大鼠海马及内嗅皮质、嗅周皮质、嗅后皮质和颞叶皮质中的一氧化氮合酶和精氨酸酶:区域差异及与年龄相关的变化

Nitric oxide synthase and arginase in the rat hippocampus and the entorhinal, perirhinal, postrhinal, and temporal cortices: regional variations and age-related changes.

作者信息

Liu Ping, Smith Paul F, Appleton Ian, Darlington Cynthia L, Bilkey David K

机构信息

Department of Pharmacology and Toxicology, School of Medical Sciences, University of Otago, Dunedin, New Zealand.

出版信息

Hippocampus. 2003;13(7):859-67. doi: 10.1002/hipo.10138.

Abstract

Increasing evidence suggests that nitric oxide synthase (NOS)/nitric oxide (NO) contributes to the aging process. By contrast, the role of arginase, which shares a common substrate with NOS, has not been determined. In the present study, regional variations and age-related changes in NOS and arginase in the hippocampus and its neighboring structures were investigated for the first time. In young adult rats, high levels of NOS activity were found in the entorhinal, perirhinal, and postrhinal cortices, whereas low values were located in the hippocampus and the temporal cortex. Interestingly, arginase activity showed an overall inverse pattern with the lowest levels in the entorhinal and perirhinal cortices. When a comparison was carried out between young (4-month-old) and aged (24-month-old) rats, significant increases in total NOS activity were found in the aged entorhinal and temporal cortices, and a significant decrease in arginase activity was observed in the aged postrhinal cortex. Western blotting demonstrated significant decreases in both neuronal and endothelial NOS expression in the aged hippocampus and postrhinal cortex, whereas arginase I and II expression did not show age-related changes in any region examined. Activity and protein expression of inducible NOS were not detected in any tissue from either group. The present findings of region-specific changes in NOS and arginase appear to support the potential involvement of NOS/NO in the aging process and raise the issue of a possible contribution of arginase to aging.

摘要

越来越多的证据表明,一氧化氮合酶(NOS)/一氧化氮(NO)参与了衰老过程。相比之下,与NOS共用一种共同底物的精氨酸酶的作用尚未确定。在本研究中,首次对海马及其邻近结构中NOS和精氨酸酶的区域差异及与年龄相关的变化进行了研究。在年轻成年大鼠中,内嗅皮质、梨状周围皮质和鼻后皮质中发现高水平的NOS活性,而海马和颞叶皮质中的活性较低。有趣的是,精氨酸酶活性呈现出总体相反的模式,在内嗅皮质和梨状周围皮质中水平最低。当对年轻(4个月大)和老年(24个月大)大鼠进行比较时,发现老年内嗅皮质和颞叶皮质中的总NOS活性显著增加,而老年鼻后皮质中的精氨酸酶活性显著降低。蛋白质印迹法显示,老年海马和鼻后皮质中神经元型和内皮型NOS表达均显著降低,而在所检查的任何区域中,精氨酸酶I和II的表达均未显示出与年龄相关的变化。两组的任何组织中均未检测到诱导型NOS的活性和蛋白质表达。本研究中关于NOS和精氨酸酶区域特异性变化的发现似乎支持了NOS/NO在衰老过程中的潜在参与,并提出了精氨酸酶对衰老可能有贡献的问题。

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