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Biochemical Properties and Effects on Mitochondrial Respiration of Aqueous Extracts of Basidiomycete Mushrooms.

Alex Graça ContatoTatiane BrugnariAna Paula Ames SibinAna Julia Dos Reis BuzzoAnacharis Babeto de Sá-NakanishiLívia BrachtCiomar Aparecida Bersani-AmadoRosane Marina PeraltaCristina Giatti Marques de Souza
Published in: Cell biochemistry and biophysics (2020)
There are different varieties of mushrooms not yet studied spread all over the planet. The objective of this study was to evaluate biochemical properties and effects on mitochondrial respiration of eight Basidiomycete mushrooms: Flaviporus venustus EF30, Hydnopolyporus fimbriatus EF41 and EF44, Inonotus splitgerberi EF46, Oudemansiella canarii EF72, Perenniporia sp. EF79, Phellinus linteus EF81, and Pleurotus albidus EF84. Total phenols, ABTS, TEAC, FRAP, and ORAC were measured in order to determine the antioxidant capacity. Antimicrobial potential was studied by disc-diffusion and microdilution method. Cytotoxicity was determined in murine peritoneal macrophages. The bioenergetic aspects were evaluated by the uncoupling of the oxidative phosphorylation in mitochondrias. The H. fimbriatus mushroom was the one that presented the most significant results for the antioxidant assays. Three mushrooms presented antimicrobial activity, indicating a potential for formulation of drugs. The results suggest that I. spligerberi has an uncoupling activity, even at the lowest concentration tested, dissipating the mitochondrial electrochemical gradient. On the other hand, P. albidus has effect only on succinate-oxidase activity without influencing mitochondrial respiratory efficiency. Therefore, both interfere negatively in mitochondrial respiration. In relation with the cytotoxicity in peritoneal macrophages, O. canarii and F. venustus were cytotoxic in this type of cells.
Keyphrases
  • oxidative stress
  • induced apoptosis
  • drug delivery
  • ionic liquid
  • staphylococcus aureus
  • nitric oxide
  • single cell
  • climate change
  • human health
  • nitric oxide synthase
  • mass spectrometry
  • risk assessment
  • signaling pathway