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Differences in D- and L-norepinephrine-H3.

作者信息

KOPIN I J, BRIDGERS W

出版信息

Life Sci (1962). 1963 May;5:356-62. doi: 10.1016/0024-3205(63)90169-3.

DOI:10.1016/0024-3205(63)90169-3
PMID:14034692
Abstract
摘要

相似文献

1
Differences in D- and L-norepinephrine-H3.D-和L-去甲肾上腺素-H3的差异
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2
The effects of tranylcypromine isomers on norepinephrine-H3 metabolism in rat brain.反苯环丙胺异构体对大鼠脑内去甲肾上腺素-H3代谢的影响。
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Functional identification of histamine H3-receptors in the human heart.人类心脏中组胺H3受体的功能鉴定
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6
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Regional differences in H3-norepinephrine and H3-dopamine uptake into rat brain homogenates.大鼠脑匀浆中H3-去甲肾上腺素和H3-多巴胺摄取的区域差异。
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8
Direct evidence for histamine H3 receptor-mediated inhibition of norepinephrine release from sympathetic terminals of guinea pig myocardium.组胺H3受体介导抑制豚鼠心肌交感神经末梢去甲肾上腺素释放的直接证据。
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N-methyl-D-aspartate (NMDA)-stimulated noradrenaline (NA) release in rat brain cortex is modulated by presynaptic H3-receptors.大鼠大脑皮层中，N-甲基-D-天冬氨酸（NMDA）刺激的去甲肾上腺素（NA）释放受突触前H3受体调节。
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Histamine H3-receptor signaling in the heart: possible involvement of Gi/Go proteins and N-type Ca++ channels.心脏中的组胺H3受体信号传导：Gi/Go蛋白和N型钙离子通道可能的参与情况。
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引用本文的文献

1
THE UPTAKE AND RELEASE OF H3-NOREPINEPHRINE BY THE GUINEA-PIG HEART IN VIVO.豚鼠心脏在体对H3-去甲肾上腺素的摄取与释放
Naunyn Schmiedebergs Arch Exp Pathol Pharmakol. 1964 Apr 21;248:85-98. doi: 10.1007/BF00247061.
2
THE UPTAKE OF NORADRENALINE BY THE ISOLATED PERFUSED RAT HEART.去甲肾上腺素在离体灌注大鼠心脏中的摄取
Br J Pharmacol Chemother. 1963 Dec;21(3):523-37. doi: 10.1111/j.1476-5381.1963.tb02020.x.
3
The uptake and release of radioactive noradrenaline by the splenic nerves of cats.猫脾神经对放射性去甲肾上腺素的摄取与释放
J Physiol. 1966 Nov;187(1):51-68. doi: 10.1113/jphysiol.1966.sp008075.
4
[Turnover times of noradrenaline in various rat organs determined by the isotope method: comparison of the the results obtained from utilizaton of l and dl noradrenaline 3H].
Pflugers Arch. 1971;323(4):297-309. doi: 10.1007/BF00592400.
5
Steric aspects of adrenergic drugs XXI. Drug-induced release of (-)- and (+)- 14 C-norepinephrine from the isolated superfused rat vas deferens.
Naunyn Schmiedebergs Arch Pharmacol. 1972;274(4):394-403. doi: 10.1007/BF00501276.