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한의약융합데이터센터


근거중심한의약 DB

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Title

Activation of amygdala opioid receptors by electroacupuncture of Feng-Chi (GB20) acupoints exacerbates focal epilepsy.

Authors

Yi PL, Lu CY, Cheng CH, Tsai YF, Lin CT, Chang FC.

Journal

BMC Complement Altern Med.

Year

2013

Vol (Issue)

13(1)

Page

290.

doi

10.1186/1472-6882-13-290.

PMID

24165229

Url

http://www.ncbi.nlm.nih.gov/pubmed/24165229

MeSH

Acupuncture Points*
Amygdala/metabolism*
Animals
Electroacupuncture*
Epilepsies, Partial/metabolism
Epilepsies, Partial/therapy*
Humans
Male
Narcotic Antagonists/pharmacology
Rats
Rats, Sprague-Dawley
Receptors, Opioid/genetics
Receptors, Opioid/metabolism*

Keywords

Electroacupuncture; Feng-Chi (GB20); Epilepsy; Amygdala; Opioid receptors

한글 키워드

전침; 풍지; 간질; 편도체; 오피오이드 수용체

KMCRIC summary and commentary

없음

Korean Study

Abstract

BACKGROUND:
The effect of seizure suppression by acupuncture of Feng-Chi (GB20) acupoints has been documented in the ancient Chinese literature, Lingshu Jing (Classic of the Miraculous Pivot), however, there is a lack of scientific evidence to prove it. This current study was designed to elucidate the effect of electroacupuncture (EA) stimulation of bilateral Feng-Chi (GB20) acupoints on the epileptic activity by employing an animal model of focal epilepsy.
METHODS:
Administration of pilocarpine into the left central nucleus of amygdala (CeA) induced the focal epilepsy in rats. Rats received a 30-min 100 Hz EA stimulation of bilateral Feng-Chi acupoints per day, beginning at 30 minutes before the dark period and performing in three consecutive days. The broad-spectrum opioid receptor antagonist (naloxone), mu-receptor antagonist (naloxonazine), delta-receptor antagonist (naltrindole) and kappa-receptor antagonist (nor-binaltorphimine) were administered directly into the CeA to elucidate the involvement of CeA opioid receptors in the EA effect.
RESULTS:
High-frequency (100 Hz) EA stimulation of bilateral Feng-Chi acupoints did not suppress the pilocarpine-induced epileptiform electroencephalograms (EEGs), whereas it further increased the duration of epileptiform EEGs. We also observed that epilepsy occurred while 100 Hz EA stimulation of Feng-Chi acupoints was delivered into naive rats. EA-induced augmentation of epileptic activity was blocked by microinjection of naloxone, mu- (naloxonazine), kappa- (nor-binaltorphimine) or delta-receptor antagonists (natrindole) into the CeA, suggesting that activation of opioid receptors in the CeA mediates EA-exacerbated epilepsy.
CONCLUSIONS:
The present study suggests that high-frequency (100 Hz) EA stimulation of bilateral Feng-Chi acupoints has no effect to protect against pilocarpine-induced focal epilepsy; in contrast, EA further exacerbated focal epilepsy induced by pilocarpine. Opioid receptors in the CeA mediated EA-induced exacerbation of focal epilepsy.

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