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果蝇抑制高盐摄入的抑制机制。

An inhibitory mechanism for suppressing high salt intake in Drosophila.

机构信息

Interdepartmental Neuroscience Program, University of California, Riverside, CA 92521, United States.

Department of Molecular, Cell & Systems Biology, University of California, Riverside, CA 92521, United States.

出版信息

Chem Senses. 2023 Jan 1;48. doi: 10.1093/chemse/bjad014.

Abstract

High concentrations of dietary salt are harmful to health. Like most animals, Drosophila melanogaster are attracted to foods that have low concentrations of salt, but show strong taste avoidance of high salt foods. Salt in known on multiple classes of taste neurons, activating Gr64f sweet-sensing neurons that drive food acceptance and 2 others (Gr66a bitter and Ppk23 high salt) that drive food rejection. Here we find that NaCl elicits a bimodal dose-dependent response in Gr64f taste neurons, which show high activity with low salt and depressed activity with high salt. High salt also inhibits the sugar response of Gr64f neurons, and this action is independent of the neuron's taste response to salt. Consistent with the electrophysiological analysis, feeding suppression in the presence of salt correlates with inhibition of Gr64f neuron activity, and remains if high salt taste neurons are genetically silenced. Other salts such as Na2SO4, KCl, MgSO4, CaCl2, and FeCl3 act on sugar response and feeding behavior in the same way. A comparison of the effects of various salts suggests that inhibition is dictated by the cationic moiety rather than the anionic component of the salt. Notably, high salt-dependent inhibition is not observed in Gr66a neurons-response to a canonical bitter tastant, denatonium, is not altered by high salt. Overall, this study characterizes a mechanism in appetitive Gr64f neurons that can deter ingestion of potentially harmful salts.

摘要

高浓度的膳食盐对健康有害。像大多数动物一样,黑腹果蝇被低浓度盐的食物所吸引,但对高盐食物表现出强烈的味觉回避。盐在已知的多种味觉神经元中被激活,激活 Gr64f 甜味感应神经元,从而驱动食物接受,另外 2 种(Gr66a 苦味和 Ppk23 高盐)则驱动食物拒绝。在这里,我们发现 NaCl 在 Gr64f 味觉神经元中引发双峰剂量依赖性反应,低盐时表现出高活性,高盐时活性降低。高盐还抑制 Gr64f 神经元对糖的反应,而这种作用与神经元对盐的味觉反应无关。与电生理分析一致的是,在盐存在的情况下摄食抑制与 Gr64f 神经元活性的抑制相关,如果高盐味觉神经元被遗传沉默,这种抑制仍然存在。其他盐,如 Na2SO4、KCl、MgSO4、CaCl2 和 FeCl3,以同样的方式作用于糖反应和摄食行为。对各种盐的影响的比较表明,抑制是由阳离子部分决定的,而不是盐的阴离子部分。值得注意的是,在 Gr66a 神经元中没有观察到高盐依赖性抑制-对经典苦味味觉剂苯甲地那铵的反应不受高盐的影响。总的来说,这项研究描述了一种在食欲性 Gr64f 神经元中可以阻止潜在有害盐摄入的机制。

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