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一种体内咖啡因反应所需的味觉受体。

A taste receptor required for the caffeine response in vivo.

作者信息

Moon Seok Jun, Köttgen Michael, Jiao Yuchen, Xu Hong, Montell Craig

机构信息

Department of Biological Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205, USA.

出版信息

Curr Biol. 2006 Sep 19;16(18):1812-7. doi: 10.1016/j.cub.2006.07.024.

Abstract

Caffeine is a methylxanthine present in the coffee tree, tea plant, and other naturally occurring sources and is among the most commonly consumed drugs worldwide. Whereas the pharmacological action of caffeine has been studied extensively, relatively little is known concerning the molecular mechanism through which this substance is detected as a bitter compound. Unlike most tastants, which are detected through cell-surface G protein-coupled receptors, it has been proposed that caffeine and related methylxanthines activate taste-receptor cells through inhibition of a cyclic nucleotide phosphodiesterase (PDE) . Here, we show that the gustatory receptor Gr66a is expressed in the dendrites of Drosophila gustatory receptor neurons and is essential for the caffeine response. In a behavioral assay, the aversion to caffeine was specifically disrupted in flies missing Gr66a. Caffeine-induced action potentials were also eliminated, as was the response to theophylline, the methylxanthine in tea. The Gr66a mutant exhibited normal tastant-induced action potentials upon presentation of theobromine, a methylxanthine in cocoa. Given that theobromine and caffeine inhibit PDEs with equal potencies , these data further support the role of Gr66a rather than a PDE in mediating the caffeine response. Gr66a is the first gustatory receptor shown to be essential for caffeine-induced behavior and activity of gustatory receptor cells in vivo.

摘要

咖啡因是一种存在于咖啡树、茶树及其他天然来源中的甲基黄嘌呤,是全球消费最为普遍的药物之一。尽管对咖啡因的药理作用已有广泛研究,但对于该物质作为苦味化合物被检测到的分子机制却知之甚少。与大多数通过细胞表面G蛋白偶联受体检测的味觉物质不同,有人提出咖啡因及相关甲基黄嘌呤是通过抑制环核苷酸磷酸二酯酶(PDE)来激活味觉受体细胞的。在此,我们表明味觉受体Gr66a在果蝇味觉受体神经元的树突中表达,并且对于咖啡因反应至关重要。在行为测定中,缺失Gr66a的果蝇对咖啡因的厌恶反应被特异性破坏。咖啡因诱导的动作电位也消失了,对茶中的甲基黄嘌呤茶碱的反应也是如此。在给予可可碱(可可中的一种甲基黄嘌呤)时,Gr66a突变体表现出正常的味觉物质诱导的动作电位。鉴于可可碱和咖啡因对PDE的抑制效力相同,这些数据进一步支持了Gr66a而非PDE在介导咖啡因反应中的作用。Gr66a是首个被证明对体内咖啡因诱导的行为和味觉受体细胞活性至关重要的味觉受体。

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