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前列腺素E2、环磷酸腺苷与吗啡镇痛

Prostaglandin E2, cyclic adenosine monophosphate and morphine analgesia.

作者信息

Vonvoigtlander P F, Losey E G

出版信息

Brain Res. 1977 Jun 10;128(2):275-83. doi: 10.1016/0006-8993(77)90994-5.

Abstract

Intravenous administration of prostaglandin E2 (PGE2) to mice results in a significant distribution of PGE2 into the brain and an elevation of cyclic adenosine monophosphate (cAMP) in the midhindbrain and corpus striatum. Neither acute morphine administration nor morphine tolerance alters this response. Morphine alone also elevates cAMP levels. Although these elevations are blocked by the narcotic antagonist, naloxone, they only occur at supra-analgesic doses. Therefore morphine analgesia does not correlate with either elevation of cAMP levels of antagonism of PGE2-induced elevations of cAMP.

摘要

给小鼠静脉注射前列腺素E2(PGE2)会导致PGE2大量分布到大脑中,并使中后脑和纹状体中的环磷酸腺苷(cAMP)水平升高。急性给予吗啡或吗啡耐受性均不会改变这种反应。单独使用吗啡也会提高cAMP水平。尽管这些升高被麻醉拮抗剂纳洛酮阻断,但它们仅在超镇痛剂量下才会出现。因此,吗啡镇痛作用与cAMP水平升高或对PGE2诱导的cAMP升高的拮抗作用均无关。

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