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Dipeptidyl peptidase-4 inhibitors and the ischemic heart: Additional benefits beyond glycemic control.

Abstract
Obese-insulin resistance and type 2 diabetes mellitus (T2DM) have become global health problems, and they are both associated with a higher risk of ischemic heart disease. Although reperfusion therapy is the treatment to increase blood supply to the ischemic myocardium, this intervention potentially causes cardiac tissue damage and instigates arrhythmias, processes known as reperfusion injury. Dipeptidyl peptidase 4 (DPP-4) inhibitors are glycemic control drugs commonly used in T2DM patients. Growing evidence from basic and clinical studies demonstrates that a DPP-4 inhibitor could exert cardioprotection and improve left ventricular function by reducing oxidative stress, apoptosis, and increasing reperfusion injury salvage kinase (RISK) activity. However, recent reports also showed potentially adverse cardiac events due to the use of a DPP-4 inhibitor. To investigate this disparity, future large clinical trials are essential in verifying whether DPP-4 inhibitors are beneficial beyond their glycemic control particularly for the ischemic heart in obese-insulin resistant subjects and T2DM patients.
AuthorsNipon Chattipakorn, Nattayaporn Apaijai, Siriporn C Chattipakorn
JournalInternational journal of cardiology (Int J Cardiol) Vol. 202 Pg. 415-6 (Jan 01 2016) ISSN: 1874-1754 [Electronic] Netherlands
PMID26432493 (Publication Type: Letter, Research Support, Non-U.S. Gov't)
CopyrightCopyright © 2015 Elsevier Ireland Ltd. All rights reserved.
Chemical References
  • Blood Glucose
  • Dipeptidyl-Peptidase IV Inhibitors
  • Hypoglycemic Agents
  • Nitriles
  • Pyrrolidines
  • Vildagliptin
  • Adamantane
  • Sitagliptin Phosphate
Topics
  • Adamantane (analogs & derivatives, pharmacology)
  • Animals
  • Blood Glucose (metabolism)
  • Diabetes Mellitus, Type 2 (blood, drug therapy)
  • Dipeptidyl-Peptidase IV Inhibitors (pharmacology)
  • Humans
  • Hypoglycemic Agents (pharmacology)
  • Insulin Resistance (physiology)
  • Myocardial Ischemia (blood, drug therapy)
  • Nitriles (pharmacology)
  • Obesity (complications, epidemiology, pathology)
  • Oxidative Stress (physiology)
  • Pyrrolidines (pharmacology)
  • Rats
  • Sitagliptin Phosphate (pharmacology)
  • Ventricular Function, Left (drug effects)
  • Vildagliptin

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