Hypoglycemic and Antioxidants Activities of Carica Papaya Leaves

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Omiyale Olumakinde Charles; Ogunniran Blessing Ifeoluwa; Ezeh Mercy Ogochukwu; Yussuf Mubaraq Damilare; Oparah Confidence Damian; Isshak Fawaz

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Journal Paper

Paper Information

Journal: INTERNATIONAL JOURNAL OF ADVANCED BIOLOGICAL AND BIOMEDICAL RESEARCH (IJABBR) Year:621 | Volume: | Issue: Page(s): 141-154

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Title

Hypoglycemic and Antioxidants Activities of Carica Papaya Leaves

Author(s)

Keywords

Carica papaya

Hypoglycemic

Antioxidant Activity

Lipid peroxidation

malondialdehyde

Abstract

The objective of the current study was to assess the ethanolic and methanolic extracts of Carica papaya's Hypoglycemic effects. Yeast glucose uptake, muscle glucose uptake, and glucose adsorption capacity were used to measure the extracts' in vitro Hypoglycemic effects. The antioxidant capacity of the extracts was assessed by investigating how they affect Lipid peroxidation brought on by iron (II) sulphate and sodium nitroprusside. The findings showed that glucose was absorbed by both the ethanolic and methanolic extracts of Carica papaya, and that this adsorption significantly increased as the concentration of glucose rose. There were no variations in their adsorption capabilities that were statistically significant (p=0.05). The yeast cells were also stimulated to take up glucose by the plant extracts, and this stimulation was influenced by the sample and glucose content. In the study's muscle glucose uptake, the ethanolic extract of Carica papaya leaves showed substantially greater (p=0.05) performance than the methanolic of the same leaves with increasing concentration. The study's findings showed that the plant's methanolic extract was substantially more potent than its ethanolic (p=0.05). In addition, the methanolic extract considerably inhibited the generation of MDA (malondialdehyde) in the liver and brain homogenates more than the ethanolic extract did. Both plant extracts also exhibit dose-dependent inhibition of the various pro-oxidant agents (Iron (II) Sulphate and sodium nitroprusside) caused fatty acid oxidation tissues present in the brain and liver.

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