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大鼠小脑衰老过程中一氧化氮体系的研究。

Study of the nitric oxide system in the rat cerebellum during aging.

机构信息

Department of Experimental Biology, University of Jaen, Campus Las Lagunillas s/n, 23071, Jaén, Spain.

出版信息

BMC Neurosci. 2010 Jun 24;11:78. doi: 10.1186/1471-2202-11-78.

Abstract

BACKGROUND

The cerebellum is the neural structure with the highest levels of nitric oxide, a neurotransmitter that has been proposed to play a key role in the brain aging, although knowledge concerning its contribution to cerebellar senescence is still unclear, due mainly to absence of integrative studies that jointly evaluate the main factors involved in its cell production and function. Consequently, in the present study, we investigate the expression, location, and activity of nitric oxide synthase isoenzymes; the protein nitration; and the production of nitric oxide in the cerebellum of adult and old rats.

RESULTS

Our results show no variation in the expression of nitric oxide synthase isoforms with aging, although, we have detected some changes in the cellular distribution pattern of the inducible isoform particularly in the cerebellar nuclei. There is also an increase in nitric oxide synthase activity, as well as greater protein-nitration levels, and maintenance of nitrogen oxides (NOx) levels in the senescent cerebellum.

CONCLUSIONS

The nitric oxide/nitric oxide synthases system suffers from a number of changes, mainly in the inducible nitric oxide synthase distribution and in overall nitric oxide synthases activity in the senescent cerebellum, which result in an increase of the protein nitration. These changes might be related to the oxidative damage detected with aging in the cerebellum.

摘要

背景

小脑是神经结构中一氧化氮含量最高的部位,一氧化氮是一种神经递质,它被认为在大脑衰老中起着关键作用,尽管由于缺乏综合评估其细胞产生和功能的主要因素的研究,因此对其在小脑衰老中的作用的了解仍不清楚。因此,在本研究中,我们研究了成年和老年大鼠小脑中一氧化氮合酶同工酶的表达、定位和活性;蛋白质硝化;以及一氧化氮的产生。

结果

我们的结果表明,随着年龄的增长,一氧化氮合酶同工酶的表达没有变化,尽管我们已经检测到诱导型同工酶的细胞分布模式发生了一些变化,特别是在小脑核中。一氧化氮合酶活性增加,蛋白质硝化水平升高,衰老小脑中的氮氧化物(NOx)水平保持不变。

结论

一氧化氮/一氧化氮合酶系统发生了多种变化,主要是诱导型一氧化氮合酶的分布和衰老小脑中总的一氧化氮合酶活性的变化,导致蛋白质硝化增加。这些变化可能与小脑衰老时检测到的氧化损伤有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20bf/2905430/ed00fe802557/1471-2202-11-78-1.jpg

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