中国医学创新
中國醫學創新
중국의학창신
MEDICAL INNOVATION OF CHINA
2014年
22期
18-20
,共3页
王玉梅%黄琼%罗鹏%段鸿侠
王玉梅%黃瓊%囉鵬%段鴻俠
왕옥매%황경%라붕%단홍협
香烟%白介素-8%谷胱甘肽%组蛋白去乙酰化酶2
香煙%白介素-8%穀胱甘肽%組蛋白去乙酰化酶2
향연%백개소-8%곡광감태%조단백거을선화매2
Smoke%IL-8%GSH%HDAC2
目的:探讨香烟暴露及戒烟对大鼠肺白介素-8、谷胱甘肽(GSH)及组蛋白去乙酰化酶2(HDAC2)的影响。方法:健康雄性SD大鼠40只随机分对照组、吸烟组(1月、2月组)、戒烟组(1月、2月组)。每组8只,吸烟组及戒烟组大鼠每天给予烟熏两次,吸烟组烟熏1月、2月取材;戒烟组烟熏2月后再继续饲养1月和2月后取材,分别检测支气管肺泡灌洗液(BALF)中白介素-8和GSH、肺组织HDAC2的表达。结果:比较吸烟组、戒烟组和对照组BALF中白介素-8含量升高、GSH浓度下降,戒烟后GSH渐升高,但仍不能达到正常;吸烟组肺组织HDAC2含量逐渐降低,戒烟后HDAC2又逐渐升高,但与对照组比较,仍有下降。结论:香烟暴露可诱导气道氧化应激反应,导致GSH减少,HDAC2减少,戒烟可有所改善。
目的:探討香煙暴露及戒煙對大鼠肺白介素-8、穀胱甘肽(GSH)及組蛋白去乙酰化酶2(HDAC2)的影響。方法:健康雄性SD大鼠40隻隨機分對照組、吸煙組(1月、2月組)、戒煙組(1月、2月組)。每組8隻,吸煙組及戒煙組大鼠每天給予煙熏兩次,吸煙組煙熏1月、2月取材;戒煙組煙熏2月後再繼續飼養1月和2月後取材,分彆檢測支氣管肺泡灌洗液(BALF)中白介素-8和GSH、肺組織HDAC2的錶達。結果:比較吸煙組、戒煙組和對照組BALF中白介素-8含量升高、GSH濃度下降,戒煙後GSH漸升高,但仍不能達到正常;吸煙組肺組織HDAC2含量逐漸降低,戒煙後HDAC2又逐漸升高,但與對照組比較,仍有下降。結論:香煙暴露可誘導氣道氧化應激反應,導緻GSH減少,HDAC2減少,戒煙可有所改善。
목적:탐토향연폭로급계연대대서폐백개소-8、곡광감태(GSH)급조단백거을선화매2(HDAC2)적영향。방법:건강웅성SD대서40지수궤분대조조、흡연조(1월、2월조)、계연조(1월、2월조)。매조8지,흡연조급계연조대서매천급여연훈량차,흡연조연훈1월、2월취재;계연조연훈2월후재계속사양1월화2월후취재,분별검측지기관폐포관세액(BALF)중백개소-8화GSH、폐조직HDAC2적표체。결과:비교흡연조、계연조화대조조BALF중백개소-8함량승고、GSH농도하강,계연후GSH점승고,단잉불능체도정상;흡연조폐조직HDAC2함량축점강저,계연후HDAC2우축점승고,단여대조조비교,잉유하강。결론:향연폭로가유도기도양화응격반응,도치GSH감소,HDAC2감소,계연가유소개선。
To evaluate the impacting of IL-8,GSH and HDAC2 in the lung of cigarette exposure and cessation rats. Method:40 SD rats were randomly divided into control group,smoking group(January,February group), smoking cessation group(January,February group),smoking group were sacrificed at 1 month and 2 month,smoking cessation group was sacrificed when smoking cessation for 1 month and 2 months. To collect the cells in BALF and lung tissue,and detect the IL-8,GSH and HDAC2 in rats’lung tissue. Result:Compared with control group,the levels of IL-8 in smoking group and smoking cessation group increased(P<0.01),the levels of GSH and HDAC2 in smoking group and smoking cessation group decreased(P<0.01),but smoking groups level was lower than that of smoking-cessation groups. Conclusion:It shows that cigarette exposure can induce airway oxidative stress. It can decrease after quitting,but still can't back to the normal.