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Clinical importance of the renin-angiotensin system in chronic heart failure: double blind comparison of captopril and prazosin.肾素-血管紧张素系统在慢性心力衰竭中的临床重要性:卡托普利与哌唑嗪的双盲比较
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10
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本文引用的文献

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Studies on water diuresis: Part I. The effect of decerebration, anaesthesia and morphia upon water diuresis.水利尿研究:第一部分。去大脑、麻醉和吗啡对水利尿的影响。
J Physiol. 1929 Aug 28;68(1):39-44. doi: 10.1113/jphysiol.1929.sp002593.
2
Evidence for dopamine as an inhibitor of vasoprotein release in man.多巴胺作为人体血管蛋白释放抑制剂的证据。
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3
Opiate receptors influence vasopressin release from nerve terminals in rat neurohypophysis.阿片受体影响大鼠神经垂体神经末梢中血管加压素的释放。
Nature. 1980 Mar 27;284(5754):350-1. doi: 10.1038/284350a0.
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Proceedings: An antibody to vasopressin in man.论文集:人体内抗血管加压素抗体
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5
An enzymatic solid-phase method for trace iodination of proteins and peptides with 125-iodine.一种用¹²⁵碘对蛋白质和肽进行微量碘化的酶促固相方法。
Anal Biochem. 1975 Jul;67(1):1-10. doi: 10.1016/0003-2697(75)90266-3.
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beta-Endorphin secretion of arginine vasopressin in vivo.体内精氨酸加压素的β-内啡肽分泌
Endocrinology. 1977 Nov;101(5):1643-6. doi: 10.1210/endo-101-5-1643.
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Central cardiovascular effects of enkephalins and C-fragment of lipotropin [proceedings].脑啡肽和促脂素C片段的中枢心血管效应[会议论文集]
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8
Release of vasopressin by enkephalin.脑啡肽释放抗利尿激素。
Br J Pharmacol. 1978 Mar;62(3):370-1. doi: 10.1111/j.1476-5381.1978.tb08472.x.
9
Central sites at which morphine acts when producing cardiovascular effects [proceedings].吗啡产生心血管效应时起作用的中枢位点[会议论文集]
J Physiol. 1978 Feb;275:57P.
10
Opiate inhibition of peptide release from the neurohumoral terminals of hypothalamic neurones.阿片类物质对下丘脑神经元神经体液终末肽释放的抑制作用。
Nature. 1979 Dec 13;282(5740):746-8. doi: 10.1038/282746a0.

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.

DOI:10.1113/jphysiol.1981.sp013592
PMID:7264975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1275417/
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。