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单次给药后吗啡在大鼠脑和血清中的持续存在情况。

Morphine persistence in rat brain and serum after single doses.

作者信息

Mullis K B, Perry D C, Finn A M, Stafford B, Sadée W

出版信息

J Pharmacol Exp Ther. 1979 Feb;208(2):228-31.

PMID:762653
Abstract

The disposition of morphine in rat brain and serum was determined over 48 hr after subcutaneous doses. Free morphine was measured by a specific assay using 3H-labeling together with high-pressure liquid chromatography separation, with a sensitivity of 1 nM (0.3 ng of morphine per ml). This study revealed the persistence of free morphine in nanomolar concentrations over at least 24 hr after a single analgesic dose. The terminal half-life of morphine elimination was 5 hours. Total radioactivity was retained in the body at much higher concentrations. Similar disposition of [C-1-3H]morphine and [N-14CH3] morphine ruled out any major metabolic alterations at these positions, including N-demethylation. Irreversible binding to insoluble tissue components, which has previously been linked to tolerance, was observed only to the extent of less than 20% of total tissue radioactivity and was not unique to brain tissue. The persistence of morphine and its metabolites may be related to protracted opiate effects such as withdrawal symptoms after addiction.

摘要

皮下给药后48小时内测定了大鼠脑和血清中吗啡的处置情况。游离吗啡通过使用3H标记并结合高压液相色谱分离的特异性测定法进行测量,灵敏度为1 nM(每毫升0.3 ng吗啡)。该研究表明,单次镇痛剂量后,游离吗啡在纳摩尔浓度下至少持续24小时。吗啡消除的终末半衰期为5小时。体内总放射性以高得多的浓度保留。[C-1-3H]吗啡和[N-14CH3]吗啡的类似处置排除了这些位置的任何主要代谢改变,包括N-去甲基化。与不溶性组织成分的不可逆结合(此前已与耐受性相关)仅在总组织放射性的不到20%的程度上观察到,并且并非脑组织所特有。吗啡及其代谢产物的持续存在可能与阿片类药物的长期效应有关,例如成瘾后的戒断症状。

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