U Wolters, J M Müller, K Wölfelschneider, H Iffland
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引用次数: 0
摘要
锌加速了许多代谢过程,因为它是许多酶促反应所必需的。锌池的改变可能影响肿瘤的生长。我们使用了一种动物模型,我们将吉田肉瘤以腹水形式腹腔内应用于肠外喂养的Sprague-Dawley大鼠。4组10只荷瘤大鼠(TBR)和10只非荷瘤大鼠(NTBR)分别给予不同的肠外营养。高热量组1和低热量组2饲喂无锌饲料。第3组(常热量组)和第3组(低热量组)用高剂量锌(0.519 mg/500 g Kg/d)代替。在第3组中,我们发现了肿瘤肿块的定量和定性最高证据。各组腹水氮含量变化不显著。我们发现锌取代的NTBR重量减轻。在我们的动物模型中,锌改善了肿瘤的合成并导致宿主体重减轻。
[Does varied parenteral zinc administration modify interaction between tumor and host? Studies based on an animal model].
Zinc speeds up a lot of metabolic processes because it is essential for a lot of enzymatic reactions. A modification of the zinc pool may influence the tumor growth. We used an animal model where we applied the Yoshida sarkoma intraperitoneally in its ascites form to parenterally fed Sprague-Dawley rats. Four groups with ten tumor bearing (TBR) and ten non-tumor-bearing rats (NTBR) each received different parenteral nutrition. The normocaloric Group 1 and the hypocaloric (reduced to 1/3 energy) Group 2 were fed without zinc. In Groups 3 (normocaloric) and (hypocaloric) high doses of zinc (0.519 mg/500 g Kg/d) were substituted. In Group 3 we found the quantitatively and qualitatively highest proof of tumor mass. The nitrogen content of the ascites wasn't significantly changed within the groups. We found a weight loss of the NTBR with zinc substitution. Zinc improves the synthesis of the tumor and leads to a weight loss of the host in our animal model.