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α-去甲肾上腺素能受体在体内介导脑多磷酸肌醇代谢中的作用。

Involvement of alpha noradrenergic receptors in mediation of brain polyphosphoinositides metabolism in vivo.

作者信息

Soukup J, Schanberg S

出版信息

J Pharmacol Exp Ther. 1982 Jul;222(1):209-14.

PMID:6283069
Abstract

The acute effects of norepinephrine (NE) on polyphosphoinositide (PPI) metabolism were examined in regions of rat brain in vivo with the techniques of intracisternal injection and microwave irradiation fixation. NE (80 nmol/g of brain) increased PPI incorporation of both [32P] orthophosphate and [3H] inositol by 50 to 100% within 5 min of the simultaneous intracisternal administration of both drug and radiolabel. These effects of NE were more pronounced in the brainstem and cerebellum than in the cerebral cortex, and were greater for triphosphoinositide than for diphosphoinositide. The increases were blocked by phentolamine and phenoxybenzamine but not by propranolol or atropine, suggesting that alpha noradrenergic receptors mediated the effect. Similar metabolic responses were observed with PPI precursors, phosphatidic acid and monophosphoinositide. However, no other phospholipid was altered in response to the agents administered in these studies (data not shown). Increased incorporation of radiolabels into PPI was never accompanied by detectable increases in endogenous PPI concentrations, suggesting that head group turnover was stimulated rather than whole molecule synthesis. Also, the increase in PPI phosphate radiolabel incorporation was not due to NE effects on the specific activity of phosphate donor precursors (nucleotides). The present data suggest that the PPI may be involved in the membrane processes that result from stimulation of alpha noradrenergic receptors in brain.

摘要

采用脑池内注射和微波辐照固定技术,在大鼠脑内区域研究了去甲肾上腺素(NE)对多磷酸肌醇(PPI)代谢的急性影响。在同时进行药物和放射性标记物脑池内给药后5分钟内,NE(80 nmol/g脑)使[32P]正磷酸盐和[3H]肌醇的PPI掺入量增加了50%至100%。NE的这些作用在脑干和小脑中比在大脑皮层中更明显,对三磷酸肌醇的作用比对二磷酸肌醇的作用更大。这些增加被酚妥拉明和酚苄明阻断,但不被普萘洛尔或阿托品阻断,提示α肾上腺素能受体介导了该作用。用PPI前体磷脂酸和单磷酸肌醇也观察到了类似的代谢反应。然而,在这些研究中,未观察到其他磷脂因给药药物而发生改变(数据未显示)。放射性标记物掺入PPI增加时,内源性PPI浓度从未检测到相应增加,提示刺激的是头部基团周转而非整个分子的合成。此外,PPI磷酸放射性标记物掺入增加并非由于NE对磷酸盐供体前体(核苷酸)比活性的影响。目前的数据提示,PPI可能参与了脑内α肾上腺素能受体受刺激所导致的膜过程。

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