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色氨酸羟化酶的抑制作用消除了运动大鼠中枢色氨酸引起的疲劳。

Inhibition of tryptophan hydroxylase abolishes fatigue induced by central tryptophan in exercising rats.

机构信息

Exercise Physiology Laboratory, Department of Physical Education, School of Physical Education, Physiotherapy and Occupational Therapy, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil; Department of Physiology and Biophysics, Institute of Biological Sciences, Universidade Federal de Minas Gerais, Belo Horizonte, Minas Gerais, Brazil.

出版信息

Scand J Med Sci Sports. 2014 Feb;24(1):80-8. doi: 10.1111/j.1600-0838.2012.01464.x. Epub 2012 Apr 29.

Abstract

Fatigue during prolonged exercise is related to brain monoamines concentrations, but the mechanisms underlying this relationship have not been fully elucidated. We investigated the effects of increased central tryptophan (TRP) availability on physical performance and thermoregulation in running rats that were pretreated with parachlorophenylalanine (p-CPA), an inhibitor of the conversion of TRP to serotonin. On the 3 days before the experiment, adult male Wistar rats were treated with intraperitoneal (ip) injections of saline or p-CPA. On the day of the experiment, animals received intracerebroventricular (icv) injections of either saline or TRP (20.3 μM) and underwent a submaximal exercise test until fatigue. Icv TRP-treated rats that received ip saline presented higher heat storage rate and a 69% reduction in time to fatigue compared with the control animals. Pretreatment with ip p-CPA blocked the effects of TRP on thermoregulation and performance. Moreover, ip p-CPA administration accelerated cutaneous heat dissipation when compared with saline-pretreated rats. We conclude that an elevated availability of central TRP interferes with fatigue mechanisms of exercising rats. This response is modulated by serotonergic pathways, because TRP effects were blocked in the presence of p-CPA. Our data also support that a depletion of brain serotonin facilitates heat loss mechanisms during exercise.

摘要

在长时间运动中感到疲劳与大脑单胺浓度有关,但这种关系的机制尚未完全阐明。我们研究了增加中枢色氨酸(TRP)供应对预先用对氯苯丙氨酸(p-CPA)处理的跑步大鼠的身体表现和体温调节的影响,p-CPA 是一种将 TRP 转化为 5-羟色胺的抑制剂。在实验前 3 天,成年雄性 Wistar 大鼠接受腹腔(ip)注射盐水或 p-CPA。在实验当天,动物接受脑室内(icv)注射盐水或 TRP(20.3 μM),并进行亚最大运动测试直到疲劳。与对照动物相比,接受 ip 盐水的 icv TRP 处理的大鼠表现出更高的热量储存率和 69%的疲劳时间减少。ip p-CPA 预处理阻断了 TRP 对体温调节和性能的影响。此外,与盐水预处理的大鼠相比,ip p-CPA 给药加速了皮肤散热。我们得出结论,中枢 TRP 的可用性增加会干扰运动大鼠的疲劳机制。这种反应受到 5-羟色胺能途径的调节,因为 p-CPA 存在时 TRP 作用被阻断。我们的数据还支持大脑 5-羟色胺耗竭促进运动过程中的散热机制。

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