TY - JOUR
T1 - Antioxidant and alpha glucosidase inhibitor screening of merremia peltata L. As potential traditional treatment for diabetes mellitus
AU - Muthi'atul Af-Idah, Bannan
AU - Hanafi, Muhammad
AU - Elya, Berna
N1 - Funding Information:
We would like to acknowledge the financial assistance obtained from the "Publikasi Terindeks Internasional (PUTI) Q3 Grant” from Universitas Indonesia with contract number BA-1517/UN2.RST/ PPM.00.03.01/2020.
Publisher Copyright:
© 2021 Phcogj.Com. This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
PY - 2021/7
Y1 - 2021/7
N2 - Introduction: Merremia peltata is ethnomedicine plant used as traditional medicine in Sulawesi, Sumatra, Maluku and Papua. M. peltata is used for diabetic. Diabetes mellitus therapy with inhibit activity of alpha glucosidase enzyme could delay absorption of monosaccharides after a meal and interrupt glucose transport into the circulation. Objective: This research purpose is to investigate in vitro antioxidant activity and alpha glucosidase enzyme inhibitor leaves and stem extract of M. peltata. Method: The Stem and leaves of M. peltata were extracted sequentially using the UAE method using hexane, ethyl acetate, and methanol as mobile phase/solvent. The M. peltata extracts were subjected to the antioxidant activity assay by the DPPH radical scavenging and FRAP method. Antidiabetic activity was determined by an enzymatic alpha glucosidase inhibitor. Result: The extract which had best performance in antioxidant activity was stem ME with value of IC50 in DPPH 47.41 μg/mL and total antioxidant power 340.04 μmol/g. This study showed that leaves and stem extract of M.peltata have potential alpha glucosidase inhibitors for diabetic therapy. Stem ME had the best activity with IC50 value 47.44 μg/mL, almost two times better than acarbose as a positive control (IC50 = 98.38 μg/mL). Leaves ME, leaves EA, and stem EA also give better activity of alpha glucosidase inhibitors than acarbose with IC50 value 67.24 μg/mL, 69.38 μg/mL, and 72.85 μg/mL, respectively. Conclusion: M. peltata has potential antioxidant and alpha glucosidase inhibitor activity for diabetic therapy.
AB - Introduction: Merremia peltata is ethnomedicine plant used as traditional medicine in Sulawesi, Sumatra, Maluku and Papua. M. peltata is used for diabetic. Diabetes mellitus therapy with inhibit activity of alpha glucosidase enzyme could delay absorption of monosaccharides after a meal and interrupt glucose transport into the circulation. Objective: This research purpose is to investigate in vitro antioxidant activity and alpha glucosidase enzyme inhibitor leaves and stem extract of M. peltata. Method: The Stem and leaves of M. peltata were extracted sequentially using the UAE method using hexane, ethyl acetate, and methanol as mobile phase/solvent. The M. peltata extracts were subjected to the antioxidant activity assay by the DPPH radical scavenging and FRAP method. Antidiabetic activity was determined by an enzymatic alpha glucosidase inhibitor. Result: The extract which had best performance in antioxidant activity was stem ME with value of IC50 in DPPH 47.41 μg/mL and total antioxidant power 340.04 μmol/g. This study showed that leaves and stem extract of M.peltata have potential alpha glucosidase inhibitors for diabetic therapy. Stem ME had the best activity with IC50 value 47.44 μg/mL, almost two times better than acarbose as a positive control (IC50 = 98.38 μg/mL). Leaves ME, leaves EA, and stem EA also give better activity of alpha glucosidase inhibitors than acarbose with IC50 value 67.24 μg/mL, 69.38 μg/mL, and 72.85 μg/mL, respectively. Conclusion: M. peltata has potential antioxidant and alpha glucosidase inhibitor activity for diabetic therapy.
KW - Alpha-glucosidase inhibitor
KW - Antidiabetic
KW - Antioxidant
KW - Merremia peltata
UR - http://www.scopus.com/inward/record.url?scp=85110968332&partnerID=8YFLogxK
U2 - 10.5530/pj.2021.13.116
DO - 10.5530/pj.2021.13.116
M3 - Article
AN - SCOPUS:85110968332
SN - 0975-3575
VL - 13
SP - 902
EP - 908
JO - Pharmacognosy Journal
JF - Pharmacognosy Journal
IS - 4
ER -