Evidence mapPaperPMID 41310896Full record

ArticleEuropean journal of medical research2025

High-fat diet-induced anorexia in rats: involving orosensory deficits, gastrointestinal dysfunction, intestinal taste receptor downregulation and dopamine signaling dysregulation.

Qina Ye, Liying Zeng, Xiangna Yang, Jing Zhang, Zhuoming Lu, Jian Deng, Zequn Liu

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Article in European journal of medical research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Qina Ye *The Second Clinical College , Guangzhou University of Chinese Medicine, Guangzhou, 510405, China. 18125344663@163.com.ORCID http://orcid.org/0000-0001-5739-9364
Liying Zeng *Basic Medicine Postdoctoral Research Station, Jinan University, Guangzhou, 510632, China.
Xiangna YangDepartment of Traditional Chinese Medicine, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No.9 Jinsui Road, Guangzhou, 510623, China.
Jing ZhangDepartment of Traditional Chinese Medicine, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No.9 Jinsui Road, Guangzhou, 510623, China.
Zhuoming LuBasic Medicine Postdoctoral Research Station, Jinan University, Guangzhou, 510632, China.
Jian DengDepartment of Traditional Chinese Medicine, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No.9 Jinsui Road, Guangzhou, 510623, China.
Zequn LiuDepartment of Obstetrics, Guangzhou Women and Children's Medical Center, Guangzhou Medical University, No.9 Jinsui Road, Guangzhou, 510623, China. perfect-qun@163.com.

Funding

Guangdong Provincial Natural Science Foundation No.2025A1515012708Scientific Research Project of the Guangdong Provincial Bureau of Traditional Chinese Medicine No. 20251285
6 · The paper itself

Abstract

objectivesTo explore how a high-fat diet (HFD) led to anorexia in rats via peripheral-central axis integrated dysfunction.

methodsTwenty male Sprague‒Dawley rats were randomly assigned to the control group (G1, standard chow; n = 10) or the high-fat diet group (G2; n = 10) for 27 days. Body weight and food consumption were recorded at regular intervals. The gastric residual rate (GRR) and small intestinal advancement rate (SIAR) were used to evaluate gastrointestinal motility. The circumvallate papillae (CVP), proximal jejunum and hypothalamus were collected postintervention. Analyses included analyses of CVP histology (H&E staining), taste receptor type 1 member expression (T1R1/T1R2/T1R3) and transient receptor potential melastatin 5 (TRPM5) through immunohistochemistry and quantitative real-time PCR (qPCR) and hypothalamic dopamine (DA) levels by enzyme-linked immunosorbent assay (ELISA).

resultsTotal food intake (41.5% lower) and final body weight (21.8% lower) were significantly lower in the HFD group than in the control group. The morphology of CVP was significantly degenerated by HFD feeding, resulting in a 49.13% reduction in the taste bud count. Gastrointestinal dysfunction was evidenced by increased GRR and decreased SIAR. Although taste receptor expression in CVP remained unchanged, the proximaljejunal mRNA expression levels of T1R1, T1R3, and TRPM5 significantly decreased. Notably, the DA concentration in the hypothalamus was also significantly lower in HFD-fed rats than in control rats.

conclusionsHFD consumption effectively induced anorexia in young rats, which was accompanied by gastrointestinal dysfunction, a reduction in taste buds, impaired gut-brain axis taste transduction and a suppressed central DA response. These results indicate that peripheral-central axis impairment may be an important pathological phenomenon in HFD-induced anorexia.

Indexed as

AnorexiaDiet, High-FatDopamineReceptors, G-Protein-CoupledAnimalsDown-RegulationMaleRatsRats, Sprague-DawleySignal TransductionDopamineReceptors, G-Protein-Coupledtaste receptors, type 1AnorexiaDopamineHigh-fat dietTaste receptors

Identifiers

PMID41310896
PMCPMC12750658

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.