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哺乳动物中枢神经系统神经元上的多种阿片受体。体内和体外研究。

Multiple opiate receptors on neurons of the mammalian central nervous system. In vivo and in vitro studies.

作者信息

Zieglgänsberger W, French E D, Mercuri N, Pelayo F, Williams J T

出版信息

Life Sci. 1982;31(20-21):2343-6. doi: 10.1016/0024-3205(82)90152-7.

DOI:10.1016/0024-3205(82)90152-7
PMID:6298526
Abstract

Experiments were performed in rat spinal cord cells in vivo and on hippocampal pyramidal cells in vitro. These investigations suggest that acute and chronic treatment renders the neurons subsensitive to opiate alkaloids without altering their sensitivity to opioid peptides. The experiments performed in the dorsal horn of the spinal cord provide evidence that in this structure mu- and delta-receptors may also be localized on the same cell. The evidence for the existence of distinct types of opiate receptors as originally proposed by (1) and suggested by the differing pattern of opiate and opioid peptide activity in various assay systems has been substantiated by investigations involving the selective development of tolerance and the protection of a particular receptor subtype by chemical manipulation. Furthermore, they have been characterized by the use of low concentrations of radiolabelled agonists and antagonists and through the ability of GTP to influence differentially their binding to the opiate receptor (for refs. see: 2). Recently autoradiographic techniques were able to provide direct evidence by mu- and delta-receptors in the mammalian brain (3; 4; 5; 6; and cits. therein). The presence of multiple opiate receptors located on the same cell is suggested by the present study.

摘要

实验在大鼠脊髓细胞体内以及海马锥体细胞体外进行。这些研究表明,急性和慢性治疗使神经元对阿片生物碱不敏感,而不改变其对阿片肽的敏感性。在脊髓背角进行的实验提供了证据,表明在该结构中μ受体和δ受体也可能定位于同一细胞。最初由(1)提出并由各种检测系统中阿片和阿片肽活性的不同模式所暗示的不同类型阿片受体存在的证据,已通过涉及耐受性的选择性发展以及通过化学操作对特定受体亚型的保护的研究得到证实。此外,它们已通过使用低浓度放射性标记激动剂和拮抗剂以及通过GTP对其与阿片受体结合的差异影响能力来表征(参考文献见:2)。最近,放射自显影技术能够提供哺乳动物脑中μ受体和δ受体的直接证据(3;4;5;6;以及其中的参考文献)。本研究表明同一细胞上存在多种阿片受体。

相似文献

1
Multiple opiate receptors on neurons of the mammalian central nervous system. In vivo and in vitro studies.哺乳动物中枢神经系统神经元上的多种阿片受体。体内和体外研究。
Life Sci. 1982;31(20-21):2343-6. doi: 10.1016/0024-3205(82)90152-7.
2
Neurons in the frontal cortex of the rat carry multiple opiate receptors.大鼠额叶皮质中的神经元携带多种阿片受体。
Brain Res. 1981 Dec 7;226(1-2):304-8. doi: 10.1016/0006-8993(81)91103-3.
3
Opiate receptor agonists regulate phosphorylation of synapsin I in cocultures of rat spinal cord and dorsal root ganglion.阿片受体激动剂可调节大鼠脊髓和背根神经节共培养物中突触素I的磷酸化。
Proc Natl Acad Sci U S A. 1993 May 1;90(9):4052-6. doi: 10.1073/pnas.90.9.4052.
4
Opioid peptides with differential affinity for mu and delta receptors decrease sensory neuron calcium-dependent action potentials.对μ和δ受体具有不同亲和力的阿片肽可降低感觉神经元钙依赖性动作电位。
J Pharmacol Exp Ther. 1983 Nov;227(2):394-402.
5
Kappa-opioid receptor stimulation abolishes mu- but not delta-mediated inhibitory control of spinal Met-enkephalin release.
Neurosci Lett. 1992 Jan 6;134(2):238-42. doi: 10.1016/0304-3940(92)90525-c.
6
A microiontophoretic study of the actions of mu-, delta- and kappa-opiate receptor agonists in the rat brain.大鼠脑中μ、δ和κ阿片受体激动剂作用的微量离子电泳研究
Br J Pharmacol. 1984 Nov;83(3):763-72. doi: 10.1111/j.1476-5381.1984.tb16231.x.
7
Enkephalins modulate excitatory synaptic transmission in the superficial dorsal horn by acting at mu-opioid receptor sites.脑啡肽通过作用于μ-阿片受体位点来调节脊髓背角浅层的兴奋性突触传递。
Brain Res. 1988 Sep 20;460(2):260-8. doi: 10.1016/0006-8993(88)90371-x.
8
Dynorphin selectively augments the M-current in hippocampal CA1 neurons by an opiate receptor mechanism.强啡肽通过阿片受体机制选择性增强海马CA1神经元的M电流。
J Neurophysiol. 1999 Oct;82(4):1768-75. doi: 10.1152/jn.1999.82.4.1768.
9
The excitatory response of in vitro hippocampal pyramidal cells to normorphine and methionine-enkephalin may be mediated by different receptor populations.体外培养的海马锥体细胞对去甲吗啡和甲硫氨酸脑啡肽的兴奋性反应可能由不同的受体群体介导。
Exp Brain Res. 1982;48(2):238-44. doi: 10.1007/BF00237219.
10
Distinct antinociceptive actions mediated by different opioid receptors in the region of lamina I and laminae III-V of the dorsal horn of the rat.大鼠背角I层和III - V层区域中不同阿片受体介导的不同抗伤害感受作用。
Br J Pharmacol. 1990 Oct;101(2):477-83. doi: 10.1111/j.1476-5381.1990.tb12733.x.

引用本文的文献

1
Antibodies to probe endogenous G protein-coupled receptor heteromer expression, regulation, and function.用于探测内源性G蛋白偶联受体异聚体表达、调控及功能的抗体。
Front Pharmacol. 2014 Dec 3;5:268. doi: 10.3389/fphar.2014.00268. eCollection 2014.
2
Revolution in GPCR signalling: opioid receptor heteromers as novel therapeutic targets: IUPHAR review 10.G蛋白偶联受体信号传导的革命:阿片受体异聚体作为新型治疗靶点:IUPHAR综述10
Br J Pharmacol. 2014 Sep;171(18):4155-76. doi: 10.1111/bph.12798.
3
Pharmacological Profiles of Oligomerized μ-Opioid Receptors.
寡聚 μ 阿片受体的药理学特性。
Cells. 2013 Oct 11;2(4):689-714. doi: 10.3390/cells2040689.
4
Heteromers of μ-δ opioid receptors: new pharmacology and novel therapeutic possibilities.μ-δ阿片受体异聚体:新药理学及新型治疗可能性
Br J Pharmacol. 2015 Jan;172(2):375-87. doi: 10.1111/bph.12663. Epub 2014 Jul 1.
5
Disruption of δ-opioid receptor phosphorylation at threonine 161 attenuates morphine tolerance in rats with CFA-induced inflammatory hypersensitivity.δ-阿片受体第 161 位苏氨酸磷酸化的破坏可减轻 CFA 诱导的炎症性超敏反应大鼠对吗啡的耐受。
Neurosci Bull. 2012 Apr;28(2):182-92. doi: 10.1007/s12264-012-1216-8.
6
Essential role of mu opioid receptor in the regulation of delta opioid receptor-mediated antihyperalgesia.μ阿片受体在调节δ阿片受体介导的抗痛觉过敏中的重要作用。
Neuroscience. 2007 Dec 19;150(4):807-17. doi: 10.1016/j.neuroscience.2007.09.060. Epub 2007 Oct 5.
7
Heterodimerization of mu and delta opioid receptors: A role in opiate synergy.μ和δ阿片受体的异源二聚化:在阿片类药物协同作用中的作用。
J Neurosci. 2000 Nov 15;20(22):RC110. doi: 10.1523/JNEUROSCI.20-22-j0007.2000.
8
Inhibition of dopamine-sensitive adenylate cyclase by opioids: possible involvement of physically associated mu- and delta-opioid receptors.阿片类物质对多巴胺敏感的腺苷酸环化酶的抑制作用:与μ和δ阿片受体物理关联的可能参与情况。
Naunyn Schmiedebergs Arch Pharmacol. 1987 Mar;335(3):278-84. doi: 10.1007/BF00172797.