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首页> 外文期刊>Biology of Sex Differences >Early progression of pulmonary hypertension in the monocrotaline model in males is associated with increased lung permeability
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Early progression of pulmonary hypertension in the monocrotaline model in males is associated with increased lung permeability

机译:雄性甲胺醛模型中肺动脉高压的早期进展与肺渗透率增加有关

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The mechanisms involved in pulmonary hypertension (PH) development in patients and pre-clinical models are poorly understood. PH has a well-established sex dimorphism in patients with increased frequency of PH in females, and more severe disease with poor survival prognosis in males. Previously, we found that heme signaling plays an essential role in the development phase of the Sugen/Hypoxia (SU/Hx) model. This study is focused on the elucidation of sex differences in mechanisms of PH development related to heme action at the early stage of the monocrotaline (MCT) PH model. Rats received MCT injection (60?mg/kg, i.p.) and followed for 14?days to investigate early disease changes. Hemodynamic parameters were recorded at the end of the study; plasma, lung homogenates, and nuclear fractions were used for the evaluation of protein levels. Our data indicate that on day 14, rats did not show any significant increase in the Fulton index due to the early disease phase. However, the right ventricular systolic pressure was significantly increased in male rats, while female rats showed only a trend. Interestingly, only males demonstrated an increased lung-to-bodyweight ratio that indicated lung edema. Indeed, lung histology confirmed severe perivascular edema in males. Previously, we have reported that the increased perivascular edema in SU/Hx model correlated with intravascular hemolysis and activated heme signaling. Here, we found that elevated free hemoglobin levels and perivascular edema were increased, specifically in males showing more rapid progress of PH. A high level of heme carrier protein 1 (HCP-1), which is involved in heme uptake from the bloodstream into the cells, was also found elevated in the lungs of males. The upregulation of heme oxygenase in males indicated increased intracellular heme catabolism. Increased heme signaling resulted in the activation of heme-mediated barrier-disruptive mechanisms. Thus, hemolysis in males can be responsible for increased permeability of the lungs and early disease development. Our study indicates the importance of barrier-disruptive mechanisms as an earlier event in the induction of pulmonary hypertension. Importantly, males are more susceptible to hemolysis and develop PH earlier than females.
机译:参与患者肺动脉高压(pH)发育和临床前模型的机制尚不清楚。 pH在女性pH频率增加的患者中具有良好的性别二态性,以及更严重的疾病,雄性存活差。以前,我们发现血红素信号在Sugen /缺氧(SU / HX)模型的发育阶段起着重要作用。本研究专注于阐明与血红素血红素(MCT)pH模型的早期血液作用有关的pH有关的性差异。大鼠接受MCT注射(60?Mg / kg,I.P.),然后进行14天进行调查早期疾病的变化。在研究结束时记录了血流动力学参数;血浆,肺匀浆和核级分用于评估蛋白质水平。我们的数据表明,在第14天,大鼠由于早期疾病阶段而没有显示出富尔顿指数的任何显着增加。然而,在雄性大鼠中,右心室收缩压显着增加,而雌性大鼠仅显示出趋势。有趣的是,只有雄性才表明肺对体重增加比例增加了肺水肿。实际上,肺组织学证实了男性中严重的血管内水肿。以前,我们据报道,SU / HX模型中的血管内水肿增加与血管内溶血和活化血红素信号相关。在这里,我们发现升高的游离血红蛋白水平和大脑水肿增加,特别是在雄性中显示出更快的pH的进展。在血液中涉及从血液进入细胞的血红素载体1(HCP-1)的高水平血红素载体蛋白1(HCP-1)也被发现在雄性肺部升高。雄性血红素氧酶的上调表明细胞内血红素分解代谢增加。增加的血红素信号引发导致血红素介导的屏障破坏机制的激活。因此,男性溶血可能是肺部和早期疾病发展的渗透性增加的原因。我们的研究表明,障碍破坏机制的重要性是患有肺动脉高压诱导的早期事件。重要的是,雄性更容易溶血和比女性早些时候发育pH。

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