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咖啡因及其他拟交感神经兴奋剂:作用方式及其对运动表现的影响

Caffeine and other sympathomimetic stimulants: modes of action and effects on sports performance.

作者信息

Jones Gareth

机构信息

Centre for Sports and Exercise Science, Department of Biological Sciences, University of Essex, Wivenhoe Park, Colchester CO4 3SQ, UK.

出版信息

Essays Biochem. 2008;44:109-23. doi: 10.1042/BSE0440109.

Abstract

Stimulants, illegal and legal, continue to be used in competitive sport. The evidence for the ergogenic properties of the most potent stimulants, amphetamines, cocaine and ephedrine, is mostly insubstantial. Low doses of amphetamines may aid performance where effects of fatigue adversely affect higher psychomotor activity. Pseudoephedrine, at high doses, has been suggested to improve high intensity and endurance exercise but phenylpropanolamine has not been proven to be ergogenic. Only caffeine has substantial experimental backing for being ergogenic in exercise. The mode of action of these stimulants centres on their ability to cause persistence of catecholamine neurotransmitters, with the exception of caffeine which is an adenosine receptor antagonist. By these actions, the stimulants are able to influence the activity of neuronal control pathways in the central (and peripheral) nervous system. Rodent models suggest that amphetamines and cocaine interact with different pathways to that affected by caffeine. Caffeine has a variety of pharmacological effects but its affinity for adenosine receptors is comparable with the levels expected to exist in the body after moderate caffeine intake, thus making adenosine receptor blockade the favoured mode of ergogenic action. However, alternative modes of action to account for the ergogenic properties of caffeine have been supported in the literature. Biochemical mechanisms that are consistent with more recent research findings, involving proteins such as DARPP-32 (dopamine and cAMP-regulated phosphoprotein), are helping to rationalize the molecular details of stimulant action in the central nervous system.

摘要

无论是非法还是合法的兴奋剂,都仍在竞技体育中被使用。最有效的兴奋剂——苯丙胺、可卡因和麻黄碱——的促力特性证据大多不足。低剂量的苯丙胺可能有助于提高成绩,因为疲劳效应会对更高的精神运动活动产生不利影响。有人认为,高剂量的伪麻黄碱可以改善高强度和耐力运动,但苯丙醇胺尚未被证明具有促力作用。只有咖啡因在运动中具有促力作用有大量实验依据。除了作为腺苷受体拮抗剂的咖啡因外,这些兴奋剂的作用方式主要在于它们能够使儿茶酚胺神经递质持续存在。通过这些作用,兴奋剂能够影响中枢(和外周)神经系统中神经元控制通路的活动。啮齿动物模型表明,苯丙胺和可卡因与咖啡因影响的不同通路相互作用。咖啡因有多种药理作用,但其对腺苷受体的亲和力与适度摄入咖啡因后体内预期存在的水平相当,因此使腺苷受体阻断成为促力作用的首选方式。然而,文献中也支持了其他解释咖啡因促力特性的作用方式。与最近的研究结果一致的生化机制,涉及如DARPP - 32(多巴胺和cAMP调节的磷蛋白)等蛋白质,有助于阐明兴奋剂在中枢神经系统中作用的分子细节。

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