从进餐模式分析角度看环氧合酶II抑制剂在调节颞下颌关节炎症中的作用。
A role for cyclooxygenase II inhibitors in modulating temporomandibular joint inflammation from a meal pattern analysis perspective.
作者信息
Kerins Carolyn, Carlson David, McIntosh James, Bellinger Larry
机构信息
Department of Biomedical Sciences, Baylor College of Dentistry, Dallas, TX 75266, USA.
出版信息
J Oral Maxillofac Surg. 2004 Aug;62(8):989-95. doi: 10.1016/j.joms.2003.09.016.
PURPOSE
Developing a valid noninvasive animal model to study temporomandibular joint (TMJ) inflammation/pain has proved difficult. However, its has been recently demonstrated that meal pattern analysis, and in particular meal duration, can be used as a biologic marker for TMJ inflammation/pain induced by bilateral injections of complete Freund's adjuvant (CFA). The present study was undertaken to confirm previous findings and extend them by using rofecoxib (VIOXX; Merck and Co, West Point, PA), a selective cyclooxygenase-2 inhibitor (COX-2-I).
MATERIALS AND METHODS
Forty-eight male rats were assigned to 1 of 4 groups: group 1, no CFA and no COX-2-I treatment; group 2, no CFA and treatment with the COX-2-I; group 3, bilateral TMJ CFA injection and no COX-2-I treatment; and group 4, CFA injection and treatment with the COX-2-I. Food intake was recorded by computer 24 hours before and for 48 hours after CFA injection. TMJ swelling, chromodacryorrhea, and meal patterns were quantified.
RESULTS
CFA increased swelling (P <.05), chromodaccryorrhea (P <.05), meal duration at 24 and 48 hours, and TMJ retrodiscal tissue interleukin-1beta (P < 0.01) in group 3, but treatment with the COX-2-I attenuated these effects in group 4, (CFA + COX-2-I).
CONCLUSIONS
These data confirm that meal pattern analysis, and in particular meal duration, is a noninvasive measure of TMJ inflammation/pain. However, this experiment has extended this model as a marker of drug treatment efficacy, specifically the efficacy of COX-2-I in treatment of orofacial inflammation/pain.
目的
事实证明,开发一种有效的非侵入性动物模型来研究颞下颌关节(TMJ)炎症/疼痛颇具难度。然而,最近有研究表明,进餐模式分析,尤其是进餐持续时间,可作为双侧注射完全弗氏佐剂(CFA)诱发的TMJ炎症/疼痛的生物学标志物。本研究旨在证实先前的研究结果,并通过使用选择性环氧化酶-2抑制剂(COX-2-I)罗非昔布(万络;默克公司,西点,宾夕法尼亚州)对其进行扩展。
材料与方法
48只雄性大鼠被分为4组中的1组:第1组,不进行CFA和COX-2-I治疗;第2组,不进行CFA但接受COX-2-I治疗;第3组,双侧TMJ注射CFA且不进行COX-2-I治疗;第4组,注射CFA并接受COX-2-I治疗。在CFA注射前24小时及注射后48小时通过计算机记录食物摄入量。对TMJ肿胀、流泪和进餐模式进行量化。
结果
第3组中,CFA增加了肿胀(P <.05)、流泪(P <.05)、24小时和48小时的进餐持续时间以及TMJ盘后组织白细胞介素-1β(P < 0.01),但第4组(CFA + COX-2-I)中COX-2-I治疗减弱了这些效应。
结论
这些数据证实进餐模式分析,尤其是进餐持续时间,是TMJ炎症/疼痛的一种非侵入性测量方法。然而,本实验扩展了该模型作为药物治疗疗效标志物的作用,特别是COX-2-I治疗口面部炎症/疼痛的疗效。