Histopathological changes induced by Hemiscorpius lepturus scorpion venom in mice

被引:35
|
作者
Heidarpour, Mojgan [2 ]
Ennaifer, Emna [3 ]
Ahari, Hamed
Srairi-Abid, Najet [4 ]
Borchani, Lamia [4 ]
Khalili, Ghader [5 ]
Amini, Hossein [1 ]
Anvar, Amir Ali [2 ]
Boubaker, Samir [3 ]
El-Ayeb, Mohamed [4 ]
Shahbazzadeh, Delavar [1 ]
机构
[1] Pasteur Inst Iran, Biotechnol Res Ctr, Med Biotechnol Grp, Venom & Toxin Lab, Tehran, Iran
[2] Inst Stand & Ind Res Iran, Karaj, Iran
[3] Pasteur Inst Tunis, Lab Human & Expt Pathol, Tunis 1002, Tunisia
[4] Inst Pasteur, Lab Venin & Toxin, Tunis 1002, Tunisia
[5] Pasteur Inst Iran, Dept Immunol, Tehran, Iran
关键词
Hemiscorpius lepturus; Scorpion venom; Histopathology; Creatine kinase (CK); Lactate dehydrogenase (LDH); TITYUS-SERRULATUS; IN-VIVO; LOXOSCELES; TOXIN; IRAN; ENVENOMATION; NECROSIS; FAILURE; SNAKE;
D O I
10.1016/j.toxicon.2011.12.011
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Envenomation by Hemiscorpius lepturus (H. lepturus) is associated with local necrosis, followed by systemic manifestations. In this work the LD50 of H. lepturus venom were determined by subcutaneous (SC) injection in white Balb/c mice (5 mg/kg). Histopathological alterations in organs such as kidney, heart, liver, lungs, stomach and intestine were determined in 3, 6, 12 and 24 h following experimental (SC) envenoming injection of one LD50 of the venom in Balb/c mice. Histological studies showed degenerative changes in the kidney with disorganized glomeruli and necrotic tubular in 3 h and reached to its climax in 6 h. Myocardium showed massive myocytolysis with interstitial necrosis in 3 h and reached to its peak after 6 h past envenoming. Bowels showed edema of lamina propria and slight villous necrosis. The enzymatic activities of creatine kinase (CK) and lactate dehydrogenase (LDH) were significantly increased in the serum in 9 h. No necrotic lesion observed in lungs and liver. The results indicate that the venom of H. lepturus is a highly cytotoxic, and induces massive tissue damages in specific organs, starting from the heart and kidney as the first target in 3 h and ends to the bowels in 6 h post envenomation. (c) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:373 / 378
页数:6
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