Allopurinol treatment reduced vascular remodeling and improved vascular functions in monocrotaline-induced pulmonary hypertensive rats

IF 3.3 3区 医学 Q2 PHARMACOLOGY & PHARMACY
Telli Gokcen , Kazkayasi Inci , Ergonul E. Inci , Onder Sevgen , Uma Serdar
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引用次数: 1

Abstract

Increased oxidative stress and high uric acid are implicated in the pathogenesis of pulmonary hypertension (PH). This provides opportunity to benefit from drugs like allopurinol which suppresses both contributing factors. Therefore, we aimed to investigate the effects of allopurinol in preventing as well as reversing the pathological changes occurring in monocrotaline (MCT)-induced rat model of PH. Male rats were assigned into three groups based on the follow-up time: 7, 21 and 35 days. Time-matched controls of each group received single injections of MCT (60 mg/kg) intraperitoneally. Test groups consisted of rats who were treated with MCT on day 0 plus oral allopurinol (60 mg/kg) daily for 7 or 21 days. 35-day group received allopurinol for two weeks starting on the 22nd day following MCT injection. At the end of all-time points, rats were killed and basal pulmonary perfusion pressure, Fulton index, pulmonary arterial wall thickness and pulmonary arterial relaxations along with oxidative stress markers (MDA, SOD, XO), NO and uric acid levels were measured in all groups. MCT-injected rats had evidence of raised oxidative stress (high MDA and XO, low SOD levels) which was reversed by allopurinol co-treatment in all-time groups. Marked elevation of uric acid seen in 21- and 35 day-groups was also reversed by allopurinol. Reduced NO levels of 21 and 35 days were unchanged in allopurinol treated groups. Apart from an increase in arterial wall thickening which was maintained in all-time groups, no alterations in other cardiovascular parameters were observed in 7-day group. However, basal lung perfusion pressure and Fulton index significantly increased, while arterial relaxations decreased in 21- and 35-day groups. Co-treatment with allopurinol for 21 days improved these functional alterations, whereas late allopurinol treatment failed to affect them. Our results indicate that early treatment of MCT-induced PH with allopurinol ameliorated the impaired functional characteristics via suppressing the increased oxidative stress and uric acid, while treatment started after progression of the disease had no significant effect.

Abstract Image

别嘌呤醇治疗可减少单芥碱诱导的肺动脉高压大鼠血管重构,改善血管功能
氧化应激增加和高尿酸与肺动脉高压(PH)的发病机制有关。这就提供了从别嘌呤醇等药物中获益的机会,别嘌呤醇可以抑制这两种因素。因此,我们旨在探讨别嘌呤醇对MCT诱导的ph大鼠模型的预防和逆转病理变化的作用。雄性大鼠按随访时间分为3组:7、21和35 d。各组时间匹配的对照组接受单次腹腔注射MCT (60 mg/kg)。试验组大鼠在第0天给予MCT治疗,同时每天口服别嘌呤醇(60 mg/kg),连续7或21天。35天组从MCT注射后第22天开始,连续2周给予别嘌呤醇治疗。在各时间点结束时处死大鼠,测定各组肺灌注压、富尔顿指数、肺动脉壁厚度、肺动脉舒张度及氧化应激标志物(MDA、SOD、XO)、NO、尿酸水平。注射mct的大鼠有氧化应激升高的证据(高MDA和XO,低SOD水平),在所有时间组中,别嘌呤醇联合治疗可以逆转。在21天和35天的组中,尿酸的显著升高也被别嘌呤醇逆转。别嘌呤醇处理组第21天和第35天一氧化氮水平降低无变化。除了动脉壁增厚在所有时间组中保持增加外,在7天组中没有观察到其他心血管参数的变化。21、35 d组肺基础灌注压和Fulton指数显著升高,动脉舒张度降低。与别嘌呤醇联合治疗21天改善了这些功能改变,而晚期别嘌呤醇治疗未能影响它们。我们的研究结果表明,早期用别嘌呤醇治疗mct诱导的PH可以通过抑制氧化应激和尿酸的增加来改善受损的功能特征,而在疾病进展后开始治疗则没有显著效果。
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来源期刊
CiteScore
6.20
自引率
0.00%
发文量
41
审稿时长
42 days
期刊介绍: Pulmonary Pharmacology and Therapeutics (formerly Pulmonary Pharmacology) is concerned with lung pharmacology from molecular to clinical aspects. The subject matter encompasses the major diseases of the lung including asthma, cystic fibrosis, pulmonary circulation, ARDS, carcinoma, bronchitis, emphysema and drug delivery. Laboratory and clinical research on man and animals will be considered including studies related to chemotherapy of cancer, tuberculosis and infection. In addition to original research papers the journal will include review articles and book reviews. Research Areas Include: • All major diseases of the lung • Physiology • Pathology • Drug delivery • Metabolism • Pulmonary Toxicology.
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