Serum biochemical evaluation following administration of imidazolyl thiazolidinedione in streptozotocin-induced diabetic rats.

IF 2.9 4区 生物学 Q3 CELL BIOLOGY
Journal of Molecular Histology Pub Date : 2024-12-01 Epub Date: 2024-10-09 DOI:10.1007/s10735-024-10272-8
Neda Shakour, Mohammad Reza Mahdinezhad, Mousa-Al-Reza Hadjzadeh, Amirhossein Sahebkar, Farzin Hadizadeh
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引用次数: 0

Abstract

Background: Diabetes mellitus represents a prominent global health concern, characterized by a rising prevalence rate. Type 2 Diabetes Mellitus (T2DM) is purported to be associated with an intricate interplay of genetic, environmental, and lifestyle factors. While some progress have been made in T2DM management, controlling associated complications remains a great challenge in medicine.

Objectives: This study investigated a synthesized Imidazolyl Thiazolidinedione antidiabetic agent (PA9), focusing on serum parameters.

Methods: Streptozotocin-induced diabetic rats (n = 6) were subjected to orally treatment with PA9 (synthesized by Shakour et al. in an equal dose of a standard drug, 0.011 mmol/kg). The study conducted to measure some specific serum factors, including lipid profiles, liver and kidney enzymes, cardiac enzymes, and oxidative stress markers, both before and after treatment.

Results: The study findings indicated that PA9 effectively ameliorates hyperlipidemia by significantly reducing total cholesterol and triglyceride levels in serum. Additionally, PA9 demonstrated hepatoprotective effects against TZD-induced injuries, as evidenced by decreased levels of alanine transaminase and, alkaline phosphatase. In addition, PA9 also exhibited a modulatory effect on a cardiac injury marker, creatine kinase MB. Moreover, PA9 demonstrated antioxidant properties by reducing oxidative stress markers and enhancing the activities of catalase, thiol, and superoxide dismutase.

Conclusions: The synthesized TZD compound (PA9) stands out as a highly promising agent for the management of diabetes. Its significant antihyperlipidemic effects, preventive influences on organ injuries, and demonstrated efficacy in reducing oxidative stress marker (SOD) make it therapeutic agent in diabetes management. This study lays the groundwork for innovative strategies in diabetes management.

对链脲佐菌素诱导的糖尿病大鼠服用咪唑噻唑烷二酮后的血清生化评估
背景:糖尿病是一个突出的全球健康问题,其特点是患病率不断上升。据称,2 型糖尿病(T2DM)与遗传、环境和生活方式等因素错综复杂的相互作用有关。虽然 T2DM 的治疗取得了一些进展,但控制相关并发症仍是医学界面临的巨大挑战:本研究对一种合成的咪唑烷基噻唑烷二酮类抗糖尿病药物(PA9)进行了研究,重点是血清参数:方法:对链脲佐菌素诱导的糖尿病大鼠(n = 6)口服 PA9(由 Shakour 等人合成,与标准药物等剂量,0.011 mmol/kg)。研究测量了治疗前后的一些特定血清因子,包括血脂、肝肾酶、心肌酶和氧化应激标记物:研究结果表明,PA9 能有效改善高脂血症,显著降低血清中的总胆固醇和甘油三酯水平。此外,PA9 还对 TZD 引起的肝损伤具有保护作用,这体现在丙氨酸转氨酶和碱性磷酸酶水平的降低上。此外,PA9 还对心脏损伤标志物肌酸激酶 MB 具有调节作用。此外,PA9 还具有抗氧化特性,可降低氧化应激指标,提高过氧化氢酶、硫醇和超氧化物歧化酶的活性:合成的 TZD 化合物(PA9)是一种极具潜力的糖尿病治疗药物。其明显的降血脂作用、对器官损伤的预防性影响以及在降低氧化应激标志物(SOD)方面的功效使其成为糖尿病治疗药物。这项研究为糖尿病管理的创新战略奠定了基础。
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来源期刊
Journal of Molecular Histology
Journal of Molecular Histology 生物-细胞生物学
CiteScore
5.90
自引率
0.00%
发文量
68
审稿时长
1 months
期刊介绍: The Journal of Molecular Histology publishes results of original research on the localization and expression of molecules in animal cells, tissues and organs. Coverage includes studies describing novel cellular or ultrastructural distributions of molecules which provide insight into biochemical or physiological function, development, histologic structure and disease processes. Major research themes of particular interest include: - Cell-Cell and Cell-Matrix Interactions; - Connective Tissues; - Development and Disease; - Neuroscience. Please note that the Journal of Molecular Histology does not consider manuscripts dealing with the application of immunological or other probes on non-standard laboratory animal models unless the results are clearly of significant and general biological importance. The Journal of Molecular Histology publishes full-length original research papers, review articles, short communications and letters to the editors. All manuscripts are typically reviewed by two independent referees. The Journal of Molecular Histology is a continuation of The Histochemical Journal.
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