Brain

Advances in the field of schizophrenia research: New genetic factors identified

Cocaine addiction linked to voluntary drug use and cellular memory, UCSF study shows

Rats that voluntarily use cocaine show a persistent cellular memory in the brain's reward center even after several months of abstinence from the drug, while their involuntary counterparts had no such memory, according to a new study by researchers at the University of California, San Francisco.

UCLA imaging study suggests Alzheimer's drug may help mild memory loss

Alzheimer's disease is the end result of gradual, progressive brain aging. Positron emission technology (PET) scans of patients' brains typically reveal a decreased rate of metabolism, a hallmark of the disorder.

Belief in God, parenthood prompt gay partners to make commitment

Which gay and lesbian couples are more likely to legalize their relationship and hold a commitment ceremony? Those with children and strong religious beliefs, says a new University of Illinois study.

Large study uncovers surprisingly diverse genome alterations that contribute to schizophrenia

A multinational group of investigators has discovered that people suffering from schizophrenia are far more likely to carry rare chromosomal structural changes of all types, particularly those that have the potential to alter gene function. In addition, the study uncovered two new specific genomic areas that, when altered, significantly increase the risk of developing the disease. The report from the International Schizophrenia Consortium, the largest and most complete such study to date, is being published online today by the journal Nature.

Brain plays key role in appetite by regulating free radicals

Researchers at Yale School of Medicine have found the brain's appetite center uses fat for fuel by involving oxygen free radicals—molecules associated with aging and neurodegeneration. The findings, reported in the journal Nature, suggest that antioxidants could play a role in weight control.

The study's lead authors were Sabrina Diano and Tamas Horvath, who are an associate professor and professor, respectively, in the Departments of Obstetrics, Gynecology & Reproductive Sciences and Neurobiology. Horvath is also chair of the Section of Comparative Medicine.

Beating the baby blues: A mouse model for postpartum depression

A new study provides critical insight into the disabling depression experienced by many women during early motherhood. The research, published by Cell Press in the July 31 issue of the journal Neuron, reveals new details about the pathogenesis of postpartum depression and provides a mouse model that may lead to development of new treatments for mood disorders associated with pregnancy.

Brain's reaction to self-administered cocaine differs

New research has uncovered a fundamental cellular mechanism that may drive pathological drug-seeking behavior. The study, published by Cell Press in the July 31 issue of the journal Neuron, examines the brain's reward circuitry and details strikingly distinct influences of self-administered cocaine compared to natural rewards or passive cocaine injection.

Mechanism for postpartum depression found in mice

Researchers have pinpointed a mechanism in the brains of mice that could explain why some human mothers become depressed following childbirth. The discovery could lead to improved treatment for postpartum depression. Supported in part by the National Institute of Mental Health, of the National Institutes of Health, the study used genetically engineered mice lacking a protein critical for adapting to the sex hormone fluctuations of pregnancy and the postpartum period.

Traumatic response to bad memories can be minimized

Irvine, Calif. — UC Irvine researchers have identified the brain mechanism that switches off traumatic feelings associated with bad memories, a finding that could lead to the development of drugs to treat panic disorders.

Scientists from UCI and the University of Muenster in Germany found that a small brain protein called neuropeptide S is involved in erasing traumatic responses to adverse memories by working on a tiny group of neurons inside the amygdala where those memories are stored.