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一种用化学改性葡聚糖聚合物治疗牙周炎组织破坏的新方法。

A new approach to treat tissue destruction in periodontitis with chemically modified dextran polymers.

作者信息

Escartin Q, Lallam-Laroye C, Baroukh B, Morvan F O, Caruelle J P, Godeau G, Barritault D, Saffar J L

机构信息

Laboratoire de Biologie et PhysioPathologie Crânio-Faciales, Faculté de Chirurgie Dentaire, Université René Descartes (Paris-5), 92120 Montrouge, France.

出版信息

FASEB J. 2003 Apr;17(6):644-51. doi: 10.1096/fj.02-0708com.

Abstract

Periodontitis are diseases of the supportive tissues of the teeth provoked by bacteria and characterized by gingival inflammation and bone destruction. We have developed a new strategy to repair tissues by administrating agents (RGTA) that mimic heparan sulfates by protecting selectively some of the growth factors naturally present within the injured tissue and interfering with inflammation. After periodontitis induction in hamsters, the animals were left untreated or received weekly i.m. injections of RGTA1507 at a dose of 100 microg/kg, 400 microg/kg, 1.5 mg/kg, or 15 mg/kg for 4 wk. RGTA treatment significantly reduced gingival tissue inflammation, thickened the pocket epithelium by increasing cell proliferation, and enhanced collagen accumulation in the gingiva. A marked reduction in bone loss was observed, resulting from depression of osteoclasia and robust stimulation of bone formation at the dose of 1.5 mg/kg. RGTA treatment for 8 wk at this dose reversed macroscopic bone loss, sharply contrasting with the extensive bone destruction in the untreated animals. RGTA treatment decreased gelatinase A (MMP-2) and B (MMP-9) pro-forms in gingival tissues. Our data indicate that a 4 wk treatment dose-dependently attenuated gingival and bone manifestations of the disease, whereas a longer treatment restored alveolar bone close to controls. By modulating and coordinating host responses, RGTA has unique therapeutic properties and is a promising candidate for the treatment of human periodontitis.

摘要

牙周炎是由细菌引发的牙齿支持组织疾病,其特征为牙龈炎症和骨质破坏。我们研发了一种新的组织修复策略,即通过给予模拟硫酸乙酰肝素的药剂(RGTA)来实现,该药剂可选择性保护受损组织中天然存在的某些生长因子,并干预炎症反应。在诱导仓鼠患上牙周炎后,部分动物不接受治疗,其余动物每周接受一次肌肉注射RGTA1507,剂量分别为100微克/千克、400微克/千克、1.5毫克/千克或15毫克/千克,持续4周。RGTA治疗显著减轻了牙龈组织炎症,通过增加细胞增殖使袋状上皮增厚,并增强了牙龈中胶原蛋白的积累。在1.5毫克/千克剂量下,观察到骨丢失显著减少,这是由于破骨作用受到抑制以及骨形成得到有力刺激所致。以该剂量进行8周的RGTA治疗逆转了宏观骨丢失,这与未治疗动物广泛的骨质破坏形成鲜明对比。RGTA治疗降低了牙龈组织中明胶酶A(MMP - 2)和B(MMP - 9)的前体形式。我们的数据表明,4周的治疗剂量依赖性地减轻了该疾病的牙龈和骨骼表现,而更长时间的治疗使牙槽骨恢复至接近对照水平。通过调节和协调宿主反应,RGTA具有独特的治疗特性,是治疗人类牙周炎的一个有前景的候选药物。

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