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苦味受体和人工甜味剂激活大鼠气管急性组织切片中的一组上皮细胞。

Bitter tastants and artificial sweeteners activate a subset of epithelial cells in acute tissue slices of the rat trachea.

机构信息

Department of Neurosciences, Biomedicine and Movement Sciences, Anatomy and Histology Section, University of Verona, School of Medicine, Verona, Italy.

Neurobiology Group, SISSA, International School for Advanced Studies, Trieste, Italy.

出版信息

Sci Rep. 2019 Jun 20;9(1):8834. doi: 10.1038/s41598-019-45456-w.

Abstract

Bitter and sweet receptors (T2Rs and T1Rs) are expressed in many extra-oral tissues including upper and lower airways. To investigate if bitter tastants and artificial sweeteners could activate physiological responses in tracheal epithelial cells we performed confocal Ca imaging recordings on acute tracheal slices. We stimulated the cells with denatonium benzoate, a T2R agonist, and with the artificial sweeteners sucralose, saccharin and acesulfame-K. To test cell viability we measured responses to ATP. We found that 39% of the epithelial cells responding to ATP also responded to bitter stimulation with denatonium benzoate. Moreover, artificial sweeteners activated different percentages of the cells, ranging from 5% for sucralose to 26% for saccharin, and 27% for acesulfame-K. By using carbenoxolone, a gap junction blocker, we excluded that responses were mainly mediated by Ca waves through cell-to-cell junctions. Pharmacological experiments showed that both denatonium and artificial sweeteners induced a PLC-mediated release of Ca from internal stores. In addition, bitter tastants and artificial sweeteners activated a partially overlapping subpopulation of tracheal epithelial cells. Our results provide new evidence that a subset of ATP-responsive tracheal epithelial cells from rat are activated by both bitter tastants and artificial sweeteners.

摘要

苦味和甜味受体(T2R 和 T1R)表达于许多口腔外组织,包括上、下呼吸道。为了研究苦味物质和人工甜味剂是否能激活气管上皮细胞的生理反应,我们在急性气管切片上进行了共聚焦 Ca2+成像记录。我们用苯甲地那铵(一种 T2R 激动剂)和人工甜味剂三氯蔗糖、糖精和安赛蜜 K 刺激细胞。为了测试细胞活力,我们测量了对 ATP 的反应。我们发现,39%对 ATP 有反应的上皮细胞也对苯甲地那铵的苦味刺激有反应。此外,人工甜味剂激活了不同比例的细胞,从 5%的三氯蔗糖到 26%的糖精,和 27%的安赛蜜 K。用瓜氨酸,缝隙连接阻断剂,我们排除了细胞间 Ca2+波主要介导反应。药理学实验表明,苯甲地那铵和人工甜味剂都诱导 PLC 介导的细胞内储存的 Ca2+释放。此外,苦味物质和人工甜味剂激活了气管上皮细胞的一个部分重叠的亚群。我们的结果提供了新的证据,即大鼠的一部分对 ATP 有反应的气管上皮细胞可以被苦味物质和人工甜味剂激活。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c141/6586933/c8232a87bcd4/41598_2019_45456_Fig1_HTML.jpg

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