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Lung Function Measurements in Rodents in Safety Pharmacology Studies

机译:安全药理研究中啮齿动物的肺功能测量

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摘要

The ICH guideline S7A requires safety pharmacology tests including measurements of pulmonary function. In the first step – as part of the “core battery” – lung function tests in conscious animals are requested. If potential adverse effects raise concern for human safety, these should be explored in a second step as a “follow-up study”. For these two stages of safety pharmacology testing, both non-invasive and invasive techniques are needed which should be as precise and reliable as possible. A short overview of typical in vivo measurement techniques is given, their advantages and disadvantages are discussed and out of these the non-invasive head-out body plethysmography and the invasive but repeatable body plethysmography in orotracheally intubated rodents are presented in detail. For validation purposes the changes in the respective parameters such as tidal midexpiratory flow (EF50) or lung resistance have been recorded in the same animals in typical bronchoconstriction models and compared. In addition, the technique of head-out body plethysmography has been shown to be useful to measure lung function in juvenile rats starting from day two of age. This allows safety pharmacology testing and toxicological studies in juvenile animals as a model for the young developing organism as requested by the regulatory authorities (e.g., EMEA Guideline 1/2008). It is concluded that both invasive and non-invasive pulmonary function tests are capable of detecting effects and alterations on the respiratory system with different selectivity and area of operation. The use of both techniques in a large number of studies in mice and rats in the last years have demonstrated that they provide useful and reliable information on pulmonary mechanics in safety pharmacology and toxicology testing, in investigations of respiratory disorders, and in pharmacological efficacy studies.
机译:ICH指南S7A需要进行安全药理学测试,包括对肺功能的测量。第一步-作为“核心电池”的一部分-要求对有意识的动物进行肺功能测试。如果潜在的不良影响引起人们对人身安全的关注,则应在第二步中将其作为“后续研究”进行探讨。对于安全药理学测试的这两个阶段,都需要尽可能精确和可靠的无创技术和有创技术。简要概述了典型的体内测量技术,讨论了它们的优缺点,并从口气管插管啮齿类动物的无创抬头人体容积描记法和有创但可重复的人体容积描记图中详细介绍了这些方法。为了验证的目的,已经在典型的支气管收缩模型中的相同动物中记录了诸如潮气中气流量(EF50)或肺阻力等各个参数的变化,并进行了比较。另外,头顶出身体体积描记法的技术已被证明可用于从第二天开始测量幼年大鼠的肺功能。根据监管机构的要求(例如,EMEA指南1/2008),这可以对幼小的动物进行安全的药理学测试和毒理学研究,作为年轻的发育中生物的模型。结论是,有创和无创肺功能测试均能够以不同的选择性和手术区域检测对呼吸系统的影响和改变。近年来,在小鼠和大鼠的大量研究中使用这两种技术已证明,它们在安全药理学和毒理学测试,呼吸系统疾病的研究以及药理功效研究中提供了有关肺力学的有用而可靠的信息。

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