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首页> 外文期刊>Toxicon: An International Journal Devoted to the Exchange of Knowledge on the Poisons Derived from Animals, Plants and Microorganisms >THERAPEUTIC EFFECTS OF ANTIVENOM SUPPLEMENTED BY ANTITHROMBIN III IN RATS EXPERIMENTALLY ENVENOMATED WITH RUSSELLS VIPER (DABOIA RUSSELLI SIAMENSIS) VENOM
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THERAPEUTIC EFFECTS OF ANTIVENOM SUPPLEMENTED BY ANTITHROMBIN III IN RATS EXPERIMENTALLY ENVENOMATED WITH RUSSELLS VIPER (DABOIA RUSSELLI SIAMENSIS) VENOM

机译:抗坏血酸III补充的抗肿瘤药对实验性被维塞尔病毒(DABOIA RUSSELLI SIAMENSIS)毒杀的大鼠的治疗作用

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摘要

The effects of equine antivenom and antithrombin III (AT-III) on the coagulopathy induced by Russell's viper venom (RVV, Daboia russelli siamensis) were investigated in the rat. After taking blood samples from the femoral vein for determination of simple blood clotting time and AT-III activity, all anaesthetized rats received an intramuscular injection of venom (2 mu g/g). Treatment (antivenom or AT-III or both) was given intravenously through another femoral vein 30 min after venom injection. All untreated rats (n = 7) developed AT-III depletion (<70%) [mean (S.D.)] 70 (36) min, and incoagulable blood 85 (53) min after venom injection. Supplementation with AT-III (either 0.25 U/g or 0.5 U/g) had no effect on the RW induced coagulopathy (n = 20). Treatment with antivenom alone (10 mu g/g) reduced the incidence of abnormal clotting significantly (8/15, 53%) (P = 0.03). When antivenom was given in combination with AT-III (0.5 U/g), abnormal clotting was prevented in all but one animal (1/15, 7%) (P = 0.007). AT-III activity declined progressively in all rats which developed non-clotting blood. These results suggest that coagulopathy in Russell's viper envenoming is associated with activation of coagulation and consumption of AT-III. Antivenom can prevent coagulopathy, but its neutralizing activity is augmented significantly by AT-III supplementation. [References: 26]
机译:在大鼠中研究了马抗蛇毒和抗凝血酶III(AT-III)对Russell蛇毒(RVV,russsia siamensis)诱发的凝血病的影响。从股静脉采集血样以确定简单的凝血时间和AT-III活性后,所有麻醉的大鼠均进行肌内注射毒液(2μg / g)。注射毒液后30分钟,通过另一股静脉静脉给予治疗(抗胆碱或AT-III或两者)。注射毒液后,所有未治疗的大鼠(n = 7)均出现AT-III耗竭(<70%)[平均值(标准差)] 70(36)min,可凝结血液85(53)min。补充AT-III(0.25 U / g或0.5 U / g)对RW引起的凝血病没有影响(n = 20)。单独使用抗蛇毒血清(10μg / g)治疗可显着降低异常凝血的发生率(8 / 15,53%)(P = 0.03)。当抗蛇毒血清与AT-III(0.5 U / g)一起使用时,除了一只动物(1/15,7%)外,其他所有动物都可以防止异常凝血(P = 0.007)。在产生不凝血的所有大鼠中,AT-III活性逐渐降低。这些结果表明,罗素毒蛇毒化中的凝血病与凝血的活化和AT-III的消耗有关。抗毒液可以预防凝血病,但是通过补充AT-III可以显着增强其中和活性。 [参考:26]

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