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The transmethylation cycle in the brain of Alzheimer patients.

机译:阿尔茨海默氏病患者大脑中的甲基化循环。

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摘要

Homocysteine accumulation, frequently observed in plasma of AD patients, may be a sign of a reduced activity of the brain methionine-homocysteine transmethylation cycle. S-Adenosylmethionine (SAM) is the main methyl donor in several transmethylation reactions. The demethylated product of SAM, S-adenosylhomocysteine (SAH), is hydrolyzed to yield homocysteine, which can be remethylated to methionine by transfer of a methyl group of 5-methyltetrahydrofolate (5-MTHF). A reduced activity of the transmethylation cycle in the brain may result in hypomethylation of the promoter of the presenilin 1 (PS1) gene, which will lead to overexpression of presenilin 1 and, consequently, to increased Abeta(1-42) (Abeta42) formation. Brain transmethylation was studied in 30 patients with 'probable' AD and 28 age-matched non-demented controls by measuring the cerebrospinal fluid (CSF) levels of SAM, SAH and 5-MTHF. 5-MTHF was determined by HPLC with electrochemical detection, while SAM and SAH were assayed by stable isotope dilution tandem mass spectrometry. We found no statistical differences between AD patients and controls for 5-MTHF, SAM and SAH levels, and the SAM/SAH-ratio in CSF. These findings argue against a possible change in methylation of the promoter and expression of PS1.
机译:在AD患者的血浆中经常观察到同型半胱氨酸的积累,这可能是脑蛋氨酸-高半胱氨酸转甲基化周期活性降低的迹象。 S-腺苷甲硫氨酸(SAM)是几个甲基转移反应中的主要甲基供体。将SAM的脱甲基产物S-腺苷同型半胱氨酸(SAH)水解,得到高半胱氨酸,可以通过转移5-甲基四氢叶酸(5-MTHF)的甲基将其再甲基化为蛋氨酸。脑中转甲基化循环活性的降低可能导致早老素1(PS1)基因启动子的甲基化不足,这将导致早老素1的过表达,并因此导致Abeta(1-42)(Abeta42)形成增加。通过测量SAM,SAH和5-MTHF的脑脊液(CSF)水平,对30位“可能” AD患者和28位年龄相匹配的非痴呆对照患者进行了脑甲基化研究。 5-MTHF通过电化学检测的HPLC测定,而SAM和SAH通过稳定同位素稀释串联质谱法测定。我们发现AD患者与对照组中5-MTHF,SAM和SAH水平以及CSF中SAM / SAH比率之间无统计学差异。这些发现反对启动子的甲基化和PS1表达的可能改变。

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