Studies on In-vitro Anti-inflammatory and Antioxidant Potentials of Annona muricata Leaf Extracts
| Autor: | G. A. Olatunji, I. Nwaehujor, S. A. Akande, O. Atolani |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2020 |
| Předmět: |
chemistry.chemical_classification
Antioxidant antioxidant extracts biology Traditional medicine lcsh:TP368-456 medicine.drug_class medicine.medical_treatment General Medicine biology.organism_classification Anti-inflammatory In vitro Enzyme assay Lipoxygenase annona muricata lcsh:Food processing and manufacture Enzyme chemistry Annona muricata anti-inflammatory medicine biology.protein Medicinal plants |
| Zdroj: | Croatian journal of food science and technology Volume 12 Issue 2 Croatian Journal of Food Science and Technology, Vol 12, Iss 2, Pp 177-183 (2020) |
| ISSN: | 1848-9923 1847-3466 |
| Popis: | Inflammation has stimulated significant worldwide scientific interest because of its implication in many human diseases. Most inflammations are caused by reactive oxygen species or free radicals. Annona muricataleaf extracts were investigated for their in-vitroantioxidant and anti-inflammatory potentials. Annona muricataleavesweredried at room temperature, blended using a mill.and extracted with solvents of varying degree of polarities. The solventsused were hexane, ethyl acetate,and ethanol. After sequential extraction, the crude extracts were examined for their in-vitroanti-inflammatory activities on lipoxygenase inhibition, proteinase inhibition, albumin denaturation inhibition,and red blood cell membrane stabilization assays,while the antioxidant activities were examined using DPPH, ABTS and hydrogen peroxide assays. The results showed that the ethanol extract had significantlyhigher albumin denaturation inhibition activity at 500 μg/mL (p < 0.01). The activity of all the extracts on proteinase inhibition decreased with the increase in concentration of the extracts. Indomethacin (standard), ethanol extract,and ethyl acetate extract exhibited a dose dependent increase in lipoxygenase activity. The ethanol extract showed highred blood cell membrane stabilization activity at 500 μg/mL and the activity was comparable with that of the standard (diclofenac). Hydrogen peroxide scavenging activity of the extracts and standard (Vitamin C) were comparable at 20 –100 μg/mL. The ethanol extract showed significantly higher(p < 0.01) DPPH radical scavenging activity compared with other extracts. A similar trend was also observed for ABTS radical scavenging activity. Generally,the ethanol extract exhibited higher anti-inflammatory and antioxidant activities in most of the assays, this could be attributed to the polar compounds present in the extract. |
| Databáze: | OpenAIRE |
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