Suppr超能文献

大气污染淀粉样变生成被γ-分泌酶调节剂 GSM-15606 减弱。

Air pollution amyloidogenesis is attenuated by the gamma-secretase modulator GSM-15606.

机构信息

Leonard Davis School of Gerontology, University of Southern California, Los Angeles, California, USA.

Capricor Therapeutics, Inc., Beverly Hills, California, USA.

出版信息

Alzheimers Dement. 2024 Sep;20(9):6107-6114. doi: 10.1002/alz.14086. Epub 2024 Aug 12.

Abstract

INTRODUCTION

Chronic air pollution (AirPoll) is associated with accelerated cognitive decline and risk of Alzheimer's disease (AD). Correspondingly, wild-type and AD-transgenic rodents exposed to AirPoll have increased amyloid peptides and behavioral impairments.

METHODS

We examined the γ-secretase modulator GSM-15606 for potential AirPoll protection by its attenuating of amyloid beta (Aβ)42 peptide production. Male and female wild-type mice were fed GSM-15606 during an 8-week inhalation exposure to AirPoll subfractions, ambient nanoparticulate matter (nPM), and diesel exhaust particles (DEP).

RESULTS

GSM-15606 decreased Aβ42 during nPM and DEP exposure without changing beta- or gamma-secretase activity or BACE1 and PS1 protein levels. DEP increased lateral ventricle volume by 25%.

DISCUSSION

These enzyme responses are relevant to AD drug treatments, as well as to the physiological functions of the Aβ42 peptide. GSM-15606 attenuation of Aβ42 may benefit human exposure to AirPoll.

HIGHLIGHTS

Gamma-secretase modulator (GSM-15606) attenuates the amyloidogenic amyloid beta (Aβ)42 peptide during exposure to air pollution, which may be a mechanism by which air pollution increases Alzheimer's disease (AD) risk. AD drug treatments may also consider Aβ homeostasis among the chronic effects of GSM-15606 and other amyloid reduction treatments on secretase enzymes.

摘要

简介

慢性空气污染(AirPoll)与认知能力加速下降和阿尔茨海默病(AD)风险增加有关。相应地,暴露于 AirPoll 的野生型和 AD 转基因啮齿动物会增加淀粉样肽和行为障碍。

方法

我们研究了 γ-分泌酶调节剂 GSM-15606,以其对淀粉样β(Aβ)42 肽产生的衰减作用,来评估其对 AirPoll 保护的潜在作用。雄性和雌性野生型小鼠在 8 周的 AirPoll 亚组分、环境纳米颗粒(nPM)和柴油废气颗粒(DEP)吸入暴露期间接受 GSM-15606 喂养。

结果

GSM-15606 在 nPM 和 DEP 暴露期间降低了 Aβ42,而不改变β-或γ-分泌酶活性或 BACE1 和 PS1 蛋白水平。DEP 使侧脑室体积增加了 25%。

讨论

这些酶反应与 AD 药物治疗以及 Aβ42 肽的生理功能有关。GSM-15606 对 Aβ42 的衰减可能有益于人类暴露于空气污染。

重点

γ-分泌酶调节剂(GSM-15606)在暴露于空气污染时会减弱淀粉样的淀粉样β(Aβ)42 肽,这可能是空气污染增加阿尔茨海默病(AD)风险的一种机制。AD 药物治疗也可能考虑到 GSM-15606 和其他淀粉样减少治疗对 secretase 酶的慢性影响中的 Aβ 动态平衡。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8e3/11497728/5c2216d236cc/ALZ-20-6107-g003.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验