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布比卡因、罗哌卡因和吗啡:对人半腱肌源性干细胞/祖细胞毒性的比较。

Bupivacaine, ropivacaine, and morphine: comparison of toxicity on human hamstring-derived stem/progenitor cells.

机构信息

Experimental Surgery and Regenerative Medicine, Department of Surgery, Ludwig-Maximilians-University Munich, Nussbaumstr. 20, 80336, Munich, Germany.

出版信息

Knee Surg Sports Traumatol Arthrosc. 2011 Dec;19(12):2138-44. doi: 10.1007/s00167-011-1564-3. Epub 2011 Jun 7.

Abstract

PURPOSE

Bupivacaine, ropivacaine, and morphine are commonly administered intraarticularly after anterior cruciate ligament (ACL) reconstruction. However, their effects on human tendon stem/progenitor cells (TSPC) have not been studied. Therefore, this study investigates the cytotoxicity of these analgetics on TSPC.

METHODS

Cells were isolated from human hamstring grafts of 3 female (age 15, 16 and 59) and 2 male patients (age 16 and 47). Cells were incubated using 0.5% bupivacaine, 0.5/0.75% ropivacaine, and 0.025% morphine. Cell viability was assessed after 0.5, 2, and 6 h using live/dead assay. Metabolic activity and apoptosis were measured by WST- and Annexin-V-FACS-assay after 2 h.

RESULTS

Cell viability remained unchanged after 0.5 h in all groups, while treatment with bupivacaine and 0.5/0.75% ropivacaine resulted in a complete cell loss after 6 h. Contrarily, morphine showed no cytotoxic effect. Cell viability and metabolism were significantly reduced after treatment with bupivacaine (22.1; 8.3%) and 0.75% ropivacaine (56.5; 23.8%), while 0.5% ropivacaine and morphine showed no significant difference compared with controls. Apoptosis was significantly induced after incubation with bupivacaine (58.1%) and 0.75% ropivacaine (26.2%), whereas 0.5% ropivacaine only led to a slight induction compared with morphine and controls.

CONCLUSIONS

Clinically administered concentrations of bupivacaine (0.5%) and ropivacaine (0.75%) have a significant cytotoxic effect on human TSPC in vitro, while ropivacaine in a concentration of 0.5% has a mild but not significant effect on apoptosis and cell metabolism. In contrast, morphine does not affect cell survival, metabolism, or apoptosis. Knowing that morphine provides comparable to even prolonged pain reduction after ACL reconstruction, the presented in vitro study suggests morphine as a potentially less toxic analgetic drug for intraarticular application in clinical practice.

摘要

目的

布比卡因、罗哌卡因和吗啡常用于前交叉韧带(ACL)重建后关节内给药。然而,它们对人肌腱干/祖细胞(TSPC)的影响尚未得到研究。因此,本研究调查了这些镇痛药对 TSPC 的细胞毒性。

方法

从 3 名女性(年龄 15、16 和 59 岁)和 2 名男性(年龄 16 和 47 岁)的人腘绳肌腱移植物中分离细胞。使用 0.5%布比卡因、0.5/0.75%罗哌卡因和 0.025%吗啡孵育细胞。使用活/死检测法在 0.5、2 和 6 h 后评估细胞活力。在用 2 h 后用 WST-和 Annexin-V-FACS 测定法测量代谢活性和凋亡。

结果

所有组在 0.5 h 后细胞活力保持不变,而用布比卡因和 0.5/0.75%罗哌卡因处理后,6 h 后完全丧失细胞活力。相反,吗啡没有显示出细胞毒性作用。用布比卡因(22.1%;8.3%)和 0.75%罗哌卡因(56.5%;23.8%)处理后,细胞活力和代谢明显降低,而 0.5%罗哌卡因和吗啡与对照相比无显著差异。用布比卡因(58.1%)和 0.75%罗哌卡因(26.2%)孵育后,细胞凋亡明显诱导,而 0.5%罗哌卡因与吗啡和对照相比仅引起轻微诱导。

结论

临床应用浓度的布比卡因(0.5%)和罗哌卡因(0.75%)在体外对人 TSPC 具有显著的细胞毒性作用,而 0.5%浓度的罗哌卡因对细胞凋亡和细胞代谢仅有轻度但无显著影响。相比之下,吗啡不影响细胞存活、代谢或凋亡。鉴于吗啡在 ACL 重建后提供类似甚至更长时间的疼痛缓解,本体外研究表明,吗啡作为一种潜在的毒性较小的关节内应用镇痛药,在临床实践中具有应用前景。

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