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对大鼠中由哈马灵和毒扁豆碱诱导的震颤和运动活动抑制进行同步定量分析。

Concurrent quantification of tremor and depression of locomotor activity induced in rats by harmaline and physostigmine.

作者信息

Wang G, Fowler S C

机构信息

Department of Pharmacology and Toxicology, University of Kansas, Lawrence, KS 66045, USA.

出版信息

Psychopharmacology (Berl). 2001 Nov;158(3):273-80. doi: 10.1007/s002130100882.

Abstract

RATIONALE

Both harmaline and physostigmine are known to produce whole-body tremors in rodents, yet there is little quantitative information on the differential frequency characteristics of these tremors or on other possible motor effects of these drugs. In addition, the degree to which tolerance develops to their tremorogenic effects is uncertain.

OBJECTIVES

The purpose of this work was to use a new kind of instrument (the force-plate actometer) to describe quantitatively the frequency characteristics of tremor induced by the two drugs and simultaneously to measure locomotor activity effects. Another aim was to detect any tolerance effects on the tremor or locomotor measurements.

METHODS

Sprague-Dawley rats in four separate groups received harmaline (0, 4.0, 8.0, and 16.0 mg/kg) while another four groups received physostigmine (0, 0.10, 0.25, and 0.50 mg/kg). Dosing continued for 4 consecutive days. Each day, every rat's whole-body tremor and locomotor activity were recorded for 30 min. Fourier analysis of the force-plate recordings was used to quantify tremor and characterize its frequency components.

RESULTS

Harmaline induced a dose-related tremor that peaked in the 10 Hz region of the spectrum, while the dose related-tremor of physostigmine was demonstrably of a broader-band frequency composition. While harmaline tremor exhibited pronounced tolerance, physostigmine tremor remained substantial across the 4 days of dosing. Both drugs suppressed locomotor activity, and there was no tolerance on this measure for either drug.

CONCLUSIONS

In regard to tremor, harmaline and physostigmine induced quantitatively different kinds of tremor, and these differences probably reflect the drugs' different sites of action in the brain (harmaline: inferior olive; physostigmine: basal ganglia). For harmaline, tolerance to the tremorogenic effect was concurrent with a lack of tolerance to locomotor suppression, and this finding suggested the presence of a strong motor effect of harmaline that continued to be expressed despite the absence of tremor.

摘要

理论依据

已知哈马灵和毒扁豆碱均可使啮齿动物全身震颤,但关于这些震颤的频率差异特征或这些药物其他可能的运动效应,几乎没有定量信息。此外,对它们致颤效应的耐受程度尚不确定。

目的

本研究旨在使用一种新型仪器(测力板活动计)定量描述这两种药物诱发震颤的频率特征,并同时测量运动活动效应。另一个目的是检测对震颤或运动测量的任何耐受效应。

方法

将四组不同的斯普拉格 - 道利大鼠分别给予哈马灵(0、4.0、8.0和16.0mg/kg),而另外四组给予毒扁豆碱(0、0.10、0.25和0.50mg/kg)。给药持续4天。每天记录每只大鼠30分钟的全身震颤和运动活动。使用测力板记录的傅里叶分析来量化震颤并表征其频率成分。

结果

哈马灵诱发剂量相关的震颤,在频谱的10Hz区域达到峰值,而毒扁豆碱的剂量相关震颤明显具有更宽的频率组成。虽然哈马灵震颤表现出明显的耐受性,但在给药的4天中,毒扁豆碱震颤仍然很明显。两种药物均抑制运动活动,且两种药物在该测量指标上均未出现耐受性。

结论

关于震颤,哈马灵和毒扁豆碱诱发了定量上不同类型的震颤,这些差异可能反映了药物在大脑中的不同作用部位(哈马灵:下橄榄核;毒扁豆碱:基底神经节)。对于哈马灵,对致颤效应的耐受性与对运动抑制的耐受性缺乏同时存在,这一发现表明哈马灵存在强烈的运动效应,尽管没有震颤但仍持续表现出来。

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