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小鼠长期使用吗啡后中枢一氧化氮合酶活性变化的时间进程:纳曲酮的逆转作用。

Time course of the changes in central nitric oxide synthase activity following chronic treatment with morphine in the mouse: reversal by naltrexone.

作者信息

Kumar S, Bhargava H N

机构信息

Department of Pharmaceutics (M/C 865), University of Illinois at Chicago, USA.

出版信息

Gen Pharmacol. 1997 Aug;29(2):223-7. doi: 10.1016/s0306-3623(96)00416-8.

DOI:10.1016/s0306-3623(96)00416-8
PMID:9251903
Abstract
  1. The time course of the effect of chronic administration of morphine on the activity of nitric oxide synthase (NOS) in the brain regions and spinal cord of the mouse was determined. The effect of naltrexone by itself on the NOS activity and that induced by morphine also were determined. 2. Male Swiss Webster mice were implanted subcutaneously with a pellet containing 25 mg of morphine free base for 4 days. Placebo pellet implanted mice served as controls. 3. Twenty-four hours after treatment with morphine, NOS activity decreased in the cerebellum, midbrain, cortex and remainder of the brain as well as in the spinal cord. Forty-eight and 72 hr after the treatment with morphine, NOS activity increased in the cerebellum and cortex, but no change was observed in the other brain regions and spinal cord. Twenty-four hours after morphine pellet removal (withdrawal), NOS activity in all brain regions and the spinal cord has returned to normal. 4. Implantation of a pellet containing 10 mg of naltrexone did not alter NOS activity in any brain region or spinal cord for 24, 48 and 72 hr or 24 hr after removal of the pellet. 5. Implantation of a naltrexone pellet in conjunction with a morphine pellet blocked the changes in NOS activity in the brain region and spinal cord induced by morphine. 6. It is concluded that the initial decrease in NOS activity by morphine may be related to enhanced motor activity, whereas the increase in NOS activity in certain brain regions may be associated with tolerance-physical dependence development. Additionally, the changes in central NOS activity by morphine appear to be mediated by opioid receptors because they were blocked by concurrent treatment with naltrexone.
摘要
  1. 测定了慢性给予吗啡对小鼠脑区和脊髓中一氧化氮合酶(NOS)活性影响的时间进程。还测定了纳曲酮自身对NOS活性的影响以及吗啡诱导的影响。2. 将含有25mg吗啡游离碱的药丸皮下植入雄性瑞士韦伯斯特小鼠体内,持续4天。植入安慰剂药丸的小鼠作为对照。3. 用吗啡治疗24小时后,小脑、中脑、皮质和脑的其余部分以及脊髓中的NOS活性降低。用吗啡治疗48小时和72小时后,小脑中的NOS活性增加,皮质中的NOS活性增加,但其他脑区和脊髓中未观察到变化。取出吗啡药丸(撤药)24小时后,所有脑区和脊髓中的NOS活性已恢复正常。4. 植入含有10mg纳曲酮的药丸在24、48和72小时或取出药丸后24小时内,未改变任何脑区或脊髓中的NOS活性。5. 与吗啡药丸联合植入纳曲酮药丸可阻断吗啡诱导的脑区和脊髓中NOS活性的变化。6. 得出的结论是,吗啡最初导致的NOS活性降低可能与运动活动增强有关,而某些脑区中NOS活性的增加可能与耐受性 - 身体依赖性的发展有关。此外,吗啡引起的中枢NOS活性变化似乎是由阿片受体介导的,因为它们被同时给予纳曲酮所阻断。

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