2009•Unpublished venueRequires access

Available online through www.jpronline.info

A. K. Asif, W. R. Shariff

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Abstract

Polyherbal formulation consists of alcoholic extract of leaves of Syzygium cumini, bark of Ficus glomerata and Flowers of Butea superba was investigated for its possible antidiabetic effect in alloxan-induced diabetic rats. The acute oral toxicity showed that the polyherbal formulation was safe until 5000mg/kg body weight and no macroscopical organ abnormalities were observed in acute oral models. Oral administration of 500mg/kg body wt. of aqueous solution of polyherbal formulation for 7 days exhibited significant reduction in blood glucose level in diabetic rats. A comparison was made between the action of prepared polyherbal formulation and a known antidiabetic drug glibenclamide 600µg/kg body wt. The antidiabetic effect of polyherbal formulation were nearly comparable than that observed with glibenclamide.

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What this paper is about

Polyherbal formulation consists of alcoholic extract of leaves of Syzygium cumini, bark of Ficus glomerata and Flowers of Butea superba was investigated for its possible antidiabetic effect in alloxan-induced diabetic rats. The acute oral toxicity showed that the polyherbal formulation was safe until 5000mg/kg body weight and no macroscopical organ abnormalities were observed in acute oral models. Oral administration of 500mg/kg body wt. of aqueous solution of polyherbal formulation for 7 days exhibited significant reduction in blood glucose level in diabetic rats. A comparison was made between the action of prepared polyherbal formulation and a known antidiabetic drug glibenclamide 600µg/kg body wt. The antidiabetic effect of polyherbal formulation were nearly comparable than that observed with glibenclamide.

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Available abstract

Polyherbal formulation consists of alcoholic extract of leaves of Syzygium cumini, bark of Ficus glomerata and Flowers of Butea superba was investigated for its possible antidiabetic effect in alloxan-induced diabetic rats. The acute oral toxicity showed that the polyherbal formulation was safe until 5000mg/kg body weight and no macroscopical organ abnormalities were observed in acute oral models. Oral administration of 500mg/kg body wt. of aqueous solution of polyherbal formulation for 7 days exhibited significant reduction in blood glucose level in diabetic rats. A comparison was made between the action of prepared polyherbal formulation and a known antidiabetic drug glibenclamide 600µg/kg body wt. The antidiabetic effect of polyherbal formulation were nearly comparable than that observed with glibenclamide.

Key concepts: Glibenclamide, Traditional medicine, Medicine, Alloxan, Acute toxicity, Diabetes mellitus, Oral administration, Syzygium

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