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采用放射受体分析法对大鼠大脑皮层切片中肌醇(1,4,5)三磷酸进行定量测定:神经递质和去极化的影响

Mass measurements of inositol(1,4,5)trisphosphate in rat cerebral cortex slices using a radioreceptor assay: effects of neurotransmitters and depolarization.

作者信息

Challiss R A, Batty I H, Nahorski S R

机构信息

Department of Pharmacology and Therapeutics, University of Leicester, U.K.

出版信息

Biochem Biophys Res Commun. 1988 Dec 15;157(2):684-91. doi: 10.1016/s0006-291x(88)80304-8.

DOI:10.1016/s0006-291x(88)80304-8
PMID:2904813
Abstract

The specific binding of [3H] and [32P]Ins(1,4,5)P3 to a particulate preparation of bovine adrenal cortex has been used as a radioreceptor assay to determine the concentration of Ins(1,4,5)P3 in agonist- and depolarization-stimulated rat cerebral cortex slices. The resting concentration of Ins(1,4,5)P3 in slices that had been preincubated in a physiological medium was 18.8 +/- 2.6 pmol/mg prot. Carbachol evoked a rapid and dose-related increase in the concentration of Ins(1,4,5)P3. Maximal stimulation (80%) was already seen at the earliest point (10 sec) examined and was maintained for at least 5 min. The EC50 for carbachol was 75 +/- 17 microM and the response was totally suppressed by the muscarinic antagonist atropine. A direct comparison in the same slices was made between mass determinations and [3H]Ins(1,4,5)P3 and [3H]Ins(1,3,4)P3 accumulation determined by h.p.l.c. Although an identical time course was observed for cold and radiolabelled Ins(1,4,5)P3, the greater stimulation of [3H]Ins(1,4,5)P3 may indicate changes in specific radioactivity. Of a variety of other receptor agonists studied, only the glutamate receptor agonist quisqualate, and noradrenaline significantly increased the mass of Ins(1,4,5)P3 in cerebral cortical slices. However, depolarizing concentrations of K+ were as effective as carbachol at elevating this second messenger.

摘要

利用[3H]和[32P]肌醇-1,4,5-三磷酸(Ins(1,4,5)P3)与牛肾上腺皮质微粒体制剂的特异性结合,作为一种放射受体分析法来测定激动剂和去极化刺激的大鼠大脑皮层切片中Ins(1,4,5)P3的浓度。在生理培养基中预孵育的切片中,Ins(1,4,5)P3的静息浓度为18.8±2.6 pmol/mg蛋白。卡巴胆碱引起Ins(1,4,5)P3浓度迅速且呈剂量相关的增加。在最早检测的时间点(10秒)就已观察到最大刺激(80%),并持续至少5分钟。卡巴胆碱的半数有效浓度(EC50)为75±17 μM,且该反应被毒蕈碱拮抗剂阿托品完全抑制。在同一切片中对通过高效液相色谱法测定的Ins(1,4,5)P3和Ins(1,3,4)P3的质量测定结果与[3H]Ins(1,4,5)P3和[3H]Ins(1,3,4)P3的积累情况进行了直接比较。尽管观察到冷的和放射性标记的Ins(1,4,5)P3具有相同的时间进程,但[3H]Ins(1,4,5)P3受到的更大刺激可能表明比放射性发生了变化。在所研究的多种其他受体激动剂中,只有谷氨酸受体激动剂quisqualate和去甲肾上腺素能显著增加大脑皮层切片中Ins(1,4,5)P3的质量。然而,去极化浓度的钾离子在升高这种第二信使方面与卡巴胆碱一样有效。

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