Kumar Vibhu, Khare Pragyanshu, Devi Kirti, Kaur Jasleen, Kumar Vijay, Kiran Kondepudi Kanthi, Chopra Kanwaljit, Bishnoi Mahendra
TR(i)P for Health Laboratory, Centre of Excellence in Functional Foods, National Agri-Food Biotechnology Institute (NABI), Knowledge City-Sector 81, SAS Nagar, Punjab, 140603, India.
Pharmacology Division, University Institute of Pharmaceutical Sciences (UIPS), Panjab University, Chandigarh, 160014, India.
Fundam Clin Pharmacol. 2021 Dec;35(6):1004-1017. doi: 10.1111/fcp.12663. Epub 2021 Mar 17.
Short-chain fatty acids (SCFAs), metabolites of colonic bacterial fermentation of complex carbohydrates, are closely related to the release of gut hormones. In this study, we examined the involvement of transient receptor potential ankyrin 1 (TRPA1) in SCFA-induced increase in intracellular calcium ([Ca ] ) and its impact on gut hormone secretion using naturally TRPA1 expressing intestinal secretin tumour cell-1 (STC-1) cell line. Individual SCFAs and their physiological mix enhanced calcium influx in TRPA1-dependent manner. SCFA mix also significantly increased membrane expression of TRPA1. Gene expression studies revealed that SCFA mix elevated the expression of genes involved in calcium-activated calcineurin pathway in TRPA1-dependent manner and cAMP-regulated transcriptional co-activators (CRTC) pathway independent to TRPA1. Genes representing synaptic vesicular exocytosis and gut hormone precursors were significantly elevated with SCFA mix treatment. Treatment with TRPA1 antagonist HC-030031 markedly reduced these effects. The release of gut hormones was elevated with 10 mm SCFA mix in TRPA1 dependent manner. Our in vivo prebiotic study results suggested presence of an environment conducive to increase in gut hormone secretion. Overall, our findings provide an evidence for the possible role of TRPA1 in SCFA-induced increase in gut hormone secretion, hence another mechanism of action for prebiotics.
短链脂肪酸(SCFAs)是复合碳水化合物经结肠细菌发酵产生的代谢产物,与肠道激素的释放密切相关。在本研究中,我们使用天然表达瞬时受体电位锚蛋白1(TRPA1)的肠促胰液素肿瘤细胞-1(STC-1)细胞系,研究了TRPA1在SCFA诱导的细胞内钙浓度([Ca²⁺])升高中的作用及其对肠道激素分泌的影响。单个SCFAs及其生理混合物以TRPA1依赖的方式增强钙内流。SCFA混合物还显著增加了TRPA1的膜表达。基因表达研究表明,SCFA混合物以TRPA1依赖的方式提高了参与钙激活钙调神经磷酸酶途径的基因表达,以及独立于TRPA1的环磷酸腺苷(cAMP)调节的转录共激活因子(CRTC)途径。SCFA混合物处理后,代表突触小泡胞吐作用和肠道激素前体的基因显著上调。用TRPA1拮抗剂HC-030031处理可显著降低这些作用。10 mM的SCFA混合物以TRPA1依赖的方式提高了肠道激素的释放。我们的体内益生元研究结果表明存在有利于肠道激素分泌增加的环境。总体而言,我们的研究结果为TRPA1在SCFA诱导的肠道激素分泌增加中可能发挥的作用提供了证据,从而为益生元的另一种作用机制提供了依据。