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去甲肾上腺素而非牛磺酸对脑钠钾ATP酶的刺激作用。

Stimulation of brain Na,K-ATPase by norepinephrine but not taurine.

作者信息

Chapman G E, Greenwood C E

机构信息

Department of Nutritional Sciences, Faculty of Medicine, University of Toronto, Ontario.

出版信息

Neurochem Res. 1988 Jan;13(1):77-82. doi: 10.1007/BF00971858.

DOI:10.1007/BF00971858
PMID:2835694
Abstract

The effect of taurine on rat and hamster brain Na,K-ATPase was examined and compared to norepinephrine (NE) stimulation of the enzyme. Although NE stimulation of microsomal Na,K-ATPase was observed in the presence of the cell cytosolic fraction, taurine was without effect in the presence and absence of this fraction. Taurine also failed to modulate pubescent and mature hamster brain Na,K-ATPase. Presence or absence of ion chelators did not change taurine's effect. These results are discussed in relation to previous reports of taurine and catecholamine stimulation of Na,K-ATPase.

摘要

研究了牛磺酸对大鼠和仓鼠脑钠钾-ATP酶的作用,并与去甲肾上腺素(NE)对该酶的刺激作用进行了比较。尽管在存在细胞胞质部分的情况下观察到NE对微粒体钠钾-ATP酶有刺激作用,但无论有无该部分,牛磺酸均无作用。牛磺酸也未能调节青春期和成年仓鼠脑钠钾-ATP酶。离子螯合剂的存在与否并未改变牛磺酸的作用。结合先前关于牛磺酸和儿茶酚胺刺激钠钾-ATP酶的报道对这些结果进行了讨论。

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1
Stimulation of brain Na,K-ATPase by norepinephrine but not taurine.去甲肾上腺素而非牛磺酸对脑钠钾ATP酶的刺激作用。
Neurochem Res. 1988 Jan;13(1):77-82. doi: 10.1007/BF00971858.
2
Taurine stimulation of isolated hamster brain Na+,K+-ATPase: activation kinetics and chemical specificity.
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[Na, K-ATPase activity of the microsomal fraction of the rat brain exposed to insulin].[暴露于胰岛素的大鼠脑微粒体部分的钠钾ATP酶活性]
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Effect of catecholamines and metal chelating agents on the brain and brown adipose tissue Na,K-ATPase.儿茶酚胺和金属螯合剂对脑及棕色脂肪组织钠钾-ATP酶的影响。
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Modulation of benthiocarb in vitro inhibited neonate rat (Wistar strain) brain Na+K+-ATPase by norepinephrine.灭草松的体外调节通过去甲肾上腺素抑制新生大鼠(Wistar品系)脑钠钾ATP酶。
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[Effect of mineralocorticoids on the Na, K-ATPase activity of the rat brain].[盐皮质激素对大鼠脑钠钾ATP酶活性的影响]
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Inhibition of hamster sperm Na+, K+-ATPase activity by taurine and hypotaurine.牛磺酸和亚牛磺酸对仓鼠精子钠钾ATP酶活性的抑制作用。
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Stimulation of brain Na+, K+-ATPase by norepinephrine in vivo: prevention by receptor antagonists and enhancement by repeated stimulation.去甲肾上腺素对体内脑钠钾ATP酶的刺激作用:受体拮抗剂的抑制作用及重复刺激的增强作用
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Buffer systems variably affect the interaction of norepinephrine with brain Na+-K+ ATPase.缓冲系统对去甲肾上腺素与脑钠钾ATP酶的相互作用有不同程度的影响。
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Noradrenaline stimulation of (Na+, K+)ATPase in homogenates of the developing rat brain.去甲肾上腺素对发育中大鼠脑匀浆中(钠,钾)ATP酶的刺激作用。
Biochem Pharmacol. 1981 Aug 15;30(16):2368-70. doi: 10.1016/0006-2952(81)90116-7.

本文引用的文献

1
Does Na,K-ATPase play a role in the regulation of neurotransmitter release by prejunctional alpha-adrenoceptors?
Biochem Pharmacol. 1981 Sep 1;30(17):2389-97. doi: 10.1016/0006-2952(81)90332-4.
2
The Na,K-ATPase of nervous tissue.神经组织的钠钾ATP酶
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3
Possible mechanisms involved in the release and modulation of release of neuroactive agents.神经活性物质释放及释放调节所涉及的可能机制。
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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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A SENSITIVE AND SPECIFIC ASSAY FOR THE ESTIMATION OF MONOAMINE OXIDASE.一种用于估算单胺氧化酶的灵敏且特异的检测方法。
Biochem Pharmacol. 1963 Dec;12:1439-41. doi: 10.1016/0006-2952(63)90215-6.
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Distribution and function of taurine in nervous tissues: an introductory review.
Prog Clin Biol Res. 1983;125:127-40.
7
Catecholamines and the brain microsomal Na, K-adenosinetriphosphatase--II. The mechanism of action.
Biochem Pharmacol. 1981 Mar 1;30(5):433-9. doi: 10.1016/0006-2952(81)90627-4.
8
Catecholamines and the brain microsomal Na, K-adenosinetriphosphatase--I. Protection against lipoperoxidative damage.儿茶酚胺与脑微粒体钠钾 - 三磷酸腺苷酶——I. 对脂质过氧化损伤的保护作用
Biochem Pharmacol. 1981 Mar 1;30(5):427-32. doi: 10.1016/0006-2952(81)90626-2.
9
The effect of desipramine on the noradrenaline stimulated Na-K ATPase of rabbit synaptic membranes.去甲丙咪嗪对兔突触膜中去甲肾上腺素刺激的钠钾ATP酶的作用。
Biochem Pharmacol. 1980 Jan 1;29(1):111-2. doi: 10.1016/0006-2952(80)90252-x.
10
Receptor independent stimulatory effect of noradrenaline on Na,K-ATPase in rat brain homogenate. Role of lipid peroxidation.去甲肾上腺素对大鼠脑匀浆中钠钾ATP酶的非受体依赖性刺激作用。脂质过氧化的作用。
Biochem Pharmacol. 1982 Jul 1;31(13):2231-6. doi: 10.1016/0006-2952(82)90106-x.