Mitochondrial metabolism in blood more reliably predicts whole-animal energy needs compared to other tissues.

Understanding energy metabolism in free-ranging animals is crucial for ecological studies. In birds, red blood cells (RBCs) offer a minimally invasive method to estimate metabolic rate (MR). In this study with European starlings Sturnus vulgaris, we examined how RBC oxygen consumption relates to oxygen use in key tissues (brain, liver, heart, and pectoral muscle) and versus the whole organism measured at basal levels. The pectoral muscle accounted for 34%-42% of organismal MR, while the heart and liver, despite their high mass-specific metabolic rate, each contributed 2.5%-3.0% to organismal MR. Despite its low contribution to organismal MR (0.03%-0.04%), RBC MR best predicted organismal MR (r = 0.70). Oxygen consumption of the brain and pectoralis was also associated with whole-organism MR, unlike that of heart and liver. Overall, our findings demonstrate that the metabolism of a systemic tissue like blood is a superior proxy for organismal energy metabolism than that of other tissues.

Quantifying Glucocorticoid Plasticity Using Reaction Norm Approaches: There Still is So Much to Discover!

Hormones are highly responsive internal signals that help organisms adjust their phenotype to fluctuations in environmental and internal conditions. Our knowledge of the causes and consequences of variation in circulating hormone concentrations has improved greatly in the past. However, this knowledge often comes from population-level studies, which generally tend to make the flawed assumption that all individuals respond in the same way to environmental changes. Here, we advocate that we can vastly expand our understanding of the ecology and evolution of hormonal traits once we acknowledge the existence of individual differences by quantifying hormonal plasticity at the individual level, where selection acts. In this review, we use glucocorticoid (GC) hormones as examples of highly plastic endocrine traits that interact intimately with energy metabolism but also with other organismal traits like behavior and physiology. First, we highlight the insights gained by repeatedly assessing an individual's GC concentrations along a gradient of environmental or internal conditions using a "reaction norm approach." This study design should be followed by a hierarchical statistical partitioning of the total endocrine variance into the among-individual component (individual differences in average hormone concentrations, i.e., in the intercept of the reaction norm) and the residual (within-individual) component. The latter is ideally further partitioned by estimating more precisely hormonal plasticity (i.e., the slope of the reaction norm), which allows to test whether individuals differ in the degree of hormonal change along the gradient. Second, we critically review the published evidence for GC variation, focusing mostly on among- and within-individual levels, finding only a good handful of studies that used repeated-measures designs and random regression statistics to investigate GC plasticity. These studies indicate that individuals can differ in both the intercept and the slope of their GC reaction norm to a known gradient. Third, we suggest rewarding avenues for future work on hormonal reaction norms, for example to uncover potential costs and trade-offs associated with GC plasticity, to test whether GC plasticity varies when an individual's reaction norm is repeatedly assessed along the same gradient, whether reaction norms in GCs covary with those in other traits like behavior and fitness (generating multivariate plasticity), or to quantify GC reaction norms along multiple external and internal gradients that act simultaneously (leading to multidimensional plasticity). Throughout this review, we emphasize the power that reaction norm approaches offer for resolving unanswered questions in ecological and evolutionary endocrinology.

Inferring Whole-Organism Metabolic Rate From Red Blood Cells in Birds.

Metabolic rate is a key ecological variable that quantifies the energy expenditure needed to fuel almost all biological processes in an organism. Metabolic rates are typically measured at the whole-organism level (woMR) with protocols that can elicit stress responses due to handling and confinement, potentially biasing resulting data. Improved, non-stressful methodology would be especially valuable for measures of field metabolic rate, which quantifies the energy expenditure of free-living individuals. Recently, techniques to measure cellular metabolic rate (cMR) in mitochondria of blood cells have become available, suggesting that blood-based cMR can be a proxy of organismal aerobic performance. Aerobic metabolism actually takes place in the mitochondria. Quantifying cMR from blood samples offers several advantages such as direct estimates of metabolism and minimized disturbance of individuals. To our knowledge, the hypothesis that blood-based cMR correlates with woMR has not yet been directly tested. We measured cMR in red blood cells of captive great tits (Parus major), first during their morning activity period and second after subjecting them to a 2.5 h day-time respirometry protocol to quantify woMR. We predicted cMR to decrease as individuals transitioned from an active to a resting state. In the two blood samples we also assessed circulating corticosterone concentrations to determine the perceived disturbance of individuals. From respirometry traces we extracted initial and final woMR measures to test for a predicted positive correlation with cMR measures, while accounting for corticosterone concentrations. Indeed, cMR declined from the first to the second measurement. Furthermore, woMR and cMR were positively related in individuals that had relatively low corticosterone concentrations and displayed little locomotor activity throughout respirometry. By contrast, woMR and cMR covaried negatively in birds that increased corticosterone concentrations and activity levels substantially. Our results show that red blood cell cMR represents a proxy for woMR when birds do not display signs of stress, i.e., either before increases in hormonal or behavioral parameters have occurred or after they have abated. This method represents a valuable tool for obtaining metabolic data repeatedly and in free-living individuals. Our findings also highlight the importance of accounting for individual stress responses when measuring metabolic rate at any level.

A comprehensive statistical classifier of foci in the cell transformation assay for carcinogenicity testing.

The identification of the carcinogenic risk of chemicals is currently mainly based on animal studies. The in vitro Cell Transformation Assays (CTAs) are a promising alternative to be considered in an integrated approach. CTAs measure the induction of foci of transformed cells. CTAs model key stages of the in vivo neoplastic process and are able to detect both genotoxic and some non-genotoxic compounds, being the only in vitro method able to deal with the latter. Despite their favorable features, CTAs can be further improved, especially reducing the possible subjectivity arising from the last phase of the protocol, namely visual scoring of foci using coded morphological features. By taking advantage of digital image analysis, the aim of our work is to translate morphological features into statistical descriptors of foci images, and to use them to mimic the classification performances of the visual scorer to discriminate between transformed and non-transformed foci. Here we present a classifier based on five descriptors trained on a dataset of 1364 foci, obtained with different compounds and concentrations. Our classifier showed accuracy, sensitivity and specificity equal to 0.77 and an area under the curve (AUC) of 0.84. The presented classifier outperforms a previously published model.