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NAFLD Aggravates Septic Shock Due to Inadequate Adrenal Response and 11β-HSDs Dysregulation in Rats.

Pharmaceutics (2020-05-02)
Hui-Chun Huang, Ming-Hung Tsai, Fa-Yauh Lee, Te-Yueh Lin, Ching-Chih Chang, Chiao-Lin Chuang, Shao-Jung Hsu, Ming-Chih Hou, Yi-Hsiang Huang
RÉSUMÉ

Non-alcoholic fatty liver disease (NAFLD) is linked with metabolic syndrome. Previous studies showed that obesity may disrupt adrenal function and adversely affect its counter-regulations against shock. This study hence evaluated adrenal function abnormalities in NAFLD with shock. Sprague-Dawley rats were fed with regular chow-diet (control) or high fat diet (HFD, 60% energy derived from fat). Blood tests were performed at the end of the 4th, 6th and 8th week, respectively. Experiments were performed at the end of the 8th week. HFD rats developed NAFLD. HFD rats had 27% and 51% increase in plasma corticosterone at the 6th and 8th week in usual status. However, HFD rats had 5 times more reduction of mean arterial pressure in response to lipopolysaccharide-induced sepsis as compared to control rats. The corticosterone increment ratio was also lower in HFD rats, even after ACTH administration. 11β-HSD system tended to generate more corticosterone in HFD rats under hemodynamic stable status without shock and the trend was lost in HFD rats with septic shock. Rats with NAFLD had profound septic shock due to inadequate corticosterone response. This is, at least partly, due to 11β-HSDs dysregulation in sepsis.

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Sigma-Aldrich
Aldosterone, ≥95% (HPLC)
Sigma-Aldrich
Rabbit Anti-Sheep IgG Antibody, HRP conjugate, Chemicon®, from rabbit