Hogstrand C, Verbost P M, Bonga S E, Wood C M
T. H. Morgan School of Biological Sciences, University of Kentucky, Lexington 40506-0225, USA.
Am J Physiol. 1996 May;270(5 Pt 2):R1141-7. doi: 10.1152/ajpregu.1996.270.5.R1141.
The uptake mechanism of Zn2+ through the gill epithelium of freshwater rainbow trout was investigated both in intact animals and in isolated basolateral membranes. Involvement of the apical Ca2+ uptake sites in Zn2+ uptake was examined in vivo by pharmacological manipulation of the apical Ca2+ permeability. The apical entries of Ca2+ and Zn2+, but not Na2+ and Cl-, were inhibited by addition of La to the water. Addition of 1.0 microM La reduced the influxes of Ca2+ and Zn2+ to 22 +/- 3 and 53 +/- 7% (mean +/- SE) of the control value, respectively. Injection of CaCl2 also reduced the branchial influxes of Ca2+ and Zn2+. This treatment decreased the influx of Ca2- to 45 +/- 4% of the control level and the Zn2+ influx to 68 +/- 5%. These results strongly imply that Zn2+ passes across the apical membrane of the chloride cells of the gills via the same pathway as Ca2+. The presence of an active basolateral transporter for Zn2+ was investigated in vitro on isolated basolateral membranes. There was no ATP-dependent or Na2+(-)gradient driven transport of Zn2+ at physiological Zn2+ activities. The same system was used to study potential effects of Zn2+ on the basolateral Ca2+(-)adenosinetri-phosphatase. Zn2+ was found to be a potent blocker of this transporter, causing a mixed inhibitory effect on the ATP driven Ca2+ transport at a free Zn2+ activity of 100 pM.
在完整动物和分离的基底外侧膜中,研究了淡水虹鳟鱼鳃上皮对锌离子(Zn2+)的摄取机制。通过药理学方法调节顶端钙离子(Ca2+)通透性,在体内研究了顶端Ca2+摄取位点在Zn2+摄取中的作用。向水中添加镧(La)可抑制Ca2+和Zn2+的顶端摄取,但不影响钠离子(Na2+)和氯离子(Cl-)。添加1.0微摩尔/升的La可分别将Ca2+和Zn2+的流入量降至对照值的22±3%和53±7%(平均值±标准误)。注射氯化钙(CaCl2)也会降低鳃对Ca2+和Zn2+的流入量。这种处理使Ca2+的流入量降至对照水平的45±4%,Zn2+的流入量降至68±5%。这些结果强烈表明,Zn2+通过与Ca2+相同的途径穿过鳃氯细胞的顶端膜。在体外对分离的基底外侧膜研究了Zn2+活性基底外侧转运体的存在情况。在生理Zn2+活性下,没有发现Zn2+的ATP依赖性或Na2+梯度驱动的转运。使用相同的系统研究了Zn2+对基底外侧Ca2+ - 三磷酸腺苷酶的潜在影响。发现Zn2+是该转运体的有效阻滞剂,在游离Zn2+活性为100皮摩尔时,对ATP驱动的Ca2+转运产生混合抑制作用。