Selective affinity labeling and molecular characterization of hepatic alpha 1-adrenergic receptors with [3H]phenoxybenzamine.

Suppr

超能文献

作者信息

Kunos G, Kan W H, Greguski R, Venter J C

出版信息

J Biol Chem. 1983 Jan 10;258(1):326-32.

PMID:6294103

Abstract

摘要

相似文献

Selective affinity labeling and molecular characterization of hepatic alpha 1-adrenergic receptors with [3H]phenoxybenzamine.

J Biol Chem. 1983 Jan 10;258(1):326-32.

Characterization and solubilization of the alpha-adrenoreceptor of rat liver plasma membranes labeled with [3H]phenoxybenzamine.用[3H]酚苄明标记的大鼠肝质膜α-肾上腺素能受体的特性鉴定及增溶作用

J Biol Chem. 1979 Nov 10;254(21):10761-8.

The hepatic alpha-adrenergic receptor.肝脏α-肾上腺素能受体。

Adv Cyclic Nucleotide Res. 1981;14:507-19.

Affinity labelling of alpha-adrenoceptors in intact liver cells by [3H]phenoxybenzamine.用[3H]酚苄明对完整肝细胞中的α-肾上腺素能受体进行亲和标记。

Biochem Biophys Res Commun. 1979 Nov 14;91(1):303-11. doi: 10.1016/0006-291x(79)90618-1.

Hepatic alpha-adrenoreceptor: specific and irreversible labeling by [3H]-phenoxybenzamine.肝脏α-肾上腺素能受体：[3H] - 酚苄明的特异性和不可逆标记

Biochem Biophys Res Commun. 1979 Aug 28;89(4):1178-85. doi: 10.1016/0006-291x(79)92132-6.

Affinity labeling of the DDT1 MF-2 cell alpha 1-adrenergic receptor with [3H]phenoxybenzamine.用[3H]酚苄明对DDT1 MF-2细胞α1-肾上腺素能受体进行亲和标记。

Biochem Pharmacol. 1986 May 15;35(10):1663-9. doi: 10.1016/0006-2952(86)90320-5.

Measurement of alpha-adrenoceptor "turnover' using phenoxybenzamine.

Eur J Pharmacol. 1982 May 21;80(2-3):279-80. doi: 10.1016/0014-2999(82)90070-x.

Studies on the alpha-adrenergic activation of hepatic glucose output. alpha-Adrenergic activation of phosphorylase by immobilized epinephrine.

J Biol Chem. 1980 May 10;255(9):3905-10.

Simultaneous loss and reappearance of alpha 1-adrenergic responses and [3H]prazosin binding sites in rat liver after irreversible blockade by phenoxybenzamine.在经苯氧苄胺不可逆阻断后，大鼠肝脏中α1-肾上腺素能反应和[3H]哌唑嗪结合位点的同时丧失与重现

Biochim Biophys Acta. 1983 May 25;757(2):156-63. doi: 10.1016/0304-4165(83)90103-4.

Identification of the subunit-binding site of alpha 2-adrenergic receptors using [3H]phenoxybenzamine.使用[3H]酚苄明鉴定α2-肾上腺素能受体的亚基结合位点。

J Biol Chem. 1984 Jun 25;259(12):7864-9.

引用本文的文献

Monoclonal antibodies detect the conservation of muscarinic cholinergic receptor structure from Drosophila to human brain and detect possible structural homology with alpha 1-adrenergic receptors.单克隆抗体检测到从果蝇到人类大脑毒蕈碱胆碱能受体结构的保守性，并检测到与α1 -肾上腺素能受体可能的结构同源性。

Proc Natl Acad Sci U S A. 1984 Jan;81(1):272-6. doi: 10.1073/pnas.81.1.272.

The role of calcium ions in the mechanism of action of alpha-adrenergic agonists in rat liver.钙离子在大鼠肝脏中α-肾上腺素能激动剂作用机制中的作用。

Biochem J. 1984 Oct 1;223(1):1-13. doi: 10.1042/bj2230001.

Time-dependent conversion of alpha 1- to beta-adrenoceptor-mediated glycogenolysis in isolated rat liver cells: role of membrane phospholipase A2.离体大鼠肝细胞中α1-肾上腺素能受体介导的糖原分解向β-肾上腺素能受体介导的糖原分解的时间依赖性转变：膜磷脂酶A2的作用

Proc Natl Acad Sci U S A. 1984 Oct;81(19):6178-82. doi: 10.1073/pnas.81.19.6178.

Effects of the irreversible alpha-adrenoceptor antagonists phenoxybenzamine and benextramine on the effectiveness of nifedipine in inhibiting alpha 1- and alpha 2-adrenoceptor mediated vasoconstriction in pithed rats.不可逆性α-肾上腺素能受体拮抗剂酚苄明和苄奈明对硝苯地平抑制去脑大鼠α1和α2肾上腺素能受体介导的血管收缩作用的影响。

Naunyn Schmiedebergs Arch Pharmacol. 1985 Jun;329(4):404-13. doi: 10.1007/BF00496376.

Molecular comparison of alpha 1- and alpha 2-adrenergic receptors suggests that these proteins are structurally related "isoreceptors".α1和α2肾上腺素能受体的分子比较表明，这些蛋白质是结构相关的“同工受体”。

Proc Natl Acad Sci U S A. 1985 Jul;82(14):4842-6. doi: 10.1073/pnas.82.14.4842.

Photoaffinity labeling of the DDT1 MF-2 cell alpha 1-adrenergic receptor.滴滴涕1 MF-2细胞α1-肾上腺素能受体的光亲和标记

Mol Cell Biochem. 1985 May;67(1):47-53. doi: 10.1007/BF00220985.

Irreversible blockade of beta-adrenergic receptors with a bromoacetyl derivative of pindolol.用吲哚洛尔的溴乙酰衍生物对β-肾上腺素能受体进行不可逆阻断。

Naunyn Schmiedebergs Arch Pharmacol. 1985 Jan;328(3):279-87. doi: 10.1007/BF00515554.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验