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PLC beta 2-Independent behavioral avoidance of prototypical bitter-tasting ligands

机译:PLC beta 2独立的行为规避原型苦味配体

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Using a brief-access taste assay, we show in the present report that although phospholipase C beta 2 knockout (PLC beta 2 KO) mice are unresponsive to low- and midrange concentrations of quinine and denatonium, they do significantly avoid licking higher concentrations of these aversive compounds. PLC beta 2 KO mice displayed no concentration-dependent licking of the prototypical sweetener sucrose but were similar to wild-type mice in their responses to citric acid and NaCl, notwithstanding some interesting exceptions. Although these findings confirm an essential role for PLC beta 2 in taste responsiveness to sucrose and to low- to midrange concentrations of quinine and denatonium in mice as previously reported, they importantly suggest that higher concentrations of the latter two compounds, which are bitter to humans, can engage a PLC beta 2-independent taste transduction pathway.
机译:使用简短的味觉分析,我们在本报告中显示,尽管磷脂酶C beta 2敲除(PLC beta 2 KO)小鼠对奎宁和地那铵的中低浓度无反应,但它们确实避免了舔食这些化合物的较高浓度厌恶化合物。尽管有一些有趣的例外,PLC beta 2 KO小鼠对原型甜味剂蔗糖没有浓度依赖性的舔食,但它们对柠檬酸和NaCl的反应与野生型小鼠相似。尽管这些发现证实了PLC beta 2在小鼠对蔗糖以及对中低浓度的奎宁和地那铵的味觉响应中的重要作用,但它们重要地表明,较高浓度的后两种化合物对人而言是苦的。可以参与PLC beta 2独立的味觉传导途径。

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