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首页> 外文期刊>Molecular Metabolism >Time-resolved hypothalamic open flow micro-perfusion reveals normal leptin transport across the blood–brain barrier in leptin resistant mice
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Time-resolved hypothalamic open flow micro-perfusion reveals normal leptin transport across the blood–brain barrier in leptin resistant mice

机译:时间分辨的下丘脑开流微灌注显示瘦素抵抗小鼠中正常的瘦素转运穿过血脑屏障

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Objective The inability of leptin to suppress food intake in diet-induced obesity, sometimes referred to as leptin resistance, is associated with several distinct pathological hallmarks. One prevailing theory is that impaired transport of leptin across the blood–brain barrier (BBB) represents a molecular mechanism that triggers this phenomenon. Recent evidence, however, has challenged this notion, suggesting that leptin BBB transport is acquired during leptin resistance. Methods To resolve this debate, we utilized a novel cerebral Open Flow Microperfusion (cOFM) method to examine leptin BBB transport in male C57BL/6J mice, fed a chow diet or high fat diet (HFD) for 20 days. Results Basal plasma leptin levels were 3.8-fold higher in HFD-fed mice (p? Conclusions These data suggest that leptin transport across the BBB is not impaired in non-obese leptin resistant mice and thus unlikely to play a direct role in the progression of pharmacological leptin resistance.
机译:目的瘦素不能抑制饮食引起的肥胖症中的食物摄入,有时被称为瘦素抵抗性,与几种明显的病理学特征有关。一种流行的理论是,瘦蛋白通过血脑屏障(BBB)的运输障碍是触发这种现象的分子机制。然而,最近的证据挑战了这一观点,表明在瘦素抵抗过程中获得了瘦素BBB转运。方法为了解决这一争论,我们利用一种新颖的脑开放流微灌流(cOFM)方法检查了以20日龄或高脂饮食喂养的雄性C57BL / 6J小鼠的瘦素BBB转运。结果饲喂HFD的小鼠的基础血浆瘦素水平高3.8倍(p?结论)这些数据表明,在非肥胖瘦素抵抗性小鼠中,瘦素在BBB中的转运不会受到损害,因此不太可能在肝癌的进展中发挥直接作用。药理瘦素抵抗。

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