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胃肠道疾病中十二指肠多巴胺受体与痕量胺相关受体1的功能相互作用模式受损。

Dopamine Receptors and TAAR1 Functional Interaction Patterns in the Duodenum Are Impaired in Gastrointestinal Disorders.

作者信息

Vaganova Anastasia N, Markina Alisa A, Belousov Aleksandr M, Lenskaia Karina V, Gainetdinov Raul R

机构信息

Institute of Translational Biomedicine, St. Petersburg State University, Universitetskaya nab. 7/9, 199034 St. Petersburg, Russia.

St. Petersburg State University Hospital, St. Petersburg State University, Universitetskaya nab. 7/9, 199034 St. Petersburg, Russia.

出版信息

Biomedicines. 2024 Jul 17;12(7):1590. doi: 10.3390/biomedicines12071590.

Abstract

Currently, there is a growing amount of evidence for the involvement of dopamine receptors and the functionally related trace amine-associated receptor, TAAR1, in upper intestinal function. In the present study, we analyzed their expression in the duodenum using publicly accessible transcriptomic data. We revealed the expression of , , , , and genes in different available datasets. The results of the gene ontology (GO) enrichment analysis for and especially co-expressed genes were consistent with the previously described localization of D2 and TAAR1 in enteric neurons and secretory cells, respectively. Considering that co-expressed genes are more likely to be involved in the same biological processes, we analyzed genes that are co-expressed with , , , and genes in healthy mucosa and duodenal samples from patients with functional dyspepsia (FD) or diabetes-associated gastrointestinal symptoms. Both pathological conditions showed a deregulation of co-expression patterns, with a high discrepancy between s and co-expressed gene sets in normal tissues and patients' samples and a loss of these genes' functional similarity. Meanwhile, we discovered specific changes in co-expression patterns that may suggest the involvement of TAAR1 and D5 receptors in pathologic or compensatory processes in FD or diabetes accordingly. Despite our findings suggesting the possible role of TAAR1 and dopamine receptors in functional diseases of the upper intestine, underlying mechanisms need experimental exploration and validation.

摘要

目前,越来越多的证据表明多巴胺受体以及功能相关的痕量胺相关受体TAAR1参与上消化道功能。在本研究中,我们使用公开可用的转录组数据分析了它们在十二指肠中的表达。我们在不同的可用数据集中揭示了 、 、 、 和 基因的表达。对 和特别是 共表达基因的基因本体(GO)富集分析结果分别与先前描述的D2和TAAR1在肠神经元和分泌细胞中的定位一致。考虑到共表达基因更有可能参与相同的生物学过程,我们分析了在健康黏膜以及功能性消化不良(FD)或糖尿病相关胃肠道症状患者的十二指肠样本中与 、 、 和 基因共表达的基因。两种病理状况均显示共表达模式失调,正常组织和患者样本中 和 共表达基因集之间存在高度差异,并且这些基因的功能相似性丧失。同时,我们发现了共表达模式的特定变化,这可能相应地表明TAAR1和D5受体参与了FD或糖尿病的病理或代偿过程。尽管我们的研究结果表明TAAR1和多巴胺受体可能在上消化道功能性疾病中发挥作用,但其潜在机制仍需实验探索和验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf56/11274761/4b4dd2d18f27/biomedicines-12-01590-g001.jpg

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