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.
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.
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.