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SK&F 96365(1-[β-[3-(4-甲氧基苯基)丙氧基]-4-甲氧基苯乙基]-1H-咪唑盐酸盐)可刺激人U373 MG星形细胞瘤细胞中的磷酸肌醇水解。

SK&F 96365 (1-[beta-[3-(4-methoxyphenyl)propoxy]-4-methoxyphenylethyl]-1H- imidazole hydrochloride) stimulates phosphoinositide hydrolysis in human U373 MG astrocytoma cells.

作者信息

Arias-Montaño J A, Gibson W J, Young J M

机构信息

Department of Pharmacology, University of Cambridge, UK.

出版信息

Biochem Pharmacol. 1998 Oct 15;56(8):1023-7. doi: 10.1016/s0006-2952(98)00125-7.

Abstract

SK&F 96365 (1-[beta-[3-(4-methoxyphenyl)propoxy]-4-methoxyphenylethyl]-1H-imi dazole hydrochloride) stimulated the accumulation of [3H]inositol monophosphates ([3H]IP1) in human U373 MG astrocytoma cells prelabelled with [3H]inositol (EC50 15 +/- 1 microM, Hill coefficient 3.8 +/- 0.4). SK&F 96365-induced accumulation of [3H]IP1 increased linearly with time, but there was no initial rapid formation of [3H]IP3. SK&F 96365 also stimulated [3H]IP1 accumulation in human HeLa cells, but only to a small extent in slices of rat cerebral cortex and guinea-pig cerebellum. SK&F 96365-induced accumulation of [3H]IP1 in U373 MG cells increased as extracellular Ca2+ was increased from nominally zero to 4 mM, but there was no evidence that SK&F 96365 induced any marked entry of Ca2+ into cells; only an inhibition of store-refilling-induced Ca2+ entry was apparent. Further, the response to SK&F 96365 was additive with that to the Ca2+ ionophore ionomycin. Depolarization of the cells with raised K+ produced only a small stimulation of phosphoinositide hydrolysis. SK&F 96365 caused the release of Ca2+ from intracellular stores in U373 MG cells (EC50 26 +/- 14 microM), but thapsigargin induced only a small accumulation of [3H]IP1. Miconazole, another N-substituted imidazole, also stimulated [3H]IP1 accumulation in U373 cells.

摘要

SK&F 96365(1-[β-[3-(4-甲氧基苯基)丙氧基]-4-甲氧基苯乙基]-1H-咪唑盐酸盐)刺激预先用[3H]肌醇标记的人U373 MG星形细胞瘤细胞中[3H]肌醇单磷酸([3H]IP1)的积累(半数有效浓度为15±1微摩尔,希尔系数为3.8±0.4)。SK&F 96365诱导的[3H]IP1积累随时间呈线性增加,但没有[3H]IP3的初始快速形成。SK&F 96365也刺激人HeLa细胞中[3H]IP1的积累,但在大鼠大脑皮层切片和豚鼠小脑切片中仅产生很小程度的刺激。随着细胞外Ca2+从名义上的零增加到4毫摩尔,SK&F 96365在U373 MG细胞中诱导的[3H]IP1积累增加,但没有证据表明SK&F 96365诱导Ca2+有任何明显进入细胞;仅明显抑制了储存再填充诱导的Ca2+内流。此外,对SK&F 96365的反应与对Ca2+离子载体离子霉素的反应具有加和性。用升高的K+使细胞去极化仅对磷酸肌醇水解产生很小的刺激。SK&F 96365导致U373 MG细胞中Ca2+从细胞内储存释放(半数有效浓度为26±14微摩尔),但毒胡萝卜素仅诱导[3H]IP1有少量积累。另一种N-取代咪唑咪康唑也刺激U373细胞中[3H]IP1的积累。

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