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High-dose sinomenine attenuates ischemia/reperfusion-induced hepatic inflammation and oxidative stress in rats with diabetes mellitus.
Hui, Bo; Zhang, Xiaogang; Dong, Dinghui; Shu, Yantao; Li, Ren; Yang, Zhengan.
Affiliation
  • Hui B; Department of General Surgery Unit-4, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
  • Zhang X; Department of Hepatobiliary Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
  • Dong D; Department of Hepatobiliary Surgery, The First Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
  • Shu Y; Department of General Surgery Unit-4, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
  • Li R; Department of General Surgery Unit-4, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
  • Yang Z; Department of General Surgery Unit-4, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.
Immun Inflamm Dis ; 12(6): e1271, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38888355
ABSTRACT

INTRODUCTION:

Ischemia-reperfusion (I/R) injury, resulting from blood flow interruption and its subsequent restoration, is a prevalent complication in liver surgery. The liver, as a crucial organ for carbohydrate and lipid metabolism, exhibits decreased tolerance to hepatic I/R in patients with diabetes mellitus (DM), resulting in a significant increase in hepatic dysfunction following surgery. This may be attributed to elevated oxidative stress and inflammation. Our prior research established sinomenine's (SIN) protective role against hepatic I/R injury. Nevertheless, the impact of SIN on hepatic I/R injury in DM rats remains unexplored. OBJECTIVE AND

METHODS:

This study aimed to investigate the therapeutic potential of SIN in hepatic I/R injury in DM rats and elucidate its mechanism. Diabetic and hepatic I/R injury models were established in rats through high-fat/sugar diet, streptozotocin injection, and hepatic blood flow occlusion. Liver function, oxidative stress, inflammatory reaction, histopathology, and Nrf-2/HO-1 signaling pathway were evaluated by using UV spectrophotometry, biochemical assays, enzyme-linked immunosorbent assay, hematoxylin-eosin staining, and Western blot analysis.

RESULTS:

High-dose SIN (300 mg/kg) significantly attenuated hepatic I/R injury in DM rats, reducing serum activities of ALT and AST, decreasing the AST/ALT ratio, enhancing tissue contents of SOD and GSH-Px, suppressing the levels of TNF-α and IL-6, improving the liver histopathology, and activating Nrf-2/HO-1 signaling by promoting Nrf-2 trans-location from cytoplasm to nucleus. Low-dose SIN (100 mg/kg) was ineffective.

CONCLUSIONS:

This study demonstrates that high-dose sinomenine's mitigates hepatic I/R-induced inflammation and oxidative stress in diabetes mellitus (DM) rats via Nrf-2/HO-1 activation, suggesting its potential as a preventive strategy for hepatic I/R injury in DM patients.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Reperfusion Injury / Rats, Sprague-Dawley / Oxidative Stress / Diabetes Mellitus, Experimental / Liver / Morphinans Limits: Animals Language: En Journal: Immun Inflamm Dis Year: 2024 Document type: Article Affiliation country: Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Reperfusion Injury / Rats, Sprague-Dawley / Oxidative Stress / Diabetes Mellitus, Experimental / Liver / Morphinans Limits: Animals Language: En Journal: Immun Inflamm Dis Year: 2024 Document type: Article Affiliation country: Country of publication: