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杜氏侏膨蝰蛇毒引起的心脏效应:形态功能证据及作用机制

Cardiac effect induced by Crotalus durissus cascavella venom: Morphofunctional evidence and mechanism of action.

作者信息

Simões Letícia O, Alves Quiara L, Camargo Samuel B, Araújo Fênix A, Hora Viviane R S, Jesus Rafael L C, Barreto Breno C, Macambira Simone G, Soares Milena B P, Meira Cássio S, Aguiar Márcio C, Couto Ricardo D, Lomonte Bruno, Menezes-Filho José Evaldo, Cruz Jader S, Vannier-Santos Marcos A, Casais-E-Silva Luciana L, Silva Darizy F

机构信息

Department of Bioregulation, Federal University of Bahia, Salvador, BA, 40110-902, Brazil.

Gonçalo Moniz Institute, FIOCRUZ, Salvador, BA, Brazil.

出版信息

Toxicol Lett. 2021 Feb 1;337:121-133. doi: 10.1016/j.toxlet.2020.11.019. Epub 2020 Nov 22.

Abstract

Envenoming, resulting from snake bites, is a global public health problem. The present study was undertaken to investigate the influence of Crotalus durissus cascavella (Cdcas) venom on cardiac activity and the mechanisms of action underlying its effect. To investigate the inotropic and chronotropic effects induced by Cdcas, studies were performed on the left and right atria. A series of tests were conducted to investigate whether the negative inotropic effect, induced by Cdcas, was related to cardiac damage. Cdcas venom (0.1-30 μg/mL) elicited a significant negative inotropic effect. The addition of Cdcas crude venom (7.5, 15 and 30 μg/mL) did not induce significant alterations in cell proliferation, nor in the enzymatic activity of total-CK and CKMB. Ultrastructural evaluation demonstrated that cardiac cells from isoproterenol and Cdcas groups revealed discreet swelling and displaced intermyofibrillar mitochondria with disorganization of the cristae. No change was observed in cardiac electrical activity in perfused isolated rat hearts with Cdcas. In addition, Cdcas reduced contractility in isolated cardiomyocytes from the rat left ventricle. The negative inotropic effect of Cdcas was reduced by l-NAME (100 μM), PTIO (100 μM), ODQ (10 μM) and KT5823 (1 μM), suggesting the participation of NO/cGMP/PKG pathway due to Cdcas. In non-anesthetized rats, Cdcas induced hypotension followed by bradycardia, the latter was also observed by ECG (anesthetized animals). Our results suggest that the negative inotropic effect induced by Cdcas venom is unrelated to cardiac toxicity, at least, at the concentrations tested; and occurs through of NO/cGMP/PKG pathway, likely leading to hypotension and bradycardia when administered in vivo.

摘要

蛇咬伤导致的中毒是一个全球性的公共卫生问题。本研究旨在调查杜氏响尾蛇(Crotalus durissus cascavella, Cdcas)毒液对心脏活动的影响及其作用机制。为了研究Cdcas诱导的变力性和变时性效应,对左右心房进行了研究。进行了一系列测试,以调查Cdcas诱导的负性变力性效应是否与心脏损伤有关。Cdcas毒液(0.1 - 30μg/mL)引起了显著的负性变力性效应。添加Cdcas粗毒液(7.5、15和30μg/mL)未引起细胞增殖、总肌酸激酶(total-CK)和肌酸激酶同工酶(CKMB)酶活性的显著变化。超微结构评估表明,异丙肾上腺素和Cdcas组的心肌细胞显示出轻微肿胀,肌原纤维间线粒体移位,嵴结构紊乱。在灌注的离体大鼠心脏中,Cdcas对心脏电活动没有影响。此外,Cdcas降低了大鼠左心室分离心肌细胞的收缩力。L- NAME(100μM)、PTIO(100μM)、ODQ(10μM)和KT5823(1μM)可降低Cdcas的负性变力性效应,提示Cdcas可激活NO/cGMP/PKG信号通路。在未麻醉的大鼠中,Cdcas引起低血压,随后出现心动过缓,在麻醉动物中通过心电图也观察到了后者。我们的结果表明,至少在所测试的浓度下,Cdcas毒液诱导的负性变力性效应与心脏毒性无关;并且是通过NO/cGMP/PKG信号通路发生的,在体内给药时可能导致低血压和心动过缓。

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