南京中医药大学学报
南京中醫藥大學學報
남경중의약대학학보
Journal of Nanjing University of Traditional Chinese Medicine
2015年
5期
475-479
,共5页
张微%李瑛%刘丽莎%罗芳丽%郑倩华
張微%李瑛%劉麗莎%囉芳麗%鄭倩華
장미%리영%류려사%라방려%정천화
电针%俞募穴%功能性便秘%GDNF
電針%俞募穴%功能性便祕%GDNF
전침%유모혈%공능성편비%GDNF
electroacupuncture%Backshu and Frontmu points%functional constipation%GDNF
目的:探讨电针大肠俞募穴治疗功能性便秘的作用机制。方法32只小鼠随机分为对照组、模型组、针刺组和 EGC 抑制组。采用复方地芬诺酯灌胃造模法,电针刺激天枢、大肠俞,每次30 min,共治疗5次。运用光镜、电镜、免疫组化及原位杂交技术,观察电针治疗前后结肠组织上皮细胞形态学改变,结肠组织中 GDNF 蛋白及 mRNA 表达水平。结果与对照组比较,模型组结肠组织 GDNF 蛋白及 mRNA 表达水平显著降低(P <0.01)。电针刺激大肠俞募穴可提高结肠中 GDNF 蛋白及其 mRNA 的表达水平(P <0.05),光镜和电镜发现针刺可修复受损上皮细胞,进而改善肠道传输功能。EGC 抑制组结肠中GDNF 蛋白表达与模型组比较无显著性差异(P >0.05),与针刺组比较显著降低(P <0.05),GDNF mRNA 的表达水平高于模型组(P <0.05),低于针刺组,但差异无统计学意义(P >0.05)。光镜和电镜下 EGC 抑制组结肠组织形态改变较为严重。结论电针刺激大肠俞募穴可提高 EGC 细胞中 GDNF 蛋白及其 mRNA 的表达水平,修复受损结肠上皮细胞,进而改善肠道传输功能。
目的:探討電針大腸俞募穴治療功能性便祕的作用機製。方法32隻小鼠隨機分為對照組、模型組、針刺組和 EGC 抑製組。採用複方地芬諾酯灌胃造模法,電針刺激天樞、大腸俞,每次30 min,共治療5次。運用光鏡、電鏡、免疫組化及原位雜交技術,觀察電針治療前後結腸組織上皮細胞形態學改變,結腸組織中 GDNF 蛋白及 mRNA 錶達水平。結果與對照組比較,模型組結腸組織 GDNF 蛋白及 mRNA 錶達水平顯著降低(P <0.01)。電針刺激大腸俞募穴可提高結腸中 GDNF 蛋白及其 mRNA 的錶達水平(P <0.05),光鏡和電鏡髮現針刺可脩複受損上皮細胞,進而改善腸道傳輸功能。EGC 抑製組結腸中GDNF 蛋白錶達與模型組比較無顯著性差異(P >0.05),與針刺組比較顯著降低(P <0.05),GDNF mRNA 的錶達水平高于模型組(P <0.05),低于針刺組,但差異無統計學意義(P >0.05)。光鏡和電鏡下 EGC 抑製組結腸組織形態改變較為嚴重。結論電針刺激大腸俞募穴可提高 EGC 細胞中 GDNF 蛋白及其 mRNA 的錶達水平,脩複受損結腸上皮細胞,進而改善腸道傳輸功能。
목적:탐토전침대장유모혈치료공능성편비적작용궤제。방법32지소서수궤분위대조조、모형조、침자조화 EGC 억제조。채용복방지분낙지관위조모법,전침자격천추、대장유,매차30 min,공치료5차。운용광경、전경、면역조화급원위잡교기술,관찰전침치료전후결장조직상피세포형태학개변,결장조직중 GDNF 단백급 mRNA 표체수평。결과여대조조비교,모형조결장조직 GDNF 단백급 mRNA 표체수평현저강저(P <0.01)。전침자격대장유모혈가제고결장중 GDNF 단백급기 mRNA 적표체수평(P <0.05),광경화전경발현침자가수복수손상피세포,진이개선장도전수공능。EGC 억제조결장중GDNF 단백표체여모형조비교무현저성차이(P >0.05),여침자조비교현저강저(P <0.05),GDNF mRNA 적표체수평고우모형조(P <0.05),저우침자조,단차이무통계학의의(P >0.05)。광경화전경하 EGC 억제조결장조직형태개변교위엄중。결론전침자격대장유모혈가제고 EGC 세포중 GDNF 단백급기 mRNA 적표체수평,수복수손결장상피세포,진이개선장도전수공능。
ABSTRACTOBJECTIVE To explore the mechanism of electroacupuncture at Back?shu and Front?mu points for functional constipation treatment.METHODS 32 mice were randomly divided into control groupmodel groupelectroacupunctureEA group and EGC group.Compound diphenoxylate were gavaged for modelingand electroacupuncture Tianshu and Dachangshu points30 min each time for a total of 5 times treatment.By light microscopyelectron microscopyimmunohisto-chemistry and in situ hybridizationthe morphology of colonic epithelial structure were observedand the level of GDNF pro-tein and mRNA expression in colon were detected.RESULTS The expression of GDNF protein and mRNA in model group was significantly decreasedP <0.01.Electroacupuncture at back?Shu and front?Mu points improved the expression of GDNF protein and mRNAP <0.05and light microscope and electron microscope showed that acupuncture repaired damaged depi-thelial cellsand then improved the intestinal transmission function.The expression of GDNF protein in EGC group showed no significant difference with the model groupP >0.05but significantly decreasedcompared with EA groupP <0.05.GD-NF mRNA was significantly higher than model groupP <0.05but lower than EA group with no significant differenceP>0.05.The morphology change of colon tissue is more serious.CONCLUSION Electroacupuncture at back?Shu and front? Mu points can improve the expression of GDNF protein and mRNA in EGC cellsrepair the colonic epithelial cellsand then improve the intestinal transmission function.