An innovative proof-of-concept approach to identify age-modulating drugs capable of reversing inflammation and re-setting the epigenetic clock

一种创新的概念验证方法，用于识别能够逆转炎症和重置表观遗传时钟的年龄调节药物

• 批准号: 10264863
• 负责人: DEAN L KELLOGG
• 金额: $ 19.34万
• 依托单位: UNIVERSITY OF TEXAS HLTH SCIENCE CENTER
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-09-30 至 2024-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10264863
• 关键词: Acarbose; Acute; Affect; Age; Aging; Animal Model; Area; Biological Assay; Biological Markers; Blood; Blood Circulation; Bulla; Cells; Clinical Trials; Collection; DNA; DNA Methylation; Dermal; Dose; Drug Controls; Elderly; Enzyme-Linked Immunosorbent Assay; Epigenetic Process; Female; Forearm; Future; Human; Individual; Inflammation; Inflammation Mediators; Inflammatory; Intercellular Fluid; Intervention; Liquid substance; Longevity; Measurable; Measures; Metformin; Methods; Methylation; Organism; Outcome; Pathology; Pharmaceutical Preparations; Pharmacodynamics; Pharmacology; Phase; Placebo Control; Placebos; Populations at Risk; Preclinical Testing; Research; Risk; Rodent; Safety; Sex Differences; Sirolimus; Site; Skin; Suction; Surgical Flaps; Surrogate Markers; Techniques; Testing; Therapeutic; Tissues; Topical application; Translating; Treatment Protocols; Validation; age effect; anti aging; arm; base; cohort; cost; cost effective; cytokine; design; drug candidate; drug testing; efficacy evaluation; epigenome; epigenomics; healthspan; healthy aging; human subject; in vivo; innovation; interstitial; keratinocyte; mTOR Inhibitor; male; methylation pattern; minimally invasive; novel; preclinical study; therapeutic candidate; treatment site

ABSTRACT In order to identify drugs and/or interventions with the potential to delay the onset and progression of age- associated pathologies, preclinical studies have used animal models where extension of lifespan could be accurately assessed. Several outstanding candidate therapeutics have been identified over the last decade; these include mTOR inhibitors (like rapamycin), senolytic agents, acarbose, and others. However, translating anti-aging results from animal models into humans has been challenging. For example, measuring extension of lifespan would be impractical in humans, so it is necessary to identify and validate parameters that can serve as surrogate markers of healthy aging. Moreover, the efficacy of age-modulating drugs is often only demonstrable with older individuals where functional deficits are already evident. Thus, testing of potential anti- aging therapeutics should be done in a cohort of human subjects of an advanced age; issues of safe administration would be even more acute in this “at risk” population. To circumvent these limitations, we propose to develop and validate an innovative, minimally invasive, cost-effective assay in human subjects ranging from 65-95 years old. The putative anti-aging test drug will be applied topically to a discrete area of skin on the subject’s forearm while a “vehicle only” (control) is applied in parallel to the opposite arm. Thus, each subject will serve as his/her own control. The pharmacodynamic outcomes at the “test” and placebo sites will be compared in both males and females since the effects of age-modulating agents often differ between the sexes. Ascertaining the efficacy of topically-applied therapeutics requires robust biomarkers of aging that can be measured in skin, but will be generalizable to the intact organism. Towards this end, we have opted to use two independent parameters that are known to be modified with aging both locally (in individual tissues) and systemically: i) the DNA methylation pattern or “epigenetic clock” and ii) biomarkers associated with inflammation. To validate the proposed technique, we have chosen a drug, rapamycin (RAPA), which has already been shown to modulate aging in rodents and which has been tested for safe systemic application in humans [1-4]. After a 6 month treatment phase, suction blisters will be generated at each site to allow collection of skin cells (blister flap) for use in the epigenomic analysis (Aim 1) and interstitial (blister) fluid for use in measuring cytokines and other inflammatory regulators (Aim 2). Once validated, our approach can be used to safely and efficiently screen the age-modulating potential of pharmacological agents in humans to identify those agents that warrant large, expensive human clinical trials with systemic agent administration.

抽象的 为了确定有可能延缓年龄增长的药物和/或干预措施， 相关的病理学，临床前研究使用了可以延长寿命的动物模型 过去十年中已经确定了几种出色的候选疗法； 这些包括 mTOR 抑制剂（如雷帕霉素）、senolytic 药物、阿卡波糖等。 例如，从动物模型到人类的抗衰老结果的测量一直具有挑战性。 人类的寿命是不切实际的，因此有必要识别和验证可以服务的参数 此外，年龄调节药物的功效往往只是健康衰老的替代标志。 对于功能缺陷已经很明显的老年人来说，可以证明这一点，因此，对潜在的抗-测试进行了测试。 衰老治疗应在高龄人类受试者群体中进行，存在安全问题； 为了规避这些限制，我们对这一“高危”人群采取更加严厉的管理措施。 提议在人类受试者中开发和验证一种创新的、微创的、具有成本效益的检测方法 假定的抗衰老测试药物将局部应用于 65-95 岁的离散区域。 受试者前臂上的皮肤，同时“仅车辆”（对照）平行于另一侧手臂。 每个受试者将作为他/她自己的对照“测试”和安慰剂站点的药效学结果。 将在男性和女性中进行比较，因为年龄调节剂的效果通常在男性和女性之间有所不同 确定局部应用治疗的疗效需要衰老的生物标志物。 可以在皮肤中进行测量，但可以推广到完整的有机体。 使用两个独立的参数，已知这些参数会随着局部（在单个组织中）老化而改变 系统地：i) DN​​A 甲基化模式或“表观遗传时钟”，以及 ii) 与相关的生物标志物 为了验证所提出的技术，我们选择了一种药物雷帕霉素（RAPA），它具有 已被证明可以调节啮齿动物的衰老，并且已在以下领域进行了安全的系统应用测试： 人类 [1-4] 经过 6 个月的治疗阶段后，每个部位都会产生吸水泡。 收集用于表观基因组分析（目标 1）的皮肤细胞（水泡瓣）和间质（水泡）液 用于测量细胞因子和其他炎症调节因子（目标 2）。 用于安全有效地筛选药物对人类的年龄调节潜力 确定那些需要进行大规模、昂贵的人体临床试验并进行全身给药的药物。