建立评估小鼠高血压危象的模型

Xuan Phuc Nguyen, Van Vien Doan, Manh Hung Tran
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摘要

高血压是导致中风和心血管并发症的主要原因。建立高血压危象模型可以快速检测降压药物的效果,满足研究和开发慢性药理模型的需要。通过腹腔注射不同剂量的木甲唑啉和皮下注射 0.4 mg/kg 剂量的阿托品,诱发急性高血压模型。这项研究应用 CODA 高通量高血压机确定了一个合适的模型。结果显示,注射 1 毫克/千克(IP)剂量的西甲唑啉和 0.4 毫克/千克(SC)剂量的阿托品可诱发收缩压大于 130 毫米汞柱的高血压,20 分钟内持续 15 圈。口服硝苯地平(6 毫克/千克)、洛沙坦(100 毫克/千克)和卡托普利(100 毫克/千克)均有降压作用。然而,比索洛尔在 50 毫克/千克的剂量下没有降压作用。该小鼠模型可用于进一步筛选和评估降压药物的治疗效果。
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Building a model to evaluate hypertensive crisis in mice
High blood pressure is a major cause of stroke and cardiovascular complications. The development of a hypertensive crisis model allows rapid testing of the effects of antihypertensive drugs, meeting the need for research and development of chronic pharmacological models. A model of acute hypertension was induced by intraperitoneal injections of xylometazoline at different doses and subcutaneous injections of atropine at a dose of 0.4 mg/kg. This study applied the CODA high-throughput hypertensive machine to determine a suitable model. The results of injecting xylometazoline at a dose of 1 mg/kg ( IP) and atropine (0.4 mg/kg) (SC) showed induced hypertension with systolic >130 mmHg constantly with 15 circles in 20 minutes. The hypotensive effect was found when oral administration of nifedipine (6 mg/kg), losartan (100 mg/kg), and captopril (100 mg/kg). However, the hypotensive effect of bisoprolol was not found at a dose of 50 mg/kg. This mouse model can be applied for further screening and evaluating the therapeutic effect of hypotensive drugs.
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