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为中年饮食中的小鼠提供 PI3K p110α 抑制剂 BYL719(阿培利司)的疗效。

Efficacy of Providing the PI3K p110α Inhibitor BYL719 (Alpelisib) to Middle-Aged Mice in Their Diet.

机构信息

Discipline of Nutrition, School of Medical Sciences, University of Auckland, Auckland 1023, New Zealand.

Maurice Wilkins Centre for Molecular Biodiscovery, University of Auckland, Auckland 1023, New Zealand.

出版信息

Biomolecules. 2021 Jan 25;11(2):150. doi: 10.3390/biom11020150.

DOI:10.3390/biom11020150
PMID:33503847
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7911305/
Abstract

BYL719 (alpelisib) is a small molecule inhibitor of PI3K p110α developed for cancer therapy. Targeted suppression of PI3K has led to lifespan extension in rodents and model organisms. If PI3K inhibitors are to be considered as an aging therapeutic, it is important to understand the potential consequences of long-term exposure, and the most practical way to achieve this is through diet administration. Here, we investigated the pharmacokinetics of BYL719 delivered in diet and the efficacy of BYL719 to suppress insulin signaling when administered in the diet of 8-month-old male and female mice. Compared to oral gavage, diet incorporation resulted in a lower peak plasma BYL719 (3.6 vs. 9.2 μM) concentration but similar half-life (~1.5 h). Consuming BYL719 resulted in decreased insulin signaling in liver and muscle within 72 h, and mice still showed impaired glucose tolerance and insulin sensitivity following 6 weeks of access to a diet containing 0.3 g/kg BYL719. However, consuming BYL719 did not affect food intake, body mass, muscle function (rotarod and hang time performance) or cognitive behaviors. This provides evidence that BYL719 has long-term efficacy without major toxicity or side effects, and suggests that administering BYL719 in diet is suitable for studying the effect of pharmacological suppression of PI3K p110α on aging and metabolic function.

摘要

BYL719(阿培利司)是一种用于癌症治疗的小分子 PI3K p110α 抑制剂。PI3K 的靶向抑制作用导致啮齿动物和模式生物的寿命延长。如果将 PI3K 抑制剂视为一种衰老治疗方法,那么了解长期暴露的潜在后果非常重要,而实现这一目标的最实际方法是通过饮食管理。在这里,我们研究了在饮食中给予 BYL719 的药代动力学以及在 8 月龄雄性和雌性小鼠饮食中给予 BYL719 抑制胰岛素信号的功效。与口服灌胃相比,饮食摄入导致血浆 BYL719 峰值浓度降低(3.6 对 9.2 μM),但半衰期相似(~1.5 h)。在 72 小时内,摄入 BYL719 导致肝脏和肌肉中的胰岛素信号降低,并且在 6 周内摄入含有 0.3 g/kg BYL719 的饮食后,小鼠仍然表现出葡萄糖耐量受损和胰岛素敏感性降低。然而,摄入 BYL719 并不影响食物摄入量、体重、肌肉功能(转棒和悬挂时间表现)或认知行为。这提供了证据表明,BYL719 具有长期疗效,没有重大毒性或副作用,并且表明在饮食中给予 BYL719 适合研究药理学抑制 PI3K p110α 对衰老和代谢功能的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/479466dd8718/biomolecules-11-00150-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/8941532140e7/biomolecules-11-00150-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/9631dea6c5fc/biomolecules-11-00150-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/3815aad4f9ce/biomolecules-11-00150-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/0ef928f0a0ad/biomolecules-11-00150-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/eb771a03fd9a/biomolecules-11-00150-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/479466dd8718/biomolecules-11-00150-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/8941532140e7/biomolecules-11-00150-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/9631dea6c5fc/biomolecules-11-00150-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/3815aad4f9ce/biomolecules-11-00150-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/0ef928f0a0ad/biomolecules-11-00150-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/eb771a03fd9a/biomolecules-11-00150-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e5/7911305/479466dd8718/biomolecules-11-00150-g006.jpg

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