中华消化杂志
中華消化雜誌
중화소화잡지
Chinese Journal of Digestion
2011年
4期
235-238
,共4页
杨琰%余跃%高显奎%陈军%王巧民
楊琰%餘躍%高顯奎%陳軍%王巧民
양염%여약%고현규%진군%왕교민
糖尿病%胰岛素%十二指肠%平滑肌细胞
糖尿病%胰島素%十二指腸%平滑肌細胞
당뇨병%이도소%십이지장%평활기세포
Diabetes mellitus%Insulin%Duodenum%Myocytes,smooth muscle
目的 探讨胰岛素(regular insulin,RI)对糖尿病(DM)小鼠小肠功能的影响.方法 一次性给予雄性BALB/c小鼠链脲佐菌素(STZ,150 mg/kg)腹腔注射造模.将造模成功小鼠分为DM组6只,DM+RI组6只,另选血糖正常小鼠6只为对照组.DM+RI组给予RI 40U·kg-1·d-1皮下注射,对照组和DM组每天给予等量的磷酸盐缓冲液(pH=7.4)腹腔注射.所有小鼠干预6周结束后,给予印度墨水灌胃测定胃肠传输速率.免疫组织化学法检测各组小鼠十二指肠组织的c-kit阳性细胞数目.最后处死所有小鼠,用细胞内记录技术记录各组小鼠十二指肠平滑肌细胞内慢波的变化.采用SPSS 17.0软件分析,多组资料间比较采用LSD检验.结果 干预6周后,DM+RI组的多饮、多食、多尿症状比DM组减轻,体重较DM组明显增加[(23.33±3.13)g比(15.42±1.40)g,P<0.01],但比对照组降低[(26.78±2.09)g,P<0.05].第6周DM组血糖值显著高于对照组(P<0.01),但比DM+RI组显著升高(P<0.01).DM组小肠推进率比DM+RI组和对照组明显降低(P值均<0.01);DM+RI组也较对照组降低(P<0.01).光镜下观察到DM组c-kit阳性细胞数明显低于DM+RI组和对照组(P值均<0.05),DM+RI组比正常组减少(P<0.05).DM组慢波频率比DM+RI组和对照组显著降低(P值均<0.01),而DM+RI组慢波频率比对照组降低(P<0.01).DM组慢波波幅比DM+RI组和对照组明显降低(P值均<0.01),而DM+RI组慢波波幅比对照组降低(P<0.01).结论 DM小鼠存在胃肠动力障碍,外源性RI可能对DM小鼠小肠动力障碍有一定的改善作用.
目的 探討胰島素(regular insulin,RI)對糖尿病(DM)小鼠小腸功能的影響.方法 一次性給予雄性BALB/c小鼠鏈脲佐菌素(STZ,150 mg/kg)腹腔註射造模.將造模成功小鼠分為DM組6隻,DM+RI組6隻,另選血糖正常小鼠6隻為對照組.DM+RI組給予RI 40U·kg-1·d-1皮下註射,對照組和DM組每天給予等量的燐痠鹽緩遲液(pH=7.4)腹腔註射.所有小鼠榦預6週結束後,給予印度墨水灌胃測定胃腸傳輸速率.免疫組織化學法檢測各組小鼠十二指腸組織的c-kit暘性細胞數目.最後處死所有小鼠,用細胞內記錄技術記錄各組小鼠十二指腸平滑肌細胞內慢波的變化.採用SPSS 17.0軟件分析,多組資料間比較採用LSD檢驗.結果 榦預6週後,DM+RI組的多飲、多食、多尿癥狀比DM組減輕,體重較DM組明顯增加[(23.33±3.13)g比(15.42±1.40)g,P<0.01],但比對照組降低[(26.78±2.09)g,P<0.05].第6週DM組血糖值顯著高于對照組(P<0.01),但比DM+RI組顯著升高(P<0.01).DM組小腸推進率比DM+RI組和對照組明顯降低(P值均<0.01);DM+RI組也較對照組降低(P<0.01).光鏡下觀察到DM組c-kit暘性細胞數明顯低于DM+RI組和對照組(P值均<0.05),DM+RI組比正常組減少(P<0.05).DM組慢波頻率比DM+RI組和對照組顯著降低(P值均<0.01),而DM+RI組慢波頻率比對照組降低(P<0.01).DM組慢波波幅比DM+RI組和對照組明顯降低(P值均<0.01),而DM+RI組慢波波幅比對照組降低(P<0.01).結論 DM小鼠存在胃腸動力障礙,外源性RI可能對DM小鼠小腸動力障礙有一定的改善作用.
목적 탐토이도소(regular insulin,RI)대당뇨병(DM)소서소장공능적영향.방법 일차성급여웅성BALB/c소서련뇨좌균소(STZ,150 mg/kg)복강주사조모.장조모성공소서분위DM조6지,DM+RI조6지,령선혈당정상소서6지위대조조.DM+RI조급여RI 40U·kg-1·d-1피하주사,대조조화DM조매천급여등량적린산염완충액(pH=7.4)복강주사.소유소서간예6주결속후,급여인도묵수관위측정위장전수속솔.면역조직화학법검측각조소서십이지장조직적c-kit양성세포수목.최후처사소유소서,용세포내기록기술기록각조소서십이지장평활기세포내만파적변화.채용SPSS 17.0연건분석,다조자료간비교채용LSD검험.결과 간예6주후,DM+RI조적다음、다식、다뇨증상비DM조감경,체중교DM조명현증가[(23.33±3.13)g비(15.42±1.40)g,P<0.01],단비대조조강저[(26.78±2.09)g,P<0.05].제6주DM조혈당치현저고우대조조(P<0.01),단비DM+RI조현저승고(P<0.01).DM조소장추진솔비DM+RI조화대조조명현강저(P치균<0.01);DM+RI조야교대조조강저(P<0.01).광경하관찰도DM조c-kit양성세포수명현저우DM+RI조화대조조(P치균<0.05),DM+RI조비정상조감소(P<0.05).DM조만파빈솔비DM+RI조화대조조현저강저(P치균<0.01),이DM+RI조만파빈솔비대조조강저(P<0.01).DM조만파파폭비DM+RI조화대조조명현강저(P치균<0.01),이DM+RI조만파파폭비대조조강저(P<0.01).결론 DM소서존재위장동력장애,외원성RI가능대DM소서소장동력장애유일정적개선작용.
Objective To investigate the effects of regular insulin (RI)on duodenal smooth muscle in diabetic mice. Methods Diabetes mellitus (DM) model was established by intraperitoneal injection of 150 mg/kg streptozotocin (STZ) in male BALB/c mice. The model mice were divided into DM group and DM treated with RI group with 6 each. Meanwhile, 6 normal mice were served as controls. The mice in treatment group were intraperitoneally injected with 40 U/kg of RI daily.Whereas the mice in DM and control groups were intraperitoneally injected with phosphate buffer solution (pH = 7. 40). After 6 weeks, the small intestinal transit rate of mice was determined by lavage of Indian ink. Interstitial cells of cajal (ICC) in duodenal myenteric plexus were counted using immunohistochemical staining. Slow waves of duodenal smooth muscle cells were recorded with intracellular recordings. Data were analysed by SPSS 17.0 software, and comparisons among three groups were done using LSD test. Results After intervention for 6 months, the clinical presentations,such as more water and food intake and polyuria, were improved in treatment group. The body weight was increased in treatment group [(23.33±3.13) g] compared with DM group [(15.42±1.40) g,P<0.01] ,but dereased compared with control group [(26.78 ± 2.09) g, P<0.05]. The level of blood glucose in DM group was significantly higher than that in control and treatment groups(P<0.01). Small intestine transmission rate was significantly reduced in DM group than that in control and treatment groups (P<0.01), but it was slower in treatment group than that in control group (P< 0. 01 ). Immunohistochemical study showed that the number of c-kit positive cells reduced obviously in DM group than that in control group and treatment group (P<0.05), whereas it was lower in treatment group than that in control group (P < 0.05). The slow wave frequency and amplitude of duodenal smooth muscle cells in DM group were reduced when compared with control and treatment groups (P<0.01) and both were lower in treatment group than that in control group (P<0. 01 ). Conclusion The findings indicate that DM mice have gastrointestinal dysmotility and exogenous insulin may improve small intestinal dysmotility in DM mice.