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在衰老大鼠中,过氧化物酶体增殖物激活受体α(PPAR-α)的表达与炎性细胞因子白细胞介素-1β(IL-1β)和肿瘤坏死因子-α(TNF-α)呈负相关。

PPAR-alpha expression inversely correlates with inflammatory cytokines IL-1beta and TNF-alpha in aging rats.

作者信息

Gelinas David S, McLaurin JoAnne

机构信息

Centre for Research in Neurodegenerative Diseases and Department of Laboratory Medicine and Pathobiology, University of Toronto, Tanz Neuroscience Building, 6 Queen's Park Crescent West, Toronto, Ontario, M5S3H2, Canada.

出版信息

Neurochem Res. 2005 Nov;30(11):1369-75. doi: 10.1007/s11064-005-8341-y.

Abstract

Dehydroepiandrosterone (DHEAS) was given the name "fountain of youth" in reference to its beneficial properties in memory, cognition and aging. Cultured cell studies showed that DHEAS may mediate its action by counteracting aging-associated inflammation via PPAR-alpha activation. In the present study, we demonstrated an age-dependent increase in IL-1beta and TNF-alpha expression in the brain and the spleen of aging rats, while PPAR-alpha expression was decreased in the spleen of 18 month-old rats. Oral treatment with DHEAS increased PPAR-alpha mRNA in 3 month-old rats and decreased PPAR-alpha protein expression in 18 month-old rats in the spleen. In contrast, DHEAS did not alter cytokine expression in spleen and brain of the three age groups. These findings underline a differential role for DHEAS in PPAR-alpha expression that is age-dependent, and also, that beneficial effects of DHEAS on cognitive function are unlikely mediated by a decrease in cytokine expression.

摘要

脱氢表雄酮(DHEAS)因其在记忆、认知和衰老方面的有益特性而被称为“青春之泉”。细胞培养研究表明,DHEAS可能通过激活PPAR-α来对抗与衰老相关的炎症,从而介导其作用。在本研究中,我们发现衰老大鼠脑和脾中IL-1β和TNF-α的表达随年龄增长而增加,而18月龄大鼠脾中PPAR-α的表达则降低。对3月龄大鼠进行DHEAS口服治疗可增加脾中PPAR-α mRNA的表达,而对18月龄大鼠进行DHEAS口服治疗则可降低脾中PPAR-α蛋白的表达。相反,DHEAS并未改变三个年龄组大鼠脾和脑中细胞因子的表达。这些发现强调了DHEAS在PPAR-α表达中具有年龄依赖性的差异作用,同时也表明DHEAS对认知功能的有益作用不太可能是通过降低细胞因子表达来介导的。

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