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Effect of Quinine Solutions on Intracellular Ca~(2+) Levels in Neuro-2a Cells-Conventional Physiological Method for the Evaluation of Bitterness-

机译:奎宁溶液对神经2a细胞内细胞内Ca〜(2+)水平的影响-评估苦味的常规生理方法-

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摘要

The purpose of the present study was to examine the effect of quinine on intracellular Ca~(2+) ([Ca~(2+)]_i) levels in cultured neuro-2a cells, and to investigate the possibility of using [Ca~(2+)]_i levels to predict the bitterness of quinine solutions. [Ca~(2+)]_i levels in neuro-2a cells increased following stimulation by quinine in a concentration-related manner. There was a good linear correlationship between the quinine-induced increase in [Ca~(2+)]_i levels increase and the bitterness scores of the quinine solutions as assessed in human gustatory sensation tests (r~2 = 0.918). The quinine-induced increase in [Ca~(2+)]_i levels was inhibited by thapsigargin (an inhibitor of the Ca~(2+) pump into intracellular stores), U73122 (an inhibitor of phospholipase C) and ω-conotoxin (an N-type Ca~(2+)-channel blocker), but not by nifedipine (an L-type Ca~(2+)-channel blocker).
机译:本研究的目的是研究奎宁对培养的神经2a细胞中细胞内Ca〜(2+)([Ca〜(2 +)] _ i)水平的影响,并探讨使用[Ca〜 (2 +)] _ i水平可预测奎宁溶液的苦味。奎宁刺激后,神经2a细胞中的[Ca〜(2 +)] _ i水平以浓度相关的方式升高。奎宁诱导的[Ca〜(2 +)] _ i水平增加与奎宁溶液的苦味评分之间存在良好的线性相关性(在人类味觉测试中评估)(r〜2 = 0.918)。 thapsigargin(一种抑制Ca〜(2+)泵进入细胞内储存的抑制剂),U73122(一种磷脂酶C的抑制剂)和ω-芋螺毒素(奎宁)抑制了奎宁诱导的[Ca〜(2 +)] _ i水平的增加。 N型Ca〜(2+)通道阻滞剂),但不是硝苯地平(L型Ca〜(2+)通道阻滞剂)。

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