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一种用于大鼠慢性疼痛研究的有限关节炎模型。

A limited arthritic model for chronic pain studies in the rat.

作者信息

Butler Stephen H, Godefroy Françoise, Besson Jean-Marie, Weil-Fugazza Jeanne

机构信息

Unité de Recherches de Physiopharmacologie du Systéme Nerveux, INSERM U. 161, 75014 ParisFrance.

出版信息

Pain. 1992 Jan;48(1):73-81. doi: 10.1016/0304-3959(92)90133-V.

Abstract

Freund's adjuvant induced polyarthritis in rats has been used extensively to study pain processes of long duration. There are limitations of this model for chronic studies of pain/arthritis since the severe systemic changes provoke ethical concerns and also affect behaviour, physiology and biochemistry. Attempts to limit adjuvant-induced arthritis by plantar injection of the inoculum have been made. In this model, however, the process evolved to produce widespread polyarthritis if followed for the 6-plus-weeks necessary for chronic studies. Therefore, although it offers the researcher a reliable limited model of inflammation and nociception at the outset, for longer studies it may have all the disadvantages of the polyarthritic rat. The purpose of the present study was to produce a limited arthritic process in rats, stable over 6 weeks and suitable for behavioural and neurochemical studies of various chronic pain treatment methods. Injection (0.05 ml) of complete adjuvant containing 300 micrograms Mycobacterium butyricum in the tibio-tarsal joint produces a predictable monoarthritis, stable clinically and behaviourly from weeks 2 through 6 post injection. As revealed by clinical observations and X-ray examinations, the arthritis produced was limited anatomically, pronounced, prolonged and stable. A marked increase in sensitivity to paw pressure was seen in the affected limb. Animals gained weight and remained active, indicating little systemic disturbance as opposed to polyarthritic rats. We propose this limited model of arthritis as a suitable alternative to the polyarthritic rat for prolonged studies.

摘要

弗氏佐剂诱导的大鼠多关节炎已被广泛用于研究长时间的疼痛过程。由于严重的全身变化引发了伦理问题,并且还影响行为、生理和生物化学,因此该模型在疼痛/关节炎的慢性研究中存在局限性。人们曾尝试通过足底注射接种物来限制佐剂诱导的关节炎。然而,在这个模型中,如果按照慢性研究所需的6周以上时间进行观察,该过程会演变成广泛的多关节炎。因此,尽管它在一开始为研究人员提供了一个可靠的有限炎症和伤害感受模型,但对于更长时间的研究,它可能具有多关节炎大鼠的所有缺点。本研究的目的是在大鼠中产生一个有限的关节炎过程,该过程在6周内稳定,适合于各种慢性疼痛治疗方法的行为和神经化学研究。在胫跗关节注射0.05毫升含有300微克丁酸分枝杆菌的完全佐剂,可产生可预测的单关节炎,在注射后第2周至第6周临床和行为上稳定。临床观察和X线检查显示,所产生的关节炎在解剖学上是有限的、明显的、持续的和稳定的。受影响肢体对 paw 压力的敏感性显著增加。动物体重增加且保持活跃,表明与多关节炎大鼠相比几乎没有全身干扰。我们提出这种有限的关节炎模型作为多关节炎大鼠长时间研究的合适替代方案。

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