CNS and anticonvulsant activity of a non-protein toxin (KC-MMTx) isolated from King Cobra (Ophiophagus hannah) venom

被引:5
|
作者
Saha, A
Gomes, A
Chakravarty, AK
Biswas, AK
Giri, B
Dasgupta, SC
Gomes, A
机构
[1] Univ Calcutta, Dept Physiol, Lab Toxicol & Expt Pharmacodynam, Kolkata 700009, W Bengal, India
[2] Indian Inst Chem Biol, Div New Drug Dev, Kolkata 700032, W Bengal, India
[3] Indian Inst Chem Biol, Div Med Chem, Kolkata 700032, W Bengal, India
关键词
snake venom; King Cobra venom; non-protein toxin; anticonvulsant potential;
D O I
10.1016/j.toxicon.2005.11.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In the present study, King Cobra (Ophiophagus hannah) venom was subjected to TLC followed by column chromatography/HPLC to isolate and purify a non-protein toxin designated as KC-MMTx. H-1 NMR, IR and EIMS studies showed KC-MMTx likely to be a 282 D unsaturated aliphatic acid having molecular formula ClsH3402. The minimum lethal dose of KC-MMTx was 200 mu g/kg (i.v.) and 350 mu g/kg (i.p.) in Swiss albino male mice. It significantly increased pentobarbitone induced sleeping time and significantly decreased the body temperature of male albino mice. It provided protection against amphetamine aggregate toxicity in mice but failed to protect amphetamine stereotypy in male albino rats. KC-MMTx provided significant protection against drug (strychnine, pentylenetetrazole, yobimbine) induced convulsions in male albino mice. It increased serum Na+ and decreased serum Ca2+ significantly in male mice. MAO activity and brain neurotransmitter levels in male mice were altered significantly. Further detailed study is warranted on the CNS, anticonvulsant potential of KC-MMTx, which may lead to the development of newer therapeutic tools in the near future. (c) 2005 Elsevier Ltd. All rights reserved.
引用
收藏
页码:296 / 303
页数:8
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