Skip to main content
Biochemical Journal logoLink to Biochemical Journal
. 1996 Jan 1;313(Pt 1):77–82. doi: 10.1042/bj3130077

Tumour growth results in changes in placental amino acid transport in the rat: a tumour necrosis factor alpha-mediated effect.

N Carbó 1, F J López-Soriano 1, W Fiers 1, J M Argilés 1
PMCID: PMC1216912  PMID: 8546713

Abstract

The implantation of a fast growing tumour (Yoshida AH-130 ascites hepatoma) to late pregnant rats resulted in no changes in fetal growth, this possibly being associated with an important increase in the fetal uptake of maternal-derived amino acids [Carbó, López-Soriano and Argilés (1995) Endocrinology 136, 3579-3584]. The present investigation was undertaken to see whether the presence of the tumour induced changes in placental transport systems. For alanine transport, although no changes in affinity (Km) were observed, tumour growth resulted in a 192% increase in Vmax in the Na(+)-independent component. Kinetic analysis of the Na(+)-dependent component resulted in two clearly different components: while the low-affinity and high-capacity component was unaffected by tumour growth, the high-affinity, low-capacity component of the tumour-bearing rats showed an important increase in Vmax. (78%). With regard to leucine transport, tumour burden induced important increases in the Na(+)-independent component, not only in Km (262%) but also in Vmax. (189%). Since elevated tumour necrosis factor-alpha (TNF) concentrations have been reported in this kind of tumour model, we performed the same type of transport experiments in rats chronically treated with TNF, the results obtained showing great similarities with those observed with tumour growth. The Vmax. of Na(+)-independent alanine transport was also increased by the cytokine (104%) while no changes were observed in affinity. TNF treatment also induced an increase in the Vmax. (67%) of the Na(+)-dependent (high-affinity, low-capacity) component while no changes in affinity were observed. Concerning leucine kinetics, TNF treatment, as in the case of tumour growth, also increased Km (155%) and Vmax. (72%) associated with Na(+)-independent transport. Interestingly, treatment with the cytokine increased both the Km (43%) and Vmax. (64%) of the Na(+)-dependent component. The inhibition patterns suggest the existence of more that one Na(+)-dependent transport for alanine although the majority of the amino acid is transported through the A system. The results presented suggest that, during gestation, the mother is able to adapt her placental amino acid transport systems to compensate for the nitrogen drainage associated with tumour growth and thus provide the fetus with enough amino acids to allow its normal growth, and that TNF could be responsible for the triggering of this compensatory mechanism.

Full Text

The Full Text of this article is available as a PDF (360.2 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. BEATON G. H., BEARE J., RYU M. H., McHENRY E. W. Protein metabolism in the pregnant rat. J Nutr. 1954 Oct 11;54(2):291–304. doi: 10.1093/jn/54.2.291. [DOI] [PubMed] [Google Scholar]
  2. Carbó N., Costelli P., Tessitore L., Bagby G. J., López-Soriano F. J., Baccino F. M., Argilés J. M. Anti-tumour necrosis factor-alpha treatment interferes with changes in lipid metabolism in a tumour cachexia model. Clin Sci (Lond) 1994 Sep;87(3):349–355. doi: 10.1042/cs0870349. [DOI] [PubMed] [Google Scholar]
  3. Carbó N., López-Soriano F. J., Argilés J. M. Administration of tumor necrosis factor-alpha results in a decreased placental transfer of amino acids in the rat. Endocrinology. 1995 Aug;136(8):3579–3584. doi: 10.1210/endo.136.8.7628396. [DOI] [PubMed] [Google Scholar]
  4. Carbó N., López-Soriano F. J., Argilés J. M. The effects of tumour growth on circulating amino acids in the late pregnant rat. Cancer Lett. 1995 Jan 6;88(1):21–25. doi: 10.1016/0304-3835(94)03606-j. [DOI] [PubMed] [Google Scholar]
  5. Carroll M. J., Young M. The relationship between placental protein synthesis and transfer of amino acids. Biochem J. 1983 Jan 15;210(1):99–105. doi: 10.1042/bj2100099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Evans R. D., Argilés J. M., Williamson D. H. Metabolic effects of tumour necrosis factor-alpha (cachectin) and interleukin-1. Clin Sci (Lond) 1989 Oct;77(4):357–364. doi: 10.1042/cs0770357. [DOI] [PubMed] [Google Scholar]
  7. Fisher S. E., Atkinson M., Holzman I., David R., Van Thiel D. H. Effect of ethanol upon placental uptake of amino acids. Prog Biochem Pharmacol. 1981;18:216–223. [PubMed] [Google Scholar]
  8. Glazier J. D., Jones C. J., Sibley C. P. Preparation of plasma membrane vesicles from the rat placenta at term and measurement of Na+ uptake. Placenta. 1990 Sep-Oct;11(5):451–463. doi: 10.1016/s0143-4004(05)80218-8. [DOI] [PubMed] [Google Scholar]
  9. Glazier J. D., Jones C. J., Sibley C. P. Purification and Na+ uptake by human placental microvillus membrane vesicles prepared by three different methods. Biochim Biophys Acta. 1988 Nov 22;945(2):127–134. doi: 10.1016/0005-2736(88)90475-0. [DOI] [PubMed] [Google Scholar]
  10. Gresham E. L., Simons P. S., Battaglia F. C. Maternal-fetal urea concentration difference in man: metabolic significance. J Pediatr. 1971 Nov;79(5):809–811. doi: 10.1016/s0022-3476(71)80396-7. [DOI] [PubMed] [Google Scholar]
  11. Hunt J. S., Atherton R. A., Pace J. L. Differential responses of rat trophoblast cells and embryonic fibroblasts to cytokines that regulate proliferation and class I MHC antigen expression. J Immunol. 1990 Jul 1;145(1):184–189. [PubMed] [Google Scholar]
  12. LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
  13. Lemons J. A., Schreiner R. L. Amino acid metabolism in the ovine fetus. Am J Physiol. 1983 May;244(5):E459–E466. doi: 10.1152/ajpendo.1983.244.5.E459. [DOI] [PubMed] [Google Scholar]
  14. Mayel-Afshar S., Grimble R. F. Tyrosine oxidation and protein turnover in maternal tissues and the fetus during pregnancy in rats. Biochim Biophys Acta. 1982 May 27;716(2):201–207. doi: 10.1016/0304-4165(82)90269-0. [DOI] [PubMed] [Google Scholar]
  15. Philipps A. F., Rosenkrantz T. S., Porte P. J., Raye J. R. The effects of chronic fetal hyperglycemia on substrate uptake by the ovine fetus and conceptus. Pediatr Res. 1985 Jul;19(7):659–666. doi: 10.1203/00006450-198507000-00005. [DOI] [PubMed] [Google Scholar]
  16. Schuger L., Varani J., Marks R. M., Kunkel S. L., Johnson K. J., Ward P. A. Cytotoxicity of tumor necrosis factor-alpha for human umbilical vein endothelial cells. Lab Invest. 1989 Jul;61(1):62–68. [PubMed] [Google Scholar]
  17. Silen M. L., Firpo A., Morgello S., Lowry S. F., Francus T. Interleukin-1 alpha and tumor necrosis factor alpha cause placental injury in the rat. Am J Pathol. 1989 Aug;135(2):239–244. [PMC free article] [PubMed] [Google Scholar]
  18. Singh J., Grigor M. R., Thompson M. P. Glucose tolerance and hormonal changes in rats bearing a transplantable sarcoma. Int J Biochem. 1981;13(10):1095–1100. doi: 10.1016/0020-711x(81)90172-5. [DOI] [PubMed] [Google Scholar]
  19. Stevens B. R., Kaunitz J. D., Wright E. M. Intestinal transport of amino acids and sugars: advances using membrane vesicles. Annu Rev Physiol. 1984;46:417–433. doi: 10.1146/annurev.ph.46.030184.002221. [DOI] [PubMed] [Google Scholar]
  20. Tessitore L., Bonelli G., Baccino F. M. Early development of protein metabolic perturbations in the liver and skeletal muscle of tumour-bearing rats. A model system for cancer cachexia. Biochem J. 1987 Jan 1;241(1):153–159. doi: 10.1042/bj2410153. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Vengesa P. B., Hopfer U. Cytochemical localization of alkaline phosphatase and Na+-pump sites in adult rat colon. J Histochem Cytochem. 1979 Sep;27(9):1231–1235. doi: 10.1177/27.9.39100. [DOI] [PubMed] [Google Scholar]
  22. Williamson D. H., Evans R. D., Wood S. C. Tumor growth and lipid metabolism during lactation in the rat. Adv Enzyme Regul. 1988;27:93–104. doi: 10.1016/0065-2571(88)90011-8. [DOI] [PubMed] [Google Scholar]

Articles from Biochemical Journal are provided here courtesy of The Biochemical Society

RESOURCES