Nox4-derived reactive oxygen species mediate cardiomyocyte injury in early type 1 diabetes

作者：Maalouf Rita M^*; Eid Assaad A; Gorin Yves C; Block Karen; Escobar Gladys Patricia; Bailey Steven; Abboud Hanna E

来源：American Journal of Physiology - Cell Physiology, 2012, 302(3): C597-C604.

DOI：10.1152/ajpcell.00331.2011

• cardiac injury
• oxidative stress
• NADPH oxidases

Maalouf RM, Eid AA, Gorin YC, Block K, Escobar GP, Bailey S, Abboud HE. Nox4-derived reactive oxygen species mediate cardiomyocyte injury in early type 1 diabetes. Am J Physiol Cell Physiol 302: C597-C604, 2012. First published October 26, 2011; doi: 10.1152/ajpcell.00331.2011.-Oxidative stress contributes to diabetic cardiomyopathy. This study explored the role of the NADPH oxidase Nox4 as a source of reactive oxygen species (ROS) involved in the development of diabetic cardiomyopathy. Phosphorothioated antisense (AS) or sense (S) oligonucleotides for Nox4 were administered for 2 wk to rats made diabetic by streptozotocin. NADPH oxidase activity, ROS generation, and the expression of Nox4, but Nox1 or Nox2, were increased in left ventricular tissue of the diabetic rats. Expression of molecular markers of hypertrophy and myofibrosis including fibronectin, collagen, alpha-smooth muscle actin, and beta-myosin heavy chain were also increased. These parameters were attenuated by the administration of AS but not S Nox4. Moreover, the impairment of contractility observed in diabetic rats was prevented in AS- but not S-treated animals. Exposure of cultured cardiac myocytes to 25 mM glucose [high glucose (HG)] increased NADPH oxidase activity, the expression of Nox4, and molecular markers of cardiac injury. These effects of HG were prevented in cells infected with adenoviral vector containing a dominant negative form of Nox4. This study provides strong evidence that Nox4 is an important source of ROS in the left ventricle and that Nox4-derived ROS contribute to cardiomyopathy at early stages of type 1 diabetes.

• 出版日期2012-2