4.4 Article

Lipoic acid effects on renal function, aminopeptidase activities and oxidative stress in Crotalus durissus terrificus envenomation in mice

期刊

TOXICON
卷 56, 期 3, 页码 402-410

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.toxicon.2010.04.003

关键词

Comparative toxinology; Snake envenomation; Acute renal failure; Peptidases; Oxidative stress; Lipoic acid

资金

  1. FAPESP (Fundacao de Amparo a Pesquisa do Estado de Sao Paulo, Brazil) [06/06926-9]
  2. CNPq (Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brazil)
  3. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [06/06926-9] Funding Source: FAPESP

向作者/读者索取更多资源

Crotalus durissus terrificus envenomation has been associated with direct nephrotoxicity, rhabdomyolysis, hyperuricemia, urinary hypoosmolality, alterations in aminopeptidase activities (AP) and oxidative stress. This study evaluated the effects of lipoic acid (LA) on renal function, lethality, AP and GSSG/GSH in mice injected with C. d. terrificus venom (vCdt). The doses and routes of administration of LA and vCdt promoted no systemic myotoxicity. LA did not alter significantly the lethality of vCdt. In nonenvenomed, LA induced hypercreatinemia, urinary hyperosmolality, decrease of urinary urea and creatinine, increase of protein in plasma and in soluble fraction (SF) and decrease in membrane-bound fraction (MF) of cortex and medulla. Decreased levels of all AP (except neutral-AP in MF-medulla) were also induced by LA in nonenvenomed. LA associated with vCdt decreased plasma osmolality, hematocrit, urinary uric acid, but increased urinary and SF-medullar protein. LA mitigated the increase of protein in SF-cortex and corrected hyperuricemia, GSSG/GSH and protein in MF-cortex and MF-medulla, as well as decreased plasma neutral AP and acid AP in MF-medulla of envenomed mice. Data suggest that LA contributes to the solubilization/remotion of proteins in MF with impairment of most AP, but it could be beneficial for the treatment of the direct nephrotoxicity of vCdt. (C) 2010 Elsevier Ltd. All rights reserved.

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