Effect of phosphamidon on convulsive behavior and biochemical parameters: modulation by progesterone and 4′-chlorodiazepam in rats

被引:0
作者
Vikas Joshi
Tarun Arora
Ashish K. Mehta
Amit K. Sharma
Naveen Rathor
Kapil D. Mehta
Prabha Mahajan
Pramod K. Mediratta
Basu D. Banerjee
Krishna K. Sharma
机构
[1] University of Delhi,Department of Pharmacology, University College of Medical Sciences
[2] University of Delhi,Department of Physiology, University College of Medical Sciences
[3] University of Delhi,Department of Biochemistry, University College of Medical Sciences
来源
Naunyn-Schmiedeberg's Archives of Pharmacology | 2010年 / 382卷
关键词
Pentylenetetrazole; Maximal electroshock seizures; Phosphamidon; Progesterone; 4′-chlorodiazepam;
D O I
暂无
中图分类号
学科分类号
摘要
Phosphamidon (PHOS) has been shown to affect nervous system adversely. The present study was designed to explore the modulation of the effects of PHOS on convulsions by neurosteroids, progesterone (PROG), and 4′-chlorodiazepam (4′-CD), in both acute and chronic seizure models. In acute study, seizures were induced by either pentylenetetrazole (PTZ) injection or maximal electroshock seizures, while in the chronic study, kindling was induced by injecting PTZ (30 mg/kg, s.c.) on alternate days three times in a week. Oxidative stress was assessed in the brain by measuring the levels of malondialdehyde (MDA), acetylcholinesterase (AChE), and non-protein thiol (NP-SH). PROG and 4′-CD were able to modulate the PHOS-induced convulsions in acute PTZ convulsions as well as in chronic kindling model. However, they failed to reverse the derangements in oxidative stress parameters of MDA and NP-SH produced by PHOS in kindled animals. PROG significantly increased the AChE activity in untreated rats, while PROG and 4′-CD reversed the AChE activity inhibition induced by PHOS. The study indicates a possible anticonvulsive mechanism of neurosteroids, since both PROG and 4′-CD reversed PHOS-induced inhibition of AChE activity. The neurosteroids seem to play a protective role in PHOS-induced convulsions besides their antioxidant property.
引用
收藏
页码:311 / 320
页数:9
相关论文
共 243 条
[31]  
Gee KW(1996)Neuroactive steroids protect against pilocarpine-and kainic acid-induced limbic seizures and status epilepticus in mice Neuropharmacology 35 1049-237
[32]  
Borekci B(1993)Stimulation on brain pregnenolone synthesis by mitochondrial diazepam binding inhibitor receptor ligands in vivo J Neurochem 61 1515-455
[33]  
Ingec M(1992)Mitochondrial benzodiazepine receptors and the regulation of steroid biosynthesis Annu Rev Pharmacol Toxicol 32 211-245
[34]  
Yilmaz M(1995)Neurosteroids: a new class of neuromodulators Drugs Today 31 433-133
[35]  
Kukula O(2004)Beta-estradiol, dehydroepiandrosterone, and dehydroepiandrosterone sulfate protect against J Pharmacol Exp Ther 311 237-151
[36]  
Karaca M(1978)-methyl- J Neurol Sci 36 119-295
[37]  
Hacimuftuoglu A(2007)-aspartate-induced neurotoxicity in rat hippocampal neurons by different mechanisms Neurosci Lett 411 147-395
[38]  
Halici Z(1979)The effect of progesterone on the spontaneous interictal spike evoked by the application of penicillin to the cat’s cerebral cortex Pharmacol Rev 31 277-48
[39]  
Suleyman H(1992)The anticonvulsant effects of allopregnanolone against amygdala-kindled seizures in female rats Prog Neurobiol 38 379-358
[40]  
Bucolo C(1990)Multiplicity of mammalian microsomal cytochrome P450 Pharmacol Toxicol 67 47-2322