SAYAMWONG (JOM) HAMMACK
Associate Professor, Biobehavioral Psychology
My research interests involve understanding the neurobiological mechanisms of stress, emotion and resilience. I use a variety of techniques to investigate these mechanisms, which include assessing conditioned and unconditioned fear and anxiety, pharmacological manipulations, neuroanatomical techniques, molecular, and intracellular electrophysiological techniques. I am particularly interested in the involvement of serotonin and stress-related neuropeptides in mediating the behavioral consequences of exposure to stressful stimuli, as well as the neurochemical changes mediating stress-resilience (for example, why does exercise reduce anxiety and make you more resilient in the face of stressors). Specific questions include:
Project 1: How does serotonin modulate brain regions associated with anxiety-like behavior?
Substantial evidence suggests that the activation of serotonin systems alters anxiety-like behavior; however, the nature of the relationship between serotonin and anxiety is still unclear. For example, selective-serotonin reuptake inhibitors (SSRIs), which elevate levels of serotonin in the central nervous system, have well-known therapeutic anxiety-reducing effects when administered chronically. But the acute effects of these drugs often include increases in indices of anxiety. Several nuclei associated with the central extended amygdala, including the bed nucleus of the stria terminalis (BNST) and central nucleus of the amygdala (CeA) have been suggested to mediate fear/anxiety-like behavior. We are currently using behavioral, anatomical, and physiological techniques to determine how these brain regions respond to serotonin, in order to better understand the relationship between serotonin and anxiety. Specific questions include:
Project 2: How does voluntary exercise modulate brain regions associated with anxiety-like behavior
Exercise is therapeutic in the treatment of anxiety, and the effects of exercise may be mediated through changes in serotonin functioning. We are currently investigating whether the effects of exercise on anxiety are mediated by serotonin changes in the BNST. Metachlorophenylpiperazine (mCPP), which is an agonist at 5-HT2B and 5-HT2C receptors (with some affinity at 5-HT2A receptors), increases signs of anxiety in both humans and animals. The BNST has been implicated in mediating anxiety in a number of paradigms in rodents and primates. Therefore, the BNST might an important brain region mediating the effects of serotonergic modulation on anxiety. Single BNST neurons can respond to 5-HT with excitation and/or inhibition, and mCPP injected into the BNST is anxiogenic likely because this drug selectively activates the excitatory response on these neurons, which is mediated, in part, by the 5-HT2 family of receptors. Consistent with reports in humans, we have shown that voluntary exercise is anxiolytic in many anxiety models in animals. Importantly, voluntary exercise reduces the increases in anxiety observed after mCPP. These studies are being conducted in a collaborative effort with Professor Bill Falls and the Falls Laboratory in the Department of Psychology. Specific question include:
Funded by a grant from the National Institute of Mental Health
Project 3: How do pituitary adenylate cyclase-activitating polypeptides modulate anxiety-like behavior?
Although evidence suggests that chronic stress is important to the etiology of anxiety disorders, ,the mechanisms by which stress alters brain anxiety circuits are still unknown. Substantial evidence has implicated the BNST as a critical structural node mediating anxiety-like behavior in humans and animals. The BNST organizes central and peripheral stress responding to unpredictable and/or persistent threats, and sustained exposure to these stressful events has been argued to result in maladaptive BNST functioning that could underlie anxiety disorders. Consistent with this hypothesis, previous reports have shown that chronic stress-induced BNST neuroplasticity leads to enhanced excitability within BNST networks to produce heightened anxiety states. Pituitary adenylate cyclase activating polypeptides (PACAP) have acute neurotransmitter functions in neuronal excitability, long term neurotrophic properties in neuroplasticity, and appear to be key components in stress signaling. In collaboration with Professor Victor May in the Departiment of Anatomy and Neurobiology and Professor Bill Falls and the Falls Laboratory in the Department of Psychology, we are currently determiningthe role of BNST PACAP in mediating stress-induce anxiety-like behavior. Specific questions include:
Funded by a grant from UVM's Vice President for Research and Graduate Studies (Research Opportunities Grant Program)
Project 4: How does the extended amygdala process long- versus short-duration stressful or threatening stimuli?
Based on a number of studies, it seems clear that the BNST mediates fear- and anxiety-like behavior using some behavioral paradigms, whereas the central nucleus of the amygdala (CeA) mediates fear- and anxiety-like behavior in other paradigms. Based on these data, Michael Davis and colleagues have argued that the BNST mediates long-duration responses to diffuse, chronic, or unpredictable stimuli, whereas the CeA mediates short duration responses when the stimuli are predictable in nature. Based on this argument, this group has suggested that during exposure to a long-duration threat, axniety-like behavior might initially be mediated by the CeA, but as the duration increased, activity within the circuit would shift from the CeA to the BNST. Interestingly, Professor Mark Bouton and his group in the Department of Psychology recently showed that the BNST was necessary to observe changes in fear-like behavior when 10-minute predicted footshock, but not when a 1-minute tone predicted the shock, and this group has suggested that during the 10-minute tone, fear-like behavior is initially mediated by the BNST, but as the time of exposure to the 10-minute tone increases (towards the end of the 10 minute tone), activity switches from the BNST to the CeA. Hence, in collaboration with Professor Bouton’s group, we are currently investigating activation within the BNST and CeA following training with 1- and 10-minute tones.
Project 5: Is the response of neurons in the extended amygdala to serotonin altered during learned helplessness?
In a project funded by the National Alliance for Research on Schizophrenia and Depression (NARSAD), we are investigating the role of 5-HT7 receptors in the BNST in learned helplessness (LH), which is currently poorly understood. We are currently using behavioral, pharmacological and electrophysiological techniques to determine whether changes in BNST 5-HT7 receptors mediate the behavioral changes associated with LH. These studies could lead to a better understanding of the brain mechanisms underlying affective disorders as well as the design of more selective pharmacological treatments for these disorders.
Funded by NARSAD
Last modified April 23 2013 09:23 AM