Stigmasterol inhibits lipopolysaccharide-induced innate immune responses in murine models

Stigmasterol is a naturally occurring steroid alcohol which occurs in vegetables, soya and a large variety of medicinal plants. Stigmasterol and other phytosterols have been documented as immunomodulators with huge therapeutic potential. We assessed the mitigating effect of stigmasterol on non-fatal...

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Veröffentlicht in:International immunopharmacology 2017-12, Vol.53, p.105-113
Hauptverfasser: Antwi, Aaron O., Obiri, David D., Osafo, Newman, Forkuo, Arnold D., Essel, Leslie B.
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container_start_page 105
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creator Antwi, Aaron O.
Obiri, David D.
Osafo, Newman
Forkuo, Arnold D.
Essel, Leslie B.
description Stigmasterol is a naturally occurring steroid alcohol which occurs in vegetables, soya and a large variety of medicinal plants. Stigmasterol and other phytosterols have been documented as immunomodulators with huge therapeutic potential. We assessed the mitigating effect of stigmasterol on non-fatal and fatal innate immune responses in murine models after intraperitoneal challenge with an endotoxin, lipopolysaccharide, LPS. The effect of stigmasterol on LPS-induced febrile response, inflammatory cell proliferation, multiple organ damage and mortality were respectively investigated. Pretreatment with stigmasterol 10, 50 and 100mg/kg reduced total LPS-induced fever response by 39.93±10.52%, 53.05±5.84% and 77.27±6.25% respectively. Neutrophil proliferation both in blood and recovered peritoneal fluid was significantly reversed by stigmasterol at 50 and 100mg/kg. Lung and liver histopathology showed stigmasterol effectively controlled organ damage. The lung inflammation score of 9.20±0.73 for the polyethylene glycol, PEG-treated disease control mice was reduced respectively to 6.50±0.54, 4.60±0.40 and 4.10±0.42 with 10, 50 and 100mg/kg of stigmasterol. Serum levels of liver enzyme markers, alanine transaminase, ALT and aspartate transaminase, AST were consistent with the observed histological changes. Stigmasterol at 50 and 100mg/kg significantly protected mice from LPS-induced mortality with 40% survival. Overall, stigmasterol inhibits LPS-induced innate immune responses in murine models. [Display omitted] •Stigmasterol alleviates lipopolysaccharide-induced pyrexia in Wistar rats.•Lipopolysaccharide-induced multiple organ damage is inhibited by stigmasterol.•Neutrophil accumulation in blood and peritoneal fluid is abated by stigmasterol.
doi_str_mv 10.1016/j.intimp.2017.10.018
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Stigmasterol and other phytosterols have been documented as immunomodulators with huge therapeutic potential. We assessed the mitigating effect of stigmasterol on non-fatal and fatal innate immune responses in murine models after intraperitoneal challenge with an endotoxin, lipopolysaccharide, LPS. The effect of stigmasterol on LPS-induced febrile response, inflammatory cell proliferation, multiple organ damage and mortality were respectively investigated. Pretreatment with stigmasterol 10, 50 and 100mg/kg reduced total LPS-induced fever response by 39.93±10.52%, 53.05±5.84% and 77.27±6.25% respectively. Neutrophil proliferation both in blood and recovered peritoneal fluid was significantly reversed by stigmasterol at 50 and 100mg/kg. Lung and liver histopathology showed stigmasterol effectively controlled organ damage. The lung inflammation score of 9.20±0.73 for the polyethylene glycol, PEG-treated disease control mice was reduced respectively to 6.50±0.54, 4.60±0.40 and 4.10±0.42 with 10, 50 and 100mg/kg of stigmasterol. Serum levels of liver enzyme markers, alanine transaminase, ALT and aspartate transaminase, AST were consistent with the observed histological changes. Stigmasterol at 50 and 100mg/kg significantly protected mice from LPS-induced mortality with 40% survival. Overall, stigmasterol inhibits LPS-induced innate immune responses in murine models. [Display omitted] •Stigmasterol alleviates lipopolysaccharide-induced pyrexia in Wistar rats.•Lipopolysaccharide-induced multiple organ damage is inhibited by stigmasterol.•Neutrophil accumulation in blood and peritoneal fluid is abated by stigmasterol.</description><identifier>ISSN: 1567-5769</identifier><identifier>EISSN: 1878-1705</identifier><identifier>DOI: 10.1016/j.intimp.2017.10.018</identifier><identifier>PMID: 29078089</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Alanine ; Alanine transaminase ; Alanine Transaminase - blood ; Alcohols ; Animal models ; Animals ; Aspartate transaminase ; Cell proliferation ; Cell Proliferation - drug effects ; Cells, Cultured ; Disease control ; Disease Models, Animal ; Female ; Fever ; Fever - chemically induced ; Fever - drug therapy ; Histopathology ; Humans ; Immune response ; Immunity, Innate ; Immunomodulation ; Immunomodulators ; Inflammation ; Inflammation - chemically induced ; Inflammation - drug therapy ; Injections, Intraperitoneal ; Innate immunity ; Lipopolysaccharide-induced ; Lipopolysaccharides ; Lipopolysaccharides - administration &amp; dosage ; Liver ; Lung - drug effects ; Lung - pathology ; Lungs ; Male ; Medicinal plants ; Mice ; Mice, Inbred C57BL ; Mortality ; Neutrophils - immunology ; Peritoneal fluid ; Peritoneum ; Phytosterols ; Plants (botany) ; Polyethylene glycol ; Rats ; Rats, Wistar ; Serum levels ; Sterols ; Stigmasterol ; Transaminase ; Vegetables</subject><ispartof>International immunopharmacology, 2017-12, Vol.53, p.105-113</ispartof><rights>2017 Elsevier B.V.</rights><rights>Copyright © 2017 Elsevier B.V. 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Stigmasterol and other phytosterols have been documented as immunomodulators with huge therapeutic potential. We assessed the mitigating effect of stigmasterol on non-fatal and fatal innate immune responses in murine models after intraperitoneal challenge with an endotoxin, lipopolysaccharide, LPS. The effect of stigmasterol on LPS-induced febrile response, inflammatory cell proliferation, multiple organ damage and mortality were respectively investigated. Pretreatment with stigmasterol 10, 50 and 100mg/kg reduced total LPS-induced fever response by 39.93±10.52%, 53.05±5.84% and 77.27±6.25% respectively. Neutrophil proliferation both in blood and recovered peritoneal fluid was significantly reversed by stigmasterol at 50 and 100mg/kg. Lung and liver histopathology showed stigmasterol effectively controlled organ damage. The lung inflammation score of 9.20±0.73 for the polyethylene glycol, PEG-treated disease control mice was reduced respectively to 6.50±0.54, 4.60±0.40 and 4.10±0.42 with 10, 50 and 100mg/kg of stigmasterol. Serum levels of liver enzyme markers, alanine transaminase, ALT and aspartate transaminase, AST were consistent with the observed histological changes. Stigmasterol at 50 and 100mg/kg significantly protected mice from LPS-induced mortality with 40% survival. Overall, stigmasterol inhibits LPS-induced innate immune responses in murine models. 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The lung inflammation score of 9.20±0.73 for the polyethylene glycol, PEG-treated disease control mice was reduced respectively to 6.50±0.54, 4.60±0.40 and 4.10±0.42 with 10, 50 and 100mg/kg of stigmasterol. Serum levels of liver enzyme markers, alanine transaminase, ALT and aspartate transaminase, AST were consistent with the observed histological changes. Stigmasterol at 50 and 100mg/kg significantly protected mice from LPS-induced mortality with 40% survival. Overall, stigmasterol inhibits LPS-induced innate immune responses in murine models. [Display omitted] •Stigmasterol alleviates lipopolysaccharide-induced pyrexia in Wistar rats.•Lipopolysaccharide-induced multiple organ damage is inhibited by stigmasterol.•Neutrophil accumulation in blood and peritoneal fluid is abated by stigmasterol.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>29078089</pmid><doi>10.1016/j.intimp.2017.10.018</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-7906-9534</orcidid></addata></record>
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subjects Alanine
Alanine transaminase
Alanine Transaminase - blood
Alcohols
Animal models
Animals
Aspartate transaminase
Cell proliferation
Cell Proliferation - drug effects
Cells, Cultured
Disease control
Disease Models, Animal
Female
Fever
Fever - chemically induced
Fever - drug therapy
Histopathology
Humans
Immune response
Immunity, Innate
Immunomodulation
Immunomodulators
Inflammation
Inflammation - chemically induced
Inflammation - drug therapy
Injections, Intraperitoneal
Innate immunity
Lipopolysaccharide-induced
Lipopolysaccharides
Lipopolysaccharides - administration & dosage
Liver
Lung - drug effects
Lung - pathology
Lungs
Male
Medicinal plants
Mice
Mice, Inbred C57BL
Mortality
Neutrophils - immunology
Peritoneal fluid
Peritoneum
Phytosterols
Plants (botany)
Polyethylene glycol
Rats
Rats, Wistar
Serum levels
Sterols
Stigmasterol
Transaminase
Vegetables
title Stigmasterol inhibits lipopolysaccharide-induced innate immune responses in murine models
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