Creative experiences such as dance, music, drawing, and strategy video games might preserve brain health. The authors show that regular practice or short training in these activities is linked to brains that look younger and work more efficiently.
Depression is a serious disorder that disrupts daily life through lethargy, sleep disturbance, and social withdrawal, and also increases the risk of suicide. The number of depression patients has steadily increased over the years, affecting more than 280 million people worldwide as of 2025. Now, researchers have uncovered a new pathological mechanism that could provide clues for the diagnosis and treatment of depression.
A research team led by C. Justin Lee and Lee Boyoung at the Institute for Basic Science (IBS) has identified a new molecular pathway in the brain that directly links abnormal sugar modifications in proteins to depressive behaviors. Specifically, chronic stress disrupts sugar chains (O-glycans) attached to proteins in the prefrontal cortex, thereby triggering depression.
The findings, published in Science Advances, open new possibilities for targeted therapies for treatment-resistant depression.
Paying less attention to faces is one of the key markers of autism spectrum disorder. But while researchers have begun to uncover the brain network that supports processing of social stimuli such as faces, gaze, and speech, little is known about how and when it begins to develop.
In a new study, Yale researchers have now found that this network is already quite active at birth or shortly thereafter, a finding that provides insight into the brain processes that underlie social behaviors later in life.
The study was published in Biological Psychiatry Global Open Science.
Trying to document how single brain cells participate in networks that govern behavior is a daunting task. Brain probes called Neuropixels, which feature high-density silicon arrays, have enabled scientists to collect electrophysiological data of this nature from a variety of animals. These include fish, reptiles, rodents and primates, as well as humans.
Neuropixels, which come in several versions, record electrical activity from hundreds to thousands of neurons simultaneously. Neurons are nerve cells that receive, process and transmit information.
While the data collected has led to insights on the neural basis of perception and decision-making, those probes cannot sample fine-scale brain structures. They also are limited in resolving (separately distinguishing) the electrical fields around individual brain cells.
To elicit VEPs, the eyelid corresponding to the stimulated retina was retracted temporarily while periodic 50 ms flashes were generated at 1 Hz from an array of white light-emitting diodes (LEDs). Neural response waveforms were temporally aligned to the stimulus onset. VEPs were calculated as the time-aligned averaged signals over 150 trials.
Electrical stimulation at the cortical surface was applied at one of the 200 µm electrodes, controlled by the Intan Technologies RHS controller and RHX software. Charge-balanced, biphasic, cathodic-first, 200 µs pulses of 100 µA peak current were delivered at 0.25 Hz. The evoked potentials were recorded over a series of trials. During analysis, for each trial and electrode, the Hjorth ‘activity’ of each trial was computed as the variance of the signal from 200 ms to 2,000 ms post-stimulation, and the average activity was taken over 40 trials.
A 1,024-channel array was placed over the sensorimotor cortex on each hemisphere following carefully sized bilateral craniectomies. Two Intan 1,024-channel RHD controllers were used to record from both arrays simultaneously.
Past neuroscience studies have consistently showed the profound effects of early life experiences on the brain’s wiring, particularly on the formation of the junctions that enable communication between neurons (i.e., synapses). The influence of early life experiences was found to be particularly pronounced during so-called sensitive periods (SPs), windows of time during which the brain’s plasticity (i.e., its ability to form or reorganize neural connections) is heightened.
Experimental evidence suggests that these periods of heightened brain plasticity are regulated by specialized neurons that release the inhibitory neurotransmitter GABA (gamma-aminobutyric acid). So-called parvalbumin-positive (PV+) interneurons have been found to play a central role in the unfolding of SPs, as their gradual enclosure into protective structures was linked to the conclusion of these periods.
Researchers at University of Milan and University of Helsinki recently carried out a study exploring the effects of early exposure to the widely prescribed antidepressant fluoxetine (FLX) on the regulation of SPs in rats. Their findings, published in Molecular Psychiatry, suggest that exposure to fluoxetine during gestation, pregnancy or breastfeeding could influence the brain development and behavior of rat pups later in life.
Bioengineers at the University of California San Diego have developed a powerful new technology that can map the entire network of RNA-protein interactions inside human cells—an achievement that could offer new strategies for treating diseases ranging from cancer to Alzheimer’s.
RNA-protein interactions regulate many essential processes in cells, from turning genes on and off to responding to stress. But until now, scientists could only capture small subsets of these interactions, leaving much of the cellular “conversation” hidden.
“This technology is like a wiring map of the cell’s conversations,” said Sheng Zhong, professor in the Shu Chien-Gene Lay Department of Bioengineering at the UC San Diego Jacobs School of Engineering, who led the study published in Nature Biotechnology.