4.4 Article

Ascorbic acid and hydrocortisone synergistically inhibit septic organ injury via improving oxidative stress and inhibiting inflammation

Journal

IMMUNOPHARMACOLOGY AND IMMUNOTOXICOLOGY
Volume 44, Issue 5, Pages 786-794

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/08923973.2022.2082978

Keywords

Sepsis; hydrocortisone; ascorbic acid; liver injury; kidney injury; oxidative stress

Funding

  1. Research Foundation of Anhui Medical University [2019xkj186]

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The combination of ascorbic acid and hydrocortisone has a synergistic effect in protecting against septic organ injury by inhibiting the inflammatory response and oxidative stress, with the antioxidative effect of ascorbic acid contributing to the anti-inflammatory action.
Background The current study aimed to investigate the effect of the combination of ascorbic acid (AscA) and hydrocortisone (Hyd) on septic organ injury and its potential mechanism. Method Sepsis was induced in mice by a single intraperitoneal injection of lipopolysaccharides. Results AscA and Hyd combined showed more effective protection of the injured liver and kidney in septic mice by decreasing alanine aminotransferase, aspartate aminotransferase, serum urea nitrogen, and serum creatinine and ameliorating pathological manifestations than Hyd or AscA alone. AscA showed a mild inhibitory effect on the secretion of proinflammatory cytokines (tumor necrosis factor-alpha (TNF-alpha), interleukin-1 beta (IL-1 beta), and interleukin-6 (IL-6)). However, Hyd showed a weak regulatory effect on septic oxidative stress markers (malondialdehyde (MDA), superoxide dismutase (SOD), and glutathione peroxidase (GSH-Px)). However, the combination of AscA and Hyd showed a more powerful inhibitory effect on the septic inflammatory response and oxidative stress than Hyd or AscA alone by decreasing TNF-alpha, IL-1 beta, and IL-6 and regulating MDA, SOD, and GSH. In an in vitro study, cotreatment of RAW 264.7 macrophages with Hyd and AscA sharply reduced reactive oxygen species (ROS) generation and synergistically inhibited TNF-alpha, IL-1 beta, and IL-6 secretion, which could be abolished by additional stimulation with the ROS donor 3-nitropropionic acid (3-NP). As expected, cotreatment of macrophages with Hyd and AscA synergistically inhibited the activation of p38 MAPK and p-p65, and the effect could be reversed by additional stimulation with 3-NP. Conclusions AscA and Hyd synergistically protect the kidney and liver from injury by inhibiting the inflammatory response and oxidative stress. The powerful inhibitory effects of AscA on oxidative stress contribute to the synergistic anti-inflammatory action.

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