中国康复
中國康複
중국강복
CHINESE JOURNAL OF REHABILITATION
2015年
2期
83-87
,共5页
任莎莎%李雪萍%林强%程凯%夏鹏%杨怀春%高明霞
任莎莎%李雪萍%林彊%程凱%夏鵬%楊懷春%高明霞
임사사%리설평%림강%정개%하붕%양부춘%고명하
低强度脉冲超声%软骨细胞%PI3K/Akt 通路%凋亡
低彊度脈遲超聲%軟骨細胞%PI3K/Akt 通路%凋亡
저강도맥충초성%연골세포%PI3K/Akt 통로%조망
ultrasound%chondrocytes%PI3K/Akt pathway%apoptosis
目的::探讨低强度脉冲超声(LIPUS)对兔膝骨性关节炎(OA)软骨细胞凋亡的影响及有关作用机制。方法:共选取30只新西兰大白兔,随机分为正常对照组(A 组)、OA 模型组(B 组)、OA+ LIPUS 组(C 组)、OA+LY294002(PI3K/Akt 抑制剂)组(D 组)、OA+LY294002+LIPUS 组(E 组),每组各6只。采用右后膝前交叉韧带切断术(ACLT)造模。于造模后第6周时采用空气栓塞法处死实验兔,切取软骨组织进行组织学观察,并进行Mankin 评分;提取软骨细胞进行体外培养并采用免疫组化染色法鉴定;应用 western blot 检测各组软骨细胞中Ⅱ型胶原(COL2)、MMP-13、Akt、pAkt、P53、Bcl-2蛋白表达情况。结果:B 组 COL2、pAkt、Bcl-2蛋白含量较 A 组降低,MMP-13、P53蛋白含量较 A 组增高(P <0.05)。与 B 组相比,C 组 COL2、pAkt、Bcl-2蛋白含量增高,MMP-13、P53蛋白含量下降(P <0.05);D 组 COL2、Bcl-2、pAkt 蛋白含量下降,MMP-13、P53蛋白含量升高(P <0.05),E 组COL2、MMP-13、P53、Bcl-2、pAkt 蛋白含量无明显变化,但与 C 组、D 组相比差异显著(P <0.05)。各组 Akt 蛋白表达无明显差异。结论:LIPUS 能通过 PI3K/Akt 通路降低兔膝骨性关节炎软骨细胞凋亡率,促进抗凋亡基因 Bcl-2表达,下调促凋亡基因 P53水平,促进关节软骨损伤修复。
目的::探討低彊度脈遲超聲(LIPUS)對兔膝骨性關節炎(OA)軟骨細胞凋亡的影響及有關作用機製。方法:共選取30隻新西蘭大白兔,隨機分為正常對照組(A 組)、OA 模型組(B 組)、OA+ LIPUS 組(C 組)、OA+LY294002(PI3K/Akt 抑製劑)組(D 組)、OA+LY294002+LIPUS 組(E 組),每組各6隻。採用右後膝前交扠韌帶切斷術(ACLT)造模。于造模後第6週時採用空氣栓塞法處死實驗兔,切取軟骨組織進行組織學觀察,併進行Mankin 評分;提取軟骨細胞進行體外培養併採用免疫組化染色法鑒定;應用 western blot 檢測各組軟骨細胞中Ⅱ型膠原(COL2)、MMP-13、Akt、pAkt、P53、Bcl-2蛋白錶達情況。結果:B 組 COL2、pAkt、Bcl-2蛋白含量較 A 組降低,MMP-13、P53蛋白含量較 A 組增高(P <0.05)。與 B 組相比,C 組 COL2、pAkt、Bcl-2蛋白含量增高,MMP-13、P53蛋白含量下降(P <0.05);D 組 COL2、Bcl-2、pAkt 蛋白含量下降,MMP-13、P53蛋白含量升高(P <0.05),E 組COL2、MMP-13、P53、Bcl-2、pAkt 蛋白含量無明顯變化,但與 C 組、D 組相比差異顯著(P <0.05)。各組 Akt 蛋白錶達無明顯差異。結論:LIPUS 能通過 PI3K/Akt 通路降低兔膝骨性關節炎軟骨細胞凋亡率,促進抗凋亡基因 Bcl-2錶達,下調促凋亡基因 P53水平,促進關節軟骨損傷脩複。
목적::탐토저강도맥충초성(LIPUS)대토슬골성관절염(OA)연골세포조망적영향급유관작용궤제。방법:공선취30지신서란대백토,수궤분위정상대조조(A 조)、OA 모형조(B 조)、OA+ LIPUS 조(C 조)、OA+LY294002(PI3K/Akt 억제제)조(D 조)、OA+LY294002+LIPUS 조(E 조),매조각6지。채용우후슬전교차인대절단술(ACLT)조모。우조모후제6주시채용공기전새법처사실험토,절취연골조직진행조직학관찰,병진행Mankin 평분;제취연골세포진행체외배양병채용면역조화염색법감정;응용 western blot 검측각조연골세포중Ⅱ형효원(COL2)、MMP-13、Akt、pAkt、P53、Bcl-2단백표체정황。결과:B 조 COL2、pAkt、Bcl-2단백함량교 A 조강저,MMP-13、P53단백함량교 A 조증고(P <0.05)。여 B 조상비,C 조 COL2、pAkt、Bcl-2단백함량증고,MMP-13、P53단백함량하강(P <0.05);D 조 COL2、Bcl-2、pAkt 단백함량하강,MMP-13、P53단백함량승고(P <0.05),E 조COL2、MMP-13、P53、Bcl-2、pAkt 단백함량무명현변화,단여 C 조、D 조상비차이현저(P <0.05)。각조 Akt 단백표체무명현차이。결론:LIPUS 능통과 PI3K/Akt 통로강저토슬골성관절염연골세포조망솔,촉진항조망기인 Bcl-2표체,하조촉조망기인 P53수평,촉진관절연골손상수복。
Objective:To investigate the effects of low intensity pulsed ultrasound (LIPUS)on the apoptosis of chondrocytes in rabbits with osteoarthritis (OA)and explore the underlying mechanism.Methods:Thirty healthy New Zealand white rabbits were selected for this study.All the cultured cells were randomly divided into five groups:a normal control group (A group),an OA model group (B group),an OA model plus LIPUS group (C group),an OA model plus PI3K/Akt inhibitor group (D group),and an OA model plus PI3K/Akt inhibitor and LI-PUS group (E group).The OA model was made by knee anterior cruciate ligament transection.At the 6th week af-ter modeling,the rabbits were sacrificed by air embolism method and pathologic changes were assessed on articular surface of femoral condyles.Meanwhile chondrocytes were isolated and cultured in vitro ,and cultured cells were i-dentified by immuohistochemistry.The expression of collagen protein type Ⅱ,MMP-13,Akt,pAkt,P53,and Bcl-2 was detected by Western blotting.Results:As compared with the A group,the expression of collagen type Ⅱ, pAkt and Bcl-2 was significantly reduced in the B group,but that of MMP-13 and P53 was significantly increased in the B group (P <0.05 ).As compared with the B group,the expression of collagen type Ⅱ,pAkt and Bcl-2 was significantly increased,and that of MMP-13 and P53 was significantly reduced in the C group (P <0.05);the ex-pression of collagen type Ⅱ,pAkt and Bcl-2 was significantly reduced (P <0.05),and that of MMP-13 and P53 was significantly increased in the D group (P <0.05).Although the expression of collagen type Ⅱ,MMP-13,pA-kt,P53,and Bcl-2 showed no significant difference be-tween the E group and the B group,the expression of collagen type Ⅱ, MMP-13, pAkt, P53 and Bcl-2 showed significant difference between C group and D group (P <0.05).There was no significant difference in the expression of Akt among all groups.Conclusions:The LIPUS can obviously decrease the apoptosis rate of chondrocytes in the knee joints of OA rabbits via activating PI3K/Akt pathway,and the underlying mechanisms are closely related to upregulation of Bcl-2 expression and downregulation of P53 expression.The LIPUS can accelerate the recovery of cartilage for the purpose of treatment of OA.