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短期给予香蜂草提取物可改善心肌缺血/再灌注损伤:聚焦于氧化应激。

Short-Term Administration of Lemon Balm Extract Ameliorates Myocardial Ischemia/Reperfusion Injury: Focus on Oxidative Stress.

作者信息

Draginic Nevena, Milosavljevic Isidora, Andjic Marijana, Jeremic Jovana, Nikolic Marina, Sretenovic Jasmina, Kocovic Aleksandar, Srejovic Ivan, Zivkovic Vladimir, Bolevich Sergey, Bolevich Stefani, Curcic Svetlana, Jakovljevic Vladimir

机构信息

Department of Pharmacy, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia.

Department of Human Pathology, First Moscow State Medical University I.M. Sechenov, 119991 Moscow, Russia.

出版信息

Pharmaceuticals (Basel). 2022 Jul 8;15(7):840. doi: 10.3390/ph15070840.

DOI:10.3390/ph15070840
PMID:35890139
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9317599/
Abstract

We aimed to investigate the cardioprotective effects of ethanolic L. extract (ME) in the rat model of myocardial ischemia/reperfusion (I/R) injury. Thirty-two rats were randomly divided into a CTRL non-treated control group with myocardial I/R injury and three experimental groups of rats treated with 50, 100, or 200 mg/kg of ME for 7 days per os. Afterward, hearts were isolated, and cardiodynamic function was assessed via the Langendorff model of global 20 min ischemia and 30 min reperfusion. Oxidative stress parameters were determined spectrophotometrically from the samples of coronary venous effluent (O, HO, TBARS, and NO,) and heart tissue homogenate (TBARS, NO, SOD, and CAT). H/E and Picrosirius red staining were used to examine cardiac architecture and cardiac collagen content. ME improved cardiodynamic parameters and achieved to preserve cardiac architecture after I/R injury and to decrease fibrosis, especially in the ME200 group compared to CTRL. ME200 and ME100 markedly decreased prooxidants TBARS, O, and HO while increasing NO. Hereby, we confirmed the ME`s ability to save the heart from I/R induced damage, even after short-term preconditioning in terms of preserving cardiodynamic alterations, cardiac architecture, fibrosis, and suppressing oxidative stress, especially in dose of 200 mg/kg.

摘要

我们旨在研究乙醇提取物(ME)在大鼠心肌缺血/再灌注(I/R)损伤模型中的心脏保护作用。32只大鼠被随机分为心肌I/R损伤的未处理对照组(CTRL)和三个实验组,每组大鼠经口给予50、100或200 mg/kg的ME,持续7天。之后,分离心脏,通过Langendorff模型评估心脏动力学功能,该模型包括20分钟全心缺血和30分钟再灌注。采用分光光度法从冠状静脉流出物样本(O、HO、TBARS和NO)和心脏组织匀浆(TBARS、NO、SOD和CAT)中测定氧化应激参数。使用苏木精/伊红(H/E)染色和天狼星红染色检查心脏结构和心脏胶原含量。与CTRL组相比,ME改善了心脏动力学参数,在I/R损伤后维持了心脏结构并减少了纤维化,尤其是在ME200组。ME200和ME100显著降低了促氧化剂TBARS、O和HO,同时增加了NO。因此,我们证实了ME即使在短期预处理后,在维持心脏动力学改变、心脏结构、纤维化以及抑制氧化应激方面,尤其是在200 mg/kg剂量下,具有保护心脏免受I/R诱导损伤的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/47f37d9ad247/pharmaceuticals-15-00840-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/58f75fc9919f/pharmaceuticals-15-00840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/069296cb0529/pharmaceuticals-15-00840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/bc34844945c6/pharmaceuticals-15-00840-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/3ca9e53b84e6/pharmaceuticals-15-00840-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/0459ccc28bb5/pharmaceuticals-15-00840-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/47f37d9ad247/pharmaceuticals-15-00840-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/58f75fc9919f/pharmaceuticals-15-00840-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/069296cb0529/pharmaceuticals-15-00840-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/bc34844945c6/pharmaceuticals-15-00840-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/3ca9e53b84e6/pharmaceuticals-15-00840-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/0459ccc28bb5/pharmaceuticals-15-00840-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a331/9317599/47f37d9ad247/pharmaceuticals-15-00840-g006.jpg

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