Antihyperalgesic Activity of Quillaic Acid Obtained from Quillaja Saponaria Mol.

Author:

Arrau Sylvia1,Rodríguez-Díaz Maité2,Cassels Bruce K.3,Valenzuela-Barra Gabriela4,Delporte Carla4,Barriga Andrés5,Miranda Hugo F.6

Affiliation:

1. Departamento Nucleo de Salud, Facultad de Medicina Veterinaria, Universidad Mayor, 8580745, Santiago, Chile

2. Escuela de Quimica y Farmacia, Facultad de Medicina, Universidad Andres Bello, 8370092, Santiago, Chile

3. Departamento de Quimica, Facultad de Ciencias, Universidad de Chile, 7800003, Santiago, Chile

4. Departamento de Quimica Farmacologica y Toxicologica, Facultad de Ciencias Quimicas y Farmaceuticas, Universidad de Chile, 8380494, Santiago, Chile

5. Unidad de Espectrometria de Masa, Facultad de Ciencias Quimicas y Farmaceuticas, Universidad de Chile. 8380492, Santiago, Chile

6. Escuela de Medicina, Programa de Farmacologia, Instituto de Ciencias Biomedicas, Facultad de Medicina, Universidad de Chile, 8380456, Santiago, Chile

Abstract

Background: Quillaja saponaria Mol. bark contains a high concentration of triterpene saponins that have been used for centuries as a cleansing, antiinflammatory and analgesic agent in Chilean folk medicine. In earlier studies, in mice, both the anti-inflammatory as well as the antinociceptive effect of the major sapogenin, quillaic acid have been demonstrated (QA). Objective: To determine the antihyperalgesic effect of QA one and seven days after itpl administration of complete Freund's adjuvant (CFA) in male mice using the hot plate test in the presence of complete Freund's adjuvant (HP/CFA) as an acute and chronic skeletal muscle pain model. Methods: The present study evaluated the antihyperalgesic activity of QA against acute and chronic skeletal muscle pain models in mice using the hot plate test in the presence of complete Freund's adjuvant (HP/CFA), at 24 h (acute assay) and 7 days (chronic assay) , with dexketoprofen (DEX) as the reference drug. Results: In acute and chronic skeletal muscle pain assays, QA at 30 mg/kg ip elicited its maximal antihyperalgesic effects (65.0% and 53.4%) at 24 h and 7 days, respectively. The maximal effect of DEX (99.0 and 94.1 at 24 h and 7 days, respectively) was induced at 100 mg/kg. Conclusion: QA and DEX elicit dose-dependent antihyperalgesic effects against acute and chronic skeletal muscle pain, but QA is more potent than DEX in the early and late periods of inflammatory pain induced by CFA.

Funder

National Fund for Scientific and Technological Development

Publisher

Bentham Science Publishers Ltd.

Subject

Drug Discovery,General Medicine

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. New Experimental and Computational Tools for Drug Discovery. - Part-VII;Current Topics in Medicinal Chemistry;2019-07-25

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