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M.D. (1975)
Tufts University School of Medicine

David A. Bushinsky
  Professor of Medicine, Nephrology Unit and of Pharmacology and Physiology, Associate Chair of Medicine

Primary Appointment:
  Medicine

GEBS Cluster Affiliations:
  CRMP- Cell Regulation and Molecular Pharmacology
  IBS - Integrative Biomedical Science
 


Research:
  Effects of Hydrogen Ions on Bone Calcium Homeostasis

Contact Information:
  E-Mail: David_Bushinsky@urmc.rochester.edu
University of Rochester
School of Medicine and Dentistry
601 Elmwood Ave, Box 675
Rochester, New York 14642
Medical Center [room]
Phone: (716) [tele]
Fax: (716) [number]
Research Overview
Our laboratory has two main areas of interest: the mechanisms by which hydrogen ions affect bone and the mechanism of hypercalciuria in our inbred strain of genetic hypercalciuric stone forming rats. We have found that acid induces calcium efflux from bone through both physicochemical and cell-mediated mechanisms, the latter involving suppression of immediate early response genes and genes controlling bone matrix formation. The hypercalciuria is due to a systemic disorder of calcium transport, thought to be secondary to an increase in vitamin D receptor number.
Recent Publications

Frick, K. K., L. Jiang and D. A. Bushinsky. Acute metabolic acidosis inhibits the induction of osteoblastic egr-1 and type 1 collagen. Am. J. Physiol. 272 (Cell Physiol. 41): C1450-C1456, 1997.

Yao, J., P. Kathpalia, D. A. Bushinsky and M. J. Favus. Hyperresponsiveness of vitamin D receptor gene expression to 1,25-dihydroxyvitamin D3: A new characteristic of genetic hypercalciuric stone-forming rats. J. Clin. Invest.: 101:2223-2232, 1998.

Frick, K and D. A. Bushinsky. Chronic metabolic acidosis reversibly inhibits extracellular matrix gene expression in mouse osteoblasts. Am. J. Physiol. (Renal Physiol. in press, 1998.



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GEBS Clusters:
CRMP

IBS