Scientists develop safer way to boost cell calorie burn

Researchers at the University of Technology Sydney have created experimental compounds that prompt mitochondria to burn more calories safely. These mild mitochondrial uncouplers could offer a new approach to treating obesity without the deadly risks of past chemicals. The findings, published in Chemical Science, highlight potential benefits for metabolic health and aging.

A team led by Associate Professor Tristan Rawling at the University of Technology Sydney (UTS) has pioneered experimental compounds designed to make cells burn additional calories by altering mitochondrial function. Mitochondria, known as the cell's powerhouses, convert food into adenosine triphosphate (ATP), the body's chemical energy. The new molecules, called mild mitochondrial uncouplers, disrupt this process mildly, causing cells to consume more fats and release excess energy as heat rather than usable power.

Rawling explains the mechanism: "Mitochondrial uncouplers disrupt this process, triggering cells to consume more fats to meet their energy needs." He likens it to a hydroelectric dam, where uncouplers create a small leak, allowing energy to escape as heat instead of generating electricity.

This innovation builds on a fraught history. About a century ago, during World War I, French munitions workers exposed to 2,4-Dinitrophenol (DNP) experienced rapid weight loss, elevated temperatures, and fatalities. In the 1930s, DNP was marketed as a weight-loss drug for its effectiveness but was banned due to its toxicity—the therapeutic dose being perilously close to the lethal one.

The UTS study, in collaboration with Memorial University of Newfoundland, modified chemical structures to produce safer uncouplers. Some variants increased mitochondrial activity without harming cells or ATP production, unlike more aggressive predecessors. These mild versions also reduce oxidative stress, potentially aiding healthier metabolism, slowing aging processes, and protecting against conditions like dementia.

Obesity, a global issue linked to diabetes and cancer, often requires injectable medications with side effects. This research, published in 2026 in Chemical Science (DOI: 10.1039/D5SC06530E), offers a roadmap for safer oral treatments that could enhance calorie burn while supporting broader health benefits. Though early-stage, it addresses a critical need in public health.

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Realistic illustration of a fatigued young adult overlaid with brain MRI and blood cell visuals highlighting altered ATP energy patterns linked to depression.
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Study links major depression in young adults to altered cellular energy patterns in brain and blood

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Researchers studying young adults with major depressive disorder have reported an unusual energy “signature” in both the brain and immune blood cells: higher ATP-related measures at rest, paired with a reduced ability to increase energy production when demand rises. The findings, published in Translational Psychiatry, may help explain common symptoms such as fatigue and low motivation, though the work is early and based on a small sample.

McGill University scientists report that glycerol released during cold-induced fat breakdown can activate the enzyme tissue-nonspecific alkaline phosphatase (TNAP), switching on a creatine-based energy-dissipating pathway in brown fat. The findings were published May 12, 2026 in Nature and may also inform research into bone disorders linked to TNAP.

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Researchers at University College London have discovered how the body naturally shuts down inflammation using fat-derived molecules called epoxy-oxylipins. These molecules prevent the buildup of immune cells linked to chronic diseases like arthritis and heart disease. A study involving a drug that boosts these molecules showed faster pain relief and reduced harmful immune activity.

Researchers at the University of Santiago de Compostela report a light-driven method that directly “allylates” methane—adding an allyl group that can be used to build more complex molecules—and they demonstrate the approach by producing the nonsteroidal estrogen dimestrol from methane.

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Researchers at Texas A&M University have developed a chemogenetic system that uses caffeine to activate CRISPR gene editing in cells, potentially aiding treatments for cancer and diabetes. The method allows precise control over gene modifications by consuming small amounts of caffeine from everyday sources like coffee or chocolate. This approach aims to enhance immune responses and insulin production with reversible activation.

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