Treatment with crocin attenuates cardiac metabolic disturbances and subsequent inflammation in streptozotocin-induced diabetes.

IF 3.5 2区 生物学 Q3 CELL BIOLOGY
Dimitra Palioura, Konstantinos Feidantsis, Antigone Lazou
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引用次数: 0

Abstract

Diabetes mellitus (DM) is a metabolic disorder closely associated with cardiac dysfunction. Natural products are considered potential candidates for the management of DM. Crocin, a natural carotenoid derived from saffron, has been reported to possess several pharmacological properties, including cardioprotective effects. The aim of the present study was to investigate the beneficial effects of crocin on the metabolic derangement of the diabetic myocardium. Streptozotocin (STZ)-induced diabetic rats were treated with 10 mg/kg of crocin daily for two weeks. Oral administration of crocin normalized blood glucose, HbA1c, triglycerides, total cholesterol, LDL, and HDL levels. Notably, crocin reduced the elevated protein levels of cardiac PPARα and PPARδ-major transcriptional regulators of cardiac metabolism-back to normal. Consequently, the expression of the fatty acid (FA) transporter CD36 was downregulated, the activity of the FA oxidation enzyme 3-hydroxyacyl-CoA dehydrogenase (HOAD) was decreased, and intramyocardial triglyceride accumulation returned to physiological levels. Furthermore, crocin improved glucose uptake and metabolism in the diabetic myocardium, as evidenced by increased Akt phosphorylation, translocation of GLUT4 to the plasma membrane, enhanced activity of pyruvate kinase, and downregulation of pyruvate dehydrogenase kinase 4 (PDK4). Importantly, the stimulatory effect of crocin on Akt phosphorylation was also confirmed in isolated cardiac myocytes exposed to high glucose, further supporting its direct role in modulating glucose signaling pathways. Crocin treatment also reduced STZ-induced elevations in the levels of inflammatory cytokines-interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α)-as well as the phosphorylation of IκBα, bringing them close to basal levels. Overall, these findings suggest that crocin activates Akt signaling and thereby alleviates diabetes-induced metabolic disturbances by restoring the balance between glucose and fatty acid utilization in the hearts of STZ-induced diabetic rats. Therefore, crocin supplementation may represent a promising approach for the development of natural compound-based adjunct therapies for diabetic cardiomyopathy.

用藏红花素治疗可减轻链脲佐菌素引起的糖尿病的心脏代谢紊乱和随后的炎症。
糖尿病是一种与心功能障碍密切相关的代谢性疾病。天然产物被认为是糖尿病治疗的潜在候选者。藏红花素是一种从藏红花中提取的天然类胡萝卜素,据报道具有多种药理特性,包括心脏保护作用。本研究旨在探讨藏红花素对糖尿病心肌代谢紊乱的有益作用。链脲佐菌素(STZ)诱导的糖尿病大鼠每天给予10 mg/kg的藏红花素治疗2周。口服藏红花素使血糖、糖化血红蛋白、甘油三酯、总胆固醇、低密度脂蛋白和高密度脂蛋白水平正常化。值得注意的是,藏红花素使升高的心脏PPARα和ppar δ(心脏代谢的主要转录调节因子)的蛋白水平恢复正常。因此,脂肪酸(FA)转运体CD36的表达下调,FA氧化酶3-羟基酰基辅酶a脱氢酶(HOAD)活性降低,心内甘油三酯积累恢复到生理水平。此外,藏红花素改善了糖尿病心肌的葡萄糖摄取和代谢,如Akt磷酸化增加,GLUT4向质膜移位,丙酮酸激酶活性增强,丙酮酸脱氢酶激酶4 (PDK4)下调。重要的是,在暴露于高糖环境下的离体心肌细胞中,藏红花素对Akt磷酸化的刺激作用也得到了证实,进一步支持其在调节葡萄糖信号通路中的直接作用。藏红花素治疗还降低了stz诱导的炎症细胞因子-白细胞介素-6 (IL-6)和肿瘤坏死因子-α (TNF-α)水平升高以及IκBα磷酸化水平,使其接近基础水平。综上所述,这些发现表明藏红花素激活Akt信号,从而通过恢复stz诱导的糖尿病大鼠心脏中葡萄糖和脂肪酸利用之间的平衡来缓解糖尿病诱导的代谢紊乱。因此,藏红花素补充剂可能代表了一种有前途的方法,为开发天然化合物为基础的辅助治疗糖尿病心肌病。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Molecular and Cellular Biochemistry
Molecular and Cellular Biochemistry 生物-细胞生物学
CiteScore
8.30
自引率
2.30%
发文量
293
审稿时长
1.7 months
期刊介绍: Molecular and Cellular Biochemistry: An International Journal for Chemical Biology in Health and Disease publishes original research papers and short communications in all areas of the biochemical sciences, emphasizing novel findings relevant to the biochemical basis of cellular function and disease processes, as well as the mechanics of action of hormones and chemical agents. Coverage includes membrane transport, receptor mechanism, immune response, secretory processes, and cytoskeletal function, as well as biochemical structure-function relationships in the cell. In addition to the reports of original research, the journal publishes state of the art reviews. Specific subjects covered by Molecular and Cellular Biochemistry include cellular metabolism, cellular pathophysiology, enzymology, ion transport, lipid biochemistry, membrane biochemistry, molecular biology, nuclear structure and function, and protein chemistry.
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