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Is Taking a 'Fart Walk' Good for Your Health?

Is Taking a 'Fart Walk' Good for Your Health?

What you once knew as an after-dinner stroll has been rebranded a 'fart walk' on social media—and the trend is having a moment. Fans of the so-called fart walk—a short stroll taken up to about an hour after eating a meal—claim it aids digestion and relieves GI symptoms like gas and bloating. But what do doctors think?
New name, old concept
'Feeling bloated after a meal is common,' says Dr. David D. Clarke, a clinical assistant professor of gastroenterology emeritus at Oregon Health & Science University and president of the Association of the Treatment of Neuroplastic Symptoms. That's because people eat too much, or they eat too quickly and swallow excess air, or they drink beverages with dissolved gas in them like soda or beer.
To counter symptoms like these and help relieve gas naturally, walking after dinner can help, doctors agree. Walking can enhance the muscle contractions of the gastrointestinal tract—a wave-like movement called peristalsis—which can help pass the gas as belches or flatulence, explains Clarke. Research has also long supported taking a postprandial walk for a different reason: it helps reduce blood sugar levels.
The varied benefits of a fart walk
This is one social media trend physicians can get behind. A fart walk helps relieve symptoms of bloating and gas and promotes motility of the bowels, says Dr. Shawn Khodadadian of Manhattan Gastroenterology in New York City. Clarke agrees; mild-to-moderate exercise, such as walking, helps the stomach empty more quickly, improving transit through the intestinal tract and clearing out gas and waste through the digestive system, all of which can help alleviate issues like bloating and constipation, he says. 'Walking promotes muscle contractions in the stomach and intestines that can lead to belching and farting,' he says. That quicker emptying will also 'decrease the time that acid is present in the stomach,' which relieves heartburn in most people, Clarke says. (However, some people with poor tone in the sphincter muscle—at the junction of the esophagus and stomach—might experience more acid reflux when stomach contractions are stimulated by walking, he warns.)
Read More: What Doctors Really Think of Sleepmaxxing
Fart walking may be particularly beneficial for those with medical conditions like irritable bowel syndrome (IBS) and metabolic syndrome. 'There have been studies that show that mobility in general can lead to decreased sensation of gas and bloating in patients with IBS symptoms,' says Khodadadian. Plus, a post-meal stroll's ability to better regulate blood sugar is especially helpful for people with metabolic syndrome, he says. Short walks after eating can also benefit the heart: helping to stave off weight gain, improve circulation, lower blood pressure, support overall cardiovascular fitness, says Khodadadian.
Other perks of fart walking might include reducing the risk of diabetes, Clarke says. 'Walking after a meal facilitates removal of blood sugar by the muscles and thereby reduces the need for insulin secretion by the pancreas,' Clarke says, which may reduce the risk for the future development of diabetes.
A postprandial amble can also brighten your mood. 'The addition of aerobic exercise has been shown to improve stress, anxiety, and mild depression,' says Khodadadian. 'This can happen by reducing baseline cortisol levels over time, by improving sleep quality, and by increasing levels of chemicals such as endorphins, dopamine and serotonin in the body.'
How to get the most out of your fart walk
Fart walks don't have to be long to be effective. Aim for at least four to five minutes of light-to-moderate paced walking within about an hour of finishing a meal. (More is better: for more sustained GI benefits, shoot for 30–60 minutes of moderate-paced walking on most days of the week, Clarke says.)
Walking is generally healthy for everyone, and it should not be strenuous—but if you have had recent surgery, motility issues, abdominal distress, arthritis, or heart or lung issues, you should check with your doctor first before proceeding, adds Khodadadian. Based on your medical history, recommendations may vary for precisely how long you walk, he says, but the goal is ultimately to be able to engage in an appropriate level of exercise—including fart walking—for you.
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The #1 Habit You Should Start If You Have IBS, According to Dietitians
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Yahoo

time6 days ago

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The #1 Habit You Should Start If You Have IBS, According to Dietitians

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Newsweek

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PTSD Drug Discovery May Help Patients Let Go of Trauma

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"It targets the pathological reactive astrocyte-derived GABA at the source," said Won. "Unlike traditional MAO inhibitors, which can have off-target effects and are irreversible, KDS2010 is highly selective, reversible, and brain-penetrant, making it safer and more targeted." They report the drug has already passed Phase 1 safety trials in humans, which makes it a "strong candidate" for future PTSD treatments. GABA can be a positive thing, helping to regulate motor function, sensory processing and emotional stability. It can also offer calming effects, including helping to reduce anxiety and stress by controlling overactive neurons. "However," Won explained, "GABA does not act uniformly across the brain, and its outcome varies depending on the target circuit. "While GABA is generally calming, in this context [of the researcher's findings], it was silencing a circuit that the brain needs to overcome fear. This highlights that the effect of GABA is not simply good or bad, but it critically depends on where it acts and what neural circuits are involved." Digital illustration showing brain waves and activity. Digital illustration showing brain waves and activity. selvanegra/Getty Images The study focused on the medial prefrontal cortex (mPFC), a region of the brain critical for regulating fear. It found that PTSD patients had unusually high levels of GABA and reduced cerebral blood flow in this area, based on brain imaging studies of more than 380 participants. On the other hand, GABA levels decreased in patients who showed clinical improvement, suggesting the chemical has a central role in recovery. To unearth the origin of the excess GABA, the researchers examined postmortem human brain tissue and used PTSD-like mouse models. They discovered that astrocytes, not neurons, were producing abnormal amounts of GABA via the MAOB enzyme. 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This confirms astrocytic MAOB as a central driver of PTSD symptoms and MAOB inhibition as a viable therapeutic path. The researchers flagged a major challenge of the study was linking clinical findings in humans with cellular mechanisms in the lab. They addressed this by applying a "reverse translational" strategy, beginning with clinical brain scans and moving backward to identify the cellular source of dysfunction. They then confirmed the mechanism and tested drug effects in animal models. This led to a new understanding of how glial cells—non-neuronal cells long thought to be passive—actively shape psychiatric symptoms. Would this type of drug be used alongside other methods like talking therapy for PTSD? "DS2010 alone has a strong potential to restore brain function by normalizing astrocytic GABA and improving fear extinction. However, we think that combining it with psychotherapy, especially exposure-based therapy, could create even greater synergy. By reducing abnormal inhibition in fear extinction circuits, KDS2010 may help the brain become more responsive to therapeutic input," Won explained. How would it be administered? "KDS2010 is an orally available small molecule. In preclinical and early-phase clinical studies, it has been administered once daily in capsule or liquid form. This makes it highly feasible for long-term outpatient use, similar to antidepressants." What about side effects? "In the Phase 1 clinical trial, KDS2010 was found to be well tolerated, with no serious adverse effects reported, even at higher doses. This safety is largely due to its selectivity for MAOB and its reversible mechanism, which avoids the long-term enzyme compensation seen with older MAO inhibitors. Nevertheless, larger trials in PTSD patients will be needed to fully assess tolerability and any rare side effects." Won said the drug is currently undergoing Phase 2 trials for other neurological disorders, which means its safety profile is already being tested extensively in patients. "Because of this, we believe it could reach the public faster than many other new drugs. If future trials for PTSD are successful and regulatory steps proceed smoothly, it could become available within a few years. Importantly, KDS2010 is part of a broader platform that may also be useful for treating other disorders involving astrocytic dysfunction, such as Parkinson's and Alzheimer's disease." Do you have a tip on a health story that Newsweek should be covering? Do you have a question about PTSD? Let us know via health@ Reference Yoon, S., Won, W., Lee, S., Han, K., Ha, E., Lee, J., Hyeon, S. J., Joo, Y., Hong, H., Lee, H., Song, Y., Park, K. D., Huber, B. R., Lee, J., Edden, R. A. E., Suh, M., Ryu, H., Lee, C. J., & Lyoo, I. K. (2025). Astrocytic gamma-aminobutyric acid dysregulation as a therapeutic target for posttraumatic stress disorder. Signal Transduction and Targeted Therapy, 10(1), 240.

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