In Vitro Antioxidant, Anti-Inflammatory, and Digestive Enzymes Inhibition Activities of Hydro-Ethanolic Leaf and Bark Extracts of Psychotria densinervia (K. Krause) Verdc.
Jean Romuald MbaDjamila ZouheiraHadidjatou DairouFanta Sabine Adeline YadangNfor Njini GaelLawrence AyongJules-Roger KuiatéGabriel Agbor AgborPublished in: Advances in pharmacological and pharmaceutical sciences (2022)
Psychotria densinervia hydro-ethanolic leaf extract (PHELE) and bark extract (PHEBE) were evaluated for antioxidant, anti-inflammatory, and inhibition of digestive enzymes activities. The antioxidant activity was characterized by 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2'-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), ferric reducing antioxidant power (FRAP), total phenolic content (TPC), and total flavonoid content (TFC) assays. The anti-inflammatory activity was characterized by protein denaturation and antiproteinase tests, while the inhibition of the enzymes was assessed using α -amylase, α -glucosidase, lipase, and cholesterol esterase activities. PHELE presented low ( p < 0.001) IC 50 (59.09 ± 5.97 μ g/ml) for DPPH compared with ascorbic acid (71.78 ± 6.37 μ g/ml) and PHEBE (115.40 ± 1.21 μ g/ml). The IC 50 of PHELE (262.4 ± 4.46 μ g/ml) and PHEBE (354.2 ± 1.97 μ g/ml) was higher ( p < 0.001) than that of catechin (33.48 ± 2.02 μ g/ml) for ABTS. PHELE had high ( p < 0.001) FRAP (341.73 ± 21.70 mg CE/g) than PHEBE (150.30 ± 0.32 mg CE/g). PHELE presented ( p < 0.001) high TPC (270.05 ± 7.53 mg CE/g) and TFC (23.43 ± 0.032 mg CE/g) than PHEBE (TPC: 138.89 ± 0.91 and TFC: 20.06 ± 0.032 mg CE/g). PHELE showed antiprotein denaturation with IC 50 (257.0 ± 7.51 μ g/ml) ( p < 0.001) and antiproteinase activity (74.37 ± 1.10 μ g/ml) lower than PHEBE (316.1 ± 6.02 μ g/ml and 177.6 ± 0.50 μ g/ml), respectively. Orlistat inhibited lipase ( p < 0.001) activity with IC 50 (37.11 ± 4.39 μ g/ml) lower than PHELE and PHEBE (50.57 ± 2.89 μ g/ml and 62.88 ± 1.74 μ g/ml, respectively). PHELE inhibited cholesterol esterase with IC 50 (34.75 ± 3.87 μ g/ml) lower than orlistat (54.61 ± 2.56) and PHEBE (80.14 ± 1.71 μ g/ml). PHELE inhibited α -amylase IC 50 (6.07 ± 4.05 μ g/ml) lower than PHEBE (19.69 ± 6.27 μ g/ml) and acarbose (20.01 ± 2.84 μ g/ml). Acarbose inhibited α -glucosidase ( p < 0.001) activity with IC 50 (4.11 ± 3.47 μ g/ml) lower than PHELE (24.41 ± 2.84 μ g/ml) and PHEBE (38.81 ± 2.46 μ g/ml). PHELE presented better antioxidant, anti-inflammatory, and enzyme inhibition activity than PHEBE.
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