4.7 Article

Polyphenols-Rich Fraction from Annona muricata Linn. Leaves Attenuates Oxidative and Inflammatory Responses in Neutrophils, Macrophages, and Experimental Lung Injury

期刊

PHARMACEUTICS
卷 14, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/pharmaceutics14061182

关键词

Annonaceae; natural products; neutrophils; macrophages; reactive oxygen species; acute lung injury

资金

  1. Foundation for Research Support of the Minas Gerais State-FAPEMIG [APQ-01856-14, APQ-01981-16]
  2. National Institute of Science and Technology in Theranostics and Nanobiotechnology-INCT-TeraNano (CNPq) [465669/2014-0]
  3. National Post-Doctoral Scholarship Program (PNPD-CAPES)
  4. FAPEMIG [PPM-00503-18]
  5. CNPq (PQ-Research productivity) [312812/2021-3]

向作者/读者索取更多资源

In this study, the antioxidant and anti-inflammatory activities of polyphenols-rich fractions from Annona muricata L. leaves were investigated. The fractions reduced the generation of reactive oxygen species and secretion of inflammatory markers in immune cells. Furthermore, these fractions attenuated oxidative damage and inflammation in experimental acute lung injury. These findings suggest that these fractions might be explored for the development of new therapies for inflammatory conditions.
Annona muricata Linn. is a common plant found in the warmest regions of South and Central America and its use in traditional medicine has been reported for the treatment of various illnesses. In the current study, we investigate the antioxidant and anti-inflammatory activities of crude extract and fractions from A. muricata L. leaves in isolated murine phagocytic immune cells as well as experimental LPS-induced acute lung injury (ALI). In a luminol-dependent chemiluminescence assay, we showed that ethyl acetate (EtOAc.f) and n-butanol (BuOH.f) fractions-both rich in polyphenols-reduced the generation of reactive oxygen species (ROS) by neutrophils stimulated with opsonized zymosan; similar results were found in culture of bone marrow-derived macrophages (BMDMs). By evaluating anti-inflammatory activity in BMDMs, EtOAc.f and BuOH.f reduced secretion of IL-6 and expression of the co-stimulatory molecule CD40. Furthermore, in LPS-induced ALI, oral administration of EtOAc.f reduced myeloperoxidase (MPO) activity in lung tissue. In addition, on a mechanism dependent on glutathione levels, the oxidative damage was also attenuated. These findings revealed direct antioxidant and anti-inflammatory activities of polyphenols-rich fractions of A. muricata L. leaves on neutrophils and macrophages. Moreover, the reduced oxidative damage and levels of inflammatory markers in experimental ALI suggest that these fractions might be explored for the development of new therapies for inflammatory conditions.

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