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单位:100029首都医科大学附属北京安贞医院心内科北京市心肺血管疾病研究所(王越、王悦、刘倍倍、陈蕾蕾、吴小凡),心血管生物学研究室(蒋宏峰)
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【摘要】目的 探讨慢性间歇低氧(CIH)环境下小鼠肝脏组织中缺氧诱导因子(HIF)2α的表达变化及对肝脏脂质代谢的影响。方法 选择无特定病原体级载脂蛋白E基因敲除雄性小鼠24只,适应性喂养1周后随机分为3组,各8只。对照组普通饲料喂养;高脂组给予高脂饲料喂养12周;高脂+低氧组于高脂饲料喂养4周后,将小鼠放入低氧舱内8 h/d,持续8周。12周后取小鼠肝脏组织,通过油红O染色法计算油滴面积占总面积的百分比,酶法检测肝脏组织中三酰甘油和总胆固醇含量,免疫组织化学染色法检测HIF-2α的表达,应用超氧化物阴离子探针检测活性氧含量。结果 高脂+低氧组肝脏组织中脂滴面积占总面积的百分比高于高脂组和对照组[(35.52±12.77)%比(11.65±7.43)%、(0.45±0.26)%],总胆固醇和三酰甘油含量高于高脂组和对照组,HIF-2α表达水平和活性氧含量高于高脂组和对照组[(45.0±6.3)%比(17.7±2.5)%、(5.2±2.4)%,(23.74±5.19)%比(4.33±2.11)%、(0.25±0.11)%],差异均有统计学意义(均P<0.05)。结论 HIF-2α在CIH诱导的肝脏脂质代谢紊乱中发挥重要作用,其对氧化应激反应的调控作用可能是引起肝脏脂质蓄积的重要通路,HIF-2α有望成为防治肝脏脂质代谢异常的重要靶点。
【Abstract】Objective To observe the expression of hypoxia inducible factor(HIF)-2α in liver tissue under chronic intermittent hypoxia(CIH) and explore the influence of CIH on liver lipid metabolism. Methods Twenty-four specific-pathogen-free apolipoprotein-E-/- mice were randomly divided into control group (n=8), high-fat diet group(n=8) and high-fat diet+CIH group(n=8). The control group was fed with normal diet; the high-fat diet group had high-fat feed for 12 weeks; the high-fat diet+CIH group was fed with high-fat diet for 4 weeks and placed in hypoxic chamber 8 h/d for 8 weeks. Liver tissue was separated after 12 weeks treatment; lipid area was determined by oil red O staining; contents of triglyceride and total cholesterol were tested by enzymatic method; expression of HIF-2α was detected by immunohistochemistry and active oxygen was detected by dihydroethidium fluorescent staining. Results Percentage of oil area in high-fat diet+CIH group was greater than that in high-fat diet group and control group[(35.52±12.77)% vs (11.65±7.43)%,(0.45±0.26)%]; contents of triglyceride and total cholesterol in high-fat diet+CIH group were higher than those in high-fat diet group and control group; expression of HIF-2α and content of active oxygen in high-fat diet+CIH group were higher than those in high-fat diet group and control group[(45.0±6.3)% vs (17.7±2.5)%,(5.2±2.4)%; (23.74±5.19)% vs (4.33±2.11)%,(0.25±0.11)%]; the differences were significant(all P<0.05). Conclusions HIF-2α plays an important role in CIH-induced hepatic lipid metabolism disorder, its regulation on oxidative stress may be a pathway for lipid accumulation. HIF-2α is expected to be an important target in preventing and treating liver lipid metabolism disorder.
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