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Revista Peruana de Medicina Experimental y Salud Publica
versión impresa ISSN 1726-4634versión On-line ISSN 1726-4642
Resumen
YARLEQUE-CHOCAS, Mirtha; DORREGARAY-LLERENA, Flor; YARLEQUE-CHOCAS, Armando y GONZALES-CHAVESTA, Celso. In vitro anti-inflammatory activity of Plantago major L. and Piper aduncum L. on phospholipase A2 from the venom of snake Lachesis muta muta. Rev. perú. med. exp. salud publica [online]. 2023, vol.40, n.3, pp.325-332. Epub 26-Sep-2023. ISSN 1726-4634. http://dx.doi.org/10.17843/rpmesp.2023.403.12191.
Objective.
To evaluate the in vitro inhibitory activity of Plantago major “llantén” and Piper aduncum “matico” extracts on phospholipase A2 (PLA2) from the venom of the snake Lachesis muta muta.
Materials and methods.
We carried out an explanatory study with experimental design. Leaves of P. major and P. aduncum were collected in the province of Huarochirí in Lima, Peru. Then, we prepared alcoholic extracts diluted in distilled water and conducted phytochemical assays, quantification of phenols and flavonoids, thin layer chromatography (TLC) on cellulose and enzymatic activity with PLA2. The ability to inhibit PLA2 with the extracts under study and their fractions was analyzed. The Kruskal Wallis test and Bonferroni multiple comparisons were used during statistical analysis.
Results.
Phenols, flavonoids and tannins were qualitatively identified in both P. major and P. aduncum; in addition, P. aduncum presented saponins. The inhibition of PLA2 activity of the venom by the total extract of P. major was 45.3%, and its fractions showed the following inhibition values: 31.1% for LLF-1, 66.3% for LLF-2 and 65.5% for LLF-3. The inhibition values for the total extract of P. aduncum were 86.9%, and its fractions showed the following inhibition rates: 34.3% for MF-1, 67.1% for MF-2 and 54.9% for MF-3. Statistical analysis showed significant differences in the inhibition of PLA2 (p=0.009) by the extracts.
Conclusion.
The tests demonstrated an association between the anti-inflammatory effect of the extracts and PLA2 inhibition.
Palabras clave : Plant extracts; Plantago; Piper; Venom; Phospholipase A2; Anti-inflammatory.