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与大鼠颞下颌关节炎症/疼痛相关的饮食模式变化;镇痛作用。

Meal pattern changes associated with temporomandibular joint inflammation/pain in rats; analgesic effects.

作者信息

Kerins C A, Carlson D S, McIntosh J E, Bellinger L L

机构信息

Department of Biomedical Sciences, Baylor College of Dentistry, Texas A&M University System Health Science Center, 3302 Gaston Avenue, Dallas, TX 75266-0677, USA.

出版信息

Pharmacol Biochem Behav. 2003 Apr;75(1):181-9. doi: 10.1016/s0091-3057(03)00072-8.

Abstract

Establishing a valid animal model to study temporomandibular joint (TMJ) pain has proven extremely difficult. Using complete Freund's adjuvant (CFA) to induce TMJ inflammation, we recently showed that meal pattern analysis could be used as a noninvasive biological marker to study TMJ pain in an animal model. The purpose of this study was to further validate our animal model by determining whether aspects of CFA-induced TMJ inflammation/pain are reversed with ibuprofen (IBU) treatment. In the first trial, 48 male rats were used and in the second trial, 32 female ovariectomized rats, given 17beta-estradiol replacement, were used. The rats were assigned to one of four groups: control (CON-CON); control+IBU (CON+IBU); CFA-CON; and CFA+IBU. In the male trial, CFA injection (P<.01) caused TMJ swelling and chromodacryorrhea (CFA-CON); IBU eliminated these changes in the CFA+IBU group. Meal pattern analysis showed the pertinent CFA-induced change and the IBU effect was that meal duration was increased in the CFA-CON group (P<.01), but normal in the CFA+IBU-treated group on the first, but not second, day postinjection. In the female trial, CFA increased TMJ swelling, but did not cause significant chromodacryorrhea (CFA-CON); IBU eliminated swelling in the CFA+IBU group. Meal duration was increased (P<.01) in the CFA-CON group, but was normal in the CFA+IBU-treated group on both the first and second days postinjection. In both trials, interleukin-1beta (IL-1beta) levels were increased similarly in CFA-CON and CFA+IBU groups (P<.01). This study shows that CFA-induced TMJ inflammation/pain can cause changes in meal patterns (i.e., meal duration), which may be used as a behavioral marker for TMJ inflammation/pain.

摘要

事实证明,建立一个有效的动物模型来研究颞下颌关节(TMJ)疼痛极其困难。我们最近利用完全弗氏佐剂(CFA)诱导TMJ炎症,发现饮食模式分析可作为一种非侵入性生物标志物,用于研究动物模型中的TMJ疼痛。本研究的目的是通过确定布洛芬(IBU)治疗是否能逆转CFA诱导的TMJ炎症/疼痛的各个方面,进一步验证我们的动物模型。在第一次试验中,使用了48只雄性大鼠,在第二次试验中,使用了32只接受17β-雌二醇替代治疗的雌性去卵巢大鼠。将大鼠分为四组之一:对照组(CON-CON);对照+IBU组(CON+IBU);CFA-对照组;CFA+IBU组。在雄性试验中,注射CFA(P<0.01)导致TMJ肿胀和泪溢(CFA-对照组);IBU消除了CFA+IBU组中的这些变化。饮食模式分析显示,相关的CFA诱导变化以及IBU的作用是,CFA-对照组的进食持续时间增加(P<0.01),但在注射后第一天而非第二天,CFA+IBU治疗组的进食持续时间正常。在雌性试验中,CFA增加了TMJ肿胀,但未引起明显的泪溢(CFA-对照组);IBU消除了CFA+IBU组中的肿胀。CFA-对照组的进食持续时间增加(P<0.01),但在注射后第一天和第二天,CFA+IBU治疗组的进食持续时间均正常。在两项试验中,CFA-对照组和CFA+IBU组的白细胞介素-1β(IL-1β)水平均以相似的幅度升高(P<0.01)。本研究表明,CFA诱导的TMJ炎症/疼痛可导致饮食模式(即进食持续时间)发生变化,这可作为TMJ炎症/疼痛的行为标志物。

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