重庆医学
重慶醫學
중경의학
CHONGQING MEDICAL JOURNAL
2013年
30期
3653-3655
,共3页
刘芹%王军%叶黎离%郑玉艳%刘文强%杨倩倩
劉芹%王軍%葉黎離%鄭玉豔%劉文彊%楊倩倩
류근%왕군%협려리%정옥염%류문강%양천천
巨细胞病毒感染%小鼠%结肠%肠三叶因子%更昔洛韦
巨細胞病毒感染%小鼠%結腸%腸三葉因子%更昔洛韋
거세포병독감염%소서%결장%장삼협인자%경석락위
cytomegalovirus infection%mice%colon%intestinal trefoil factor%ganciclovir
目的:观察肠三叶因子(ITF/TFF3)在鼠巨细胞病毒(MCMV)感染小鼠结肠中的表达及更昔洛韦的干预作用。方法将48只4周龄BALB/c小鼠,随机分为空白组、病毒组及更昔洛韦(GCV)组,每组8只。病毒组和GCV组分别腹腔接种致半数细胞感染量(TCID50=105.31/mL)的MCMV病毒悬液100μL ,GCV组在接种MCMV 24 h后GCV 50 mg/kg ,每天1次,腹腔注射,连续14 d ,同时病毒组和空白组分别给予同等剂量的生理盐水作为对照。定量PCR检测肝脏、结肠MCMV-DNA ;采用实时定量逆转录-聚合酶链反应(RT-PCR)法检测ITF mRNA表达水平。结果病毒组小鼠明显出现食欲差、活动少;皮毛稀松、对刺激反应迟钝、生长迟缓、体质量不增等表现。病毒组肝脏、结肠组织有MCMV-DNA表达,GCV组亦有表达,但弱于病毒组。GCV组与病毒组相比ITF mRNA表达升高,差异有统计学意义(P<0.05);病毒组与空白组相比ITF mRNA表达水平升高,差异有统计学意义(P<0.05)。结论 ITF是一类较新的肠黏膜保护因子,在MCMV感染后所导致的急性肠道炎症损伤过程中发挥着重要的保护作用。
目的:觀察腸三葉因子(ITF/TFF3)在鼠巨細胞病毒(MCMV)感染小鼠結腸中的錶達及更昔洛韋的榦預作用。方法將48隻4週齡BALB/c小鼠,隨機分為空白組、病毒組及更昔洛韋(GCV)組,每組8隻。病毒組和GCV組分彆腹腔接種緻半數細胞感染量(TCID50=105.31/mL)的MCMV病毒懸液100μL ,GCV組在接種MCMV 24 h後GCV 50 mg/kg ,每天1次,腹腔註射,連續14 d ,同時病毒組和空白組分彆給予同等劑量的生理鹽水作為對照。定量PCR檢測肝髒、結腸MCMV-DNA ;採用實時定量逆轉錄-聚閤酶鏈反應(RT-PCR)法檢測ITF mRNA錶達水平。結果病毒組小鼠明顯齣現食欲差、活動少;皮毛稀鬆、對刺激反應遲鈍、生長遲緩、體質量不增等錶現。病毒組肝髒、結腸組織有MCMV-DNA錶達,GCV組亦有錶達,但弱于病毒組。GCV組與病毒組相比ITF mRNA錶達升高,差異有統計學意義(P<0.05);病毒組與空白組相比ITF mRNA錶達水平升高,差異有統計學意義(P<0.05)。結論 ITF是一類較新的腸黏膜保護因子,在MCMV感染後所導緻的急性腸道炎癥損傷過程中髮揮著重要的保護作用。
목적:관찰장삼협인자(ITF/TFF3)재서거세포병독(MCMV)감염소서결장중적표체급경석락위적간예작용。방법장48지4주령BALB/c소서,수궤분위공백조、병독조급경석락위(GCV)조,매조8지。병독조화GCV조분별복강접충치반수세포감염량(TCID50=105.31/mL)적MCMV병독현액100μL ,GCV조재접충MCMV 24 h후GCV 50 mg/kg ,매천1차,복강주사,련속14 d ,동시병독조화공백조분별급여동등제량적생리염수작위대조。정량PCR검측간장、결장MCMV-DNA ;채용실시정량역전록-취합매련반응(RT-PCR)법검측ITF mRNA표체수평。결과병독조소서명현출현식욕차、활동소;피모희송、대자격반응지둔、생장지완、체질량불증등표현。병독조간장、결장조직유MCMV-DNA표체,GCV조역유표체,단약우병독조。GCV조여병독조상비ITF mRNA표체승고,차이유통계학의의(P<0.05);병독조여공백조상비ITF mRNA표체수평승고,차이유통계학의의(P<0.05)。결론 ITF시일류교신적장점막보호인자,재MCMV감염후소도치적급성장도염증손상과정중발휘착중요적보호작용。
Objective To observe the expression of ITF in colon of mice infected by mouse cytomegalovirus (MCMV) and the in-volvement of ganciclovir(GCV) .Methods Forty-eight BALB/c young mice were randomly divided into blank group ,virus group and GCV group ,each with 8 mice .Mice in virus group and GCV group received injection of 100 μL MCMV virus suspension (TCID50105 .31 /mL) ,and GCV group was given intraperitoneal injection of GCV once a day at the dose of 50 mg/kg from day 0 (24 hours after vaccination of virus ) ,for 14 days .At the same time the virus group and blank group were given the same dose of normal saline as controls .Murine cytomegalovirus loads in livers and colons were measured by PCR .The expression levels of ITF in mRNA in colon were detected by RT-PCR .Results After MCMV injection ,mice in virus group manifested aggressively apparent poor appetite ,less activity ,fur laxly ,unresponsiveness to stimuli ,growth retardation ,body weight not increased .All liver and colon tissue MCMV-DNA PCR electrophoresis of virus group had positive strip ,while the blank group did not .GCV group also showed less bright positive strip when compared with the virus group .Expression level of ITF mRNA was significant higher in GCV group than virus group ,there was statistically significant difference(P<0 .05) .Expression of ITF mRNA in virus group were higher than that in blank group ,there was statistical difference(P<0 .05) .Conclusion ITF is regarded as a fast reaction peptide in the course of mucosa impairments ,so ITF plays a protective role in delayed healing process after acute MCMV infection .