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应激期间大鼠大脑中的阿片受体结合

Opiate receptor binding in the brain of rat during stress.

作者信息

Sirakova I, Panova D, Georgiev P, Sirakov L M

机构信息

Department of Biochemistry, Medical Academy, Sofia, Bulgaria.

出版信息

Pavlov J Biol Sci. 1988 Apr-Jun;23(2):54-6. doi: 10.1007/BF02995655.

DOI:10.1007/BF02995655
PMID:2838796
Abstract

Two types of opioid receptors were studied in the brain of rats: Delta (for endogenous opiate) and mu (for exogenous opiates). 3H derivates: D-Ala2-enkephalin and Naloxone were used as labeled ligands. The results obtained were calculated by computer program for automatic estimation of the data using approximation equations. An increase of binding delta receptors is observed in both types of stress (2-8 times), while to the mu receptors the binding is less effective mainly after irradiation. These data suggest that a close interaction exists between sympathoadrenal system and opioid mechanisms during stress.

摘要

在大鼠大脑中研究了两种阿片受体

δ受体(针对内源性阿片)和μ受体(针对外源性阿片)。使用了3H衍生物:D-丙氨酸2-脑啡肽和纳洛酮作为标记配体。通过计算机程序使用近似方程对获得的结果进行自动数据估计计算。在两种应激类型中均观察到δ受体结合增加(2至8倍),而对于μ受体,主要在照射后结合效果较差。这些数据表明,应激期间交感肾上腺系统与阿片机制之间存在密切相互作用。

相似文献

1
Opiate receptor binding in the brain of rat during stress.应激期间大鼠大脑中的阿片受体结合
Pavlov J Biol Sci. 1988 Apr-Jun;23(2):54-6. doi: 10.1007/BF02995655.
2
The occurrence and receptor specificity of endogenous opioid peptides within the pancreas and liver of the rat. Comparison with brain.大鼠胰腺和肝脏内源性阿片肽的发生及受体特异性。与脑的比较。
Biochem J. 1990 Apr 1;267(1):233-40. doi: 10.1042/bj2670233.
3
Leucine enkephalin noncompetitively inhibits the binding of [3H]naloxone to the opiate mu-recognition site: evidence for delta----mu binding site interactions in vitro.亮氨酸脑啡肽非竞争性抑制[3H]纳洛酮与阿片μ-识别位点的结合:体外δ----μ结合位点相互作用的证据。
Neuropeptides. 1985 Jul;6(4):351-63. doi: 10.1016/0143-4179(85)90008-3.
4
Regional interactions of opioid peptides at mu and delta sites in rat brain.
Peptides. 1983 Nov-Dec;4(6):853-8. doi: 10.1016/0196-9781(83)90080-3.
5
Naloxonazine effects on the interaction of enkephalin analogs with mu-1, mu and delta opioid binding sites in rat brain membranes.纳洛酮嗪对脑啡肽类似物与大鼠脑膜中μ-1、μ和δ阿片样物质结合位点相互作用的影响。
J Pharmacol Exp Ther. 1987 Jul;242(1):15-20.
6
Effect of electroconvulsive treatment on cerebral opioid receptors in the rat: changes in delta but not mu receptors.电休克治疗对大鼠脑阿片受体的影响:δ受体而非μ受体发生变化。
Naunyn Schmiedebergs Arch Pharmacol. 1984 Nov;328(1):87-9. doi: 10.1007/BF00496112.
7
[Stability of opiate receptors of wet and lyophilized preparations of rat brain membranes].[大鼠脑膜湿制剂和冻干制剂中阿片受体的稳定性]
Biokhimiia. 1984 Jul;49(7):1127-33.
8
Opiate and opioid peptide binding in rat goldfish: further evidence for opiate receptor heterogeneity.
Brain Res. 1982 Sep 23;248(1):192-5. doi: 10.1016/0006-8993(82)91164-7.
9
[Selectivity of [D-Ala2-O-benzyl-Ser5]-enkephalin on mu and delta opiate receptor subtypes].
Zhongguo Yao Li Xue Bao. 1985 Mar;6(1):3-5.
10
Antagonist-induced opioid receptor up-regulation. II. Regionally specific modulation of mu, delta and kappa binding sites in rat brain revealed by quantitative autoradiography.拮抗剂诱导的阿片受体上调。II. 定量放射自显影揭示大鼠脑中μ、δ和κ结合位点的区域特异性调节。
J Pharmacol Exp Ther. 1988 Nov;247(2):729-36.

本文引用的文献

1
Opioid and nonopioid mechanisms of stress analgesia.应激镇痛的阿片类和非阿片类机制。
Science. 1980 May 9;208(4444):623-5. doi: 10.1126/science.7367889.
2
Enkephalins as possible adrenomedullary hormones: storage, secretion, and regulation of synthesis.脑啡肽作为潜在的肾上腺髓质激素:储存、分泌及合成调控
Adv Biochem Psychopharmacol. 1980;22:191-204.
3
The role of endorphins in stress: evidence and speculations.内啡肽在应激反应中的作用:证据与推测。
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4
Stereospecific interaction between narcotic analgesics and a synaptic plasm a membrane fraction of rat cerebral cortex.麻醉性镇痛药与大鼠大脑皮质突触质膜部分之间的立体特异性相互作用。
Acta Pharmacol Toxicol (Copenh). 1973;32(3):317-20. doi: 10.1111/j.1600-0773.1973.tb01477.x.
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Opiate receptor: demonstration in nervous tissue.阿片受体:在神经组织中的显示
Science. 1973 Mar 9;179(4077):1011-4. doi: 10.1126/science.179.4077.1011.
6
Corticotropin-releasing factor stimulation of adrenocorticotropin and beta-endorphin release: effects of acute and chronic stress.促肾上腺皮质激素释放因子对促肾上腺皮质激素和β-内啡肽释放的刺激作用:急性和慢性应激的影响
Endocrinology. 1985 Jul;117(1):23-30. doi: 10.1210/endo-117-1-23.
7
Identification of two related pentapeptides from the brain with potent opiate agonist activity.从大脑中鉴定出两种具有强效阿片激动剂活性的相关五肽。
Nature. 1975 Dec 18;258(5536):577-80. doi: 10.1038/258577a0.
8
Opioid activity of a peptide, beta-lipotropin-(61-91), derived from beta-lipotropin.源自β-促脂素的一种肽β-促脂素-(61-91)的阿片样活性。
Proc Natl Acad Sci U S A. 1976 Jun;73(6):1821-3. doi: 10.1073/pnas.73.6.1821.
9
beta-Endorphin and adrenocorticotropin are selected concomitantly by the pituitary gland.
Science. 1977 Sep 30;197(4311):1367-9. doi: 10.1126/science.197601.