Mahaffey S M, Copeland E M, Economides E, Talbert J L, Baumgartner T G, Sitren H S
J Surg Res. 1987 Feb;42(2):159-65. doi: 10.1016/0022-4804(87)90114-4.
The influence of alternate forms of nutritional support on primary tumor growth rate, tumor DNA synthesis rate, and number of lung metastases was examined in Swiss mice bearing subcutaneously implanted Lewis lung carcinoma (LLC). From Day 14 through 22 postimplant, mice were fed by continuous intravenous infusion of dextrose/amino acid (TPN), were offered the same solution from a feeding bottle (PO), were offered a casein-based, solid diet (CASEIN), or were infused with an electrolyte (ELECT) solution while energy and nitrogen were provided from the casein diet. Tumor weight and doubling time were decreased in the PO group compared to CASEIN; however, host weight decreased by 22% in the PO group. Tumor weight and DNA synthesis were decreased in the TPN group compared to CASEIN, and host weight increased by 4.6%. The decreased rate of tumor growth in the PO group was not reflected in a decrease in DNA synthesis, perhaps a result of the circadian pattern of DNA synthesis as previously reported for LLC. The number of metastatic lung nodules was significantly decreased in both the TPN and ELECT groups compared to PO and CASEIN, suggesting that intravenous fluid load rather than nutrient intake was the causative factor. In this host-tumor system, parenteral feeding was associated with a decrease in primary tumor weight and DNA synthesis rate, maintenance of host weight, and a decrease in pulmonary metastatic disease compared to mice fed a conventional diet.
在皮下植入Lewis肺癌(LLC)的瑞士小鼠中,研究了不同形式的营养支持对原发性肿瘤生长速率、肿瘤DNA合成速率和肺转移数量的影响。从植入后第14天到第22天,通过持续静脉输注葡萄糖/氨基酸(全胃肠外营养,TPN)喂养小鼠,或从奶瓶中给予相同溶液(经口,PO),或给予基于酪蛋白的固体饮食(酪蛋白,CASEIN),或输注电解质(ELECT)溶液,同时从酪蛋白饮食中提供能量和氮。与酪蛋白组相比,经口组的肿瘤重量和倍增时间降低;然而,经口组的宿主体重下降了22%。与酪蛋白组相比,全胃肠外营养组的肿瘤重量和DNA合成降低,宿主体重增加了4.6%。经口组肿瘤生长速率的降低并未反映在DNA合成的降低上,这可能是如先前报道的LLC中DNA合成昼夜模式的结果。与经口组和酪蛋白组相比,全胃肠外营养组和电解质组的肺转移结节数量均显著减少,表明静脉液体负荷而非营养摄入是致病因素。在这个宿主-肿瘤系统中,与喂食传统饮食的小鼠相比,肠外营养与原发性肿瘤重量和DNA合成速率的降低、宿主体重的维持以及肺转移疾病的减少有关。