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血清素能激动剂和拮抗剂会影响大鼠的耐力表现。

Serotonergic agonists and antagonists affect endurance performance in the rat.

作者信息

Bailey S P, Davis J M, Ahlborn E N

机构信息

Department of Exercise Science, School of Public Health, University of South Carolina.

出版信息

Int J Sports Med. 1993 Aug;14(6):330-3. doi: 10.1055/s-2007-1021187.

DOI:10.1055/s-2007-1021187
PMID:8407063
Abstract

The purpose of this experiment was to examine the effects of administration of serotonergic (5-HT) agonist and antagonist drugs on run-time to exhaustion (RUN-EXH) in male and female rats. RUN-EXH was reduced (p < 0.05) in a dose related manner by increasing dosages of quipazine dimaleate (QD: general 5-HT agonist) (0-5 mg.kg-1 i.p.) administered immediately prior to exercise (treadmill running at 20 m.min-1 and 5% grade). Conversely, RUN-EXH was increased (p < 0.05) by the greatest dosage of LY 53,857 (LY: 5-HT1C and 5-HT2 antagonist) (1.5 mg.kg-1 i.p.). Drug effects were similar in male and female rats. The negative effects of QD administration on RUN-EXH were not attenuated by administration of the peripherally restricted antagonist, xylamidine tosylate (up to 200 ug.kg-1 i.p.). The results of this investigation indicated that fatigue during prolonged exercise can be influenced by direct pharmacological administration of a serotonergic agonist and antagonist and that the mechanisms underlying these effects are likely to be central (brain) in nature.

摘要

本实验的目的是研究给予血清素能(5-羟色胺,5-HT)激动剂和拮抗剂药物对雄性和雌性大鼠运动至疲惫时间(RUN-EXH)的影响。在运动(以20米/分钟的速度和5%的坡度在跑步机上跑步)前立即腹腔注射不同剂量的马来酸喹哌嗪(QD:一般5-HT激动剂)(0 - 5毫克/千克),RUN-EXH以剂量相关的方式缩短(p < 0.05)。相反,腹腔注射最大剂量的LY 53,857(LY:5-HT1C和5-HT2拮抗剂)(1.5毫克/千克)可使RUN-EXH延长(p < 0.05)。药物对雄性和雌性大鼠的作用相似。给予外周限制拮抗剂甲苯磺酸赛拉米定(腹腔注射剂量高达200微克/千克)并不能减弱QD给药对RUN-EXH的负面影响。本研究结果表明,长时间运动期间的疲劳可受到血清素能激动剂和拮抗剂的直接药理学给药的影响,并且这些作用的潜在机制可能本质上是中枢性的(大脑)。

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