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作 者:梁颖[1] 刘金宝[1] 王军[2] 叶章群[3] 宋波[2] 金锡御[2]
机构地区:[1]新疆医科大学公共卫生学院营养与食品卫生学教研室,新疆乌鲁木齐830054 [2]第三军医大学西南医院全军泌尿外科,重庆400038 [3]华中科技大学同济医学院附属同济医院泌尿外科,湖北武汉430030
出 处:《新疆医科大学学报》2006年第5期415-417,420,共4页Journal of Xinjiang Medical University
摘 要:目的: 探讨尿纤溶活性在尿结石形成过程中的保护作用以及α-亚麻酸(α-LNA)对草酸钙结石鼠纤溶活性的影响.方法: 75只雄性Wistar成年大鼠随机分成5组,阴性对照组饲以普通饲料,阳性对照组饲以高脂饲料,成石组饲以高脂饲料加诱石剂饮水,苏子油组饲以高脂饲料加诱石剂饮水并每日苏子油灌胃(2 g/只),葵花籽油组饲以高脂饲料加诱石剂饮水并每日葵花籽油灌胃(2 g/只).实验8周后检测各组大鼠血清总胆固醇(TC)、甘油三酯(TG)、血纤溶酶原激活物(tPA)水平,并对各组进行比较.结果:苏子油组和葵花籽油组血清TC和TG水平显著低于阳性对照组(P〈0.05~0.01),成石组tPA水平明显低于阴性对照组和苏子油组(P〈0.01).结论: 尿纤溶活性是一种重要的抗结石形成而保护机体健康的因素,α-LNA可提高草酸钙结石鼠尿纤溶活性,抑制尿结石形成.Objective: To investigate the protective role of urinary fibrinolytic activity in urinary stone for mation and the effect of α-Linolenic acid on the fibrinolytic activity in calcium oxalate urolithiasis rats. Methods: The 75 male adult rats were random divided into five groups: negative control group rats were administered with common forage, positive control group rats were administered with high fat forage , stone group rats were administered with high fat diet and drinking 1% of ethylene glycol plus 1% of muri ate water, perilla frutescens (L · ) Britt · oil group rats were administered with high fat diet and drinking 1% of ehtylene glycol plus 1% of muriate water, meanwhil, tube feeding with perilla frutescens (L · ) Britt ·oil (10 g · kg^-1 · d^-1) and sunflower seeds oil group rats were administered with high fat diet and drinking 1% of ehtylene glycol plus 1% of muriate water, and tube feeding with sunflower seeds oil (10 g · kg ^-1· d ^-1). 8 weeks later, serum cholesterol (TC), the triglyceride (TG) and tissue type plasminogen activator(tPA) were detected and compared with. Results: Perilla frutescens (L ·) Britt · oil group and sunflower seeds oil group rats, the serum cholesterol and the triglyceride were signficantly lower than stone group (P 〈0.05-0.01). Stone group tissue type plasminogen activator were significantly lower compared with negative control group and perilla frutescens (L · ) Britt · oil group (P 〈C0.01). Conclusions: Urinary fibrinolytic activity was a important protective factor of urinary calculi formation, α-Linolenic acid may prevent calcium oxalate urolithiasis formation by increasing urinary fibrinolytic activity.
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