回到子宫:哺乳动物冬眠的围产期视角。

IF 1.8 3区 生物学 Q3 PHYSIOLOGY
Dominique Singer
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引用次数: 1

摘要

在行星际太空飞行中,让宇航员进入类似冬眠状态的想法引发了人们对冬眠和麻木的进化根源的新兴趣。在这种情况下,应该指出的是,哺乳动物胎儿和新生儿对围产期环境挑战的反应具有许多生理机制,这些机制与冬眠和冬眠有着惊人的相似之处。这主要包括三点:一是产前偏离整体代谢大小关系,使胎儿适应子宫内低氧条件,对应冬眠和睡眠期间的代谢减少;第二,出生时氧气供应缩短导致的产后潜水性心动过缓,类似于进入麻木状态时体温下降前的心率下降;第三,出生后棕色脂肪组织的非寒战产热,伴随着基础代谢率的增加,达到了身体大小的预期水平,比如在从冬眠中唤醒时。围产期出现的类似冬眠的适应表明,相反,冬眠和冬眠可能是由所有哺乳动物在出生时共有的机制组成的。这一假设为冬眠的起源提供了新的线索,并支持了包括人类在内的非冬眠物种的潜在可及性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Back to the Womb: A Perinatal Perspective on Mammalian Hibernation.

AbstractThe idea of putting astronauts into a hibernation-like state during interplanetary spaceflights has sparked new interest in the evolutionary roots of hibernation and torpor. In this context, it should be noted that mammalian fetuses and neonates respond to the environmental challenges in the perinatal period with a number of physiological mechanisms that bear striking similarity to hibernation and torpor. These include three main points: first, prenatal deviation from the overall metabolic size relationship, which adapts the fetus to the low-oxygen conditions in the womb and corresponds to the metabolic reduction during hibernation and estivation; second, intranatal diving bradycardia in response to shortened O2 supply during birth, comparable to the decrease in heart rate preceding the drop in body temperature upon entry into torpor; and third, postnatal onset of nonshivering thermogenesis in the brown adipose tissue, along with the increase in basal metabolic rate up to the level expected from body size, such as during arousal from hibernation. The appearance of hibernation-like adaptations in the perinatal period suggests that, conversely, hibernation and torpor may be composed of mechanisms shared by all mammals around birth. This hypothesis sheds new light on the origins of hibernation and supports its potential accessibility to nonhibernating species, including humans.

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来源期刊
CiteScore
3.20
自引率
6.20%
发文量
62
审稿时长
6-12 weeks
期刊介绍: Physiological and Biochemical Zoology: Ecological and Evolutionary Approaches primarily publishes original research in animal physiology and biochemistry as considered from behavioral, ecological, and/or evolutionary perspectives. Studies at all levels of biological organization from the molecular to the whole organism are welcome, and work that integrates across levels of organization is particularly encouraged. Studies that focus on behavior or morphology are welcome, so long as they include ties to physiology or biochemistry, in addition to having an ecological or evolutionary context. Subdisciplines of interest include nutrition and digestion, salt and water balance, epithelial and membrane transport, gas exchange and transport, acid-base balance, temperature adaptation, energetics, structure and function of macromolecules, chemical coordination and signal transduction, nitrogen metabolism and excretion, locomotion and muscle function, biomechanics, circulation, behavioral, comparative and mechanistic endocrinology, sensory physiology, neural coordination, and ecotoxicology ecoimmunology.
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