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John H. Winston, Ph.D.
Associate Professor, Division of Gastroenterology and Hepatology



John H. Winston, Ph.D.

John H. Winston, Ph.D.
Associate Professor
Department of Internal Medicine

University of Texas Medical Branch
301 University Blvd.
Galveston, TX 77555-0764
Phone: 409.772.1501
Fax: 409.772.5841
jhwinsto@utmb.edu

Biosketch

Dr. Winston received a B.S. from Louisiana State University in 1983 and a Ph.D. from UT Southwestern Medical School in Dallas in 1990. He completed a two year Molecular Genetics fellowship at Baylor College of Medicine and then worked as a Research Associate at Baylor College of Medicine for four years in the laboratory of Rodney Kellums. Here, Dr. Winston identified genetic regulatory elements directing expression of the murine Adenosine Deaminase gene to the fetal placenta and to the forestomach using transgenic mice as an assay system. Dr. Winston was promoted to Instructor in the GI division, Department of Pediatrics, Baylor College of Medicine. He joined the Division of Gastroenterology and Hepatology, Department of Internal Medicine at UTMB in June 1997 as an Instructor and was promoted to Assistant Professor after three years. Dr. WinstonÂ's principle function was to establish a lab capable of studying molecular mechanisms of pain in inflammatory and functional G-I disorders using rodent models.

Research Interests

Although pain is a cardinal feature of pancreatitis, the underlying biological mechanisms are poorly understood. The vanilloid receptor (TRPV1) is an ion channel that is activated by heat and by various inflammatory mediators and functions as a molecular transducer of noxious stimuli into nerve impulses in primary sensory afferent neurons. This channel is expressed on 80% of pancreatic afferent neurons. Capsaicin activated current is increased 2 to 4 fold in rats with acute necrotizing pancreatitis, but there is no increase in TRPV1 expression. Recent findings indicate that increased production of nerve growth factor in pancreatitis may be linked to increased TRPV1 activity. Further experiments are in progress to define the molecular mechanisms responsible for this increase in TRPV1 function in pancreatitis. Additional studies address the efficacy of various TRPV1 antagonists in the treatment of pain and inflammation in pancreatitis.

Irritable Bowel Syndrome (IBS) is a functional bowel disorder of unknown etiology defined by symptoms including abdominal pain and alterations in bowel habits that occur in the absence of detectable ongoing organic disease. Human studies demonstrate that IBS is associated with a state of chronic visceral hypersensitivity suggesting that processing of visceral sensory information is altered. However, little is known about changes in the processing of visceral information occur. Our long-term objective is to identify key molecular events responsible for the perpetuation of the sensitized state and provide targets for new pharmacological approaches to the treatment of this syndrome. To attain this goal, we have developed a rat model of chronic visceral hyperalgesia produced by irritation of the colon of neonatal rats. We have identified gene expression profiles in the colon, sensory neurons and spinal chord associated with chronic visceral hyperalgesia. There are an ongoing collaborative studies with clinicians to determine whether any of the genes identified in the colon can serve as biological marker (s) of post-infectious IBS. Gene expression profiles in colon show alterations in genes that regulate smooth muscle contractility; studies are in progress to determine whether there is an increase in smooth muscle contractility in this model.

Selected Publications

Winston JH, Xu GY, Sarna SK. Adrenergic Stimulation Mediates Visceral Hypersensitivity to Colorectal Distension following Heterotypic Chronic Stress. Gastroenterology. 2010 Jan;138(1):294-304.e3.

Xu GY, Winston JH, Shenoy M, Zhou S, Chen JD, Pasricha PJ.The endogenous hydrogen sulfide producing enzyme cystathionine-beta synthase contributes to visceral hypersensitivity in a rat model of irritable bowel syndrome. Mol Pain. 2009 Aug 6;5:44.

Xu GY, Winston JH, Chen JD. Electroacupuncture attenuates visceral hyperalgesia and inhibits the enhanced excitability of colon specific sensory neurons in a rat model of irritable bowel syndrome. Neurogastroenterol Motil. 2009 Dec;21(12):1302-e125.

Liu LS, Winston JH, Shenoy MM, Song GQ, Chen JD, Pasricha PJ. Rat Model of Chronic Gastric Sensorimotor Dysfunction Resulting From Transient Neonatal Gastric Irritation. Gastroenterology. 2008 Jun;134(7):2070-9. PMID: 18448102

Xu GY, Winston JH, Shenoy M, Yin H, Pendyala S, Pasricha PJ. Transient receptor potential vanilloid 1 mediates hyperalgesia and is up-regulated in rats with chronic pancreatitis. Gastroenterology. 2007;133(4):1282-92. PMID: 17698068

Winston JH, Shenoy M, Medley M, Naniwadekar A, Pasricha PJ. The vanilloid receptor initiates and maintains colonic hypersensitivity induced by neonatal colon irritation in rats. Gastroenterology. 2007;132(2):615-27. PMID 17258176

Xu GY, Winston JH, Shenoy MM, Yin H, Pasricha PJ. Enhanced excitability and suppression of A-type potassium current of pancreas specific afferent neurons in a rat model of chronic pancreatitis. Am J Physiol Gastrointest Liver Physiol. 2006; 291:424-431.PMID 16645160

Winston JH, He ZJ, Shenoy M, Xiao SY, Pasricha PJ. Molecular and behavioral changes in nociception in a novel rat model of chronic pancreatitis for the study of pain. Pain 2005; 117(1-2):214-22. PMID: 16098667

John H. Winston, Hiroki Toma, Mohan Shenoy, Zhi-Jun He, Lei Zou, Shu-Yuan Xiao, Maria-Adelaide Micci, Pankaj J. Pasricha (2003) Acute pancreatitis results in referred mechanical hypersensitivity and neuropeptide up-regulation that can be suppressed by the protein kinase inhibitor k252a. Journal of Pain 4:329-337.

Winston, J., Toma, H., Shenoy, M.,. And Pasricha, P.J. (2001) Nerve Growth Factor regulates VR-1 nRNA levels in cultures of adult dorsal root ganglion neurons. Pain 89:181-186.

»Pub Med Search

The department of internal medicine is developing evidence based clinical protocols which will be available in EPIC (as order sets) for use when admitting patients with these diagnoses. Their AIM is to standardize care and decrease length of stay and readmission rates.

Currently available protocols are:
  • CAP - Community Acquired Pneumonia Orderset
  • Congestive Heart Failure (CHF)
  • Chronic Obstructive Pulmonary Disease (COPD)
  • Diabetic Ketoacidosis Adult, ICU
  • General Medicine Admission
  • Immunodeficiency Flow Panel
  • MICU/CCU Admission Order Set
  • Oral Analgesic Medicaitons
  • Parenteral Opioids
  • Sepsis, Adult ICU

All protocols can be found in the EPIC order set section.

» For more information

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