Combining Thiophene-Triazole Hybrids with Bothropic Antivenom to Enhance Its Inhibitory Effect Against the Coagulant Activity of Bothrops Jararaca, B. Neuwiedi, and B. Jararacussu Snake Venoms.

IF 3.6 4区 医学 Q3 CHEMISTRY, MEDICINAL
Brenda Bairral de Oliveira, Eladio Flores Sanchez, Danielle Pagliaminuto Portella, Vitor Francisco Ferreira, Fernando de Carvalho da Silva, Daniel Tadeu Gomes Gonzaga, Andre Lopes Fuly
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引用次数: 0

Abstract

Introduction: Snakebite envenomation causes approximately 5 million incidents, 130,000 deaths, and 400,000 amputations annually worldwide. Thus, the objective of this work was to assess the ability of 16 thiophene-triazole hybrid compounds (6a-6h and 7a-7h) to inhibit the coagulant activity of Bothrops jararaca, B. neuwiedi, and B. jararacussu venoms in combination with commercial antibothropic antivenom.

Method: In the experimental prevention protocol, human plasma or commercial fibrinogen was incubated for 60 seconds at 37°C with the study compounds, with or without antivenom, followed by the addition of snake venoms. In the treatment protocol, each venom was incubated with plasma or fibrinogens for 60 seconds at 37°C, and then the study compounds, with or without antivenom, were added to the medium. Clotting was monitored using a digital coagulometer.

Results: The study compounds inhibited the coagulation of plasma and fibrinogen caused by B. neuwiedi venom under both protocols, but they did not inhibit B. jararacussu venom under the treatment protocol. Overall, the coagulation inhibition was more effective when the study compounds were mixed with antivenom, and some compounds achieved complete prevention of venom- induced coagulation.

Discussion: A combination of compounds with antivenom enhanced efficacy in preventing the coagulant activity of Bothrops venoms.

Conclusion: A drug cocktail comprising the most active compounds mixed with antivenom may be a promising strategy to improve the treatment of envenomation by these snake species.

噻吩-三唑复合物与Bothropic抗蛇毒血清联合增强对Jararaca、B. Neuwiedi和B. Jararacussu蛇毒凝血活性的抑制作用。
简介:全世界每年大约有500万起毒蛇咬伤事件,13万人死亡,40万人截肢。因此,本研究的目的是评估16种噻吩-三唑杂化化合物(6a-6h和7a-7h)与商业抗蛇毒血清联合抑制jararacussu Bothrops、B. newiedi和B. jararacussu毒液的凝血活性。方法:在实验预防方案中,人血浆或商品纤维蛋白原与研究化合物(含或不含抗蛇毒血清)在37℃下孵育60秒,然后加入蛇毒。在治疗方案中,每种毒液与血浆或纤维蛋白原在37℃下孵育60秒,然后将研究化合物(含或不含抗蛇毒血清)添加到培养基中。使用数字凝血仪监测凝血情况。结果:在两种治疗方案下,化合物均能抑制新魏氏小蠊毒液引起的血浆凝血和纤维蛋白原,而在治疗方案下,化合物均无抑制作用。总的来说,当研究化合物与抗蛇毒血清混合使用时,凝血抑制更有效,一些化合物可以完全预防蛇毒诱导的凝血。讨论:化合物与抗蛇毒血清的组合增强了预防Bothrops毒液凝固活性的功效。结论:用抗蛇毒血清混合抗蛇毒血清中最有效的化合物组成的药物鸡尾酒可能是改善这些蛇毒中毒治疗的一种有希望的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.40
自引率
2.90%
发文量
186
审稿时长
3-8 weeks
期刊介绍: Current Topics in Medicinal Chemistry is a forum for the review of areas of keen and topical interest to medicinal chemists and others in the allied disciplines. Each issue is solely devoted to a specific topic, containing six to nine reviews, which provide the reader a comprehensive survey of that area. A Guest Editor who is an expert in the topic under review, will assemble each issue. The scope of Current Topics in Medicinal Chemistry will cover all areas of medicinal chemistry, including current developments in rational drug design, synthetic chemistry, bioorganic chemistry, high-throughput screening, combinatorial chemistry, compound diversity measurements, drug absorption, drug distribution, metabolism, new and emerging drug targets, natural products, pharmacogenomics, and structure-activity relationships. Medicinal chemistry is a rapidly maturing discipline. The study of how structure and function are related is absolutely essential to understanding the molecular basis of life. Current Topics in Medicinal Chemistry aims to contribute to the growth of scientific knowledge and insight, and facilitate the discovery and development of new therapeutic agents to treat debilitating human disorders. The journal is essential for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important advances.
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