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5-羟色胺乙酸水平升高与身体依赖性的分离:纳洛酮的作用

Dissociation of increased 5-hydroxyindoleacetic acid levels and physical dependence: the effects of naloxone.

作者信息

Laska F J, Fennessy M R

出版信息

Clin Exp Pharmacol Physiol. 1977 Nov-Dec;4(6):515-23. doi: 10.1111/j.1440-1681.1977.tb02681.x.

Abstract
  1. A slow release emulsion of naloxone (naloxone SR) was administered subcutaneously to rats in an attempt to induce physical dependence of the morphine type. 2. Naltrexone (2.5 mg/kg), injected i.p., failed to elicit an abstinence syndrome in rats treated with 75, 100 or 150 mg/kg naloxone SR for 24, 48, or 72 h. 3. Naloxone SR had no effect on the whole brain levels of noradrenaline, dopamine, homovanillic acid or serotonin. 4. Naloxone SR caused an apparent dose-related increase in the brain levels of 5-hydroxyindoleacetic acid. 5. These results show that while naloxone does not induce physical dependence of the morphine type, it may, like morphine, increase the brain serotonin turnover rate. 6. It is proposed that the increase in brain serotonin turnover rate may not be causally related to physical dependence on morphine-like drugs but may be a property of drugs containing the basic opiate molecular structure.
摘要
  1. 将纳洛酮缓释乳剂(naloxone SR)皮下注射给大鼠,试图诱导吗啡型身体依赖性。2. 腹腔注射纳曲酮(2.5毫克/千克),对接受75、100或150毫克/千克纳洛酮SR治疗24、48或72小时的大鼠未引发戒断综合征。3. 纳洛酮SR对全脑去甲肾上腺素、多巴胺、高香草酸或5-羟色胺水平无影响。4. 纳洛酮SR导致脑内5-羟吲哚乙酸水平出现明显的剂量相关增加。5. 这些结果表明,虽然纳洛酮不会诱导吗啡型身体依赖性,但它可能像吗啡一样,增加脑5-羟色胺转换率。6. 有人提出,脑5-羟色胺转换率的增加可能与对吗啡样药物的身体依赖性没有因果关系,而是含基本阿片分子结构药物的一种特性。

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