[Reoxygenation improves reduced hypothalamic leptin responsiveness induced by intermittent hypoxia in obese rats].

M Dong, T Zhu, J Ma, X DU, Y Feng
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Abstract

Objective: To evaluate the effects of intermittent hypoxia-reoxygenation (IHR) on body weight, diet and water intake, circulating metabolites, and responses to central leptin injection in a rat model of diet-induced obesity (DIO).

Methods: Rat models of DIO established by 12-week high-fat diet (HFD) feeding were randomized into normoxia group (n=15), intermittent hypoxia group (6% O2, 30 cycles/h, 8 h/day for 4 weeks; n=15), and IHR group (2 weeks of intermittent hypoxia followed by 2 weeks of reoxygenation; n=15). Body weight, diet and water intake of the rats were recorded, and circulating leptin, IL-6, and Ang-II levels were detected. After IHR treatment, the rats received intracerebroventricular injection of 4 μg leptin, and the hypothalamus and liver were taken 1 h later for detecting POMC, FRA-1 and FRA-2 expressions in the hypothalamus using immunohistochemistry, POMC, pSTAT3 and LepR expressions in the hypothalamus using Western blotting, and LepR mRNA expression in the hypothalamus and liver using RT-PCR.

Results: The rats in intermittent hypoxia group showed significantly increased weight gain, food intake and elevated systemic inflammatory cytokine levels. Intermittent hypoxia obviously inhibited the expression of POMC, lowered the expressions of FRA-1 and pSTAT3, reduced the responsiveness of the rats to exogenous leptin, and downregulated the mRNA and protein expression of LepR. Two weeks of reoxygenation treatment obviously reduced intermittent hypoxia-induced weight gain and metabolic disorder and improved leptin sensitivity of the rats.

Conclusion: Prolonged intermittent hypoxia impairs hypothalamic leptin signaling by downregulating LepR expression to promote weight gain in obese rats, which can be improved by reoxygenation treatment.

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[再吸氧可改善肥胖大鼠因间歇性缺氧而导致的下丘脑瘦素反应性降低]。
目的评估间歇性低氧-复氧(IHR)对饮食诱导肥胖(DIO)大鼠模型的体重、饮食和水摄入量、循环代谢物以及中枢瘦素注射反应的影响:方法:将饲喂12周高脂饮食(HFD)建立的DIO大鼠模型随机分为常氧组(n=15)、间歇性缺氧组(6%氧气,30次/小时,8小时/天,4周;n=15)和IHR组(间歇性缺氧2周,然后复氧2周;n=15)。记录大鼠的体重、饮食和饮水量,并检测循环瘦素、IL-6和Ang-II水平。IHR治疗后,大鼠脑室内注射4 μg瘦素,1小时后取下丘脑和肝脏,用免疫组化法检测下丘脑中POMC、FRA-1和FRA-2的表达,用Western印迹法检测下丘脑中POMC、pSTAT3和LepR的表达,用RT-PCR法检测下丘脑和肝脏中LepR mRNA的表达:结果:间歇性缺氧组大鼠的体重增加、摄食量和全身炎性细胞因子水平均显著增加。间歇性缺氧明显抑制了POMC的表达,降低了FRA-1和pSTAT3的表达,降低了大鼠对外源性瘦素的反应性,下调了LepR的mRNA和蛋白表达。两周的复氧治疗明显减少了间歇性缺氧引起的体重增加和代谢紊乱,并改善了大鼠对瘦素的敏感性:结论:长期间歇性缺氧会通过下调 LepR 的表达来损害下丘脑瘦素信号转导,从而促进肥胖大鼠体重增加,而复氧治疗可以改善肥胖大鼠的体重增加。
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来源期刊
南方医科大学学报杂志
南方医科大学学报杂志 Medicine-Medicine (all)
CiteScore
1.50
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0.00%
发文量
208
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