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.

संबंधित लेख

Realistic depiction of sticky mitochondrial DNA damage (glutathionylated adducts) disrupting cell energy, activating stress pathways, and linking to diseases like diabetes, cancer, and neurodegeneration.
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Researchers identify sticky mitochondrial DNA damage tied to cellular stress and disease risk

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Scientists at the University of California, Riverside have identified a previously unknown form of mitochondrial DNA damage known as glutathionylated DNA adducts, which build up at dramatically higher levels in mitochondrial DNA than in nuclear DNA. The lesions disrupt energy production and activate stress-response pathways, and researchers say the work could help explain how damaged mitochondrial DNA contributes to inflammation and diseases including diabetes, cancer and neurodegeneration.

Researchers in Japan have discovered that boosting a protein called COX7RP in mice improves mitochondrial function, leading to longer lives and better health. The engineered mice lived 6.6% longer on average, with enhanced metabolism and reduced signs of aging. This finding points to potential ways to promote healthier aging in humans.

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Biomedical engineers at Texas A&M University have used nanoflowers to make stem cells produce roughly twice the usual number of mitochondria. These enhanced stem cells then transfer the extra energy-producing organelles to damaged or aging cells, restoring their energy production and resilience in lab studies, according to a new report in the Proceedings of the National Academy of Sciences.

Researchers working at Harvard University and collaborators in Brazil have identified metabolites produced by gut bacteria that travel through the portal vein to the liver and appear to influence energy use and insulin sensitivity in mice. The findings, published in Cell Metabolism, suggest possible new strategies for preventing or treating obesity and type 2 diabetes by targeting gut–liver communication.([sciencedaily.com](https://www.sciencedaily.com/releases/2025/12/251214100926.htm?utm_source=openai))

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Weill Cornell Medicine researchers report that free radicals generated at a specific mitochondrial site in astrocytes appear to promote neuroinflammation and neuronal injury in mouse models. Blocking those radicals with tailored compounds curbed inflammation and protected neurons. The findings, published Nov. 4, 2025, in Nature Metabolism, point to a targeted approach that could inform therapies for Alzheimer’s disease and frontotemporal dementia.

Researchers at Case Western Reserve University report they have identified an abnormal interaction between the Parkinson’s-linked protein alpha-synuclein and the enzyme ClpP that disrupts mitochondrial function in experimental models. They also describe an experimental compound, CS2, designed to block that interaction, which they say improved movement and cognitive performance and reduced brain inflammation in lab and mouse studies.

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An international team of researchers has identified trimethylamine (TMA), a gut microbe metabolite produced from dietary nutrients such as choline, as a compound that inhibits the immune-signalling protein IRAK4, dampening inflammation and improving insulin action in experimental models. The discovery, reported in Nature Metabolism, suggests a potential new way to counter some of the harmful metabolic effects of high-fat diets and opens avenues for future type 2 diabetes therapies, a disease affecting more than 500 million people worldwide.

 

 

 

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