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抗组胺药的抗胆碱能特性对随意和不随意运动的影响。

The effects of antihistamines with varying anticholinergic properties on voluntary and involuntary movement.

机构信息

School of Pharmacy, Griffith University, Gold Coast, Australia.

出版信息

Clin Neurophysiol. 2013 Sep;124(9):1840-5. doi: 10.1016/j.clinph.2013.04.003. Epub 2013 May 3.

Abstract

OBJECTIVE

Recent evidence indicates that antihistamines can affect movement, which is most likely due to altered neurotransmission in cholinergic and histaminergic pathways. The purpose of this study was to determine if antihistamines with varying anticholinergic properties differentially affect voluntary and involuntary movement control.

METHODS

Eleven healthy subjects were enlisted into a human double blind, placebo-controlled, five-way crossover study. Drowsiness, reaction time, and physiological tremor were examined 1-, 2-, and 3-hr post-ingestion of antihistamines with known anticholinergic profiles. These were the first-generation promethazine, and second-generation loratadine, desloratadine, and fexofenadine. Hyoscine butylbromide was used in an additional experiment to determine how a peripheral antimuscarinic drug influenced neuromotor function.

RESULTS

Promethazine, desloratadine and fexofenadine increased drowsiness. Promethazine increased simple and choice reaction time and reduced tremor. Desloratadine increased choice reaction time and tremor, while loratadine slowed simple and choice reaction time.

CONCLUSION

Central anticholinergic and antihistaminergic properties of antihistamines potentially contribute to movement dysfunction.

SIGNIFICANCE

Second-generation antihistamines have provided the consumer with a safer alternative to the first-generation sedating antihistamine. However, the results of this study suggest that loratadine and desloratadine have the potential to affect movement control, and further research is warranted to understand the clinical relevance of these findings.

摘要

目的

最近的证据表明,抗组胺药会影响运动,这很可能是由于胆碱能和组胺能途径中的神经递质传递发生改变。本研究的目的是确定具有不同抗胆碱能特性的抗组胺药是否会对自主和非自主运动控制产生不同的影响。

方法

11 名健康受试者参加了一项人类双盲、安慰剂对照、五向交叉研究。在摄入具有已知抗胆碱能特性的抗组胺药 1、2 和 3 小时后,检查嗜睡、反应时间和生理性震颤。这些抗组胺药包括第一代的异丙嗪,以及第二代的氯雷他定、地氯雷他定和非索非那定。在额外的实验中使用了氢溴酸莨菪碱,以确定外周抗毒蕈碱药物如何影响神经运动功能。

结果

异丙嗪、地氯雷他定和非索非那定增加了嗜睡。异丙嗪增加了简单和选择反应时间,降低了震颤。地氯雷他定增加了选择反应时间和震颤,而氯雷他定则减缓了简单和选择反应时间。

结论

抗组胺药的中枢抗胆碱能和抗组胺能特性可能导致运动功能障碍。

意义

第二代抗组胺药为消费者提供了比第一代镇静性抗组胺药更安全的选择。然而,这项研究的结果表明,氯雷他定和地氯雷他定有可能影响运动控制,需要进一步研究以了解这些发现的临床意义。

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