Anti-aging drug combo damages myelin in mouse brains

A widely studied anti-aging treatment triggered significant brain damage in mice, according to new research from the University of Connecticut. The drug combination dasatinib plus quercetin caused myelin loss and changes resembling those seen in multiple sclerosis. The findings raise questions about its use in longevity studies and off-label therapies.

Researchers at the University of Connecticut tested the dasatinib-quercetin combination on both young and old mice. They found that the treatment reduced protective myelin layers around nerve fibers in the brain, with younger animals showing greater damage than older ones. The corpus callosum also deteriorated in treated mice, producing effects similar to those described as chemo brain in humans undergoing chemotherapy.

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Researchers at Texas A&M University have developed a nasal spray that appears to reverse aspects of brain aging after just two doses. The treatment reduced inflammation and restored memory function in models for months afterward. The findings were published in the Journal of Extracellular Vesicles.

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A 2023 study found that falling levels of the protein Menin in the hypothalamus drive multiple signs of aging in mice. Restoring the protein or supplementing with the amino acid D-serine improved memory and other measures.

A study involving 73 people with mild cognitive impairment or early dementia found that tailored treatment plans targeting nutritional deficiencies, infections and other factors led to significant cognitive improvements after nine months. Participants in the intervention group saw their overall cognitive scores rise by 13.7 points, while the control group declined by 4.5 points. The approach combines medical interventions with lifestyle changes like diet, exercise and cognitive training.

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A major Cochrane review of 17 clinical trials involving over 20,000 participants has concluded that drugs targeting amyloid beta in the brain provide no meaningful benefits for patients with mild cognitive impairment or early Alzheimer’s. These treatments also raise the risk of brain swelling and bleeding. Researchers urge a shift to alternative pathways for future treatments.

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