Oxidative stress-mediated - mediated proapoptosis signaling A novel theory on the mechanism underlying the pathogenesis of burning mouth syndrome

被引:1
|
作者
Heiliczer, Shimrit [1 ]
Yanko, Robert [1 ]
Sharav, Yair [1 ]
Aframian, Doron J. [1 ]
Klutstein, Michael [2 ]
Wilensky, Asaf [3 ]
Haviv, Yaron [1 ]
机构
[1] Hebrew Univ Jerusalem Hadassah Hosp & Med Sch, Sch Dent Med, Dept Oral Med Sedat & Imaging, POB 12272, IL-91120 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Inst Biomed & Oral Res, Fac Dent Med, Jerusalem, Israel
[3] Hebrew Univ Jerusalem, Fac Dent Med, Hadassah Med Ctr, Dept Periodontol, Jerusalem, Israel
来源
关键词
Burning mouth syndrome; pathogenesis; molecular mechanisms; proapoptosis calcium oxidative stress; reactive; GENE-RELATED PEPTIDE; ESTROGEN; BCL-2; PAIN; CALCIUM; TRPV1; PROLIFERATION; OVARIECTOMY; TRAFFICKING; ACTIVATION;
D O I
10.1016/j.adaj.2023.08.014
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Background. Burning mouth syndrome (BMS) is a chronic oral pain disorder characterized by a generalized burning sensation in the oral mucosa without apparent medical or dental causes. Despite various hypotheses proposed to explain BMS pathogenesis, a clear understanding of the cellular- level events and associated histologic and molecular findings is lacking. Advancing our understanding of BMS pathogenesis could facilitate the development of more targeted therapeutic interventions. Types of Studies Reviewed. The authors conducted an extensive literature search and review of cellular mechanisms, focusing on evidence-based data that support a comprehensive hypothesis for BMS pathogenesis. The authors explored novel and detailed mechanisms that may account for the characteristic features of BMS. Results. The authors proposed that BMS symptoms arise from the uncontrolled activation of proapoptotic transmembrane calcium permeable channels expressed in intraoral mucosal nerve fibers. Elevated levels of reactive oxygen species or dysfunctional antiapoptosis pathways may lead to uncontrolled oxidative stress-mediated apoptosis signaling, resulting in upregulation of trans- membrane transient receptor potential vanilloid type 1 and P2X 3 calcium channels in nociceptive fibers. Activation of these channels can cause nerve terminal depolarization, leading to generation of action potentials that are centrally interpreted as pain. Conclusions and Practical Implications. The authors present a novel hypothesis for BMS pathogenesis, highlighting the role of proapoptotic transmembrane calcium permeable channels and oxidative stress-mediated apoptosis signaling in the development of BMS symptoms. Understanding these underlying mechanisms could provide new insights into the development of targeted therapeutic interventions for BMS. Additional research is warranted to validate this hypothesis and explore potential avenues for effective management of BMS.
引用
收藏
页码:258 / 267
页数:10
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