摘要
CuCl_2/抗坏MK体系产生的羟自由基(·OH)在离体条件下可抑制血浆及纯品抗凝血酶Ⅲ(AT-Ⅲ)活性,诱发AT-Ⅲ纯品解聚,这种损伤呈明显的量效。时效关系。且血浆稀释度越高。AT-Ⅲ损伤越重。0.1-0.6mmol·L ̄(-1)没食子酸乙酯。丙酯和异丁酯抑制血浆AT-Ⅲ氧化呈量效关系。0.6mmol·L ̄(-1)时,上述三种酯对AT-Ⅲ氧化的抑制率依次为48.5%,39.1%和40.0%,比较结果表明。这些酯与另三种抗血栓药抑制AT-Ⅲ纯品解聚的作用强度为川芎嗪<阿魏酸钠<儿茶精<没食子酸酯.
The activities of plasma antithrombin Ⅲ(AT-Ⅲ),crude or purified,can be in-hibited by hydroxyl radical produced byCuCl_2/ascorbic acid svstem in vitro,and the purifiedAT-Ⅲ also can be cleavaged by this system,The inhi-bition was dosage-and time-dependent.The higherthe dilution of plasma, the heavier the AT-Ⅲdamagewas observed. The protective effects of 0-0.6mmol·L ̄(-1)ethyl gallate, propyl gallate and isobutyl gallateagainst plasma AT-Ⅲ oxidation were dosage-depen-dent. At 0.6mmol· ̄(-1),the protection percentageagainst plasma AT-Ⅲ oxidation of these esters wereethyl gallate 48.5%,propyl gallate 39.1%and isobutylgallate 40.0%,respectively. The order of the protectivepotency of these esters and other three anti-thrombotic drugs was pyrazine < sodium ferulate <catechuicine<gallic esters.
出处
《中国药理学与毒理学杂志》
CAS
CSCD
北大核心
1995年第1期50-53,共4页
Chinese Journal of Pharmacology and Toxicology