Evidence map›Paper›PMID 41484271›Full record

ArticleBiogerontology2026

Curcumin attenuates PM2.5-triggered pulmonary senescence via the mTOR/S6K1 signaling pathway.

Kai Liu, Meng Shi, Xin Li, Xiaoli Zeng, Xiaoju Liu

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Article in Biogerontology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Kai LiuThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.
Meng ShiThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.
Xin LiThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.
Xiaoli ZengThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.
Xiaoju LiuThe First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China. liuxiaoju835@126.com.

Funding

Hospital Fund of The First Hospital of Lanzhou University ldyyyn2023-115Key Research and Development Plan of Gansu Province 22YF7FA083National Natural Science Foundation of China 82260010
6 · The paper itself

Abstract

Exposure to fine particulate matter (PM2.5) triggers pulmonary inflammation and oxidative stress, which can lead to cellular senescence and a decline in lung function. Curcumin, a yellow polyphenol derived from the rhizome of Curcuma longa, is traditionally used to treat respiratory ailments. However, its potential to counteract PM2.5-induced pulmonary senescence remains underexplored. In this study, we established a murine model of PM2.5-triggered lung senescence and used BEAS-2B cells to investigate the mechanisms of curcumin. We assessed senescence markers (p16, p21, and senescence-associated β-galactosidase [SA-β-gal]) and evaluated pulmonary function. Levels of inflammatory cytokines (e.g., interleukin-1β [IL-1β], interleukin-6 [IL-6], and tumor necrosis factor-α [TNF-α]) and oxidative stress markers (e.g., malondialdehyde [MDA], superoxide dismutase [SOD], catalase [CAT], and reactive oxygen species [ROS]) were also measured. To elucidate the underlying mechanism, we examined the expression of proteins in the mammalian target of rapamycin (mTOR)/S6K1 pathway. PM2.5 exposure induced senescence, as shown by increased levels of p16, p21, and SA-β-gal, accompanied by impaired lung function. These changes coincided with elevated pro-inflammatory mediators and increased oxidative stress. PM2.5 exposure also activated the mTOR/S6K1 pathway. Curcumin treatment attenuated the senescence markers and improved lung function. It reduced oxidative stress (e.g., lowered MDA and ROS levels) and enhanced the activity of antioxidant enzymes (SOD and CAT). Curcumin also effectively inhibited mTOR/S6K1 signaling. However, its protective effects were diminished by MHY1485, an mTOR activator, which exacerbated senescence, inflammation, and oxidative stress. These findings suggest that curcumin alleviates PM2.5-induced pulmonary senescence, likely through a hormetic effect that inhibits excessive activation of the mTOR/S6K1 axis. This study highlights the translational potential of curcumin as a phytochemical intervention against PM2.5-associated respiratory damage.

Indexed as

Cellular SenescenceCurcuminLungParticulate MatterTOR Serine-Threonine KinasesAnimalsHumansMaleMiceMice, Inbred C57BLOxidative StressRibosomal Protein S6 Kinases, 90-kDaSignal TransductionCurcuminmTOR protein, mouseParticulate MatterRibosomal Protein S6 Kinases, 90-kDaRps6ka1 protein, mouseTOR Serine-Threonine KinasesCurcuminmTOR/S6K1PM2.5Pulmonary senescence

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.