Bai Nan, Chen Yuan-Zheng, Mao Kai-Ping, Fu Yanjie, Lin Qiang, Xue Yan
Department of Surgery, Linyi People's Hospital Linyi, 276000, Shandong Province, China.
Department of Thoracic Surgery, Qingdao Municipal Hospital Qingdao, Shandong Province, China.
Int J Clin Exp Pathol. 2014 Apr 15;7(5):2324-36. eCollection 2014.
To explore whether lidocaine has the synergistic effect with pingyangmycin (PYM) in the venous malformations (VMs) treatment.
The mouse spleen was chosen as a VM model and injected with different concentration of lidocaine or PYM or jointly treated with lidocaine and PYM. After 2, 5, 8 or 14 days, the mouse spleen tissues were acquired for hematoxylin-eosin (HE) staining, transmission electron microscopy (TEM) analysis, TUNEL assay and quantitative RT-PCR analysis to examine the toxicological effects of lidocaine and PYM on splenic vascular endothelial cells.
0.4% of lidocaine mildly promoted the apoptosis of endothelial cells, while 2 mg/ml PYM significantly elevated the apoptotic ratios. However, the combination of 0.2% lidocaine and 0.5 mg/ml PYM notably elevated the apoptotic ratios of splenic cells and severely destroyed the configuration of spleen, compared to those of treatment with 0.5 mg/ml PYM alone.
Lidocaine exerts synergistic effects with PYM in promoting the apoptosis of mouse splenic endothelial cells, indicating that lidocaine possibly promotes the therapeutic effects of PYM in VMs treatment via synergistically enhancing the apoptosis of endothelial cells of malformed venous lesions.
探讨利多卡因在静脉畸形(VMs)治疗中是否与平阳霉素(PYM)具有协同作用。
选用小鼠脾脏作为VM模型,注射不同浓度的利多卡因或PYM,或利多卡因与PYM联合处理。在2、5、8或14天后,获取小鼠脾脏组织进行苏木精-伊红(HE)染色、透射电子显微镜(TEM)分析、TUNEL检测和定量RT-PCR分析,以检测利多卡因和PYM对脾血管内皮细胞的毒理学作用。
0.4%的利多卡因轻度促进内皮细胞凋亡,而2mg/ml的PYM显著提高凋亡率。然而,与单独使用0.5mg/ml的PYM相比,0.2%的利多卡因与0.5mg/ml的PYM联合使用显著提高了脾细胞的凋亡率,并严重破坏了脾脏结构。
利多卡因与PYM在促进小鼠脾内皮细胞凋亡方面具有协同作用,表明利多卡因可能通过协同增强畸形静脉病变内皮细胞的凋亡来促进PYM在VMs治疗中的疗效。