Dose-dependent effects of lanthanum chloride on wear particle-induced aseptic inflammation in a murine air-pouch model
Dose-dependent effects of lanthanum chloride on wear particle-induced aseptic inflammation in a murine air-pouch model作者机构:Department of Orthopaedicsthe First Affiliated HospitalNanchang University
出 版 物:《Journal of Rare Earths》 (稀土学报(英文版))
年 卷 期:2013年第31卷第4期
页 面:420-427页
核心收录:
学科分类:08[工学] 080502[工学-材料学] 0805[工学-材料科学与工程(可授工学、理学学位)]
基 金:supported by National Natural Science Foundation of China (81160222) the Foundation of Health Department of JiangxiProvince (20121044)
主 题:lanthanum chloride wear particle aseptic inflammation pro-inflammatory cytokine nuclear factor-KB air-pouch model
摘 要:To investigate the effects of local injection of different doses of lanthanum chloride (LaCl3) on aseptic inflammation in mice stimulated by wear particles from artificial joints, the particles were prepared by vacuum ball mill in vitro and air-pouch models were performed with 45 male BALB/c mice that were randomly divided into blank control group, wear particle group and wear parti- cle + LaCl3 (0.1, 0.9 and 8.1 μmol) group. All animals were sacrificed and tissue specimens were harvested 7 days after treatment. Hematoxylin and eosin (H&E) staining, enzyme-linked immunosorbent assay (ELISA), reverse transcription-polymerase chain reac- tion (RT-PCR) and western blot were applied to observe inflammatory reaction and detect the expression of pro-inflammatory cyto- kines (TNF-et, IL-1β) and nuclear factor-κB (NF-κB) in mRNA and protein levels in air-pouch membrances. The results showed that wear particles could stimulate aseptic inflammation in vivo effectively; 0.9 μmol LaCl3 could significantly inhibit wear parti- cle-induced gene and protein expression of pro-inflammatory cytokines and NF-Id3 (P〈0.05); 0.1 and 8. 1 μmol LaCl3 did not exert an inflammation-inhibiting effect and even caused adverse effects at 8.1 μmol. In conclusion, LaC13 played a protective role against wear particle-induced aseptic inflammation dose-dependently, which was involved in NF-κB related signaling pathways.