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pubmed-article:11072139pubmed:dateCreated2000-12-27lld:pubmed
pubmed-article:11072139pubmed:abstractTextThis work was designed to examine whether brain endomorphins (EM1 and EM2), the endogenous mu-opioid ligands, are involved in electroacupuncture (EA)-induced analgesia in the mice. C57BL/6J mice were given EA for 30 min and the effect of EA-induced analgesia was assessed by radiant heat tail flick latency (TFL). Intracerebroventricular (i.c.v.) injection of mu-opioid receptor antagonist D-Phe-Cys-Tyr-D-Tyr-Orn-Thr-Pen-Thr-NH(2) (CTOP), or antiserum against EM1 or EM2 was performed to see whether EA analgesia could be blocked. The results showed that: (1) i.c.v. injection of CTOP at 25-100 ng dose-dependently antagonized the analgesia induced by EA of 2 Hz, but not 100 Hz. (2) Intracerebroventricular injection of EM1 antiserum (5 ml, 1:1 or 1:10 dilution) dose-dependently antagonized 2 Hz, but not 100 Hz EA analgesia. (3) EM2 antiserum showed similar effect at 1:1 dilution. The results are interpreted to mean that endogenously released EM1 and EM2 and the cerebral mu-receptors are involved in mediating 2 Hz but not 100 Hz EA analgesia in the mice.lld:pubmed
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pubmed-article:11072139pubmed:authorpubmed-author:RAOT TTTlld:pubmed
pubmed-article:11072139pubmed:authorpubmed-author:HuangCClld:pubmed
pubmed-article:11072139pubmed:authorpubmed-author:WangYYlld:pubmed
pubmed-article:11072139pubmed:authorpubmed-author:ChangJ KJKlld:pubmed
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pubmed-article:11072139pubmed:volume294lld:pubmed
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pubmed-article:11072139pubmed:pagination159-62lld:pubmed
pubmed-article:11072139pubmed:dateRevised2007-11-14lld:pubmed
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pubmed-article:11072139pubmed:articleTitleEndomorphin and mu-opioid receptors in mouse brain mediate the analgesic effect induced by 2 Hz but not 100 Hz electroacupuncture stimulation.lld:pubmed
pubmed-article:11072139pubmed:affiliationNeuroscience Research Institute, Peking University, 38 Xue Yuan Road, 100083, PR, Beijing, China.lld:pubmed
pubmed-article:11072139pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:11072139pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
pubmed-article:11072139pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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