首页> 外文期刊>Biochemistry >Hemostatic Interference of Indian King Cobra (Ophiophagus hannah) Yenom. Comparison with Three Other Snake Venoms of the Subcontinent
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Hemostatic Interference of Indian King Cobra (Ophiophagus hannah) Yenom. Comparison with Three Other Snake Venoms of the Subcontinent

机译:印度眼镜王蛇(Ophiophagus hannah)Yenom的止血干扰。与次大陆其他三种蛇毒的比较

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摘要

Unlike Naja naja, Bungarus caeruleus, Echis carinatus, and Daboia/Vipera russellii venoms, Ophiophagus hannah venom is medically ignored in the Indian subcontinent. Being the biggest poisonous snake, O. hannah has been presumed to inject several lethal doses of venom in a single bite. Lack of therapeutic antivenom to O. hannah bite in India makes any attempt to save the victim a difficult exercise. This study was initiated to compare O. hannah venom with the above said venoms for possible interference in hemostasis. Ophiophagus hannah venom was found to actively interfere in hemostatic stages such as fibrin clot formation, platelet activation/aggregation, and fibrin clot dissolution. It decreased partial thromboplastin time (aPTT), prothrombin time (PT), and thrombin clotting time (TCT). These activities are similar to that shown by E. carinatus and D. russellii venoms, and thus O. hannah venom was found to exert procoagulant activity through the common pathway of blood coagulation, while N. naja venom increased aPTT and TCT but not PT, and hence it was found to exert anticoagulant activity through the intrinsic pathway. Venoms of 0. hannah, E. carinatus, and D. russellii lack plasminogen activation property as they do not hydrolyze azocasein, while they all show plasmin-like activity by degrading the fibrin clot. Although N. naja venom did not degrade azocasein, unlike other venoms, it showed feeble plasmin-like activity on fibrin clot. Venom of E. carinatus induced clotting of human platelet rich plasma (PRP), while the other three venoms interfered in agonist-induced platelet aggregation in PRP. Venom of O. hannah least inhibited the ADP induced platelet aggregation as compared to D. russellii and N. naja venoms. All these three venoms showed complete inhibition of epineph-rine-induced aggregation at varied doses. However, O. hannah venom was unique in inhibiting thrombin induced aggregation.
机译:与印度眼镜蛇眼镜蛇,印度洋蛇眼镜蛇和印度大蛇ia蛇毒不同,印度次大陆在医学上忽略了印度蛇眼(Ophiophagus hannah)蛇毒。作为最大的毒蛇,汉娜·奥纳(O. hannah)被认为可以一次咬入几剂致命的毒液。在印度缺乏对O. hannah咬伤的治疗性抗癫痫药,使拯救受害者的任何尝试都很困难。发起该研究以将汉娜O. hannah毒液与上述毒液对止血的可能干扰进行比较。人们发现,食腐汉娜毒液会积极干扰止血阶段,例如血纤蛋白凝块形成,血小板活化/聚集和血纤蛋白凝块溶解。它减少了部分凝血活酶时间(aPTT),凝血酶原时间(PT)和凝血酶凝血时间(TCT)。这些活性与Carinatus和D. russellii毒液所显示的活性相似,因此,发现O. hannah毒液通过血液的共同通路发挥促凝活性,而N. naja毒液增加了aPTT和TCT,但不增加PT,因此发现通过内在途径发挥抗凝活性。 0. hannah,E。carinatus和D. russellii的毒液缺乏纤溶酶原激活特性,因为它们不水解偶氮酪蛋白,而它们都通过降解纤维蛋白凝块而显示出类似纤溶酶的活性。尽管与其他毒液不同,眼镜蛇毒液不降解偶氮酪蛋白,但对纤维蛋白凝块显示出微弱的纤溶酶样活性。大肠杆菌的毒液诱导人血小板富集血浆(PRP)凝结,而其他三种毒液则干扰激动剂诱导的血小板在PRP中聚集。与罗氏梭菌和眼镜蛇毒相比,汉娜的毒液对ADP诱导的血小板聚集的抑制作用最小。所有这三种毒液在不同剂量下均显示出完全抑制肾上腺素诱导的聚集的作用。然而,汉娜毒液在抑制凝血酶诱导的聚集方面是独特的。

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