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Primary pulmonary arterial hypertension: Protocol to assess comprehensively in the rat the response to pharmacologic treatments

机译:原发性肺动脉高压:全面评估大鼠对药物治疗反应的方案

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摘要

The identification of new treatments for primary pulmonary arterial hypertension (PAH) is a critical unmet need since there is no a definitive cure for this disease yet. Due to the complexity of PAH, a wide set of methods are necessary to assess the response to a pharmacological intervention. Thus, a rigorous protocol is crucial when experimental studies are designed. In the present experimental protocol, a stepwise approach was followed in a monocrotaline-induced PAH model in the rat, moving from the dose finding study of treatment compounds to the recognition of the onset of disease manifestation, in order to identify when to start a curative treatment. A complete multidimensional evaluation of treatment effects represented the last step. The primary study endpoint was the change in right ventricular systolic pressure after 14 days of treatment; echocardiographic and biohumoral markers together with heart and pulmonary arterial morphometric parameters were considered as secondary efficacy and/or safety endpoints and for the evaluation of the biologic coherence in the different results.
机译:由于目前尚无确切的治疗方法,因此寻找新的治疗原发性肺动脉高压(PAH)的方法是一项亟待解决的关键问题。由于PAH的复杂性,需要多种方法来评估对药理干预的反应。因此,设计实验研究时,严格的方案至关重要。在本实验方案中,在大鼠中由一克他croline诱导的PAH模型中采用了逐步方法,从治疗化合物的剂量寻找研究到识别疾病表现的开始,以识别何时开始治疗。治疗。最后一个步骤是对治疗效果的完整多维评估。主要研究终点是治疗14天后右心室收缩压的变化。超声心动图和生物体液标记物以及心脏和肺动脉形态计量学参数被认为是次要功效和/或安全性终点,并被用于评估不同结果中的生物学一致性。

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