Increasing doses of 0.2 and 0.6 mg/kg talsaclidine were injected alternately into the third cerebral ventricle and intravenously in 6 guinea pigs before and after blockade of peripheral muscarinic receptors with 1 mg/kg ipratropium bromide i.v. In another group of 6 animals the injections were given into the cisterna cerebellomedullaris using the same protocol. In both groups central administration of talsaclidine caused dose-related hypertension while intravenous injections were hypotensive. Ipratropium bromide, a peripheral antimuscarinic drug, reversed this hypotensive action of intravenous talsaclidine into hypertension, but did not inhibit the effects of central administration. In contrast, atropine, an antimuscarinic drug which passes the blood-brain barrier, abolished the effect of 0.6 mg/kg talsaclidine injected into the cisterna cerebellomedullaris of 8 guinea pigs. The hypertensive effect of a first injection of 0.6 mg/kg talsaclidine into the cisterna cerebellomedullaris of 6 guinea pigs was approximately twice as large as that of a second given 90 min after bilateral adrenalectomy. Sham operation in another 6 animals was not inhibitory. The results demonstrate that talsaclidine, a selective muscarinic M1-receptor agonist, activates central parts of the sympathetic nervous system, including central projections of the adrenals by an action mediated by central muscarinic receptors.

摘要

他索氯定是一种用于阿尔茨海默病胆碱能替代疗法的新型M1受体选择性毒蕈碱激动剂,在豚鼠和犬中,它可在交感神经节和神经节旁肾上腺激活交感神经系统。豚鼠实验结果为其额外的中枢作用位点提供了间接证据。本研究在麻醉且切断迷走神经的豚鼠中进行,旨在通过比较小剂量他索氯定脑室内注射和静脉注射对血压的影响,直接证明其对交感神经系统的中枢激活作用。在6只豚鼠中,先用1mg/kg异丙托溴铵静脉注射阻断外周毒蕈碱受体,然后交替脑室内和静脉注射递增剂量的0.2mg/kg和0.6mg/kg他索氯定。在另一组6只动物中,采用相同方案将药物注射到小脑延髓池。在两组中,他索氯定中枢给药均引起剂量相关的高血压,而静脉注射则导致低血压。外周抗毒蕈碱药物异丙托溴铵将静脉注射他索氯定的低血压作用逆转为高血压,但不抑制中枢给药的作用。相比之下,能透过血脑屏障的抗毒蕈碱药物阿托品消除了8只豚鼠小脑延髓池注射0.6mg/kg他索氯定的作用。6只豚鼠小脑延髓池首次注射0.6mg/kg他索氯定的高血压作用约为双侧肾上腺切除90分钟后第二次注射的两倍。另外6只动物的假手术无抑制作用。结果表明,选择性毒蕈碱M1受体激动剂他索氯定可激活交感神经系统的中枢部分,包括通过中枢毒蕈碱受体介导的作用激活肾上腺的中枢投射。

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