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How Fear and the 'Love Hormone' Connect: Mouse Brain Cells Found by Japanese Scientists

Взаємозв'язок між страхом і гормоном любові: дослідження японських вчених виявили нові клітини мозку мишей. Photo: НВ — Техно

When Bonding Chemistry Meets Fear

Oxytocin, often called the 'love hormone' for its role in social bonding, also shapes how the brain responds to danger. Japanese researchers have identified a cluster of oxytocin-sensitive neurons in the paraventricular thalamus (PVT) of mice. These cells appear to influence both social interest and the ability to stop being afraid once a threat is gone. The experiments used genetically modified male mice and focused specifically on neurons carrying oxytocin receptors.

Suppressing those neurons reduced the animals' interest in unfamiliar mice. This change could not be explained by reduced mobility or increased anxiety. In a fear-conditioning test, the mice learned to link a specific place with a mild electric shock. Blocking the neurons did not prevent them from remembering the original threat, but when they were later placed back in the same area without any shock, mice with suppressed neurons continued to freeze in fear. Brief activation of the neurons during the early phase lowered the freezing response, but the effect disappeared by the next day and was absent after a week.

Social Behavior and Brain Imaging

The researchers also examined data from 30 Japanese adolescents: 19 had autism spectrum disorder and 11 did not. The team compared oxytocin levels in saliva, MRI scans of the thalamus, and behavioral indicators. The sample was small, however, and oxytocin measured in saliva does not necessarily reflect oxytocin activity in the brain. The study also has limitations because it relied mainly on male mice, and artificially activating neurons is not the same as natural oxytocin release. So these findings do not demonstrate that natural oxytocin directly controls social behavior or fear extinction in humans.

The authors suggest that further research into this mechanism could improve understanding of disrupted social behavior and fear regulation, particularly in autism and anxiety disorders.

These results could eventually contribute to treatment strategies for social difficulties such as autism or anxiety disorders. A clearer picture of how oxytocin regulates social behavior and fear might lead to new approaches that modify specific neural pathways. Since this work was conducted in animals, future studies in humans will be needed to confirm or challenge the conclusions and expand our knowledge of the neural basis of social behavior.

Understanding the complex interactions between hormones and brain functions can shed light on various behavioral responses. For instance, a recent study explored how specific brain signals influence physical reactions, such as why surprised eyes widen. This research adds another layer to our comprehension of the intricate relationship between emotions and biological processes.