Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Aug 29;23(1):302.
doi: 10.1186/s12906-023-04138-x.

The mechanism of Qijing Mingmu decoction on cellular senescence of conjunctivochalasis

Affiliations

The mechanism of Qijing Mingmu decoction on cellular senescence of conjunctivochalasis

Minhong Xiang et al. BMC Complement Med Ther. .

Abstract

Background: Qijing Mingmu decoction (QJMM), a compound Chinese medicine preparation, which consists of Lycium barbarum, Polygonatum, Ophiopogon japonicus, Poria cocos, Glycyrrhiza, Eclipta prostrata and Ligusticum striatum, has been confirmed to be effective for the treatment of conjunctivochalasis (CCH) in clinic and reduce cellular senescence. However, the underlying mechanism is still unknown. Our previous study revealed that p38-mediated cellular senescence contributed to the pathogenesis of CCH.

Methods: To explore whether p38 might be the potential therapeutic target of QJMM for CCH, CCH fibroblasts were treated with QJMM granule and then the effect of QJMM granule on the expression and promoter activity of p38α was determined by western blot and dual luciferase reporter gene assay, respectively. Meanwhile, the influence of QJMM granule on cell proliferation, oxidative stress, cellular senescence and the expression of the cellular senescence-associated genes were measured by corresponding methods.

Results: QJMM granule significantly decreased the protein expression of p38α and p-p38α in CCH fibroblasts in a dose-dependent manner and inhibited p38α promoter activity. QJMM granule as well as the p38 inhibitor SB203580 reduced the level of reactive oxygen species and increased the activity of superoxide dismutase in CCH fibroblasts. QJMM granule and SB203580 promoted cell proliferation and reduced the percentage of SA-β-Gal-positive cells. The mRNA and protein expression of p53 and p21 was remarkably down-regulated by QJMM granule as well as SB203580 and that of SMP30 was up-regulated in CCH fibroblasts.

Conclusions: Our findings demonstrated that QJMM granule was effective for alleviating cellular senescence of CCH fibroblasts by p38 MAPK signaling and the followed p53/p21 signaling.

Keywords: Cellular senescence; Chinese herbal medicine; Conjunctivochalasis; p38 MAPK signaling.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no competing interests.

Figures

Fig. 1
Fig. 1
QJMM granule affected p38 MAPK signaling in CCH fibroblasts. A The protein expression of p38α and p-p38α in CCH fibroblasts treated with different concentration of QJMM granule. B The promoter activity of p38α in CCH fibroblasts treated with 1.61 mg/L QJMM. **P < 0.001 compared with CCH group; ## P < 0.001 compared with CCH + 0.805 mg/L QJMM group; & P < 0.05 compared with CCH + 1.61 mg/L QJMM group; n = 3
Fig. 2
Fig. 2
QJMM granule affected oxidative stress in CCH fibroblasts. A Reactive oxygen species (ROS) level in CCH fibroblasts treated with QJMM granule. B Superoxide dismutase (SOD) activity in CCH fibroblasts treated with QJMM granule. *P < 0.05, **P < 0.001 compared with normal group; ## P < 0.001 compared with CCH group; & P < 0.05 compared with CCH + QJMM group; n = 3
Fig. 3
Fig. 3
QJMM granule affected cell proliferation of CCH fibroblasts. *P < 0.05, **P < 0.001 compared with normal group; ## P < 0.001 compared with CCH group; n = 3
Fig. 4
Fig. 4
QJMM granule affected cellular senescence in CCH fibroblasts. **P < 0.001 compared with normal group; ## P < 0.001 compared with CCH group; n = 3
Fig. 5
Fig. 5
The mRNA (A-D) and protein (E) levels of p38 and senescence-associated genes in CCH fibroblasts treated with QJMM granule. *P < 0.05, **P < 0.001 compared with normal group; # P < 0.05, ## P < 0.001 compared with CCH group; & P < 0.05, && P < 0.001 compared with CCH + QJMM group; n = 3
Fig. 6
Fig. 6
Molecular mechanism of QJMM on cellular senescence of CCH

Similar articles

Cited by

References

    1. Meller D, Tseng SC. Conjunctivochalasis: literature review and possible pathophysiology. Surv Ophthalmol. 1998;43(3):225–232. doi: 10.1016/S0039-6257(98)00037-X. - DOI - PubMed
    1. Di Pascuale MA, Espana EM, Kawakita T, Tseng SC. Clinical characteristics of conjunctivochalasis with or without aqueous tear deficiency. Br J Ophthalmol. 2004;88(3):388–392. doi: 10.1136/bjo.2003.025460. - DOI - PMC - PubMed
    1. Mimura T, Yamagami S, Usui T, Funatsu H, Mimura Y, Noma H, et al. Changes of conjunctivochalasis with age in a hospital-based study. Am J Ophthalmol. 2009;147(1):171–177. doi: 10.1016/j.ajo.2008.07.010. - DOI - PubMed
    1. Zhang X, Li Q, Zou H, Peng J, Shi C, Zhou H, et al. Assessing the severity of conjunctivochalasis in a senile population: a community-based epidemiology study in Shanghai, China. BMC Public Health. 2011;11:198. doi: 10.1186/1471-2458-11-198. - DOI - PMC - PubMed
    1. Gumus K, Pflugfelder SC. Increasing prevalence and severity of conjunctivochalasis with aging detected by anterior segment optical coherence tomography. Am J Ophthalmol. 2013;155(2):238–42. doi: 10.1016/j.ajo.2012.07.014. - DOI - PubMed

Substances