The secretion of glucocorticoids (GCs) is a classic endocrine response to stress. Despite that, it remains controversial as to what purpose GCs serve at such times. One view, stretching back to the time of Hans Selye, posits that GCs help mediate the ongoing or pending stress response, either via basal levels of GCs permitting other facets of the stress response to emerge efficaciously, and/or by stress levels of GCs actively stimulating the stress response. In contrast, a revisionist viewpoint posits that GCs suppress the stress response, preventing it from being pathologically overactivated. In this review, we consider recent findings regarding GC action and, based on them, generate criteria for determining whether a particular GC action permits, stimulates, or suppresses an ongoing stressresponse or, as an additional category, is preparative for a subsequent stressor. We apply these GC actions to the realms of cardiovascular function, fluid volume and hemorrhage, immunity and inflammation, metabolism, neurobiology, and reproductive physiology. We find that GC actions fall into markedly different categories, depending on the physiological endpoint in question, with evidence for mediating effects in some cases, and suppressive or preparative in others. We then attempt to assimilate these heterogeneous GC actions into a physiological whole. (Endocrine Reviews 21: 55‐ 89, 2000)

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How do glucocorticoids influence stress responses? Integrating permissive, suppressive, stimulatory, and preparative actions.

A DNA test to sex most birds.

ION, GENERAL CONCEPTIONS, SELF-CONSCIOUSNESS, MENTAL INDIVIDUALITY. It would be very difficult for any one with even much more knowledge than I possess, to determine how far animals exhibit any traces of these high mental powers. This difficulty arises from the impossibility of judging what passes through the mind of an animal; and again, the fact that writers differ to a great extent in the meaning which they attribute to the above terms, causes a further difficulty. If one may judge from various articles which have been published lately, the greatest stress seems to be laid on the supposed entire absence in animals of the power of abstraction, or of forming general concepts. But when a dog sees another dog at a distance, it is often clear that he perceives that it is a dog in the abstract; for when he gets nearer his whole manner suddenly changes, if the other dog be a friend. A recent writer remarks, that in all such cases it is a pure assumption to assert that the mental act is not essentially of the same nature in the animal as in man. If either refers what he perceives with his senses to a mental concept, then so do both. (44. Mr. Hookham, in a letter to Prof. Max Muller, in the 'Birmingham News,' May, 1873.) When I say to my terrier, in an eager voice (and I have made the trial many times), "Hi, hi, where is it?" she at once takes it as a sign that something is to be hunted, and generally first looks quickly all around, and then rushes into the nearest thicket, to scent for any game, but finding nothing, she looks up into any neighbouring tree for a squirrel. Now do not these actions clearly shew that she had in her mind a general idea or concept that some animal is to be discovered and hunted? It may be freely admitted that no animal is self-conscious, if by this term it is implied, that he reflects on such points, as whence he comes or whither he will go, or what is life and death, and so forth. But how can we feel sure that an old dog with an excellent memory and some power of imagination, as shewn by his dreams, never reflects on his past pleasures or pains in the chase? And this would be a form of self-consciousness. On the other hand, as Buchner (45. 'Conferences sur la Theorie Darwinienne,' French translat. 1869, p. 132.) has remarked, how little can the hardworked wife of a degraded Australian savage, who uses very few abstract words, and cannot count above four, exert her self-consciousness, or reflect on the nature of her own existence. It is generally admitted, that the higher animals possess memory, attention, association, and even some imagination and reason. If these powers, which differ much in different animals, are capable of improvement, there seems no great improbability in more complex faculties, such as the higher forms of abstraction, and selfconsciousness, etc., having been evolved through the development and combination of the simpler ones. It has been urged against the views here maintained that it is impossible to say at what point in the ascending scale animals become capable of abstraction, etc.; but who can say at what age this occurs in our young children? We see at least that such powers

https://www.jstage.jst.go.jp/article/ase1887/22/257/22_257_458/_pdf

The descent of man and selection in relation to sex

This chapter presents basic concepts related to avian clinical biochemistry. Avian medicine and surgery is recognized as an official specialty in veterinary medicine in three continents: Europe, Australia, and North America. The increasing demand for veterinary care for individual birds with a high sentimental or economical value and efforts to conserve endangered species facilitated this awareness. The introduction of micromethods in clinical laboratories and the public demand for veterinary care for individual birds have removed many obstacles of this field. This chapter begins with discussing how blood samples of birds can be collected in the most efficient way. The chapter then discusses starvation, flight, and postprandial effects. The chapter also elaborates the biochemistry of plasma proteins, renal function, and hepatobiliary disease in birds. The chapter emphasizes that all efforts should be made to obtain a blood sample before any treatment is given. Treatments administered before samples are collected may severely affect plasma chemical values, which may jeopardize a correct diagnosis at a later stage. The time interval between restraint and blood sampling should be kept to a minimum to prevent stress-associated changes in clinical chemistry parameters. Blood samples should be obtained before an extensive clinical examination is performed to avoid iatrogenic changes in the samples.

Avian Clinical Biochemistry

Publisher Summary This chapter reviews the present empirical and theoretical work on antipredator decision making. The ways in which predators influence the behavioral decisions made by their prey is now the subject of a large and growing literature. Some notable recent advances include clear demonstrations that antipredatory decision making (1) may influence many aspects of reproductive behavior, (2) has demonstrable long-term consequences for individual fitness, and (3) may influence the nature of ecological systems themselves. There have also been many advances in the theory of antipredator behavior, which should provide a sound conceptual basis for further progress. Attention is needed for further work on the effects that predator and prey have on the other's behavioral decisions. The range of reproductive behaviors influenced by the risk of predation also requires much more investigation. Work on the long-term costs of antipredator decision making needs more empirical documentation and greater taxonomic diversity. Work on the ecological implications of antipredatory decision making has only scratched the surface, especially with regard to population-level effects and species interactions. Theoretical investigations should also play a prominent role in future work.

Stress and Decision Making under the Risk of Predation: Recent Developments from Behavioral, Reproductive, and Ecological Perspectives

Various bird species regularly fast in connection with breeding, migration, or drastic climatic conditions. The metabolic response of penguins and domestic geese to fasting has been studied in deta...

Physiology and biochemistry of long-term fasting in birds

During long-term fasting in birds and mammals, protein utilization initially decreases (phase I), is thereafter maintained at a low value (phase II), and then further increases (phase III). To delineate hormonal and biochemical changes responsible for these modifications, the effect of food deprivation for 50 days was studied in 6 male king penguins captured at the beginning of their natural breeding fast. During phase II, both rate of mass loss and plasma uric acid concentration remained at low levels, whereas plasma beta-hydroxybutyrate concentration increased. In phase III there was by contrast a 2.5-fold increase in the rate of mass loss, an eightfold increase in plasma uric acid, and an 80% drop in plasma beta-hydroxybutyrate. Plasma corticosterone was low and steady in phase II and increased three times in phase III. During the overall fast, there were no significant variations in plasma insulin, but there was a fourfold increase in plasma glucagon and a decrease in plasma thyroxine and triiodothyronine. These findings suggest that protein sparing (phase II) requires low levels of corticosterone, insulin, and thyroid hormones, whereas the further increase in protein utilization (phase III) is due to an increase in plasma corticosterone. The high plasma glucagon concentration in phase III is presumably responsible for a transient increase in plasma glucose observed at this stage; such increase in glucagon could enhance gluconeogenesis from amino acids.

Fasting in king penguin. I. Hormonal and metabolic changes during breeding

SUMMARY Microstructure–function relationships remain poorly understood in
primary bone tissues. The relationship between bone growth rate and bone
tissue type, although documented in some species by previous works, remains
somewhat unclear and controversial. We assessed this relationship in a species
with extreme adaptations, the king penguin ( Aptenodytes patagonicus ).
These birds have a peculiar growth, interrupted 3 months after hatching by the
austral winter. Before this interruption, chicks undergo extremely rapid
statural and ponderal growth. We recorded experimentally (by means of
fluorescent labelling) the growth rate of bone tissue in four long bones
(humerus, radius, femur and tibiotarsus) of four king penguin chicks during
their fastest phase of growth (3–5 weeks after hatching) and identified
the associated bone tissue types (`laminar9, `longitudinal9, `reticular9 or
`radial9 fibro-lamellar bone tissue). We found the highest bone tissue growth
rate known to date, up to 171 μm day –1 (mean 55 μm
day –1 ). There was a highly significant relationship between
bone tissue type and growth rate ( P –6 ).
Highest rates were obtained with the radial microarchitecture of
fibro-lamellar bone, where cavities in the woven network are aligned radially.
This result supports the heuristic value of a relationship between growth rate
and bone primary microstructure. However, we also found that growth rates of
bone tissue types vary according to the long bone considered
( P –5 ) (e.g. growth rates were 38% lower in the
radius than in the other long bones), a result that puts some restriction on
the applicability of absolute growth rate values (e.g. to fossil species). The
biomechanical disadvantages of accelerated bone growth are discussed in
relation to the locomotor behaviour of the chicks during their first month of
life.

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Assessing a relationship between bone microstructure and growth rate: a fluorescent labelling study in the king penguin chick (Aptenodytes patagonicus).

The body mass of male emperor penguins is approximately 38 kg at the beginning of the 4-mo winter fast connected with breeding, and it is an estimated approximately 18 kg in leanest birds at time of spontaneous refeeding. For a 38- to 18-kg range, we investigated the changes in the rate of body mass loss, body composition, and plasma concentrations of uric acid and urea. After the first few days (phase I) a steady state (phase II) was reached in the proportions of the energy derived from proteins and lipids with proteins accounting for a constant 4%, and the remaining 96% being from lipids. The same proportions were maintained until body mass had decreased to 24 kg. Below this value the proportion of energy derived from proteins increased progressively (phase III), being 14 times higher at 18 kg than during phase II. Rate of body mass loss and plasma uric acid and urea concentrations closely reflected the changes in protein utilization: being at a low and steady value throughout phase II and increasing during phase III. Emperor penguins also fast during the spring, but for periods of only 2-3 wk. We found a 2.5 times higher value for rate of body mass loss, uric acid, and urea during spring phase II, suggesting lower effectiveness in protein sparing at that time. It may be attributed to the lower initial lipid reserves of spring birds. Would these findings be generalized to the wide variety of birds and mammals that spontaneously fast under natural conditions?(ABSTRACT TRUNCATED AT 250 WORDS)

Protein and lipid utilization during long-term fasting in emperor penguins

Mammals and birds adapt to prolonged fasting by mobilizing fat stores and minimizing protein loss. This strategy ends with an increase in protein utilization associated with behavioural changes promoting food foraging. Using the Zucker rat as a model, we have investigated the effect of severe obesity on this pattern of protein loss during long-term fasting. Two interactions between the initial adiposity and protein utilization were found. First, protein conservation was more effective in obese than in lean rats: fatty rats had a three times lower daily nitrogen excretion and proportion of energy expenditure deriving from proteins, and a lower daily protein loss in various muscles. This phase of protein sparing is moreover nine times longer in the fatty rats. Second, obese animals did not show the late increase in nitrogen excretion that occurred in their lean littermates. Total body protein loss during starvation was larger in fatty rats (57% versus 29%) and, accordingly, total protein loss was greater in their muscles. At the end of the experiment, lean and obese rats had lost 98% and 82%, respectively, of their initial lipid reserves, and fatty rats still had an obese body composition. These results support the hypothesis that in severely obese humans and animals a lethal cumulative protein loss is reached long before the exhaustion of fat stores, while the phase of protein conservation is still continuing. In contrast, in lean rats, survival of fasting seems to depend on the availability of lipid fuels.(ABSTRACT TRUNCATED AT 250 WORDS)

Jean-Patrice Robin

Papers

Physiology and biochemistry of long-term fasting in birds

Fasting in king penguin. I. Hormonal and metabolic changes during breeding

Assessing a relationship between bone microstructure and growth rate: a fluorescent labelling study in the king penguin chick (Aptenodytes patagonicus).

Protein and lipid utilization during long-term fasting in emperor penguins

Relationships between lipid availability and protein utilization during prolonged fasting.