Hepatotoxicity and oxidative stress induced by Naja haje crude venom

被引:35
作者
Al-Quraishy, Saleh [1 ]
Dkhil, Mahamed A. [1 ,2 ]
Moneim, Ahmed Esmat Abdel [2 ,3 ]
机构
[1] King Saud Univ, Coll Sci, Dept Zool, Riyadh, Saudi Arabia
[2] Helwan Univ, Fac Sci, Dept Zool & Entomol, Cairo, Egypt
[3] Univ Oviedo, Asturias Inst Biotechnol, Dept Biochem & Mol Biol, E-33006 Oviedo, Spain
关键词
Naja haje venom; Hepatotoxicity; Oxidative stress; Apoptosis; Rats; AMINO-ACID OXIDASE; PHOSPHOLIPASES A(2); SEQUENCE-ANALYSIS; SNAKE-VENOMS; MOUSE MODEL; MECHANISMS; APOPTOSIS; COMPLEX; INHIBITION; TISSUES;
D O I
10.1186/1678-9199-20-42
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Background: Snake venoms are synthesized and stored in venom glands. Most venoms are complex mixtures of several proteins, peptides, enzymes, toxins and non-protein components. In the present study, we investigated the oxidative stress and apoptosis in rat liver cells provoked by Naja haje crude injection (LD50) after four hours. Methods: Wistar rats were randomly divided into two groups, the control group was intraperitoneally injected with saline solution while LD50-dose envenomed group was intraperitoneally injected with venom at a dose of 0.025 mu g/kg of body weight. Animals were killed four hours after the injection. Lipid peroxidation, nitric oxide and glutathione levels were measured as oxidative markers in serum and liver homogenate. In addition, liver function parameters and activities of antioxidant enzymes were determined. Results: N. haje crude venom (0.025 mu g/kg of body weight) enhanced lipid peroxidation and nitric oxide production in both serum and liver with concomitant reduction in glutathione, catalase, glutathione reductase and glutathione-Stransferase activities. Superoxide dismutase and glutathione peroxidase activities were significantly increased in liver of envenomed rats. These findings were associated with apoptosis induction in the liver. In addition, N. haje crude venom caused hepatic injury as indicated by histopathological changes in the liver tissue with an elevation in total bilirubin, serum alanine aminotransferase, aspartate aminotransferase, gamma-glutamyl transpeptidase, and alkaline phosphatase. Conclusions: Based on the present results, it can hypothesized that N. haje crude venom is a potent inducer of toxin-mediated hepatotoxicity associated with apoptosis in the liver.
引用
收藏
页数:10
相关论文
共 49 条
[1]  
Abdel Moneim AE., 2014, TOXICOL IND HEALTH, V32, P1064
[2]  
Aebi H, 1984, Methods Enzymol, V105, P121
[3]   Mechanisms of cell death induction by L-amino acid oxidase, a major component of ophidian venom [J].
Ande, Sudharsana Rao ;
Kommoju, Phaneeswara Rao ;
Draxl, Sigrid ;
Murkovic, Michael ;
Macheroux, Peter ;
Ghisla, Sandro ;
Ferrando-May, Elisa .
APOPTOSIS, 2006, 11 (08) :1439-1451
[4]   Induction of cytotoxicity of Pelagia noctiluca venom causes reactive oxygen species generation, lipid peroxydation induction and DNA damage in human colon cancer cells [J].
Ayed, Yosra ;
Boussabbeh, Manel ;
Zakhama, Wiem ;
Bouaziz, Chayma ;
Abid, Salwa ;
Bacha, Hassen .
LIPIDS IN HEALTH AND DISEASE, 2011, 10
[5]  
Barraviera B, 1989, Rev Soc Bras Med Trop, V22, P5, DOI 10.1590/S0037-86821989000100002
[6]  
Barraviera Benedito, 1995, Revista do Instituto de Medicina Tropical de Sao Paulo, V37, P63, DOI 10.1590/S0036-46651995000100008
[7]   REVISED ASSAY FOR SERUM PHENYL PHOSPHATASE-ACTIVITY USING 4-AMINO-ANTIPYRINE [J].
BELFIELD, A ;
GOLDBERG, DM .
ENZYME, 1971, 12 (05) :561-&
[8]  
Carleton HM., 1980, Carleton's Histological Technique, V5, P147
[9]   Anti-inflammatory properties of Lactobacillus gasseri expressing manganese superoxide dismutase using the interleukin 10-deficient mouse model of colitis [J].
Carroll, Ian M. ;
Andrus, Jason M. ;
Bruno-Barcena, Jose M. ;
Klaenhammer, Todd R. ;
Hassan, Hosni M. ;
Threadgill, Deborah S. .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2007, 293 (04) :G729-G738
[10]   Mapping structural determinants of biological activities in snake venom phospholipases A(2) by sequence analysis and site directed mutagenesis [J].
Chioato, L ;
Ward, RJ .
TOXICON, 2003, 42 (08) :869-883