Bulterijs Sven, Braeckman Bart P
Laboratory of Aging Physiology and Molecular Evolution, Department of Biology, Ghent University, 9000 Ghent, Belgium.
Pharmaceuticals (Basel). 2020 Jul 25;13(8):164. doi: 10.3390/ph13080164.
Population aging is one of the largest challenges of the 21st century. As more people live to advanced ages, the prevalence of age-related diseases and disabilities will increase placing an ever larger burden on our healthcare system. A potential solution to this conundrum is to develop treatments that prevent, delay or reduce the severity of age-related diseases by decreasing the rate of the aging process. This ambition has been accomplished in model organisms through dietary, genetic and pharmacological interventions. The pharmacological approaches hold the greatest opportunity for successful translation to the clinic. The discovery of such pharmacological interventions in aging requires high-throughput screening strategies. However, the majority of screens performed for geroprotective drugs in so far are rather low throughput. Therefore, the development of high-throughput screening strategies is of utmost importance.
人口老龄化是21世纪最大的挑战之一。随着越来越多的人活到高龄,与年龄相关的疾病和残疾的患病率将会增加,给我们的医疗系统带来越来越大的负担。解决这一难题的一个潜在办法是开发通过降低衰老过程速率来预防、延缓或减轻与年龄相关疾病严重程度的治疗方法。通过饮食、基因和药物干预,在模式生物中已经实现了这一目标。药物方法在成功转化到临床方面具有最大的机会。发现此类衰老方面的药物干预需要高通量筛选策略。然而,到目前为止,针对老年保护药物进行的大多数筛选通量相当低。因此,开发高通量筛选策略至关重要。