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炔丙基甘氨酸输注对胃肠外营养生长大鼠组织谷胱甘肽水平、血浆氨基酸浓度及组织形态的影响

Propargylglycine infusion effects on tissue glutathione levels, plasma amino acid concentrations and tissue morphology in parenterally-fed growing rats.

作者信息

Cho E S, Hovanec-Brown J, Tomanek R J, Stegink L D

机构信息

Department of Home Economics, University of Iowa, Iowa City 52242.

出版信息

J Nutr. 1991 Jun;121(6):785-94. doi: 10.1093/jn/121.6.785.

Abstract

Amino acid solutions currently used for total parenteral nutrition (TPN) contain little cysteine or cystine. Some premature human infants have low liver activities of gamma-cystathionase and presumably require preformed cysteine or cystine. Growing animals tend to have higher liver gamma-cystathionase activity, which makes them unsuitable as models to study effects of CSH precursors. Because propargylglycine (PPG) inhibits gamma-cystathionase specifically, rats infused with PPG as part of a TPN regimen were evaluated as a potential model. Two groups of rats (120-160 g) were infused for 15 d with TPN regimens, one without and one with PPG (40 mumols/d). A third group received the TPN-control regimen, with methionine added at toxic levels. Propargylglycine treatment significantly decreased plasma cystine and taurine concentrations and significantly increased plasma cystathionine concentration without affecting methionine concentration. Propargylglycine treatment significantly decreased brain, muscle, liver, intestine and stomach glutathione concentration without affecting erythrocyte or heart glutathione concentrations. Electron microscopic examination showed no abnormalities in heart and kidney of PPG-treated rats. Hepatocyte glycogen was lower in TPN-fed controls than in orally fed rats and was further reduced in TPN-PPG-fed animals. Growing rats infused with low doses of PPG show promise as an animal model to study a number of important issues concerning human sulfur amino acid metabolism.

摘要

目前用于全胃肠外营养(TPN)的氨基酸溶液中半胱氨酸或胱氨酸含量很少。一些早产的人类婴儿肝脏中γ-胱硫醚酶的活性较低,可能需要预先形成的半胱氨酸或胱氨酸。生长中的动物肝脏γ-胱硫醚酶活性往往较高,这使得它们不适宜作为研究半胱氨酸(CSH)前体作用的模型。由于炔丙基甘氨酸(PPG)能特异性抑制γ-胱硫醚酶,因此对作为TPN方案一部分输注PPG的大鼠作为潜在模型进行了评估。两组大鼠(120 - 160克)接受TPN方案输注15天,一组不添加PPG,另一组添加PPG(40微摩尔/天)。第三组接受TPN对照方案,并添加毒性水平的蛋氨酸。炔丙基甘氨酸处理显著降低了血浆胱氨酸和牛磺酸浓度,并显著提高了血浆胱硫醚浓度,而不影响蛋氨酸浓度。炔丙基甘氨酸处理显著降低了脑、肌肉、肝脏、肠道和胃中的谷胱甘肽浓度,但不影响红细胞或心脏中的谷胱甘肽浓度。电子显微镜检查显示,接受PPG处理的大鼠心脏和肾脏没有异常。TPN喂养的对照大鼠肝细胞糖原含量低于经口喂养的大鼠,而TPN - PPG喂养的动物中糖原含量进一步降低。输注低剂量PPG的生长大鼠有望成为研究许多有关人类含硫氨基酸代谢重要问题的动物模型。

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