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The effect of a series of clonidine analogues on [3H] clonidine binding in rat cerebral cortex.

作者信息

Jarrott B, Louis W J, Summers R J

出版信息

Biochem Pharmacol. 1979;28(1):141-4. doi: 10.1016/0006-2952(79)90282-x.

DOI:10.1016/0006-2952(79)90282-x
PMID:215166
Abstract
摘要

相似文献

1
The effect of a series of clonidine analogues on [3H] clonidine binding in rat cerebral cortex.一系列可乐定类似物对大鼠大脑皮层中[3H]可乐定结合的影响。
Biochem Pharmacol. 1979;28(1):141-4. doi: 10.1016/0006-2952(79)90282-x.
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Binding characteristics of [3H]guanfacine to rat brain alpha-adrenoceptors. Comparison with [3H]clonidine.[3H]胍法辛与大鼠脑α-肾上腺素能受体的结合特性。与[3H]可乐定的比较。
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5
Specific binding of 3H-guanfacine to alpha 2-adrenoceptors in rat brain. Comparison with 3H-clonidine.3H-胍法辛与大鼠脑内α2-肾上腺素能受体的特异性结合。与3H-可乐定的比较。
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Receptor interactions of imidazolines. XI. Alpha-adrenergic and antihypertensive effects of clonidine and its methylene-bridged analog, St 1913.咪唑啉的受体相互作用。XI. 可乐定及其亚甲基桥连类似物St 1913的α-肾上腺素能和降压作用。
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[Relative affinities of S 3341 and clonidine for the alpha 2- and alpha 2-adrenoceptors of the rat brain (author's transl)].[S 3341与可乐定对大鼠脑α₂-和α₁-肾上腺素能受体的相对亲和力（作者译）]
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[3H]Para-amino-clonidine: a novel ligand which binds with high affinity to alpha-adrenergic receptors.[3H]对氨基可乐定：一种与α-肾上腺素能受体高亲和力结合的新型配体。
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3H-clonidine and 3H-p-aminoclonidine interactions in vitro with central and peripheral alpha 2-adrenergic receptors.3H-可乐定和3H-对氨基可乐定在体外与中枢和外周α2-肾上腺素能受体的相互作用。
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Displacement of [3H]clonidine binding by clonidine analogues in membranes from rat cerebral cortex.大鼠大脑皮层膜中可乐定类似物对[3H]可乐定结合的置换作用。
Eur J Pharmacol. 1980 Aug 29;66(2-3):233-41. doi: 10.1016/0014-2999(80)90147-8.

引用本文的文献

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Adrenoceptors: Receptors, Ligands and Their Clinical Uses, Molecular Pharmacology and Assays.肾上腺素能受体：受体、配体及其临床用途，分子药理学和检测。
Handb Exp Pharmacol. 2024;285:55-145. doi: 10.1007/164_2024_713.
2
Double-blind trial comparing guanfacine and methyldopa in patients with essential hypertension.比较胍法辛和甲基多巴治疗原发性高血压患者的双盲试验。
Eur J Clin Pharmacol. 1981;19(5):309-15. doi: 10.1007/BF00544579.
3
Guanabenz. A review of its pharmacodynamic properties and therapeutic efficacy in hypertension.胍那苄。其药效学特性及治疗高血压疗效的综述。
Drugs. 1983 Sep;26(3):212-29. doi: 10.2165/00003495-198326030-00003.
4
[3H]-Clonidine binding to alpha-adrenoceptors in membranes prepared from regions of guinea-pig kidney: alteration by monovalent and divalent cations.[3H] -可乐定与豚鼠肾脏各区域制备的膜中α-肾上腺素能受体的结合：单价和二价阳离子的影响
Br J Pharmacol. 1980;71(1):57-63. doi: 10.1111/j.1476-5381.1980.tb10909.x.
5
[3H]-guanfacine: a radioligand that selectively labels high affinity alpha2-adrenoceptor sites in homogenates of rat brain.[3H]-胍法辛：一种能选择性标记大鼠脑匀浆中高亲和力α2-肾上腺素能受体位点的放射性配体。
Br J Pharmacol. 1982 Feb;75(2):401-8. doi: 10.1111/j.1476-5381.1982.tb08801.x.
6
Pharmacological characterization of the alpha adrenoceptors of the dog basilar artery.犬基底动脉α肾上腺素能受体的药理学特性
Naunyn Schmiedebergs Arch Pharmacol. 1982 Apr;319(1):1-7. doi: 10.1007/BF00491469.
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A comparison of the cardiovascular and sedative actions of the alpha-adrenoceptor agonists, FLA-136 and clonidine, in the rat.大鼠体内α-肾上腺素能受体激动剂FLA - 136与可乐定的心血管及镇静作用比较
Br J Pharmacol. 1982 Jan;75(1):13-21. doi: 10.1111/j.1476-5381.1982.tb08753.x.
8
A comparison of pre- and post-junctional potencies of several alpha-adrenoceptor agonists in the cardiovascular system and anococcygeus muscle of the rat. Evidence for two types of post-junctional alpha-adrenoceptor.几种α-肾上腺素能激动剂在大鼠心血管系统和尾骨肌中节前和节后效能的比较。两种节后α-肾上腺素能受体的证据。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jun;312(2):107-16. doi: 10.1007/BF00569718.
9
Renal effects of antihypertensive drugs.抗高血压药物对肾脏的影响。
Drugs. 1989 Jun;37(6):900-25. doi: 10.2165/00003495-198937060-00005.