Inflammation Archives | Experience Life https://experiencelife.lifetime.life/category/health/health-conditions/inflammation/ Mon, 06 Oct 2025 14:00:27 +0000 en-US hourly 1 https://wordpress.org/?v=6.8.2 Aging With Brain Power: How to Boost Your Mental Acuity and Cognition (Performance & Longevity Series) https://experiencelife.lifetime.life/podcast/aging-with-brain-power-how-to-boost-your-mental-acuity-and-cognition-performance-longevity-series/ Thu, 02 Oct 2025 10:00:04 +0000 https://experiencelife.lifetime.life/?post_type=podcast&p=124563 The post Aging With Brain Power: How to Boost Your Mental Acuity and Cognition (Performance & Longevity Series) appeared first on Experience Life.

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Are Autoimmune Diseases Becoming More Common? https://experiencelife.lifetime.life/article/are-autoimmune-diseases-becoming-more-common/ https://experiencelife.lifetime.life/article/are-autoimmune-diseases-becoming-more-common/#view_comments Thu, 11 Sep 2025 13:01:54 +0000 https://experiencelife.lifetime.life/?post_type=article&p=120138 Yes, and many experts suspect environmental triggers. Here's why.

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If it feels as if a startling number of people in your life now struggle with at least one autoimmune ­disease, it’s not your imagination.

“Autoimmunity” encompasses more than 100 conditions in which the immune system attacks the body’s own tissues, and the incidence of these disorders is increasing by up to 12 percent each year in the United States, warns Molly Murray, CAE, president and CEO of the Autoimmune Association. These conditions include psoriasis, celiac disease, multiple sclerosis, type 1 diabetes, rheumatoid arthritis, and lupus.

Today, between 15 million and 50 million Americans have an ­autoimmune condition, with estimates varying widely due to the difficulty in assessing the scope of these diseases.

And because of the complexity of diagnosing autoimmunity itself, 50 million is likely to be an under­estimate, Murray writes in a 2024 National Health Council guest blog post.

Women make up 80 percent of those with autoimmunity and are twice as likely as men to be diagnosed.

Susceptibility to autoimmune disorders appears to run in families. A particular disease may not be genetic, but if one family member has lupus, the likelihood that another may have Sjögren’s disease and a third may have rheumatoid arthritis is much higher.

The rise of autoimmune diseases in many parts of the world is an epidemic,” says Frederick W. Miller, MD, PhD, former deputy chief of the Clinical Research Branch and retired chief of the Environmental Autoimmunity Group at the National Institute of Environmental Health Sciences at the National Institutes of Health. “We do not know the specific causes, but given the rapid increase, it cannot be genetic changes.”

Since genetics alone are not enough to explain the rapid rise in autoimmunity, many experts — including Miller — suspect environmental triggers.

“More evidence is becoming available that the evolution of autoimmune disease … results from multiple exposures that alter susceptible genomes and immune systems over time,” Miller writes in a 2024 review. “We pay a price for altering our environment, changing our lifestyles, and ignoring climate change.”

Then there’s stress. “Chronic stress can challenge the immune system and trigger inflammation,” explains neurologist David Perlmutter, MD, FACN, ABIHM. This can lead to immune dysfunction.

And these are especially stressful times, he adds. “Unlike historical stressors that were often immediate and survival based, modern stress tends to be chronic, stemming from work demands, financial insecurity, and, importantly, social comparisons.”

We’ve also lost many of the things that softened the impact of everyday stress, such as strong community ties and time in nature.

Stress increases cortisol levels, which can disrupt sleep and drive cravings for unhealthy foods, while toxins in the environment add to the body’s inflammatory burden,” ­Perlmutter says. “Together, these factors weaken resilience, impair detoxification, and accelerate the development of autoimmune diseases.” (For more on autoimmunity and how to cope, see “Autoimmune Disorders: When Your Body Turns on You.”)

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How Melatonin Reduces Inflammation https://experiencelife.lifetime.life/article/how-melatonin-reduces-inflammation/ https://experiencelife.lifetime.life/article/how-melatonin-reduces-inflammation/#view_comments Mon, 18 Aug 2025 12:00:15 +0000 https://experiencelife.lifetime.life/?post_type=article&p=118775 Melatonin does more than just regulate your sleep cycle — it also helps tamp down inflammation. Here's how.

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During the COVID-19 pandemic, melatonin received heightened attention for its capacity to both help fight infections and reduce inflammation. A paper published in Clinical Nutrition ESPEN in 2021 listed it among the key preventive and therapeutic nutraceuticals for COVID, along with zinc, selenium, and vitamins C and D.

Melatonin can stimulate cytokine production to help the body fight off invading viruses, bacteria, or other pathogens, notes John ­Lieurance, ND, DC, in his book Melatonin: Miracle ­Molecule. It can also help slow down cyto­kine production when the body needs to reverse or prevent potential inflammatory damage.

“Being chronically underslept will increase the likelihood of illness and chronic inflammation.”

“It is this dual action of melatonin on the immune system that has been of particularly great interest to scientists,” Lieurance writes. It makes melatonin especially valuable in treating conditions like COVID, where the potential overreaction of the ­immune system — known as a cytokine storm — can be as damaging as the infection itself.

Because inflammation is managed in part by optimal sleep, melatonin’s role in promoting sleep is key, says Samantha McKinney, RD, who helps lead nutrition education at Life Time. “Being chronically underslept will increase the likelihood of illness and chronic inflammation.”

Emerging research suggests that symptoms associated with inflammatory autoimmune conditions, such as multiple sclerosis, may be eased with melatonin supplementation. This is most likely due to the hormone’s anti-­inflammatory properties and its ability to reduce oxidative stress and regulate the gut microbiome.

 Discover More of Melatonin’s Many Wonders

Melatonin is much more than just a sleep compound. It helps to regulate hormone regulator, boost immunity, and support mitochondira. Learn about the many roles this important and versatile molecule plays at “The Powerful — and Surprising — Health Benefits of Melatonin,” from which this article was excerpted.

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Becoming Heart Smart (Performance & Longevity Series) https://experiencelife.lifetime.life/podcast/becoming-heart-smart-performance-longevity-series/ Thu, 14 Aug 2025 10:00:23 +0000 https://experiencelife.lifetime.life/?post_type=podcast&p=121785 The post Becoming Heart Smart (Performance & Longevity Series) appeared first on Experience Life.

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Breaking Insulin Resistance: Your Guide to Blood-Sugar Mastery (Performance & Longevity Series) https://experiencelife.lifetime.life/podcast/breaking-insulin-resistance-your-guide-to-blood-sugar-mastery-performance-longevity-series/ Thu, 07 Aug 2025 10:00:40 +0000 https://experiencelife.lifetime.life/?post_type=podcast&p=121297 The post Breaking Insulin Resistance: Your Guide to Blood-Sugar Mastery (Performance & Longevity Series) appeared first on Experience Life.

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Inflammation and Aging: The Hidden Connection (Performance & Longevity Series) https://experiencelife.lifetime.life/podcast/inflammation-and-aging-the-hidden-connection-performance-longevity-series/ Thu, 31 Jul 2025 10:00:15 +0000 https://experiencelife.lifetime.life/?post_type=podcast&p=121069 The post Inflammation and Aging: The Hidden Connection (Performance & Longevity Series) appeared first on Experience Life.

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Learning How to Manage Gestational Hypertension — Naturally https://experiencelife.lifetime.life/article/learning-how-to-manage-gestational-hypertension-naturally/ https://experiencelife.lifetime.life/article/learning-how-to-manage-gestational-hypertension-naturally/#view_comments Tue, 15 Jul 2025 13:01:13 +0000 https://experiencelife.lifetime.life/?post_type=article&p=115973 How healthcare researcher Michelle Emebo learned to manage gestational hypertension with quality nutrition and exercise.

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See Michelle’s Top 3 Takeaways

Before giving birth in May 2015, I developed gestational hypertension. Despite concerns that it could lead to additional health complications — such as placental abruption, premature birth, or organ damage — I delivered a healthy baby girl.

Over the next year, my blood pressure remained high, and I wasn’t able to lose weight. At a checkup, my doctor noted that Black women tend to be overweight, and he recommended increasing the dose of the hypertension medication I’d started after my daughter was born. He did not suggest lifestyle modifications, like changing my diet or exercising more.

I’m a healthcare researcher, so I knew that his statement concerning Black women was statistically correct. Based on the data, the number of higher-weight Black women is disproportionate compared with other demographic groups for reasons that aren’t entirely understood. A partial explanation is well-established, however: Body mass index overestimates obesity in Black people because it doesn’t account for differences in body composition.

Nevertheless, this didn’t necessarily apply to me — I hadn’t been hypertensive or overweight before I tried to get pregnant. I wanted to find the root cause of my hypertension and weight retention, and I wanted to focus on lifestyle changes before I treated the problem with more medication. I hoped to find another physician to partner with on this wellness journey.

 

Rising Pressure

I got pregnant in 2014, about a year after marrying my college sweetheart. I was a little underweight after my first trimester, so I started drinking protein shakes with breakfast.

Living in Chicago helped too — the city is full of great food. My husband and I ­enjoyed eating at nearby burger joints, taco bars, and pizza places. I made friends with the baker at a local doughnut shop, who always waved me in and gave me one of my favorite glazed long johns.

By the middle of my third trimester, I had gained almost 55 pounds. My blood pressure had also increased — so much so that my physician advised me to come in every other week for checkups. At the time, I didn’t think much about the condition. I felt OK and I’d been reassured that my numbers would normalize after giving birth.

People with hypertension may not experience symptoms, so the condition is not always taken seriously. But it is a genuine threat to health, known as a “silent killer.” Gestational hypertension increases blood-vessel resistance, reducing blood flow to the mother’s essential organs and the placenta. This has the potential to deprive the developing baby of necessary nutrients and oxygen.

We were lucky. Although my blood pressure remained high during the weeks leading to my due date, my baby, Sarai, was born in good health.

The Fourth Trimester

Four months after I gave birth, my healthcare provider advised that I start taking a low-dose medication to manage my blood pressure.

I was having a difficult time ­recovering physically and emotionally from childbirth. The experience had been hard on my body, and adjusting to life with a newborn was a challenge — even with the help of my mother and mother-in-law. Sarai wasn’t feeding well, and she was sleeping all day and awake all night.

At a six-week follow-up visit, I was diagnosed with postpartum depression. I started seeing a therapist on a regular basis, and she helped me learn how to prioritize my own needs while figuring out how to take care of Sarai. I began by simply making sure I was eating, showering, and getting some sleep.

By November 2015, I was starting to adjust to my new life. But my blood pressure remained high. For months I had been living in survival mode. I ate as I had during pregnancy, not thinking about sodium or macronutrients, and I felt more stressed. I lacked the capacity to focus on better nutrition or exercise.

But now that I was finding balance in other areas of my life, I felt ready to address the root causes of my high blood pressure.

I found a new doctor who was willing to focus on nutrition and exercise before increasing my medication. It was the ­motivation I needed to make a change.

Taking Back My Power

I began working with a nutritionist who recommended I reduce sodium and take a month off from eating out. To follow this advice, my husband and I became more intentional about grocery shopping. I focused on produce and meat and was mindful of food labels. On Sundays, I prepped food for the week ahead.

I also made exercise a priority. I’d been athletic as a child and young adult: I played basketball and volleyball in high school and continued with basketball through college. But fitness took a back seat after I graduated. With my health on the line, it was time to tune in to my once-active spirit. I started by attending fitness classes two or three times a week.

Although ­results came slowly and gradually, I never felt like I was sacrificing. I maintained a regular workout routine; chose whole foods over processed ones; modified portion sizes to match my nutritional needs; opted for a salad over a burger when I ate out; and ­requested one pump of syrup instead of two in my ­coffee drink.

It all took about 18 months, but I was committed. Consistency was more important than a quick fix.

By fall 2018, my blood pressure had normalized and I had lost 75 pounds.

My doctor said I could go off the meds — cold turkey. My blood pressure was stable when I saw him again a month later, and it’s remained stable ever since. Today, it’s in the range of 110–120/80, and I only see my doctor once a year for a wellness exam.

I now know what my body needs to be healthy.

Reaching and Keeping the Goal

My goals have changed since my blood pressure stabilized. In 2018, I joined Life Time, motivated by the amenities offered for children. Sarai was an active toddler by then, and I wanted her to learn how to have fun with fitness at a young age.

I started working with a personal trainer who created a routine that I can adjust as needed. I add more yoga classes during stressful times. I’ve also trained for and competed in a variety of races, including obstacle-course events and a half-marathon. I like the opportunity to modify my training and connect with other people in the fitness community.

I love being active with Sarai, who is now 10. We like to throw the football or shoot hoops together, and I’ll run alongside while she bikes.

Nutrition is an important part of our lives, and my husband and I have ­incorporated the phrase “nutrient-dense foods” into the family vocabulary. I hope my journey ­teaches Sarai she has the power to take control of her physical, mental, and spiritual health.

I’m also preparing to return to medical school. I hope to join an emerging field of physician nutrition specialists who work with patients with chronic disease. My dream is to run my own team and conduct research that incorporates nutrition. I want to help more patients learn how to improve their health outcomes through manageable lifestyle adjustments — like I was able to do for myself.

Michelle’s Top 3 Takeaways

1. Take control of your health. “I was waiting on doctors to cure me, until I realized I had to partner with my doctor and help myself,” says Michelle.

2. Take hypertension seriously. “What starts with obesity and hypertension becomes cardiac disease, then kidney disease, [and this can] lead to death. Try to prevent that early on.”

3. Make small changes over time. We often expect a quick snapback after birth, she notes. Huge change is not realistic. Reach the goal, then keep the goal.

 My Turnaround

For more real-life success stories of people who have embraced healthy behaviors and changed their lives, visit our My Turnaround department.

Tell Us Your Story! 
Have a transformational healthy-living tale of your own? Share it with us!

This article originally appeared as “Easing the Pressure” in the the July/August 2025 issue of Experience Life.

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Redefining Obesity https://experiencelife.lifetime.life/article/redefining-obesity/ https://experiencelife.lifetime.life/article/redefining-obesity/#view_comments Tue, 20 May 2025 12:56:42 +0000 https://experiencelife.lifetime.life/?post_type=article&p=115294 Rather than looking just at a person’s weight, some progressive healthcare providers are seeking to identify obesity by its metabolic effects.

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In my late 30s, I was in the best shape of my life, cycling 20 to 30 miles daily, pumping iron regularly, and eating a plant-forward Mediterranean diet. Digestive issues I’d been dealing with had dissipated, and I was sleeping well after years of insomnia. I felt healthier than ever.

Imagine my surprise when my doctor told me I was overweight.

Many of us have faced this puzzling experience. Definitions of overweight and obesity often stem from misleading metrics such as the body mass index (BMI) my doctor used. These classifications can lead to a range of misunderstandings about what a higher body weight means for your health — not to mention the significant stress of being told you’re unhealthy solely because of your weight.

Given this confusion, some healthcare providers are turning to other metrics, including measurements of metabolic health, to determine whether a patient’s weight poses a health risk. They may deploy tests that measure stress hormones, glucose regulation, hormonal balance, thyroid and gut health, and inflammation, all of which affect how well your body converts food into energy and offer insight into your metabolic functioning.

The questions that follow examine why a metabolic framework for obesity might be a better starting point for determining the true status of your health.

Why do we gain weight?

While we typically assume weight gain is primarily about dietary choices — and they certainly can play a role — it can be influenced by a variety of factors. These include genetics, hormone dysregulation, sleep, stress, and certain medications.

Researchers are also investigating the role played by exposure to environmental toxins, sometimes called “obesogens.” These chemicals are often found in everyday items and include bisphenol A (BPA), which is employed in making plastics, and phthalates, endocrine disruptors commonly used in personal-care products. They can disrupt the body’s normal metabolic processes and endocrine function, promoting fat accumulation.

Excess weight can contribute to impaired cardiovascular function, joint stress, and breathing challenges, like sleep apnea. These physical impacts can be significant. Still, weight alone doesn’t provide a complete picture of a person’s overall metabolic health.

What’s wrong with relying on BMI as a measure of weight health?

Your body mass index is the measure of your weight in kilograms divided by the square of your height in meters. It’s widely used by healthcare providers to classify people as underweight, normal weight, overweight, or obese. (Learn more at “Beyond BMI: Why True Health Is About More Than What You Weigh.”)

“Physicians typically use BMI to measure a patient’s ‘weight health,’” explains Stewart Lonky, MD, in his book, Outsmarting Obesity: A Doctor Reveals Why We Gain Weight, Why It Matters, and What We Can Do About It.

Yet BMI is a blunt tool with significant limitations. It was first developed in the early 19th century — and updated by physiologist Ancel Keyes in 1972 — strictly as a research tool for measuring weight trends in populations. Neither of its creators were medical professionals, and they never intended BMI for medical use.

It was first developed in the early 19th century — and updated by physiologist Ancel Keyes in 1972 — strictly as a research tool for measuring weight trends in populations. Neither of its creators were medical professionals, and they never intended BMI for medical use.

The original study in which BMI was used didn’t include women and most of its participants were white men. This means its current status as a universal metric misdiagnoses a wide diversity of body types.

Most importantly, BMI reveals nothing about body composition. “The most significant drawback of BMI is its inability to differentiate between fat and muscle,” explains Lonky. “While it’s not accurate to say that muscle weighs more than fat, it is denser. This density is why a cubic inch of muscle weighs more than a cubic inch of fat.”

In a recent paper published in The Lancet Diabetes and Endocrinology, a commission of global experts argue that BMI-based definitions lead to overdiagnosis and underdiagnosis, labeling people as unhealthy when they aren’t and missing those who may be at risk despite a “normal” BMI. This can result in poorer health outcomes for everyone.

For example, a fit, muscular athlete might have a BMI over 30, qualifying them as obese strictly because of their weight-to-height ratio. On the other hand, someone with a “healthy” BMI of less than 25 might have metabolically active visceral fat (more on why that matters later) that puts them at risk for cardiovascular disease.

In neither case does their BMI explain anything about their actual health status.

Does the location of fat matter?

Where fat is stored may be more indicative of its risks than weight alone. “BMI tells you nothing about body composition or where you’re putting on weight,” explains holistic nurse practitioner Monique Class, MS, APRN-BC.

Visceral fat stored around vital organs in the abdomen appears to be particularly risky. Unlike subcutaneous fat, which is stored under the skin, visceral fat is sometimes described as “metabolically active” because it can produce hormones and inflammatory molecules. Fat around the midsection has been associated with systemic inflammation, insulin resistance, and cardiovascular risks.

Visceral fat can also be an indication of metabolic syndrome, a cluster of conditions — including high blood pressure, high blood triglycerides, low levels of HDL cholesterol, and insulin resistance — that occurs together. Metabolic syndrome increases a person’s risk of heart disease, stroke, and type 2 diabetes.  (Listen as Jim LaValle, RPh, CCN, explains the factors that contribute to insulin resistance, how to measure and monitor blood sugar, and the habits we can adopt to manage blood sugar effectively at “Breaking Insulin Resistance: Your Guide to Blood-Sugar Mastery.”)

What is “metabolic obesity”?

The global commission of experts involved in The Lancet Diabetes and Endocrinology report recommend defining obesity through clinical signs — such as tissue and organ alterations — that better capture when excess fat genuinely impacts health. This definition ensures a more precise identification of those in need of intervention and could lead to more effective treatment.

This approach acknowledges that caloric intake or physical-activity level are not the only factors influencing a person’s metabolic health. Chronic stress, sleep quality, thyroid health, hormone regulation, gut health, and genetics all play an important role. Understanding the root causes of disruptions in metabolic health would be the focus of any intervention.

By this definition, a thin person with metabolic syndrome could be classifiably obese while a heavier person may or may not. What matters most are factors like insulin regulation, blood pressure, and cardiovascular function.

By focusing on metabolic health, clinicians can identify and address issues such as hormonal imbalances and the role of visceral fat in driving inflammation and cardiovascular risks.

Are there other ways to classify higher weight and obesity?

Some researchers classify weight metabolically using these phenotypes:

  • Metabolically Unhealthy Normal Weight: People who have a BMI of between 18.5 and 24.9 but exhibit metabolic problems commonly associated with obesity or metabolic syndrome, such as insulin resistance and high blood pressure. Despite their lower weight, these individuals may face health risks due to underlying metabolic dysfunction.
  • Metabolically Unhealthy Obesity (MUO): Individuals with high weight and additional metabolic complications, such as high blood pressure, insulin resistance, and abnormal cholesterol levels. MUO is associated with higher risks for cardiovascular disease and type 2 diabetes.
  • Metabolically Healthy Obesity (MHO): People with a BMI over 30 without metabolic risk factors typically linked to obesity. Even if a person categorized as MHO has healthy metabolic markers, it’s important to manage those markers over time by remaining active and eating a quality diet. While MHO offers a lower immediate risk, studies have shown that up to 50 percent of individuals with MHO develop metabolic complications within a decade or so, driven by aging, weight gain, and declining insulin sensitivity.

Weight is only one aspect of overall metabolic health, so it’s important to recognize that the number on the scale tells the whole story. It makes perfect sense to question an obesity diagnosis, especially if it’s based on BMI, if you know you’re healthy, rested, and strong. The metabolic numbers are the ones that count.

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The Connection Between Your Gut and Your Mental Health https://experiencelife.lifetime.life/article/your-gut-and-your-mental-health/ https://experiencelife.lifetime.life/article/your-gut-and-your-mental-health/#view_comments Tue, 15 Apr 2025 13:01:05 +0000 https://experiencelife.lifetime.life/?post_type=article&p=116264 In his new book, The Gut-Brain Paradox, Steven Gundry, MD, talks about how maintaining a healthy gut microbiome may improve your mood.

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Back in the 1800s, one of the most hotly contested “celebrity” feuds was between two French chemists: Louis Pasteur and Antoine Béchamp. Chances are, you’ve only heard of one of these scientists, which means that he ostensibly “won” the debate. This is true, but it does not tell the full story, or even come close.

Pasteur and Béchamp were fighting about germs, also known as microbes or microorganisms. These tiny living things include viruses, bacteria, archaea, fungi, and protists — all too small to be seen by the naked eye. Both men agreed that these microbes existed. What they disagreed about was whether they were good or bad.

Pasteur believed microbes were bad. One of his signature contributions to public health was pasteurization, which kills microbes in milk and makes it safe to drink. Pasteur took this idea a step further, claiming that all microbes caused disease and that killing them was therefore always the cure. This became known as the germ theory of diseases, and today this framework informs much of modern medicine.

We now generally assume that killing off germs is the best way to prevent and cure disease, so we do it routinely. Just think about that hand sanitizer that you carry around with you, or the last round of antibiotics your doctor prescribed. And some specific bacteria, such as some E. coli and Salmonella, are pathogenic and therefore dangerous to us. But Pasteur’s germ theory was only partially correct. And Béchamp knew it.

To Béchamp, germs themselves were not strictly the problem. He believed they only caused disease when their environmental “terrain” was disrupted, making their host susceptible to disease. In other words, most microbes could only cause disease when the conditions in the body allowed them to overgrow.

Béchamp also believed that microbes were an essential part of human beings and all living things, so he viewed killing off germs as both impossible and terribly dangerous. Unfortunately, his argument failed to gain any traction. Pasteur was a brilliant public speaker, and in 1863 he allegedly gained Emperor Napoleon III’s undying support when he “proved” that wine went “bad” from bacterial contamination.

In vino veritas, as they say. But not always.

Thanks to recent research, we now know that it was Béchamp — not Pasteur — who had the better understanding of the microbial world.

Every day we discover new things about the sheer numbers of microbes living in and around us, not to mention the countless, complex ways they influence our health and behavior. Our bodies are host to multiple microbial communities — in our mouths, lungs, skin, and, most significantly, in our guts. Together, these are known as the “holobiome,” and they give us good reason to reconsider who and what we are as humans.

Are we lone creatures, or symbiotic communities made up of a combination of human and microbial cells? If you believe you are the former, I hope to change your mind.

 

Mental Health and the Gut

Not long after the debate between Pasteur and Béchamp, a Portuguese physician named Antonio Maria de Bettencourt Rodrigues became the first doctor we know of to make the connection between bacteria and mental health. In 1889, at a mental health congress in Paris, Rodrigues presented the idea that depression could be caused by “autointoxication,” a theory that bacterial waste products could build up in the body and cause disease. He treated depressed patients with a combination of dietary changes and gut detoxification.

The idea of autointoxication went hand in hand with Pasteur’s belief that all bacteria were harmful, and it became the prevailing theory of the day. Throughout the 19th century, autointoxication was widely viewed as a cause of or contributor to most diseases, leading to such interventions as colonic irrigation to clear out those bacterial waste products.

Rodrigues may have been the first to suggest autointoxication as a cause for depression, but some of his contemporaries also saw a potential connection between mental health and the gut. A scientist named François-André Chevalier-Lavaure observed that many of his psychiatric patients suffered from digestive conditions and saw improvements in their psychiatric symptoms after their digestive issues were treated.

Although the term “autointoxication” was imprecise and incorrect, these scientists were onto something. As the field of psychology grew over the course of the 20th century, the connection between gut health and mental health was mostly abandoned in favor of the idea that the mind and body were basically disconnected and should be treated separately.

But things have a way of coming full circle. Today, we see that a vast majority of mental health conditions involve neuroinflammation. Numerous studies have noted the connections between mental illness and leaky gut, a leaky blood-brain barrier, increased cytokines, and microglial activation.

Put another way, it seems that waste products and toxins may contribute to mental health challenges, if not in the way autointoxication proposed.

When mice are given lipopolysaccharides (LPSs), which are fragments of cell walls from dead bacteria, it leads directly to anxiety-related behaviors. Adult humans with major depressive disorder (MDD), schizophrenia, and bipolar disorder have all been shown to have increased cytokine levels as well as higher-than-normal amounts of mitochondrial content in their bloodstreams. That mitochondrial content has been released from the cells during a process of cellular cleansing known as apoptosis. Because of its bacterial DNA, that content is then recognized by the immune system as invasive bacteria. This triggers neuroinflammation and, by extension, higher potential for mental health struggles.

 

The Depressed Microbiome

Let’s take a look at the connections between depression and the gut — of which there are many.

Our gut bacteria can lead to depression via neuroinflammation stemming from dysbiosis and leaky gut. Dysbiosis can also lead to a change in neurotransmitter levels, which can lead to depression, and inflammation can also cause worsening dysbiosis and leaky gut.

Although the role of neurotransmitters in depression is widely known, many researchers leave the microbiome out of this discussion. But gut bacteria produce neurotransmitters either directly or they produce the precursors that your body needs to make neurotransmitters. Simply put, with an altered terrain, neurotransmitter levels become dysregulated. This is a major factor in depression.

Research shows that patients suffering from MDD have significantly altered microbiomes compared with healthy patients. Notably, patients with MDD have enriched proinflammatory bacteria and depleted anti-inflammatory, butyrate-producing bacteria. Patients with MDD also have a higher chance of suffering from leaky gut and higher levels of circulating cytokines.

Further, in 2022, a groundbreaking study looked at the microbiomes of more than a thousand patients with depression. They found alterations in 13 specific bacteria associated with depression. These specific bacteria are all known to be involved in the synthesis of glutamate, butyrate, serotonin, and GABA. And in patients with severe mental illness, increases in dysbiosis, levels of zonulin (with causes leaky gut), LPSs, and inflammation are all correlated with the severity of disease.

Inflammation doesn’t discriminate. Once your immune system gets the message that the fortress of your gut lining has been breached, that inflammation will become widespread and eventually get to your brain.

One study looked at the metabolites in the blood of three groups of people: those suffering from depression, those who were in remission from depression, and a control group. The people suffering from depression had significantly higher levels of glutamate and alanine and significantly lower levels of myo-inositol, GABA, phenylalanine, creatine, methionine, oleic acid, and tryptophan compared with the other two groups.

 

The Metabolite Problem

Balance is key when it comes to metabolites. Either too many or too few can cause problems. A balanced inner terrain should produce just the right amount of these substances; in patients suffering from depression, their microbiomes are not able to do their jobs correctly.

Low levels of tryptophan are especially notable in depression. Tryptophan is a precursor to serotonin and plays a role in its synthesis. It is also a precursor of 5-hydroxytryptamine, an amino acid needed to activate serotonin receptors — the main targets for conventional antidepressants.

What’s interesting is that antidepressants actually work their magic less on the serotonin receptors than on the microbiome. Research has found that SSRIs (selective serotonin reuptake inhibitors) change the makeup of the gut and even have direct antibacterial effects. One study compared the microbiomes of patients with MDD before and after they had been treated with an SSRI. Before treatment, their microbiomes showed reduced diversity and richness compared with controls. After treatment, their microbiomes had “normalized” and were comparable to those of healthy patients.

So, if SSRIs work by fixing the microbiome, then why not just go straight to the source and … fix the microbiome? That’s what I do in my practice. Meanwhile, have patience: The effects of SSRIs usually take a month to kick in, because it takes about that long to change your inner terrain.

 

Some Examples of Treating Depression Through the Gut

Treating depression by way of the gut can be done through several mechanisms:

 

Fecal Microbiota Transplant

A review of 21 human studies found that fecal microbiota transplants — repopulating the gut microbiome with diverse and healthy microbes — consistently led to a decrease in depression and anxiety symptoms among patients suffering from depression. A recent review also found that transplanting fecal microbiota from patients suffering from depression to healthy patients led to depression and anxiety symptoms in those previously healthy patients.

 

Probiotics and Prebiotics

Probiotics, which help rebalance the gut microbiome, can help regulate serotonin levels and reduce inflammation, leading to a reduction in symptoms of depression. And prebiotics (which feed our gut microbes) also seem to have antidepressant and antianxiety effects. A recent review looked at human studies from 2015 to 2023 on probiotics and prebiotics being used to treat depression. Researchers concluded that by attenuating inflammation and making serotonin more available, both prebiotics and probiotics significantly improved mood and reduced the severity of symptoms in patients suffering from depression.

 

Hydrogen Sulfide

Hydrogen sulfide (H2S) is a signaling molecule made by your gut microbes, specifically when they ferment sulfur-containing compounds. H2S plays an important role in nociception, which is your nervous system’s process of understanding noxious stimuli (heat, cold, mechanical force, or chemical stimulation).

When you experience pain, your gut microbes produce H2S and send it to your brain to let you know you’re hurt. The H2S then activates nociception neurons in the brain, which leads to the release of inflammatory cytokines and growth factors to heal the damage. When nociceptors are removed, the result is a defective tissue-protective reparative process. This happens because neurons do not get the signal that you’re in pain and need to heal.

Too little H2S can lead to depression. When mice were treated with LPSs, it led to an increase in neuroinflammation and symptoms of depression. Both the inflammation and the symptoms were reversed with the administration of H2S.

 

Vitamin D

Depression and vitamin D deficiency often occur together, so vitamin D supplements are another potential treatment for depression. It comes as no surprise that vitamin D has a positive impact on the gut. It increases gut diversity and the relative abundance of butyrate-producing bacteria, as well as some other particularly helpful gut microbes, like Akkermansia and Bifidobacterium. The result of these changes is less leaky gut and less inflammation. This may be why vitamin D also helps prevent dementia.

 

Psychedelics

Much like SSRIs, psychedelic drugs work with the gut to help alleviate depression. Ketamine, for example, can profoundly reduce inflammation by making changes to the microbiome. When depressed mice were injected with ketamine for seven days, they had a significant increase in friendly gut microbes and a reduction of pathogens.

Our gut microbes also play a big role in the bioavailability of these drugs and their effects, because they play a big role in metabolizing psychedelic substances. The uniqueness of our inner terrains may help explain why the effects of psychedelics tend to vary so much between individuals.

For instance, Bifidobacterium, which is linked to dopamine and addiction, modulates the metabolism of DMT, the psychoactive compound in ayahuasca. Another species of bacteria, Enterococcus faecalis, produces a critical enzyme to degrade LSD. There are specific bacterial strains that can metabolize mescaline, a psychoactive compound found in the peyote cactus. An insufficient microbial terrain will make it difficult to receive any benefit from these treatments.

That means patients with dysbiosis and leaky gut, which can cause inflammation and depression, are the least likely to be able to metabolize psychedelics. This is just one reason I think it’s critical to heal the microbiome before attempting to treat depression with any of these substances.

 

The Root of the Problem

The gut is the real root of neuroinflammation, which, in turn, is the real root of neurodegeneration and many common mental health and cognitive issues. With our disrupted inner terrains, many of us now have leaky gut, causing a near-constant activation of the immune system and chronic neuroinflammation. It’s a recipe for disaster, but it can be turned around, along with the diseases and symptoms that it causes.

Adapted from “THE GUT-BRAIN PARADOX” by Dr. Steven R. Gundry. Copyright © 2025 by Dr. Steven R. Gundry. Reprinted courtesy of Harper, an imprint of HarperCollins Publishers. Available wherever books are sold.

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How Ultraprocessed Foods Wreak Havoc on Your Metabolism https://experiencelife.lifetime.life/article/how-ultraprocessed-foods-wreak-havoc-on-your-metabolism/ https://experiencelife.lifetime.life/article/how-ultraprocessed-foods-wreak-havoc-on-your-metabolism/#view_comments Wed, 09 Apr 2025 12:00:54 +0000 https://experiencelife.lifetime.life/?post_type=article&p=111402 Eating UPFs can undermine your digestion, gut health, and metabolism. Here's why.

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There are several hypotheses about how UPFs harm the body, though there’s still no consensus about the exact mechanism that causes the damage. Still, the research is moving quickly, says Schmidt. “Finding . . . [that mechanism] is the holy grail of nutrition science right now.” These are some of those theories.

1) Calorie Density

In 2019, a study correlated UPFs and weight gain for the first time. The randomized controlled trial, conducted by the National Institutes of Health, divided 20 healthy adults into two groups. For two weeks, one group ate only ultraprocessed foods while the other ate foods that were minimally processed. Then the groups switched diets and continued for two more weeks.

To increase the study’s accuracy, participants lived at the research center. Their meals contained an identical number of calories and grams of sugar, fat, sodium, fiber, and macronutrients. At mealtimes, both groups had an hour to eat as much or as little as they chose.

Researchers found that the subjects who were eating the UPFs consumed about 500 calories more per day than those eating minimally processed foods. After two weeks, members of the UPF group had gained an average of about 2 pounds.

By the end, researchers found that the subjects who were eating the UPFs consumed about 500 calories more per day than those eating minimally processed foods. After two weeks, members of the UPF group had gained an average of about 2 pounds.

2) Speed of Digestion

The body perceives industrially processed foods as essentially prechewed and predigested. That perception produces a host of repercussions along the digestive tract, starting in the mouth. Studies have shown that the longer a food must be chewed before it’s swallowed, the more satisfying it is to eat and the fuller a person feels afterward.

Research has also shown that people who chew their food longer consume fewer calories. In the NIH study, participants eating the ultraprocessed diet swallowed more calories per minute than did their counterparts. The combined eating speed and caloric density is what led to the extra 500 calories a day.

When we eat whole foods, the foods’ cells don’t break down completely, explains Juul. She compares whole ­almonds and almond flour: Whole almonds involve some serious chewing. After you swallow, your body absorbs only about 75 percent of their calories, she says, because the nut’s structure is still partly intact.

Once almonds are turned into almond flour, a higher percentage of their calories is absorbed into the bloodstream. This speed of absorption affects everything from blood-sugar levels to satiety hormones.

Evidence has suggested that highly palatable foods can dampen the body’s satiety signals, which can lead to over­eating. As van Tulleken writes, “The signals that tell you to stop eating haven’t evolved to handle food this soft and ­easily digested.”

(After the gut, the mouth contains the most diverse microbial community in the body. As a result, the oral microbiome has a significant influence on your overall health. Learn more at “Everything You Need to Know About the Oral Microbiome.”)

3) Missing Nutrients

Studies suggest that UPFs are crowding out the nutrient-dense foods on our plates. In a 2021 meta-analysis, researchers noted a correlation between the increasing number of UPFs in meals and decreasing amounts of dietary fiber, protein, potassium, zinc, niacin, and vitamins A, C, D, E, and B12.

4) Novel Molecules

On a cellular level, nutrients exist in a certain structure within a food, and synergies exist between different nutrients and non-nutrients, says Juul. This is known as the food matrix, and it’s destroyed by industrial processing.

Our digestive system is designed to slowly and methodically break down a food’s matrix to glean the greatest nourishment for the body — and specifically for the microbiome.

Likewise, our signaling pathways evolved over millions of years to distinguish good molecules from bad. A molecule that is a shade different from one found in food can cause real problems with human chemistry, says Robert ­Rountree, MD, a Boulder, Colo.-based integrative family medicine practitioner. “Xenobiotic molecules gum up the works.”

5) Inflamed Gut

New evidence suggests that food ­additives, such as emulsifiers, thickeners, and artificial sweeteners, may cause gut inflammation. This can lead to a variety of gastrointestinal issues, including IBS.

Presently, more than 60 types of emulsifiers are used in UPFs, including polysorbate 80, carboxymethylcellulose, and carrageenan. Studies have found that mice exposed to these substances developed gut inflammation after 12 weeks.

There’s also a potential cocktail effect from multiple food additives in a single UPF, as well as in the many combinations that might be eaten in a handful of foods at one sitting.

“All of us are subjects in a food experiment that humans have never encountered before,” says Devries. “As a result, we are seeing a greater spectrum of digestive problems than have ever been observed before.”

Ultraprocessed Foods are Everywhere

Take a closer look at the many ways these food products can harm your health — and why it’s worth the effort to avoid them when you can at “The Truth About Ultraprocessed Foods,” from which this article was excerpted.

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