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Antidiabetic Activity of an Optimized Polyherbal Dispersible Tablet of Terminalia arjuna, Moringa oleifera, and Syzygium cumini in Streptozotocin-Induced Diabetic Rats

Priyanka Shrivastava, Vishal Gupta

GSC Biological and Pharmaceutical Sciences11 June 2026
View paper DOI: 10.30574/gscbps.2026.35.3.0217
20
Early
Animal In VivoPositiveBlood Sugar

Priyanka Shrivastava, Vishal Gupta (2026). Antidiabetic Activity of an Optimized Polyherbal Dispersible Tablet of Terminalia arjuna, Moringa oleifera, and Syzygium cumini in Streptozotocin-Induced Diabetic Rats. GSC Biological and Pharmaceutical Sciences. doi:10.30574/gscbps.2026.35.3.0217

A combination of three medicinal plants — Terminalia arjuna (arjuna bark), Moringa oleifera (moringa leaf), and Syzygium cumini (black plum) — was formulated into a dispersible tablet and tested for blood sugar-lowering effects in diabetic rats. Rats had diabetes artificially induced using streptozotocin, a chemical that destroys the insulin-producing beta cells of the pancreas, mimicking type 1 or severe type 2 diabetes. Animals treated with either the raw polyherbal formulation or the compressed tablet form at 150 mg/kg for 14 days showed meaningfully lower blood glucose levels and better body weight maintenance compared to untreated diabetic rats. Microscopic examination of pancreatic tissue in treated animals showed partial recovery of the islets of Langerhans — the clusters of cells responsible for insulin production — suggesting the combination may support pancreatic repair or protection rather than simply masking blood sugar readings. Safety testing following OECD guideline No. 423 found no deaths or severe toxic effects at doses up to 2000 mg/kg, which is a standard benchmark for acute oral safety screening. The study is notable for comparing a loose herbal formulation against a tablet form, testing whether the manufacturing process itself affects efficacy. While the results are promising at a preclinical level, this is an animal study only, and the findings cannot be directly applied to human use without further clinical investigation. The three-herb combination draws on traditional medicine systems where each plant has an independent history of use in metabolic conditions, making this a formulation-focused study rather than a single-ingredient investigation.

Study details

Population

Streptozotocin-induced diabetic rats (35 mg/kg i.p.); group sizes not specified in abstract; acute toxicity arm also conducted in rats per OECD guideline No. 423

Duration

14 days

Plant part

Mixed

Preparation

Other

Dosage

150 mg (150 mg/kg/day oral dose used for antidiabetic efficacy assessment over 14 days in rats; this is an animal study dose and cannot be converted to a human equivalent without further pharmacokinetic data)

Country

India

Dosage protocol

150 mg/kg orally per day for 14 days (both polyherbal formulation and polyherbal tablet forms tested at this dose in streptozotocin-induced diabetic rats); acute toxicity tested up to 2000 mg/kg single oral dose

Key compounds

quercetinkaempferolbeta-caroteneisothiocyanates

Original paper

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