Upregulation of PCSK9, rho kinase and cardiac troponin by Eucalyptus globulus leaf extract improves fructose-streptozotocin-induced diabetic cardiac dysfunction in rats.

IF 2.5 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Afolabi C Akinmoladun, Morenikejimi Bello, Emmanuel Oluwafemi Ibukun
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Abstract

Context: The effect of Eucalyptus globulus in diabetic cardiac dysfunction and the possible mechanisms involved have not been explored.

Objective: To evaluate the effect of ethanol leaf extract of E. globulus (NEE) on the cardiac function of fructose/streptozotocin-induced diabetic rats.

Materials and methods: Type-2 diabetes was induced in rats with 10% fructose feeding for 14 days and an intraperitoneal administration of 40 mg/kg streptozotocin. Diabetic animals were treated with NEE (100-400 mg/kg) or 5 mg/kg glibenclamide orally for 21 days. Biochemical assays, histopathological examination and analyses of PCSK9, Rho kinase and Cardiac troponin expression were performed.

Results: The untreated diabetic group showed decreased expression of the genes, oxidative stress, dyslipidemia, increased activities of creatine kinase MB and lactate dehydrogenase, reduced nitric oxide level, and depletion of cardiomyocytes, which were reversed in NEE treated groups.

Conclusions: Eucalyptus globulus ameliorated diabetic cardiac dysfunction through increased PCSK9, Rho kinase and Cardiac troponin expression.

蓝桉叶提取物上调PCSK9、rho激酶和心肌肌钙蛋白可改善果糖-链脲佐菌素诱导的大鼠糖尿病心功能障碍。
背景:巨桉对糖尿病心功能障碍的影响及其可能的机制尚未探讨。目的:探讨金莲叶乙醇提取物(NEE)对果糖/链脲霉素诱导的糖尿病大鼠心功能的影响。材料与方法:采用10%果糖喂养大鼠14 d,腹腔注射链脲佐菌素40 mg/kg诱导2型糖尿病。糖尿病动物口服NEE (100-400 mg/kg)或5 mg/kg格列本脲21 d。进行生化、组织病理学检查及PCSK9、Rho激酶、心肌肌钙蛋白表达分析。结果:糖尿病未治疗组出现基因表达降低、氧化应激、血脂异常、肌酸激酶MB和乳酸脱氢酶活性升高、一氧化氮水平降低、心肌细胞耗竭等症状,NEE治疗组逆转上述情况。结论:蓝桉通过增加PCSK9、Rho激酶和心肌肌钙蛋白的表达改善糖尿病心功能障碍。
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来源期刊
Archives of Physiology and Biochemistry
Archives of Physiology and Biochemistry ENDOCRINOLOGY & METABOLISM-PHYSIOLOGY
CiteScore
6.90
自引率
3.30%
发文量
21
期刊介绍: Archives of Physiology and Biochemistry: The Journal of Metabolic Diseases is an international peer-reviewed journal which has been relaunched to meet the increasing demand for integrated publication on molecular, biochemical and cellular aspects of metabolic diseases, as well as clinical and therapeutic strategies for their treatment. It publishes full-length original articles, rapid papers, reviews and mini-reviews on selected topics. It is the overall goal of the journal to disseminate novel approaches to an improved understanding of major metabolic disorders. The scope encompasses all topics related to the molecular and cellular pathophysiology of metabolic diseases like obesity, type 2 diabetes and the metabolic syndrome, and their associated complications. Clinical studies are considered as an integral part of the Journal and should be related to one of the following topics: -Dysregulation of hormone receptors and signal transduction -Contribution of gene variants and gene regulatory processes -Impairment of intermediary metabolism at the cellular level -Secretion and metabolism of peptides and other factors that mediate cellular crosstalk -Therapeutic strategies for managing metabolic diseases Special issues dedicated to topics in the field will be published regularly.
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