Instituto Clodomiro Picado, Facultad de Microbiología, Universidad de Costa Rica, San José, 11501, Costa Rica.
Laboratorio de Hematología, Hospital Nacional de Niños 'Dr Carlos Sáenz Herrera', Caja Costarricense Del Seguro Social, San José, Costa Rica.
Toxicon. 2022 Jul 30;214:121-129. doi: 10.1016/j.toxicon.2022.05.042. Epub 2022 May 27.
Viperid snakebite envenoming is often characterized by a venom-induced consumption coagulopathy due to the procoagulant effect of venom components, resulting in the alteration of clotting laboratory tests. There is a growing trend to use rotational thromboelastometry in the assessment of clotting disturbances in a variety of pathologies, although its use in experimental models of envenoming has been limited. An in vivo murine model was implemented to assess the coagulopathy induced by three Central American viperid venoms which have different mechanisms of action on clotting factors, i.e., Bothrops asper, Crotalus simus and Bothriechis lateralis. Venom was injected by the intravenous route and blood samples were collected at 1, 3, 5 and 24 h after envenoming. Coagulopathy was assessed by standard clotting tests and by routine rotational thromboelastometric parameters. In addition, the changes in platelet number were followed. B. asper and C. simus venoms induced coagulopathy and thrombocytopenia 1 h after injection, followed by a slow recovery at 3, 5 and 24 h, although the majority of clotting parameters were still significantly affected by 3 and 5 h, and were corrected by 24 h. In general, a similar time-course of alterations was observed for standard clotting tests and most rotational thromboelastomeric assays. However, some thromboelastometric parameters, especially those related to Fibtem, showed more drastic alterations than standard tests and remained altered even at 24 h in some cases. This is likely related to the low fibrinogen concentration observed at most time intervals. B. lateralis venom did not induce a consumption coagulopathy, although it caused a marked thrombocytopenia.
响尾蛇咬伤中毒常因毒液成分的促凝作用导致消耗性凝血病,从而改变凝血实验室检查结果。尽管在蛇毒中毒的实验模型中应用有限,但旋转血栓弹性测定法在评估各种病理情况下的凝血紊乱方面有不断增长的应用趋势。本研究建立了一种体内小鼠模型,以评估三种中美洲响尾蛇毒液引起的凝血紊乱,这三种毒液对凝血因子的作用机制不同,分别为矛头蝮蛇(Bothrops asper)、矛头蝮蛇(Crotalus simus)和矛头蝮蛇(Bothriechis lateralis)。毒液通过静脉途径注射,在中毒后 1、3、5 和 24 小时采集血液样本。通过标准凝血试验和常规旋转血栓弹性测量参数评估凝血紊乱,并监测血小板数量的变化。B. asper 和 C. simus 毒液在注射后 1 小时引起凝血紊乱和血小板减少,随后在 3、5 和 24 小时缓慢恢复,但大多数凝血参数在 3 和 5 小时仍受到显著影响,24 小时时得到纠正。一般来说,标准凝血试验和大多数旋转血栓弹性测定法观察到的变化具有相似的时间过程。然而,一些血栓弹性参数,尤其是与 Fibtem 相关的参数,比标准试验表现出更剧烈的变化,在某些情况下甚至在 24 小时时仍保持改变。这可能与大多数时间间隔观察到的低纤维蛋白原浓度有关。B. lateralis 毒液不会引起消耗性凝血病,尽管它会导致明显的血小板减少。