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作 者:王俊科[1] 孙瑞[1] 盛卓人[1] 许国忠[1] 常天辉[1]
出 处:《临床麻醉学杂志》1997年第1期2-5,共4页Journal of Clinical Anesthesiology
摘 要:为观察血液稀释下多培沙明(DPX)、多巴胺(DOP)和多巴酚丁胺(DOB)对外周血管阻力的影响及前者的影响机制,将48只大鼠随机分为Ia、Ib、Ⅱ和Ⅲ四组(每组12只)进行后肢恒流灌注,分别在血液稀释或阻断多巴胺受体2(DA2)及β受体(Ib组)前后注药,记录后肢灌注压(PP)的变化。结果显示:Ia组DPX3、10、30μg/kg使PP下降20%、20%和32%(P<0.01),释稀后DPX不改变PP;Ib组DA2阻断后,PP升高23%(P<0.01),注入DPX使其下降(P<0.05);β受体阻断后PP升高34%(P<0.01),DPX仍使PP明显增高(P<0.01);Ⅱ组DOP小剂量PP无变化,大于10μg/kg使PP增加23%(P<0.05),稀释后DOP使PP更明显升高(P<0.01);Ⅲ,DOB1、3和10μg/kg使PP下降13%、20%和37%(P<0.01),但稀释后DOB不改变PP。提示:血液稀释可减弱DPX及DOB对外周血管的舒缩效应;DPX激动β2受体发挥其扩血管作用;大剂量DOP有明显缩血管作用,血液稀释使其作用增强。To investigate the effects of dopexamine(DPX),dopamine(DOP)and dobutamine(DOB)on peripheral vascular resistance (PR) following acute normovolemic hemodilution,fourty eight rat hindlimb perfused preparations were randomly divided into four groups(n=12 each group):group Ⅰ a given DPX 3,10,30μg/kg,group Ⅱ given DOP 1,3,10,30μg/kg; group Ⅲ given DOB 1,3,10μg/kg;DPX, DOP and DOB were administered before and after hemodilution(Hct to 20%) resulted from blood withdrawal(25ml/kg) and replacement of an equal volume of 6% dextran(mean molecular weight is 7000,000)in 5% glucose and in normal saline,and group Ⅰ b.given DPX 3,10,30μg/kg after selective dopamine receptor 2(DA 2) blockade with haloperidol or β receptors blockade with propranolol.The changes of hindlimb perfusion pressure(PP)were continuously measured to evaluate the responses of PVR to DPX,DOP and DOB.The results:DPX at the dose of 3,10 and 30 μg/kg caused a dosedependent decreases in PP but no changes following hemodilution;After selective DA 2 blockade which resulted in increase of 23% in PP,DPX still caused PP decrease,but DPX increased PP significantly(P<0 01) after β receptors blockade;DOP at the dose of 1 and 3μg/kg had no effect on PP,while DOP at the dose of 10 and 30 μg/kg produced 12% and 23% increases in PP,respectively and more increase(P<0 01) after hemodilution;DOB at the dose of 1,3,10μg/kg resulted in a dose dependent decrease in PP but no change following hemodilution.It is concluded that the vasoactivities of DPX and DOB can be attenuated and vasoconstriction of DOP be potentiated following hemodilution,and that DPX produces vasodilation effect through stimulating β 2 adrenergic receptor.
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