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机构地区:[1]桂林医学院附属医院消化内科,桂林541001
出 处:《郑州大学学报(医学版)》2013年第1期47-50,共4页Journal of Zhengzhou University(Medical Sciences)
基 金:广西壮族自治区卫生厅中医药科技专项课题GZKZ10-125;广西壮族自治区科学基金资助项目桂科回0342027
摘 要:目的:探讨伴有胃肠动力障碍的重症急性胰腺炎(SAP)大鼠结肠黏膜下神经节一氧化氮合酶(NOS)阳性神经元的改变。方法:20只SD大鼠随机分为假手术组与模型组,用逆行胰胆管注射牛磺胆酸钠的方法制作大鼠SAP模型。24h后,测定2组小肠推进比、结肠蠕动频率、粪便含水量,并进行胰腺病理评分;制作结肠黏膜下神经丛全层标本,运用免疫荧光技术观察黏膜下神经节NOS阳性神经元的变化。结果:与假手术组相比,模型组小肠推进比减少[(41.04±4.36)%vs(14.54±2.30)%,t=15.477,P<0.001],结肠蠕动频率减慢[(13.40±1.35)min-1vs(4.00±0.93)min-1,t=16.748,P<0.001],粪便含水量降低[(41.56±6.69)%vs(12.98±6.56)%,t=8.869,P<0.001],胰腺病理评分增高[(1.20±0.63)vs(15.75±1.72),t=23.569,P<0.001],但其结肠黏膜下NOS阳性神经元计数无明显改变[(22.49±5.14)%vs(26.36±2.57)%,Z=-1.955,P=0.055]。结论:伴胃肠动力障碍的SAP大鼠结肠黏膜下NOS阳性神经元可能未发生明显重塑。Aim:To investigate the change of nitric oxide synthase(NOS) immunoreactive neurons in colonic submucous ganglia of rats with severe acute pancreatitis(SAP) accompanied by gastrointestinal dysmotility.Methods:Twenty SD rats were randomly divided into two groups:sham operation group and model group.SAP model was established by retrograde injecting sodium taurocholate into the bile-pancreatic duct.After 24 h,small intestinal transit index,frequency of colonic peristalisis,water content of the fecal matter,and pathological damage of pancreas were measured.Whole-mount samples were prepared and double immunofluorescence was employed to observe NOS immunoactive neurons in colonic submucous ganglia.Results:Compared with sham operation group,small intestinal transit index,frequency of colonic peristalisis and water content of fecal matter of the model group were significantly lower[(41.04±4.36)% vs (14.54±2.30)%,(13.40±1.35) min-1 vs (4.00±0.93) min-1,(41.56±6.69)% vs (12.98±6.56)%,t=15.477,16.748,8.869,P0.001],and score of pancreatic pathological damage was higher[(1.20±0.63) vs (15.75±1.72),t=23.569,P0.001],however,there was no significant changes in NOS immunoreactive neurons count[(22.49±5.14)% vs (26.36±2.57)%,Z=-1.955,P=0.055].Conclusion:NOS immunoreactive neurons in colonic submucous ganglia may be no significant plasticity in SAP rats complicated with gastrointestinal dysmotility.
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