Gurgel Bruno César de Vasconcelos, Duarte Poliana Mendes, Nociti Francisco H, Sallum Enilson A, Casati Márcio Zaffalon, Sallum Antonio Wilson, de Toledo Sérgio
Department of Periodontics and Prosthodontics, School of Dentistry at Piracicaba (UNICAMP), São Paulo, Brazil.
J Periodontol. 2004 Dec;75(12):1613-8. doi: 10.1902/jop.2004.75.12.1613.
Anti-inflammatory agents have been reported as a bone loss mediator in periodontitis. This study aimed to investigate in rats the impact of a selective cyclooxygenase-2 inhibitor (meloxicam) on bone loss in ligature-induced periodontitis and its post-treatment effect after administration withdrawal.
Seventy-five adult male Wistar rats were included. After anesthesia, a mandibular first molar was randomly assigned to receive the cotton ligature in the sulcular position, while the contralateral tooth was left unligated. The animals were randomly assigned to one of the following five treatment groups (15 animals each), including daily subcutaneous injections: 1) saline solution for 15 days; 2) saline solution for 45 days; 3) 3 mg/kg of meloxicam for 15 days; 4) 3 mg/kg of meloxicam for 45 days; or 5) 3 mg/kg of meloxicam for 15 days followed by saline solution for 30 days. The animals were sacrificed and the specimens routinely processed. The volume of bone loss was histometrically measured and statistical analysis performed.
Intergroup comparisons demonstrated that the drug may significantly reduce periodontitis-related bone loss (group 3: 5.83 +/- 2.04); however, this effect is less evident when the drug is administered in a short period (group 4: 3.59 +/- 1.57). Moreover, after drug withdrawal, no residual effect was observed (6.86 +/- 3.59, 6.09 +/- 2.66, groups 2 and 5, respectively) (P > 0.05).
Within the limits of the present study, it can be concluded that selective cyclooxygenase-2 inhibitors may reduce bone loss associated with experimental periodontitis and that no remaining effect can be expected after its withdrawal.
抗炎药已被报道为牙周炎中骨质流失的介质。本研究旨在探讨选择性环氧化酶-2抑制剂(美洛昔康)对大鼠结扎诱导性牙周炎骨质流失的影响及其停药后的治疗效果。
纳入75只成年雄性Wistar大鼠。麻醉后,将下颌第一磨牙随机分配接受龈沟位置的棉线结扎,对侧牙齿不结扎。动物被随机分配到以下五个治疗组之一(每组15只动物),包括每日皮下注射:1)生理盐水注射15天;2)生理盐水注射45天;3)3mg/kg美洛昔康注射15天;4)3mg/kg美洛昔康注射45天;或5)3mg/kg美洛昔康注射15天,随后生理盐水注射30天。处死动物并对标本进行常规处理。通过组织计量学测量骨质流失体积并进行统计分析。
组间比较表明,该药物可显著减少与牙周炎相关的骨质流失(第3组:5.83±2.04);然而,短期给药时这种效果不太明显(第4组:3.59±1.57)。此外,停药后未观察到残留效应(第2组和第5组分别为6.86±3.59、6.09±2.66)(P>0.05)。
在本研究的范围内,可以得出结论,选择性环氧化酶-2抑制剂可能减少与实验性牙周炎相关的骨质流失,且停药后无残留效应。