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Anticonvulsion effect of acupuncture might be related to the decrease of neuronal and inducible nitric oxide
1Department of Neurobiology, Institute of Acupuncture Research, Shanghai Medical University, PR China.
Acupuncture & Electro-Therapeutics Research
|March 23, 2001
Summary
Electroacupuncture (EA) treatment reduced nitric oxide synthase (NOS) levels in rats with penicillin-induced epilepsy. This suggests EA
Area of Science:
- Neuroscience
- Pharmacology
- Biochemistry
Background:
- Epilepsy is a neurological disorder characterized by recurrent seizures.
- Nitric oxide synthase (NOS) plays a role in neuronal function and has been implicated in epilepsy.
- Understanding the role of different NOS isoforms in epilepsy is crucial for developing effective treatments.
Purpose of the Study:
- To investigate the changes in hippocampal nitric oxide synthase (NOS) isoform levels during penicillin-induced epilepsy in rats.
- To evaluate the effect of electroacupuncture (EA) on these NOS isoform levels in the epileptic model.
Main Methods:
- Epilepsy was induced in Wistar rats by injecting penicillin into the hippocampus.
- Electroacupuncture (EA) was applied to "Feng Fu" (DU 16) and "Jin Suo" (DU 8) acupoints.
- Hippocampal nitric oxide synthase (NOS) mRNA levels were quantified using reverse transcription-polymerase chain reaction (RT-PCR).
Main Results:
- Penicillin-induced epilepsy significantly increased neuronal nitric oxide synthase (nNOS) and inducible nitric oxide synthase (iNOS) mRNA levels in the hippocampus (P<0.01).
- Epithelial nitric oxide synthase (eNOS) mRNA levels showed no significant change.
- EA treatment inhibited epilepsy and correspondingly decreased nNOS and iNOS mRNA levels (P<0.01), without affecting eNOS mRNA.
Conclusions:
- Penicillin-induced epilepsy is associated with increased hippocampal expression of nNOS and iNOS.
- The anticonvulsant effects of EA may be mediated by the downregulation of nNOS and iNOS.
- These findings highlight the potential of EA as a therapeutic strategy for epilepsy by modulating NOS pathways.