首页> 外文期刊>American Journal of Physiology >Nocturnal reduction in circulating adiponectin concentrations related to hypoxic stress in severe obstructive sleep apnea-hypopnea syndrome
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Nocturnal reduction in circulating adiponectin concentrations related to hypoxic stress in severe obstructive sleep apnea-hypopnea syndrome

机译:严重阻塞性睡眠呼吸暂停低通气综合征与低氧应激相关的循环脂联素浓度的夜间降低

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Previous reports demonstrated that adiponectin has antiatherosclerotic properties. Obstructive sleep apnea-hypopnea syndrome (OSAHS) is reported to exacerbate atherosclerotic diseases. We investigated nocturnal alternation of serum adiponectin levels before sleep and after wake-up in OSAHS patients and the effect of sustained hypoxia on adiponectin in vivo and in vitro. We measured serum adiponectin concentrations in 75 OSAHS patients and 18 control subjects before sleep and after wake-up and examined the effect of one-night nasal continuous positive airway pressure (nCPAP) on adiponectin in 24 severe OSAHS patients. We investigated the effects of hypoxia on adiponectin in mice and cultured adipocytes with a sustained hypoxia model. Circulating adiponectin levels before sleep and after wake-up were lower in severe OSAHS patients than in control subjects [before sleep: 5.9 +- 2.9 vs. 8.8 +- 5.6 mug/ml (P < 0.05); after wake-up: 5.2 +- 2.6 vs. 8.5 +- 5.5 mug/ml (P < 0.01), respectively; means +- SD]. Serum adiponectin levels diminished significantly during sleep in severe OSAHS patients (P < 0.0001), but one-night nCPAP improved the drop in serum adiponectin levels [-18.4 +- 13.4% vs. -10.4 +- 12.4% (P < 0.05)]. In C57BL/6J mice and 3T3-L1 adipocytes, hypoxic exposure decreased adiponectin concentrations by inhibiting adiponectin regulatory mechanisms at secretion and transcriptional levels. The present study demonstrates nocturnal reduction in circulating adiponectin levels in severe OSAHS. Our experimental studies showed that hypoxic stress induced adiponectin dysregulation at transcriptional and posttranscriptional levels. Hypoxic stress is, at least partly, responsible for the reduction of serum adiponectin in severe OSAHS. Nocturnal reduction in adiponectin in severe OSAHS may be an important risk for cardiovascular events or other OSAHS-related diseases during sleep.
机译:先前的报道表明脂联素具有抗动脉粥样硬化特性。据报道阻塞性睡眠呼吸暂停低通气综合征(OSAHS)加剧了动脉粥样硬化疾病。我们调查了OSAHS患者睡眠前和唤醒后血清脂联素水平的夜间变化以及体内和体外持续缺氧对脂联素的影响。我们测量了75名OSAHS患者和18名对照组受试者的睡眠前和唤醒后的血清脂联素浓度,并检查了24例重症OSAHS患者一整夜的鼻持续气道正压通气(nCPAP)对脂联素的影响。我们调查了持续性缺氧模型对小鼠和培养的脂肪细胞中缺氧对脂联素的影响。重症OSAHS患者的睡眠前和苏醒后循环脂联素水平低于对照组[睡眠前:5.9±2.9比8.8±5.6杯/毫升(P <0.05);唤醒后:5.2±2.6和8.5±5.5杯/毫升(P <0.01);表示+-SD]。严重OSAHS患者在睡眠期间血清脂联素水平显着降低(P <0.0001),但是一夜nCPAP改善了血清脂联素水平的下降[-18.4 +-13.4%vs. -10.4 +-12.4%(P <0.05)] 。在C57BL / 6J小鼠和3T3-L1脂肪细胞中,低氧暴露通过在分泌和转录水平上抑制脂联素调节机制而降低脂联素浓度。本研究证明了严重OSAHS患者夜间脂联素水平的夜间降低。我们的实验研究表明,低氧应激在转录和转录后水平上引起脂联素失调。低氧应激至少部分是导致严重OSAHS患者血清脂联素降低的原因。严重OSAHS中夜间脂联素的减少可能是睡眠期间发生心血管事件或其他OSAHS相关疾病的重要风险。

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