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利用福尔马林试验对裸鼹鼠抗伤害感受中去甲肾上腺素能受体系统的研究()。 (注:括号里内容原文缺失,翻译时保留原样)

Investigation of noradrenergic receptor system in anti-nociception using formalin test in the naked mole rat ().

作者信息

Mwobobia R M, Kanui T I, Abelson K S P

机构信息

School of Agriculture and Veterinary Sciences, South Eastern Kenya University, P O Box 170-90200, Kitui, Kenya.

Department of Experimental Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamvej 3B, 2200, Copenhagen, Denmark.

出版信息

Heliyon. 2020 Oct 23;6(10):e05216. doi: 10.1016/j.heliyon.2020.e05216. eCollection 2020 Oct.

DOI:10.1016/j.heliyon.2020.e05216
PMID:33134574
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7586093/
Abstract

The naked mole rat (NMR) is a rodent that has gained importance as a biomedical research model for various conditions like hypoxic brain injury, cancer and nociception. This study was designed to investigate possible involvement of the noadrenergic receptor system in antinoception in the NMR, using the alpha-2 adrenergic receptor specific ligands clonidine (agonist) and yohimbine (antagonist) in the formalin test. Formalin test followed 30 min after intraperitoneal administration of ligands or control. A total of 96 naked mole rats were used. A significant reduction in nociceptive behaviours was demonstrated after administration of clonidine in the doses 1,3,10 and 30 μg/kg (n = 8 per group). Doses of clonidine above 30 μg/kg caused loss of motor and proprietion skills exhibited by prostration and failure to turn over when placed on their backs. The antinociception by 3 μg/kg clonidine was reversed by administration of 30 μg/kg of yohimbine. The present study demonstrates that the noradrenergic receptor system is present and involved in formalin test-related antinociceptive mechanisms in the NMR, similar to other mammals. Given the increasing importance of the NMR as a model for pain and nociception, the species may prove useful as an animal model for noradrenergic mechanisms in pain modulation.

摘要

裸鼹鼠是一种啮齿动物,作为多种病症(如缺氧性脑损伤、癌症和痛觉感受)的生物医学研究模型,其重要性日益凸显。本研究旨在通过在福尔马林试验中使用α-2肾上腺素能受体特异性配体可乐定(激动剂)和育亨宾(拮抗剂),来探究去甲肾上腺素能受体系统在裸鼹鼠痛觉感受中的可能作用。在腹腔注射配体或对照后30分钟进行福尔马林试验。总共使用了96只裸鼹鼠。给予1、3、10和30μg/kg剂量的可乐定后,伤害性反应行为显著减少(每组n = 8)。剂量高于30μg/kg的可乐定导致运动和本体感觉技能丧失,表现为俯卧以及仰卧时无法翻身翻转。给予30μg/kg育亨宾可逆转3μg/kg可乐定的镇痛作用。本研究表明,与其他哺乳动物类似,去甲肾上腺素能受体系统存在于裸鼹鼠中,并参与福尔马林试验相关的镇痛机制。鉴于裸鼹鼠作为疼痛和痛觉感受模型的重要性日益增加,该物种可能被证明是一种用于研究去甲肾上腺素能机制在疼痛调节中作用的有用动物模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/cea55c24ad09/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/a34442902354/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/77a1d66c8194/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/d0e4a3bb5ebc/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/cea55c24ad09/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/a34442902354/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/77a1d66c8194/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/d0e4a3bb5ebc/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/13b9/7586093/cea55c24ad09/gr4.jpg

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本文引用的文献

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Inbred or Outbred? Genetic Diversity in Laboratory Rodent Colonies.近亲繁殖还是远亲繁殖?实验鼠群体中的遗传多样性。
G3 (Bethesda). 2018 Feb 2;8(2):679-686. doi: 10.1534/g3.117.300495.
2
Modulation of formalin-induced pain-related behaviour by clonidine and yohimbine in the Speke's hinged tortoise (Kiniskys spekii).可乐定和育亨宾对斯氏铰链陆龟(Kiniskys spekii)福尔马林诱导的疼痛相关行为的调节作用。
J Vet Pharmacol Ther. 2017 Oct;40(5):439-446. doi: 10.1111/jvp.12374. Epub 2016 Nov 27.
3
Locus Ceruleus Norepinephrine Release: A Central Regulator of CNS Spatio-Temporal Activation?
蓝斑去甲肾上腺素释放:中枢神经系统时空激活的核心调节因子?
Front Synaptic Neurosci. 2016 Aug 26;8:25. doi: 10.3389/fnsyn.2016.00025. eCollection 2016.
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Investigation of the presence and antinociceptive function of muscarinic acetylcholine receptors in the African naked mole-rat (Heterocephalus glaber).非洲裸鼹鼠(裸鼹形鼠)中毒蕈碱型乙酰胆碱受体的存在及其抗伤害感受功能的研究
J Comp Physiol A Neuroethol Sens Neural Behav Physiol. 2016 Jan;202(1):7-15. doi: 10.1007/s00359-015-1048-x. Epub 2015 Oct 31.
5
Yohimbine is a 5-HT1A agonist in rats in doses exceeding 1 mg/kg.育亨宾在大鼠体内剂量超过1毫克/千克时是一种5-羟色胺1A受体激动剂。
Neurosci Lett. 2015 Oct 8;606:215-9. doi: 10.1016/j.neulet.2015.09.008. Epub 2015 Sep 12.
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In Vivo. 2014 Jan-Feb;28(1):39-48.