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缺血再灌注心脏模型中血管黏附分子-1的机制。

The mechanism of vascular adhesion molecule-1 in an ischemia-reperfusion cardia model.

作者信息

Zarei Seyedamirhossein, Nazari Afshin, Chehelcheraghi Farzaneh, Birjandi Mehdi, Karbaschi Roxana

机构信息

Student Research Committee, School of Medicine, Lorestan University of Medical Sciences, Khorramabad, Iran.

Department of Physiology and Pharmacology, School of Medicine, Cardiovascular Research Center, Lorestan University of Medical Sciences, Khorramabad, Lorestan, Iran.

出版信息

ARYA Atheroscler. 2025;21(4):44-54. doi: 10.48305/arya.2025.43457.3025.

Abstract

BACKGROUND

Vascular adhesion molecule-1 (VCAM-1) is involved in promoting inflammation within blood vessels, activating endothelial cells, and is a key factor in the progression of diabetic vasculopathy in rats with diabetes, contributing to the underlying pathophysiological processes. This study focused on the expression level of VCAM-1 in diabetic rats subjected to a six-week schedule of aerobic training and valerian supplements.

METHODS

Fifty male Wistar rats' hearts were removed under deep anesthesia and were studied using Lutgendorf's apparatus. They were divided into five groups (10 each): Healthy control (C), Diabetic control (DC), Diabetic with valerian (DV), Diabetic with exercise (DE), and Diabetic with valerian and exercise (DVE). Diabetes was induced in the animals by administering a shot of STZ (50 mg/kg) in their abdominal area. Following confirmation of diabetes in the animals, moderate exercise five days a week, combined with intraperitoneal administration of 200 mg/kg/day of valerian, was maintained for six weeks. Heart tissue was obtained from diabetic cardiac ischemia-reperfusion model (CI/RM) injury (n=40) and control rats (n=10).

RESULTS

VCAM-1 expression and histological parameters were not observed when comparing experimental and control groups. However, the exercise/valerian treatment (E + V) notably reduced the irregularity in cardiac tissue and increased the size of cardiomyocytes.

CONCLUSION

These findings suggest that E + V extract could diminish the levels of diabetic cardiac complications. Also, it had a dual effect: it corrected cardiac tissue abnormalities and increased the size of cardiomyocytes, enhancing the overall structure and function of the heart. More research is needed to understand non-pharmacological complementary treatments in this area.

摘要

背景

血管细胞黏附分子-1(VCAM-1)参与促进血管内炎症、激活内皮细胞,是糖尿病大鼠糖尿病血管病变进展的关键因素,在潜在病理生理过程中起作用。本研究聚焦于接受六周有氧训练和缬草补充剂的糖尿病大鼠中VCAM-1的表达水平。

方法

在深度麻醉下取出50只雄性Wistar大鼠的心脏,使用Lutgendorf仪器进行研究。它们被分为五组(每组10只):健康对照组(C)、糖尿病对照组(DC)、糖尿病+缬草组(DV)、糖尿病+运动组(DE)和糖尿病+缬草+运动组(DVE)。通过在动物腹部注射一剂链脲佐菌素(STZ,50mg/kg)诱导糖尿病。在确认动物患有糖尿病后,每周进行五天的适度运动,并腹腔注射200mg/kg/天的缬草,持续六周。从糖尿病心脏缺血再灌注模型(CI/RM)损伤的大鼠(n = 40)和对照大鼠(n = 10)获取心脏组织。

结果

比较实验组和对照组时,未观察到VCAM-1表达和组织学参数的差异。然而,运动/缬草治疗(E + V)显著减少了心脏组织的不规则性,并增加了心肌细胞的大小。

结论

这些发现表明,E + V提取物可以降低糖尿病心脏并发症的水平。此外,它具有双重作用:纠正心脏组织异常并增加心肌细胞大小,增强心脏的整体结构和功能。需要更多研究来了解该领域的非药物补充治疗。

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