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  1. Article: Nuclear control of the inflammatory response in mammals by peroxisome proliferator-activated receptors.

    Mandard, Stéphane / Patsouris, David

    PPAR research

    2013  Volume 2013, Page(s) 613864

    Abstract: Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that play pivotal roles in the regulation of a very large number of biological processes including inflammation. Using specific examples, this paper focuses on ...

    Abstract Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors that play pivotal roles in the regulation of a very large number of biological processes including inflammation. Using specific examples, this paper focuses on the interplay between PPARs and innate immunity/inflammation and, when possible, compares it among species. We focus on recent discoveries establishing how inflammation and PPARs interact in the context of obesity-induced inflammation and type 2 diabetes, mostly in mouse and humans. We illustrate that PPAR γ ability to alleviate obesity-associated inflammation raises an interesting pharmacologic potential. In the light of recent findings, the protective role of PPAR α and PPAR β / δ against the hepatic inflammatory response is also addressed. While PPARs agonists are well-established agents that can treat numerous inflammatory issues in rodents and humans, surprisingly very little has been described in other species. We therefore also review the implication of PPARs in inflammatory bowel disease; acute-phase response; and central, cardiac, and endothelial inflammation and compare it along different species (mainly mouse, rat, human, and pig). In the light of the data available in the literature, there is no doubt that more studies concerning the impact of PPAR ligands in livestock should be undertaken because it may finally raise unconsidered health and sanitary benefits.
    Language English
    Publishing date 2013-03-07
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2237981-2
    ISSN 1687-4765 ; 1687-4757
    ISSN (online) 1687-4765
    ISSN 1687-4757
    DOI 10.1155/2013/613864
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Immune response of BV-2 microglial cells is impacted by peroxisomal beta-oxidation.

    Tawbeh, Ali / Raas, Quentin / Tahri-Joutey, Mounia / Keime, Céline / Kaiser, Romain / Trompier, Doriane / Nasser, Boubker / Bellanger, Emma / Dessard, Marie / Hamon, Yannick / Benani, Alexandre / Di Cara, Francesca / Cunha Alves, Tânia / Berger, Johannes / Weinhofer, Isabelle / Mandard, Stéphane / Cherkaoui-Malki, Mustapha / Andreoletti, Pierre / Gondcaille, Catherine /
    Savary, Stéphane

    Frontiers in molecular neuroscience

    2023  Volume 16, Page(s) 1299314

    Abstract: Microglia are crucial for brain homeostasis, and dysfunction of these cells is a key driver in most neurodegenerative diseases, including peroxisomal leukodystrophies. In X-linked adrenoleukodystrophy (X-ALD), a neuroinflammatory disorder, very long- ... ...

    Abstract Microglia are crucial for brain homeostasis, and dysfunction of these cells is a key driver in most neurodegenerative diseases, including peroxisomal leukodystrophies. In X-linked adrenoleukodystrophy (X-ALD), a neuroinflammatory disorder, very long-chain fatty acid (VLCFA) accumulation due to impaired degradation within peroxisomes results in microglial defects, but the underlying mechanisms remain unclear. Using CRISPR/Cas9 gene editing of key genes in peroxisomal VLCFA breakdown (
    Language English
    Publishing date 2023-12-18
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2452967-9
    ISSN 1662-5099
    ISSN 1662-5099
    DOI 10.3389/fnmol.2023.1299314
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Human cholesteryl ester transfer protein lacks lipopolysaccharide transfer activity, but worsens inflammation and sepsis outcomes in mice.

    Dusuel, Aloïs / Deckert, Valérie / Pais de Barros, Jean-Paul / van Dongen, Kevin / Choubley, Hélène / Charron, Émilie / Le Guern, Naig / Labbé, Jérôme / Mandard, Stéphane / Grober, Jacques / Lagrost, Laurent / Gautier, Thomas

    Journal of lipid research

    2020  Volume 62, Page(s) 100011

    Abstract: Bacterial lipopolysaccharides (LPSs or endotoxins) can bind most proteins of the lipid transfer/LPS-binding protein (LT/LBP) family in host organisms. The LPS-bound LT/LBP proteins then trigger either an LPS-induced proinflammatory cascade or LPS binding ...

    Abstract Bacterial lipopolysaccharides (LPSs or endotoxins) can bind most proteins of the lipid transfer/LPS-binding protein (LT/LBP) family in host organisms. The LPS-bound LT/LBP proteins then trigger either an LPS-induced proinflammatory cascade or LPS binding to lipoproteins that are involved in endotoxin inactivation and detoxification. Cholesteryl ester transfer protein (CETP) is an LT/LBP member, but its impact on LPS metabolism and sepsis outcome is unclear. Here, we performed fluorescent LPS transfer assays to assess the ability of CETP to bind and transfer LPS. The effects of intravenous (iv) infusion of purified LPS or polymicrobial infection (cecal ligation and puncture [CLP]) were compared in transgenic mice expressing human CETP and wild-type mice naturally having no CETP activity. CETP displayed no LPS transfer activity in vitro, but it tended to reduce biliary excretion of LPS in vivo. The CETP expression in mice was associated with significantly lower basal plasma lipid levels and with higher mortality rates in both models of endotoxemia and sepsis. Furthermore, CETPTg plasma modified cytokine production of macrophages in vitro. In conclusion, despite having no direct LPS binding and transfer property, human CETP worsens sepsis outcomes in mice by altering the protective effects of plasma lipoproteins against endotoxemia, inflammation, and infection.
    MeSH term(s) Cholesterol Ester Transfer Proteins
    Chemical Substances CETP protein, human ; Cholesterol Ester Transfer Proteins
    Language English
    Publishing date 2020-12-15
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80154-9
    ISSN 1539-7262 ; 0022-2275
    ISSN (online) 1539-7262
    ISSN 0022-2275
    DOI 10.1194/jlr.RA120000704
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: Physiological and Nutritional Roles of PPAR across Species.

    Bionaz, Massimo / Hausman, Gary J / Loor, Juan J / Mandard, Stéphane

    PPAR research

    2013  Volume 2013, Page(s) 807156

    Language English
    Publishing date 2013-05-15
    Publishing country United States
    Document type Journal Article
    ZDB-ID 2237981-2
    ISSN 1687-4765 ; 1687-4757
    ISSN (online) 1687-4765
    ISSN 1687-4757
    DOI 10.1155/2013/807156
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Role of Diet and Nutrients in SARS-CoV-2 Infection: Incidence on Oxidative Stress, Inflammatory Status and Viral Production.

    Brahmi, Fatiha / Vejux, Anne / Ghzaiel, Imen / Ksila, Mohamed / Zarrouk, Amira / Ghrairi, Taoufik / Essadek, Soukena / Mandard, Stéphane / Leoni, Valerio / Poli, Giuseppe / Vervandier-Fasseur, Dominique / Kharoubi, Omar / El Midaoui, Adil / Atanasov, Atanas G / Meziane, Smail / Latruffe, Norbert / Nasser, Boubker / Bouhaouala-Zahar, Balkiss / Masmoudi-Kouki, Olfa /
    Madani, Khodir / Boulekbache-Makhlouf, Lila / Lizard, Gérard

    Nutrients

    2022  Volume 14, Issue 11

    Abstract: Coronavirus illness (COVID-19) is an infectious pathology generated by intense severe respiratory syndrome coronavirus 2 (SARS-CoV-2). This infectious disease has emerged in 2019. The COVID-19-associated pandemic has considerably affected the way of life ...

    Abstract Coronavirus illness (COVID-19) is an infectious pathology generated by intense severe respiratory syndrome coronavirus 2 (SARS-CoV-2). This infectious disease has emerged in 2019. The COVID-19-associated pandemic has considerably affected the way of life and the economy in the world. It is consequently crucial to find solutions allowing remedying or alleviating the effects of this infectious disease. Natural products have been in perpetual application from immemorial time given that they are attested to be efficient towards several illnesses without major side effects. Various studies have shown that plant extracts or purified molecules have a promising inhibiting impact towards coronavirus. In addition, it is substantial to understand the characteristics, susceptibility and impact of diet on patients infected with COVID-19. In this review, we recapitulate the influence of extracts or pure molecules from medicinal plants on COVID-19. We approach the possibilities of plant treatment/co-treatment and feeding applied to COVID-19. We also show coronavirus susceptibility and complications associated with nutrient deficiencies and then discuss the major food groups efficient on COVID-19 pathogenesis. Then, we covered emerging technologies using plant-based SARS-CoV-2 vaccine. We conclude by giving nutrient and plants curative therapy recommendations which are of potential interest in the COVID-19 infection and could pave the way for pharmacological treatments or co-treatments of COVID-19.
    MeSH term(s) Antiviral Agents/therapeutic use ; COVID-19 ; COVID-19 Vaccines ; Diet ; Humans ; Incidence ; Nutrients ; Oxidative Stress ; SARS-CoV-2
    Chemical Substances Antiviral Agents ; COVID-19 Vaccines
    Language English
    Publishing date 2022-05-25
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2518386-2
    ISSN 2072-6643 ; 2072-6643
    ISSN (online) 2072-6643
    ISSN 2072-6643
    DOI 10.3390/nu14112194
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Protective Effect of Cactus Cladode Extracts on Peroxisomal Functions in Microglial BV-2 Cells Activated by Different Lipopolysaccharides.

    Saih, Fatima-Ezzahra / Andreoletti, Pierre / Mandard, Stéphane / Latruffe, Norbert / El Kebbaj, M'Hammed Saïd / Lizard, Gérard / Nasser, Boubker / Cherkaoui-Malki, Mustapha

    Molecules (Basel, Switzerland)

    2017  Volume 22, Issue 1

    Abstract: In this study, we aimed to evaluate the antioxidant and anti-inflammatory properties ... ...

    Abstract In this study, we aimed to evaluate the antioxidant and anti-inflammatory properties of
    MeSH term(s) Animals ; Anti-Inflammatory Agents/pharmacology ; Antioxidants/pharmacology ; Catalase/metabolism ; Cell Line ; Escherichia coli ; Fatty Acids/metabolism ; Lipopolysaccharides ; Mice ; Microglia/cytology ; Microglia/drug effects ; Microglia/metabolism ; Neuroprotective Agents/pharmacology ; Nitric Oxide/metabolism ; Opuntia/chemistry ; Oxidation-Reduction/drug effects ; Oxidative Stress/drug effects ; Peroxisomes/metabolism ; Plant Extracts/pharmacology ; Reactive Oxygen Species/metabolism ; Salmonella
    Chemical Substances Anti-Inflammatory Agents ; Antioxidants ; Fatty Acids ; Lipopolysaccharides ; Neuroprotective Agents ; Plant Extracts ; Reactive Oxygen Species ; Nitric Oxide (31C4KY9ESH) ; Catalase (EC 1.11.1.6)
    Language English
    Publishing date 2017-01-07
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 1413402-0
    ISSN 1420-3049 ; 1431-5165 ; 1420-3049
    ISSN (online) 1420-3049
    ISSN 1431-5165 ; 1420-3049
    DOI 10.3390/molecules22010102
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Inhibition of mitophagy drives macrophage activation and antibacterial defense during sepsis.

    Patoli, Danish / Mignotte, Franck / Deckert, Valérie / Dusuel, Alois / Dumont, Adélie / Rieu, Aurélie / Jalil, Antoine / Van Dongen, Kevin / Bourgeois, Thibaut / Gautier, Thomas / Magnani, Charlène / Le Guern, Naig / Mandard, Stéphane / Bastin, Jean / Djouadi, Fatima / Schaeffer, Christine / Guillaumot, Nina / Narce, Michel / Nguyen, Maxime /
    Guy, Julien / Dargent, Auguste / Quenot, Jean-Pierre / Rialland, Mickaël / Masson, David / Auwerx, Johan / Lagrost, Laurent / Thomas, Charles

    The Journal of clinical investigation

    2020  Volume 130, Issue 11, Page(s) 5858–5874

    Abstract: Mitochondria have emerged as key actors of innate and adaptive immunity. Mitophagy has a pivotal role in cell homeostasis, but its contribution to macrophage functions and host defense remains to be delineated. Here, we showed that lipopolysaccharide ( ... ...

    Abstract Mitochondria have emerged as key actors of innate and adaptive immunity. Mitophagy has a pivotal role in cell homeostasis, but its contribution to macrophage functions and host defense remains to be delineated. Here, we showed that lipopolysaccharide (LPS) in combination with IFN-γ inhibited PINK1-dependent mitophagy in macrophages through a STAT1-dependent activation of the inflammatory caspases 1 and 11. In addition, we demonstrated that the inhibition of mitophagy triggered classical macrophage activation in a mitochondrial ROS-dependent manner. In a murine model of polymicrobial infection (cecal ligature and puncture), adoptive transfer of Pink1-deficient bone marrow or pharmacological inhibition of mitophagy promoted macrophage activation, which favored bactericidal clearance and led to a better survival rate. Reciprocally, mitochondrial uncouplers that promote mitophagy reversed LPS/IFN-γ-mediated activation of macrophages and led to immunoparalysis with impaired bacterial clearance and lowered survival. In critically ill patients, we showed that mitophagy was inhibited in blood monocytes of patients with sepsis as compared with nonseptic patients. Overall, this work demonstrates that the inhibition of mitophagy is a physiological mechanism that contributes to the activation of myeloid cells and improves the outcome of sepsis.
    MeSH term(s) Animals ; Bacteria/immunology ; Female ; Humans ; Interferon-gamma/immunology ; Lipopolysaccharides/immunology ; Macrophage Activation ; Macrophages, Peritoneal/immunology ; Macrophages, Peritoneal/microbiology ; Macrophages, Peritoneal/pathology ; Male ; Mice ; Mitophagy/immunology ; Protein Kinases/immunology ; RAW 264.7 Cells ; Sepsis/immunology ; Sepsis/microbiology ; Sepsis/pathology
    Chemical Substances IFNG protein, human ; IFNG protein, mouse ; Lipopolysaccharides ; Interferon-gamma (82115-62-6) ; Protein Kinases (EC 2.7.-) ; PTEN-induced putative kinase (EC 2.7.11.1)
    Language English
    Publishing date 2020-08-05
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 3067-3
    ISSN 1558-8238 ; 0021-9738
    ISSN (online) 1558-8238
    ISSN 0021-9738
    DOI 10.1172/JCI130996
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  8. Article ; Online: A role for peroxisome proliferator-activated receptor gamma in resveratrol-induced colon cancer cell apoptosis.

    Aires, Virginie / Brassart, Bertrand / Carlier, Annie / Scagliarini, Alessandra / Mandard, Stéphane / Limagne, Emeric / Solary, Eric / Martiny, Laurent / Tarpin, Michel / Delmas, Dominique

    Molecular nutrition & food research

    2014  Volume 58, Issue 9, Page(s) 1785–1794

    Abstract: Scope: Resveratrol may function as a chemopreventive agent. A recent clinical study demonstrates a reduction in tumor cell proliferation in colorectal patients receiving repeated oral ingestion of resveratrol. However, gaps remain in our knowledge of ... ...

    Abstract Scope: Resveratrol may function as a chemopreventive agent. A recent clinical study demonstrates a reduction in tumor cell proliferation in colorectal patients receiving repeated oral ingestion of resveratrol. However, gaps remain in our knowledge of the molecular mechanisms by which resveratrol exerts its chemopreventive effect. We have previously demonstrated that resveratrol induces apoptosis in colon cancer cells and that resveratrol can sensitize chemoresistant colon cancer cells to various drugs. Based on its ability to activate peroxisome proliferator-activated receptor gamma (PPARγ) in colon cancer cells, we sought to determine the implication of this nuclear transcription factor in resveratrol-induced apoptosis.
    Methods and results: Transient transfection of cancer cells with a dominant-negative PPARγ mutant or treatment with a PPARγ antagonist (GW9662) reversed the inhibitory effect of resveratrol. Moreover, GW9662 prevented disruption of the cell cycle induced by resveratrol and consequently abrogated resveratrol-induced apoptosis. Tumor cell death was potentiated by combining resveratrol with rosiglitazone, a PPARγ agonist.
    Conclusion: The results show that PPARγ plays a role in resveratrol-induced apoptosis of colon carcinoma cells. The combination of resveratrol with a PPARγ agonist could be a promising pharmacological approach for treatment of colorectal cancer.
    MeSH term(s) Anilides/pharmacology ; Apoptosis/drug effects ; Cell Line, Tumor/drug effects ; Cell Proliferation/drug effects ; Colonic Neoplasms/drug therapy ; Colonic Neoplasms/pathology ; Humans ; PPAR gamma/agonists ; PPAR gamma/antagonists & inhibitors ; PPAR gamma/genetics ; PPAR gamma/metabolism ; S Phase Cell Cycle Checkpoints/drug effects ; Stilbenes/pharmacology ; Thiazolidinediones/pharmacology
    Chemical Substances 2-chloro-5-nitrobenzanilide ; Anilides ; PPAR gamma ; Stilbenes ; Thiazolidinediones ; rosiglitazone (05V02F2KDG) ; resveratrol (Q369O8926L)
    Language English
    Publishing date 2014-09
    Publishing country Germany
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2160372-8
    ISSN 1613-4133 ; 1613-4125
    ISSN (online) 1613-4133
    ISSN 1613-4125
    DOI 10.1002/mnfr.201300962
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  9. Article ; Online: Lipopolysaccharides-mediated increase in glucose-stimulated insulin secretion: involvement of the GLP-1 pathway.

    Nguyen, Anh Thoai / Mandard, Stéphane / Dray, Cédric / Deckert, Valérie / Valet, Philippe / Besnard, Philippe / Drucker, Daniel J / Lagrost, Laurent / Grober, Jacques

    Diabetes

    2014  Volume 63, Issue 2, Page(s) 471–482

    Abstract: Lipopolysaccharides (LPS) of the cell wall of gram-negative bacteria trigger inflammation, which is associated with marked changes in glucose metabolism. Hyperglycemia is frequently observed during bacterial infection and it is a marker of a poor ... ...

    Abstract Lipopolysaccharides (LPS) of the cell wall of gram-negative bacteria trigger inflammation, which is associated with marked changes in glucose metabolism. Hyperglycemia is frequently observed during bacterial infection and it is a marker of a poor clinical outcome in critically ill patients. The aim of the current study was to investigate the effect of an acute injection or continuous infusion of LPS on experimentally induced hyperglycemia in wild-type and genetically engineered mice. The acute injection of a single dose of LPS produced an increase in glucose disposal and glucose-stimulated insulin secretion (GSIS). Continuous infusion of LPS through mini-osmotic pumps was also associated with increased GSIS. Finally, manipulation of LPS detoxification by knocking out the plasma phospholipid transfer protein (PLTP) led to increased glucose disposal and GSIS. Overall, glucose tolerance and GSIS tests supported the hypothesis that mice treated with LPS develop glucose-induced hyperinsulinemia. The effects of LPS on glucose metabolism were significantly altered as a result of either the accumulation or antagonism of glucagon-like peptide 1 (GLP-1). Complementary studies in wild-type and GLP-1 receptor knockout mice further implicated the GLP-1 receptor-dependent pathway in mediating the LPS-mediated changes in glucose metabolism. Hence, enhanced GLP-1 secretion and action underlies the development of glucose-mediated hyperinsulinemia associated with endotoxemia.
    MeSH term(s) Animals ; Blood Glucose ; Glucagon-Like Peptide 1/genetics ; Glucagon-Like Peptide 1/metabolism ; Glucagon-Like Peptide-1 Receptor ; Glucose/metabolism ; Insulin/metabolism ; Lipopolysaccharides/metabolism ; Lipopolysaccharides/toxicity ; Mice ; Mice, Knockout ; Phospholipid Transfer Proteins/genetics ; Phospholipid Transfer Proteins/metabolism ; Receptors, Glucagon/genetics ; Receptors, Glucagon/metabolism
    Chemical Substances Blood Glucose ; Glp1r protein, mouse ; Glucagon-Like Peptide-1 Receptor ; Insulin ; Lipopolysaccharides ; Phospholipid Transfer Proteins ; Receptors, Glucagon ; phospholipid transfer protein, mouse ; Glucagon-Like Peptide 1 (89750-14-1) ; Glucose (IY9XDZ35W2)
    Language English
    Publishing date 2014-02
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 80085-5
    ISSN 1939-327X ; 0012-1797
    ISSN (online) 1939-327X
    ISSN 0012-1797
    DOI 10.2337/db13-0903
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article ; Online: Protective Effect of Argan and Olive Oils against LPS-Induced Oxidative Stress and Inflammation in Mice Livers.

    El Kamouni, Soufiane / El Kebbaj, Riad / Andreoletti, Pierre / El Ktaibi, Abderrahim / Rharrassi, Issam / Essamadi, Abdelkhalid / El Kebbaj, M'hammed Saïd / Mandard, Stéphane / Latruffe, Norbert / Vamecq, Joseph / Nasser, Boubker / Cherkaoui-Malki, Mustapha

    International journal of molecular sciences

    2017  Volume 18, Issue 10

    Abstract: Sepsis causes severe dysregulation of organ functions, via the development of oxidative stress and inflammation. These pathophysiological mechanisms are mimicked in mice injected with bacterial lipopolysaccharide (LPS). Here, protective properties of ... ...

    Abstract Sepsis causes severe dysregulation of organ functions, via the development of oxidative stress and inflammation. These pathophysiological mechanisms are mimicked in mice injected with bacterial lipopolysaccharide (LPS). Here, protective properties of argan oil against LPS-induced oxidative stress and inflammation are explored in the murine model. Mice received standard chow, supplemented with argan oil (AO) or olive oil (OO) for 25 days, before septic shock was provoked with a single intraperitoneal injection of LPS, 16 hours prior to animal sacrifice. In addition to a rise in oxidative stress and inflammatory markers, injected LPS also caused hepatotoxicity, accompanied by hyperglycemia, hypercholesterolemia and hyperuremia. These LPS-associated toxic effects were blunted by AO pretreatment, as corroborated by normal plasma parameters and cell stress markers (glutathione: GSH) and antioxidant enzymology (catalase, CAT; superoxide dismutase, SOD and glutathione peroxidase, GPx). Hematoxylin-eosin staining revealed that AO can protect against acute liver injury, maintaining a normal status, which is pointed out by absent or reduced LPS-induced hepatic damage markers (i.e., alanine aminotransferase (ALT) and aspartate transaminase (AST)). Our work also indicated that AO displayed anti-inflammatory activity, due to down-regulations of genes encoding pro-inflammatory cytokines Interleukin-6 (IL-6) and Tumor Necrosis Factor-α (TNF-α) and in up-regulations of the expression of anti-inflammatory genes encoding Interleukin-4 (IL-4) and Interleukin-10 (IL-10). OO provided animals with similar, though less extensive, protective changes. Collectively our work adds compelling evidence to the protective mechanisms of AO against LPS-induced liver injury and hence therapeutic potentialities, in regard to the management of human sepsis. Activations of IL-4/Peroxisome Proliferator-Activated Receptors (IL-4/PPARs) signaling and, under LPS, an anti-inflammatory IL-10/Liver X Receptor (IL-10/LXR) route, obviously indicated the high potency and plasticity of the anti-inflammatory properties of argan oil.
    MeSH term(s) Animals ; Anti-Inflammatory Agents/administration & dosage ; Anti-Inflammatory Agents/pharmacology ; Anti-Inflammatory Agents/therapeutic use ; Antioxidants/administration & dosage ; Antioxidants/pharmacology ; Antioxidants/therapeutic use ; Dietary Supplements ; Lipopolysaccharides/toxicity ; Liver/drug effects ; Liver/metabolism ; Liver Diseases/drug therapy ; Liver Diseases/etiology ; Liver Diseases/prevention & control ; Mice ; Olive Oil/administration & dosage ; Olive Oil/pharmacology ; Olive Oil/therapeutic use ; Oxidative Stress ; Plant Oils/administration & dosage ; Plant Oils/pharmacology ; Plant Oils/therapeutic use
    Chemical Substances Anti-Inflammatory Agents ; Antioxidants ; Lipopolysaccharides ; Olive Oil ; Plant Oils ; argan oil (4V59G5UW9X)
    Language English
    Publishing date 2017-10-19
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms18102181
    Database MEDical Literature Analysis and Retrieval System OnLINE

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