My primary research interest focuses on the central nervous system regulation of visceral pain with a strategic objective of using preclinical rodent models and multiple state-of-the-art techniques, from molecular and cellular to behavioral, pharmacological and electrophysiological methods to advance basic scientific knowledge that has direct relevance to the diagnosis and treatment of veterans with visceral pain. Below I have summarized the main research projects in my laboratory. 1. Central Neural Circuitry Underlying Anxiety and Visceral pain: Mechanisms of Resilience and Novel Treatments: In one aspect of my research we are studying the neuroanatomical and neuropharmacological substrates involved in the interaction between visceral pain and anxiety. My research focuses on the role of amygdala-mediated mechanisms in the control of visceral and somatic pain and the mechanisms connecting anxiety and visceral (colonic) hypersensitivity. We are attempting to identify at least one potential neural substrate that might be involved in the central processing of visceral pain. From there we hope to identify a receptor mechanism within the neural substrate that mediates central processing of visceral pain. A long-term goal is to investigate how the neural substrate modulates visceral pain sensitivity within the larger neural pathway controlling anxiety, and use this knowledge to identify potential pharmacotherapeutic targets in the central processing pathway that mediates visceral pain. We have demonstrated long lasting increases in anxiety-like behavior and viscerosomatic sensitivity in response to the local exposure of the amygdala to corticosterone (CORT). We found persistent down-regulation of GR expression and increases in the expression of CRF and HCN1 channels leading to hyper-excitability of the CeA neurons. These changes in gene expression represent a potential mechanism leading to chronic anxiety and pain, via facilitation of the HPA axis. The objective of latest experiments has been to use gene knockdown to directly manipulate CRF and GR expression in the central amygdala. We found that knockdown of CRF within the amygdala inhibits stress-induced chronic visceral and somatic pain, and that loss of GR within the amygdala is key to triggering visceral and somatic pain. Such findings are relevant for the future development of gene targeted therapeutics to treat stress-induced visceral and somatic pain (Funded by the Department of Veteran's Affairs Merit Award: 2013-2017). 2. Early life stress on visceral and somatic pain in adulthood: Sex differences. In women, IBS is the most prevalent GI disorders. Emotional stressors, increased anxiety or uni- and bipolar associative disorders often exacerbate symptoms. Despite this knowledge and evidence that females embody strong connections to life stressors, physical/sexual abuse and an emotionally reactive disposition related to the outbreak of symptomatology, there has been very little progress made to enhance our understanding of the descending connections between the brain and the GI tract in female Veterans. Our latest project was designed to investigate the mechanisms by which the context of the early life stress (ELS) can affect nociception in adulthood. We are also exploring evidence for a two hit hypothesis underlying the vulnerability to visceral pain in females. Specifically, we will investigate the mechanisms by which an unpredictable stress in early life leads to chronic abdominal pain in adulthood. Additionally we will assess the impact of ELS on the amygdala response to an adult stressor (Funded by the Department of Veteran's Affairs Merit Award: 2010-2014; 2015- 2019).
Many Veterans report that life stressors worsen or even initiate gastrointestinal symptomatology, including abdominal pain and abnormal bowel habits resembling those seen in patients with irritable bowel syndrome (IBS). My research is highly relevant to the patient-care mission of the VA, since the VA cares for a Veteran population that has been exposed to severe stress during deployment. When combined with a history of early life stress, deployment stress may lead to the development of chronic abdominal pain and may increase the susceptibility of a soldier, especially a female soldier, to the adverse effects of combat-related stress. Successful completion of the research within my laboratory will offer new insights into the mechanisms of brain-gut dysfunction that likely lead to chronic abdominal pain. Importantly our findings may identify novel targets for new therapies directed at the brain to improve the treatment or even reduce the risk for visceral pain in veterans.
|Greenwood-Van Meerveld, Beverley; Mohammadi, Ehsan; Latorre, Rocco et al. (2018) Preclinical Animal Studies of Intravesical Recombinant Human Proteoglycan 4 as a Novel Potential Therapy for Diseases Resulting From Increased Bladder Permeability. Urology 116:230.e1-230.e7|
|Johnson, Anthony C; Latorre, Rocco; Ligon, Casey O et al. (2018) Visceral hypersensitivity induced by optogenetic activation of the amygdala in conscious rats. Am J Physiol Gastrointest Liver Physiol 314:G448-G457|
|Yang, Qing; Xia, Ding; Towner, Rheal A et al. (2018) Reduced urothelial regeneration in rat bladders augmented with permeable porcine small intestinal submucosa assessed by magnetic resonance imaging. J Biomed Mater Res B Appl Biomater 106:1778-1787|
|Ligon, C; Mohammadi, E; Ge, P et al. (2018) Linaclotide inhibits colonic and urinary bladder hypersensitivity in adult female rats following unpredictable neonatal stress. Neurogastroenterol Motil 30:e13375|
|Hattay, Priya; Prusator, Dawn K; Johnson, Anthony C et al. (2018) Stereotaxic Exposure of the Central Nucleus of the Amygdala to Corticosterone Increases Colonic Permeability and Reduces Nerve-Mediated Active Ion Transport in Rats. Front Neurosci 12:543|
|Meerveld, Beverley Greenwood-Van; Johnson, Anthony C (2018) Mechanisms of Stress-induced Visceral Pain. J Neurogastroenterol Motil 24:7-18|
|Louwies, Tijs; Ligon, Casey O; Johnson, Anthony C et al. (2018) Targeting epigenetic mechanisms for chronic visceral pain: A valid approach for the development of novel therapeutics. Neurogastroenterol Motil :e13500|
|Mohammadi, Ehsan N; Ligon, Casey O; Silos-Santiago, Ada et al. (2018) Linaclotide Attenuates Visceral Organ Crosstalk: Role of Guanylate Cyclase-C Activation in Reversing Bladder-Colon Cross-Sensitization. J Pharmacol Exp Ther 366:274-281|
|Hattay, P; Prusator, D K; Tran, L et al. (2017) Psychological stress-induced colonic barrier dysfunction: Role of immune-mediated mechanisms. Neurogastroenterol Motil 29:|
|Johnson, Anthony C; Greenwood-Van Meerveld, Beverley (2017) Critical Evaluation of Animal Models of Gastrointestinal Disorders. Handb Exp Pharmacol 239:289-317|
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