BLOCKADE OF ACUPUNCTURE ANALGESIA BY INTRAVENTRICULAR INJECTION OF NALOXONE OR CINANSERIN IN THE RABBIT
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BLOCKADE OF ACUPUNCTURE ANALGESIA BY INTRAVENTRICULAR INJECTION OF NALOXONE OR CINANSERIN IN THE RABBIT
Acupuncture ResearchIssue 1, Pages: 31-35(1982)
作者机构:
北京医学院针麻原理研究室中枢介质组
作者简介:
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DOI:
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Published:1982
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Zhou Zhongfu, Xuan yuting, Han Jisheng. BLOCKADE OF ACUPUNCTURE ANALGESIA BY INTRAVENTRICULAR INJECTION OF NALOXONE OR CINANSERIN IN THE RABBIT[J]. Acupuncture research, 1982, (1): 31-35.
DOI:
Zhou Zhongfu, Xuan yuting, Han Jisheng. BLOCKADE OF ACUPUNCTURE ANALGESIA BY INTRAVENTRICULAR INJECTION OF NALOXONE OR CINANSERIN IN THE RABBIT[J]. Acupuncture research, 1982, (1): 31-35.DOI:
BLOCKADE OF ACUPUNCTURE ANALGESIA BY INTRAVENTRICULAR INJECTION OF NALOXONE OR CINANSERIN IN THE RABBIT
Intraventricular (ivt) injection of 40 μg of naloxone
which is sufficient to block completely analgesia elicited by i. v. injection of 6mg/kg of morphine
caused only a partial (50~55%) blockade of electroacupuncture analgesia (EAA) in the rabbit. It implies that the mechanism for EAA is smilar to
but not identical with
that of morphine analgesia. The effect of EAA could also be blocked by 40% by ivt injection of 60 μg of cinanserin
the serotonin antagonist. While doubling the dose of nal oxone or cinanserin brought about no further attenuation of EAA
the combined administration of both antagonists reduced the effect of EAA by 74%. The results imply that; (1) both endogenous opioids and serotonin are important for mediation of EAA
(2) there may be a certain degree of overlapping between these two mechanisms
and (3) neurochemical me chanisms other than endogenous opioids and serotonin may be operating for mediation of EAA.