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一种药物性胃饥饿素激动剂对 C57BL/6J 雄性小鼠寿命的影响:一项对照实验。

The effect of a pharmaceutical ghrelin agonist on lifespan in C57BL/6J male mice: A controlled experiment.

机构信息

Department of Health Behavior, School of Public Health, University of Alabama at Birmingham, Birmingham, Alabama, USA.

Department of Cell, Developmental and Integrative Biology, School of Medicine, University of Alabama at Birmingham, Birmingham, Alabama, USA.

出版信息

Aging Cell. 2023 Apr;22(4):e13787. doi: 10.1111/acel.13787. Epub 2023 Feb 3.

DOI:10.1111/acel.13787
PMID:36734122
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10086516/
Abstract

Interventions for animal lifespan extension like caloric restriction (CR) have identified physiologic and biochemical pathways related to hunger and energy-sensing status as possible contributors, but mechanisms have not been fully elucidated. Prior studies using ghrelin agonists show greater food intake but no effect on lifespan in rodent models. This experiment in male C57BL/6J mice tested the influence of ghrelin agonism for perceived hunger, in the absence of CR, on longevity. Mice aged 4 weeks were allowed to acclimate for 2 weeks prior to being assigned (N = 60/group). Prior to lights off daily (12:12 cycle), animals were fed a ghrelin agonist pill (LY444711; Eli Lilly) or a placebo control (Ctrl) until death. Treatment (GhrAg) animals were pair-fed daily based on the group mean food intake consumed by Ctrl (ad libitum feeding) the prior week. Results indicate an increased lifespan effect (log-rank p = 0.0032) for GhrAg versus placebo Ctrl, which weighed significantly more than GhrAg (adjusted for baseline weight). Further studies are needed to determine the full scope of effects of this ghrelin agonist, either directly via increased ghrelin receptor signaling or indirectly via other hypothalamic, systemic, or tissue-specific mechanisms.

摘要

干预动物寿命延长,如热量限制 (CR),已确定与饥饿和能量感应状态相关的生理和生化途径可能是其贡献者,但机制尚未完全阐明。先前使用胃饥饿素激动剂的研究表明,在啮齿动物模型中,食欲增加,但对寿命没有影响。本实验在雄性 C57BL/6J 小鼠中测试了在没有 CR 的情况下,胃饥饿素激动剂对感知饥饿的影响对长寿的影响。4 周龄的小鼠适应环境 2 周后,被分配(每组 60 只)。在每日熄灯前(12:12 周期),动物服用胃饥饿素激动剂药丸(LY444711;礼来)或安慰剂对照(Ctrl),直至死亡。治疗(GhrAg)动物根据前一周 Ctrl(自由喂养)组平均食物摄入量进行每日配对喂养。结果表明,与安慰剂对照(Ctrl)相比,GhrAg 具有延长寿命的作用(对数秩检验 p = 0.0032),GhrAg 比 GhrAg 重(根据基线体重调整)。需要进一步研究来确定这种胃饥饿素激动剂的全部作用范围,无论是通过增加胃饥饿素受体信号直接作用,还是通过其他下丘脑、全身或组织特异性机制间接作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4406/10086516/0b92c7248b31/ACEL-22-e13787-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4406/10086516/0b92c7248b31/ACEL-22-e13787-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4406/10086516/0b92c7248b31/ACEL-22-e13787-g001.jpg

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Contribution of Ghrelin to the Pathogenesis of Growth Hormone Deficiency.生长激素缺乏症发病机制中Ghrelin 的作用。
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