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脑室内注射吗啡对大鼠血管加压素释放的影响。

The effect of intracerebroventricular injections of morphine on vasopressin release in the rat.

作者信息

Aziz L A, Forsling M L, Woolf C J

出版信息

J Physiol. 1981 Feb;311:401-9. doi: 10.1113/jphysiol.1981.sp013592.

Abstract
  1. An investigation was carried out to determine the effect of intracerebroventricular (I.C.V.) micro-injections of morphine on vasopressin (AVP) release in the urethane-anaesthetized rat. 2. Plasma AVP levels at different time intervals, following I.C.V. injection of 10-150 microgram morphine, were measured by radioimmunoassay. The effect of I.C.V. micro-injections of morphine on urine outflow was also studied in a group of water-loaded rats. 3. The vasopressin response to I.C.V. micro-injections of morphine was both dose- and time-dependent. High dose of 50 and 150 microgram morphine produced short latency stimulation of AVP release, followed by a fall. The low dose of 10 microgram morphine produced only a long latency inhibition. The most consistent response of I.C.V. injection of morphine was an inhibition of release. 4. Both stimulatory and inhibitory effects of morphine on vasopressin release were naloxone reversible and stereospecific. 5. I.C.V. micro-injections of morphine produced a dose-dependent rise in mean arterial blood pressure of short latency. Naloxone (0.5 mg/kg) completely abolished the rise seen with 10 microgram morphine and diminished the rise with 50 microgram. 6. Doses of 10 and 50 microgram morphine injected I.C.V. produced an immediate antidiuresis in water-loaded rats under urethane anaesthesia. 7. The vasopressin response to I.C.V. micro-injections of morphine is independent of the effects on the cardiovascular system and may involve different opiate receptor populations. The results also suggest the possibility that opiate receptors with different affinities for morphine may be responsible for the stimulatory and inhibitory effects of morphine on vasopressin release.
摘要
  1. 进行了一项研究,以确定脑室内(I.C.V.)微量注射吗啡对乌拉坦麻醉大鼠血管加压素(AVP)释放的影响。2. 通过放射免疫分析法测量了I.C.V.注射10 - 150微克吗啡后不同时间间隔的血浆AVP水平。还在一组水负荷大鼠中研究了I.C.V.微量注射吗啡对尿量流出的影响。3. 对I.C.V.微量注射吗啡的血管加压素反应呈剂量和时间依赖性。高剂量的50和150微克吗啡引起AVP释放的短潜伏期刺激,随后下降。低剂量的10微克吗啡仅产生长潜伏期抑制。I.C.V.注射吗啡最一致的反应是释放抑制。4. 吗啡对血管加压素释放的刺激和抑制作用均为纳洛酮可逆且具有立体特异性。5. I.C.V.微量注射吗啡使平均动脉血压在短潜伏期内呈剂量依赖性升高。纳洛酮(0.5毫克/千克)完全消除了10微克吗啡引起的血压升高,并减弱了50微克吗啡引起的升高。6. I.C.V.注射10和50微克吗啡在乌拉坦麻醉的水负荷大鼠中立即产生抗利尿作用。7. 对I.C.V.微量注射吗啡的血管加压素反应独立于对心血管系统的影响,可能涉及不同的阿片受体群体。结果还提示,对吗啡具有不同亲和力的阿片受体可能是吗啡对血管加压素释放的刺激和抑制作用的原因。

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