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布比卡因对培养的腱细胞的影响。

Effect of bupivacaine on cultured tenocytes.

作者信息

Scherb Michael B, Han Seung-Hwan, Courneya Jean-Paul, Guyton Gregory P, Schon Lew C

机构信息

Department of Orthopedic Surgery, Union Memorial Hospital, Baltimore, MD 21218, USA.

出版信息

Orthopedics. 2009 Jan;32(1):26. doi: 10.3928/01477447-20090101-19.

Abstract

Proliferation of cultured human fibroblasts and other types of cells has been shown to be hindered by exposure to local anesthetics, which are widely used in musculoskeletal medicine for their use in regional anesthesia, selective nerve blocks, bursography, and brisement. We hypothesized that bupivacaine would decrease cell proliferation and production of extracellular matrix components collagen and proteoglycan in healthy human tenocytes in culture. Primary human tenocyte cultures were prepared from samples of normal tendons obtained from healthy tissue that would otherwise have been discarded during lower extremity tendon transfer surgery. Samples were obtained from 6 patients, 5 women and 1 man with an average age of 69 years (range, 17-73 years). Five flexor digitorum longus tendon samples and 1 peroneus longus tendon sample were used. Harvested tendon tissues (5 mm(3)) were used as explants for primary cell cultures. To measure the proliferative response to bupivacaine, seeded cells were exposed to saline control or to various concentrations of bupivacaine in 1% fetal bovine serum DMEM/F12 or 10% fetal bovine serum DMEM/F12. The 1% fetal bovine serum medium demonstrated the pure bupivacaine effect, and 10% fetal bovine serum more closely approximated the in vivo environment. Seeded cells were starved of fetal bovine serum for 12 hours before exposure to phosphate-buffered saline (control group) and 500 microM bupivacaine (experimental group). This concentration of bupivacaine was selected because it was found to significantly hinder proliferation in both the 1% and 10% fetal bovine serum groups in our proliferation assay. Tenocyte proliferation and extracellular matrix component production were significantly lower (P<or=.05) at >or=1 time points up to 6 days in bupivacaine-treated groups as compared with controls.

摘要

已表明,暴露于局部麻醉剂会阻碍培养的人成纤维细胞和其他类型细胞的增殖,局部麻醉剂因其在区域麻醉、选择性神经阻滞、滑囊造影和手法松解中的应用而广泛用于肌肉骨骼医学。我们假设布比卡因会降低培养的健康人肌腱细胞中细胞的增殖以及细胞外基质成分胶原蛋白和蛋白聚糖的产生。从健康组织获取的正常肌腱样本中制备原代人肌腱细胞培养物,这些样本在下肢肌腱转移手术中原本会被丢弃。样本取自6名患者,5名女性和1名男性,平均年龄69岁(范围17 - 73岁)。使用了5个趾长屈肌腱样本和1个腓骨长肌腱样本。收获的肌腱组织(5立方毫米)用作原代细胞培养的外植体。为了测量对布比卡因的增殖反应,将接种的细胞暴露于生理盐水对照或1%胎牛血清DMEM/F12或10%胎牛血清DMEM/F12中的各种浓度的布比卡因。1%胎牛血清培养基显示了布比卡因的纯效应,10%胎牛血清更接近体内环境。在暴露于磷酸盐缓冲盐水(对照组)和500微摩尔布比卡因(实验组)之前,将接种的细胞在无胎牛血清的条件下饥饿12小时。选择该布比卡因浓度是因为在我们的增殖试验中发现它在1%和10%胎牛血清组中均显著阻碍增殖。与对照组相比,布比卡因处理组在长达6天的≥1个时间点时,肌腱细胞增殖和细胞外基质成分产生显著更低(P≤0.05)。

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