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Anatomic and energetic correlates of divergent selection for basal metabolic rate in laboratory mice.

The aerobic capacity model postulates that high basal metabolic rates (BMR) associated with endothermy evolved as a correlated response to the selection on maximum, peak metabolic rate Vo2max. Furthermore, the model assumes that BMR and Vo2max are causally linked, and therefore, evolutionary changes in their levels cannot occur independently. To test this, we compared metabolic and anatomical correlates of selection for high and low body mass-corrected BMR in males of laboratory mice of F18 and F19 selected generations. Divergent selection resulted in between-line difference in BMR equivalent to 2.3 phenotypic standard deviation units. Vo2max elicited by forced swimming in 20 degrees C water was higher in the low BMR than high BMR line and did not differ between the lines when elicited by exposure to heliox at -2.5 degrees C. Moreover, the magnitude of swim- and heliox-induced hypothermia was significantly smaller in low BMR mice, whereas their interscapular brown adipose tissue was larger than in high BMR mice. Our results are therefore at variance with the predictions of aerobic capacity model. The selection also resulted in correlated response in food consumption (C) and masses of metabolically active internal organs: kidneys, liver, small intestine, and heart, which fuel maximum, sustained metabolic rate (SusMR) rather than Vo2max. These correlated responses were strong enough to claim the existence of positive, genetic correlations between BMR and the mass of viscera as well as C. Thus, our findings support the suggestion that BMR evolved as a correlated response to selection for SusMR, not Vo2max. In functional terms BMR should therefore be interpreted as a measure of energetic costs of maintenance of metabolic machinery necessary to sustain high levels of energy assimilation rate.

Adaptation, Physiological↗

Climatic influences on basal metabolic rates among circumpolar populations.

This article examines evidence for elevations in basal metabolic rate (BMR) among indigenous Northern (circumpolar) populations and considers potential mechanisms and the adaptive basis for such elevations. Data on BMR among indigenous (n = 109 males; 122 females) and nonindigenous (n = 15 males; 22 females) circumpolar groups of North America and Siberia are compiled and compared to predicted BMRs based on three different references: body surface area (Consolazio et al., 1963), body mass (Schofield, 1985), and fat-free mass (Poehlman and Toth, 1995). Regardless of which reference is used, indigenous circumpolar groups show systematic and statistically significant elevations in BMR ranging from +7% to +19% above predicted values for indigenous men and from +3 to +17% for indigenous women. Nonindigenous males also show elevations in BMR, although not to the same extent as in indigenous men (deviations = +3 to +14%), whereas nonindigenous females show no clear evidence of elevated BMRs (deviations = -7 to +5%). This pattern of variation between indigenous and nonindigenous groups suggests that both functional and genetic factors play a role in metabolic adaptation to northern climes. Recent studies on the ecology and genetics of thyroid function offer insights into the mechanisms through which indigenous circumpolar populations may regulate metabolic rates. Studies of seasonal variation in thyroid hormone levels suggest that indigenous circumpolar populations may have a greater capacity to elevate BMR during severe cold than nonindigenous groups. Recent twin studies indicate a significant genetic component of thyroid responses to environmental stressors. Further research exploring the genetics of seasonal variation in thyroid function and BMR among circumpolar groups would advance understanding of the role that selection may have played in shaping metabolic variation.

Acclimatization↗

The influence of different methods on basal metabolic rate measurements in human subjects.

While collating basal metabolic rate (BMR) measurements made worldwide it becomes important to know how different instruments compare with each other and whether errors in methodology could account for the differences in BMRs measured. BMRs of 34 healthy individuals were measured by using five different instruments in various combinations. Results show that energy outputs were comparable between the oxylog. Hartmann and Braun Metabolator, ventilated tent and hood, and whole-body indirect calorimeter: small differences, if any, were not statistically significant. However, significant interactions existed between subjects with the ventilated tent and hood and calorimeter when measurements were taken in subjects who were unaccustomed to the apparatus. When converting O2-consumption measurements to energy output, some instruments make assumptions that introduce a variable error in the final result, which may lead to systematic errors during the compilation of large databases of human BMRs.

Adult↗

Long-term repeatability makes basal metabolic rate a likely heritable trait in the zebra finch Taeniopygia guttata.

Basal metabolic rate (BMR) is a physiological trait believed to show adaptational changes. Few studies have tested whether BMR shows stable between-individual variations. Repeatability indicates that the trait might be heritable and therefore a possible target for natural selection. We tested whether BMR was repeatable over a considerable time of the lifespan of a small passerine bird: the zebra finch Taeniopygia guttata. BMR was measured six times over a 2.5 year period in captive zebra finches. BMR residuals showed significant repeatabilities over a short (1.5 months) and a long (2.5 years) period for each sex as well as for both sexes pooled. In contrast to earlier studies on metabolism, our calculated repeatability (R) did not change significantly from the short to the long period in either males (R from 0.501 to 0.465), females (R from 0.413 to 0.522) or the pooled data (R from 0.571 to 0.567). Our results show that there are consistent between-individual variations in BMR on which natural selection can work, provided that this trait is heritable.

Adaptation, Physiological↗

Basal metabolic rate of normal and marginally undernourished mestizo children in Colombia.

The basal metabolic rate (BMR) was measured in mestizo children 6-16 years of age living under economically deprived conditions in Colombia. Of a total of 239 boys and 126 girls, 137 boys and 72 girls were classified as marginally malnourished. Differences in BMR by age, sex and nutritional group could be accounted for by differences in lean body mass. The Schofield equations were found to overestimate BMR significantly in the boys. However, the estimates in girls were not significantly different from measured values.

Adolescent↗

The difference between the basal metabolic rate and the sleeping metabolic rate in Japanese.

Previous studies have demonstrated the difference between the basal metabolic rate (BMR) and the sleeping metabolic rate (SMR): however, the difference in the Japanese population has not yet been explored. This study examined the relationship between the BMR and SMR in ninety-four healthy Japanese subjects (37 males and 57 females, 39 +/- 12 y of age and 22.0 +/- 7.4% body fat) in a respiratory chamber. The SMR was significantly lower than the BMR (1416 +/- 245 vs. 1492 +/- 256 kcal/d): however, there was a highly significant correlation between the two (r = 0.867; p < 0.001). The ratio of SMR/BMR largely varied among individuals (0.95 +/-0.08, 8.4% of the coefficient of variation). The ratio was significantly lower in males than in females (0.93 +/- 0.10 vs. 0.97 +/- 0.06, p < 0.05). None of the anthropometric measures (age, weight, body mass index, body surface area or percent body fat) correlated with the ratio. These results showed that SMR was 95%, of BMR on average in a healthy Japanese group. However, when applied over a longer time period (24 h or more), the difference tends to become negligible for most analyses in a group. Although the difference between SMR and BMR will induce a 5% gap of physical activity level defined as the total energy expenditure divided by the BMR or SMR, this factor seems to have little practical importance in epidemiological research.

Adult↗

Effects of body mass and reproduction on the basal metabolic rate of brown long-eared bats (Plecotus auritus).

We measured basal metabolic rate (BMR) of nonreproductive and of breeding (pregnant and lactating) female brown long-eared bats (Plecotus auritus) to investigate the effects of intra- and interindividual variation in body mass and of reproduction on metabolism. The BMR of six nonreproductive females was measured between five and seven times at approximately 2-wk intervals over a period of 2.5 mo. There was a highly significant effect (P<0.001) of body mass on BMR of these nonreproductive females. The pooled within-individual scaling exponent (1.88) significantly exceeded the established mammalian interspecific exponent (0.75). In addition, we made single observations on 14 nonreproductive females to establish the effects of differences in mass between individuals. The mean BMR across all 14 individuals was 82 mW (+/-24 SD). There was a significant positive relationship between BMR and body mass across these individuals (r2=0.39), with a between-individual scaling exponent of 0.75. Inter- and intraindividual effects of mass on BMR were combined in a regression analysis that included mean body mass and deviation from mean mass on any given day as predictors. This regression model explained 55% of the variation in BMR. We made longitudinal measurements of BMR throughout reproduction and compared these with the predicted BMR of nonreproductive bats of the same body mass. Reproductive females exhibited temporal flexibility in BMR. BMR during pregnancy increased on a whole-animal basis but was significantly lower (by, on average, 15%) than BMR predicted for nonreproductive females of the same mass. Over a period of 1-75 d following birth, whole-animal BMR was greater than that during pregnancy, even though body mass declined after parturition. Hence, postbirth BMR was greater than the level predicted for nonreproductive females of the same mass. This study indicates that the scaling of BMR with body mass differs significantly within and between individuals and that there is a reduction of BMR in pregnancy and an elevation of BMR during lactation.

Animals↗

Additional anthropometric measures may improve the predictability of basal metabolic rate in adult subjects.

BACKGROUND: The most commonly used predictive equation for basal metabolic rate (BMR) is the Schofield equation, which only uses information on body weight, age and sex to derive the prediction. However, because body composition is a key influencing factor, there will be error in calculating an individual's basal requirements based on this prediction. OBJECTIVE: To investigate whether adding additional anthropometric measures to the standard measures can enhance the predictability of BMR and to cross-validate this within a separate subgroup. DESIGN: Cross-sectional study of 150 Caucasian adults from Scotland, with a body mass index range of 16.7-49.3 kg/m(2). All subjects underwent measurement of BMR, body composition, and 148 also had basic skinfold and circumference measures taken. The resultant equation was tested in a subgroup of 39 obese males. RESULTS: The average difference between the predicted (Schofield equation) and measured BMR was 502 kJ/day. There was a slight systematic bias in this error, with the Schofield equation underestimating the lowest values. The average discrepancy between predicted and actual BMR was reduced to 452 kJ/day, with the addition of fat mass, fat-free mass, an overall 10% improvement on the Schofield equation (P=0.054). Using an equation derived from principal components analysis of anthropometry measurements similarly decreased the difference to 458 kJ/day (P=0.039). Testing the equation in a separate group indicated a 33% improvement in predictability of BMR, compared to the Schofield equation. CONCLUSIONS: In the absence of detailed information on body composition, utilizing anthropometric data provides a useful alternative methodology to improve the predictability of BMR beyond that achieved from the standard Schofield prediction equation. This should be confirmed in more individuals, both within the obese and normal weight category.

Adult↗

Basal metabolic rate and the evolution of the adaptive immune system.

Vertebrates have evolved an adaptive immune system in addition to the ancestral innate immune system. It is often assumed that a trade-off between costs and benefits of defence governs the evolution of immunological defence, but the costs and benefits specific to the adaptive immune system are poorly known. We used genetically engineered mice lacking lymphocytes (i.e. mice without adaptive, but with innate, immunity) as a model of the ancestral state in the evolution of the vertebrate immune system. To investigate if the magnitude of adaptive defence is constrained by the energetic costs of producing lymphocytes etc., we compared the basal metabolic rate of normal and lymphocyte-deficient mice. We found that lymphocyte-deficient mice had a higher basal metabolic rate than normal mice with both innate and adaptive immune defence. This suggests that the evolution of the adaptive immune system has not been constrained by energetic costs. Rather, it should have been favoured by the energy savings associated with a combination of innate and adaptive immune defence.

Adaptation, Physiological↗

Basal metabolic state of hearts of patients with congenital heart disease: the effects of cyanosis, age, and pathology.

BACKGROUND: Experimental models have established numerous myocardial metabolic changes with chronic hypoxia and maturation. We conducted this study to specifically look at the effects of cyanosis, age, and pathology upon the basal metabolic state of the immature human heart. METHODS: One hundred and eighty-one pediatric patients (37 cyanotic, 144 acyanotic) undergoing open heart surgery were recruited. A myocardial biopsy was collected before ischemia and analyzed for adenine nucleotides, purines, and lactate. The effect of cyanosis was estimated by an analysis of age-matched pairs of children with either ventricular septal defects or tetralogy of Fallot, and by multiple regression modeling. The effects of age and pathology were estimated in acyanotic children also by multiple regression modeling (adjustments were made for baseline differences). RESULTS: The only effect of cyanosis was for lactate where the paired t test, and unadjusted and adjusted regression analyses were all consistent (ranging from 1.33 to 1.48 times higher in cyanotic than acyanotic children). The concentrations of adenosine triphosphate (ATP), adenosine diphosphate (ADP), and adenosine monophosphate (AMP) declined with age, whereas the ATP/ADP ratio increased; these associations remained significant even in the adjusted regression analysis. None of the effects of acyanotic pathology were highly significant (p < 0.01), implying that few important metabolic differences were attributable to pathology. CONCLUSIONS: Cyanosis and age are important factors that determine the basal metabolic state of the pediatric heart. Cyanotic patients have higher myocardial lactate concentrations, whereas young age is associated with lower ATP/ADP ratios and higher adenine nucleotide levels.

Adenine Nucleotides↗

A reanalysis of the factors influencing basal metabolic rate in normal adults.

A multiple regression analysis of several factors influencing basal metabolic rate (BMR) was performed using data for 223 subjects from the classic metabolism studies published by Harris and Benedict in 1919. These data had previously been analyzed by Kleiber using metabolic body size, the three-fourths power of body mass, as a predictor of BMR. His prediction equations were separated by sex and each contained components for age and height. Factors in the present analysis included sex, age, height, body mass, and estimated lean body mass (LBM). Lean body mass was found to be the single predictor of BMR. A best estimate prediction equation: BMR(cal/day) = 500 + 22 (LBM) is proposed. The previously presumed influences of sex and age are shown to add little to this estimation.

Adolescent↗

[Historical and methodological aspects of the measurement and prediction of basal metabolic rate: a review].

This paper reviews the most relevant aspects of measuring basal metabolic rate (BMR). The authors discuss individual and lifestyle factors (age, anthropometry, smoking, physical activity, diet, menses, and ethnicity) as well as possible environmental factors at time of measurement which may alter BMR values. Various available predictive equations, especially those recommended by the World Health Organization in 1985, and subsequent validation studies, particularly in populations living in the tropics, are presented. The review indicates the need for more information on BMR from populations living in different parts of the world so that better estimates can be provided for clinicians and epidemiologists.

Age Factors↗

Basal metabolic rate, fat-free mass, and body cell mass during energy restriction.

Basal metabolic rate (BMR) has been reported to decrease during semistarvation and during hypocaloric treatment of obesity. However, it remains controversial whether the decrease is due to change in body composition, or if it represents a downregulation in cellular metabolism. To examine this relationship, we reviewed studies of BMR in children, adolescents, adults, semistarved non-obese, anorexics, and weight-reducing obese. The relationship between BMR and fat-free mass (FFM) of children, lean adolescents, and lean and obese adults consuming sufficient energy could be described by a single line, BMR (MJ/d) = 2.44 + 0.084 FFM (SEE = 0.63, R2 = .80). Obese adolescents demonstrated BMRs greater than predicted and semistarved lean individuals demonstrated BMRs less than predicted by this relationship. Obese individuals demonstrated a reduced BMR during underfeeding, but less so than semistarved lean individuals. The reduction in BMR relative to FFM in semistarved lean individuals could not be explained by disproportionate reductions in body cell mass (BCM).

Adipose Tissue↗