Reduction of reactive oxygen species in diabetes-associated nephrology

(Press-News.org) Contact information: Corinne Williams
press_releases@the-jci.org
Journal of Clinical Investigation
Reduction of reactive oxygen species in diabetes-associated nephrology Diabetes-associated complications, including retinopathy, neuropathy, and nephropathy are associated with increased glucose levels, but it is not understood how glucose drives these manifestations. There is evidence that cultured cells exposed to high levels of glucose produce reactive oxygen species (ROS); however it is unknown if ROS contributes directly to diabetes complications. In this issue of the Journal of Clinical Investigation, Kumar Sharma and colleagues at the University of California, San Diego determined that ROS production was actually reduced in kidneys of diabetic mice, and this decrease was associated with lowered activity of the major energy-sensing enzyme, AMPK. Furthermore, AMPK activity was also reduced in kidneys of diabetic patients. Treatment of diabetic mice with a compound that increased AMPK activity reduced kidney-associated symptoms, including fibrosis and albuminuria. In the companion commentary, Dwight Towler of the Sanford-Burnham Medical Institute discusses how this view of ROS in diabetes will require a new look at therapeutic approaches for relieving diabetes complications.### TITLE: AMPK dysregulation promotes diabetes-related reduction of superoxide and mitochondrial function AUTHOR CONTACT: Kumar Sharma
UCSD, La Jolla, CA, USA
Phone: 858-822-0870; Fax: 858-822-7483; E-mail: kusharma@ucsd.edu View this article at: http://www.jci.org/articles/view/66218?key=5fad8f958699794ef103 ACCOMPANYING COMMENTARY TITLE: Mitochondrial ROS deficiency and diabetic complications: AMP[K]-lifying the adaptation to hyperglycemia AUTHOR CONTACT: Dwight Towler
Sanford-Burnham Medical Research Institute, orlando, , USA
Phone: 407-745-2079; Fax: ; E-mail: dtowler@sanfordburnham.org View this article at: http://www.jci.org/articles/view/72326?key=dcdae15a08a5b61c4 END