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在一系列大鼠组织中,响应叶酸营养改变时蝶酰多谷氨酸浓度和长度的调节。

Modulation of pteroylpolyglutamate concentration and length in response to altered folate nutrition in a comprehensive range of rat tissues.

作者信息

Ward G J, Nixon P F

机构信息

Department of Biochemistry, University of Queensland, St. Lucia, Australia.

出版信息

J Nutr. 1990 May;120(5):476-84. doi: 10.1093/jn/120.5.476.

Abstract

For a range of rat tissue extracts, the concentrations of total folates and of short-chain pteroylpolyglutamates were assayed by Lactobacillus casei with and without conjugase treatment, respectively, and the concentration and chain length of H4PteGlnn and 5,10-CH2-H4PteGlnn together were assayed after binding to thymidylate synthase and tritiated fluorodeoxyuridylate. For rats fed a nonpurified diet and consuming 26 micrograms of folic acid daily, the respective concentrations of these total folates, short-chain folates and thymidylate synthase bindable folates were, in nmol/g, 10.2, 2.5 and 3.5 in liver, 3.9, 1.8 and 2.0 in kidney, 4.2, 1.2 and 1.0 in bone marrow, 2.3, 0.6 and 0.2 in adrenal, 2.1, 0.3 and 0.5 in spleen, 2.1, 0.9 and 0.8 in jejunal smooth muscle, 1.2, 0.9 and 0.2 in jejunal mucosa, 1.0, 0.3 and 0.6 in testis, 0.7, 0.1 and 0.2 in heart, 0.3, 0.1 and 0.1 in skeletal muscle, 0.5, 0.1 and 0.3 in brain and 0.7, 0.002 and 0 in erythrocytes. The predominant pteroylpolyglutamate chain length was 6 residues in all tissues except kidney, jejunal mucosa, skeletal muscle and brain, in which the value was 5 residues. A folate-deficient diet (30 ng/d) fed for 3 wk resulted in a depression in the total folate concentration of all tissues (except brain); the depression was generally greater for short-chain than for long-chain folates and was accompanied by a lengthening of the pteroylpolyglutamate chain. Opposite results followed folate excess of 4 to 5.4 mg/d. The fractional change in the folate concentration of the individual tissues, following perturbation of dietary folate, did not vary greatly among tissues.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

对于一系列大鼠组织提取物,分别用干酪乳杆菌在有和没有结合酶处理的情况下测定总叶酸和短链蝶酰多聚谷氨酸的浓度,并在与胸苷酸合成酶和氚化氟脱氧尿苷酸结合后测定H4PteGlnn和5,10-CH2-H4PteGlnn的浓度和链长。对于喂食非纯化日粮且每日摄入26微克叶酸的大鼠,这些总叶酸、短链叶酸和胸苷酸合成酶可结合叶酸的各自浓度(以nmol/g计)在肝脏中分别为10.2、2.5和3.5,在肾脏中为3.9、1.8和2.0,在骨髓中为4.2、1.2和1.0,在肾上腺中为2.3、0.6和0.2,在脾脏中为2.1、0.3和0.5,在空肠平滑肌中为2.1、0.9和0.8,在空肠黏膜中为1.2、0.9和0.2,在睾丸中为1.0、0.3和0.6,在心脏中为0.7、0.1和0.2,在骨骼肌中为0.3、0.1和0.1,在大脑中为0.5、0.1和0.3,在红细胞中为0.7、0.002和0。除肾脏、空肠黏膜、骨骼肌和大脑中主要的蝶酰多聚谷氨酸链长为5个残基外,所有组织中的主要链长均为6个残基。喂食3周叶酸缺乏日粮(30 ng/d)导致所有组织(除大脑外)的总叶酸浓度降低;短链叶酸的降低通常比长链叶酸更大,并且伴随着蝶酰多聚谷氨酸链的延长。叶酸过量摄入4至5.4 mg/d则产生相反的结果。饮食中叶酸受到干扰后,各个组织中叶酸浓度的分数变化在不同组织之间差异不大。(摘要截取自250字)

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