Galvez Fernando, Franklin Natasha M, Tuttle Ryan B, Wood Chris M
Department of Biological Sciences, Louisiana State University, Baton Rouge, LA 70803, USA.
Aquat Toxicol. 2007 Aug 30;84(2):208-14. doi: 10.1016/j.aquatox.2007.04.013. Epub 2007 Jun 16.
Recent studies have shown that dietary Ca(2+) supplementation strongly inhibits uptake of Ca(2+) and Cd at the fish gill. To better understand the influence of dietary Ca(2+) on branchial Ca(2+) transport, we examined the expression of two trout gill calcium transporters during waterborne and dietary Cd exposure, at two different levels of dietary Ca(2+). Quantitative polymerase chain reaction (PCR) was used to monitor epithelial calcium channel (ECaC) and sodium-calcium exchange (NCX) mRNA levels following 7-28 days of exposure to these treatments. In brief, juvenile rainbow trout (Oncorhynchus mykiss) were exposed to control, 3 microg/L waterborne Cd, 500 mg/kg dietary Cd, or a combined 3 microg/L waterborne plus 500 mg/kg dietary Cd exposure, supplemented with either 20 mg/g or 60 mg/g dietary calcium (Ca(2+)). Two-way analysis of variance was used to discern the main effects of Cd exposure and dietary Ca(2+) supplementation on ECaC and NCX mRNA levels. We found that dietary Ca(2+) supplementation decreased significantly ECaC mRNA expression on days 14 and 21. In comparison, NCX mRNA levels were not influenced by dietary Ca(2+) supplementation, but rather were significantly inhibited in the combined waterborne and dietary Cd exposure on day 7 alone. Statistical analysis found no interactive effects between Cd exposure and dietary Ca(2+) exposure at any time point, except for day 28. This study provides evidence of the importance of nutritional status on the transcriptional regulation of ion transport at the fish gill. We discuss the importance of diet and nutritional status to the development of new regulatory approaches, such as the biotic ligand model, which currently do not account for the significance of diet on metal bioavailability in aquatic organisms.
近期研究表明,膳食补充Ca(2+)能强烈抑制鱼类鳃对Ca(2+)和Cd的摄取。为了更好地理解膳食Ca(2+)对鳃部Ca(2+)转运的影响,我们在两种不同膳食Ca(2+)水平下,研究了虹鳟鱼鳃中两种钙转运蛋白在水体和膳食Cd暴露过程中的表达情况。采用定量聚合酶链反应(PCR)监测暴露于这些处理7 - 28天后上皮钙通道(ECaC)和钠钙交换体(NCX)的mRNA水平。简而言之,将幼年虹鳟(Oncorhynchus mykiss)暴露于对照组、3 μg/L水体Cd、500 mg/kg膳食Cd或3 μg/L水体加500 mg/kg膳食Cd的联合暴露组,同时分别补充20 mg/g或60 mg/g膳食钙(Ca(2+))。采用双向方差分析来识别Cd暴露和膳食Ca(2+)补充对ECaC和NCX mRNA水平的主要影响。我们发现,膳食补充Ca(2+)在第14天和第21天显著降低了ECaC mRNA的表达。相比之下,NCX mRNA水平不受膳食Ca(2+)补充的影响,而是仅在第7天的水体和膳食Cd联合暴露中受到显著抑制。统计分析发现,除第28天外,在任何时间点Cd暴露和膳食Ca(2+)暴露之间均无交互作用。本研究提供了营养状况对鱼类鳃部离子转运转录调控重要性的证据。我们讨论了饮食和营养状况对新调控方法(如生物配体模型)发展的重要性,目前该模型未考虑饮食对水生生物中金属生物有效性的影响。