Vieira-Coelho M A, Teixeira V A, Finkel Y, Soares-Da-Silva P, Bertorello A M
Departments of Molecular Medicine and Woman and Child Health, Karolinska Institute, Karolinska Hospital, 171 76 Stockholm, Sweden.
Am J Physiol. 1998 Dec;275(6):G1317-23. doi: 10.1152/ajpgi.1998.275.6.G1317.
During high-salt diet endogenous dopamine (DA) reduces jejunal sodium transport in young but not in adult rats. This study was designed to evaluate whether this effect is mediated, at the cellular level, by inhibition of Na+-K+-ATPase activity. Enzyme activity was determined in isolated jejunal cells by the rate of [gamma-32P]ATP hydrolysis. Cells were obtained from weanling and adult rats fed either with high- or normal-salt diet. In 20-day-old but not in 40-day-old rats Na+-K+-ATPase activity was significantly reduced during high-salt diet. This inhibition was abolished by a blocker of DA synthesis. The decreased activity was associated with a decreased alpha1-subunit at the plasma membrane. During high-salt diet there was an increase in DA content in jejunal cells from 20-day-old rats, associated with a parallel decrease in 5-hydroxytryptamine, compared with normal-salt diet. In 40-day-old rats, however, the catecholamine level remained unchanged during high-salt diet. Incubation of isolated jejunal cells with DA resulted in a dose-dependent inhibition of Na+-K+-ATPase activity in 20- but not in 40-day-old rats. We conclude that during high-salt diet, jejunal Na+-K+-ATPase in 20-day-old rats is inhibited, and this effect is likely to be mediated by locally formed DA.
在高盐饮食期间,内源性多巴胺(DA)可降低幼龄大鼠空肠的钠转运,但对成年大鼠无此作用。本研究旨在评估这种效应在细胞水平上是否通过抑制钠钾ATP酶活性介导。通过[γ-32P]ATP水解速率测定分离的空肠细胞中的酶活性。细胞取自喂食高盐或正常盐饮食的断奶大鼠和成年大鼠。在20日龄而非40日龄大鼠中,高盐饮食期间钠钾ATP酶活性显著降低。DA合成阻滞剂可消除这种抑制作用。活性降低与质膜上α1亚基减少有关。与正常盐饮食相比,高盐饮食期间20日龄大鼠空肠细胞中DA含量增加,5-羟色胺含量相应减少。然而,在40日龄大鼠中,高盐饮食期间儿茶酚胺水平保持不变。用DA孵育分离的空肠细胞导致20日龄而非40日龄大鼠的钠钾ATP酶活性呈剂量依赖性抑制。我们得出结论,在高盐饮食期间,20日龄大鼠的空肠钠钾ATP酶受到抑制,这种效应可能由局部生成的DA介导。