In vitro alpha glucosidase inhibition, in vivo antidiabetic activity and hypolipidemic effect of tepal extracts of Musa paradisiaca in stz-induced diabetic mice

The use of medicinal plants as source of remedies for the treatment of many diseases dated back to prehistory and people of all continents have this old tradition. In the present study, tepals of Musa paradisiaca was evaluated for phytochemical screenin, the total content of flavonoid and phenolics,...

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Bibliographic Details
Main Author: Muhammad Abdurrazak (Author)
Corporate Author: Universiti Sultan Zainal Abidin . Faculty of Medicine
Format: Thesis Book
Language:English
Subjects:

MARC

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100 0 |a Muhammad Abdurrazak ,   |e author 
245 1 0 |a In vitro alpha glucosidase inhibition, in vivo antidiabetic activity and hypolipidemic effect of tepal extracts of Musa paradisiaca in stz-induced diabetic mice   |c Muhammad Abdurrazak 
264 0 |c 2015 
300 |a xv, 144 leaves :   |b ill. (some col.) ;   |c 30 cm. 
336 |a text  |2 rdacontent 
337 |a unmediated  |2 rdamedia 
338 |a volume  |2 rdacarrier 
502 |a Thesis (Master of Science) - Universiti Sultan Zainal Abidin, 2015 
504 |a Includes bibliographical references (leaves 107-135) 
505 0 |a 1. Introduction -- 2. Literature review -- 3. Materials and methods -- 4. Results and discussion -- 5. Conclusion and recommendation 
520 |a The use of medicinal plants as source of remedies for the treatment of many diseases dated back to prehistory and people of all continents have this old tradition. In the present study, tepals of Musa paradisiaca was evaluated for phytochemical screenin, the total content of flavonoid and phenolics, in vitro a-glucosidase inhibition and in vivo antidiabetic efficacy in streptozotocin (STZ)- induced diabetic mice. Diabetic mice were administered 500 mg/kg per day of methanolic tepal extract (MTE) orally for one month and compared with untreated mice for the following studies. The mice were sacrificed and blood collected for key biochemical markers such as, blood glucose, creatinine, urea, uric acid, total protein, lipid profile, aminotransferases and alkaline phosphatase. The histopathological studies of pancreas, liver and kidney were also performed. Preliminary phytochemical screening reveals the presence of phenolics, flavonoids, glycosides, terpenoids, tannins and alkaloids. MTE has the richest content of both phenolics (4.27 mg GAE/g) and flavonoids (0.25mg QE/g) in comparison with aqueous and ethanolic tepal extracts. The result of the inhibitory effect of these extracts on a-glucosidase activities also revealed that MTE was the most potent inhibitor of a-glucosidase (with IC50 60±0.14 µg/mL) followed by ethanolic tepal extract (ETE) and then aqueous tepal extract (ATE) in a dose dependent manner, though the various extracts were not significantly different (p>0.05) at 1 mg/mL. Elevated blood glucose, creatinine, urea and uric acid levels were significantly (p<0.05) reverted back to near normal in STZ-induced diabetic mice with oral administration of MTE. Plasma protein, lipid profile, transaminases and alkaline phosphatase were also significantly reverted back to near normalcy (p<0.05) after the treatment. Histopathological analysis indicated tissue damages in the diabetic untreated mice; treatment with MTE exhibits the tissue protective role (of pancreas and liver) against peroxidation damage, thus signifying tissue integrity maintenance of MTE. In conclusion, it can be inferred that the in vitro and in vivo antidiabetic therapeutic efficacy of tepals of Musa paradisiaca may be attributed to the presence of phytochemicals such as phenolics, flavonoids, alkaloids etc. 
610 2 0 |a Universiti Sultan Zainal Abidin   |x Dissertations 
610 2 0 |a Universiti Sultan Zainal Abidin   |x Faculty of Medicine   |v Dissertations 
650 0 |a alpha-Glucosidases 
650 0 |a Diabetes   |x Research 
650 0 |a Hypoglycemic Agents 
650 0 |a In Vitro Techniques 
650 0 |a Plantain banana 
650 0 |a Plants 
650 0 |a Plants, Medicinal 
655 0 |a Dissertations, Academic 
710 2 |a Universiti Sultan Zainal Abidin .   |b Faculty of Medicine 
999 |a 1000165451   |b Thesis   |c Reference   |e Medical Campus