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Specific binding of [3H]sulpiride to rat striatal preparations.

作者信息

Theodorou A, Crockett M, Jenner P, Marsden C D

出版信息

J Pharm Pharmacol. 1979 Jun;31(6):424-6. doi: 10.1111/j.2042-7158.1979.tb13545.x.

DOI:10.1111/j.2042-7158.1979.tb13545.x
PMID:39154
Abstract
摘要

相似文献

1
Specific binding of [3H]sulpiride to rat striatal preparations.[3H]舒必利与大鼠纹状体制剂的特异性结合。
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The effect of guanosine nucleotides of [3H]sulpiride binding to rat striatal membranes.
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Development of inhibitory activity of sulpiride for synaptic [3H]-spiperone binding in the rat striatum.舒必利对大鼠纹状体突触[3H] - 螺哌隆结合抑制活性的研究进展
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Kainic acid lesions of striatum and decortication reduce specific [3H]sulpiride binding in rats, so D-2 receptors exist post-synaptically on corticostriate afferents and striatal neurons.纹状体的海人酸损伤和去皮质作用可降低大鼠体内特异性[3H]舒必利结合,因此D-2受体存在于皮质纹状体传入纤维和纹状体神经元的突触后。
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Specific [3H]piflutixol binding to CHAPS-solubilised rat striatal preparations involves dopamine D-2 but not D-1 binding sites.特异性[3H]匹氟噻吨与CHAPS增溶的大鼠纹状体制剂的结合涉及多巴胺D-2而非D-1结合位点。
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Effect of guanine nucleotides on dopaminergic agonist and antagonist affinity for [3H]sulpiride binding sites in rat striatal membrane preparations.鸟嘌呤核苷酸对大鼠纹状体膜制剂中多巴胺能激动剂和拮抗剂与[³H]舒必利结合位点亲和力的影响。
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A study on the localization of [3H]sulpiride binding sites in rat striatal membranes.大鼠纹状体膜中[3H]舒必利结合位点的定位研究。
Neuropharmacology. 1981 Dec;20(12A):1151-5. doi: 10.1016/0028-3908(81)90056-3.

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J Neural Transm. 1989;76(1):13-28. doi: 10.1007/BF01244988.
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Quantitative autoradiographic distribution and pharmacological characterization of (3H)buspirone binding to sections from rat, bovine and marmoset brain.(3H)丁螺环酮与大鼠、牛和狨猴脑切片结合的定量放射自显影分布及药理学特征
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Dopamine acts on D2 receptors to increase potassium conductance in neurones of the rat substantia nigra zona compacta.多巴胺作用于D2受体,以增加大鼠黑质致密部神经元的钾离子电导率。
J Physiol. 1987 Nov;392:397-416. doi: 10.1113/jphysiol.1987.sp016787.
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Effects of selective D1 and D2 dopamine antagonists on cocaine self-administration in the rat.
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