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转化生长因子 β3 预防颊黏膜瘢痕形成。

Prevention of buccal mucosa scarring with transforming growth factor β3.

机构信息

Department of Otolaryngology, Head and Neck Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Japan.

出版信息

Laryngoscope. 2011 Jul;121(7):1404-9. doi: 10.1002/lary.21759. Epub 2011 Jun 6.

Abstract

OBJECTIVES/HYPOTHESIS: In the treatment of tumorous diseases, scarring often forms after resection or irradiation. Scarring of the buccal mucosa causes difficulty in opening the mouth and mastication, decreasing quality of life. Transforming growth factor (TGF) β3 is an isoform of TGFβ1 that is known to accelerate scarring, although it has different effects on wound healing. TGFβ3 administration into wounds has been associated with improvement in the quality of healing skin in vivo. TGFβ3 is also considered to be an important anti-scarring factor in buccal mucosa. The present study aimed to examine whether TGFβ3 is effective for prevention and treatment of buccal mucosa scarring.

STUDY DESIGN

Prospective study using an animal model.

METHODS

Thirty Sprague-Dawley rats were involved in this study. We injected 0.5 mL of TGFβ3 (0.005 μg/mL, 0.05 μg/mL, 0.5 μg/mL, 5 μg/mL) or saline was injected into the buccal submucosa. Fifteen minutes after the injection, the mucosa was removed down to the masseter muscle or orbicularis oris muscle layer using a 6-mm biopsy punch. Six weeks after the operation, the buccal mucosae were harvested after euthanasia. Morphologic and histologic examinations were performed.

RESULTS

The administration of 0.5 μg/mL TGFβ3 induced rapid re-epithelialization and suppressed scar formation. In the submucosal layer, favorable restoration of hyaluronic acid and elastin was seen in the TGFβ3-treated groups compared to the saline-treated group.

CONCLUSIONS

TGFβ3 is considered to be effective for better restoration of extracellular matrices of injured buccal mucosa, suggesting a preventative effect of buccal mucosa scarring.

摘要

目的/假设:在治疗肿瘤性疾病时,切除或放疗后常形成瘢痕。颊黏膜瘢痕导致张口和咀嚼困难,降低生活质量。转化生长因子 (TGF)β3 是 TGFβ1 的一种同工型,已知其可加速瘢痕形成,尽管它对伤口愈合有不同的影响。TGFβ3 给药到伤口中与体内愈合皮肤质量的改善相关。TGFβ3 也被认为是颊黏膜中重要的抗瘢痕形成因子。本研究旨在研究 TGFβ3 是否对预防和治疗颊黏膜瘢痕有效。

研究设计

前瞻性动物模型研究。

方法

本研究纳入 30 只 Sprague-Dawley 大鼠。我们将 0.5mL 的 TGFβ3(0.005μg/mL、0.05μg/mL、0.5μg/mL、5μg/mL)或生理盐水注入颊黏膜下。注射后 15 分钟,使用 6mm 活检冲孔将黏膜从咬肌或口轮匝肌层向下切除。手术后 6 周,安乐死后采集颊黏膜。进行形态学和组织学检查。

结果

0.5μg/mL TGFβ3 的给药诱导快速再上皮化并抑制瘢痕形成。在黏膜下层,与生理盐水处理组相比,TGFβ3 处理组的透明质酸和弹性蛋白得到了更好的恢复。

结论

TGFβ3 被认为对受损颊黏膜细胞外基质的更好恢复有效,提示其对颊黏膜瘢痕具有预防作用。

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