Department of Oral Biology, Indiana University School of Dentistry, Indianapolis, IN, USA.
Oral Dis. 2011 Apr;17(3):291-7. doi: 10.1111/j.1601-0825.2010.01739.x. Epub 2010 Sep 23.
Osteonecrosis of the jaw is a serious complication of bisphosphonate treatment for which the pathophysiology is unknown. The purpose of this study was to investigate whether in vivo zoledronic acid (ZA) induces alterations in cell proliferation, apoptosis, and matrix metalloproteinases (MMPs) expression in oral mucosal epithelial cells.
One-year-old dogs were either untreated (control group) or given high doses of intravenous ZA (ZA group) for 3 months. The doses of ZA were equivalent to those given to cancer patients, yet were administered two times more frequently (every 2 weeks). Mucosal tissues were assessed immunohistochemically for cell proliferation (proliferating cell nuclear antigen, PCNA), matrix metalloproteinase (MMP) expression, and apoptosis (caspase 3 and TUNEL).
There were no significant differences between the groups with respect to PCNA, MMP-2, MMP-14, and TUNEL positive cells. However, the expression of MMP-9 was significantly higher in the control group than in the ZA group (P < 0.05), whereas the expression of caspase 3 was significantly lower in the control group than in the ZA group (P < 0.05).
These results suggest that high doses of ZA resulted in higher levels of apoptosis and lower levels of MMP-9 in the oral epithelial cells supporting the idea of bisphosphonate treatment affects the oral mucosa.
颌骨坏死是双膦酸盐治疗的一种严重并发症,其病理生理学尚不清楚。本研究旨在探讨唑来膦酸(ZA)体内诱导口腔黏膜上皮细胞增殖、凋亡和基质金属蛋白酶(MMPs)表达改变的情况。
1 岁犬分别给予未治疗(对照组)或高剂量静脉 ZA(ZA 组)治疗 3 个月。ZA 剂量与癌症患者相同,但给药频率增加两倍(每 2 周 1 次)。用免疫组织化学法评估黏膜组织细胞增殖(增殖细胞核抗原,PCNA)、MMP 表达和凋亡(半胱氨酸天冬氨酸蛋白酶 3 和 TUNEL)。
两组之间 PCNA、MMP-2、MMP-14 和 TUNEL 阳性细胞无显著差异。然而,MMP-9 的表达在对照组明显高于 ZA 组(P < 0.05),而对照组 caspase 3 的表达明显低于 ZA 组(P < 0.05)。
这些结果表明,高剂量 ZA 导致口腔上皮细胞凋亡增加和 MMP-9 水平降低,支持双膦酸盐治疗影响口腔黏膜的观点。