Journal
BIOORGANIC CHEMISTRY
Volume 88, Issue -, Pages -Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bioorg.2019.102972
Keywords
Dipyridamole; Hydrolyzing enzymes; Enzyme inhibition; Hypoglycemia
Funding
- Research Council of Kermanshah University of Medical Sciences
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Dipyridamole (DP) elevates cyclic Adenosine Monophosphate (cAMP) levels in platelets, erythrocytes, and endothelial cells and also blocks adenosine reuptake. It is used to dilate blood vessels in people with peripheral arterial disease and coronary artery disease (CAD). The flexible backbone, hydrophobic nature, and several available hydrogen bond (H-bond) donors and acceptors are well suited structural features of DP for inhibition/activation of enzymes. Substrates of alpha-amylase (alpha-Amy) and alpha-Glucosidase (alpha-Glu), known as key absorbing enzymes, have functional groups (OH groups) similar to DP. Since hypoglycemia can occur in diabetes disease and there is a significant link between diabetes and cardiovascular diseases (CVD), thus this study aimed to evaluate the inhibitory properties of DP against alpha-Amy and alpha-Glu, as enzyme targets of interest under hypoglycemia condition. DP inhibited the alpha-Glu and alpha-Amy activity in a dose dependent manner with IC50 values 19.4 +/- 0.3 and 30.1 +/- 0.4 mu M, respectively. Further, the (K) over bar (i) values of DP for alpha-Glu and alpha-Amy were determined as 2.9 +/- 0.2 and 3.1 +/- 0.4 mu M in a competitive-mode and mixed-mode inhibition, respectively. Also, DP had binding energies of -7.3 and -6.5 kcal/mol, to communicate with the active site of alpha-Glu and alpha-Amy, respectively. In addition, in-vivo studies revealed that the blood glucose concentration diminished after taking of DP compared to positive control group (p < 0.01). Accordingly, the results of the current work may prompt the scientific community to investigate the possible interconnection between DP clinical (side) effects and its alpha-Glu and alpha-Amy inhibitory properties.
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