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评价重复性关节痛动物模型中稳定型透明质酸制剂(NASHA)的长期抗伤害作用。

Evaluation of long-term antinociceptive properties of stabilized hyaluronic acid preparation (NASHA) in an animal model of repetitive joint pain.

机构信息

Institute of Physiology I/Neurophysiology, Jena University Hospital-Friedrich Schiller University, Teichgraben 8, D-07743 Jena, Germany.

出版信息

Arthritis Res Ther. 2011 Jul 7;13(4):R110. doi: 10.1186/ar3394.

Abstract

INTRODUCTION

Clinical trials provided controversial results on whether the injection of hyaluronan preparations into osteoarthritic joints reduces pain. Problems of clinical studies may be the substantial placebo effects of intra-articular injections, different severity and rate of progression of the disease and others. We hypothesize that the use of preclinical pain models may help to clarify whether a certain hyaluronan exerts antinociceptive effects upon intra-articular injection. In the present study we tested in the bradykinin/prostaglandin E(2) (PGE(2)) model primarily the putative antinociceptive effect of stabilized hyaluronic acid from a non animal source (NASHA), a stabilized hyaluronic acid based gel for intra-articular treatment of OA. We established a dose-response relationship for NASHA and we compared NASHA to other hyaluronans with different formulations that are in clinical use.

METHODS

To induce transient joint pain episodes bradykinin and PGE(2) were repetitively administered intra-articularly and unilaterally into rat knee joints during short anaesthesia. After establishment of the predrug nociceptive responses, a single intra-articular injection of saline or NASHA at different concentrations was administered and pain responses to further bradykinin/PGE(2) injections were monitored up to 56 days after NASHA. Furthermore, the obtained effective dose was compared to clinically defined concentrations of Hylan GF20 and sodium hyaluronate. The primary outcome measures were primary mechanical hyperalgesia at the knee joint and pain-induced weight bearing.

RESULTS

On day 1 after injection, all tested hyaluronan preparations showed an antinociceptive effect >50% compared to saline. Single injections of higher doses of NASHA (50, 75 and 100 μl) were antinociceptive up to 56 days. When injection volumes in rat knee joints were adapted to clinical injection volumes in humans, the antinociceptive effects of the cross-linked NASHA and Hylan GF20 had a longer duration than that of the non cross-linked sodium hyaluronate (with a slightly better effect of NASHA than Hylan GF20).

CONCLUSIONS

In the bradykinin/PGE(2) model of joint pain a single injection of all hyaluronan preparations provided significant antinociceptive effects compared to saline. It appeared that the duration of the antinociceptive effect of the cross-linked hyaluronan preparations NASHA and Hylan GF20 was more prolonged. In addition, the gel beads structure allowing only a slow release of hyaluronic acid (NASHA) may even enhance this prolonged antinociceptive effect.

摘要

简介

临床研究对透明质酸制剂注射到骨关节炎关节中是否减轻疼痛提供了有争议的结果。临床研究的问题可能是关节内注射的明显安慰剂效应、疾病的严重程度和进展速度不同等。我们假设使用临床前疼痛模型可能有助于澄清某种透明质酸在关节内注射时是否具有抗伤害作用。在本研究中,我们在缓激肽/前列腺素 E2(PGE2)模型中主要测试了一种非动物来源的稳定透明质酸(NASHA)的潜在的抗伤害作用,NASHA 是一种稳定的透明质酸凝胶,用于治疗骨关节炎的关节内治疗。我们建立了 NASHA 的剂量-反应关系,并将其与其他具有不同配方的透明质酸进行了比较,这些透明质酸正在临床使用中。

方法

为了诱导短暂的关节疼痛发作,在短暂麻醉期间,将缓激肽和 PGE2 反复注入大鼠膝关节的关节内和单侧。在建立预给药痛觉反应后,在不同浓度下给予关节内注射盐水或 NASHA,并监测进一步的缓激肽/PGE2 注射后 56 天的疼痛反应。此外,将获得的有效剂量与临床上定义的 Hylan GF20 和透明质酸钠的浓度进行比较。主要的观察指标是膝关节的原发性机械性痛觉过敏和疼痛引起的负重。

结果

在注射后第 1 天,与盐水相比,所有测试的透明质酸制剂均显示出 >50%的镇痛作用。单次高剂量 NASHA(50、75 和 100μl)注射可在 56 天内镇痛。当将大鼠膝关节中的注射体积适应于临床上对人类的注射体积时,交联的 NASHA 和 Hylan GF20 的镇痛作用持续时间长于非交联的透明质酸钠(NASHA 的效果略优于 Hylan GF20)。

结论

在缓激肽/PGE2 关节疼痛模型中,与盐水相比,所有透明质酸制剂的单次注射均提供了显著的镇痛作用。交联的透明质酸制剂 NASHA 和 Hylan GF20 的镇痛作用持续时间似乎更长。此外,允许缓慢释放透明质酸的凝胶珠结构(NASHA)甚至可能增强这种延长的镇痛作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e25d/3239347/6373821fd067/ar3394-1.jpg

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