Key result
Short-term high glucose treatment increased miRNA-21 expression (p < 0.05) without cellular damage, whereas miRNA-21 reduction at 7 days induced damage pathways and compromised mitochondrial function.
Why the study?
miRNA-21 is a crucial regulator of developing cardiac diseases, but its role remains controversial, requiring clarification of its involvement in high glucose-induced acute and chronic cardiac damage.
p-value: p=<0.05
In human cardiomyocytes, miRNA-21 acts as an early defense mechanism against high glucose-induced injury, regulating mitochondrial respiration and metabolic flexibility.
miRNA-21 modulation warrants in vivo validation before any therapeutic consideration in diabetic cardiomyopathy; leaves open its role in metabolic flexibility.
AIM: miRNA-21 is a crucial regulator of developing cardiac diseases, but its role is still controversial, and therefore it is necessary to clarify, at cardiac level, its involvement in high glucose induced-acute and chronic cardiac damage. METHODS: Human ventricular cardiac myoblasts AC16, treated and not with miRNA-21 inhibitor, were exposed to high glucose for 2 and 7 days, and the expression of damage markers were investigated. Further, cardiac energetic metabolism was evaluated by measuring both the expression of glucose transporters and lipids regulators. RESULTS: Short-term high glucose treatment induced a significant increase in miRNA-21 expression (p < 0.05) that was associated with an increase in hydrogen ion flux and energy potential dissipation without any change in energy production or increase in genes expression involved in cellular damage. miRNA-21 reduction observed (p < 0.05) at 7 days of high glucose treatment, induced the activation of damage pathways and compromised mitochondrial function (p < 0.05). CONCLUSION: In human cardiomyocytes, the abundance of miRNA-21 takes part in first defense mechanism against cardiac insult and its cardioprotective effect depends on time of exposure to injury. Moreover, miRNA-21 regulates mitochondrial respiration and the ability of cells to select the most appropriate substrate for ATP production in given environment.
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Scisciola et al. (2022) studied High glucose induced-acute and chronic cardiac damage. High glucose treatment with or without miRNA-21 inhibitor vs. Untreated cells was evaluated on miRNA-21 expression, damage markers, and cardiac energetic metabolism (p=<0.05). Short-term high glucose treatment increased miRNA-21 expression (p < 0.05) without cellular damage, whereas miRNA-21 reduction at 7 days induced damage pathways and compromised mitochondrial function.
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