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美托洛尔和抗坏血酸联合治疗可预防糖尿病性心肌病期间心脏的内在损伤。

Combined metoprolol and ascorbic acid treatment prevents intrinsic damage to the heart during diabetic cardiomyopathy.

作者信息

Saran Varun, Sharma Vijay, Wambolt Richard, Yuen Violet G, Allard Michael, McNeill John Hugh

机构信息

a James Hogg Research Centre, Department of Pathology and Laboratory Medicine, University of British Columbia, St. Paul's Hospital, 1081 Burrard Street, Vancouver, BC V6Z 1Y6, Canada.

出版信息

Can J Physiol Pharmacol. 2014 Oct;92(10):827-37. doi: 10.1139/cjpp-2014-0078. Epub 2014 Aug 14.

Abstract

Metabolic disturbances and oxidative stress have been highlighted as potential causative factors for the development of diabetic cardiomyopathy. The β-blocker metoprolol is known to improve function in the diabetic rat heart and ameliorates the sequelae associated with oxidative stress, without lowering oxidative stress. The antioxidant ascorbic acid is known to improve function in the diabetic rat heart. We tested whether a combination of ascorbic acid and metoprolol treatment would improve function further than each drug individually. Control and streptozotocin-induced diabetic Wistar rats were treated with metoprolol (15 mg·(kg body mass)(-1)·day(-1), via an osmotic pump) and (or) ascorbic acid (1000 mg·(kg body mass)(-1)·day(-1), via their drinking water). To study the effect of treatment on the development of dysfunction, we examined time points before (5 weeks diabetic) and after (7 weeks diabetic) development of overt systolic dysfunction. Echocardiography and working-heart-perfusion were used to assess cardiac function. Blood and tissue samples were collected to assess the severity of disease and oxidative stress. While both drugs improved function, only ascorbic acid had effects on oxidative damage. Combination treatment had a more pronounced improvement in function. Our β-blocker + antioxidant treatment strategy focused on oxidative stress, not diabetes specifically; therefore, it may prove useful in other diseases where oxidative stress contributes to the pathology.

摘要

代谢紊乱和氧化应激已被视为糖尿病性心肌病发展的潜在致病因素。已知β受体阻滞剂美托洛尔可改善糖尿病大鼠心脏功能,并减轻与氧化应激相关的后遗症,且不会降低氧化应激水平。已知抗氧化剂抗坏血酸可改善糖尿病大鼠心脏功能。我们测试了抗坏血酸和美托洛尔联合治疗是否比单独使用每种药物能进一步改善心脏功能。将对照大鼠和链脲佐菌素诱导的糖尿病Wistar大鼠用美托洛尔(15 mg·(kg体重)(-1)·天(-1),通过渗透泵给药)和(或)抗坏血酸(1000 mg·(kg体重)(-1)·天(-1),通过饮用水给药)进行治疗。为了研究治疗对功能障碍发展的影响,我们在明显的收缩功能障碍出现之前(糖尿病5周)和之后(糖尿病7周)的时间点进行了检查。使用超声心动图和工作心脏灌注来评估心脏功能。采集血液和组织样本以评估疾病严重程度和氧化应激水平。虽然两种药物都改善了心脏功能,但只有抗坏血酸对氧化损伤有影响。联合治疗在功能改善方面更为显著。我们的β受体阻滞剂 + 抗氧化剂治疗策略关注的是氧化应激,而非特定的糖尿病;因此,它可能在氧化应激导致病理变化的其他疾病中证明是有用的。

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