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机构地区:[1]徐州医学院生理学教研室徐州医学院神经生物学研究中心,江苏徐州221002
出 处:《徐州医学院学报》2007年第12期771-774,共4页Acta Academiae Medicinae Xuzhou
基 金:国家自然科学基金(30570671);江苏省教育厅科学研究基金(05KJB310134);徐州医学院科研课题(07KJ58)
摘 要:目的研究室旁核(paraventricular nucleus,PVN)内注射血管紧张素Ⅱ(angiotensinⅡ,AngⅡ)对大鼠胃缺血/再灌注(gastric ischemia/reperfusion,GI/R)后的胃黏膜核因子κB(NF-κB)表达的影响。方法采用核团微量注射法以及夹闭大鼠腹腔动脉30 min后松开动脉夹血流复灌1 h的GI/R模型,计数胃黏膜损伤指数并应用免疫组化方法检测胃黏膜NF-κB p65的表达。结果①GI/R可引起胃黏膜损伤,PVN内微量注射AngⅡ(0.3μl含30 ng)后GI/R损伤显著减轻;侧脑室注射(icv)AngⅡ受体拮抗剂洛沙坦,能阻断AngⅡ对GI/R损伤的保护作用,使GI/R损伤明显加重;②正常大鼠胃黏膜可见NF-κB表达,并主要在胞质表达;GI/R后,NF-κB表达增多,尤其是胞核表达明显增加;PVN内微量注射AngⅡ后,可使胃黏膜NF-κB表达量减少;icv给予洛沙坦可阻断AngⅡ的效应,即GI/R损伤后胃黏膜NF-κB阳性细胞数表达量增加。结论PVN内微量注射AngⅡ对大鼠GI/R损伤有明显的保护作用,且该作用可被洛沙坦翻转;NF-κB在PVN内微量注射AngⅡ减轻大鼠GI/R损伤过程中可能发挥着重要作用。Objective To study the effect of angiotensin Ⅱ ( Ang Ⅱ ) in the paraventricular nucleus (PVN) on the expression of NF -κB in gast,ic mucosa following gastric ischemia/reperfusion (GI/R) in rats. Methods Intranuclear microinjection and model of GI/R were employed in the experiment. The GI/R model was established by clamping the celiac artery for 30 rain to induce ischemia and allowing reperfusion for 1 h. The animals were finally sacrificed to investigate the gastric mucosal damage index and the expression of NF -κB in the gastric mucosa by immunohistochemistry. Results ① GI/R induced gastric mucosal injury; microinjection of Ang Ⅱ (30 ng)into PVN obviously attenuated the GI/R injury; intracerebroventricular injection (icy) of losartan, an Ang Ⅱ AT1 receptor antagonist, could eliminate the protective effect of Ang Ⅱ against the I/R - induced gastric mucosal injury. ② NF -κB ( p65 ) was mainly expressed in the cytoplasm in the middle and bottom layers of gastric mucosa in normal rat, NF -κB was obviously expressed in both nucleus and cytoplasm and translocated to the nuclei of gastric mucosal cells after 1 h of L/R. Microinjection of Ang Ⅱ (30 ng) into the PVN significantly suppressed the translocation of p65 to the nuclei, and losartan blocked the effect of Ang Ⅱ. The expression of NF -κB varied with the changes of the gastric mucosal damage index. Conclusion Microinjection of AngⅡ into the PVN protects against GI/R injury, and the protective effect of Ang Ⅱ can be reversed by losartan. NF-κB may play an important role in the PVN, where Ang Ⅱ mediates the protection against GI/R injury .
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