New research from UTHealth Houston reveals that substance use disorders accelerate biological aging in the brain through substance-specific molecular mechanisms. The study, published in Genomic Psychiatry, identified distinct genetic and biological pathways that contribute to premature aging in individuals with alcohol, opioid, and stimulant use disorders, offering potential targets for future therapeutic interventions.

Researchers at the University of Michigan have demonstrated that a single dose of a psychedelic compound significantly improves cognitive flexibility in mice for at least three weeks after administration. This groundbreaking finding suggests potential therapeutic applications for conditions characterized by cognitive rigidity, including depression, PTSD, and Alzheimer's disease.

New research on the biological basis of addiction has found that the critical epigenetic enzyme histone deacetylase 5 (HDAC5) limits the expression of the gene Scn4b, regulating neuronal activity and thereby the formation of strong drug-related memories, which can trigger relapse in individuals with substance use disorders (SUDs). The study in Biological Psychiatry, published by Elsevier, detailing these epigenetic mechanisms in the brain, uncovers a new molecular target for the development of novel SUD treatments.