Jia Shan-shan, Liu Yue-hua
Department of Orthodontics, School of Stomatology, Tongji University, Shanghai 200072, China.
Zhonghua Kou Qiang Yi Xue Za Zhi. 2010 Oct;45(10):627-30.
To investigate the effects of estrogen on the expression of phosphofructokinase muscle-specific isoform (PFK-M) in genioglossus of chronic intermittent hypoxia (CIH) rats.
Fifty male SD rats were randomly divided into five groups: the normal control group (NC), the chronic intermittent hypoxia group (CIH), and three doses of estrogen plus hypoxia groups (LE, ME, HE). Rats in the latter four groups were used to build CIH models (8 h/d, 5 weeks). In the mean time, rats in the latter three groups were injected with three dose levels of estrogen (0.1, 0.2, 0.3 mg/kg), and rats in NC and CIH groups were injected with sterile olive oil as control. At the end of the treatment, the genioglossus was isolated and quickly removed. The mRNA levels of PFK-M were determined by real-time RT-PCR and the protein content of PFK-M was detected by Western blotting analysis.
PFK-M mRNA and protein in CIH group (2.144 ± 0.260, 0.875 ± 0.025) were both higher than those (1.000 ± 0.259, 0.413 ± 0.013) in NC group (P < 0.05). The expression of PFK-M mRNA in LE, ME and HE groups were 1.424 ± 0.193, 1.395 ± 0.251 and 1.310 ± 0.094, respectively. The expression of protein in LE, ME and HE groups were 0.638 ± 0.015, 0.576 ± 0.017 and 0.505 ± 0.021, respectively. Compared with CIH group, the expression of PFK-M mRNA and protein in LE, ME and HE groups were all inhibited significantly (P < 0.05). Among the three treatment groups, decreased protein content of PFK-M was observed only in HE group when compared with LE group (P < 0.05), but no significant difference was detected in the expression of PFK-M mRNA.
CIH exposure could increase the expression of PFK-M mRNA and protein in rat genioglossus, while estrogen administration could dose dependently inhibit the overexpression.
探讨雌激素对慢性间歇性缺氧(CIH)大鼠颏舌肌中磷酸果糖激酶肌肉特异性同工酶(PFK-M)表达的影响。
将50只雄性SD大鼠随机分为5组:正常对照组(NC)、慢性间歇性缺氧组(CIH)以及三个雌激素加缺氧组(低剂量组LE、中剂量组ME、高剂量组HE)。后四组大鼠用于建立CIH模型(每天8小时,共5周)。同时,后三组大鼠分别注射三种剂量水平的雌激素(0.1、0.2、0.3mg/kg),NC组和CIH组大鼠注射无菌橄榄油作为对照。治疗结束时,分离并迅速取出颏舌肌。通过实时逆转录聚合酶链反应(RT-PCR)测定PFK-M的mRNA水平,通过蛋白质印迹分析检测PFK-M的蛋白质含量。
CIH组的PFK-M mRNA和蛋白质水平(2.144±0.260,0.875±0.025)均高于NC组(1.000±0.259,0.413±0.013)(P<0.05)。LE组、ME组和HE组的PFK-M mRNA表达分别为1.424±0.193、1.395±0.251和1.310±0.094。LE组、ME组和HE组蛋白质表达分别为0.638±0.015、0.576±0.017和0.505±0.021。与CIH组相比,LE组、ME组和HE组的PFK-M mRNA和蛋白质表达均显著受到抑制(P<0.05)。在三个治疗组中,与LE组相比,仅HE组观察到PFK-M蛋白质含量降低(P<0.05),但PFK-M mRNA表达未检测到显著差异。
暴露于CIH可增加大鼠颏舌肌中PFK-M mRNA和蛋白质的表达,而给予雌激素可剂量依赖性地抑制这种过表达。