Literature DB >> 3476146

The significance of learned food aversions in the aetiology of anorexia associated with cancer.

J A Levine, P W Emery.   

Abstract

The results of 24 h food preference tests have suggested that learned food aversions may be involved in the development of anorexia in tumour bearing rats and in patients with cancer. We have performed similar tests over longer periods, up to 10 days, in male rats implanted with Leydig cell tumours, using semisynthetic diets containing differing proportions of fat, protein and carbohydrate. Tumour growth caused anorexia (16-30% decrease in food intake) and cachexia (78% decrease in body fat and 18% decrease in body protein, but 16% increase in body water). Both tumour bearing and control rats preferred a high carbohydrate diet to a high fat diet regardless of their previous diet: tumour bearing rats showed no evidence of a learned food aversion in these experiments. Tumour bearing rats did show an initial preference for a novel high protein diet when this was offered as an alternative to the normal protein diet they had previously been consuming, but this apparent learned food aversion disappeared on the second day of the test and was in fact reversed on all the subsequent days of the test. However, tumour bearing rats did show a sustained preference for a novel low protein diet when this was offered as an alternative to the normal protein diet they had previously been consuming. These results suggest that anorexia in the tumour bearing rats was not caused by a learned food aversion. However the results do indicate that the tumour bearing rats may have developed a specific aversion to protein in the diet. Leydig cell tumours are known to secrete large amounts of oestradiol. However injections of oestradiol in normal male rats caused an increase in body fat content and had no effect on the rats' preference for dietary protein. Clearly hypersecretion of oestradiol was not responsible for the loss of body fat, the fluid retention and the aversion to dietary protein which characterised the tumour bearing rats. The mechanisms by which tumour growth causes anorexia and cachexia in these rats remains obscure.

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Year:  1987        PMID: 3476146      PMCID: PMC2001665          DOI: 10.1038/bjc.1987.157

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  15 in total

1.  Different patterns of protein turnover in skeletal and gastrointestinal smooth muscle and the production of N tau-methylhistidine during fasting in the rat.

Authors:  P W Emery; L Cotellessa; M Holness; C Egan; M J Rennie
Journal:  Biosci Rep       Date:  1986-02       Impact factor: 3.840

Review 2.  Cachexia, the metabolic component of neoplastic diseases.

Authors:  G Costa
Journal:  Cancer Res       Date:  1977-07       Impact factor: 12.701

3.  Ovarian-adrenal interactions in regulation of body weight by female rats.

Authors:  D G Mook; N J Kenney; S Roberts; A I Nussbaum; W I Rodier
Journal:  J Comp Physiol Psychol       Date:  1972-11

4.  Protein-calorie undernutrition in hospitalized cancer patients.

Authors:  D W Nixon; S B Heymsfield; A E Cohen; M H Kutner; J Ansley; D H Lawson; D Rudman
Journal:  Am J Med       Date:  1980-05       Impact factor: 4.965

5.  A salt mixture supplying the national research council estimates of the mineral requirements of the rat.

Authors:  F W Bernhart; R M Tomarelli
Journal:  J Nutr       Date:  1966-08       Impact factor: 4.798

6.  A Leydig cell tumour: a model for the study of lutropin action.

Authors:  B A Cooke; L M Lindh; F H Janszen; M J van Driel; C P Bakker; M P van der Plank; H J van der Molen
Journal:  Biochim Biophys Acta       Date:  1979-03-22

7.  Comparative response of castrate and intact male rats to diethylstilbestrol.

Authors:  P E Moffitt; G R Wilson; R L Preston
Journal:  Proc Soc Exp Biol Med       Date:  1975-03

8.  Energy balances in obese mice.

Authors:  A Djazayery; D S Miller; M J Stock
Journal:  Nutr Metab       Date:  1979       Impact factor: 4.169

9.  Effect of glucocorticoid administration on the rate of muscle protein breakdown in vivo in rats, as measured by urinary excretion of N tau-methylhistidine.

Authors:  F M Tomas; H N Munro; V R Young
Journal:  Biochem J       Date:  1979-01-15       Impact factor: 3.857

10.  Tumor anorexia: a learned food aversion?

Authors:  I L Bernstein; R A Sigmundi
Journal:  Science       Date:  1980-07-18       Impact factor: 47.728

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