Scientific illustration showing intestinal tuft cells signaling the brain via acetylcholine, serotonin, and the vagus nerve to suppress appetite during parasitic infections.
Scientific illustration showing intestinal tuft cells signaling the brain via acetylcholine, serotonin, and the vagus nerve to suppress appetite during parasitic infections.
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Intestinal cells signal brain to curb hunger during parasitic infections

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A team led by David Julius, the 2021 Nobel Prize winner in Medicine, has described the molecular mechanism by which intestinal tuft cells signal the brain to suppress appetite during parasitic infections. Published today in Nature, the study identifies communication via acetylcholine and serotonin that activates the vagus nerve. The finding could aid treatments for conditions like irritable bowel syndrome.

David Julius's team at the University of California, San Francisco (UCSF), has traced the pathway linking the intestinal immune system to the brain during parasitic worm infections. Tuft cells detect parasites via succinate and release acetylcholine in two phases: an initial brief burst and a sustained release after full immune response. This acetylcholine stimulates enterochromaffin (EC) cells, which release serotonin and activate vagus nerve fibers to the brain, causing appetite loss akin to gastroenteritis, according to the study published Wednesday in Nature. First author Koki Tohara explained: “Tuft cells do something neurons do, but through a completely different mechanism,” using acetylcholine without typical neuronal machinery. Julius noted: “The gut waits to confirm the threat is real and persistent before telling the brain to change your behavior,” explaining delayed symptoms. Coauthor and UCSF immunologist Richard Locksley highlighted interest in how these non-synaptically connected cells alter behavior. Mouse experiments confirmed the mechanism: animals with intact tuft cells ate less, while genetically modified ones lacking acetylcholine production maintained normal intake. The authors suggest applications for managing infection responses and conditions like food intolerances or chronic visceral pain, as tuft cells exist in other epithelia like airways. Spanish experts such as Félix Viana from the Alicante Institute of Neurosciences call it “interesting” and relevant for defenses in other tissues, while José Luis Trejo from the Cajal Neuroscience Center views it as a “sensory interface” with therapeutic potential.

Что говорят люди

Initial reactions on X to the Nature study on intestinal tuft cells signaling the brain to curb hunger during parasitic infections are positive and informative. Nutritionists and scientists shared summaries in English and Spanish, highlighting the role of acetylcholine and serotonin via the vagus nerve. Posts linked to the study and ScienceDaily, noting potential IBS treatment implications. Some connected findings to vagus nerve function and gut-brain axis.

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Scientists in a lab visualize VLK enzyme from neurons enabling targeted pain relief, shown with 3D neuron model and mouse pain reduction experiment.
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Researchers pinpoint enzyme that could enable safer pain relief

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Scientists at Tulane University and collaborating institutions have found that neurons release an enzyme called vertebrate lonesome kinase (VLK) outside cells to help switch on pain signals after injury. Removing VLK from pain-sensing neurons in mice sharply reduced post-surgical pain–like responses without impairing normal movement or basic sensation, according to a study in Science, suggesting a potential new route to more targeted pain treatments.

Astrocytes—cells once widely described primarily as neuronal support—may be key intermediaries in how the brain translates a post-meal rise in glucose into satiety signals, according to a study published April 6, 2026, in the Proceedings of the National Academy of Sciences.

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Researchers have discovered a cluster of sensory neurons that link the brain and heart, triggering an immune response crucial for recovery after a heart attack. This finding reveals a feedback loop involving the nervous and immune systems that could lead to new therapies. Experiments in mice showed that manipulating these neurons speeds up healing and reduces scarring.

Scientists are probing brain circuits affected by GLP-1 medicines such as Ozempic, Wegovy, Mounjaro, and Zepbound to preserve weight-loss benefits while curbing nausea. The findings, presented at Neuroscience 2025, outline strategies that could refine treatments for obesity and type 2 diabetes.

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Researchers at Cold Spring Harbor Laboratory report that support cells known as myofibroblastic cancer-associated fibroblasts (myCAFs) can recruit sympathetic nerve fibers into early pancreatic lesions, creating a feedback loop that may help pancreatic cancer take hold before full tumors form. In mouse experiments, disrupting sympathetic nerve activity reduced fibroblast activation and was associated with nearly a 50% reduction in tumor growth.

Recent research shows that body fat is more than a calorie store; it actively regulates immune responses and blood pressure. Scientists have identified specialized fat depots near the intestines that coordinate immunity against gut microbes, while another study links beige fat around blood vessels to vascular health. These findings challenge simplistic views of fat as merely harmful.

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A study in obese mice has found that the gut-derived hormone FGF19 can signal the brain to increase energy expenditure and activate fat-burning cells. Acting through the hypothalamus and the sympathetic nervous system, this mechanism enhances thermogenesis and cold tolerance and may help guide new treatments for obesity and diabetes.

 

 

 

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