J. Pharm. Pharmacogn. Res., vol. 13, no. 2, pp. 444-458, Mar-Apr 2025.

DOI: https://doi.org/10.56499/jppres24.2100_13.2.444

Original Article

Anti-inflammatory effect of the total flavonoid content of the hydroalcoholic extract of the leaves of Senna alata (L.) Roxb. in an experimental model of acute inflammation

[Efecto anti-inflamatorio del contenido total de flavonoides del extracto hidroalcohólico de las hojas de Senna alata (L.) Roxb. en un modelo experimental de inflamación aguda]

Haydee Chávez1, Angel T. Alvarado2*, Nesquen Tasayco-Yataco3, Mario Pineda Pérez4, Jorge A. García1, María R. Bendezú1, Felipe Surco-Laos1, Juan J. Palomino-Jhong1, Doris Laos-Anchante1, Elizabeth J. Melgar-Merino1, Nelly Vega-Ramos1, Carmela Ferreyra-Paredes1, Paulina Eliades Yarasca-Carlos5, Dante Fermín Calderón- Huamaní6, Mario Bolarte-Arteaga7, Berta Loja-Herrera8

1Faculty of Pharmacy and Biochemistry, San Luis Gonzaga National University of Ica, 11004, Ica, Peru.

2Research Unit in Molecular Pharmacology and Genomic Medicine (UNIPHARMOGEM), VRI, San Ignacio de Loyola University, La Molina 15024, Lima, Peru.

3Human Medicine, Faculty of Health Sciences, Norbert Wiener University, 15046, Lima, Peru.

4Pharmacy and Biochemistry, Faculty of Health Sciences, Scientific University of the South, UCSUR, Campus Villa II, 15067, Lima, Peru.

5Biological Sciences Faculty, San Luis Gonzaga National University of Ica, 11004, Ica, Peru.

6Faculty of Environmental and Sanitary Engineering, San Luis Gonzaga National University of Ica, 11004, Ica, Peru.

7Human Medicine, Continental University, Los Olivos 15304, Lima, Peru.

8General Studies, FII, National University of San Marcos, 15081, Lima, Peru.

*E-mail: aalvarado@usil.edu.pe

Abstract

Context: Acute inflammation due to persistent stimulation of noxes evolves into chronic inflammation that contributes to the pathogenesis of asthma, arthritis, atherosclerosis, diabetes, aging, and cancer; therefore, it is justified to study plants with anti-inflammatory activity and fewer adverse effects.

Aims: To evaluate the potential anti-inflammatory effect of the total flavonoid content of the hydroalcoholic extract of the leaves of Senna alata (L.) Roxb (HELSA) in an experimental model of acute inflammation induced by carrageenan in rats.

Methods: The total flavonoid content (TFC) was determined by spectrophotometry at 510 nm, total polyphenolic content (TPC) by the Folin-Ciocalteu method, and antioxidant activity by two in vitro methods. The oral median lethal dose (LD50) was determined by the logarithmic method, and acute inflammation was induced by 1% carrageenan in rats.

Results: The TFC was 1.63 ± 0.02 mg QE/100 mg and TPC was 22.90 ± 0.05 mg GAE/100 mg. Antioxidant capacity: DPPH IC50 2.89 ± 0.04 µg/µL; ABTS 11.67 ± 0.03 mM TEAC/100 mg dry extract. Correlation relationship TFC/DPPH (r = -0.9941; R2 = 0.9884), TFC/ABTS (r = 0.9971; R2 = 0.9944), TPC/DPPH (r = 0.5694; R2 = 0.3243) and TPC/ABTS (r = -0.5960; R2 = 0.3553). The LD50 was 9602 mg/kg. A significant decrease in rat paw edema (p<0.05) was evident from the first hour, in contrast to the negative control. The highest percentage of anti-inflammatory inhibition (75.75%) was at 7 hours with a dose of 500 mg/kg of HELSA, being higher than the effect of ibuprofen (39.40%) and lower than dexamethasone (87.87%).

Conclusions: The total flavonoid content and polyphenols of the hydroalcoholic extract of the leaves of S. alata exhibit potential anti-inflammatory activity in a model of acute inflammation that should be examined with other experimental models to initiate clinical trials in humans.

Keywords: Senna alata; anti-inflammatory effect; flavonoids; biophenols; antioxidant activity in vitro.

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Resumen

Contexto: La inflamación aguda por estimulación persistente de noxas evoluciona a inflamación crónica que contribuye a la patogénesis del asma, artritis, aterosclerosis, diabetes, envejecimiento, y cáncer; por ello, se justifica estudiar plantas con actividad antiinflamatoria y con menos efectos adversos.

Objetivos: Evaluar el potencial efecto antiinflamatorio del contenido total de flavonoides del extracto hidroalcohólico de las hojas de Senna alata (L.) Roxb (HELSA) en un modelo experimental de inflamación aguda inducida por carragenina en ratas.

Métodos: El contenido total de flavonoides (TFC) se determinó por espectrofotometría a 510 nm, contenido total polifenólico (TPC) por el método Folin-Ciocalteu y la actividad antioxidante por dos métodos in vitro. La dosis letal media oral (LD50) se determinó por el método logarítmico y la inflamación aguda inducida por carragenina 1% en ratas.

Resultados: El TFC fue 1,63 ± 0,02 mg QE/100 mg y TPC fue 22,90 ± 0,05 mg GAE/100 mg. Actividad antioxidante: DPPH IC50 2,89 ± 0,04 µg/µL; ABTS 11,67 ± 0,03 mM TEAC/100 mg de extracto seco. Relación de correlación TFC/DPPH (r= -0,9941; R2 = 0,9884), TFC/ABTS (r= 0,9971; R2 = 0,9944), TPC/DPPH (r = 0,5694; R2 = 0,3243) y TPC/ABTS (r = -0,5960; R2 = 0,3553). La DL50 fue 9602 mg/kg. Se evidenció disminución significativa del edema de la pata de rata (p<0.05) desde la primera hora, en contraste con el control negativo. El mayor porcentaje de inhibición antiinflamatoria (75,75 %) fue a las 7 horas con una dosis de 500 mg/kg de HELSA, siendo superior al efecto del ibuprofeno (39,40%) y menor a la dexametasona (87,87%).

Conclusiones: El contenido total de flavonoides y polifenoles del extracto hidroalcohólico de las hojas de S. alata exhiben potencial actividad antiinflamatoria en un modelo de inflamación aguda que debería examinarse con otros modelos experimentales para iniciar los ensayos clínicos en humanos.

Palabras Clave: actividad antioxidante in vitro; biofenoles; efecto antiinflamatorio; flavonoides; Senna alata.

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Citation Format: Chávez H, Alvarado AT, Tasayco N, Pineda M, García JA, Bendezú MR, Surco F, Palomino JJ, Laos D, Melgar EJ, Vega N, Ferreyra C, Yarasca PE, Calderon DF, Bolarte M, Loja B (2025) Anti-inflammatory effect of the total flavonoid content of the hydroalcoholic extract of the leaves of Senna alata (L.) Roxb. in an experimental model of acute inflammation. J Pharm Pharmacogn Res 13(1): 444–458. https://doi.org/10.56499/jppres24.2100_13.2.444
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