Research Project
Grant-in-Aid for Young Scientists (B)
DPP4 activity was increased in the diabetic state and blocked by anagliptin administration. The HMGB1 plasma levels were reduced in the diabetic TG compared with the non-diabetic TG mice, but DPP4 inhibition with anagliptin increased HMGB1 plasma levels in the diabetic TG mice. The infarct area was significantly larger in the diabetic TG than in the non-diabetic TG mice, and was reduced by DPP4 inhibition. Cardiac function, angiogenesis, and VEGF expression were impaired in the diabetic TG mice, but ameliorated by the DPP4 inhibition to levels similar to those found in the non-diabetic TG mice.The DPP4 inhibitor ameliorated cardiac function by inhibiting the inactivation of HMGB1 in diabetic mice after MI.
All 2017 2016 2015
All Journal Article (7 results) (of which Int'l Joint Research: 5 results, Peer Reviewed: 7 results, Open Access: 7 results, Acknowledgement Compliant: 2 results) Presentation (26 results) (of which Int'l Joint Research: 7 results)
International Heart Journal
Volume: 印刷中
130006179202
Int J Cardiol
Volume: 207 Pages: 368-369
10.1016/j.ijcard.2016.01.189
Journal of Atherosclerosis and Thrombosis
Volume: 22 Issue: 6 Pages: 570-581
10.5551/jat.27235
130005078031
Circulation Journal
Volume: 79 Issue: 4 Pages: 785-793
10.1253/circj.CJ-14-1280
130005130257
Journal of Cardiac Failure
Volume: 21 Issue: 8 Pages: 621-627
10.1016/j.cardfail.2015.04.015
American Journal of Physiology-Heart and Circulatory Physiology
Volume: 309 Issue: 7 Pages: H1123-H1129
10.1152/ajpheart.00533.2015
Journal of Molecular and Cellular Cardiology
Volume: 89 Pages: 306-313
10.1016/j.yjmcc.2015.10.013