中华实验外科杂志
中華實驗外科雜誌
중화실험외과잡지
CHINESE JOURNAL OF EXPERIMENTAL SURGERY
2011年
7期
1133-1135
,共3页
焦华波%黄志强%许勇%朱自满%涂玉亮%刘荣
焦華波%黃誌彊%許勇%硃自滿%塗玉亮%劉榮
초화파%황지강%허용%주자만%도옥량%류영
胆管栓塞%门静脉结扎%模型,动物%肝脏铸型%CT扫描
膽管栓塞%門靜脈結扎%模型,動物%肝髒鑄型%CT掃描
담관전새%문정맥결찰%모형,동물%간장주형%CT소묘
Bile duct embolization%Portal vein ligation%Model,animal%Liver casting specimen%CT scan
目的 建立大鼠去胆管肝叶和去门静脉肝叶自身对照模型,观察两肝叶之间胆管及门静脉是否存在交通支及其大体形态变化.方法 SD大鼠40只,分为S、BL、PL和BPL共4组,分别应用氰基丙烯酸酯对肝右叶胆管进行栓塞结扎制备去胆管肝叶;对肝方叶行门静脉结扎制备去门静脉肝叶.通过测量肝重/体重和方叶重/右叶重及对各组大鼠胆管和门静脉分别灌注硫酸钡明胶混悬液制备铸型标本,并运用Micro-CT扫描来观察两叶肝脏胆道和门静脉形态变化.结果 (1)大鼠手术后在本观察期内存活率达到100%,无黄疸表现.肝叶大体形态观察和两叶肝重量比指标显示,S、BL、PL组肝重/体重为3.5%,与BPL组比较差异有统计学意义(P<0.01).S、BL组方叶/右叶重量比为60%~70%,PL及BPL组则为20%左右,提示去胆管和去门脉肝叶之间的重量比差异有统计学意义(P<0.05或P<0.01).(2)Micro-CT铸型扫描可以直观地显示胆管和门静脉形态变化,未发现两个肝叶之间存在交通支或侧枝循环.结论 去胆管肝叶无明显萎缩.胆管及门静脉灌注造影显示两叶胆管及门静脉无明显的侧枝循环.Micro-CT扫描可以直观地显示胆管及门静脉形态变化,硫酸钡明胶灌注铸型为小动物肝脏Glissons系统形态学研究提供了一种借鉴方法.
目的 建立大鼠去膽管肝葉和去門靜脈肝葉自身對照模型,觀察兩肝葉之間膽管及門靜脈是否存在交通支及其大體形態變化.方法 SD大鼠40隻,分為S、BL、PL和BPL共4組,分彆應用氰基丙烯痠酯對肝右葉膽管進行栓塞結扎製備去膽管肝葉;對肝方葉行門靜脈結扎製備去門靜脈肝葉.通過測量肝重/體重和方葉重/右葉重及對各組大鼠膽管和門靜脈分彆灌註硫痠鋇明膠混懸液製備鑄型標本,併運用Micro-CT掃描來觀察兩葉肝髒膽道和門靜脈形態變化.結果 (1)大鼠手術後在本觀察期內存活率達到100%,無黃疸錶現.肝葉大體形態觀察和兩葉肝重量比指標顯示,S、BL、PL組肝重/體重為3.5%,與BPL組比較差異有統計學意義(P<0.01).S、BL組方葉/右葉重量比為60%~70%,PL及BPL組則為20%左右,提示去膽管和去門脈肝葉之間的重量比差異有統計學意義(P<0.05或P<0.01).(2)Micro-CT鑄型掃描可以直觀地顯示膽管和門靜脈形態變化,未髮現兩箇肝葉之間存在交通支或側枝循環.結論 去膽管肝葉無明顯萎縮.膽管及門靜脈灌註造影顯示兩葉膽管及門靜脈無明顯的側枝循環.Micro-CT掃描可以直觀地顯示膽管及門靜脈形態變化,硫痠鋇明膠灌註鑄型為小動物肝髒Glissons繫統形態學研究提供瞭一種藉鑒方法.
목적 건립대서거담관간협화거문정맥간협자신대조모형,관찰량간협지간담관급문정맥시부존재교통지급기대체형태변화.방법 SD대서40지,분위S、BL、PL화BPL공4조,분별응용청기병희산지대간우협담관진행전새결찰제비거담관간협;대간방협행문정맥결찰제비거문정맥간협.통과측량간중/체중화방협중/우협중급대각조대서담관화문정맥분별관주류산패명효혼현액제비주형표본,병운용Micro-CT소묘래관찰량협간장담도화문정맥형태변화.결과 (1)대서수술후재본관찰기내존활솔체도100%,무황달표현.간협대체형태관찰화량협간중량비지표현시,S、BL、PL조간중/체중위3.5%,여BPL조비교차이유통계학의의(P<0.01).S、BL조방협/우협중량비위60%~70%,PL급BPL조칙위20%좌우,제시거담관화거문맥간협지간적중량비차이유통계학의의(P<0.05혹P<0.01).(2)Micro-CT주형소묘가이직관지현시담관화문정맥형태변화,미발현량개간협지간존재교통지혹측지순배.결론 거담관간협무명현위축.담관급문정맥관주조영현시량협담관급문정맥무명현적측지순배.Micro-CT소묘가이직관지현시담관급문정맥형태변화,류산패명효관주주형위소동물간장Glissons계통형태학연구제공료일충차감방법.
Objective To establish a rat self-control model with the bile duct deprived (BDD) and the portal vein deprived (PVD) hepatic lobe and to observe whether there were communicated branches between the two lobes.Methods Forty SD rats were divided into four groups: group S with sham operation as an undisposed blank control, group BL with the right lobe bile duct embolized and ligated, group PL with the quadrate lobe portal vein ligated, and group BPL with the right lobe bile duct embolized and ligated and meanwhile the quadrate lobe portal vein ligated. The right hepatic bile ducts were embolized with cyanoacrylate and then ligated to prepare the BDD lobe. The portal vein of quadrate hepatic lobes was ligated as the PVD lobes. The observation period was 1 month after the bile duct or portal vein ligated. The values of liver weight/body weight and the quadrate lobe weight/the right lobe weight were recorded. The bile duct and portal vein casting specimens of these four groups were prepared by a perfusion with barium and gelatin solution. Three-dimensional micro-computerized tomography (Micro-CT) data sets were acquired to observe the morphological changes of bile duct and portal vein of the livers and whether there were communicated branches between the right and quadrate lobes in order to estimate the feasibility of the model.Results (1) The survival rate of rats after operation was 100%. No jaundice was observed. The ratio of liver/body weight in groups S, BL and PL was about 3.5%, significantly lower than that in group BPL (P<0.01). The ratio of quadrate/right lobe weight in groups S and BL was about 60%-70%, while that was about 20% in groups PL and BPL (P<0.05, or P<0.01); (2) Micro-CT images exhibited directly the morphological changes of the hepatic bile duct and portal vein, and no communicated branches or side circulation situation were observed between the two lobes.Conclusion No collateral branches were found between the two lobes and the model was successfully established. The barium casting liver specimen scanned by micro-CT provided a useful method for the morphological observation of rat liver Glissons system.