Protective Effect of Nopal Cactus (Opuntia ficus-indica) Seed Oil against Short-Term Lipopolysaccharides-Induced Inflammation and Peroxisomal Functions Dysregulation in Mouse Brain and Liver

• Published in: International journal of molecular sciences 2022-10, Vol.23 (19), p.11849
• Main Authors: Tahri-Joutey, Mounia, Saih, Fatima-Ezzahra, El Kebbaj, Riad, Gondcaille, Catherine, Vamecq, Joseph, Latruffe, Norbert, Lizard, Gérard, Savary, Stéphane, Nasser, Boubker, Cherkaoui-Malki, Mustapha, Andreoletti, Pierre
• Format: Article
• Language: English
• Subjects: ACOX1; Animals; Antioxidants; Brain; cactus seed oil; Carbon monoxide; CAT gene; Catalase; Cytokines; Endocrinology and metabolism; Endotoxins; Enzymatic activity; Enzymes; Fatty acids; Flavonoids; Gene expression; Glutathione Peroxidase; GPx; Human health and pathology; IL-1β; Il-6; Inflammation; Interleukin 6; Life Sciences; Lipids; Lipopolysaccharides; Liver; Metabolism; Mice; Neuroprotection; Oils & fats; Oilseeds; Olive Oil; Opuntia; Opuntia ficus-indica; Oxidation; Peroxidase; Polyphenols; Proteins; Sepsis
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms231911849

Exposure to endotoxins (lipopolysaccharides, LPS) may lead to a potent inflammatory cytokine response and a severe impairment of metabolism, causing tissue injury. The protective effect provided by cactus seed oil (CSO), from Opuntia ficus-indica, was evaluated against LPS-induced inflammation, dysregulation of peroxisomal antioxidant, and β-oxidation activities in the brain and the liver. In both tissues, a short-term LPS exposure increased the proinflammatory interleukine-1β (Il-1β), inducible Nitroxide synthase (iNos), and Interleukine-6 (Il-6). In the brain, CSO action reduced only LPS-induced iNos expression, while in the liver, CSO attenuated mainly the hepatic Il-1β and Il-6. Regarding the peroxisomal antioxidative functions, CSO treatment (as Olive oil (OO) or Colza oil (CO) treatment) induced the hepatic peroxisomal Cat gene. Paradoxically, we showed that CSO, as well as OO or CO, treatment can timely induce catalase activity or prevent its induction by LPS, respectively, in both brain and liver tissues. On the other hand, CSO (as CO) pretreatment prevented the LPS-associated Acox1 gene and activity decreases in the liver. Collectively, CSO showed efficient neuroprotective and hepato-protective effects against LPS, by maintaining the brain peroxisomal antioxidant enzyme activities of catalase and glutathione peroxidase, and by restoring hepatic peroxisomal antioxidant and β-oxidative capacities.