Abstract
To study whether mounting an immune response is energetically costly, mice from two lines divergently selected for high (H-BMR) and low (L-BMR) basal metabolic rate (BMR) were immunized with sheep red blood cells. Their energy budgets were then additionally burdened by sudden transfer from an ambient temperature of 23 degrees C to 5 degrees C. We found that the immune response of H-BMR mice was lower than that of L-BMR mice. However, the interaction between line affiliation and ambient temperature was not significant and cold exposure did not result in immunosuppression in either line. At 23 degrees C the animals of both lines seemed to cover the costs of immune response by increasing food consumption and digestive efficiency. This was not observed at 5 degrees C, so these costs must have been covered at the expense of other components of the energy budget. Cold exposure itself elicited a considerable increase in food intake and the mass of internal organs, which were also heavier in H-BMR than in L-BMR mice. However, irrespective of the temperature or line affiliation, immunized mice had smaller intestines, while cold-exposed immunized mice had smaller hearts. Furthermore, the observed larger mass of the liver and kidneys in immunized mice of both lines kept at 23 degrees C was not observed at 5 degrees C. Hence, immunization compromised upregulation of the function of metabolically active internal organs, essential for meeting the energetic demands of cold. We conclude that the difficulties with a straightforward demonstration of the energetic costs of immune responses in these animals stem from the extreme flexibility of their energy budgets.
Full Text
The Full Text of this article is available as a PDF (293.4 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Cichoń Mariusz, Chadzińska Magdalena, Ksiazek Aneta, Konarzewski Marek. Delayed effects of cold stress on immune response in laboratory mice. Proc Biol Sci. 2002 Jul 22;269(1499):1493–1497. doi: 10.1098/rspb.2002.2054. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Demas G. E., Chefer V., Talan M. I., Nelson R. J. Metabolic costs of mounting an antigen-stimulated immune response in adult and aged C57BL/6J mice. Am J Physiol. 1997 Nov;273(5 Pt 2):R1631–R1637. doi: 10.1152/ajpregu.1997.273.5.R1631. [DOI] [PubMed] [Google Scholar]
- Desjardins P. J., Norris L. H., Cooper S. A., Reynolds D. C. Analgesic efficacy of intranasal butorphanol (Stadol NS) in the treatment of pain after dental impaction surgery. J Oral Maxillofac Surg. 2000 Oct;58(10 Suppl 2):19–26. doi: 10.1053/joms.2000.17884. [DOI] [PubMed] [Google Scholar]
- Hammond K. A., Janes D. N. The effects of increased protein intake on kidney size and function. J Exp Biol. 1998 Jul;201(Pt 13):2081–2090. doi: 10.1242/jeb.201.13.2081. [DOI] [PubMed] [Google Scholar]
- Ots I., Kerimov A. B., Ivankina E. V., Ilyina T. A., Hõrak P. Immune challenge affects basal metabolic activity in wintering great tits. Proc Biol Sci. 2001 Jun 7;268(1472):1175–1181. doi: 10.1098/rspb.2001.1636. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Råberg Lars, Vestberg Mikael, Hasselquist Dennis, Holmdahl Rikard, Svensson Erik, Nilsson Jan-Ake. Basal metabolic rate and the evolution of the adaptive immune system. Proc Biol Sci. 2002 Apr 22;269(1493):817–821. doi: 10.1098/rspb.2001.1953. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Secor S. M., Diamond J. A vertebrate model of extreme physiological regulation. Nature. 1998 Oct 15;395(6703):659–662. doi: 10.1038/27131. [DOI] [PubMed] [Google Scholar]
- Toloza E. M., Lam M., Diamond J. Nutrient extraction by cold-exposed mice: a test of digestive safety margins. Am J Physiol. 1991 Oct;261(4 Pt 1):G608–G620. doi: 10.1152/ajpgi.1991.261.4.G608. [DOI] [PubMed] [Google Scholar]