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KMID : 1040620220280020232
Clinical and Molecular Hepatology
2022 Volume.28 No. 2 p.232 ~ p.241
Galectin-3 inhibits cardiac contractility via a tumor necrosis factor alpha-dependent mechanism in cirrhotic rats
Yoon Ki-Tae

Liu Hongqun
Zhang Jing
Han So-Jung
Lee Samuel S.
Abstract
Background/Aims: Galectin-3 plays a key pathogenic role in cardiac hypertrophy and heart failure. The present study aimed to investigate the effects of galectin-3 on cardiomyopathy ? related factors and cardiac contractility in a rat model of cirrhotic cardiomyopathy.

Methods: Rats were divided into two sets, one for a functional study, the other for cardiac contractile-related protein evaluation. There were four groups in each set: sham operated and sham plus N-acetyllactosamine (N-Lac, a galectin-3 inhibitor; 5 mg/kg); bile duct ligated (BDL) and BDL plus N-Lac. Four weeks after surgery, ventricular level of galectin-3, collagen I and III ratio, tumor necrosis factor alpha (TNF¥á), and brain natriuretic peptide (BNP) were measured either by Western blots or immunohistochemistry or enzyme-linked immunosorbent assay. Blood pressure was measured by polygraph recorder. Cardiomyocyte contractility was measured by inverted microscopy.

Results: Galectin-3 and collagen I/III ratio were significantly increased in cirrhotic hearts. TNF¥á and BNP were significantly increased in BDL serum and heart compared with sham controls. Galectin-3 inhibitor significantly decreased galectin-3, TNF¥á, and BNP in cirrhotic hearts but not in sham controls. N-Lac also significantly improved the blood pressure, and systolic and diastolic cardiomyocyte contractility in cirrhotic rats but had no effect on sham controls.

Conclusion: Increased galectin-3 in the cirrhotic heart significantly inhibited contractility via TNF¥á. Inhibition of galectin-3 decreased the cardiac content of TNF¥á and BNP and reversed the decreased blood pressure and depressed contractility in the cirrhotic heart. Galectin-3 appears to play a pathogenic role in cirrhotic cardiomyopathy.
KEYWORD
Cardiomyopathy, cirrhosis, Galectin-3, Tumor necrosis factor alpha, Heart failure
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