Why the study?
Given its regulation of lipid dysfunction and anti-inflammatory and antioxidative effects, this study investigated the cardioprotective effect and mechanism of Fufang Zhenzhu Tiao Zhi formula in diabetic cardiomyopathy.
Does Fufang Zhenzhu Tiao Zhi (FTZ) formula improve cardiac function and reduce oxidative stress and inflammasome activation in diabetic cardiomyopathy mice?
Does Fufang Zhenzhu Tiao Zhi (FTZ) formula improve cardiac function and reduce oxidative stress and inflammasome activation in diabetic cardiomyopathy mice?
The Chinese herbal medicine FTZ protects against diabetic cardiomyopathy in preclinical models by alleviating lipotoxicity-induced oxidative stress and NLRP3 inflammasome activation.
FTZ attenuates diabetic cardiomyopathy in mice; hypothesis-generating and requires human trials before any clinical consideration.
BACKGROUND: Fufang Zhenzhu Tiao Zhi (FTZ) formula is a Chinese herbal preparation used in the clinical treatment of disorders of glucolipid metabolism. Given its effective actions on the regulation of lipid dysfunction and its anti-inflammatory and antioxidative effects, we designed this study to investigate the cardioprotective effect and possible mechanism of FTZ in diabetic cardiomyopathy (DCM) mice. METHODS: FTZ was administered to diabetic mice by oral gavage daily at a dose of 1.2 g/kg or 2.4 g/kg bodyweight for 8 weeks. Doppler echocardiography, H&E, and WGA staining were used to evaluate cardiac function and structure in the mice. The levels of proinflammatory cytokines and lipids in serum were detected with corresponding commercial kits. Immunofluorescence staining and flow cytometry were used to detect oxidation damage and pyroptosis in myocardial cells. RT-PCR and western blotting were used to analyze the protein and mRNA expression levels of NLRP3 inflammasome-related genes. RESULTS: Our study indicated that FTZ improved cardiac function, attenuated heart hypertrophy, improved serum lipid and proinflammatory cytokine levels, and restrained oxidative stress and NLRP3 inflammasome-induced inflammatory activities in diabetic mouse hearts. The in vitro data suggested that FTZ suppressed intercellular lipid accumulation as well as palmitic acid (PA)-induced oxidative stress and NLRP3 inflammasome-dependent pyroptosis in cardiomyocytes. CONCLUSION: Our present findings indicate that FTZ inhibits DCM by inhibiting both oxidative stress and NLRP3 inflammasome activation induced by cardiac lipotoxicity.
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Yan et al. (2022) studied this question.
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