Silva-Magalhães Rafaela, Gomes Dos Santos Ayla Mel, Silva-Araújo Ana Luiza, Peres-Damásio Pamella Luize, Gonçalves de Alvarenga Valéria, Souza de Oliveira Luciana, Sanchez Eladio Flores, Chávez-Olórtegui Carlos, Varela Luana Silveira da Rocha Nowicki, Paiva Ana Luiza Bittencourt, Guerra-Duarte Clara
Molecular Toxinology Lab, Research and Development Department, Ezequiel Dias Foundation-FUNED, Belo Horizonte 30510-010, MG, Brazil.
Animal Venoms Biochemistry Lab, Research and Development Department, Ezequiel Dias Foundation-FUNED, Belo Horizonte 30510-010, MG, Brazil.
Toxins (Basel). 2024 Dec 10;16(12):532. doi: 10.3390/toxins16120532.
Spiders of the genus represent a public health problem in Brazil due to the severity of the cutaneous and systemic effects that may result from their bite. In the systemic form of loxoscelism, hemolytic anemia, thrombocytopenia, and disseminated intravascular coagulation can occur. Despite the seriousness of accidents, the venom of some species has not yet been properly characterized considering these hemotoxic effects, such as that of , , and . To better understand their toxic potential, this study aimed to characterize the hematotoxic properties of these venoms. The crude venom was obtained from specimens of , , and available from Funed's arachnidary. In washed platelets, inhibited platelet aggregation induced by collagen and convulxin, whereas and venoms were able to induce platelet aggregation. In the in vitro hemolysis assays, all venoms experimentally induced direct hemolysis of human erythrocytes in a concentration-dependent manner, with different intensities. Furthermore, evidence suggest that the ABO and Rh systems may influence hemolytic activity. Finally, the studied venoms degraded fibrinogen, suggesting possible alterations in the coagulation cascade. Based in the here-presented preliminary study, in vivo assays in model animals are needed to verify the real toxic potential of these species' venom, building up knowledge to elucidate the action of venoms in blood.
由于蜘蛛叮咬可能导致的皮肤和全身效应的严重性,该属蜘蛛在巴西构成公共卫生问题。在系统性洛矶山蜘蛛中毒形式中,可发生溶血性贫血、血小板减少和弥散性血管内凝血。尽管蜘蛛叮咬事故严重,但考虑到这些血液毒性作用,某些种类蜘蛛的毒液尚未得到充分表征,例如[蜘蛛种类1]、[蜘蛛种类2]和[蜘蛛种类3]的毒液。为了更好地了解它们的毒性潜力,本研究旨在表征这些[蜘蛛种类]毒液的血液毒性特性。粗毒液取自富内德蛛形纲动物馆提供的[蜘蛛种类1]、[蜘蛛种类2]和[蜘蛛种类3]标本。在洗涤后的血小板中,[蜘蛛种类1]毒液抑制胶原和convulxin诱导的血小板聚集,而[蜘蛛种类2]和[蜘蛛种类3]毒液能够诱导血小板聚集。在体外溶血试验中,所有毒液均以浓度依赖性方式实验性地诱导人红细胞直接溶血,但强度不同。此外,有证据表明ABO和Rh系统可能影响溶血活性。最后,所研究的[蜘蛛种类]毒液降解纤维蛋白原,提示凝血级联可能发生改变。基于本初步研究,需要在模型动物中进行体内试验,以验证这些种类蜘蛛毒液的实际毒性潜力,积累知识以阐明[蜘蛛种类]毒液在血液中的作用。