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龚晋, 吴东波, 张兰兰等. PCO模型大鼠卵巢组织氧化应激水平的研究[J]. 四川大学学报(医学版), 2015, 46(2): 238-242.
引用本文: 龚晋, 吴东波, 张兰兰等. PCO模型大鼠卵巢组织氧化应激水平的研究[J]. 四川大学学报(医学版), 2015, 46(2): 238-242.
GONG Jin, WU Dong-bo, ZHANG Lan-lan. et al. Study on the Oxidative Stress in the Ovaries of a Rat Model of Polycystic Ovary[J]. Journal of Sichuan University (Medical Sciences), 2015, 46(2): 238-242.
Citation: GONG Jin, WU Dong-bo, ZHANG Lan-lan. et al. Study on the Oxidative Stress in the Ovaries of a Rat Model of Polycystic Ovary[J]. Journal of Sichuan University (Medical Sciences), 2015, 46(2): 238-242.

PCO模型大鼠卵巢组织氧化应激水平的研究

Study on the Oxidative Stress in the Ovaries of a Rat Model of Polycystic Ovary

  • 摘要: 目的 应用来曲唑建立多囊卵巢(PCO)大鼠模型,从组织及细胞水平测定模型大鼠卵巢氧化应激状态,探讨卵巢氧化应激在多囊卵巢综合征(PCOS)发病中的作用,为PCOS治疗提供新的思路。 方法 将6周龄清洁级雌性SD大鼠,随机编为实验组〔45只,予1%羧甲基纤维素溶液1 mL/d+来曲唑1 mg/(kg·d)灌胃〕和对照组(45只,仅予1%羧甲基纤维素溶液1 mL/d灌胃),均持续28 d。每日定时行阴道细胞涂片巴氏染色镜检,判断动情周期,每7 d测量体质量了解生长情况,第29 d两组大鼠统一处死、采血。测量指标:血清雌二醇(E2)、孕酮(P)、促卵泡刺激素(FSH)、促黄体生成素(LH)、睾酮(T)、性激素结合蛋白(SHBG),计算游离雄激素指数(FAI);解剖子宫、卵巢,称重后计算器官质量指数;所得两侧卵巢,一侧固定后石蜡切片HE染色,另一侧制备组织匀浆、单细胞悬液,测定组织匀浆总氧化态(TOS)、总抗氧化态(TAS)、脂质过氧化物丙二醛(MDA)含量、超氧化物歧化酶(SOD)活力;检测卵巢单细胞悬液细胞内活性氧(ROS)水平。通过比较两组大鼠上述指标的差异,验证造模是否成功,分析卵巢组织氧化应激水平与PCOS的关系。 结果 ①实验组用药12~15 d后动情周期消失,体质量增长明显超过对照组(\P\P\P\P\P均<0.05)。 结论 ①应用来曲唑可成功诱导大鼠PCO模型,适于研究卵巢病变。 ②本方法所制备的PCO模型卵巢处于明显的氧化应激状态,存在细胞氧化损伤,推测人类PCOS卵巢组织内可能也存在氧化应激,因此对于PCOS的处理,在常规药物治疗同时,应注重抗氧化治疗。

     

    Abstract: Objective To establish a pathological animal model of polycystic ovary (PCO) by letrozole in rats. Investigate whether PCO were mediated by the effect of oxidative stress by measuring oxidative stress levels in this cohort of rats with PCO, and proceed a new way of treatment for polycystic ovary syndrom (PCOS). Methods 90 SD female rats aged 6 weeks were randomly divided into two groups, including a control group of 45 rats that received vehicle only 〔1% aqueous solution of carboxmethlycellulose (CMC), 1 mL/d〕 once daily orally (p.o.), and an experimental group of 45 rats, which were administered letrozole at concentrations of 1 mg/kg p.o. dissolved in 1% CMC (1 mL/d) once daily. The treatment period was 28 d. During this period, vaginal smears were collected daily for estrus cycle determination and body masses were measured every 7 d. On the day subsequent to the last letrozole dose administration, rats were killed; Uteri and ovaries were then excised and weighed for the calculation of organ indexes. Serum hormone levels, SHBG and histologic changes in the ovaries were examined. Then

     

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