TY - JOUR
T1 - Obesity Exacerbates Sepsis-Induced Oxidative Damage in Organs
AU - Petronilho, Fabricia
AU - Giustina, Amanda Della
AU - Nascimento, Diego Zapelini
AU - Zarbato, Graciela Freitas
AU - Vieira, Andriele Aparecida
AU - Florentino, Drielly
AU - Danielski, Lucinéia Gainski
AU - Goldim, Mariana Pereira
AU - Rezin, Gislaine Tezza
AU - Barichello, Tatiana
N1 - Publisher Copyright:
© 2016, Springer Science+Business Media New York.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Sepsis progression is linked to the imbalance between reactive oxygen species and antioxidant enzymes. Sepsis affects multiple organs, but when associated with a chronic inflammatory disease, such as obesity, it may be exacerbated. We hypothesized that obesity could aggravate the oxidative damage to peripheral organs of rats submitted to an animal model of sepsis. Male Wistar rats aged 8 weeks received hypercaloric nutrition for 2 months to induce obesity. Sepsis was induced by cecal ligation and puncture (CLP) procedure, and sham-operated rats were considered as control group. The experimental groups were divided into sham + eutrophic, sham + obese, CLP + eutrophic, and CLP + obese. Twelve and 24 h after surgery, oxidative damage to lipids and proteins and superoxide dismutase (SOD) and catalase (CAT) activities were evaluated in the liver, lung, kidney, and heart. The data indicate that obese rats subjected to sepsis present oxidative stress mainly in the lung and liver. This alteration reflected an oxidative damage to lipids and proteins and an imbalance of SOD and CAT levels, especially 24 h after sepsis. It follows that obesity due to its pro-inflammatory phenotype can aggravate sepsis-induced damage in peripheral organs.
AB - Sepsis progression is linked to the imbalance between reactive oxygen species and antioxidant enzymes. Sepsis affects multiple organs, but when associated with a chronic inflammatory disease, such as obesity, it may be exacerbated. We hypothesized that obesity could aggravate the oxidative damage to peripheral organs of rats submitted to an animal model of sepsis. Male Wistar rats aged 8 weeks received hypercaloric nutrition for 2 months to induce obesity. Sepsis was induced by cecal ligation and puncture (CLP) procedure, and sham-operated rats were considered as control group. The experimental groups were divided into sham + eutrophic, sham + obese, CLP + eutrophic, and CLP + obese. Twelve and 24 h after surgery, oxidative damage to lipids and proteins and superoxide dismutase (SOD) and catalase (CAT) activities were evaluated in the liver, lung, kidney, and heart. The data indicate that obese rats subjected to sepsis present oxidative stress mainly in the lung and liver. This alteration reflected an oxidative damage to lipids and proteins and an imbalance of SOD and CAT levels, especially 24 h after sepsis. It follows that obesity due to its pro-inflammatory phenotype can aggravate sepsis-induced damage in peripheral organs.
KW - inflammation
KW - obesity
KW - organs
KW - oxidative stress
KW - sepsis
UR - https://www.scopus.com/pages/publications/84988421361
UR - https://www.scopus.com/inward/citedby.url?scp=84988421361&partnerID=8YFLogxK
U2 - 10.1007/s10753-016-0444-x
DO - 10.1007/s10753-016-0444-x
M3 - Article
C2 - 27645696
AN - SCOPUS:84988421361
SN - 0360-3997
VL - 39
SP - 2062
EP - 2071
JO - Inflammation
JF - Inflammation
IS - 6
ER -