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人工诱导的大鼠冬眠状态下的多器官超微结构变化

Multiorgan ultrastructural changes in rats induced in synthetic torpor.

作者信息

Salucci Sara, Hitrec Timna, Piscitiello Emiliana, Occhinegro Alessandra, Alberti Luca, Taddei Ludovico, Burattini Sabrina, Luppi Marco, Tupone Domenico, Amici Roberto, Faenza Irene, Cerri Matteo

机构信息

Department of Biomedical and Neuromotor Sciences - University of Bologna, Bologna, Italy.

Department of Biomolecular Sciences, Carlo Bo Urbino University, Urbino, Italy.

出版信息

Front Physiol. 2024 Nov 19;15:1451644. doi: 10.3389/fphys.2024.1451644. eCollection 2024.

DOI:10.3389/fphys.2024.1451644
PMID:39628940
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11611833/
Abstract

Torpor is a state used by several mammals to survive harsh winters and avoid predation, characterized by a drastic reduction in metabolic rate followed by a decrease in body temperature, heart rate, and many physiological variables. During torpor, all organs and systems must adapt to the new low-energy expenditure conditions to preserve physiological homeostasis. These adaptations may be exploited in a translational perspective in several fields. Recently, many features of torpor were shown to be mimicked in non-hibernators by the inhibition of neurons within the brainstem region of the Raphe Pallidus. The physiological resemblance of this artificial state, called synthetic torpor, with natural torpor has so far been described only in physiological terms, but no data have been shown regarding the induced morphological changes. Here, we show the first description of the ultrastructural changes in the liver, kidney, lung, skeletal muscle, and testis induced by a 6-hours inhibition of Raphe Pallidus neurons in a non-hibernating species, the rat.

摘要

蛰伏是几种哺乳动物用来度过严冬并避免被捕食的一种状态,其特征是代谢率急剧下降,随后体温、心率和许多生理变量也随之降低。在蛰伏期间,所有器官和系统都必须适应新的低能量消耗状态,以维持生理稳态。这些适应性变化可以从转化医学的角度在多个领域加以利用。最近研究表明,通过抑制中缝苍白核脑干区域内的神经元,非冬眠动物可以模拟出蛰伏的许多特征。到目前为止,这种被称为合成蛰伏的人工状态与自然蛰伏在生理方面的相似性仅在生理层面有所描述,但尚未有关于其诱导形态变化的数据。在此,我们首次描述了在非冬眠物种大鼠中,通过抑制中缝苍白核神经元6小时所诱导的肝脏、肾脏、肺、骨骼肌和睾丸的超微结构变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/5ba1d9d66373/fphys-15-1451644-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/626125b9e181/fphys-15-1451644-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/b3111ab7413a/fphys-15-1451644-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/2e320844bc42/fphys-15-1451644-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/9788ad1ee17a/fphys-15-1451644-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/e9caf424c990/fphys-15-1451644-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/c25e5950658c/fphys-15-1451644-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/bba0dbc1c9c5/fphys-15-1451644-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/3da853a93fb6/fphys-15-1451644-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/5ba1d9d66373/fphys-15-1451644-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/626125b9e181/fphys-15-1451644-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/b3111ab7413a/fphys-15-1451644-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/2e320844bc42/fphys-15-1451644-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/9788ad1ee17a/fphys-15-1451644-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/e9caf424c990/fphys-15-1451644-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/c25e5950658c/fphys-15-1451644-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/bba0dbc1c9c5/fphys-15-1451644-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/3da853a93fb6/fphys-15-1451644-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/230a/11611833/5ba1d9d66373/fphys-15-1451644-g009.jpg

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本文引用的文献

1
Remodeling of skeletal muscle myosin metabolic states in hibernating mammals.冬眠哺乳动物骨骼肌肌球蛋白代谢状态的重塑。
Elife. 2024 May 16;13:RP94616. doi: 10.7554/eLife.94616.
2
Cold resistance of mammalian hibernators ∼ a matter of ferroptosis?哺乳动物冬眠者的抗寒能力 ∼ 与铁死亡有关?
Front Physiol. 2024 Apr 25;15:1377986. doi: 10.3389/fphys.2024.1377986. eCollection 2024.
3
Induction of a torpor-like hypothermic and hypometabolic state in rodents by ultrasound.超声诱导啮齿动物进入类似冬眠的低体温和低代谢状态。
Nat Metab. 2023 May;5(5):789-803. doi: 10.1038/s42255-023-00804-z. Epub 2023 May 25.
4
Why hibernate? Predator avoidance in the edible dormouse.为什么要冬眠?榛睡鼠的避敌策略。
Mamm Res. 2023;68(1):1-11. doi: 10.1007/s13364-022-00652-4. Epub 2022 Oct 6.
5
Regulation of protein and oxidative energy metabolism are down-regulated in the skeletal muscles of Asiatic black bears during hibernation.在冬眠期间,亚洲黑熊骨骼肌中的蛋白质和氧化能量代谢受到调节。
Sci Rep. 2022 Nov 16;12(1):19723. doi: 10.1038/s41598-022-24251-0.
6
Synthetic torpor protects rats from exposure to accelerated heavy ions.合成休眠可保护大鼠免受加速重离子辐射。
Sci Rep. 2022 Sep 30;12(1):16405. doi: 10.1038/s41598-022-20382-6.
7
Mitochondrial respiration in rats during hypothermia resulting from central drug administration.中枢给药导致大鼠低温时的线粒体呼吸。
J Comp Physiol B. 2022 Mar;192(2):349-360. doi: 10.1007/s00360-021-01421-6. Epub 2022 Jan 10.
8
European space agency's hibernation (torpor) strategy for deep space missions: Linking biology to engineering.欧洲航天局的深空任务休眠(蛰伏)策略:将生物学与工程学联系起来。
Neurosci Biobehav Rev. 2021 Dec;131:618-626. doi: 10.1016/j.neubiorev.2021.09.054. Epub 2021 Oct 1.
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Be cool to be far: Exploiting hibernation for space exploration.酷在远方:利用冬眠进行太空探索。
Neurosci Biobehav Rev. 2021 Sep;128:218-232. doi: 10.1016/j.neubiorev.2021.03.037. Epub 2021 Jun 16.
10
Reversible Tau Phosphorylation Induced by Synthetic Torpor in the Spinal Cord of the Rat.大鼠脊髓中由人工诱导的冬眠所引起的可逆性 Tau 蛋白磷酸化
Front Neuroanat. 2021 Feb 2;15:592288. doi: 10.3389/fnana.2021.592288. eCollection 2021.