Knych H K, Harrison L, Chouicha N, Kass P H
K.L. Maddy Equine Analytical Chemistry Laboratory, School of Veterinary Medicine, University of California, Davis, California, USA.
Department of Veterinary Molecular Biosciences, School of Veterinary Medicine, University of California, Davis, California, USA.
Equine Vet J. 2018 Jul;50(4):504-512. doi: 10.1111/evj.12771. Epub 2017 Nov 17.
Intra-articular use of corticosteroids is commonplace in performance horses. Isoflupredone acetate (IPA) is one of four Food and Drug Administration approved corticosteroids for intra-articular use in horses. The lack of published reports describing the efficacy and duration of effects of this drug warrant further study.
To assess the effects of intra-articular administration of IPA on the expression of selected anti- and pro-inflammatory and structural matrix genes following intra-articular administration to exercised Thoroughbred horses and to correlate these effects with drug concentrations.
Block design in vivo experiment.
Twelve exercised horses received either a single intra-articular administration of 8 mg of IPA or 0.9% saline solution. Synovial fluid samples were collected prior to and up to 42 days post drug administration from the treated joints. Microarray and qRT-PCR analysis were used to assess changes in expression levels of various inflammatory and structural genes post drug administration.
On microarray analysis, 855, 23,358 and 26,411 genes had a measurable fold change (increase or decrease in expression levels) when comparing baseline samples to 24 h, baseline samples to day 7 and 24 h samples to day 7, respectively. Of the genes selected for further study by qRT-PCR analysis, expression of ANXA-1 (lipocortin) was significantly increased and IL23A and MMP1 and MMP9 significantly decreased following IPA administration. Expression levels of collagen genes were not significantly different from baseline.
Limitations include the use of a noninflammatory model as results may differ in the presence of an acute inflammatory insult and the inability to measure protein concentrations of inflammatory mediators due to limited synovial fluid sample volume.
Expression relative to baseline, for both inflammatory and matrix genes for up to 42 days post IPA administration, suggests a prolonged effect relative to detection time in both plasma and synovial fluid.
皮质类固醇关节内给药在竞技马匹中很常见。醋酸异氟泼尼龙(IPA)是美国食品药品监督管理局批准的四种可用于马匹关节内给药的皮质类固醇之一。目前缺乏关于该药物疗效和作用持续时间的公开报道,因此有必要进一步研究。
评估向运动中的纯种马关节内注射IPA后,对所选抗炎、促炎和结构基质基因表达的影响,并将这些影响与药物浓度相关联。
体内实验的区组设计。
12匹运动马匹接受单次关节内注射8mg IPA或0.9%盐溶液。在给药前及给药后长达42天,从治疗关节采集滑液样本。采用微阵列和定量逆转录聚合酶链反应(qRT-PCR)分析评估给药后各种炎症和结构基因表达水平的变化。
微阵列分析显示,将基线样本与24小时样本、基线样本与第7天样本、24小时样本与第7天样本进行比较时,分别有855、23358和26411个基因有可测量的倍数变化(表达水平增加或降低)。在通过qRT-PCR分析选择进一步研究的基因中,IPA给药后,膜联蛋白A-1(脂皮质素)的表达显著增加,白细胞介素23A、基质金属蛋白酶1和基质金属蛋白酶9显著降低。胶原蛋白基因的表达水平与基线无显著差异。
局限性包括使用了非炎症模型,因为在存在急性炎症损伤的情况下结果可能不同,以及由于滑液样本量有限,无法测量炎症介质的蛋白质浓度。
IPA给药后长达42天,炎症和基质基因相对于基线的表达表明,相对于血浆和滑液中的检测时间,其作用持续时间延长。