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作 者:汪正芳[1] 郭前坤[2] 张声生[1] 赵鲁卿[1] 杨成[1] 李晓玲[3] 吴震宇[3]
机构地区:[1]首都医科大学附属北京中医医院消化中心,北京100010 [2]天津中医药大学第一附属医院脾胃病科,天津300193 [3]北京中医药大学,北京100029
出 处:《北京中医药》2013年第6期406-409,共4页Beijing Journal of Traditional Chinese Medicine
基 金:国家自然科学基金(30973746);北京市自然科学基金(7102083);北京市教委基金(KM201010025027)
摘 要:目的观察疏肝健脾方对腹泻型肠易激综合征(D-IBS)模型大鼠结肠黏膜5-羟色胺(5-HT),5-羟色胺3受体(5-HT3R)及5-羟色胺4受体(5-HT4R)表达的影响。方法将60只SD雄性大鼠随机分为正常组、模型组、得舒特组和疏肝健脾高、中、低剂量组,除正常组外其余各组使用乙酸灌肠加束缚应激的方法制备D-IBS大鼠模型,造模成功后各组分别予生理盐水、得舒特、疏肝健脾方灌胃2周。取大鼠结肠黏膜,采用酶联免疫法检测5-HT,免疫组化法检测5-HT3R及5-HT4R的表达。结果疏肝健脾方可以明显降低D-IBS大鼠粪便含水量(P<0.01);疏肝健脾方可以明显增加D-IBS大鼠的最小容量阈值(P<0.01);疏肝健脾方可以降低D-IBS大鼠结肠黏膜5-HT和5-HT3R的表达(P<0.01),升高5-HT4R的表达(P<0.01)。结论疏肝健脾方对D-IBS模型大鼠的治疗作用可能是通过调节结肠5-HT及其受体,减弱神经元兴奋性、提高内脏痛阈、消除肠道敏感而达到的。Objective To investigate the effects of Shuganjianpi prescription(SGJP) on the expression of 5-hydroxytryptamine(5-HT),5-HT3receptor(5-HT3R) and 5-HT4receptor(5-HT4R) of colon mucosa in the irritable bowel syndrome-diarrhea predominant(D-IBS) rats.Methods Sixty male Sprague-Dawley(SD) rats were randomly divided into six groups: a normal group,a model group,a Pinaverium Bromide(PB) group and a high-,medium-and low-dose of SGJP group(Group H,M and L).All groups except the normal group received enema of acetic acid and restraint stress for preparation of D-IBS model,which were intragastric administrated with saline,PB,and SGJP for two weeks respectively after modeling successfully.The colon mucosa of rats was taken for detecting the expression of 5-HT,5-HT3R and 5-HT4R by enzymelinked immunosorbent assay and immunohistochemical assay.Results The SGJP significantly reduced the fecal water content of D-IBS rats(P 0.01);the SGJP significantly increased the minimum capacity threshold of D-IBS rats(P 0.01);the SGJP significantly reduced the expression of 5-HT and 5-HT3R of colon mucosa in D-IBS rats(P 0.01),while significantly increased expression of 5-HT4R(P 0.01).Conclusion The therapeutic action of SGJP on the D-IBS rats might be realized through regulating 5-HT and its receptors,reducing neuronal excitability,increasing visceral pain threshold and eliminating intestinal sensitivity.
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