Department of Pharmacology and Toxicology, College of Pharmacy, Hawler Medical University, Erbil, 44001, Iraq.
Cell Mol Biol (Noisy-le-grand). 2023 Sep 30;69(9):106-112. doi: 10.14715/cmb/2023.69.9.15.
This study investigated the effects of trelagliptin and remogliflozin, alone and in combination with alpha lipoic acid (ALA), on cardiac biomarkers in diabetic cardiomyopathy (DCM). We aimed to assess the management of glucotoxicity consequences in streptozotocin-induced diabetic rats by measuring serum levels of pharmacologically active endogenous ligands. Forty-eight male rats were divided into different treatment groups, including negative control, positive control, and four experimental groups. After inducing diabetes, the rats were treated for 28 days, and serum levels of biomarkers associated with oxidative stress (malondialdehyde and thioredoxin-interacting protein), inflammation (nuclear factor NF-kappa-B p105 and lipoprotein-associated phospholipase A2), and myopathy (neprilysin and high selective cardiac troponin T) were measured. Immunohistochemical analysis of heart cells was also performed. The results showed that inducing hyperglycemia increased serum glucose levels and biomarkers associated with DCM. However, all treatment groups exhibited a significant decrease in these biomarkers and an increase in insulin levels compared to the diabetic control group. The groups receiving combination therapy with ALA showed greater improvements in cardiac biomarkers compared to the individual treatments. The immunohistochemical analysis supported these findings by demonstrating a reduction in the percentage area of cathepsin B, a protein involved in DCM pathophysiology. In conclusion, supplementing the base treatments with ALA showed promise in enhancing cardiac biomarkers associated with DCM. The combination of trelagliptin, remogliflozin, and ALA may have additional clinical value in managing DCM by targeting oxidative stress, inflammation, and glucotoxicity. However, further research is needed to validate these findings and explore their potential clinical applications.
本研究旨在探讨单独使用特立帕肽和瑞格列净,以及联合使用α-硫辛酸(ALA),对糖尿病心肌病(DCM)心脏生物标志物的影响。我们旨在通过测量药理学活性内源性配体的血清水平来评估链脲佐菌素诱导的糖尿病大鼠中糖毒性后果的管理。将 48 只雄性大鼠分为不同的治疗组,包括阴性对照组、阳性对照组和四个实验组。在诱导糖尿病后,大鼠接受 28 天治疗,测量与氧化应激(丙二醛和硫氧还蛋白相互作用蛋白)、炎症(核因子 NF-κB p105 和脂蛋白相关磷脂酶 A2)和肌病( Neprilysin 和高选择性心脏肌钙蛋白 T)相关的生物标志物的血清水平。还对心脏细胞进行了免疫组织化学分析。结果表明,诱导高血糖会增加血清葡萄糖水平和与 DCM 相关的生物标志物。然而,与糖尿病对照组相比,所有治疗组的这些生物标志物均显著降低,胰岛素水平升高。与单独治疗相比,接受 ALA 联合治疗的组在心脏生物标志物方面表现出更大的改善。免疫组织化学分析通过证明 DCM 病理生理学中涉及的蛋白酶 B 蛋白的百分比面积减少支持了这些发现。总之,用 ALA 补充基础治疗有望增强与 DCM 相关的心脏生物标志物。特立帕肽、瑞格列净和 ALA 的联合治疗可能通过靶向氧化应激、炎症和糖毒性具有额外的临床价值,用于治疗 DCM。然而,需要进一步的研究来验证这些发现并探索其潜在的临床应用。