Accession Number : AD1048417


Title :   Cellular Energy Pathways as Novel Targets for the Therapy of Autosomal Dominant Polycystic Kidney Disease


Descriptive Note : Technical Report,01 Sep 2016,31 Aug 2017


Corporate Author : UNIVERSITY OF SOUTHERN CALIFORNIA LOS ANGELES LOS ANGELES


Personal Author(s) : Hallows,Kenneth R ; Caplan,Michael J


Full Text : https://apps.dtic.mil/dtic/tr/fulltext/u2/1048417.pdf


Report Date : 01 Sep 2017


Pagination or Media Count : 24


Abstract : Autosomal dominant polycystic kidney disease (ADPKD) is a common inherited disorder where patients, over the course of decades, develop large fluid filled cysts that damage the normal kidney tissue and can lead ultimately to kidney failure that necessitates transplantation or dialysis. There are currently no FDA-approved medications for this condition. Recent research reveals that the formation of cysts is due in part both to inappropriate cell growth, fluid secretion, and dysregulation of cellular energy metabolism. The enzyme AMPK regulates a number of cellular pathways, including these disease-causing features. Drugs that activate AMPK, therefore, may constitute an effective therapeutic option for slowing or preventing cyst growth in ADPKD. This research project is aimed at examining the potential of approved, widely used, inexpensive and low-toxicity drugs that can activate AMPK (metformin, simvastatin, and salicylates) and or promote oxidative metabolism (dichloroacetic acid) as potential therapies for the treatment of ADPKD. During this past research period, we measured and analyzed various metabolomic biomarkers in samples derived from cell lysates and urine and continued collecting cyst growth data in ADPKD in vitro cell culture models and urine specimens derived from a broad cross-section of patients with ADPKD. We also began collecting in vivo data by performing dose-ranging studies of metformin and salicylates in mice.


Descriptors :   Kidney Diseases , statins , Salicylates , kinases , proteins , biological markers , Metabolism , Mass Spectrometry , inhibition , cysts , metabolomics


Subject Categories : Medicine and Medical Research
      Biochemistry
      Anatomy and Physiology


Distribution Statement : APPROVED FOR PUBLIC RELEASE