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Mice chronically fed high-fat diet have increased mortality and disturbed immune response in sepsis.

Louise Strandberg ; Margareta Verdrengh ; Maria Enge ; Niklas Andersson ; Sylvie Amu ; Karin Önnheim ; Anna Benrick ; Mikael Brisslert ; Johan Bylund ; Maria Bokarewa ; Staffan Nilsson (Institutionen för matematiska vetenskaper, matematisk statistik) ; John-Olov Jansson
PloS one (1932-6203). Vol. 4 (2009), 10, p. e7605.
[Artikel, refereegranskad vetenskaplig]

BACKGROUND: Sepsis is a potentially deadly disease that often is caused by gram-positive bacteria, in particular Staphylococcus aureus (S. aureus). As there are few effective therapies for sepsis, increased basic knowledge about factors predisposing is needed. METHODOLOGY/PRINCIPAL FINDINGS: The purpose of this study was to study the effect of Western diet on mortality induced by intravenous S. aureus inoculation and the immune functions before and after bacterial inoculation. Here we show that C57Bl/6 mice on high-fat diet (HFD) for 8 weeks, like genetically obese Ob/Ob mice on low-fat diet (LFD), have increased mortality during S. aureus-induced sepsis compared with LFD-fed C57Bl/6 controls. Bacterial load in the kidneys 5-7 days after inoculation was increased 10-fold in HFD-fed compared with LFD-fed mice. At that time, HFD-fed mice had increased serum levels and fat mRNA expression of the immune suppressing cytokines interleukin-1 receptor antagonist (IL-1Ra) and IL-10 compared with LFD-fed mice. In addition, HFD-fed mice had increased serum levels of the pro-inflammatory IL-1beta. Also, HFD-fed mice with and without infection had increased levels of macrophages in fat. The proportion and function of phagocytosing granulocytes, and the production of reactive oxygen species (ROS) by peritoneal lavage cells were decreased in HFD-fed compared with LFD-fed mice. CONCLUSIONS: Our findings imply that chronic HFD disturb several innate immune functions in mice, and impairs the ability to clear S. aureus and survive sepsis.



Denna post skapades 2010-02-03. Senast ändrad 2015-01-16.
CPL Pubid: 111473

 

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Institutioner (Chalmers)

Institutionen för neurovetenskap och fysiologi, sektionen för fysiologi (GU)
Institutionen för medicin, avdelningen för reumatologi och inflammationsforskning (GU)
Institutionen för matematiska vetenskaper, matematisk statistik (2005-2016)

Ämnesområden

Fysiologi

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