Cantor Jerome
St John's School of Pharmacy and Allied Health Sciences, St John's University, 8000 Utopia Parkway Queens, Queens, NY 11439, USA.
Int J Mol Sci. 2025 Aug 28;26(17):8386. doi: 10.3390/ijms26178386.
Animal models provide a controlled and reproducible environment for investigating the pathogenesis of human lung diseases. In many cases, the morphological changes associated with a particular model may resemble those seen in their human counterparts, but the corresponding biochemical events may differ, and their timeframe may be significantly reduced. Nevertheless, gaining insight into human disease mechanisms may be possible by employing experimental approaches that minimize the problems associated with extrapolating data from animal studies. Such strategies include using more than one model of a particular disease, employing different routes of administration of the injurious agent, using a variety of animal strains or species, or focusing on biochemical mechanisms common to both the animal model and its human counterpart. For example, rodent models that replicate elastic fiber injury in human pulmonary emphysema have been used to test aerosolized hyaluronan's ability to slow the disease's progression. The same models facilitated the identification of a new biomarker for pulmonary emphysema that may be a real-time indicator of therapeutic efficacy in clinical trials. Therefore, the appropriate use of these models can provide a necessary road map for designing appropriate dosages, delivery routes, timeframes, and endpoints in clinical trials of novel agents for the treatment of lung disease.
动物模型为研究人类肺部疾病的发病机制提供了一个可控且可重复的环境。在许多情况下,与特定模型相关的形态学变化可能与人类疾病中的变化相似,但相应的生化事件可能不同,而且其时间进程可能会显著缩短。然而,通过采用能尽量减少动物研究数据外推相关问题的实验方法,有可能深入了解人类疾病机制。这些策略包括使用特定疾病的多种模型、采用不同的损伤因子给药途径、使用多种动物品系或物种,或者关注动物模型及其人类对应物共有的生化机制。例如,复制人类肺气肿弹性纤维损伤的啮齿动物模型已被用于测试雾化透明质酸减缓疾病进展的能力。同样的模型有助于识别一种新的肺气肿生物标志物,它可能是临床试验中治疗效果的实时指标。因此,合理使用这些模型可为设计治疗肺部疾病新药物的临床试验中的合适剂量、给药途径、时间进程和终点提供必要的路线图。