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松果体中苯二氮䓬类“外周型”结合位点的调节。

Regulation of "peripheral-type" binding sites for benzodiazepines in the pineal gland.

作者信息

Weissman B A, Skolnick P, Klein D C

出版信息

Pharmacol Biochem Behav. 1984 Dec;21(6):821-4. doi: 10.1016/s0091-3057(84)80059-3.

DOI:10.1016/s0091-3057(84)80059-3
PMID:6097917
Abstract

The density of "peripheral-type" binding sites for benzodiazepines (PBS) in the rat pineal gland was reduced by approximately 50% three weeks after superior cervical ganglionectomy or exposure to constant light; the apparent affinity of [3H]Ro 5-4864 (the prototype ligand for these sites) remained unchanged. In contrast, neither the density of PBS nor the apparent affinity of [3H]Ro 5-4864 for these sites was altered in cerebral cortex by these procedures. The demonstration that PBS density is under neural control in the pineal gland suggests that these sites may have a physiologic role. The high density of PBS in pineal (approximately 24 pmol/mg protein) suggests that this tissue may be a useful model to study both the physiologic and pharmacologic function of these sites.

摘要

大鼠松果体中苯二氮䓬“外周型”结合位点(PBS)的密度,在颈上神经节切除术后三周或持续光照三周后降低了约50%;[3H]Ro 5-4864(这些位点的原型配体)的表观亲和力保持不变。相比之下,这些操作并未改变大脑皮层中PBS的密度以及[3H]Ro 5-4864对这些位点的表观亲和力。松果体中PBS密度受神经控制这一发现表明,这些位点可能具有生理作用。松果体中PBS的高密度(约24 pmol/mg蛋白质)表明,该组织可能是研究这些位点生理和药理功能的有用模型。

相似文献

1
Regulation of "peripheral-type" binding sites for benzodiazepines in the pineal gland.松果体中苯二氮䓬类“外周型”结合位点的调节。
Pharmacol Biochem Behav. 1984 Dec;21(6):821-4. doi: 10.1016/s0091-3057(84)80059-3.
2
Endogenous inhibitors of [3H] Ro 5-4864 binding to "peripheral-type" binding sites for benzodiazepines are present in peripheral tissues and brain.与苯二氮䓬“外周型”结合位点结合的[3H] Ro 5-4864的内源性抑制剂存在于外周组织和大脑中。
Prog Clin Biol Res. 1985;192:167-73.
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High density of [3H]Ro 5-4864 'peripheral' benzodiazepine binding sites in the pineal gland.松果体中[3H]Ro 5 - 4864“外周”苯二氮䓬结合位点的高密度。
Eur J Pharmacol. 1984 Jul 20;102(3-4):559-60. doi: 10.1016/0014-2999(84)90582-x.
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Characterization of benzodiazepine receptors in the bovine pineal gland: evidence for the presence of an atypical binding site.牛松果体中苯二氮䓬受体的特性:存在非典型结合位点的证据。
Brain Res. 1986 Nov;387(2):127-35. doi: 10.1016/0169-328x(86)90004-5.
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[3H]AHN 086 acylates peripheral benzodiazepine receptors in the rat pineal gland.[3H]AHN 086使大鼠松果体中的外周苯二氮䓬受体发生酰化作用。
FEBS Lett. 1989 Feb 27;244(2):263-7. doi: 10.1016/0014-5793(89)80541-1.
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Benzodiazepine binding sites in human pineal gland.人类松果体中的苯二氮䓬结合位点。
Eur J Pharmacol. 1984 Nov 13;106(2):399-403. doi: 10.1016/0014-2999(84)90728-3.
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In vitro uptake of benzodiazepines by rat pineal gland.大鼠松果体对苯二氮䓬类药物的体外摄取。
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Characterization of a [3H]glutamate binding site in rat pineal gland: enhanced affinity following superior cervical ganglionectomy.大鼠松果体中[3H]谷氨酸结合位点的特性:颈上神经节切除术后亲和力增强。
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Benzodiazepines decrease norepinephrine release from rat pineal nerves by acting on peripheral type binding sites.苯二氮䓬类药物通过作用于外周型结合位点来减少大鼠松果体神经中去甲肾上腺素的释放。
Acta Physiol Pharmacol Latinoam. 1985;35(4):441-9.

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