河北医科大学学报
河北醫科大學學報
하북의과대학학보
JOURNAL OF HEBEI MEDICAL UNIVERSITY
2014年
6期
625-627
,共3页
朱建忠%刘冀%王国明%王娟%隋月林%石葛明
硃建忠%劉冀%王國明%王娟%隋月林%石葛明
주건충%류기%왕국명%왕연%수월림%석갈명
肝硬化%大鼠%中缝背核%5-HT%神经元
肝硬化%大鼠%中縫揹覈%5-HT%神經元
간경화%대서%중봉배핵%5-HT%신경원
cirrhosis%rat%dorsal raphe nucleus%5-HT%neuron
目的:观察肝硬化大鼠中缝背核五羟色胺(5-hydroxytryptamine,5-HT)能神经元以及双标神经元的表达变化。方法健康雄性Wistar大鼠20只,分为模型组和对照组各10只,模型组大鼠经皮下注射CCl4结合饮用酒精14周,对照组皮下注射等剂量的生理盐水。应用5-HT免疫组织化学及5-HT复合NADPH-d免疫组织化学染色双标方法,观察中缝背核5-HT能神经元以及双标神经元的表达变化。结果与对照组相比,模型组大鼠中缝背核5-HT能神经元的数量未见明显变化,直径明显变小,模型组免疫反应阳性强度明显较对照组增强,神经元的光密度(0.54±0.04)vs(0.48±0.04)(P<0.01);双标神经元未见明显变化。结论肝硬化影响了大鼠中缝背核5-HT能神经元。
目的:觀察肝硬化大鼠中縫揹覈五羥色胺(5-hydroxytryptamine,5-HT)能神經元以及雙標神經元的錶達變化。方法健康雄性Wistar大鼠20隻,分為模型組和對照組各10隻,模型組大鼠經皮下註射CCl4結閤飲用酒精14週,對照組皮下註射等劑量的生理鹽水。應用5-HT免疫組織化學及5-HT複閤NADPH-d免疫組織化學染色雙標方法,觀察中縫揹覈5-HT能神經元以及雙標神經元的錶達變化。結果與對照組相比,模型組大鼠中縫揹覈5-HT能神經元的數量未見明顯變化,直徑明顯變小,模型組免疫反應暘性彊度明顯較對照組增彊,神經元的光密度(0.54±0.04)vs(0.48±0.04)(P<0.01);雙標神經元未見明顯變化。結論肝硬化影響瞭大鼠中縫揹覈5-HT能神經元。
목적:관찰간경화대서중봉배핵오간색알(5-hydroxytryptamine,5-HT)능신경원이급쌍표신경원적표체변화。방법건강웅성Wistar대서20지,분위모형조화대조조각10지,모형조대서경피하주사CCl4결합음용주정14주,대조조피하주사등제량적생리염수。응용5-HT면역조직화학급5-HT복합NADPH-d면역조직화학염색쌍표방법,관찰중봉배핵5-HT능신경원이급쌍표신경원적표체변화。결과여대조조상비,모형조대서중봉배핵5-HT능신경원적수량미견명현변화,직경명현변소,모형조면역반응양성강도명현교대조조증강,신경원적광밀도(0.54±0.04)vs(0.48±0.04)(P<0.01);쌍표신경원미견명현변화。결론간경화영향료대서중봉배핵5-HT능신경원。
Objective To study the expression of 5-hydroxytryptamine( 5-HT ) and double-labeled neurons in dorsal raphe of cirrhosis rats. Methods The healthy male Wistar rats were divided into model and control groups(n=10). Within 14 weeks,model group rats were subcutaneously injected by CCl4 plus drinking ethonal. Control group rats received subcutaneously injection of sodium chloride. 5-HT immunohistochemistry and 5-HT immunohistochemistry combined with NADPH-d staining were used to detect the expression of 5-HT and double-labeled neurons in dorsal raphe of rats. Results The average diameter 5-HT neurons in dorsal raphe decreased significantly in the model group compared with that of control group. The optical density value of 5-HT neurons in dorsal raphed increased sinificantly in the mode of group(0. 54 ± 0. 04)compared with that of control group(0. 48 ± 0. 04)(P <0. 01). The quantity of 5-HT neurons and the double-labeled neurons in dorsal raphe hasd no significant difference between two groups. Conclusion Cirrhosis influenced 5-HT neurons in dorsal raphe of rats.