A new experimental model of human cachexia.

Investigative & cell pathology Pub Date : 1979-04-01
A J Strain, G C Easty, A M Neville
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Abstract

A hypernephroma removed from a male patient who had lost 30 kg in weight in the two months preceding surgery was grown as a non-metastasizing transplantable xenograft in immune-suppressed mice. The tumour produced a considerable weight loss (greater than 25 per cent) in the mice at a stage when it comprised less than 5 per cent of the total body weight. A slight fall in food intake of the tumour-bearing mice was noted, but animals bearing other non-cachectic mouse and human tumours had much lower food intakes without accompanying weight loss. No obvious defects in gastrointestinal absorption were detected nor was any gross increase in basal metabolic rate observed. The precise mechanism producing the severe cachexia remains to be established, but elaboration of humoral factors by the tumour seems probable. This model of cachexia bears a closer relation to the clinical situation than do other experimental animal tumour models currently available.

一种新的人类恶病质实验模型。
一名男性患者在手术前两个月体重减轻了30公斤,从患者身上切除的高肾瘤在免疫抑制小鼠体内生长为非转移性可移植异种移植物。在肿瘤占小鼠总体重不到5%的阶段,肿瘤使小鼠的体重减轻了相当大的幅度(超过25%)。携带肿瘤的小鼠的食物摄入量略有下降,但携带其他非恶病性小鼠和人类肿瘤的动物的食物摄入量要低得多,但体重却没有减轻。没有发现胃肠道吸收的明显缺陷,也没有观察到基础代谢率的明显增加。产生严重恶病质的确切机制仍有待确定,但肿瘤对体液因素的阐述似乎是可能的。这种恶病质模型比目前可用的其他实验动物肿瘤模型与临床情况的关系更密切。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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