Recombinant Human Annexin A5 Alleviated Traumatic-Brain-Injury Induced Intestinal Injury by Regulating the Nrf2/HO-1/HMGB1 Pathway
Open Access
- 6 September 2022
- Vol. 27 (18) , 5755
Abstract
Aims: Annexin A5 (ANXA5) exhibited potent antithrombotic, antiapoptotic, and anti-inflammatory properties in a previous study. The role of ANXA5 in traumatic brain injury (TBI)-induced intestinal injury is not fully known. Main methods: Recombinant human ANXA5 (50 µg/kg) or vehicle (PBS) was administered to mice via the tail vein 30 min after TBI. Mouse intestine tissue was gathered for hematoxylin and eosin staining 0.5 d, 1 d, 2 d, and 7 d after modeling. Intestinal Western blotting, immunofluorescence, TdT-mediated dUTP nick-end labeling staining, and enzyme-linked immunosorbent assays were performed 2 days after TBI. A series of kits were used to assess lipid peroxide indicators such as malonaldehyde, superoxide dismutase activity, and catalase activity. Key findings: ANXA5 treatment improved the TBI-induced intestinal mucosa injury at different timepoints and significantly increased the body weight. It significantly reduced apoptosis and matrix metalloproteinase-9 and inhibited the degradation of tight-junction-associated protein in the small intestine. ANXA5 treatment improved intestinal inflammation by regulating inflammation-associated factors. It also mitigated the lipid peroxidation products 4-HNE, 8-OHDG, and malonaldehyde, and enhanced the activity of the antioxidant enzymes, superoxide dismutase and catalase. Lastly, ANXA5 significantly enhanced nuclear factor E2-related factor 2 (Nrf2) and hemeoxygenase-1, and decreased high mobility group box 1 (HMGB1). Significance: Collectively, the results suggest that ANXA5 inhibits TBI-induced intestinal injury by restraining oxidative stress and inflammatory responses. The mechanisms involved sparking the Nrf2/hemeoxygenase-1-induced antioxidant system and suppressing the HMGB1 pathway. ANXA5 may be an attractive therapeutic candidate for protecting against TBI-induced intestinal injury.Keywords
Funding Information
- National Natural Science Foundation of China (81330029)
This publication has 42 references indexed in Scilit:
- Cerebroprotection by the neuronal PGE2 receptor EP2 after intracerebral hemorrhage in middle-aged miceJournal of Cerebral Blood Flow & Metabolism, 2016
- Higenamine regulates Nrf2-HO-1-Hmgb1 axis and attenuates intestinal ischemia–reperfusion injury in miceInflammation Research, 2015
- Stimulating the Central Nervous System to Prevent Intestinal Dysfunction After Traumatic Brain InjuryJournal of Trauma: Injury, Infection & Critical Care, 2010
- Increased intestinal inflammatory response and gut barrier dysfunction in Nrf2-deficient mice after traumatic brain injuryCytokine, 2008
- Molecular mechanisms of Nrf2‐mediated antioxidant responseMolecular Carcinogenesis, 2008
- Extracellular annexin A5: Functions of phosphatidylserine-binding and two-dimensional crystallizationBiochimica et Biophysica Acta (BBA) - Molecular Cell Research, 2008
- Heme Oxygenase-1 Protects against Neutrophil-Mediated Intestinal Damage by Down-Regulation of Neutrophil p47 phox and p67 phox Activity and O2− Production in a Two-Hit Model of Alcohol Intoxication and Burn InjuryThe Journal of Immunology, 2008
- High-mobility group box 1 protein (HMGB1): nuclear weapon in the immune arsenalNature Reviews Immunology, 2005
- Alterations of intestinal mucosa structure and barrier function following traumatic brain injury in ratsWorld Journal of Gastroenterology, 2003
- Intestinal Mucosal Lesion in Low-Flow StatesArchives of Surgery, 1970