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Expanding the body mass range: associations between BMR and tissue morphology in wild type and mutant dwarf mice (David mice)

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Abstract

We sought to identify associations of basal metabolic rate (BMR) with morphological traits in laboratory mice. In order to expand the body mass (BM) range at the intra-strain level, and to minimize relevant genetic variation, we used male and female wild type mice (C3HeB/FeJ) and previously unpublished ENU-induced dwarf mutant littermates (David mice), covering a body mass range from 13.5 g through 32.3 g. BMR was measured at 30°C, mice were killed by means of CO2 overdose, and body composition (fat mass and lean mass) was subsequently analyzed by dual X-ray absorptiometry (DEXA), after which mice were dissected into 12 (males) and 10 (females) components, respectively. Across the 44 individuals, 43% of the variation in the basal rates of metabolism was associated with BM. The latter explained 47% to 98% of the variability in morphology of the different tissues. Our results demonstrate that sex is a major determinant of body composition and BMR in mice: when adjusted for BM, females contained many larger organs, more fat mass, and less lean mass compared to males. This could be associated with a higher mass adjusted BMR in females. Once the dominant effects of sex and BM on BMR and tissue mass were removed, and after accounting for multiple comparisons, no further significant association between individual variation in BMR and tissue mass emerged.

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Abbreviations

BAT:

Brown adipose tissue

BM :

Body mass

BMR:

Basal metabolic rate

CET :

Central European time

DEE :

Daily energy expenditure

ENU:

Ethyl-nitroso-urea

eWAT:

Epididymal white adipose tissue

GLM:

General linear modeling

iBAT:

Inter-scapular brown adipose tissue

MR :

Metabolic rate

RMR:

Resting metabolic rate

WAT:

White adipose tissue

WT:

Wildtype

Reference

  • Bartke A, Coschigano K, Kopchick J, Chandrashekar V, Mattison J, Kinney B, Hauck S (2001) Genes that prolong life: relationships of growth hormone and growth to aging and life span. J. Gerontol A Biol Sci Med Sci 56:B340–B349

    PubMed  CAS  Google Scholar 

  • Brommage R (2003) Validation and calibration of DEXA body composition in mice. Am J Physiol Endocrinol Metab 285:E454–E459

    PubMed  CAS  Google Scholar 

  • Butler A, Le Roith D (2001) Control of growth by the somatropic axis: growth hormone and the insulin-like growth factors have related and independent roles. Annu Rev Physiol 63:141–164

    Article  PubMed  CAS  Google Scholar 

  • Cannon B, Nedergaard J (2004) Brown adipose tissue: function and physiological significance. Physiol Rev 84:277–359

    Article  PubMed  CAS  Google Scholar 

  • Daan S, Masman D, Groenewold A (1990) Avian basal metabolic rates: their association with body composition and energy expenditure in nature. Am J Physiol 259:R333–R340

    PubMed  CAS  Google Scholar 

  • Daan S, Masman D, Strijkstra AM, Verhulst S (1989) Intraspecific allometry of basal metabolic rate: relations with body size, temperature, composition, and circadian phase in the Kestrel, Falco tinnunculus. J Biol Rhythms 4(2):267–283

    PubMed  CAS  Google Scholar 

  • Drent RH, Daan S (1980) The prudent parent: energetic adjustments in avian breeding. Ardea 68:225–252

    Google Scholar 

  • Elgar MA, Harvey PH (1987) Basal metabolic rates in mammals: allometry, phylogeny and ecology. Funct Ecol 25–36

  • Field J, Belding HS, Martin AW (1939) An analysis of the relation between basal metabolism and summated tissue respiration in the rat. 1. The post-pubertal albino rat. J Cell Comp Physiol 14:143–157

    Article  CAS  Google Scholar 

  • Foster DO, Frydman ML (1978) Brown adipose tissue: the dominant site of nonshivering thermogenesis in the rat. Experientia Suppl 32:147–151

    PubMed  CAS  Google Scholar 

  • Fuchs H, Schughart K, Wolf E, Balling R, Hrabe dA (2000) Screening for dysmorphological abnormalities—a powerful tool to isolate new mouse mutants. Mamm Genome 11:528–530

    Article  PubMed  CAS  Google Scholar 

  • Geluso K, Hayes JP (1999) Effects of dietary quality on basal metabolic rate and internal morphology of European starlings (Sturnus vulgaris). Physiol Biochem Zool 72:189–197

    Article  PubMed  CAS  Google Scholar 

  • Gillooly JF, Brown JH, West GB, Savage VM, Charnov EL (2001) Effects of size and temperature on metabolic rate. Science 293:2248–2251

    Article  PubMed  CAS  Google Scholar 

  • Glazier DS (2005) Beyond the ‘3/4-power law’: variation in the intra-and interspecific scaling of metabolic rate in animals. Biol Rev Camb Philos Soc 80:611–662

    Article  PubMed  Google Scholar 

  • Hammond KA, Diamond J (1997) Maximal sustained energy budgets in humans and animals. Nature 386:457–462

    Article  PubMed  CAS  Google Scholar 

  • Hart JS (1971) Rodents. In: Whittow GC (ed) Comparative physiology of thermoregulation. Academic, New York , pp 1–149

    Google Scholar 

  • Harvey PH, Pagel MD, Rees JA (1991) Mammalian metabolism and life histories. Am Nat 137:556–566

    Article  Google Scholar 

  • Hayssen V, Lacy RC (1985) Basal metabolic rates in mammals: taxonomic differences in the allometry of BMR and body mass. Comp Biochem Physiol A 81:741–754

    Article  PubMed  CAS  Google Scholar 

  • Heldmaier G (1974) Temperature adaptation and brown adipose tissue in hairless and albino mice. J Comp Physiol 92:281–292

    Article  Google Scholar 

  • Heldmaier G (1975) The effect of short daily cold exposures on development of brown adipose tissue in mice. J Comp Physiol 98:161–168

    Google Scholar 

  • Heldmaier G, Buchberger A (1985) Sources of heat during nonshivering thermogenesis in Djungarian hamsters: a dominant role of brown adipose tissue during cold adaptation. J Comp Physiol [B] 156:237–245

    CAS  Google Scholar 

  • Heldmaier G, Ruf T (1992) Body temperature and metabolic rate during natural hypothermia in endotherms. J Comp Physiol [B] 162:696–706

    CAS  Google Scholar 

  • Hemmingsen AM (1960) Energy metabolism as related to body size and respiratory surfaces, and its evolution. Rep Steno Memorial Hospital Nord Insulin lab 9:1–110

    Google Scholar 

  • Hull KL, Harvey S (1999) Growth hormone resistance: clinical states and animal models. J Endocrinol 163:165–172

    Article  PubMed  CAS  Google Scholar 

  • Johnson MS, Speakman JR (2001) Limits to sustained energy intake. V. Effect of cold-exposure during lactation in Mus musculus. J Exp Biol 204:1967–1977

    PubMed  CAS  Google Scholar 

  • Johnston SL, Peacock WL, Bell LM, Lonchampt M, Speakman JR (2005) PIXImus DXA with different software needs individual calibration to accurately predict fat mass. Obes Res 13:1558–1565

    PubMed  Google Scholar 

  • Kanzleiter T, Schneider T, Walter I, Bolze F, Eickhorst C, Heldmaier G, Klaus S, Klingenspor M (2005) Evidence for Nr4a1 as a cold-induced effector of brown fat thermogenesis. Physiol Genomics 24:37–44

    Article  PubMed  CAS  Google Scholar 

  • Klaus S (2004) Adipose tissue as a regulator of energy balance. Curr Drug Targets 5:241–250

    Article  PubMed  CAS  Google Scholar 

  • Kleiber M (1961) The fire of life. Wiley, New York

    Google Scholar 

  • Klingenspor M (2003) Cold-induced recruitment of brown adipose tissue thermogenesis. Exp Physiol 88:141–148

    Article  PubMed  CAS  Google Scholar 

  • Konarzewski M, Diamond J (1995) Evolution of basal metabolic rate and organ masses in laboratory mice. Evolution 49:1239–1248

    Article  Google Scholar 

  • Koteja P (1996) Limits to energy budget in a rodent (Peromyscus maniculatus): does gut capacity set the limit? Physiol Zool 69:994–1020

    Google Scholar 

  • Krebs HA (1950) Body size and tissue respiration. Biochim Biophys Acta 4:249–269

    Article  PubMed  CAS  Google Scholar 

  • Krol E, Johnson MS, Speakman JR (2003) Limits to sustained energy intake. VIII. Resting metabolic rate and organ morphology of laboratory mice lactating at thermoneutrality. J Exp Biol 206:4283–4291

    Article  PubMed  CAS  Google Scholar 

  • Ksiazek A, Konarzewski M, Lapo IB (2004) Anatomic and energetic correlates of divergent selection for basal metabolic rate in laboratory mice. Physiol Biochem Zool 77:890–899

    Article  PubMed  Google Scholar 

  • Labocha MK, Sadowska ET, Baliga K, Semer AK, Koteja P (2004) Individual variation and repeatability of basal metabolism in the bank vole, Clethrionomys glareolus. Proc Biol Sci 271:367–372

    Article  PubMed  Google Scholar 

  • Laron Z (2002) Growth hormone insensitivity (Laron syndrome). Rev Endocr Metab Disord 3:347–355

    Article  PubMed  CAS  Google Scholar 

  • Lovegrove BG (2000) The zoogeography of mammalian basal metabolic rate. Am Nat 156:201–219

    Article  PubMed  Google Scholar 

  • Lovegrove BG (2003) The influence of climate on the basal metabolic rate of small mammals: a slow-fast metabolic continuum. J Comp Physiol [B] 173:87–112

    CAS  Google Scholar 

  • McNab BK (1986) The influence of food habits on te energetics of eutherian mammals. Ecol Monographs 56:1–19

    Article  Google Scholar 

  • McNab BK (1992) A statistical analysis of mammalian rates of metabolism. Funct Ecol 12:672–679

    Article  Google Scholar 

  • Meerlo P, Bolle L, Visser GH, Masman D, Daan S (1997) Basal metabolic rate in relation to body composition and daily energy expenditure in the field vole, Microtus agrestis. Physiol Zool 70:362–369

    PubMed  CAS  Google Scholar 

  • Meyer CW, Klingenspor M, Rozman J, Heldmaier G (2004) Gene or size: metabolic rate and body temperature in obese growth hormone-deficient dwarf mice. Obes Res 12:1509–1518

    PubMed  CAS  Google Scholar 

  • Munoz-Garcia A, Williams JB (2005) Basal metabolic rate in carnivores is associated with diet after controlling for phylogeny. Physiol Biochem Zool 78:1039–1056

    Article  PubMed  Google Scholar 

  • Nagy TR, Clair AL (2000) Precision and accuracy of dual-energy X-ray absorptiometry for determining in vivo body composition of mice. Obes Res 8:392–398

    Article  PubMed  CAS  Google Scholar 

  • Nespolo RF, Bacigalupe LD, Sabat P, Bozinovic F (2002) Interplay among energy metabolism, organ mass and digestive enzyme activity in the mouse-opossum Thylamys elegans: the role of thermal acclimation. J Exp Biol 205:2697–2703

    PubMed  Google Scholar 

  • Noveroske JK, Weber JS, Justice MJ (2000) The mutagenic action of N-ethyl-N-nitrosourea in the mouse. Mamm Genome 11:478–483

    Article  PubMed  CAS  Google Scholar 

  • Porter RK (2001) Allometry of mammalian cellular oxygen consumption. Cell Mol Life Sci 58:815–822

    Article  PubMed  CAS  Google Scholar 

  • Ricklefs RE, Konarzewski M, Daan S (1996) The relationship between basal metabolic rate and daily energy expenditure in birds and mammals. Am Nat 147:1047–1071

    Article  Google Scholar 

  • Schmid PE, Tokeshi M, Schmid-Araya JM (2000) Relation between population density and body size in stream communities. Science 289:1557–1560

    Article  PubMed  CAS  Google Scholar 

  • Selman C, Korhonen TK, Bunger L, Hill WG, Speakman JR (2001) Thermoregulatory responses of two mouse Mus musculus strains selectively bred for high and low food intake. J Comp Physiol [B] 171:661–668

    CAS  Google Scholar 

  • Silver LM (1995) Mouse genetics. Concepts and applications. Oxford University Press, Oxford

  • Speakman JR, Ergon T, Cavanagh R, Reid K, Scantlebury DM, Lambin X (2003) Resting and daily energy expenditures of free-living field voles are positively correlated but reflect extrinsic rather than intrinsic effects. Proc Natl Acad Sci USA 100:14057–14062

    Article  PubMed  CAS  Google Scholar 

  • Speakman JR, Krol E (2005) Limits to sustained energy intake IX: a review of hypotheses. J Comp Physiol [B] 175:375–394

    Google Scholar 

  • Speakman JR, Krol E, Johnson MS (2004) The functional significance of individual variation in basal metabolic rate. Physiol Biochem Zool 77:900–915

    Article  PubMed  Google Scholar 

  • Speakman JR, McQueenie J (1996) Limits to sustained metabolic rate: the link between food intake, basal metabolic rate, and morphology in reproducing Mice, Mus musculus. Physiol Zool. 69:746–769

    Google Scholar 

  • Storey J (2003) The positive false discovery rate: A Bayesian interpretation and the Q-value. Ann Stat 31:2013–2035

    Article  Google Scholar 

  • White CR, Seymour RS (2003) Mammalian basal metabolic rate is proportional to body mass2/3. Proc Natl Acad Sci USA 100:4046–4049

    Article  PubMed  CAS  Google Scholar 

  • Wiedmer P, Boschmann M, Klaus S (2004) Gender dimorphism of body mass perception and regulation in mice. J Exp Biol 207:2859–2866

    Article  PubMed  Google Scholar 

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Acknowledgments

This work was supported by NGFN2 NeuroNet “Obesity and Related Disorders” (NGFN2 grant 01GS0483 to MK and GH). The authors would like to thank two anonymous reviewers for improving the manuscript.

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Correspondence to Carola W. Meyer.

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Communicated by H.V. Carey.

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Meyer, C.W., Neubronner, J., Rozman, J. et al. Expanding the body mass range: associations between BMR and tissue morphology in wild type and mutant dwarf mice (David mice). J Comp Physiol B 177, 183–192 (2007). https://doi.org/10.1007/s00360-006-0120-9

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  • DOI: https://doi.org/10.1007/s00360-006-0120-9

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