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在马非炎性关节模型中评估关节腔内注射阿米卡星,以确定有效的杀菌浓度,同时将细胞毒性降至最低。

Evaluation of Intra-Articular Amikacin Administration in an Equine Non-inflammatory Joint Model to Identify Effective Bactericidal Concentrations While Minimizing Cytotoxicity.

作者信息

Pezzanite Lynn, Chow Lyndah, Hendrickson Dean, Gustafson Daniel L, Russell Moore A, Stoneback Jason, Griffenhagen Gregg M, Piquini Gabriella, Phillips Jennifer, Lunghofer Paul, Dow Steven, Goodrich Laurie R

机构信息

Department of Clinical Sciences, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, United States.

Department of Microbiology, Immunology and Pathology, College of Veterinary Medicine and Biomedical Sciences, Colorado State University, Fort Collins, CO, United States.

出版信息

Front Vet Sci. 2021 May 21;8:676774. doi: 10.3389/fvets.2021.676774. eCollection 2021.

Abstract

Septic arthritis causes significant morbidity and mortality in veterinary and human clinical practice and is increasingly complicated by multidrug-resistant infections. Intra-articular (IA) antibiotic administration achieves high local drug concentrations but is considered off-label usage, and appropriate doses have not been defined. Using an equine joint model, we investigated the effects of amikacin injected at three different doses (500, 125, and 31.25 mg) on the immune and cartilage responses in tibiotarsal joints. Synovial fluid (SF) was sampled at multiple time points over 24 h, the cell counts determined, and amikacin concentrations measured by liquid chromatography-mass spectrometry. Cytokine concentrations and collagen degradation products in SF were measured by ELISA and multiplex immunoassays. The mean amikacin concentrations in SF were greater than or equal to the minimum inhibitory concentration (MIC) (0.004 mg/ml) for most common equine joint pathogens at all time points tested to 24 h for all three amikacin doses evaluated. The inflammatory cytokines tumor necrosis factor-alpha (TNF-α) and interleukin-1 beta (IL-1β) increased significantly in SF in the highest amikacin dose group, despite the fact that increases in SF cell counts were not observed. Similarly, the biomarkers of cartilage type II collagen cleavage (C2C and C12C) were increased in SF following amikacin injection. Mechanistically, we further demonstrated using studies that chondrocytes and synoviocytes killed by exposure to amikacin underwent apoptotic cell death and were phagocytosed by macrophages in a non-inflammatory process resembling efferocytosis. Neutrophils and T cells were susceptible to amikacin cytotoxicity at clinically relevant doses, which may result in blunting of cellular inflammatory responses in SF and account for the lack of increase in total nucleated cell counts following amikacin injection. In summary, decisions on whether to inject cytotoxic antibiotics such as aminoglycosides intra-articularly and what doses to use should take into account the potential harm that antibiotics may cause and consider lower doses than those previously reported in equine practice.

摘要

脓毒性关节炎在兽医和人类临床实践中会导致严重的发病和死亡,并且越来越多地受到多重耐药感染的困扰。关节内(IA)给药可使局部药物浓度升高,但被视为超说明书用药,且尚未确定合适的剂量。我们使用马关节模型,研究了三种不同剂量(500、125和31.25毫克)的阿米卡星注射对跗关节免疫和软骨反应的影响。在24小时内的多个时间点采集滑液(SF),确定细胞计数,并通过液相色谱 - 质谱法测量阿米卡星浓度。通过酶联免疫吸附测定(ELISA)和多重免疫测定法测量SF中的细胞因子浓度和胶原蛋白降解产物。在评估的所有三种阿米卡星剂量下,在测试至24小时的所有时间点,SF中的平均阿米卡星浓度均大于或等于大多数常见马关节病原体的最低抑菌浓度(MIC)(0.004毫克/毫升)。尽管未观察到SF细胞计数增加,但在最高阿米卡星剂量组中,炎症细胞因子肿瘤坏死因子 - α(TNF - α)和白细胞介素 - 1β(IL - 1β)在SF中显著增加。同样,注射阿米卡星后,SF中软骨II型胶原蛋白裂解的生物标志物(C2C和C12C)增加。从机制上讲,我们进一步通过研究证明,暴露于阿米卡星而死亡的软骨细胞和滑膜细胞经历了凋亡性细胞死亡,并在类似于胞葬作用的非炎症过程中被巨噬细胞吞噬。中性粒细胞和T细胞在临床相关剂量下易受阿米卡星细胞毒性的影响,这可能导致SF中细胞炎症反应减弱,并解释了注射阿米卡星后总核细胞计数缺乏增加的原因。总之,关于是否关节内注射氨基糖苷类等细胞毒性抗生素以及使用何种剂量的决定,应考虑到抗生素可能造成的潜在危害,并考虑低于马实践中先前报道的剂量。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/92db/8175670/29fadc2969f0/fvets-08-676774-g0001.jpg

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