首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effect of the platelet-activating factor antagonist TCV-309 and the cyclo-oxygenase inhibitor ibuprofen on the haemodynamic changes in canine experimental endotoxic shock.
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Effect of the platelet-activating factor antagonist TCV-309 and the cyclo-oxygenase inhibitor ibuprofen on the haemodynamic changes in canine experimental endotoxic shock.

机译:血小板活化因子拮抗剂TCV-309和环加氧酶抑制剂布洛芬对犬实验性内毒素性休克血流动力学变化的影响。

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摘要

1. The present study was conducted in order to examine the effects of the platelet-activating factor (PAF) antagonist, TCV-309, and the cyclo-oxygenase inhibitor, ibuprofen, on the acute haemodynamic responses to endotoxin in anaesthetized dogs. 2. Endotoxin (2 mg kg-1, i.v.) induced a severe hypotension by decreasing both total peripheral resistance (TPR) and cardiac output. Endotoxin also decreased central venous pressure and increased effective vascular compliance (EVC), indicating a blood pooling in the capacitance vessels. 3. The endotoxin-induced hypotension but not the fall in cardiac output, was markedly attenuated by ibuprofen. Ibuprofen abolished the decrease in TPR and even caused a systemic vasoconstriction. Ibuprofen abolished the increase in EVC. 4. The hypotension caused by endotoxin was attenuated by TCV-309 to a lesser extent than ibuprofen. However, the reduction in cardiac output produced by endotoxin was markedly attenuated by the PAF antagonist. TCV-309 also abolished the increase in EVC. In contrast to ibuprofen, TCV-309 did not affect the decrease in TPR caused by endotoxin. 5. Combined treatment with ibuprofen and TCV-309 markedly attenuated the endotoxin-induced hypotension, but not the fall in cardiac output. Nevertheless, when compared with animals treated with ibuprofen alone, treatment with ibuprofen and TCV-309 partly attenuated the endotoxin-induced reduction in cardiac output and systemic vasoconstriction. 6. These data indicate that dilatation of both resistance vessels and capacitance vessels contributes to the endotoxin-induced hypotension.(ABSTRACT TRUNCATED AT 250 WORDS)
机译:1.进行本研究是为了研究血小板活化因子(PAF)拮抗剂TCV-309和环加氧酶抑制剂布洛芬对麻醉犬对内毒素的急性血液动力学反应的影响。 2.内毒素(2 mg kg-1,i.v.)通过降低总外周阻力(TPR)和心输出量引起严重的低血压。内毒素还降低了中心静脉压并增加了有效血管顺应性(EVC),表明在电容血管中积聚了血液。 3.布洛芬可明显减轻内毒素引起的低血压,但不会降低心输出量。布洛芬废除了TPR的降低,甚至引起全身性血管收缩。布洛芬废除了EVC的增加。 4.与布洛芬相比,TCV-309对内毒素引起的低血压的减弱程度较小。但是,PAF拮抗剂可明显减轻内毒素产生的心输出量降低。 TCV-309也取消了EVC的增加。与布洛芬相反,TCV-309不影响内毒素引起的TPR降低。 5.布洛芬和TCV-309联合治疗可明显减轻内毒素引起的低血压,但不会降低心输出量。但是,与仅用布洛芬治疗的动物相比,用布洛芬和TCV-309治疗可部分减轻内毒素诱导的心输出量减少和全身血管收缩。 6.这些数据表明,阻力血管和电容血管的扩张均会导致内毒素引起的低血压。(摘要截断为250字)

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