Alpha‐Ketoglutarate Regulates Intestinal Motility and Health by OXGR1 in Nitrergic Neuron of Enteric Nervous System

ABSTRACT Intestinal health could be affected by intestinal motility, which is controlled by the enteric nervous system. In this study, we found that α‐ketoglutarate (AKG) inhibits intestinal motility and improves intestinal permeability, accompanied by an increased count of intestinal flora. We also identified that the AKG receptor, oxoglutarate receptor 1 (OXGR1), is expressed in the myenteric plexus (MP). Meanwhile, OXGR1 knockout enhanced intestinal motility. Furthermore, we found that AKG activates nitrergic neurons to synthesize nitric oxide through OXGR1, thereby suppressing intestinal smooth muscle contractility. Finally, we demonstrate that AKG/OXGR1 activates nitric oxide synthase in combination with calmodulin in nitrergic neurons. Taken together, this study may identify novel therapeutic targets for intestinal disease, such as diarrhea or colitis.

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Publication Details

Journal
Food Frontiers
Published
2026-01-01
DOI
https://doi.org/10.1002/fft2.70216
Primary Topic
Gastrointestinal motility and disorders
Type
article
Field-Weighted Citation Impact
0.00

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article

Alpha‐Ketoglutarate Regulates Intestinal Motility and Health by OXGR1 in Nitrergic Neuron of Enteric Nervous System

Ishwari Gyawali, Zewei Ma, Dan Du, PINGWEN XU et al.
Food Frontiers
Gastrointestinal motility and disorders
article

Alpha‐Ketoglutarate Regulates Intestinal Motility and Health by OXGR1 in Nitrergic Neuron of Enteric Nervous System

Ishwari Gyawali, Zewei Ma, Dan Du, PINGWEN XU, Chang Xu, Gang Shu, Jinping Yang, Jingjing Zhou, Guli Xu, Qingyan Jiang
article en

Abstract

ABSTRACT Intestinal health could be affected by intestinal motility, which is controlled by the enteric nervous system. In this study, we found that α‐ketoglutarate (AKG) inhibits intestinal motility and improves intestinal permeability, accompanied by an increased count of intestinal flora. We also identified that the AKG receptor, oxoglutarate receptor 1 (OXGR1), is expressed in the myenteric plexus (MP). Meanwhile, OXGR1 knockout enhanced intestinal motility. Furthermore, we found that AKG activates nitrergic neurons to synthesize nitric oxide through OXGR1, thereby suppressing intestinal smooth muscle contractility. Finally, we demonstrate that AKG/OXGR1 activates nitric oxide synthase in combination with calmodulin in nitrergic neurons. Taken together, this study may identify novel therapeutic targets for intestinal disease, such as diarrhea or colitis.

Food FrontiersVol. 7(1)
South China Agricultural University (CN), University of Georgia (US), University of Illinois Chicago (US), Guangzhou Women and Children Medical Center (CN), Guangzhou Medical University (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China
Openalex Percentile: Top 94%
Gastrointestinal motility and disorders
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