重庆医学
重慶醫學
중경의학
CHONGQING MEDICAL JOURNAL
2015年
4期
442-445
,共4页
陈光宇%戴睿武%罗皓%陈振宇%陈涛%黎冬暄%吕润华%汤礼军
陳光宇%戴睿武%囉皓%陳振宇%陳濤%黎鼕暄%呂潤華%湯禮軍
진광우%대예무%라호%진진우%진도%려동훤%려윤화%탕례군
模型,动物%细胞增殖%胰腺创伤%Bcl-2%Bax
模型,動物%細胞增殖%胰腺創傷%Bcl-2%Bax
모형,동물%세포증식%이선창상%Bcl-2%Bax
model,animal%cell regeneration%pancreatic trauma%Bcl-2%Bax
目的:构建大鼠单纯性胰腺创伤模型观察胰腺细胞增殖变化特点并探讨胰腺细胞增殖与组织损伤的关系。方法将60只Wistar大鼠分为2组:撞击组(采用BIM‐Ⅲ生物撞击机构建胰腺创伤大鼠模型,40只)和对照组(假手术组,20只),每组大鼠于建模后6、24、72 h ,7 d处死,采用分光光度法检测各组大鼠血清淀粉酶(AMS)、脂肪酶(LPS)活性,通过TUNEL染色和流式细胞技术测定胰腺组织细胞死亡并分析细胞周期分布特点,Western blot测定胰腺组织Bcl‐2、Bax蛋白的表达。结果撞击组大鼠LPS活性升高时相点晚于AMS且持续时间较长,TUNEL染色、流式细胞检测、Western blot结果揭示胰腺创伤可诱导胰腺组织细胞凋亡和代偿性增生。胰腺细胞增殖变化特点表明胰腺创伤后的最佳治疗时间是发病24 h内。结论同时检测AMS和L PS有助于判定胰腺的外分泌功能受损情况。
目的:構建大鼠單純性胰腺創傷模型觀察胰腺細胞增殖變化特點併探討胰腺細胞增殖與組織損傷的關繫。方法將60隻Wistar大鼠分為2組:撞擊組(採用BIM‐Ⅲ生物撞擊機構建胰腺創傷大鼠模型,40隻)和對照組(假手術組,20隻),每組大鼠于建模後6、24、72 h ,7 d處死,採用分光光度法檢測各組大鼠血清澱粉酶(AMS)、脂肪酶(LPS)活性,通過TUNEL染色和流式細胞技術測定胰腺組織細胞死亡併分析細胞週期分佈特點,Western blot測定胰腺組織Bcl‐2、Bax蛋白的錶達。結果撞擊組大鼠LPS活性升高時相點晚于AMS且持續時間較長,TUNEL染色、流式細胞檢測、Western blot結果揭示胰腺創傷可誘導胰腺組織細胞凋亡和代償性增生。胰腺細胞增殖變化特點錶明胰腺創傷後的最佳治療時間是髮病24 h內。結論同時檢測AMS和L PS有助于判定胰腺的外分泌功能受損情況。
목적:구건대서단순성이선창상모형관찰이선세포증식변화특점병탐토이선세포증식여조직손상적관계。방법장60지Wistar대서분위2조:당격조(채용BIM‐Ⅲ생물당격궤구건이선창상대서모형,40지)화대조조(가수술조,20지),매조대서우건모후6、24、72 h ,7 d처사,채용분광광도법검측각조대서혈청정분매(AMS)、지방매(LPS)활성,통과TUNEL염색화류식세포기술측정이선조직세포사망병분석세포주기분포특점,Western blot측정이선조직Bcl‐2、Bax단백적표체。결과당격조대서LPS활성승고시상점만우AMS차지속시간교장,TUNEL염색、류식세포검측、Western blot결과게시이선창상가유도이선조직세포조망화대상성증생。이선세포증식변화특점표명이선창상후적최가치료시간시발병24 h내。결론동시검측AMS화L PS유조우판정이선적외분비공능수손정황。
Objective To study the relationships between tissue damage and the ability of the pancreatic cells to regenerate ,and analyze the alteration of the pancreatic cells regeneration .Methods Sixty rats were divided into two groups :impact group(the pan‐creas was injured by a BIM‐Ⅲ biotical impact machine ,40 rats) and control group(sham operated ,20 rats) .All rats were sacrificed at 6 h ,24 h ,72 h ,7 d after operation .The level of AMS ,LPS in the serum were detected by spectrophotometry ,pancreatic cells re‐generation were examined and analyzed by TUNEL staining and flow cytomertry ,and the Bcl‐2 and Bax expression were measured by Western blot .Results In the impact groups ,LPS was activated later than AMS ,and lasted persistently .The results from TUNEL stain ,flow cytometry and Western blot indicated that pancreatic trauma induces cell death and the compensatory prolifera‐tion of pancreatic cells .The characteristics of pancreatic cells regeneration in the animal model of isolated pancreatic trauma indicate that the proper remedial time is in the first 24h after the pancreatic trauma .Conclusion Detecting AMS and LPS at the same time can help us to determine the exocrine function of pancrease .