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离体灌注大鼠肝脏的细胞容积调节反应。氨基酸的作用。

Cell volume regulatory responses of isolated perfused rat liver. The effect of amino acids.

作者信息

Wettstein M, vom Dahl S, Lang F, Gerok W, Häussinger D

机构信息

Medizinische Universitätsklinik Freiburg.

出版信息

Biol Chem Hoppe Seyler. 1990 Jun;371(6):493-501. doi: 10.1515/bchm3.1990.371.1.493.

Abstract
  1. Addition of glutamine, glycine, alanine, serine, phenylalanine, proline at a concentration of 3mM, each, or of an amino-acid mixture resembling the physiological amino-acid composition of portal venous blood, to influent perfusate of isolated perfused rat liver led to a 4-6% increase of liver mass without increase of the [3H]inulin space, and biphasic K+ movements across the plasma membrane. These K+ movements consisted of an initial net K+ uptake (0.4-0.9 mumol X g-1 liver) for about 2 min, being followed by a net K+ release (1.0-2.8 mumol X g-1 liver) during the next 10 min. Withdrawal of the amino acids from influent perfusate caused a slow net K+ reuptake by the liver and restored the initial liver mass. No effects on liver mass and K+ fluxes were observed following addition of glutamate or glucose at a concentration of 3mM, each. 2) Aminooxyacetate did not affect the alanine (3 mM) induced increase in liver mass. However, in presence of aminooxyacetate the alanine-induced net K+ release from the liver (i.e. K+ release from 2-10 min minus initial K+ uptake) increased from 0.1 to 2.2 mumol X g-1 liver, whereby simultaneously the alanine tissue level rose from 6.8 to 13.3 mumol X g-1 (corresponding to an increase of the intracellular alanine concentration from about 12 to 25 mM) in presence of aminooxyacetate. 3) When livers were perfused with different glutamine concentrations, a maximal increase in liver mass of 5-6% was observed at glutamine concentrations above 1.5-2mM. A halfmaximal increase in liver mass was observed at 0.6-1.0mM glutamine in influent, i.e. at the physiological portal glutamine concentration.(ABSTRACT TRUNCATED AT 250 WORDS)
摘要
  1. 向离体灌注大鼠肝脏的流入灌注液中分别添加浓度为3mM的谷氨酰胺、甘氨酸、丙氨酸、丝氨酸、苯丙氨酸、脯氨酸,或添加类似于门静脉血生理氨基酸组成的氨基酸混合物,可使肝脏重量增加4 - 6%,而[³H]菊粉空间无增加,且钾离子跨质膜呈双相移动。这些钾离子移动包括最初约2分钟的净钾离子摄取(0.4 - 0.9微摩尔×克⁻¹肝脏),随后在接下来的10分钟内出现净钾离子释放(1.0 - 2.8微摩尔×克⁻¹肝脏)。从流入灌注液中撤除氨基酸会导致肝脏缓慢净摄取钾离子,并使肝脏恢复初始重量。分别添加浓度为3mM的谷氨酸或葡萄糖后,未观察到对肝脏重量和钾离子通量的影响。2) 氨氧基乙酸不影响丙氨酸(3mM)诱导的肝脏重量增加。然而,在氨氧基乙酸存在的情况下,丙氨酸诱导的肝脏净钾离子释放(即2 - 10分钟的钾离子释放减去初始钾离子摄取)从0.1增加到2.2微摩尔×克⁻¹肝脏,同时在氨氧基乙酸存在时,丙氨酸组织水平从6.8上升到13.3微摩尔×克⁻¹(对应细胞内丙氨酸浓度从约12mM增加到25mM)。3) 当用不同谷氨酰胺浓度灌注肝脏时,在谷氨酰胺浓度高于1.5 - 2mM时观察到肝脏重量最大增加5 - 6%。在流入液中谷氨酰胺浓度为0.6 - 1.0mM时观察到肝脏重量增加到最大值的一半,即处于门静脉谷氨酰胺生理浓度时。(摘要截短于250字)

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