Literature DB >> 12368112

Renal toxicity of Bothrops moojeni snake venom and its main myotoxins.

P S F Barbosa1, A Havt, P E G Facó, T M Sousa, I S A M Bezerra, M C Fonteles, M H Toyama, S Marangoni, J C Novello, H S A Monteiro.   

Abstract

Acute renal failure is one the most common systemic complications after snakebite, however, its pathogenesis remains obscure. In this study we evaluated the renal effects of Bothrops moojeni venom and its myotoxins (Bmtx-I and BmtxII) in rat isolated perfused kidneys. The myotoxins were purified by ion-exchange chromatography and reverse phase HPLC. The whole venom (10 microg/ml) and myotoxins (5 microg/ml) were added to the perfusion system 30 min after the beginning of each perfusion. The renal effects were compared to a control group perfused with modified Krebs-Henseleit solution alone. B. moojeni venom decreased the perfusion pressure (PP), renal vascular resistance (RVR), and the percent sodium, potassium and chloride tubular transport (%TNa(+), %TK(+), %TCl(-)). In contrast, the venom increased the urinary flow (UF), glomerular filtration rate (GFR), and the sodium, potassium and chloride excretion (ENa(+), EK(+), ECl(-)). The renal effects of myotoxin I was very similar to those of the whole venom, but there was an increase rather than a decrease in the PP and RVR. Myotoxin II had no effect on renal physiology, except for a transient decrease in %TK(+). In conclusion, B. moojeni venom caused intense alterations in renal physiology, including a drop in vascular resistance associated with diuresis, natriuresis and kaliuresis. Bmtx-I had an opposite effect when compared to whole venom, showed in the parameters of PP and RVR. Bmtx-II had a mild effect in %TK(+). The apparent inability of Bmtx-II to induce the renal effect similarly to Bmtx-I should be explained by the absence in the Bmtx-II of the C-terminal lysine rich region. Copyright 2002 Elsevier Science Ltd.

Entities:  

Mesh:

Substances:

Year:  2002        PMID: 12368112     DOI: 10.1016/s0041-0101(02)00156-3

Source DB:  PubMed          Journal:  Toxicon        ISSN: 0041-0101            Impact factor:   3.033


  4 in total

1.  Systemic alterations induced by phospholipase A2 , BmooTX-I, isolated from Bothrops moojeni snake venom.

Authors:  Kellen Cristina Torres Costa; Bruna Barbosa de Sousa; Edigar Henrique Vaz Dias; Déborah Fernanda da Cunha Pereira; Mariana Santos Matias; Wilson Júnior Oliveira; Antônio Vicente Mundim; Carla Cristine Neves Mamede; Luíz Fernando Moreira Izidoro; Júnia de Oliveira Costa; Fábio de Oliveira
Journal:  Int J Exp Pathol       Date:  2018-11-20       Impact factor: 1.925

2.  Predicting acute renal failure in Bothrops snakebite patients in a tertiary reference center, Western Brazilian Amazon.

Authors:  Eliane Campos Alves; Jacqueline de Almeida Gonçalves Sachett; Vanderson Souza Sampaio; José Diego de Brito Sousa; Sâmella Silva de Oliveira; Elizandra Freitas do Nascimento; Alessandra Dos Santos Santos; Iran Mendonça da Silva; Ana Maria Moura da Silva; Fan Hui Wen; Mônica Colombini; Marcus Vinicius Guimarães de Lacerda; Wuelton Marcelo Monteiro; Luiz Carlos de Lima Ferreira
Journal:  PLoS One       Date:  2018-08-17       Impact factor: 3.240

3.  CCL-2 and CXCL-8: Potential Prognostic Biomarkers of Acute Kidney Injury after a Bothrops atrox Snakebite.

Authors:  Juliana Costa Ferreira Neves; Hiochelson Najibe Santos Ibiapina; Fábio Magalhães-Gama; Jacqueline Almeida Gonçalves Sachett; Iran Mendonça Silva; Kerolaine Fonseca Coelho; Eliane Campos Alves; Andréa Monteiro Tarragô; Luiz Carlos de Lima Ferreira; Adriana Malheiro; Wuelton Marcelo Monteiro; Allyson Guimarães Costa
Journal:  Mediators Inflamm       Date:  2022-09-07       Impact factor: 4.529

Review 4.  Exploiting the nephrotoxic effects of venom from the sea anemone, Phyllodiscus semoni, to create a hemolytic uremic syndrome model in the rat.

Authors:  Masashi Mizuno; Yasuhiko Ito; B Paul Morgan
Journal:  Mar Drugs       Date:  2012-07-23       Impact factor: 6.085

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.