Department of Surgery »  Faculty »  General Surgery »  Aditi Bhargava, Ph.D.
 
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Department of Surgery »  Faculty »  General Surgery »  Aditi Bhargava, Ph.D.

Aditi Bhargava, Ph.D.

Associate Professor
Division of General Surgery

Contact Information

UCSF Center for the Neurobiology of Digestive Diseases
Department of Surgery
513 Parnassus Avenue, Room S-1268
Campus Box 0660
San Francisco, CA 94143-0660

415-502-8453
415-476-6978 (Alternate)
415-476-3336 Lab
415-476-0936 Fax
aditi.bhargava@ucsfmedctr.org

Education

  • 1984-86, University of Rajasthan, B.S., Zoology (Honors)
  • 1986-88, University of Poona, M.S., Molecular Biology
  • 1990-1995, University of Poona, Ph.D., Molecular Biology

Residencies

Fellowships

Postdoctoral Training

  • 1995-96, New York Medical Col., Postdoctoral Fellow, Medicine
  • 1996-00, University of California, San Francisco School of Medicine, Postdoctoral Fellow, Medicine/Physiology
  • 2000-03, University of California, San Francisco School of Medicine, Postdoctoral Fellow, Medicine/Physiology (laboratories of Drs. Mary F. Dallman and David Pearce)

Board Certification

Program Affiliations

Clinical Expertise

Research Interests

  • Exploring and elucidating the molecular mechanisms by which components of the corticotropin releasing factor (CRF) system mediate the effect of stress on cellular function.

Biography

Aditi Bhargava, Ph.D. is an Associate Professor in the Department of Surgery at UCSF. Her research laboratory is in the UCSF Center for the Neurobiology of Digestive Diseases.

Dr. Bhargava is a recipient of the several awards including: Certificate of Merit (1986); Graduate Research Fellowship (1988-1993), CSIR, India; UNESCO/TWAS Human Genome Fellowship (1992); Senior Research Fellowship, Department of Biotechnology, India (1994-1995); Quest Diagnostic Young Investigator Award, Endocrine Society (2003); Young Investigator Travel Award, GIRI Conference, Canada (2004); New Investigator Award from the American Physiological Society (2010); and FASEB MARC Mentor Travel Award (2010). Dr. Bhargava is also a fellow of the American Gastroenterological Association (AGAF).


Research Summary

My work has far-reaching implications for many diseases in which components of the CRF system are being clinically tested. An estimated 57 million people in the US alone suffer from stress-related disorders. Stress is a major contributor towards development of Type 2 diabetes; 26 million Americans over the age of 18 are Type 2 diabetics, and an additional 79 million are thought to be pre-diabetic. Twice as many women as men suffer from stress-related disorders, including anxiety, depression, and inflammatory as well as functional bowel disease. Despite the preponderance of stress-related diseases in females, use of female animal subjects is perpetually lacking and knowledge of the sex-specific molecular pathogenesis in disease responses remain vastly understudied. Furthermore, as the dynamic relationship between stress and inflammation has become evident, CRF receptor antagonists and related molecular targets have been intensely studied and tried as promising therapeutic targets for these pathophysiologic mechanisms. Clinical trials have attempted to treat major depression, PTSD, cardiac injury, congestive heart failure and IBS using CRF-related therapeutics. Most of the therapeutics, while extremely promising in animal models, were are ineffective in clinical trials. Thus, given the myriad diseases and disorders that stress are exacerbatesd by stress, my work seeks to understand both the mechanisms that initiate a stress response and result in stress-coping action in experimental models that include both male and female subjects.

Selected Publications

  1. Hasdemir B, Mahajan S, Bunnett NW, Liao M, Bhargava A. 2012. Endothelin-Converting Enzyme-1 Actions Determine Differential Trafficking and Signaling of Corticotropin-Releasing Factor Receptor 1 at High Agonist Concentrations. Mol Endocrinol. 26(4):681-95. .
  2. Chang J, Adams MR, Clifton MS, Liao M, Brooks JH, Hasdemir B, and Bhargava A. Urocortin 1 Modulates Immunosignaling in a Rat Model of Colitis via Corticotropin-Releasing Factor Receptor 2. Am J Physiol Gastrointest Liver Physiol. 2011 Feb 17; 300:G884-G894. .
  3. Cureton EL, Ereso AQ, Victorino G, Poole PD, Liao M, Currian B, Harken AH and Bhargava A. Local Secretion of Urocortin 1 Promotes Microvascular Permeability During Lipopolysaccharide-induced Inflammation (2009). Endocrinology. 150(12):5428-37.
  4. la Fleur SF, Wick EC, Idumalla PS, Grady EF and Bhargava A. (2005). Role of peripheral corticotropin-releasing factor and urocortin II in intestinal inflammation and motility in terminal ileum. Proc Natl Acad Sci. 102 (21): 7647-7652.
  5. Bhargava A†, Chen S-Y†, Mastroberardino L, Meijer OC, Wang J, Buse P, Firestone G, Verrey, F, and Pearce D. (1999) Epithelial sodium channel regulated by aldosterone-induced protein sgk. Proc. Natl. Acad. Sci., 96: 2514-2519. (†: equal contribution by two authors).

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