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艾司洛尔对高血压性心脏病冠状动脉结构和功能产生的效应随时间的维持情况

Maintenance over Time of the Effect Produced by Esmolol on the Structure and Function of Coronary Arteries in Hypertensive Heart Diseases.

作者信息

Martín-Oropesa Raquel, Rodríguez-Rodríguez Pilar, Pazó-Sayós Laia, Arnalich-Montiel Ana, Arribas Silvia Magdalena, González Maria Carmen, Quintana-Villamandos Begoña

机构信息

Department of Anesthesiology, Hospital General Universitario Gregorio Marañón, 28007 Madrid, Spain.

Department of Physiology, Faculty of Medicine, Universidad Autónoma de Madrid, 28029 Madrid, Spain.

出版信息

Antioxidants (Basel). 2022 Oct 17;11(10):2042. doi: 10.3390/antiox11102042.

Abstract

We previously observed that esmolol treatment for 48 h reduced vascular lesions in spontaneously hypertensive rats (SHRs). Therefore, we investigated whether this beneficial effect is persistent after withdrawal. Fourteen-month-old SHRs (SHR-Es) were treated with esmolol (300 μg/kg/min) or a vehicle for 48 h. Two separate groups were also given identical treatment, but they were then monitored for a further 1 week and 1 month after drug withdrawal. We analyzed the geometry and composition of the coronary artery, vascular reactivity and plasma redox status. Esmolol significantly decreased wall thickness (medial layer thickness and cell count), external diameter and cross-sectional area of the artery, and this effect persisted 1 month after drug withdrawal. Esmolol significantly improved endothelium-dependent relaxation by ACh (10-10 mol/L); this effect persisted 1 week (10-10 mol/L) and 1 month (10-10 mol/L) after withdrawal. Esmolol reduced the contraction induced by 5-HT (3 × 10-3 × 10 mol/L), and this effect persisted 1 week after withdrawal (10-3 × 10 mol/L). Esmolol increased nitrates and reduced glutathione, and it decreased malondialdehyde and carbonyls; this enhancement was maintained 1 month after withdrawal. This study shows that the effect of esmolol on coronary remodeling is persistent after treatment withdrawal in SHRs, and the improvement in plasma oxidative status can be implicated in this effect.

摘要

我们之前观察到,艾司洛尔治疗48小时可减少自发性高血压大鼠(SHR)的血管病变。因此,我们研究了停药后这种有益作用是否持续存在。对14月龄的SHR(SHR-Es)用艾司洛尔(300μg/kg/min)或赋形剂治疗48小时。另外两组也给予相同的治疗,但在停药后再监测1周和1个月。我们分析了冠状动脉的几何形状和组成、血管反应性和血浆氧化还原状态。艾司洛尔显著降低了动脉壁厚度(中层厚度和细胞计数)、外径和横截面积,且停药1个月后这种作用仍然存在。艾司洛尔显著改善了乙酰胆碱(10-10mol/L)诱导的内皮依赖性舒张;停药后1周(10-10mol/L)和1个月(10-10mol/L)这种作用仍然存在。艾司洛尔减少了5-羟色胺(3×10-3×10mol/L)诱导的收缩,且停药1周后(10-3×10mol/L)这种作用仍然存在。艾司洛尔增加了硝酸盐并减少了谷胱甘肽,且降低了丙二醛和羰基;停药1个月后这种增强作用仍然保持。本研究表明,在SHR中,停药后艾司洛尔对冠状动脉重塑的作用仍然持续存在,血浆氧化状态的改善可能与这种作用有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/036a/9598983/d9373d135992/antioxidants-11-02042-g001.jpg

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