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High-fat feeding alters the clock synchronization to light.

机译:高脂喂养会改变时钟同步。

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High-fat feeding in rodents leads to metabolic abnormalities mimicking the human metabolic syndrome, including obesity and insulin resistance. These metabolic diseases are associated with altered temporal organization of many physiological functions. The master circadian clock located in the suprachiasmatic nuclei controls most physiological functions and metabolic processes. Furthermore, under certain conditions of feeding (hypocaloric diet), metabolic cues are capable of altering the suprachiasmatic clock's responses to light. To determine whether high-fat feeding (hypercaloric diet) can also affect resetting properties of the suprachiasmatic clock, we investigated photic synchronization in mice fed a high-fat or chow (low-fat) diet for 3 months, using wheel-running activity and body temperature rhythms as daily phase markers (i.e. suprachiasmatic clock's hands). Compared with the control diet, mice fed with the high-fat diet exhibited increased body mass index, hyperleptinaemia, higher blood glucose, and increased insulinaemia. Concomitantly, high-fat feeding led to impaired adjustment to local time by photic resetting. At the behavioural and physiological levels, these alterations include slower rate of re-entrainment of behavioural and body temperature rhythms after 'jet-lag' test (6 h advanced light-dark cycle) and reduced phase-advancing responses to light. At a molecular level, light-induced phase shifts have been correlated, within suprachiasmatic cells, with a high induction of c-FOS, the protein product of immediate early gene c-fos, and phosphorylation of the extracellular signal-regulated kinases I/II (P-ERK). In mice fed a high-fat diet, photic induction of both c-FOS and P-ERK in the suprachiasmatic nuclei was markedly reduced. Taken together, the present data demonstrate that high-fat feeding modifies circadian synchronization to light.
机译:啮齿动物的高脂喂养会导致模仿人类代谢综合征的代谢异常,包括肥胖和胰岛素抵抗。这些代谢疾病与许多生理功能的时间组织改变有关。位于视交叉上核的生物钟主时钟控制着大多数生理功能和代谢过程。此外,在某些喂养条件(低热量饮食)下,代谢线索能够改变跨视交叉钟对光的反应。为了确定高脂喂养(高热量饮食)是否也会影响视交叉钟的复位特性,我们使用轮转活动和轮转运动研究了高脂饮食或低脂饮食3个月的小鼠的光合作用。体温节律作为每日相位标记(即,视交叉钟的指针)。与对照饮食相比,高脂饮食喂养的小鼠表现出更高的体重指数,高脂血症,更高的血糖和更高的胰岛素血症。随之而来的是,高脂喂养会因光复归而导致对当地时间的调节能力受损。在行为和生理学水平上,这些改变包括“时差反应”测试(6 h提前的明暗循环)后行为和体温节律的重新夹带速率降低,以及光的相位超前响应降低。在分子水平上,在视交叉上细胞中,光诱导的相移与c-FOS,立即早期基因c-fos的蛋白质产物的高诱导以及细胞外信号调节激酶I / II的磷酸化相关。 (P-ERK)。在高脂饮食喂养的小鼠中,视交叉上核中c-FOS和P-ERK的光诱导显着降低。综上所述,本数据证明高脂喂养改变了昼夜节律对光的同步。

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