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成年幼犬与老龄犬脊髓中芳基烷基胺N - 乙酰基转移酶和褪黑素1B型受体免疫反应性的比较

Comparison of arylalkylamine N-acetyltransferase and melatonin receptor type 1B immunoreactivity between young adult and aged canine spinal cord.

作者信息

Ahn Ji Hyeon, Park Joon Ha, Kim In Hye, Lee Jae-Chul, Yan Bing Chun, Yong Min Sik, Lee Choong Hyun, CHoi Jung Hoon, Yoo Ki-Yeon, Hwang In Koo, Moon Seung Myung, Shin Hyung-Cheul, Won Moo-Ho

机构信息

Department of Neurobiology, School of Medicine, and 5Department of Anatomy, College of Veterinary Medicine, Kangwon National University, Chuncheon 200-701, Korea.

出版信息

J Vet Sci. 2014;15(3):335-42. doi: 10.4142/jvs.2014.15.3.335. Epub 2014 Jun 20.

Abstract

Melatonin affects diverse physiological functions through its receptor and plays an important role in the central nervous system. In the present study, we compared immunoreactivity patterns of arylalkylamine N-acetyltransferase (AANAT), an enzyme essential for melatonin synthesis, and melatonin receptor type 1B (MT2) in the spinal cord of young adult (23 years) and aged (1012 years) beagle dogs using immunohistochemistry and Western blotting. AANAT-specific immunoreactivity was observed in the nuclei of spinal neurons, and was significantly increased in aged dog spinal neurons compared to young adult spinal neurons. MT2-specific immunoreactivity was found in the cytoplasm of spinal neurons, and was predominantly increased in the margin of the neuron cytoplasm in aged spinal cord compared to that in the young adult dogs. These increased levels of AANAT and MT2 immunoreactivity in aged spinal cord might be a feature of normal aging and associated with a feedback mechanism that compensates for decreased production of melatonin during aging.

摘要

褪黑素通过其受体影响多种生理功能,并在中枢神经系统中发挥重要作用。在本研究中,我们使用免疫组织化学和蛋白质印迹法,比较了成年幼犬(2至3岁)和老年犬(10至12岁)脊髓中芳基烷基胺N-乙酰基转移酶(AANAT,一种褪黑素合成所必需的酶)和1B型褪黑素受体(MT2)的免疫反应模式。在脊髓神经元的细胞核中观察到AANAT特异性免疫反应,与成年幼犬脊髓神经元相比,老年犬脊髓神经元中的该反应显著增加。在脊髓神经元的细胞质中发现了MT2特异性免疫反应,与成年幼犬相比,老年脊髓中该反应主要在神经元细胞质边缘增加。老年脊髓中AANAT和MT2免疫反应性的这些增加水平可能是正常衰老的一个特征,并与一种反馈机制相关,该机制可补偿衰老过程中褪黑素分泌的减少。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ce8/4178134/83f2b63f1313/jvs-15-335-g001.jpg

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