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Transforming the understanding
and treatment of mental illnesses.

Heather Cameron

Heather Cameron, Ph.D.

Research Topics

The granule cells of the hippocampus are one of the only neuronal populations in the brain that continue to be generated throughout life. The goal of our research is to understand how and why these new neurons alter hippocampal structure, network activity, and behavior.

Much of our current work is aimed at identifying situations and tasks in which behavior is most strongly affected by adult-born neurons and teasing apart the specific cognitive processes underlying behavioral changes. Suppressing adult neurogenesis in mice and rats alters physiological and behavioral responses to psychosocial stress and alters motivation, strategy testing, and shifting of attention. We are particularly interested in the role of the new neurons in motivational conflict situations, when animals are forced to choose between multiple goals, and in driving investigation under conditions of uncertainty. By biasing behavior during motivational conflicts, ongoing neurogenesis may help optimize behavior in novel or unpredictable situations according to levels of threat in the environment.

We are also working to understand how adult neurogenesis alters network activity within the hippocampus and in downstream areas such as the prefrontal cortex. Inhibiting adult neurogenesis decreases activation across the hippocampal network when animals are faced with an unpredictable threat. We are interested in identifying the features of the new neurons that interact with particular features of the environment to drive adaptive changes in behavior. 

Biography

Dr. Cameron received her B.S. from Yale University and her Ph.D. from the Rockefeller University, where she worked with Bruce McEwen and Elizabeth Gould investigating adult neurogenesis in the adult rat dentate gyrus. During a postdoctoral fellowship with Ron McKay at NINDS, she determined the magnitude of adult neurogenesis in the dentate gyrus and investigated the effects of stress hormones on neurogenesis in the aging rat hippocampus. Dr. Cameron joined the Mood and Anxiety Disorders Program at NIMH as an Investigator in 2001 and is currently a Senior Investigator in the NIMH Intramural Research Program and Co-Director of the Brown-NIH Graduate Partnership Program.

Selected Publications

Swiercz AP, Tsuda MC, Cameron HA (2025). The curious interpretation of novel object recognition tests. Trends Neurosci 48, 250-256. https://doi.org/10.1016/j.tins.2025.02.003. [Pubmed Link ]

Tsuda MC, Akoh-Arrey T, Mercurio JC, Rucker A, Airey ML, Jacobs H, Lukasz D, Wang L, Cameron HA (2024). Adult Neurogenesis and the Initiation of Social Aggression in Male Mice. Hippocampus 34, 711-728. https://doi.org/10.1002/hipo.23643. [Pubmed Link ]

Schoenfeld TJ, Rhee D, Smith JA, Padmanaban V, Brockett AT, Jacobs HN, Cameron HA (2023). Rewarded Maze Training Increases Approach Behavior in Rats Through Neurogenesis-Dependent Growth of Ventral Hippocampus-Prelimbic Circuits. Biol Psychiatry Glob Open Sci 3, 725-733. https://doi.org/10.1016/j.bpsgos.2023.04.003. [Pubmed Link ]

Schoenfeld TJ, Smith JA, Sonti AN, Cameron HA (2020). Adult neurogenesis alters response to an aversive distractor in a labyrinth maze without affecting spatial learning or memory. Hippocampus 31, 102-114. https://doi.org/10.1002/hipo.23267. [Pubmed Link ]

Schoenfeld TJ, Rhee D, Martin L, Smith JA, Sonti AN, Padmanaban V, Cameron HA (2019). New neurons restore structural and behavioral abnormalities in a rat model of PTSD. Hippocampus 29, 848-861. https://doi.org/10.1002/hipo.23087. [Pubmed Link ]

Porter Bldg, Room 3C-915, MSC 3718
BETHESDA, MD 20814

Phone: +1 301 496 3814

Fax: +1 301 480 4564

heathercameron@mail.nih.gov