Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8880773 | Industrial Crops and Products | 2018 | 11 Pages |
Abstract
In vitro inhibition of diabetes key enzymes (α-glucosidase and α-amylase) was evaluated. The study of kinetics inhibition showed that the FSLE demonstrated a strong inhibition of both α-glucosidase (IC50â¯=â¯8.0â¯Â±â¯0.2â¯Î¼g/mL) and α-amylase (IC50â¯=â¯70.20â¯Â±â¯0.8â¯Î¼g/mL) in non-competitive manner. The acute toxicity of FSLE on Wistar rats at the doses of 200, 500 and 2000â¯mg/kg body weight (BW) was investigated. Our findings revealed that leaves extract at such doses as up to 2000â¯mg/kg did not cause any signs of toxicity or deaths in rats. Based on hematological and biochemical analyses of hepato-biliary and renal functions, we concluded that the FSLE is tolerated by rats. The analgesic effect of FSLE was assayed using the acetic acid writhing test in mice. At 100â¯mg/kg, the FSLE showed a higher analgesic activity (88.08â¯Â±â¯0.73%) than that of acetylsalicylic acid (ASL) (62.69â¯Â±â¯0.26%) used as positive control.
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Authors
Habib Mosbah, Hanen Louati, Mohamed Ali Boujbiha, Hassiba Chahdoura, Mejdi Snoussi, Guido Flamini, Roberta Ascrizzi, Ali Bouslema, Lotfi Achour, Boulbaba Selmi,