白杨素防治牙周炎的信号通路机制的研究进展*

陈亚冰 ,  杜思雨 ,  郭怡婧 ,  郑义 ,  王雷

国际老年医学杂志 ›› 2025, Vol. 46 ›› Issue (06) : 737 -741.

PDF (1119KB)
国际老年医学杂志 ›› 2025, Vol. 46 ›› Issue (06) : 737 -741. DOI: 10.3969/j.issn.1674-7593.2025.06.019
综述

白杨素防治牙周炎的信号通路机制的研究进展*

作者信息 +

Targeting inflammatory signaling pathways with Chrysin in periodontitis: current research and future directions

Author information +
文章历史 +
PDF (1145K)

摘要

牙周炎是一种非传染病性疾病, 随着我国步入老龄化时期, 牙周炎已成为老年人日益突出的口腔健康问题, 是老年人牙齿缺失的主要原因。 白杨素是一种天然类黄酮, 具有抗炎、 抗菌等多种生物学作用, 且安全无毒, 不良反应小, 在牙周炎的预防和治疗中具有广泛的应用前景。 白杨素通过抑制核转录因子-κB (NF-κB) 信号通路、Jauns 激酶/ 信号转导和转录激活子 (JAK / STAT) 信号通路和丝裂原活化蛋白激酶 (MAPK) 信号通路, 抑制炎症因子的表达, 从而达到防治牙周炎的目的。 本文就白杨素在牙周炎防治方面的信号转导机制的研究进展进行综述, 为临床提供参考。

Abstract

Periodontitis is a non-communicable disease. As China transitions into an aging culture, periodontitis has emerged as a significant oral health concern among the senior population. It is the primary cause of edentulism in the geriatric population. Chrysin, demonstrates a diverse array of biological actions, encompassing anti-inflammatory and antibacterial properties. Chrysin possesses considerable potential for the prevention and treatment of periodontal disease because to its safety, non-toxicity, and minimum adverse responses. Chrysin can prevent and treat periodontitis by inhibiting the expression of inflammatory factors via the suppression of nuclear factor-κB (NF-κB) signaling pathway, Janus kinase (JAK) / signal transducer and activator of transcription (STAT) signaling pathway (JAK/ STAT), and mitogen-activated protein kinase (MAPK) signaling pathways. This article reviews advancements in research regarding the signal transduction mechanism of Chrysin in the prevention and treatment of periodontitis, offering a reference for clinical practice.

关键词

白杨素 / 牙周炎 / 抗炎作用 / 抗菌作用 / 信号通路

Key words

Chrysin / Periodontitis / Anti-inflammatory effect / Antibacterial effect / Signaling pathway

引用本文

引用格式 ▾
陈亚冰,杜思雨,郭怡婧,郑义,王雷. 白杨素防治牙周炎的信号通路机制的研究进展*[J]. 国际老年医学杂志, 2025, 46(06): 737-741 DOI:10.3969/j.issn.1674-7593.2025.06.019

登录浏览全文

4963

注册一个新账户 忘记密码

参考文献

[1]

杨祺婧, 张洪浦, 岳靓, . 细胞焦亡在口腔感染性疾病中的研究进展[J]. 国际老年医学杂志, 2024, 45(6): 734-737.

[2]

Yang Q J, Zhang H P, Yue L, Li C Y. The role of pyroptosis in oral infectious diseases: current research progress[J]. Int J Geriatr, 2024, 45(6): 734-737.

[3]

Hu D, Zhong T, Dai Q . Clinical efficacy of probiotics as an adjunctive therapy to scaling and root planning in the management of periodontitis: a systematic review and meta—analysis of randomized controlled trails[J]. J Evid Based Dent Pract, 2021, 21(2): 101547.

[4]

Paternò Holtzman L, Valente N A, Vittorini Orgeas G, et al. Change in clinical parameters after subgingival instrumentation for the treatment of periodontitis and timing of periodontal re—evaluation: a systematic review and meta—analysis[J]. J Clin Periodontol, 2025, 52(1): 137-158.

[5]

Nawrot—Hadzik I, Matkowski A, Hadzik J, et al. Proanthocyanidins and flavan—3—ols in the prevention and treatment of periodontitis—antibacterial effects[J]. Nutrients, 2021, 13(1): 165.

[6]

Talebi M, Talebi M, Farkhondeh T, et al. A review on hepatoprotective effect of Chrysin: preclinical implications and molecular cascades came into focus[J]. Curr Diabetes Rev, 2024. doi: 10.2174/0115733998329724240918091335.

[7]

Falbo F, Aiello F . Chrysin: a polyedric flavone as a tool to explore new phytotherapeutic applications and drug design[J]. Arch Pharm (Weinheim), 2023, 356(2): e2200347.

[8]

Garg A, Chaturvedi S . A comprehensive review on Chrysin: emphasis on molecular targets, pharmacological actions and bio—pharmaceutical aspects[J]. Curr Drug Targets, 2022, 23(4): 420-436.

[9]

Hajishengallis G, Lamont R J . Polymicrobial communities in periodontal disease: their quasi—organismal nature and dialogue with the host[J]. Periodontol 2000, 2021, 86(1): 210-230.

[10]

Zhang M, Liu Y, Afzali H, et al. An update on periodontal inflammation and bone loss[J]. Front Immunol, 2024, 15: 1385436.

[11]

Alipour M, Pouya B, Aghazadeh Z, et al. The antimicrobial, antioxidative, and anti—inflammatory effects of polycaprolactone/gelatin scaffolds containing Chrysin for regenerative endodontic purposes[J]. Stem Cells Int, 2021, 2021: 3828777.

[12]

Siddhardha B, Pandey U, Kaviyarasu K, et al. Chrysin—loaded chitosan nanoparticles potentiates antibiofilm activity against Staphylococcus aureus[J]. Pathogens, 2020, 9(2): 115.

[13]

Tian Y, Li Y, Liu J, et al. Photothermal therapy with regulated Nrf2/NF—κB signaling pathway for treating bacteria—induced periodontitis[J]. Bioact Mater, 2022, 9: 428-445.

[14]

Papadatos S S, Mitselou A, Lampri E, et al. NF—kB p65 and NF—kB p50 of the rel family. A comparison between irritable bowel syndrome and inflammatory bowel disease patients[J]. Maedica (Bucur), 2024, 19(3): 478-485.

[15]

潘中武, 李泽朋, 陈晓, . 基于线粒体氧化应激损伤探讨白杨素对溃疡性结肠炎大鼠的保护作用及机制[J]. 中药材, 2023, 46(12): 3081-3090.

[16]

Pan Z W, Li Z P, Chen X, et al. Study on the protective effect and mechanism of Chrysin in ulcerative colitis of rats based on mitochondrial oxidative stress damage[J]. J Chin Med Mater, 2023, 46(12): 3081-3090.

[17]

Guldenpfennig C, Teixeiro E, Daniels M . NF—kB's contribution to B cell fate decisions[J]. Front Immunol, 2023, 14: 1214095.

[18]

Dou W, Zhang J, Zhang E, et al. Chrysin ameliorates chemically induced colitis in the mouse through modulation of a PXR/NF—κB signaling pathway[J]. J Pharmacol Exp Ther, 2013, 345(3): 473-482.

[19]

Alanazi S T, Salama S A, El—Ebiary A M, et al. Targeting SIRT1, NLRP3 inflammasome, and Nrf2 signaling with Chrysin alleviates the iron—triggered hepatotoxicity in rats[J]. Toxicology, 2024, 504: 153766.

[20]

辛本凯, 郭磊, 唐一鑫, . 丁酸钠诱导癌细胞凋亡的分子机制研究进展[J]. 国际老年医学杂志, 2022, 43(4): 472-475.

[21]

Xin B K, Guo L, Tang Y X, et al. Advances in molecular mechanisms of sodium butyrate inducing poptosis of cancer cells[J]. Int J Geriatr, 2022, 43(4): 472-475.

[22]

Martínez—Aguilar V M, Carrillo—Ávila B A, Sauri—Esquivel E A, et al. Quantification of TNF—α in patients with periodontitis and type 2 diabetes[J]. Biomed Res Int, 2019, 2019: 7984891.

[23]

Cheng R, Wu Z, Li M, et al. Interleukin—1β is a potential therapeutic target for periodontitis: a narrative review[J]. Int J Oral Sci, 2020, 12(1): 2.

[24]

Kim M J, Kim H J . Anti—inflammatory effects of Apostichopus japonicus extract in porphyromonas gingivalis—stimulated RAW 264.7 Cells[J]. Curr Issues Mol Biol, 2024, 46(12): 13405-13417.

[25]

Jinesh S, Radhakrishnan R . Pharmaceutical aspects of JAK inhibitors: a comparative review[J]. Inflammopharmacology, 2025, 33(1): 91-104.

[26]

Shi Z, Li M, Zhang C, et al. Butyrate—producing Faecalibacterium prausnitzii suppresses natural killer/T—cell lymphoma by dampening the JAK—STAT pathway[J]. Gut, 2025, 74(4): 557-570.

[27]

Al Hasan M S, Bhuia M S, Sheikh S, et al. Assessment of sedative activity of Chrysin: behavioral approach with pharmacokinetics, toxicological profile and molecular docking[J]. Sleep Med, 2025, 126: 88-96.

[28]

Qi S M, Li Q, Jiang Q, et al. [Chrysin inhibits lipopolysaccharide—induced inflammatory responses of macrophages via JAK—STATs signaling pathway][J]. Nan Fang Yi Ke Da Xue Xue Bao, 2018, 38(3): 243-250.

[29]

Wen X, Jiao L, Tan H . MAPK/ERK pathway as a central regulator in vertebrate organ regeneration[J]. Int J Mol Sci, 2022, 23(3): 1464.

[30]

Martinez M L, Nan K, Bao Z, et al. Novel kinase regulators of extracellular matrix internalisation identified by high—content screening modulate invasive carcinoma cell migration[J]. PLoS Biol, 2024, 22(12): e3002930.

[31]

Saleh D O, El—Nasr N, Fayez A M, et al. Uro—protective role of Chrysin against cyclophosphamide—induced hemorrhagic cystitis in rats involving the turning—off NF—κB/P38—MAPK, NO/PARP—1 and STAT—3 signaling cascades[J]. Chem Biol Interact, 2023, 382: 110585.

[32]

Cao Y, Tan Y J, Huang D . Molecular mechanism of 5,6—dihydroxyflavone in suppressing LPS—induced inflammation and oxidative stress[J]. Int J Mol Sci, 2024, 25(19): 10694.

[33]

石志群, 田贻婷, 张朋朋, . 白杨素生物利用度的影响因素及提高办法研究进展[J]. 中南药学, 2022, 20(6): 1379-1384.

[34]

Shi Z Q, Tian Y T, Zhang P P, et al. Research progress on influencing factors and improving methods of Chrysin bioavailability[J]. Central South Pharm, 2022, 20(6): 1379-1384.

[35]

Jangid A K, Solanki R, Patel S, et al. Improving anticancer activity of Chrysin using tumor microenvironment pH—responsive and self—assembled nanoparticles[J]. ACS Omega, 2022, 7(18): 15919-15928.

[36]

Dabiri S, Jafari S, Molavi O . Advances in nanocarrier—mediated delivery of Chrysin: enhancing solubility, bioavailability, and anticancer efficacy[J]. Bioimpacts, 2025, 15: 30269.

[37]

Roy S, Kant S, Das Saha K, et al. Chrysin—functionalized gold nanoparticles and paclitaxel exhibit synergistic impact on lung cancer cell lines via regulating the AKT/PPAR—Upsilon/beta—catenin pathway[J]. Drug Dev Ind Pharm, 2024: 1-14.

[38]

Farhadi A, Homayouni Tabrizi M, Sadeghi S, et al. Targeted delivery and anticancer effects of Chrysin—loaded chitosan—folic acid coated solid lipid nanoparticles in pancreatic malignant cells[J]. J Biomater Sci Polym Ed, 2023, 34(3): 315-333.

[39]

Alshetaili A S, Ali R, Qamar W, et al. Preparation, optimization, and characterization of Chrysin—loaded TPGS—b—PCL micelles and assessment of their cytotoxic potential in human liver cancer (Hep G2) cell lines[J]. Int J Biol Macromol, 2023, 246: 125679.

[40]

Luo D, Wang X, Zhong X, et al. MPEG—PCL Nanomicelles platform for synergistic metformin and Chrysin delivery to breast cancer in mice[J]. Anticancer Agents Med Chem, 2022, 22(2): 280-293.

[41]

Sassa—Deepaeng T, Pikulkaew S, Okonogi S . Development of Chrysin loaded poloxamer micelles and toxicity evaluation in fish embryos[J]. Drug Discov Ther, 2016, 10(3): 150-155.

基金资助

*吉林省科技发展计划项目(YDZJ202301ZYTS013)

吉林省财政厅课题(Jcsz2023481-19)

AI Summary AI Mindmap
PDF (1119KB)

0

访问

0

被引

详细

导航
相关文章

AI思维导图

/