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大鼠和犬肾中肾小管多巴胺外向转运体的动力学研究。

Kinetic study of the tubular dopamine outward transporter in the rat and dog kidney.

作者信息

Soares-da-Silva P

机构信息

Department of Pharmacology and Therapeutics, Faculty of Medicine, Porto, Portugal.

出版信息

Br J Pharmacol. 1993 Jun;109(2):577-80. doi: 10.1111/j.1476-5381.1993.tb13609.x.

Abstract
  1. The present study has determined the kinetic characteristics of the outflow of dopamine of renal origin in slices of rat and dog renal cortex loaded with exogenous L-dihydroxyphenylalanine (L-DOPA 5 to 5000 microM). 2. In both dog and rat renal tissues the production of dopamine was found to be dependent on the concentration of L-DOPA used and reached its maximum at 2500 microM L-DOPA. The decarboxylation of L-DOPA in rat cortical slices (16.4 +/- 2.6 to 1479.2 +/- 85.2 nmol g-1) was 6 fold that in the dog (2.2 +/- 0.4 to 252.1 +/- 21.2 nmol g-1). In the rat kidney a large amount (approximately 50%) of the dopamine (5.2 +/- 0.6 to 743.4 +/- 58.3 nmol g-1) was found to escape into the incubation medium, whereas in dog renal slices the amount of newly-formed dopamine escaping into the incubation medium (0.7 +/- 0.2 to 46.5 +/- 9.3 nmol g-1) was less than 25% of the total amount of the amine formed. 3. The application of the Michaelis-Menten equation to the net transport of newly-formed dopamine has allowed the identification of a saturable (carrier-mediated transfer) and a non-saturable component (diffusion). The Vmax (nmol g-1 15 min-1) and Km (nM) values for the saturable component were, respectively, 340 +/- 41 and 396 +/- 45 in the rat kidney and 112 +/- 16 and 319 +/- 35 in the dog kidney. In both rat and dog renal tissues, the magnitude of the non-saturable component was found to be of minor importance up to a concentration of 250 nmol g-1 of dopamine to be transported. At high concentrations of the amine (greater then 250 nmol g-1), only attainable in rat kidney slices, most of the dopamine was found to leave the compartment where the synthesis did occur through a non-saturable transport system.4. In conclusion, the results presented here show that the outflow of newly-formed dopamine in both dog and rat kidney slices loaded with exogenous L-DOPA follows Michaelis-Menten kinetics with a saturable component and a non-saturable one, the latter assuming particular importance only at higher concentrations of the amine.
摘要
  1. 本研究测定了在加载外源性L - 二羟基苯丙氨酸(L - DOPA,5至5000微摩尔)的大鼠和犬肾皮质切片中,肾源性多巴胺流出的动力学特征。2. 在犬和大鼠的肾组织中,均发现多巴胺的生成依赖于所使用的L - DOPA浓度,并在2500微摩尔L - DOPA时达到最大值。大鼠皮质切片中L - DOPA的脱羧作用(16.4±2.6至1479.2±85.2纳摩尔/克)是犬的6倍(2.2±0.4至252.1±21.2纳摩尔/克)。在大鼠肾脏中,大量(约50%)的多巴胺(5.2±0.6至743.4±58.3纳摩尔/克)逸出到孵育培养基中,而在犬肾切片中,逸出到孵育培养基中的新形成多巴胺量(0.7±0.2至46.5±9.3纳摩尔/克)不到所形成胺总量的25%。3. 将米氏方程应用于新形成多巴胺的净转运,已确定了一个可饱和成分(载体介导转运)和一个非可饱和成分(扩散)。大鼠肾脏中可饱和成分的Vmax(纳摩尔/克15分钟-1)和Km(纳摩尔)值分别为340±41和396±45,犬肾脏中分别为112±16和319±35。在大鼠和犬的肾组织中,在所转运多巴胺浓度高达250纳摩尔/克时,发现非可饱和成分的量不太重要。在高浓度胺(大于250纳摩尔/克)时,仅在大鼠肾切片中可达到,发现大多数多巴胺通过非可饱和转运系统离开合成发生的隔室。4. 总之,此处呈现的结果表明,在加载外源性L - DOPA的犬和大鼠肾切片中,新形成多巴胺的流出遵循米氏动力学,具有一个可饱和成分和一个非可饱和成分,后者仅在较高胺浓度时具有特别重要性。

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Dopamine receptors modulate sodium excretion in denervated kidney.多巴胺受体调节去神经支配肾脏的钠排泄。
Am J Physiol. 1986 Jun;250(6 Pt 2):F1033-8. doi: 10.1152/ajprenal.1986.250.6.F1033.

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