Stigmasterol inhibits lipopolysaccharide-induced innate immune responses in murine models

被引:49
作者
Antwi, Aaron O. [1 ]
Obiri, David D. [1 ]
Osafo, Newman [1 ]
Forkuo, Arnold D. [1 ]
Essel, Leslie B. [1 ]
机构
[1] Kwame Nkrumah Univ Sci & Technol, Coll Hlth Sci, Fac Pharm & Pharmaceut Sci, Dept Pharmacol, Kumasi, Ghana
关键词
Stigmasterol; Lipopolysaccharide-induced; Inflammation; OXIDATIVE STRESS; LIPOIC ACID; TNF-ALPHA; INFLAMMATION; EXPRESSION; SEPSIS; CELLS; LPS; PHYTOSTEROLS; RECEPTORS;
D O I
10.1016/j.intimp.2017.10.018
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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 100 mg/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 100 mg/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 100 mg/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 100 mg/kg significantly protected mice from LPS-induced mortality with 40% survival. Overall, stigmasterol inhibits LPS-induced innate immune responses in murine models.
引用
收藏
页码:105 / 113
页数:9
相关论文
共 51 条
  • [1] Bacterial lipopolysaccharides and innate immunity
    Alexander, C
    Rietschel, ET
    [J]. JOURNAL OF ENDOTOXIN RESEARCH, 2001, 7 (03): : 167 - 202
  • [2] Endothelium-derived toll-like receptor-4 is the key molecule in LPS-induced neutrophil sequestration into lungs
    Andonegui, G
    Bonder, CS
    Green, F
    Mullaly, SC
    Zbytnuik, L
    Raharjo, E
    Kubes, P
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (07) : 1011 - 1020
  • [3] Anochie P., 2013, INT J MICROBIOL IMMU, V2, P37
  • [4] Stigmasterol Modulates Allergic Airway Inflammation in Guinea Pig Model of Ovalbumin-Induced Asthma
    Antwi, Aaron Opoku
    Obiri, David Darko
    Osafo, Newman
    [J]. MEDIATORS OF INFLAMMATION, 2017, 2017
  • [5] Severe sepsis and septic shock - Definitions, epidemiology, and clinical manifestations
    Balk, RA
    [J]. CRITICAL CARE CLINICS, 2000, 16 (02) : 179 - +
  • [6] Host defense mechanisms triggered by microbial lipoproteins through toll-like receptors
    Brightbill, HD
    Libraty, DH
    Krutzik, SR
    Yang, RB
    Belisle, JT
    Bleharski, JR
    Maitland, M
    Norgard, MV
    Plevy, SE
    Smale, ST
    Brennan, PJ
    Bloom, BR
    Godowski, PJ
    Modlin, RL
    [J]. SCIENCE, 1999, 285 (5428) : 732 - 736
  • [7] Chen WP, 2012, ACTA BIOCHIM POL, V59, P537
  • [8] Infiltration of inflammatory cells plays an important role in matrix metalloproteinase expression and activation in the heart during sepsis
    Cuenca, Jimena
    Martin-Sanz, Paloma
    Alvarez-Barrrientos, Alberto M.
    Bosca, Lisardo
    Goren, Nora
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2006, 169 (05) : 1567 - 1576
  • [9] Bacterial manipulation of innate immunity to promote infection
    Diacovich, Lautaro
    Gorvel, Jean-Pierre
    [J]. NATURE REVIEWS MICROBIOLOGY, 2010, 8 (02) : 117 - 128
  • [10] Infection, fever, and exogenous and endogenous pyrogens: some concepts have changed
    Dinarello, CA
    [J]. JOURNAL OF ENDOTOXIN RESEARCH, 2004, 10 (04): : 201 - 222