Hyperbilirubinemia Protects against Aging-Associated Inflammation and Metabolic Deterioration.
Jaroslav ZelenkaAleš DvořákLukáš AlánMarie ZadinováMartin HaluzíkLibor VítekPublished in: Oxidative medicine and cellular longevity (2016)
Mild constitutive hyperbilirubinemia is associated with a reduced risk of cardiovascular diseases, diabetes, and cancer. Since these pathologies are associated with aging, inflammation, and oxidative stress, we investigated whether hyperbilirubinemia interferes with ROS homeostasis in cell cultures and with inflammation, senescence, and mitochondrial dysfunction in aged rats. Human embryonic kidney cells and rat primary fibroblasts showed a dose-dependent decrease in the ratio of oxidized/reduced glutathione, intracellular H2O2 levels, and mitochondrial ROS production, with increasing bilirubin concentrations in the culture media. Compared to their normobilirubinemic siblings, aged hyperbilirubinemic Gunn rats showed significantly smaller amounts of visceral fat, better glucose tolerance, and decreased serum levels of proinflammatory cytokines TNFα, IL-1β, and IL-18. Simultaneously, livers from Gunn rats showed decreased expression of senescence markers and cell cycle inhibitors p21 and p16. Mitochondria from aged Gunn rats showed higher respiration and lower H2O2 production compared to controls. In conclusion, we demonstrated that mildly elevated serum bilirubin is generally associated with attenuation of oxidative stress and with better anthropometric parameters, decreased inflammatory status, increased glucose tolerance, fewer signs of cellular senescence, and enhanced mitochondrial function in aged rats.
Keyphrases
- oxidative stress
- dna damage
- induced apoptosis
- cell cycle
- endothelial cells
- cardiovascular disease
- cell death
- ischemia reperfusion injury
- diabetic rats
- reactive oxygen species
- type diabetes
- adipose tissue
- body composition
- stress induced
- insulin resistance
- skeletal muscle
- cell cycle arrest
- mass spectrometry
- poor prognosis
- metabolic syndrome
- long non coding rna
- high resolution
- endoplasmic reticulum stress
- induced pluripotent stem cells
- bone marrow
- heat shock protein
- autism spectrum disorder