2012Zhonghua shiyan waike zazhiRequires access

The changes of hippocampal NO on pentylenetetrazol induced epileptic rats and its effect to hippocampal neuronal apoptosis

Zhengang Tang

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Abstract

Objective To study the changes of nitric oxide (NO) content in hippocampus of rat by Pentylenetetrazol ( PTZ)-induced seizures models and its effect of toxicity and apoptosis.Methods SD male rats were random divided into three groups,each group has 14 rats.Group A is the saline control group,group B is the pentylenetetrazol induced epileptic group and group C is aminoguanidine ( NOS inhibitor) pretreatment plus pentylenetetrazol induced epileptic group.NO content in rat hippocampus was detected by ultraviolet spectrophotometry,glutamate ( Glu ) immunoreactivity in rat hippocampus was detected by immunohistochemistry (SABC) and caspase-3 mRNA levels in rat hippocampus were detected by reverse transcription-polymerase chain reaction (RT-PCR) respectively at 2,48 h after modeling.Results Group A had no seizure,group B had epilepsia gravior over Ⅴ grade,rats in group C had seizure over Ⅱ Ⅲ grade.The NO content on group B (75.67 ± 2.04) μ mol/L was significantly higher than group A (11.90±0.64) μmol/L and group C (36.19 ±4.48) μmol/L (P<0.05) ; Glu immunoreactivity and caspase-3 mRNA leves of group A and group C were lower than group B ( P < 0.05 ).Conclusion PTZinduced seizures may lead to excessive production of NO in hippocampus,which had excited toxicity to hippocampal neurons.The intervention of NOS synthetic inhibitor had neuroprotective effects. Key words: Epilepsy;  Nitric oxide;  Glutamate;  Caspase-3 ;  Apoptosis

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Objective To study the changes of nitric oxide (NO) content in hippocampus of rat by Pentylenetetrazol ( PTZ)-induced seizures models and its effect of toxicity and apoptosis.Methods SD male rats were random divided into three groups,each group has 14 rats.Group A is the saline control group,group B is the pentylenetetrazol induced epileptic group and group C is aminoguanidine ( NOS inhibitor) pretreatment plus pentylenetetrazol induced epileptic group.NO content in rat hippocampus was detected by ultraviolet spectrophotometry,glutamate ( Glu ) immunoreactivity in rat hippocampus was detected by immunohistochemistry (SABC) and caspase-3 mRNA levels in rat hippocampus were detected by reverse transcription-polymerase chain reaction (RT-PCR) respectively at 2,48 h after modeling.Results Group A had no seizure,group B had epilepsia gravior over Ⅴ grade,rats in group C had seizure over Ⅱ Ⅲ grade.The NO content on group B (75.67 ± 2.04) μ mol/L was significantly higher than group A (11.90±0.64) μmol/L and group C (36.19 ±4.48) μmol/L (P<0.05) ; Glu immunoreactivity and caspase-3 mRNA leves of group A and group C were lower than group B ( P < 0.05 ).Conclusion PTZinduced seizures may lead to excessive production of NO in hippocampus,which had excited toxicity to hippocampal neurons.The intervention of NOS synthetic inhibitor had neuroprotective effects. Key words: Epilepsy;  Nitric oxide;  Glutamate;  Caspase-3 ;  Apoptosis

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Available abstract

Objective To study the changes of nitric oxide (NO) content in hippocampus of rat by Pentylenetetrazol ( PTZ)-induced seizures models and its effect of toxicity and apoptosis.Methods SD male rats were random divided into three groups,each group has 14 rats.Group A is the saline control group,group B is the pentylenetetrazol induced epileptic group and group C is aminoguanidine ( NOS inhibitor) pretreatment plus pentylenetetrazol induced epileptic group.NO content in rat hippocampus was detected by ultraviolet spectrophotometry,glutamate ( Glu ) immunoreactivity in rat hippocampus was detected by immunohistochemistry (SABC) and caspase-3 mRNA levels in rat hippocampus were detected by reverse transcription-polymerase chain reaction (RT-PCR) respectively at 2,48 h after modeling.Results Group A had no seizure,group B had epilepsia gravior over Ⅴ grade,rats in group C had seizure over Ⅱ Ⅲ grade.The NO content on group B (75.67 ± 2.04) μ mol/L was significantly higher than group A (11.90±0.64) μmol/L and group C (36.19 ±4.48) μmol/L (P<0.05) ; Glu immunoreactivity and caspase-3 mRNA leves of group A and group C were lower than group B ( P < 0.05 ).Conclusion PTZinduced seizures may lead to excessive production of NO in hippocampus,which had excited toxicity to hippocampal neurons.The intervention of NOS synthetic inhibitor had neuroprotective effects. Key words: Epilepsy;  Nitric oxide;  Glutamate;  Caspase-3 ;  Apoptosis

Key concepts: Pentylenetetrazol, Hippocampal formation, Hippocampus, Epilepsy, Apoptosis, Nitric oxide synthase, Epileptogenesis, Nitric oxide

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