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首页> 外文期刊>American Journal of Physiology >Contribution of thermogenic mechanisms by male and female mice lacking pituitary adenylate cyclase-activating polypeptide in response to cold acclimation
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Contribution of thermogenic mechanisms by male and female mice lacking pituitary adenylate cyclase-activating polypeptide in response to cold acclimation

机译:缺乏垂体腺苷酸环酶激活多肽的男性和雌性小鼠的热机理响应于冷适应的贡献

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Pituitary adenylate cyclase-activating polypeptide (PACAP) is a neuropeptide critical to the regulation of the stress response, including having a role in energy homeostasis. Mice lacking PACAP are cold-sensitive and have impaired adrenergic-induced thermogenesis. Interestingly, Pacap null mice can survive cold housing if acclimated slowly, similar to observations in uncoupling protein 1 (UCPI)-deficient mice. We hypothesized that Pacap null mice use alternate thermogenic pathways to compensate for impaired adaptive thermogenesis when acclimated to cold. Observations of behavior and assessment of fiber type in skeletal muscles did not show evidence of prolonged burst shivering or changes in oxidative metabolism in male or female Pacap~-/-mice during cold acclimation compared with Pacap~+/+ mice. Despite previous work that has established impaired capacity for adaptive thermogenesis in Pacap null mice, adaptive thermogenesis can be induced in mice lacking PACAP to support survival with cold housing. Interestingly, sex-specific morphological and molecular differences in adipose tissue remodeling were observed in Pacap null mice compared with controls. Thus, sexual dimorphisms are highlighted in adipose tissue remodeling and thermogenesis with cold acclimation in the absence of PACAP. NEW & NOTEWORTHY This manuscript adds to the literature of endocrine regulation of adaptive thermogenesis and energy balance. It specifically describes the role of pituitary adenylate cyclase-activating polypeptide on the regulation of brown adipose tissue via the sympathetic nervous system with a focus on compensatory mechanisms of thermogenesis. We highlight sex-specific differences in energy metabolism.
机译:垂体腺苷酸环化酶激活肽(PACAP)是一种对应激反应的调节至关重要的神经肽,包括在能量稳态中起作用。缺乏PACAP的小鼠对冷敏感,并损害肾上腺素能诱导的产热。有趣的是,如果缓慢适应,没有Pacap基因的小鼠可以在寒冷的环境中存活,这与解偶联蛋白1(UCPI)缺陷小鼠的观察结果相似。我们假设Pacap基因缺失的小鼠在适应寒冷环境时,使用交替的产热途径来补偿适应性产热受损。与Pacap~+/+小鼠相比,对骨骼肌中纤维类型的观察和评估没有显示出雄性或雌性Pacap~-/-小鼠在冷习服期间长时间爆发性颤抖或氧化代谢变化的证据。尽管之前的研究已经证实,Pacap缺失小鼠的适应性产热能力受损,但缺乏Pacap的小鼠可以诱导适应性产热,以支持冷环境下的生存。有趣的是,与对照组相比,在Pacap阴性小鼠中观察到脂肪组织重塑的性别特异性形态学和分子差异。因此,在缺乏PACAP的情况下,通过冷习服,脂肪组织重塑和产热过程中的性别二型性尤为突出。新的和值得注意的是,这本手稿补充了适应性产热和能量平衡的内分泌调节文献。它特别描述了垂体腺苷酸环化酶激活多肽通过交感神经系统调节棕色脂肪组织的作用,重点是产热的代偿机制。我们强调了能量代谢中的性别差异。

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