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速尿对马运动期间血流动力学反应的影响。

Influence of furosemide on hemodynamic responses during exercise in horses.

作者信息

Olsen S C, Coyne C P, Lowe B S, Pelletier N, Raub E M, Erickson H H

机构信息

Departments of Anatomy and Physiology, College of Veterinary Medicine, Kansas State University, Manhattan 66506.

出版信息

Am J Vet Res. 1992 May;53(5):742-7.

PMID:1524299
Abstract

Four hours prior to exercise on a high-speed treadmill, 4 dosages of furosemide (0.25, 0.50, 1.0, and 2.0 mg/kg of body weight) and a control treatment (10 ml of 0.9% NaCl) were administered IV to 6 horses. Carotid arterial pressure (CAP), pulmonary arterial pressure (PAP), and heart rate were not different in resting horses before and 4 hours after furosemide administration. Furosemide at dosage of 2 mg/kg reduced resting right atrial pressure (RAP) 4 hours after furosemide injection. During exercise, increases in treadmill speed were associated with increases in RAP, CAP, PAP, and heart rate. Furosemide (0.25 to 2 mg/kg), administered 4 hours before exercise, reduced RAP and PAP during exercise in dose-dependent manner, but did not influence heart rate. Mean CAP was reduced by the 2-mg/kg furosemide dosage during exercise at 9 and 11 m/s, but not at 13 m/s. During recovery, only RAP was decreased by furosemide administration. Plasma lactate concentration was not significantly influenced by furosemide administration. Furosemide did not influence PCV or hemoglobin concentration at rest prior to exercise, but did increase both variables in dose-dependent manner during exercise and recovery. However, the magnitude of the changes in PCV and hemoglobin concentration were small in comparison with changes in RAP and PAP, and indicate that furosemide has other properties in addition to its diuretic activities. Furosemide may mediate some of its cardiopulmonary effects by vasodilatory activities that directly lower pulmonary arterial pressure, but also increase venous capacitance, thereby reducing venous return to the atria and cardiac filling.

摘要

在高速跑步机上运动前4小时,对6匹马静脉注射4种剂量的呋塞米(0.25、0.50、1.0和2.0mg/kg体重)以及一种对照处理(10ml 0.9%氯化钠)。在给予呋塞米前和给药后4小时,静息状态下的马的颈动脉压(CAP)、肺动脉压(PAP)和心率没有差异。注射呋塞米4小时后,2mg/kg剂量的呋塞米降低了静息右心房压(RAP)。运动期间,跑步机速度的增加与RAP、CAP、PAP和心率的增加相关。运动前4小时给予的呋塞米(0.25至2mg/kg),在运动期间以剂量依赖性方式降低了RAP和PAP,但不影响心率。在9和11m/s的运动速度下,2mg/kg呋塞米剂量降低了平均CAP,但在13m/s时没有降低。恢复期间,只有给予呋塞米降低了RAP。血浆乳酸浓度未受呋塞米给药的显著影响。呋塞米在运动前静息状态下不影响红细胞压积(PCV)或血红蛋白浓度,但在运动和恢复期间以剂量依赖性方式增加了这两个变量。然而,与RAP和PAP的变化相比,PCV和血红蛋白浓度变化的幅度较小,这表明呋塞米除了具有利尿活性外还有其他特性。呋塞米可能通过血管舒张活性介导其一些心肺效应,这种活性直接降低肺动脉压,但也增加静脉容量,从而减少静脉回流至心房和心脏充盈。

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