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尼古丁诱发震颤的药理学特征:抗震颤和抗癫痫药物的反应。

Pharmacological characterization of nicotine-induced tremor: Responses to anti-tremor and anti-epileptic agents.

机构信息

Department of Pharmacology, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan.

Department of Pharmacology, Osaka University of Pharmaceutical Sciences, 4-20-1 Nasahara, Takatsuki, Osaka 569-1094, Japan.

出版信息

J Pharmacol Sci. 2018 Jun;137(2):162-169. doi: 10.1016/j.jphs.2018.05.007. Epub 2018 Jun 7.

Abstract

We previously showed that nicotine evoked kinetic tremor by activating the inferior olive, which is implicated in the pathogenesis of essential tremor, via α7 nicotinic acetylcholine receptors. Here, we evaluated the effects of various anti-tremor and anti-epileptic agents on nicotine-induced tremor in mice to clarify the pharmacological characteristics of nicotine tremor. Drugs effective for essential tremor, propranolol, diazepam and phenobarbital, all significantly inhibited kinetic tremor induced by an intraperitoneal (i.p.) injection of nicotine (1 mg/kg). In contrast, none of the medications for Parkinson's disease, l-DOPA, bromocriptine or trihexyphenidyl, affected the nicotine tremor. Among the anti-epileptic agents examined, valproate, carbamazepine and ethosuximide, significantly inhibited nicotine-induced tremor. In addition, a selective T-type Ca channel blocker, TTA-A2, also suppressed the nicotine tremor. However, neither gabapentin, topiramate, zonisamide nor levetiracetam significantly affected nicotine-induced tremor. The present results show that nicotine-induced tremor resembles essential tremor not only on the neural basis, but also in terms of the pharmacological responses to anti-tremor agents, implying that nicotine-induced tremor can serve as a model for essential tremor. In addition, it is suggested that anti-epileptic agents, which have stimulant actions on the GABAergic system or blocking actions on voltage-gated Na channels and T-type Ca channels, can alleviate essential tremor.

摘要

我们之前的研究表明,尼古丁通过激活橄榄下核(该核与原发性震颤的发病机制有关),经由α7 烟碱型乙酰胆碱受体引起运动性震颤。在这里,我们评估了各种抗震颤和抗癫痫药物对小鼠尼古丁诱导震颤的影响,以阐明尼古丁震颤的药理学特征。对原发性震颤有效的药物普萘洛尔、地西泮和苯巴比妥均能显著抑制腹腔注射(i.p.)尼古丁(1mg/kg)引起的运动性震颤。相比之下,帕金森病的治疗药物左旋多巴、溴隐亭或苯海索均不影响尼古丁震颤。在所检查的抗癫痫药物中,丙戊酸钠、卡马西平和乙琥胺显著抑制尼古丁诱导的震颤。此外,选择性 T 型钙通道阻滞剂 TTA-A2 也能抑制尼古丁震颤。然而,加巴喷丁、托吡酯、唑尼沙胺和左乙拉西坦均不能显著影响尼古丁诱导的震颤。本研究结果表明,尼古丁诱导的震颤不仅在神经基础上与原发性震颤相似,而且在抗震颤药物的药理反应方面也相似,这意味着尼古丁诱导的震颤可以作为原发性震颤的模型。此外,提示抗癫痫药物,其对 GABA 能系统具有兴奋作用或对电压门控 Na 通道和 T 型钙通道具有阻断作用,可缓解原发性震颤。

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