Etomidate Depresses Spontaneous Complex Spikes Activity of Cerebellar Purkinje Cells via Cannabinoid 1 Receptor in vivo in Mice.

IF 2.9 4区 医学 Q2 PHARMACOLOGY & PHARMACY Pharmacology Pub Date : 2023-01-01 Epub Date: 2023-08-22 DOI:10.1159/000531680
Wen Pan, Chun-Ping Chu, De-Lai Qiu
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引用次数: 0

Abstract

Introduction: Complex spikes (CSs) activity of cerebellar Purkinje cells plays critical roles in motor coordination and motor learning by transferring information to cerebellar cortex, which is an accessible and useful model for neurophysiological investigation. Etomidate is an ultrashort-acting nonbarbiturate intravenous anesthetic, which inhibits the spontaneous activity of cerebellar Purkinje cells through activation of GABAA and glycine receptors in vivo in mice. However, the effect of etomidate on the spontaneous CSs activity of cerebellar Purkinje cells in living mouse is not clear.

Methods: We here investigated the effects of etomidate on spontaneous CSs activity of cerebellar Purkinje cell in urethane-anesthetized mice by electrophysiology recording technique and pharmacological methods.

Results: Our results showed that cerebellar surface perfusion of etomidate significantly depressed the activity of spontaneous CSs, which exhibited decreases in the number of spikelets and the area under curve (AUC) of the CSs. The etomidate-produced inhibition of CSs activity was persisted in the presence of GABAA and glycine receptors antagonists. However, application of cannabinoid 1 (CB1) receptor antagonist, AM-251, completely blocked the etomidate-induced inhibition of CSs. Furthermore, application of the CB1 receptor agonist, WIN55212-2, induced a decrease of CSs. Moreover, in the presence of a specific protein kinase A (PKA) inhibitor, KT5720, etomidate failed to produce decreases in the spikelets number and the AUC of the spontaneous CSs.

Conclusion: These results indicate that cerebellar surface application of etomidate facilitates CB1 receptor activity resulting in a depression of spontaneous CSs activity of Purkinje cells via PKA signaling pathway in mouse cerebellar cortex. Our present results suggest that the etomidate administration may impair the function of cerebellar cortical neuronal circuitry by inhibition of the climbing fiber - Purkinje cells synaptic transmission through activation of CB1 receptors in vivo in mice.

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依托咪酯在小鼠体内通过大麻素1受体抑制小脑浦肯野细胞的自发复合物尖峰活性。
引言:小脑浦肯野细胞的复杂棘波(CS)活动通过将信息传递到小脑皮层,在运动协调和运动学习中发挥着关键作用,这是一种可获得且有用的神经生理学研究模型。依托咪酯是一种超短效非巴比妥类静脉麻醉药,通过激活小鼠体内GABAA和甘氨酸受体来抑制小脑浦肯野细胞的自发活动。然而,依托咪酯对活体小鼠小脑浦肯野细胞自发CSs活性的影响尚不清楚。方法:采用电生理记录技术和药理学方法研究依托咪酯对氨基甲酸乙酯麻醉小鼠小脑浦肯野细胞自发CSs活性的影响。结果:我们的结果表明,小脑表面灌注依托咪酯显著降低了自发CSs的活性,表现为CSs的小穗数和曲线下面积(AUC)降低。依托咪酯对CS活性的抑制作用在GABAA和甘氨酸受体拮抗剂的存在下持续存在。然而,大麻素1(CB1)受体拮抗剂AM-251的应用完全阻断了依托咪酯诱导的CS的抑制作用。此外,CB1受体激动剂WIN55212-2的应用诱导了CS的减少。此外在特异性蛋白激酶a(PKA)抑制剂KT5720存在下,依托咪酯不能降低自发CSs的小穗数和AUC。我们目前的研究结果表明,依托咪酯给药可能通过激活小鼠体内CB1受体来抑制攀爬纤维-浦肯野细胞的突触传递,从而损害小脑皮层神经元回路的功能。
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来源期刊
Pharmacology
Pharmacology 医学-药学
CiteScore
5.60
自引率
0.00%
发文量
52
审稿时长
6-12 weeks
期刊介绍: ''Pharmacology'' is an international forum to present and discuss current perspectives in drug research. The journal communicates research in basic and clinical pharmacology and related fields. It covers biochemical pharmacology, molecular pharmacology, immunopharmacology, drug metabolism, pharmacogenetics, analytical toxicology, neuropsychopharmacology, pharmacokinetics and clinical pharmacology. In addition to original papers and short communications of investigative findings and pharmacological profiles the journal contains reviews, comments and perspective notes; research communications of novel therapeutic agents are encouraged.
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