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人类脊髓中的阿片受体结合位点。

Opiate receptor binding sites in human spinal cord.

作者信息

Członkowski A, Costa T, Przewłocki R, Pasí A, Herz A

出版信息

Brain Res. 1983 May 16;267(2):392-6. doi: 10.1016/0006-8993(83)90897-1.

DOI:10.1016/0006-8993(83)90897-1
PMID:6307472
Abstract

Opiate receptor binding sites were analyzed in various regions of human spinal cord and compared to results obtained in spinal cord and brain of certain animals. mu-, delta- and kappa binding sites were individually monitored by the overall labeling of opiate binding sites with [3H]diprenorphine followed by the sequential elimination of binding to particular sites by the use of selective ligands. kappa-Receptors were the predominant type (approximately 50%), followed by mu-receptors (approximately 40%), and, in rather small amounts, delta-receptors. A similar proportion of receptor types was found in the spinal cord of guinea pigs.

摘要

对人类脊髓的各个区域进行了阿片受体结合位点分析,并与在某些动物的脊髓和大脑中获得的结果进行了比较。通过用[3H]二丙诺啡对阿片结合位点进行整体标记,然后使用选择性配体依次消除与特定位点的结合,分别监测了μ、δ和κ结合位点。κ受体是主要类型(约50%),其次是μ受体(约40%),δ受体的含量较少。在豚鼠的脊髓中也发现了类似比例的受体类型。

相似文献

1
Opiate receptor binding sites in human spinal cord.人类脊髓中的阿片受体结合位点。
Brain Res. 1983 May 16;267(2):392-6. doi: 10.1016/0006-8993(83)90897-1.
2
Pre- and postnatal development of opiate receptor subtypes in rat spinal cord.大鼠脊髓中阿片受体亚型的产前和产后发育
Brain Res Dev Brain Res. 1990 Apr 1;53(1):97-102. doi: 10.1016/0165-3806(90)90128-l.
3
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.
4
Analogues of beta-LPH61-64 possessing selective agonist activity at mu-opiate receptors.在μ-阿片受体上具有选择性激动剂活性的β-促脂解素61-64类似物。
Eur J Pharmacol. 1981 Apr 9;70(4):531-40. doi: 10.1016/0014-2999(81)90364-2.
5
Opioid receptor ligands in the neonatal rat spinal cord: binding and in vitro depression of the nociceptive responses.新生大鼠脊髓中的阿片受体配体:结合与伤害性反应的体外抑制
Br J Pharmacol. 1990 Mar;99(3):503-8. doi: 10.1111/j.1476-5381.1990.tb12958.x.
6
Traumatic injury alters opiate receptor binding in rat spinal cord.
Ann Neurol. 1986 May;19(5):498-501. doi: 10.1002/ana.410190514.
7
Characterisation of kappa-opioid binding sites in rat and guinea-pig spinal cord.
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8
Differential effects of two kappa-opiate agonists, U-50,488H and U-69,593, on the binding of 3H-(3-MeHis2) thyrotropin-releasing hormone to rat spinal cord and amygdala membranes.两种κ-阿片受体激动剂U-50,488H和U-69,593对3H-(3-甲基组氨酸2)促甲状腺激素释放激素与大鼠脊髓和杏仁核膜结合的不同影响。
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Multiple opiate binding sites in the central nervous system of the rabbit. Large predominance of a mu subtype in the cerebellum and characterization of a kappa subtype in the thalamus.兔中枢神经系统中的多个阿片类结合位点。小脑内μ亚型占主导,丘脑内κ亚型的特征描述。
Mol Pharmacol. 1983 Jul;24(1):23-9.
10
Characterisation of opioid binding sites using selective antagonists.
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The effect of µ-opioid receptor activation on GABAergic neurons in the spinal dorsal horn.μ-阿片受体激活对脊髓背角GABA能神经元的影响。
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3
Opioid receptor binding in rat spinal cord.大鼠脊髓中的阿片受体结合
Neurochem Res. 1987 Mar;12(3):231-5. doi: 10.1007/BF00972131.
4
Distinct distribution of opioid receptor types in rat lumbar spinal cord.大鼠腰段脊髓中阿片受体类型的独特分布。
Naunyn Schmiedebergs Arch Pharmacol. 1987 Aug;336(2):240-3. doi: 10.1007/BF00165811.
5
Spinal antinociceptive actions and naloxone reversibility of intravenous mu- and kappa-opioids in spinalized rats: potency mismatch with values reported for spinal administration.脊髓麻醉大鼠静脉注射μ和κ阿片类药物的脊髓抗伤害感受作用及纳洛酮可逆性:与脊髓给药报道值的效价不匹配
Br J Pharmacol. 1989 Oct;98(2):533-43. doi: 10.1111/j.1476-5381.1989.tb12627.x.
6
Delta-opioid receptor binding sites in rodent spinal cord.啮齿动物脊髓中的δ阿片受体结合位点。
Br J Pharmacol. 1990 Jun;100(2):319-23. doi: 10.1111/j.1476-5381.1990.tb15802.x.
7
Central non-opioid physiological and pathophysiological effects of dynorphin A and related peptides.强啡肽A及相关肽的中枢非阿片类生理和病理生理作用。
J Psychiatry Neurosci. 1992 Sep;17(3):106-19.