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毒蕈碱拮抗剂哌仑西平和加拉明对大鼠大脑皮层神经元自发反应和诱发反应的影响。

Effects of the muscarinic antagonists pirenzepine and gallamine on spontaneous and evoked responses of rat cerebral cortical neurones.

作者信息

Swanson T H, Phillis J W

机构信息

Department of Physiology, Wayne State University School of Medicine, Detroit, MI 48201.

出版信息

Br J Pharmacol. 1988 May;94(1):192-8. doi: 10.1111/j.1476-5381.1988.tb11515.x.

Abstract
  1. The muscarinic receptor antagonists gallamine and pirenzepine were iontophoretically applied to rat cerebral cortical cholinoceptive neurones, including corticospinal neurones, to assess their effects on spontaneous firing, and firing induced by: stimulation of the nucleus basalis magnocellularis (NBM); contralateral hindpaw stimulation; application of acetylcholine (ACh); and application of glutamate. 2. Both compounds potently inhibited firing induced by ACh iontophoresis, whilst neither compound consistently altered firing induced by application of glutamate. 3. Gallamine was very effective and pirenzepine less effective, at inhibiting both spontaneous firing and the delayed firing induced by NBM stimulation. The short-latency excitations elicited by NBM stimulation were enhanced by these muscarinic antagonists. 4. Gallamine and pirenzepine enhanced cortical cholinoceptive cell firing induced by contralateral hindpaw stimulation. 5. It is concluded that gallamine depresses spontaneous activity more than pirenzepine, and that both compounds can affect the cortical cell firing evoked by stimulation of the NBM and of thalamo-cortical afferent fibres.
摘要
  1. 将毒蕈碱受体拮抗剂加拉明和哌仑西平通过离子电泳法施加于大鼠大脑皮质胆碱能感受神经元,包括皮质脊髓神经元,以评估它们对自发放电以及由以下刺激诱导的放电的影响:刺激大细胞基底核(NBM);对侧后爪刺激;施加乙酰胆碱(ACh);以及施加谷氨酸。2. 这两种化合物均能有效抑制由ACh离子电泳诱导的放电,而这两种化合物均未持续改变由谷氨酸施加诱导的放电。3. 加拉明在抑制自发放电和由NBM刺激诱导的延迟放电方面非常有效,而哌仑西平效果较差。这些毒蕈碱拮抗剂增强了由NBM刺激引起的短潜伏期兴奋。4. 加拉明和哌仑西平增强了由对侧后爪刺激诱导的皮质胆碱能感受细胞放电。5. 得出的结论是,加拉明比哌仑西平更能抑制自发活动,并且这两种化合物都能影响由NBM刺激和丘脑-皮质传入纤维刺激诱发的皮质细胞放电。

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