Qi M, Jones S B
Department of Physiology, Loyola University of Chicago, Stritch School of Medicine, Maywood, Illinois.
Circ Shock. 1990 Oct;32(2):153-63.
The effect of the platelet activating factor (PAF) antagonist WEB 2086 on blood pressure; heart rate; and plasma glucose, lactate, and catecholamine concentrations were examined following either PAF or endotoxin administration in conscious rats. PAF infusion (50 ng/kg/min for 60 min) resulted in a sustained hypotension, with tachycardia and elevated plasma norepinephrine (NE; 1.8-fold increase), epinephrine (E; 6.7-fold increase), and dopamine (DA; 1.0-fold increase) at 30 min after beginning infusion. Plasma NE, E, and DA became 4.1 (NE)-, 17.4 (E)-, and 3.3 (DA)-fold higher than control at 60 min after beginning infusion. Both the hemodynamic and plasma catecholamine alterations induced with PAF were completely blocked with WEB 2086 pretreatment. Bacterial endotoxin treatment (5 mg/kg, i.v. bolus) produced well-characterized responses of hypotension, tachycardia, hyperglycemia, hyperlactacidemia, and an elevation in plasma catecholamines. Whereas complete blockade of the hypotensive and tachycardic effect of endotoxin was achieved with WEB 2086 at 30 min following endotoxin, the increases in plasma catecholamines and lactate elicited by endotoxin were attenuated but remained significantly higher than control levels. Hyperglycemia following endotoxin was not altered by WEB 2086 treatment. In endotoxic rats pretreated with WEB 2086 there was significant hypotension, tachycardia, and hyperlactacidemia and an elevation in plasma catecholamines at both 60 and 120 min, but all were less severe compared to non-WEB 2086-treated endotoxic animals. The results demonstrate that WEB 2086 completely blocked early endotoxin-induced hypotension and tachycardia but not catecholamine elevation following endotoxin. This work suggests that sympathetic activation following endotoxin may be mediated by factors other than hypotension.
在清醒大鼠中,分别给予血小板活化因子(PAF)或内毒素后,研究了PAF拮抗剂WEB 2086对血压、心率以及血浆葡萄糖、乳酸和儿茶酚胺浓度的影响。输注PAF(50 ng/kg/分钟,持续60分钟)导致持续低血压,输注开始30分钟时出现心动过速,血浆去甲肾上腺素(NE;增加1.8倍)、肾上腺素(E;增加6.7倍)和多巴胺(DA;增加1.0倍)升高。输注开始60分钟时,血浆NE、E和DA分别比对照高4.1(NE)、17.4(E)和3.3(DA)倍。PAF诱导的血流动力学和血浆儿茶酚胺改变均被WEB 2086预处理完全阻断。细菌内毒素处理(5 mg/kg,静脉推注)产生了典型的低血压、心动过速、高血糖、高乳酸血症和血浆儿茶酚胺升高反应。虽然在内毒素给药后30分钟时,WEB 2086完全阻断了内毒素的降压和心动过速作用,但内毒素引起的血浆儿茶酚胺和乳酸升高有所减弱,但仍显著高于对照水平。WEB 2086处理未改变内毒素后的高血糖。在预先用WEB 2086处理的内毒素大鼠中,60分钟和120分钟时均出现明显的低血压、心动过速、高乳酸血症和血浆儿茶酚胺升高,但与未用WEB 2086处理的内毒素动物相比,所有这些情况都较轻。结果表明,WEB 2086完全阻断了早期内毒素诱导的低血压和心动过速,但未阻断内毒素后的儿茶酚胺升高。这项研究表明,内毒素后的交感神经激活可能由低血压以外的因素介导。