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Guanine nucleotides modulate muscarinic receptor binding in the heart.

作者信息

Berrie C P, Birdsall N J, Burgen A S, Hulme E C

出版信息

Biochem Biophys Res Commun. 1979 Apr 27;87(4):1000-5. doi: 10.1016/s0006-291x(79)80006-6.

DOI:10.1016/s0006-291x(79)80006-6
PMID:465020
Abstract
摘要

相似文献

1
Guanine nucleotides modulate muscarinic receptor binding in the heart.鸟嘌呤核苷酸调节心脏中的毒蕈碱受体结合。
Biochem Biophys Res Commun. 1979 Apr 27;87(4):1000-5. doi: 10.1016/s0006-291x(79)80006-6.
2
The regulation of muscarinic cholinergic receptors by guanine nucleotides in cardiac tissue.鸟嘌呤核苷酸对心脏组织中毒蕈碱型胆碱能受体的调节作用。
Eur J Pharmacol. 1979 Jun;56(1-2):179-80. doi: 10.1016/0014-2999(79)90451-5.
3
Guanine nucleotide-induced positive cooperativity in muscarinic-cholinergic antagonist binding.鸟嘌呤核苷酸诱导的毒蕈碱型胆碱能拮抗剂结合中的正协同性。
Biochem Biophys Res Commun. 1986 Jan 14;134(1):172-7. doi: 10.1016/0006-291x(86)90543-7.
4
Cardiac muscarinic cholinergic receptor binding is regulated by Na+ and guanyl nucleotides.心肌毒蕈碱胆碱能受体结合受钠离子和鸟苷核苷酸调节。
J Biol Chem. 1980 Feb 10;255(3):820-3.
5
Hepatic alpha 1-adrenergic receptors show agonist-specific regulation by guanine nucleotides. Loss of nucleotide effect after adrenalectomy.肝脏α1 - 肾上腺素能受体显示出鸟嘌呤核苷酸对激动剂的特异性调节作用。肾上腺切除术后核苷酸效应丧失。
J Biol Chem. 1982 Oct 10;257(19):11577-83.
6
Guanine nucleotides preferentially inhibit binding of antagonists (male) and agonists (female) to muscarinic receptors of rat adenohypophysis.鸟嘌呤核苷酸优先抑制拮抗剂（雄性）和激动剂（雌性）与大鼠腺垂体毒蕈碱受体的结合。
Biochem Biophys Res Commun. 1981 Sep 30;102(2):753-60. doi: 10.1016/s0006-291x(81)80196-9.
7
MgCl2-sensitive and Gpp(NH)p-sensitive antagonist binding states of rat heart muscarinic receptors: preferential detection at ambient temperature assay and location in two subcellular fractions.大鼠心脏毒蕈碱受体的MgCl2敏感性和Gpp(NH)p敏感性拮抗剂结合状态：在环境温度测定中优先检测及在两个亚细胞组分中的定位
Mol Cell Biochem. 1990 May 10;94(2):133-46. doi: 10.1007/BF00214120.
8
Agonist specific effects of guanine nucleotides on muscarinic cholinergic receptors in rat anterior pituitary membranes.鸟嘌呤核苷酸对大鼠垂体前叶膜毒蕈碱胆碱能受体的激动剂特异性作用。
Biochim Biophys Acta. 1981 Apr 17;674(1):160-5. doi: 10.1016/0304-4165(81)90358-5.
9
Agonist and guanine nucleotide modulation of muscarinic cholinergic receptors in cultured heart cells.培养心肌细胞中毒蕈碱型胆碱能受体的激动剂和鸟嘌呤核苷酸调节
J Biol Chem. 1980 Oct 25;255(20):9571-9.
10
Cardiac muscarinic cholinergic receptor sites: opposing regulation by divalent cations and guanine nucleotides of receptor-agonist interaction.
Eur J Pharmacol. 1980 Apr 4;62(4):345-7. doi: 10.1016/0014-2999(80)90103-x.

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The expanding roles and mechanisms of G protein-mediated presynaptic inhibition.G 蛋白介导电突触前抑制的作用不断扩大及其机制。
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Muscarinic receptor oligomerization.毒蕈碱型乙酰胆碱受体寡聚化。
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Coupling of g proteins to reconstituted monomers and tetramers of the M2 muscarinic receptor.G蛋白与重组的M2毒蕈碱受体单体及四聚体的偶联。
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Estimation of ligand affinity constants for receptor states in functional studies involving the allosteric modulation of G protein-coupled receptors: implications for ligand bias.在涉及G蛋白偶联受体变构调节的功能研究中，受体状态配体亲和常数的估计：对配体偏向性的影响
J Pharmacol Toxicol Methods. 2014 May-Jun;69(3):253-79. doi: 10.1016/j.vascn.2014.01.002. Epub 2014 Jan 13.
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Molecular properties of muscarinic acetylcholine receptors.毒蕈碱型乙酰胆碱受体的分子特性。
Proc Jpn Acad Ser B Phys Biol Sci. 2013;89(6):226-56. doi: 10.2183/pjab.89.226.
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Oligomeric size of the m2 muscarinic receptor in live cells as determined by quantitative fluorescence resonance energy transfer.定量荧光共振能量转移法测定活细胞中 m2 毒蕈碱型乙酰胆碱受体的寡聚体大小。
J Biol Chem. 2010 May 28;285(22):16723-38. doi: 10.1074/jbc.M109.069443. Epub 2010 Mar 19.
7
On the analysis of ligand-directed signaling at G protein-coupled receptors.关于G蛋白偶联受体配体导向信号传导的分析。
Naunyn Schmiedebergs Arch Pharmacol. 2008 Jun;377(4-6):549-77. doi: 10.1007/s00210-008-0260-4. Epub 2008 Feb 6.
8
Inverse agonism at G protein-coupled receptors: (patho)physiological relevance and implications for drug discovery.G蛋白偶联受体的反向激动作用：（病理）生理学相关性及对药物发现的影响
Br J Pharmacol. 2000 May;130(1):1-12. doi: 10.1038/sj.bjp.0703311.
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Brain soluble fractions which modulate Na+, K+-ATPase activity likewise modify muscarinic receptor.调节钠钾ATP酶活性的脑可溶性组分同样会修饰毒蕈碱受体。
Neurochem Res. 1999 Nov;24(11):1417-22. doi: 10.1023/a:1022536824190.
10
Inverse agonist activity of pirenzepine at M2 muscarinic acetylcholine receptors.哌仑西平对M2毒蕈碱型乙酰胆碱受体的反向激动剂活性。
Br J Pharmacol. 1999 Mar;126(5):1246-52. doi: 10.1038/sj.bjp.0702407.