Abstract
Fatty liver is highly sensitive to inflammatory activation. Peroxisome proliferator-activated receptors (PPAR) have anti-inflammatory effects and regulate lipid metabolism in the fatty liver. We hypothesized that fatty liver leads to endotoxin sensitivity through an imbalance between pro- and anti-inflammatory signals. Leptin-deficient, ob/ob mice and their lean littermates were challenged with single or double insults and pro- and anti-inflammatory pathways were tested on cytokine production and activation of nuclear regulatory factors NF-κB and peroxisome proliferator receptor element (PPRE). Ob/ob mice produced significantly higher serum tumor necrosis factor α (TNF-α) and interleukin (IL) 6 and showed increased hepatic NF-κB activation compared to lean littermates after stimulation with a single dose of lipopolysaccharide (LPS) or alcohol. In ob/ob mice, double insults with alcohol and LPS augmented proinflammatory responses mediated by increased degradation of inhibitory κB (IκB)-α and IκB-β and preferential induction of the p65/p50 NF-κB heterodimer. In lean mice, in contrast, acute alcohol attenuated LPS-induced TNF-α, IL-6 production, and NF-κB activation through reduced IκB-α degradation and induction of p50/p50 homodimers. PPRE binding was increased in fatty but not in lean livers after alcohol or LPS stimulation. However, cotreatment with alcohol and LPS reduced both PPRE binding and nuclear levels of PPAR-α in fatty livers but increased those in lean livers. In conclusion, our results show opposite PPRE and NF-κB activation in fatty and lean livers. PPAR activation may represent an anti-inflammatory mechanism that fails in the fatty liver on increased proinflammatory pressure. Thus, an imbalance between PPAR-mediated anti-inflammatory and NF-κB-mediated proinflammatory signals may contribute to increased inflammation in the fatty liver.
| Original language | English |
|---|---|
| Pages (from-to) | 376-385 |
| Number of pages | 10 |
| Journal | Hepatology |
| Volume | 40 |
| Issue number | 2 |
| DOIs | |
| Publication status | Published - Aug 2004 |
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- Hepatology
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Diverse regulation of NF-κB and peroxisome proliferator-activated receptors in murine nonalcoholic fatty liver. / Romics, Laszlo; Kodys, Karen; Dolganiuc, Angela; Graham, Lucia; Velayudham, Arumugam; Mandrekar, Pranoti; Szabó, G.
In: Hepatology, Vol. 40, No. 2, 08.2004, p. 376-385.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Diverse regulation of NF-κB and peroxisome proliferator-activated receptors in murine nonalcoholic fatty liver
AU - Romics, Laszlo
AU - Kodys, Karen
AU - Dolganiuc, Angela
AU - Graham, Lucia
AU - Velayudham, Arumugam
AU - Mandrekar, Pranoti
AU - Szabó, G.
PY - 2004/8
Y1 - 2004/8
N2 - Fatty liver is highly sensitive to inflammatory activation. Peroxisome proliferator-activated receptors (PPAR) have anti-inflammatory effects and regulate lipid metabolism in the fatty liver. We hypothesized that fatty liver leads to endotoxin sensitivity through an imbalance between pro- and anti-inflammatory signals. Leptin-deficient, ob/ob mice and their lean littermates were challenged with single or double insults and pro- and anti-inflammatory pathways were tested on cytokine production and activation of nuclear regulatory factors NF-κB and peroxisome proliferator receptor element (PPRE). Ob/ob mice produced significantly higher serum tumor necrosis factor α (TNF-α) and interleukin (IL) 6 and showed increased hepatic NF-κB activation compared to lean littermates after stimulation with a single dose of lipopolysaccharide (LPS) or alcohol. In ob/ob mice, double insults with alcohol and LPS augmented proinflammatory responses mediated by increased degradation of inhibitory κB (IκB)-α and IκB-β and preferential induction of the p65/p50 NF-κB heterodimer. In lean mice, in contrast, acute alcohol attenuated LPS-induced TNF-α, IL-6 production, and NF-κB activation through reduced IκB-α degradation and induction of p50/p50 homodimers. PPRE binding was increased in fatty but not in lean livers after alcohol or LPS stimulation. However, cotreatment with alcohol and LPS reduced both PPRE binding and nuclear levels of PPAR-α in fatty livers but increased those in lean livers. In conclusion, our results show opposite PPRE and NF-κB activation in fatty and lean livers. PPAR activation may represent an anti-inflammatory mechanism that fails in the fatty liver on increased proinflammatory pressure. Thus, an imbalance between PPAR-mediated anti-inflammatory and NF-κB-mediated proinflammatory signals may contribute to increased inflammation in the fatty liver.
AB - Fatty liver is highly sensitive to inflammatory activation. Peroxisome proliferator-activated receptors (PPAR) have anti-inflammatory effects and regulate lipid metabolism in the fatty liver. We hypothesized that fatty liver leads to endotoxin sensitivity through an imbalance between pro- and anti-inflammatory signals. Leptin-deficient, ob/ob mice and their lean littermates were challenged with single or double insults and pro- and anti-inflammatory pathways were tested on cytokine production and activation of nuclear regulatory factors NF-κB and peroxisome proliferator receptor element (PPRE). Ob/ob mice produced significantly higher serum tumor necrosis factor α (TNF-α) and interleukin (IL) 6 and showed increased hepatic NF-κB activation compared to lean littermates after stimulation with a single dose of lipopolysaccharide (LPS) or alcohol. In ob/ob mice, double insults with alcohol and LPS augmented proinflammatory responses mediated by increased degradation of inhibitory κB (IκB)-α and IκB-β and preferential induction of the p65/p50 NF-κB heterodimer. In lean mice, in contrast, acute alcohol attenuated LPS-induced TNF-α, IL-6 production, and NF-κB activation through reduced IκB-α degradation and induction of p50/p50 homodimers. PPRE binding was increased in fatty but not in lean livers after alcohol or LPS stimulation. However, cotreatment with alcohol and LPS reduced both PPRE binding and nuclear levels of PPAR-α in fatty livers but increased those in lean livers. In conclusion, our results show opposite PPRE and NF-κB activation in fatty and lean livers. PPAR activation may represent an anti-inflammatory mechanism that fails in the fatty liver on increased proinflammatory pressure. Thus, an imbalance between PPAR-mediated anti-inflammatory and NF-κB-mediated proinflammatory signals may contribute to increased inflammation in the fatty liver.
UR - http://www.scopus.com/inward/record.url?scp=4043109947&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=4043109947&partnerID=8YFLogxK
U2 - 10.1002/hep.20304
DO - 10.1002/hep.20304
M3 - Article
C2 - 15368442
AN - SCOPUS:4043109947
VL - 40
SP - 376
EP - 385
JO - Hepatology
JF - Hepatology
SN - 0270-9139
IS - 2
ER -