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作 者:魏兵[1] 刘亚丽[1] 张超[1] 尚云晓[2] 张晗[2] 李淼[2]
机构地区:[1]沈阳军区总医院儿科,辽宁沈阳110016 [2]中国医科大学附属盛京医院儿科,辽宁沈阳110004
出 处:《中国当代儿科杂志》2015年第11期1248-1252,共5页Chinese Journal of Contemporary Pediatrics
基 金:辽宁省博士启动基金(20121115)
摘 要:目的探讨哮喘气道重塑大鼠中气管平滑肌细胞迁移的变化及神经激肽-1受体(NK-1R)拮抗剂WIN62577对其的影响。方法将Sprague-Dawley(SD)大鼠随机分为对照组和哮喘气道重塑组,应用卵清蛋白对模型组大鼠激发8周,原代培养纯化气管平滑肌细胞(ASMC),通过免疫荧光、实时定量PCR等方法,检测ASMC中NK-1R的表达,并给予不同剂量WIN62577干预,应用transwell小室检测ASMC迁移的变化。结果哮喘气道重塑组ASMC中NK-1R主要分布在细胞质和细胞膜,其m RNA的表达高于对照组(P<0.01)。哮喘气道重塑组ASMC迁移数目较对照组明显增高(P<0.01),而分别给予不同浓度(10-11 mol/L、10-10 mol/L、10-9 mol/L、10-8 mol/L)的WIN62577干预后ASMC迁移数目较哮喘气道重塑组明显减少(P<0.05)。结论 NK-1R能通过促进ASMC迁移能力而影响哮喘气道重塑。Objective To study the changes in the migration of airway smooth muscle cells(ASMC) in asthmatic rats with airway remodeling and the effect of NK-1R inhibitor WIN62577 on the migration of ASMC. MethodsSprague-Dawley rats were randomly assigned into two groups: airway remodeling induced by asthma and normal control. ASMC from rats with asthma and airway remodeling induced by ovalbumin(OVA) inhalation for 8 weeks were primary cultured and purified. Immunofluorescence and real-time PCR were used to measure the expression of NK-1R. With NK-1R inhibitor WIN62577 treatment, the changes in the migration of ASMC were measured by transwell chambers. Results NK-1R in ASMC was expressed mainly in the cytoplasm and cell membrane in the airway remodeling group, and the m RNA expression of NK-1R was higher than the normal control group(P〈0.01). The number of the migrated ASMC in the airway remodeling group was significantly higher than that in the normal control group(P〈0.01). Various concentrations(10^-11 mol/L, 10^-10 mol/L, 10^-9 mol/L and 10^-8 mol/L) of WIN62577 treatment decreased the number of the migrated ASMC(P〈0.05). Conclusions NK-1R may affect airway remodeling possibly through promoting the migration ability of ASMC in rats with asthma.
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