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乙醇对大鼠脑内刺激的肌醇磷脂水解的影响。

Effects of ethanol on stimulated inositol phospholipid hydrolysis in rat brain.

作者信息

Gonzales R A, Theiss C, Crews F T

出版信息

J Pharmacol Exp Ther. 1986 Apr;237(1):92-8.

PMID:3007745
Abstract

The effect of ethanol in vitro on inositol lipid metabolism in brain slices was investigated under nonstimulating and stimulating conditions. In cerebral cortical slices 100 microM norepinephrie (NE), 1 mM carbachol, 100 microM serotonin, 20 mM KCl, 1 mM glutamate and 30 microM A23187 stimulated inositide hydrolysis as measured by the release of [3H]inositol phosphates from [3H]myoinositol labeled slices. Ethanol (500 mM) inhibited nonstimulated inositide hydrolysis but had variable effects on stimulated inositide breakdown. NE-, KCl- and glutamate-stimulated [3H]inositol phosphate release was inhibited by 500 mM ethanol in the cortex. The inhibitory effect of ethanol on NE-stimulated inositide hydrolysis was concentration dependent and significant at concentrations as low as 100 mM. Inhibition by ethanol appeared to be noncompetitive. A similar pattern of inhibition by ethanol was observed when KCl was the stimulant. In hippocampal and hypothalamic slices, similar to cortical slices. NE- and KCl-stimulated inositide breakdown was significantly inhibited by ethanol. However, in brain stem slices, only KCl-stimulated [3H]inositol phosphate release was inhibited. Striatal slices stimulated by carbachol, NE and KCl were sensitive to the inhibitory effects of ethanol on inositol lipid breakdown. These results suggest that ethanol in vitro has specific effects on inositol lipid metabolism depending on the brain region studied and the type of stimulation. Moreover, the differential sensitivity to ethanol of stimulated inositide hydrolysis in the brain may contribute, at least in part, to some of the pharmacological effects of ethanol in vivo.

摘要

在非刺激和刺激条件下,研究了乙醇在体外对脑片肌醇脂质代谢的影响。在大脑皮层切片中,100微摩尔去甲肾上腺素(NE)、1毫摩尔卡巴胆碱、100微摩尔血清素、20毫摩尔氯化钾、1毫摩尔谷氨酸和30微摩尔A23187刺激了肌醇磷脂水解,这是通过从[3H]肌醇标记的切片中释放[3H]肌醇磷酸来测量的。乙醇(500毫摩尔)抑制了非刺激状态下的肌醇磷脂水解,但对刺激状态下的肌醇磷脂分解有不同的影响。在皮层中,500毫摩尔乙醇抑制了NE、氯化钾和谷氨酸刺激的[3H]肌醇磷酸释放。乙醇对NE刺激的肌醇磷脂水解的抑制作用呈浓度依赖性,在低至100毫摩尔的浓度时就具有显著作用。乙醇的抑制作用似乎是非竞争性的。当氯化钾作为刺激物时,观察到乙醇有类似的抑制模式。在海马体和下丘脑切片中,与皮层切片类似,NE和氯化钾刺激的肌醇磷脂分解受到乙醇的显著抑制。然而,在脑干切片中,只有氯化钾刺激的[3H]肌醇磷酸释放受到抑制。由卡巴胆碱、NE和氯化钾刺激的纹状体切片对乙醇抑制肌醇脂质分解的作用敏感。这些结果表明,体外乙醇对肌醇脂质代谢具有特定影响,这取决于所研究的脑区和刺激类型。此外,大脑中刺激状态下的肌醇磷脂水解对乙醇的不同敏感性可能至少部分地导致了乙醇在体内的一些药理作用。

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