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机构地区:[1]河北省中药研究与开发重点实验室,承德067000 [2]承德医学院肛肠医院,承德067000
出 处:《实验动物科学》2013年第5期15-19,共5页Laboratory Animal Science
基 金:河北省科学技术研究与发展计划项目(No.10276105D-45)
摘 要:目的观察健脾化湿颗粒对腹泻型肠易激综合征(DIARRHEA-PREDOMINANT of Irritable Bowel Syndrome,D-IBS)模型大鼠内脏敏感性和脑中促肾上腺皮质激素释放因子(Corticotropin-Releasing Factor,CRF)及促肾上腺皮质激素释放因子受体1(Corticotropin-Releasing Factor Receptor 1,CRF-R1)mRNA表达的影响。方法 72只SD大鼠随机分为正常组、模型组、得舒特组和健脾化湿颗粒低、中、高剂量组;用番泻叶灌胃结合束缚应激法复制D-IBS大鼠模型;采用直肠扩张腹壁撤退反射(Abdominal With drawal Reflex,AWR)评分评价大鼠的内脏敏感性;采用PCR法检测大鼠脑中CRF、CRF-R1 mRNA的表达。结果与正常组相比,模型组AWR评分为3的注水量明显降低(P<0.01),脑中CRF、CRF-R1 mRNA的表达明显升高(P<0.01);与模型组比较,健脾化湿颗粒中、高剂量组、得舒特组AWR评分为3的注水量明显升高(P<0.01),脑中CRF、CRF-R1mRNA的表达明显降低(P<0.01)。结论健脾化湿颗粒中、高剂量组可降低大鼠的内脏敏感性,其作用机制可能与降低中枢CRF及CRF-R1 mRNA的表达有关。Objective To explore the effects of Jianpi Huashi Granule on visceral sensitivity and CRF/CRF-R1expression in brain of D-IBS model rat.Method Seventy-two male Sprague-Dawley rats were equally and randomly divided into six groups:normal group,model group,dicetel group,low-,medium-,and high-dose Jianpi Huashi Granule groups; D-IBS was induced by restraint stress combined with administration of sennae decoction; The visceral sensitivity of rats was evaluated by colorectal distention,and recorded the water injection rate when the score of abdominal withdrawal reflex (AWR) was 3.The expression of CRF and CRF-R1mRNA in the brain was detected by PCR.Result Compared with normal group,the water injection rate of the model group showed a significant decrease when the score of AWR was 3 (P < 0.01),and the expression of CRF and CRF-R1 mRNA in the brain significantly increased (P < 0.01) ; compared with model group,the water injection rate of the dicetel group,medium-,and high-dose Jianpi Huashi Granule groups showed a significant increase when the score of AWR was 3 (P < 0.01),and the expression of CRF and CRF-R1 mRNA in the brain significantly decreased (P < 0.01).Conclusion medium-,and high-dose Jianpi Huashi Granule groups reduces visceral sensitivity in the rats with D-IBS possibly by modulating the expression of CRF and CRF-R1mRNA in the brain.
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