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Rosalind Franklin University Researcher Awarded $2 Million From NIH to Study Role Of Hormone Oxytocin In Stress, Fear and Anxiety

Project may help identify new drug therapies for PTSD, OCD, and other anxiety-driven mental illnesses


News provided by

Rosalind Franklin University of Medicine and Science

Aug 18, 2017, 09:47 ET

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NORTH CHICAGO, Ill., Aug. 18, 2017 /PRNewswire-USNewswire/ -- Rosalind Franklin University of Medicine and Science researcher Joanna Dabrowska has been awarded a five-year, $2 million grant from the National Institute of Mental Health (NIMH) to investigate the role of the hormone oxytocin in stress-induced psychiatric disorders. Her findings could lead to urgently needed new drug therapies for generalized anxiety and post-traumatic stress disorders.

The bed nucleus of the stria terminalis (BNST) plays an important role in the regulation of defensive behaviors like fear and anxiety. The image, taken from a female rat brain, reveals a variety of neuronal populations intermingling in the oval nucleus of the of the BNST, including neurons expressing tyrosine phosphatase STEP (blue) and protein kinase C delta (pink). These neurons also express oxytocin receptors, but their function is not well understood. Credit: RFU/Rachyl Shanker
The bed nucleus of the stria terminalis (BNST) plays an important role in the regulation of defensive behaviors like fear and anxiety. The image, taken from a female rat brain, reveals a variety of neuronal populations intermingling in the oval nucleus of the of the BNST, including neurons expressing tyrosine phosphatase STEP (blue) and protein kinase C delta (pink). These neurons also express oxytocin receptors, but their function is not well understood. Credit: RFU/Rachyl Shanker

Dabrowska, principal investigator for the study, and co-investigator Jeremy Amiel Rosenkranz, both faculty in the Department of Cellular and Molecular Pharmacology, will study "Modulation of the BNST activity by oxytocin — role in stress, fear and anxiety." Because BNST, the bed nucleus of the stria terminalis, a limbic structure in the forebrain, is key to the translation of stress into sustained anxiety, factors that regulate its activity have untapped potential as novel therapeutic targets.

Oxytocin, which regulates a variety of social behaviors including maternal-infant and pair bonding, has garnered substantial interest as a potential pharmacotherapeutic agent for stress-induced mental disorders in humans, because it has repeatedly shown promising anti-anxiety effects observed in animal models. But despite its unique potential, the central sites and mechanisms of important oxytocin actions are poorly understood.

"Uncovering the role of oxytocin in the BNST will be a key to understanding the mechanisms underlying the neurobiology of stress-induced psychiatric disorders," Dr. Dabrowska said. "As women are more likely to develop stress-induced psychiatric disorders than men, we will explore the role of oxytocin in both male and female brains. This will shed light on commonalities and differences in fear and anxiety circuitry between males and females."

By refining cellular targets of oxytocin effects in the BNST, the study will reveal new downstream substrates of oxytocin and can contribute to the identification of potential new targets for pharmacotherapy of stress-induced mental disorders.

Impact of stress on health
Chronic stress and the anxiety it produces can precipitate the onset of psychiatric disorders, including PTSD and phobias, and it also increases the risk of numerous other health problems, including diabetes, coronary vascular disease and autoimmune disorders. Current pharmacotherapies for anxiety have limited efficacy.

Stress-induced abnormalities in neuronal activity can cause permanent changes in brain function that in addition to anxiety, can lead to depression, obesity and sleep and memory problems. Targeting the mechanisms underlying the effects of stress in sensitive brain regions could provide new insight for treatment.

Anxiety-related disorders often go untreated
According to the NIH, 18 percent of the population struggles with anxiety disorders and nearly 23 percent of these cases are classified as "severe." Women are 60 percent more likely than men to experience anxiety over their lifetime. Approximately 37 percent of those with the disorder are receiving treatment. Anxiety is a normal reaction to stress and can actually be beneficial in some situations. For some people, however, anxiety can become excessive and negatively affect their day-to-day living.

PTSD, obsessive-compulsive disorder (OCD), and specific phobias are among many medically recognized anxiety disorders that collectively are the most common mental illnesses affecting people in the U.S. PTSD can develop after exposure to trauma or the threat of trauma, including violence, combat or natural disasters. People with PTSD have persistent frightening thoughts and memories of their ordeal, may experience sleep problems, feel detached or numb, or be easily startled. The NIH estimates that 4 percent of the U.S. adult population suffers from PTSD; about 50 percent are receiving treatment.

"Rosalind Franklin University is committed to understanding the science behind psychiatric disorders, which pose such a heavy burden on our society," said Ronald Kaplan, the university's executive vice president for research. "Approaching stress and anxiety at a molecular and pharmacological level offers great hope for a healthier future."

About Rosalind Franklin University of Medicine and Science
Formed in 1912 as the Chicago Hospital-College of Medicine, Rosalind Franklin University of Medicine and Science is a national leader in interprofessional medical and healthcare education and biomedical research. RFU includes the Chicago Medical School, School of Graduate and Postdoctoral Studies, College of Health Professions, Dr. William M. Scholl College of Podiatric Medicine and College of Pharmacy. More than 18,000 RFU degreed alumni are active throughout the United States and around the world. Learn more at rosalindfranklin.edu.         

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SOURCE Rosalind Franklin University of Medicine and Science

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