中国医药科学
中國醫藥科學
중국의약과학
CHINA MEDICINE AND PHARMACY
2013年
23期
38-41
,共4页
林也容%林进皇%吴芳芳%郁毅刚
林也容%林進皇%吳芳芳%鬱毅剛
림야용%림진황%오방방%욱의강
孕兔%子宫动脉结扎%宫内缺血缺氧%NMDAr1
孕兔%子宮動脈結扎%宮內缺血缺氧%NMDAr1
잉토%자궁동맥결찰%궁내결혈결양%NMDAr1
Pregnant rabbit%Uterine artery ligation%Intrauterine ischemia hypoxia%NMDAr1
目的:建立孕兔宫内窘迫模型,观察胎兔脑组织病理及NMDAr1表达情况。方法新西兰大白兔孕兔30只,随机分为缺血模型组(n=9)、假手术组(n=9)和空白组(n=12)。缺血模型组孕兔行开腹子宫动脉结扎术,建立急性胎兔宫内窘迫模型;假手术组行开腹术,不结扎子宫动脉;空白组不行任何手术处理。除空白组胎兔直接断头取脑外,其他组胎兔都在术后6h断头取脑,观察各组胎兔脑组织病理形态及NMDAr1表达情况。结果与空白组及假手术组比较,缺血模型组胎兔脑组织NMDAr1表达呈强阳性,病理形态学为明显的脑组织细胞损伤表现;空白组和假手术组胎兔脑组织NMDAr1表达基本相同,均为少量表达,病理形态学均无脑组织细胞损伤表现。结论急性宫内窘迫可致胎兔脑组织NMDAr1表达增加,可能是造成其脑组织病理损伤的重要机制。
目的:建立孕兔宮內窘迫模型,觀察胎兔腦組織病理及NMDAr1錶達情況。方法新西蘭大白兔孕兔30隻,隨機分為缺血模型組(n=9)、假手術組(n=9)和空白組(n=12)。缺血模型組孕兔行開腹子宮動脈結扎術,建立急性胎兔宮內窘迫模型;假手術組行開腹術,不結扎子宮動脈;空白組不行任何手術處理。除空白組胎兔直接斷頭取腦外,其他組胎兔都在術後6h斷頭取腦,觀察各組胎兔腦組織病理形態及NMDAr1錶達情況。結果與空白組及假手術組比較,缺血模型組胎兔腦組織NMDAr1錶達呈彊暘性,病理形態學為明顯的腦組織細胞損傷錶現;空白組和假手術組胎兔腦組織NMDAr1錶達基本相同,均為少量錶達,病理形態學均無腦組織細胞損傷錶現。結論急性宮內窘迫可緻胎兔腦組織NMDAr1錶達增加,可能是造成其腦組織病理損傷的重要機製。
목적:건립잉토궁내군박모형,관찰태토뇌조직병리급NMDAr1표체정황。방법신서란대백토잉토30지,수궤분위결혈모형조(n=9)、가수술조(n=9)화공백조(n=12)。결혈모형조잉토행개복자궁동맥결찰술,건립급성태토궁내군박모형;가수술조행개복술,불결찰자궁동맥;공백조불행임하수술처리。제공백조태토직접단두취뇌외,기타조태토도재술후6h단두취뇌,관찰각조태토뇌조직병리형태급NMDAr1표체정황。결과여공백조급가수술조비교,결혈모형조태토뇌조직NMDAr1표체정강양성,병리형태학위명현적뇌조직세포손상표현;공백조화가수술조태토뇌조직NMDAr1표체기본상동,균위소량표체,병리형태학균무뇌조직세포손상표현。결론급성궁내군박가치태토뇌조직NMDAr1표체증가,가능시조성기뇌조직병리손상적중요궤제。
Objective Building rabbits acute fetal distress model to observe NMDAr1 expression and pathology research on brain tissue. Methods 30 Zelanian pregnant rabbits were divided into model group(n=9), sham group(n=9) and blank group(n=12)randomly. Rabbits of model group were performed and Uterine artery ligation to build acute fetal distress model. Rabbits of sham group were just performed laparotomy, and blank group did not receive any operation. Except the blank group's fetal rabbits were beheaded and take the brain directly, other groups's fetal rabbits were beheaded and take the brain after 6 hours of postoperation. Then, observe NMDAr1 expression and pathology research on brain tissue. Results 3 groups were compared multiply. In model group, the NMDAr1 expression of the fetal rabbits were strong positive, and pathomorphism significantly showed brain tissue and cell injury. Blank group' result is similar to sham group's, which were different from model group's. The NMDAr1 expression of two group's fetal rabbits were little positive, and pathomorphism did not show brain tissue and cell injury. Conclusion Acute fetal distress can cause the fetal rabbits's NMDAr1 expression higher, that may be a critical mechanism causing the brain pathological injury.