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CCK-8对LPS攻击小鼠IL-1β、IL-6、IL-4、IL-10表达的影响
引用本文:倪志宇,丛斌,李淑瑾,马春玲,闫玉仙,徐锦荣,张国忠.CCK-8对LPS攻击小鼠IL-1β、IL-6、IL-4、IL-10表达的影响[J].中国病理生理杂志,2007,23(2):331-335.
作者姓名:倪志宇  丛斌  李淑瑾  马春玲  闫玉仙  徐锦荣  张国忠
作者单位:河北医科大学法医学系,河北 石家庄 050017
基金项目:国家自然科学基金;河北省博士科研项目
摘    要:目的: 观察LPS攻击小鼠IL-1β、IL-6、IL-4、IL-10的动态变化规律及八肽胆囊收缩素(CCK-8)对其表达的影响。方法: 将小鼠分为4组:对照组、LPS组(腹腔注射LPS)、LPS+CCK-8组(注射LPS前 30 min 腹腔注射CCK-8)及CCK-8组(单独注射CCK-8)。用ELISA及PT-PCR方法检测各组小鼠血清、肺组织中IL-1β、IL-6、IL-4、IL-10的含量及mRNA的表达情况。结果: LPS攻击可使小鼠血清及肺组织中 IL-1β、IL-6、IL-4、IL-10蛋白及mRNA的表达增加,预先注入CCK-8可显著抑制IL-1β、IL-6的表达,并使 IL-4、IL-10的表达进一步增加。结论: CCK-8可能通过抑制LPS攻击小鼠IL-1β、IL-6的表达和进一步增加 IL-4、IL-10的表达参与抗炎反应过程,从而减轻LPS引起的肺组织炎症反应。

关 键 词:缩胆囊素  脂多糖类  白细胞介素类  
文章编号:1000-4718(2007)02-0331-05
收稿时间:2006-4-12
修稿时间:2006-04-122006-06-19

Effects of cholecystokinin octapeptide on expression of IL-1β, IL-6, IL-4 and IL-10 in lipopolysaccharide-attacked mice
NI Zhi-yu,CONG Bin,LI Shu-jin,MA Chun-ling,YAN Yu-xian,XU Jin-rong,ZHANG Guo-zhong.Effects of cholecystokinin octapeptide on expression of IL-1β, IL-6, IL-4 and IL-10 in lipopolysaccharide-attacked mice[J].Chinese Journal of Pathophysiology,2007,23(2):331-335.
Authors:NI Zhi-yu  CONG Bin  LI Shu-jin  MA Chun-ling  YAN Yu-xian  XU Jin-rong  ZHANG Guo-zhong
Affiliation:Faculty of Forensic Medicine, Hebei Medical University, Shijiazhuang 050017, China. E-mail: nzy0603@126.com
Abstract:AIM:To observe the effects of cholecystokinin octapeptide (CCK-8) on the expression of proinflammatory cytokines IL-1β, IL-6 and anti-inflammatory cytokines IL-10, IL-4 in LPS- attacked mice. METHODS:Kunming mice were randomly assigned and injected intraperitoneally with LPS alone or/and CCK-8 at different time points. The expression of IL-1β, IL-6, IL-10 and IL-4 in the serum and lung tissues were assayed by ELISA and RT-PCR. RESULTS:The expression of IL-1β, IL-6, IL-10 and IL-4 were upregulated in LPS-attacked mice. Pre-treatment of CCK-8 decreased both IL-1β and IL-6 expression and augmented IL-10 and IL-4 expression in LPS-attacked mice. CONCLUSIONS:CCK-8 exerts an anti-inflammatory effect by inhibiting the expression of IL-1β, IL-6 and increasing the expression of IL-10, IL-4 in LPS-attacked mice, which could alleviate the inflammatory response in lung tissue.
Keywords:Cholecystokinin  Lipopolysaccharides  Interleukins
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