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大鼠大脑皮层切片中肌醇1,3,4,5 - 四磷酸生成的放射性标记和质谱测定:肌醇的不同影响

Radio-label and mass determinations of inositol 1,3,4,5-tetrakisphosphate formation in rat cerebral cortical slices: differential effects of myo-inositol.

作者信息

Kurian P, Narang N, Chandler L J, Crews F T

机构信息

Department of Pharmacology, University of Florida College of Medicine, Gainesville 32610-0267.

出版信息

Neurochem Res. 1993 May;18(5):639-45. doi: 10.1007/BF00966943.

Abstract

To investigate the effects of increasing concentrations of myo-inositol (inositol) on receptor stimulated [3H]inositol polyphosphate formation in the absence of lithium, slices of rat cerebral cortex were incubated with various concentrations of [3H]inositol (1 to 30 microM). Carbachol stimulated formation of [3H]inositol trisphosphate (InsP3) and [3H]inositol 1,3,4,5-tetrakisphosphate (Ins(1,3,4,5)P4) increased several fold when the inositol concentration was increased reaching a plateau at approximately 12 microM inositol. Time course studies revealed that in the presence of low concentrations of inositol (1 microM), [3H]InsP3 and [3H]Ins(1,3,4,5)P4 formation in response to carbachol stimulation increased slowly over a 10 to 20 min time period, whereas in the presence of 4 and 12 microM inositol, carbachol stimulated [3H]InsP3 and [3H]Ins(1,3,4,5)P4 formation was rapid and essentially complete within 3 to 5 min after carbachol addition. Although the carbachol dose response in 12 microM inositol had a much greater maximal efficacy, there was no change in potency. Similar to the effects of carbachol on [3H]Ins(1,3,4,5)P4 formation from prelabeled phosphoinositides, muscarinic receptor stimulation increased Ins(1,3,4,5)P4 mass formation by seven fold. Furthermore, Li+ (8 mM) completely inhibited carbachol stimulated increases in Ins(1,3,4,5)P4 mass formation. In contrast to the effects of increasing inositol on carbachol stimulated formation of radiolabeled inositol phosphates, increasing inositol had no effect upon mass formation of Ins(1,3,4,5)P4. These results show that when measuring inositol polyphosphate formation by the radiolabeling technique in the absence of Li+, increasing the inositol concentration greatly increases the stimulated component of [3H]InsP3 and [3H]Ins(1,3,4,5)P4 formation. However, this inositol induced increase in agonist stimulated Ins(1,3,4,5)P4 formation is not reflected as an increase in mass formation.

摘要

为研究在无锂情况下,增加肌醇浓度对受体刺激的[3H]肌醇多磷酸形成的影响,将大鼠大脑皮层切片与不同浓度的[3H]肌醇(1至30微摩尔)一起孵育。当肌醇浓度增加时,卡巴胆碱刺激的[3H]肌醇三磷酸(InsP3)和[3H]肌醇1,3,4,5-四磷酸(Ins(1,3,4,5)P4)形成增加了几倍,在约12微摩尔肌醇时达到平台期。时间进程研究表明,在低浓度肌醇(1微摩尔)存在下,对卡巴胆碱刺激的[3H]InsP3和[3H]Ins(1,3,4,5)P4形成在10至20分钟时间段内缓慢增加,而在4和12微摩尔肌醇存在下,卡巴胆碱刺激的[3H]InsP3和[3H]Ins(1,3,4,5)P4形成迅速,在加入卡巴胆碱后3至5分钟内基本完成。尽管在12微摩尔肌醇中卡巴胆碱剂量反应的最大效能要大得多,但效力没有变化。与卡巴胆碱对由预先标记的磷酸肌醇形成[3H]Ins(1,3,4,5)P4的影响相似,毒蕈碱受体刺激使Ins(1,3,4,5)P4质量形成增加了7倍。此外,Li+(8毫摩尔)完全抑制了卡巴胆碱刺激的Ins(1,3,4,5)P4质量形成增加。与增加肌醇对卡巴胆碱刺激的放射性标记肌醇磷酸形成的影响相反,增加肌醇对Ins(1,3,4,5)P4质量形成没有影响。这些结果表明,在无Li+情况下通过放射性标记技术测量肌醇多磷酸形成时,增加肌醇浓度会大大增加[3H]InsP3和[3H]Ins(1,3,4,5)P4形成的刺激成分。然而,这种肌醇诱导的激动剂刺激的Ins(1,3,4,5)P4形成增加并未反映为质量形成的增加。

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