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- 1*
- 1Department of Pharmacology, Indira Gandhi Medical College and.
- 2Research Institute, Kadhirkamam, Puducherry, India.
Published in Journal of Pharmacology and Pharmacotherapeutics
Correspondence: Sivagnanam G
Department of Pharmacology, Indira Gandhi Medical College and.
Email: drsivagnanam@gmail.com
Copyright: © 2012 The Author(s). This is an open access article.
Published: Jan 1, 2012
- DOI
- Not available yet
Abstract
Pendrin is expressed on the cells of distal convoluted tubule and the collecting duct. It is involved in Cl-/HCO3- exchange (mediates HCO3- secretion and Cl- absorption) and has been demonstrated to play an important role in compensatory salt absorption in response to thiazide and loop diuretics. It has been proposed that pharmacological inhibition of pendrin and thiazide- sensitive NaCl co-transporter can provide a novel and strong diuretic regimen in fluid overload conditions such as congestive heart failure, nephrotic syndrome, etc.
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