1.Mobola plum seed methanolic extracts exhibit mixed type inhibition of angiotensin Ⅰ-converting enzyme in vitro
Crown Olajusi OLAMIDE ; Olayeriju Sam OLANREWAJU ; Kolawole Oluwaseyi AYODELE ; Akinmoladun Clement AFOLABI ; Olaleye Tolulope MARY ; Akindahunsi Akintunde AFOLABI
Asian Pacific Journal of Tropical Biomedicine 2017;7(12):1079-1084
Objective:To explore the possible inhibitory potentials and mechanism by Mobola plum (Parinari curatellifolia) seeds crude methanol (CE) and flavonoid-rich (FE) extracts on angiotensin-1-converting enzyme (ACE I).Methods:The sensitivity and kinetic model of inhibition of CE and FE on ACE I using N-[3-(2-furyl)-acryloyl]-Phe-Gly-Gly as enzyme substrate for ACE I was evaluated by Michealis Menten approach.The inhibition mechanism was explored from LineweaverBurk model and IC50 was determined from Cheng-Prusoff empirical analysis.Results:The IC50 of CE and FE were 13.54 and 39.38 μg/mL,respectively.Both extracts exhibited mixed type inhibition with the inhibitory constant (Ki) of CE was between 0.38 and 0.37 μg/mL while that of FE showed a two-fold increase (1.62 μg/mL and 0.28 μg/mL).FE on ACE I demonstrated positive cooperativity with a Hill's coefficient of 1.89.Conclusions:The study reveals the superior ACE I inhibitory potential of CE over FE and suggest that mixed inhibition pattern of the enzyme might be the underlying mechanism of antihypertensive activity.
2. Mobola plum seed methanolic extracts exhibit mixed type inhibition of angiotensin -converting enzyme in vitro
Olamide Olajusi CROWN ; Olanrewaju Sam OLAYERIJU ; Ayodele Oluwaseyi KOLAWOLE ; Afolabi Clement AKINMOLADUN ; Mary Tolulope OLALEYE ; Afolabi Akintunde AKINDAHUNSI
Asian Pacific Journal of Tropical Biomedicine 2017;7(12):1079-1084
Objective To explore the possible inhibitory potentials and mechanism by Mobola plum (Parinari curatellifolia) seeds crude methanol (CE) and flavonoid-rich (FE) extracts on angiotensin-1-converting enzyme (ACE ). Methods The sensitivity and kinetic model of inhibition of CE and FE on ACE using N-[3-(2-furyl)-acryloyl]-Phe-Gly-Gly as enzyme substrate for ACE was evaluated by Michealis Menten approach. The inhibition mechanism was explored from Lineweaver–Burk model and IC