体育科学
體育科學
체육과학
China Sport Science
2013年
8期
64~72
,共null页
中等强度 低负荷 增龄 骨骼肌 蛋白质组 差异表达 鼠 动物实验
中等彊度 低負荷 增齡 骨骼肌 蛋白質組 差異錶達 鼠 動物實驗
중등강도 저부하 증령 골격기 단백질조 차이표체 서 동물실험
medium intensity;low-loads;aged;skeletal muscle;proteome;differential expression;rat;animal experiment
目的:运用比较蛋白质组学方法研究8周中等强度低负荷量运动对增龄大鼠腓肠肌蛋白质组表达图谱的影响,初步筛选出体育运动延缓骨骼肌衰老的差异蛋白。方法:将12只18月龄雌性SD大鼠随机分为实验组(n=6)和平行对照组(n=6)。实验组经中等强度(60%~75%VO2max)、低负荷量(每天每次15min,5天/周)跑台运动,与对照组一起提取腓肠肌全蛋白,进行蛋白质固相-pH梯度聚丙烯酰胺凝胶电泳(2-DE)分离,随后采用PDQuest软件进行图像分析和数据采集。选择运动后差异表达量大于2倍的备选目标蛋白点进行胶内原位酶解与质谱鉴定。结果:运动后腓肠肌重量增加30.0%(P〈0.05),腓肠肌指数增加37.5%(P〈0.01);差异表达量大于1倍的蛋白点共19个,取大于2倍的6个蛋白点经质谱鉴定为热应激同源蛋白70(HSC70)、26S蛋白酶体调节亚基6B分子(S6B)、肌动蛋白结合蛋白(Cofilin)、线粒体乙醛脱氢酶2(ALDH2)、α-酮戊二酸脱氢酶复合体(α-KG-DHC)、细胞膜修复相关蛋白(TRIM72)。结论:1)8周中等强度低负荷量运动后增龄大鼠腓肠肌蛋白质组发生显著性变化;2)成功筛选出6种目标差异蛋白,其表达量发生的适应性变化表明,8周中等强度低负荷量运动可能通过同时调控3个途径保护Sarcopenia:①调控衰老骨骼肌的线粒体代谢酶、肌动蛋白结合蛋白、热休克同源蛋白70的表达来抑制肌细胞凋亡;②下调26S蛋白水解酶表达抑制蛋白质分解,进而拮抗Sarcopenia的骨骼肌蛋白质丢失;③促进细胞膜修复蛋白表达改善Sarcopenia的肌细胞膜修复功能。
目的:運用比較蛋白質組學方法研究8週中等彊度低負荷量運動對增齡大鼠腓腸肌蛋白質組錶達圖譜的影響,初步篩選齣體育運動延緩骨骼肌衰老的差異蛋白。方法:將12隻18月齡雌性SD大鼠隨機分為實驗組(n=6)和平行對照組(n=6)。實驗組經中等彊度(60%~75%VO2max)、低負荷量(每天每次15min,5天/週)跑檯運動,與對照組一起提取腓腸肌全蛋白,進行蛋白質固相-pH梯度聚丙烯酰胺凝膠電泳(2-DE)分離,隨後採用PDQuest軟件進行圖像分析和數據採集。選擇運動後差異錶達量大于2倍的備選目標蛋白點進行膠內原位酶解與質譜鑒定。結果:運動後腓腸肌重量增加30.0%(P〈0.05),腓腸肌指數增加37.5%(P〈0.01);差異錶達量大于1倍的蛋白點共19箇,取大于2倍的6箇蛋白點經質譜鑒定為熱應激同源蛋白70(HSC70)、26S蛋白酶體調節亞基6B分子(S6B)、肌動蛋白結閤蛋白(Cofilin)、線粒體乙醛脫氫酶2(ALDH2)、α-酮戊二痠脫氫酶複閤體(α-KG-DHC)、細胞膜脩複相關蛋白(TRIM72)。結論:1)8週中等彊度低負荷量運動後增齡大鼠腓腸肌蛋白質組髮生顯著性變化;2)成功篩選齣6種目標差異蛋白,其錶達量髮生的適應性變化錶明,8週中等彊度低負荷量運動可能通過同時調控3箇途徑保護Sarcopenia:①調控衰老骨骼肌的線粒體代謝酶、肌動蛋白結閤蛋白、熱休剋同源蛋白70的錶達來抑製肌細胞凋亡;②下調26S蛋白水解酶錶達抑製蛋白質分解,進而拮抗Sarcopenia的骨骼肌蛋白質丟失;③促進細胞膜脩複蛋白錶達改善Sarcopenia的肌細胞膜脩複功能。
목적:운용비교단백질조학방법연구8주중등강도저부하량운동대증령대서비장기단백질조표체도보적영향,초보사선출체육운동연완골격기쇠로적차이단백。방법:장12지18월령자성SD대서수궤분위실험조(n=6)화평행대조조(n=6)。실험조경중등강도(60%~75%VO2max)、저부하량(매천매차15min,5천/주)포태운동,여대조조일기제취비장기전단백,진행단백질고상-pH제도취병희선알응효전영(2-DE)분리,수후채용PDQuest연건진행도상분석화수거채집。선택운동후차이표체량대우2배적비선목표단백점진행효내원위매해여질보감정。결과:운동후비장기중량증가30.0%(P〈0.05),비장기지수증가37.5%(P〈0.01);차이표체량대우1배적단백점공19개,취대우2배적6개단백점경질보감정위열응격동원단백70(HSC70)、26S단백매체조절아기6B분자(S6B)、기동단백결합단백(Cofilin)、선립체을철탈경매2(ALDH2)、α-동무이산탈경매복합체(α-KG-DHC)、세포막수복상관단백(TRIM72)。결론:1)8주중등강도저부하량운동후증령대서비장기단백질조발생현저성변화;2)성공사선출6충목표차이단백,기표체량발생적괄응성변화표명,8주중등강도저부하량운동가능통과동시조공3개도경보호Sarcopenia:①조공쇠로골격기적선립체대사매、기동단백결합단백、열휴극동원단백70적표체래억제기세포조망;②하조26S단백수해매표체억제단백질분해,진이길항Sarcopenia적골격기단백질주실;③촉진세포막수복단백표체개선Sarcopenia적기세포막수복공능。
Objective:The differential proteome expression map of rats’skeletal muscle between aging and exercise group was established to screen significant target protein response to 8 weeks low-loads of medium intensity exercise by means of proteomics,and filtrating out the objective proteins which exercise postpone skeletal muscle aging.Methods:Dividing 12 male Aged(16-month-old) SD rats into exercise and parallel control groups at random(n=6),the exercise group had a 8 weeks treadmill training with medium intensity(60%~75%VO2max),low-loads(15 min/days,5 days/week),together with the control group,preparing for whole proteins samples of gastrocnemius,and separating the protein samples by utilizing two dimensional gel electrophoresis(2-DG),and analyzing image and collecting data by using PD Quest.The alternatively objective protein spots whose differential expression volume>2 folds were selected for elenzymologic extraction and MS/ MS identification.Result:There were 19 points expressed>1 folds.Taking out 6 whose differential expression volume>2 folds were selected for elenzymologic extraction and MS/MS identification,they were heat shock cognate 70 kDa protein(HSC70),26S protease regulatory subunit 6B(S6B),actin binding protein(Cofilin),aldehyde dehydrogenase 2(ALDH2),α-ketoglutarate dehydrogenase complex(α-KGDH),membrane repair relative protein tripartite motif-containing protein 72(TRIM72).Conclusion:1) Using the methods of proteoimcs,the change of gastrocnemius protein in exercise rat s were identified.2) We succeeded in filtrating 6 objective proteins which their expression volume had an adaptive changes,it indicated that 8 weeks of low-loads medium intensity exercise may protect sarcopenia by regulation three pathways:① it could bring a series of well changes such as improving the aging skeletal muscle muscle mitochondrial metabolizing enzymes,Cofilin,HSC70 inhibit muscle cell apoptosis;② it could downregulate S6B expression to inhibit protein degradation,which antagonizes the aged rat’s skeletal muscle protein loss;③it could upregulate TRIM72 expression to improve the sarcopenia myocyte plasma membrane repair dysfunction.