Full text loading...
Diabetes mellitus is a rapidly escalating global health concern, and numerous ethnobotanical remedies are under investigation for their antidiabetic properties. Tinospora sinensis has long been used in traditional medicine by indigenous populations for glycemic control. This study aimed to characterize the phytochemical profile of T. sinensis and evaluate its in vitro- α-glucosidase inhibition, antioxidant and antimicrobial activities.
Standard qualitative assays were used to identify secondary metabolites. Total phenolic content (TPC) was quantified via Folin–Ciocalteu reagent (expressed as mg gallic acid equivalents [GAE]/g), and total flavonoid content (TFC) via aluminum chloride colorimetric method (mg quercetin equivalents [QE]/g). Antioxidant potential was determined using the DPPH radical scavenging assay. α-Glucosidase inhibition was measured spectrophotometrically using p-nitrophenyl-α-D-glucopyranoside as a substrate. Antimicrobial efficacy against Staphylococcus aureus was tested using the agar well diffusion technique.
Phytochemical screening confirmed the presence of alkaloids, flavonoids, glycosides, terpenoids, saponins, phenols, tannins, steroids, and quinones. TPC and TFC values were 181.41 ± 1.57 mg GAE/g and 12.08 ± 0.11 mg QE/g, respectively. The methanolic extract demonstrated considerable antioxidant activity (DPPH IC50 = 111.43 ± 1.13 µg/mL).
Both crude and ethyl acetate extracts exhibited significant α-glucosidase inhibition (comparable or superior to control). Notable antibacterial activity was observed against S. aureus, with a 9 mm inhibition zone.
The presence of diverse bioactive phytochemicals in T. sinensis supports its traditional use in diabetes management. Its potent α-glucosidase inhibition suggests a mechanism for attenuating postprandial hyperglycemia, while antioxidant and antimicrobial activities substantiate additional therapeutic roles. These findings warrant further in vivo studies and mechanistic exploration to validate its potential as a source of enzyme inhibitors and therapeutic agents for metabolic disorders.