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局部麻醉药和皮质类固醇对软骨细胞及滑膜细胞活力和代谢的体外毒性

In Vitro Toxicity of Local Anesthetics and Corticosteroids on Chondrocyte and Synoviocyte Viability and Metabolism.

作者信息

Sherman Seth L, Khazai Ravand S, James Christopher H, Stoker Aaron M, Flood David L, Cook James L

机构信息

Department of Orthopaedic Surgery, University of Missouri, Columbia, MO, USA.

Department of Orthopaedic Surgery, University of Chicago, Chicago, IL, USA.

出版信息

Cartilage. 2015 Oct;6(4):233-40. doi: 10.1177/1947603515594453.

DOI:10.1177/1947603515594453
PMID:26425261
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4568732/
Abstract

OBJECTIVE

There is growing concern that intra-articular injection of local anesthetic and/or corticosteroids may cause significant morbidity, including potential toxicity to chondrocytes and synoviocytes, after even a single exposure. We demonstrate that full thickness canine chondral and synovial samples exposed to various local anesthetics and corticosteroids exhibit decreased loss of cell viability compared with prior in vitro studies using monolayer culture, due to the protective effects of intact extracellular matrix and cell heterogeneity.

METHODS

Full-thickness cartilage and synovial explants were obtained from canine cadavers and exposed in culture media to the following for 24 hours: 1% lidocaine, 0.5% lidocaine, 0.25% bupivacaine, 0.125% bupvacaine, 0.0625% bupivacaine, betamethasone acetate, methylprednisolone acetate, triamcinolone acetonide, or culture media only (control). Cell viability was determined on days 1 and 7 of culture using a microscopic live-dead and alamar blue metabolic assays.

RESULTS

Complete loss of chondrocyte and synoviocyte viability was noted in the 1% and 0.5% lidocaine group, 0.25% and 0.125% bupivacaine group, betamethasone group, and methylprednisolone groups after 1 and 7 days of culture. Treatment with 0.0625% bupivacaine and triamcinolone demonstrated no decrease in cell viability or metabolism when compared to negative control.

CONCLUSIONS

In this canine explant model, 1% and 0.5% lidocaine, 0.25% and 0.125% bupivacaine, betamethasone acetate, and methylpresdnisolone acetate were severely chondrotoxic and synoviotoxic after a single exposure, despite intact extracellular matrix. In contrast, chondrocytes and synoviocytes exposed to 0.0625% bupivacaine and triamcinolone remained viable after treatment. Further in vivo study is needed before definitive recommendations can be made.

摘要

目的

越来越多的人担心,即使单次关节内注射局部麻醉剂和/或皮质类固醇也可能导致严重的发病情况,包括对软骨细胞和滑膜细胞的潜在毒性。我们证明,与之前使用单层培养的体外研究相比,暴露于各种局部麻醉剂和皮质类固醇的全层犬软骨和滑膜样本,由于完整细胞外基质和细胞异质性的保护作用,细胞活力丧失减少。

方法

从犬尸体获取全层软骨和滑膜外植体,并在培养基中暴露于以下物质24小时:1%利多卡因、0.5%利多卡因、0.25%布比卡因、0.125%布比卡因、0.0625%布比卡因、醋酸倍他米松、醋酸甲泼尼龙、曲安奈德,或仅用培养基(对照)。在培养的第1天和第7天,使用显微镜下活死细胞和alamar蓝代谢测定法测定细胞活力。

结果

在培养1天和7天后,1%和0.5%利多卡因组、0.25%和0.125%布比卡因组、倍他米松组和甲泼尼龙组的软骨细胞和滑膜细胞活力完全丧失。与阴性对照相比,用0.0625%布比卡因和曲安奈德处理未显示细胞活力或代谢下降。

结论

在这个犬外植体模型中,单次暴露后,1%和0.5%利多卡因、0.25%和0.125%布比卡因、醋酸倍他米松和醋酸甲泼尼龙具有严重的软骨毒性和滑膜毒性,尽管细胞外基质完整。相比之下,暴露于0.0625%布比卡因和曲安奈德的软骨细胞和滑膜细胞在处理后仍保持活力。在做出明确建议之前,需要进一步的体内研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/859b5dc3667c/10.1177_1947603515594453-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/5bb6b15714f1/10.1177_1947603515594453-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/0bcb5d855b23/10.1177_1947603515594453-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/584ede40d507/10.1177_1947603515594453-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/6efa797aa265/10.1177_1947603515594453-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/78ed5fcd39e0/10.1177_1947603515594453-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/859b5dc3667c/10.1177_1947603515594453-fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/5bb6b15714f1/10.1177_1947603515594453-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/0bcb5d855b23/10.1177_1947603515594453-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/584ede40d507/10.1177_1947603515594453-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/6efa797aa265/10.1177_1947603515594453-fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/78ed5fcd39e0/10.1177_1947603515594453-fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fe34/4568732/859b5dc3667c/10.1177_1947603515594453-fig6.jpg

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