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Paper ID:IJSREM66747

In Vitro Evaluation of the Antidiabetic Potential of Bergera koenigii (Curry Leaf) Leaf Extract through Inhibition of α-Amylase, α-Glucosidase and Dipeptidyl Peptidase-4 (DPP-4) Enzymes

Stream/Area:

-

Subject:

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Paper ID:

IJSREM66747

Volume:

10 |

8 |

Aug 2026

Pages:

1-6

Publication Frequency:

Monthly (12 issues per year)

DOI
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Not assigned

License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.

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Authors

N

N.SUNDHARRAJ

PHARMACOLOGY

SRI VIJAY VIDYALAYA COLLEGE OF PHARMACY DHARMAPURI

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P

P.SUBHASHINI

PHARMACOLOGY

SRI VIJAY VIDYALAYA COLLEGE OF PHARMACY DHARMAPURI

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R

R.SUGANYA

PHARMACOLOGY

SRI VIJAY VIDYALAYA COLLEGE OF PHARMACY DHARMAPURI

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Mentors

S

S.ANANTHI

PHARMACOLOGY

SRI VIJAY VIDYALAYA COLLEGE OF PHARMACY DHARMAPURI

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Abstract

Type 2 Diabetes Mellitus (T2DM) is a chronic metabolic disorder characterized by insulin resistance and progressive β-cell dysfunction, and its management increasingly targets carbohydrate-digesting and incretin-degrading enzymes. The present study evaluated the in vitro antidiabetic potential of an ethanolic leaf extract of Bergera koenigii (curry leaf) through inhibition of α-amylase, α-glucosidase and dipeptidyl peptidase-4 (DPP-4). Leaves were shade-dried, powdered and extracted by Soxhlet extraction using ethanol. Preliminary phytochemical screening confirmed the presence of alkaloids, flavonoids, tannins, saponins, glycosides, phenolics, terpenoids and steroids. Enzyme inhibition assays were performed at extract concentrations of 25–400 µg/mL, using acarbose and sitagliptin as reference standards. The extract exhibited concentration-dependent inhibition of all three enzymes: α-amylase inhibition increased from 5.91% to 39.18%, α-glucosidase inhibition from 6.20% to 40.02%, and DPP-4 inhibition from 18% to 78% across the tested range, compared with 85% inhibition for sitagliptin at the highest concentration. The pronounced DPP-4 inhibitory response, together with a broad phytochemical profile rich in flavonoids and carbazole alkaloids, suggests that Bergera koenigii leaf extract is a promising natural candidate for further development as an antidiabetic agent, warranting IC₅₀ determination and in vivo validation.

KEYWORDS

Bergera koenigii; Type 2 Diabetes Mellitus; α-amylase; α-glucosidase; DPP-4 inhibition; phytochemical screening; natural antidiabetic agent.

Cite This Article

N.SUNDHARRAJ, P.SUBHASHINI, R.SUGANYA, S.ANANTHI, "In Vitro Evaluation of the Antidiabetic Potential of Bergera koenigii (Curry Leaf) Leaf Extract through Inhibition of α-Amylase, α-Glucosidase and Dipeptidyl Peptidase-4 (DPP-4) Enzymes," International Journal of Scientific Research in Engineering and Management, vol. 10, no. 8, pp. 1-6, Aug 2026.

Full Article/Conclusion

The ethanolic leaf extract of Bergera koenigii showed a positive and broad phytochemical profile and exhibited concentration-dependent inhibitory activity against α-amylase, α-glucosidase and DPP-4, three key enzymatic targets in the management of Type 2 Diabetes Mellitus. α-Amylase inhibition increased from 5.91% to 39.18%, α-glucosidase inhibition from 6.20% to 40.02%, and DPP-4 inhibition from 18% to 78% across the 25–400 µg/mL concentration range, with the extract's DPP-4 inhibition at 400 µg/mL (78%) approaching that of sitagliptin (85%). These findings support Bergera koenigii as a promising natural source of antidiabetic enzyme inhibitors and justify further investigation, including IC₅₀ determination, active-constituent isolation, and in vivo evaluation, before its potential therapeutic application can be established.

References

[1] Ahren B. DPP-4 inhibitors: clinical data and clinical implications. Diabetes Care. 2007;30(6):1344-1350. [2] American Diabetes Association Professional Practice Committee. Classification and diagnosis of diabetes: Standards of Care in Diabetes—2024. Diabetes Care. 2024;47(Suppl 1):S20-S42. [3] American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care. 2010;33(Suppl 1):S62-S69. [4] Bhat M, Zinjarde SS, Bhargava SY, Kumar AR, Joshi BN. Antidiabetic Indian plants: a good source of potent amylase inhibitors. Evid Based Complement Alternat Med. 2011;2011:810207. [5] Sales PM, Souza PM, Simeoni LA, Magalhães PO, Silveira D. α-Amylase inhibitors: a review of raw material and isolated compounds from plant source. J Pharm Pharm Sci. 2012;15(1):141-183. [6] Chang CC, Yang MH, Wen HM, Chern JC. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. J Food Drug Anal. 2002;10(3):178-182. [7] Deacon CF. Dipeptidyl peptidase-4 inhibition with sitagliptin: a new therapy for type 2 diabetes. Expert Opin Pharmacother. 2007;8(13):2059-2071. [8] DeFronzo RA. From the triumvirate to the ominous octet: a new paradigm for the treatment of type 2 diabetes mellitus. Diabetes. 2009;58(4):773-795. [9] Drucker DJ, Nauck MA. The incretin system: glucagon-like peptide-1 receptor agonists and dipeptidyl peptidase-4 inhibitors in type 2 diabetes. Lancet. 2006;368(9548):1696-1705. [10] Kahn SE. The importance of the β-cell in the pathogenesis of type 2 diabetes mellitus. Am J Med. 2000;108(Suppl 6a):2S-8S.

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Publication Date

8/13/2026

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