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一种基于生物材料的疗法,使用透明质酸钠/生物玻璃复合水凝胶治疗口腔黏膜下纤维化。

A biomaterial-based therapy using a sodium hyaluronate/bioglass composite hydrogel for the treatment of oral submucous fibrosis.

作者信息

Guo Zhen-Xing, Zhang Zhaowenbin, Yan Jian-Fei, Xu Hao-Qing, Wang Shu-Yan, Ye Tao, Han Xiao-Xiao, Wang Wan-Rong, Wang Yue, Gao Jia-Lu, Niu Li-Na, Chang Jiang, Jiao Kai

机构信息

State Key Laboratory of Military Stomatology & National Clinical Research Center for Oral Diseases & Shaanxi Key Laboratory of Stomatology, School of Stomatology, The Fourth Military Medical University, Xi'an, Shaanxi 710032, China.

Wenzhou Institute, University of Chinese Academy of Sciences, Wenzhou, Zhejiang 325000, China; State Key Laboratory of High-Performance Ceramics and Superfine Microstructure, Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China.

出版信息

Acta Biomater. 2023 Feb;157:639-654. doi: 10.1016/j.actbio.2022.12.006. Epub 2022 Dec 10.

Abstract

Oral submucous fibrosis (OSF) is a chronic, inflammatory and potentially malignant oral disorder. Its pathophysiology is extremely complex, including excessive collagen deposition, massive inflammatory infiltration, and capillary atrophy. However, the existing clinical treatment methods do not fully take into account all the pathophysiological processes of OSF, so they are generally low effective and have many side effects. In the present study, we developed an injectable sodium hyaluronate/45S5 bioglass composite hydrogel (BG/HA), which significantly relieved mucosal pallor and restricted mouth opening in OSF rats without any obvious side effects. The core mechanism of BG/HA in the treatment of OSF is the release of biologically active silicate ions, which inhibit collagen deposition and inflammation, and promote angiogenesis and epithelial regeneration. Most interestingly, silicate ions can overall regulate the physiological environment of OSF by down-regulating α-smooth muscle actin (α-SMA) and CD68 and up-regulating CD31 expression, as well as regulating the expression of pro-fibrotic factors [transforming growth factor-β1 (TGF-β1), interleukin-10 (IL-10), tumor necrosis factor-α (TNF-α) and tissue inhibitors of metalloproteinase-1 (TIMP-1)] and anti-fibrotic factors [interleukin-1β (IL-1β)] in macrophage. In conclusion, our study shows that BG/HA has great potential in the clinical treatment of OSF, which provides an important theoretical basis for the subsequent development of new anti-fibrotic clinical preparations. STATEMENT OF SIGNIFICANCE: : Oral submucous fibrosis (OSF) is a chronic, inflammatory and potentially malignant mucosal disease with significant impact on the quality of patients' life. However, the existing clinical treatments have limited efficacy and many side effects. There is an urgent need for development of specific drugs for OSF treatment. In the present study, bioglass (BG) composited with sodium hyaluronate solution (HA) was used to treat OSF in an arecoline-induced rat model. BG/HA can significantly inhibit collagen deposition, regulate inflammatory response, promote angiogenesis and repair damaged mucosal epithelial cells, and thereby mitigate the development of fibrosis in vivo.

摘要

口腔黏膜下纤维化(OSF)是一种慢性、炎症性且具有潜在恶性的口腔疾病。其病理生理学极其复杂,包括胶原蛋白过度沉积、大量炎症浸润和毛细血管萎缩。然而,现有的临床治疗方法并未充分考虑OSF的所有病理生理过程,因此总体疗效较低且有许多副作用。在本研究中,我们研制了一种可注射的透明质酸钠/45S5生物玻璃复合水凝胶(BG/HA),其能显著缓解OSF大鼠的黏膜苍白并改善张口受限情况,且无任何明显副作用。BG/HA治疗OSF的核心机制是释放具有生物活性的硅酸根离子,其可抑制胶原蛋白沉积和炎症反应,并促进血管生成和上皮再生。最有趣的是,硅酸根离子可通过下调α平滑肌肌动蛋白(α-SMA)和CD68以及上调CD31表达,全面调节OSF的生理环境,还可调节巨噬细胞中促纤维化因子[转化生长因子-β1(TGF-β1)、白细胞介素-10(IL-10)、肿瘤坏死因子-α(TNF-α)和基质金属蛋白酶-1组织抑制剂(TIMP-1)]和抗纤维化因子[白细胞介素-1β(IL-1β)]的表达。总之,我们的研究表明BG/HA在OSF的临床治疗中具有巨大潜力,为后续新型抗纤维化临床制剂的研发提供了重要的理论依据。意义声明:口腔黏膜下纤维化(OSF)是一种慢性、炎症性且具有潜在恶性的黏膜疾病,对患者生活质量有重大影响。然而,现有的临床治疗疗效有限且副作用众多。迫切需要研发用于治疗OSF的特效药物。在本研究中,将生物玻璃(BG)与透明质酸钠溶液(HA)复合用于治疗槟榔碱诱导的大鼠OSF模型。BG/HA可显著抑制胶原蛋白沉积,调节炎症反应,促进血管生成并修复受损的黏膜上皮细胞,从而减轻体内纤维化的发展。

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