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Frontiers in Endocrinology 2020Hormones are largely responsible for the integrated communication of several physiological systems responsible for modulating cellular growth and development. Although... (Review)
Review
Hormones are largely responsible for the integrated communication of several physiological systems responsible for modulating cellular growth and development. Although the specific hormonal influence must be considered within the context of the entire endocrine system and its relationship with other physiological systems, three key hormones are considered the "anabolic giants" in cellular growth and repair: testosterone, the growth hormone superfamily, and the insulin-like growth factor (IGF) superfamily. In addition to these anabolic hormones, glucocorticoids, mainly cortisol must also be considered because of their profound opposing influence on human skeletal muscle anabolism in many instances. This review presents emerging research on: (1) Testosterone signaling pathways, responses, and adaptations to resistance training; (2) Growth hormone: presents new complexity with exercise stress; (3) Current perspectives on IGF-I and physiological adaptations and complexity these hormones as related to training; and (4) Glucocorticoid roles in integrated communication for anabolic/catabolic signaling. Specifically, the review describes (1) Testosterone as the primary anabolic hormone, with an anabolic influence largely dictated primarily by genomic and possible non-genomic signaling, satellite cell activation, interaction with other anabolic signaling pathways, upregulation or downregulation of the androgen receptor, and potential roles in co-activators and transcriptional activity; (2) Differential influences of growth hormones depending on the "type" of the hormone being assayed and the magnitude of the physiological stress; (3) The exquisite regulation of IGF-1 by a family of binding proteins (IGFBPs 1-6), which can either stimulate or inhibit biological action depending on binding; and (4) Circadian patterning and newly discovered variants of glucocorticoid isoforms largely dictating glucocorticoid sensitivity and catabolic, muscle sparing, or pathological influence. The downstream integrated anabolic and catabolic mechanisms of these hormones not only affect the ability of skeletal muscle to generate force; they also have implications for pharmaceutical treatments, aging, and prevalent chronic conditions such as metabolic syndrome, insulin resistance, and hypertension. Thus, advances in our understanding of hormones that impact anabolic: catabolic processes have relevance for athletes and the general population, alike.
Topics: Adaptation, Physiological; Animals; Exercise; Growth Hormone; Growth and Development; Humans; Hydrocortisone; Muscle, Skeletal; Somatomedins; Testosterone
PubMed: 32158429
DOI: 10.3389/fendo.2020.00033 -
Journal of Applied Physiology... Mar 2017The complexity and redundancy of the endocrine pathways during recovery related to anabolic function in the body belie an oversimplistic approach to its study. The... (Review)
Review
The complexity and redundancy of the endocrine pathways during recovery related to anabolic function in the body belie an oversimplistic approach to its study. The purpose of this review is to examine the role of resistance exercise (RE) on the recovery responses of three major anabolic hormones, testosterone, growth hormone(s), and insulin-like growth factor 1. Each hormone has a complexity related to differential pathways of action as well as interactions with binding proteins and receptor interactions. Testosterone is the primary anabolic hormone, and its concentration changes during the recovery period depending on the upregulation or downregulation of the androgen receptor. Multiple tissues beyond skeletal muscle are targeted under hormonal control and play critical roles in metabolism and physiological function. Growth hormone (GH) demonstrates differential increases in recovery with RE based on the type of GH being assayed and workout being used. IGF-1 shows variable increases in recovery with RE and is intimately linked to a host of binding proteins that are essential to its integrative actions and mediating targeting effects. The RE stress is related to recruitment of muscle tissue with the glandular release of hormones as signals to target tissues to support homeostatic mechanisms for metabolism and tissue repair during the recovery process. Anabolic hormones play a crucial role in the body's response to metabolism, repair, and adaptive capabilities especially in response to anabolic-type RE. Changes of these hormones following RE during recovery in the circulatory biocompartment of blood are reflective of the many mechanisms of action that are in play in the repair and recovery process.
Topics: Adaptation, Physiological; Exercise; Human Growth Hormone; Humans; Insulin-Like Growth Factor I; Male; Muscle Fatigue; Muscle, Skeletal; Recovery of Function; Resistance Training; Testosterone; Young Adult
PubMed: 27856715
DOI: 10.1152/japplphysiol.00599.2016 -
Alcohol Health and Research World 1998A plethora of hormones regulate many of the body's functions, including growth and development, metabolism, electrolyte balances, and reproduction. Numerous glands... (Review)
Review
A plethora of hormones regulate many of the body's functions, including growth and development, metabolism, electrolyte balances, and reproduction. Numerous glands throughout the body produce hormones. The hypothalamus produces several releasing and inhibiting hormones that act on the pituitary gland, stimulating the release of pituitary hormones. Of the pituitary hormones, several act on other glands located in various regions of the body, whereas other pituitary hormones directly affect their target organs. Other hormone-producing glands throughout the body include the adrenal glands, which primarily produce cortisol; the gonads (i.e., ovaries and testes), which produce sex hormones; the thyroid, which produces thyroid hormone; the parathyroid, which produces parathyroid hormone; and the pancreas, which produces insulin and glucagon. Many of these hormones are part of regulatory hormonal cascades involving a hypothalamic hormone, one or more pituitary hormones, and one or more target gland hormones.
Topics: Endocrine Glands; Ethanol; Hormones; Humans
PubMed: 15706790
DOI: No ID Found -
Endocrine, Metabolic & Immune Disorders... 2019An overview of the history of endocrinology indicates that definitions of some initially developed concepts, including the term 'hormone' have been changed over time.... (Review)
Review
BACKGROUND AND OBJECTIVE
An overview of the history of endocrinology indicates that definitions of some initially developed concepts, including the term 'hormone' have been changed over time. This review provides a historical overview of current definitions of 'hormone' and the criteria of a true hormone. In addition, a brief history of hormone-related concepts and their transformation over time are discussed.
RESULTS
Classically, a hormone is a chemical substance secreted into the bloodstream and acts on distant tissues, usually in a regulatory fashion. Several newly discovered bioregulators and chemical signaling molecules are far from the classical definition of a true hormone and could not fulfill many relevant criteria. Major developments in the field of endocrinology accompanied by the complex terminology, currently used to describe hormonal actions of chemical messengers, underscore the need of the revision of such classical concepts.
CONCLUSION
Complex terminology currently used to describe different hormonal actions of chemical messengers, suggests that it is time to conceptualize the term hormone and revise its classical definition.
Topics: Animals; Biomedical Research; Circadian Rhythm; Endocrine Glands; Endocrinology; History, 19th Century; History, 20th Century; History, 21st Century; Hormones; Humans; Second Messenger Systems; Secretory Pathway; Terminology as Topic
PubMed: 30914038
DOI: 10.2174/1871530319666190326142908 -
Hormones and Behavior Aug 2022When selection favors a new relationship between a cue and a hormonally mediated response, adaptation can proceed by altering the hormonal signal that is produced or by...
When selection favors a new relationship between a cue and a hormonally mediated response, adaptation can proceed by altering the hormonal signal that is produced or by altering the phenotypic response to the hormonal signal. The field of evolutionary endocrinology has made considerable progress toward understanding the evolution of hormonal signals, but we know much less about the evolution of hormone-phenotype couplings, particularly at the hormone-genome interface. We briefly review and classify the mechanisms through which these hormone-phenotype couplings likely evolve, using androgens and their receptors and genomic response elements to illustrate our view. We then present two empirical studies of hormone-phenotype couplings, one rooted in evolutionary quantitative genetics and another in comparative transcriptomics, each focused on the regulation of sexually dimorphic phenotypes by testosterone (T) in the brown anole lizard (Anolis sagrei). First, we illustrate the potential for hormone-phenotype couplings to evolve by showing that coloration of the dewlap (an ornament used in behavioral displays) exhibits significant heritability in its responsiveness to T, implying that anoles harbor genetic variance in the architecture of hormonal pleiotropy. Second, we combine T manipulations with analyses of the liver transcriptome to ask whether and how statistical methods for characterizing modules of co-expressed genes and in silico techniques for identifying androgen response elements (AREs) can improve our understanding of hormone-genome interactions. We conclude by emphasizing important avenues for future work at the hormone-genome interface, particularly those conducted in a comparative evolutionary framework.
Topics: Androgens; Animals; Biological Evolution; Genomics; Lizards; Phenotype; Testosterone
PubMed: 35777215
DOI: 10.1016/j.yhbeh.2022.105216 -
The Journal of Endocrinology Apr 2024Polycystic ovary syndrome (PCOS) is a common endocrinopathy occurring in reproductive-age women. Hyperandrogenism, polycystic ovaries, chronic anovulation, and metabolic... (Review)
Review
Polycystic ovary syndrome (PCOS) is a common endocrinopathy occurring in reproductive-age women. Hyperandrogenism, polycystic ovaries, chronic anovulation, and metabolic aberrations are the common features in PCOS. Hormonal changes are causing pathological symptoms in women with PCOS. The various hormone alterations in PCOS have been demonstrated. Hormones, such as insulin, growth hormones (GH), ghrelin, LEAP-2, gonadotropin-releasing hormone (GnRH), insulin, the luteinizing hormone/follicle-stimulating hormone (LH/FSH) ratio, androgens, and estrogens, are all abnormal in PCOS women. These hormones are related to metabolic disorders, such as diabetes and insulin resistance, overweight and obesity, infertility, and disturbed menstrual cycle in PCOS patients. The pathological changes of these hormones, such as increased insulin, reduced GH, increased ghrelin, and leptin resistance, result in an increased prevalence of diabetes and obesity in PCOS women. A reduced GH, increased LEAP-2 levels, high LH basal, increased LH/FSH ratio, high androgens, and low estrogen are demonstrated in PCOS and linked to infertility. This narrative review aims to clarify the changes of hormone profiles, such as insulin, GH, LH, FSH, androgens, estrogen, progesterone, ghrelin, LEAP-2, asprosin, and subfatin, in PCOS, which may reveal novel targets for better diagnosis and treatment of PCOS.
Topics: Female; Humans; Polycystic Ovary Syndrome; Ghrelin; Luteinizing Hormone; Follicle Stimulating Hormone; Androgens; Estrogens; Insulin; Obesity; Infertility; Diabetes Mellitus
PubMed: 38285626
DOI: 10.1530/JOE-23-0342 -
Klinische Wochenschrift Oct 1972
Review
Topics: Adenosine Triphosphatases; Animals; Anura; Biological Transport, Active; Cattle; Chromatography, Gel; Dogs; Edema; Extracellular Space; Hormones; Humans; Kidney; Kidney Tubules; Molecular Weight; Natriuresis; Oxytocics; Rats; Sodium
PubMed: 4263583
DOI: 10.1007/BF01487918 -
Best Practice & Research. Clinical... Oct 2013The free hormone hypothesis states that a hormone's physiological effects depend on the free hormone concentration, not the total hormone concentration. Although the... (Review)
Review
The free hormone hypothesis states that a hormone's physiological effects depend on the free hormone concentration, not the total hormone concentration. Although the in vivo relationship between free hormone and protein-bound hormone is complex, most experts have applied this view to the design of assays used to assess the free hormone concentration in the blood sampled for testing in vitro. The history of the measurement of free thyroxine, probably the most frequently requested free hormone determination, offers a good example of the approaches that have been taken. Methods that require physical separation of the free hormone from the protein-bound hormone must address both the potential disturbance in the equilibrium between the two, as well as the challenge of quantifying small levels of hormone accurately and precisely. The implementation of mass spectrometry in the clinical laboratory has helped to develop proposed reference measurement procedures. These must be utilized to standardize the variety of immunoassay approaches that currently represent options commercially available to the routine clinical laboratory. Practicing endocrinologists should discuss the details of the free hormone assays offered by the clinical laboratory they utilize for patient result reporting, and clinical laboratories should implement the recommendations of published guidelines to ensure that free hormone results using commercially available immunoassays are as accurate and precise as possible.
Topics: Dialysis; Female; Hormones; Humans; Hydrocortisone; Immunoassay; Insulin-Like Growth Factor I; Male; Protein Binding; Sex Hormone-Binding Globulin; Testosterone; Thyroxine; Triiodothyronine
PubMed: 24094635
DOI: 10.1016/j.beem.2013.06.007 -
Frontiers in Neuroendocrinology Oct 2022Extant animal and human data suggest endogenous ovarian hormones increase risk for binge eating in females, possibly via gene × hormone interactions and hormonally... (Review)
Review
Extant animal and human data suggest endogenous ovarian hormones increase risk for binge eating in females, possibly via gene × hormone interactions and hormonally induced increases in genetic influences. Approximately 85 % of women will take combined oral contraceptives (COCs) that mimic the riskiest hormonal milieu for binge eating (i.e., post-ovulation when both estrogen and progesterone are present). The purpose of this narrative review is to synthesize findings of binge eating risk in COC users. Few studies have been conducted, but results suggest that COCs may increase risk for binge eating and related phenotypes (e.g., craving for sweets), particularly in genetically vulnerable women. Larger, more systematic human and animal studies of COCs and binge eating are needed. The goal of this work should be to advance personalized medicine by identifying the extent of COC risk as well as the role of gene × hormone interactions in susceptibility.
Topics: Animals; Humans; Female; Contraceptives, Oral, Combined; Binge-Eating Disorder; Progesterone; Estrogens
PubMed: 36181777
DOI: 10.1016/j.yfrne.2022.101039 -
The Journal of Endocrinology Mar 2005Hormonal effects on behaviours in animals and humans are now well enough understood for general statements about causal steps to be proposed. Facilitation or repression... (Review)
Review
Hormonal effects on behaviours in animals and humans are now well enough understood for general statements about causal steps to be proposed. Facilitation or repression of a given behaviour by a given hormone can depend on the person's genetic and developmental history, on the temporal and spatial parameters of the hormone's administration, on the hormone's metabolism and on the specific receptor isoform available in a given neuron. The gene for oestrogen receptor-alpha is required for an entire chain of behaviours essential for reproduction, from courtship through maternal behaviours. In order to show that it is possible to use endocrine tools to explain a mammalian behaviour, we analysed lordosis behaviour neuronal circuitry as well as the molecular mechanisms of its facilitation by oestrogens. The functional genomics of oestrogenic effects on lordosis arrange themselves in modules for neuronal Growth, Amplification (by progestins), Preparatory behaviours, Permissive actions by hypothalamic neurons, and Synchronization of mating behaviour with ovulation (GAPPS). A related four-gene micronet involving the amygdala and the paraventricular nucleus of the hypothalamus supports social recognition. Underlying all sociosexual behaviour is the fundamental arousal of brain and behaviour. Elementary arousal depends on a bilateral, bidirectional system universal among mammalian brains, and it can be altered by null deletion of the gene for oestrogen receptor-alpha. Future molecular and biophysical studies will specify how hormone effects in the brain change central nervous system state in such a manner as to alter the frequencies of entire sets of behavioural responses.
Topics: Animals; Arousal; Behavior; Central Nervous System; Estrogen Receptor alpha; Estrogens; Female; Gene Expression Regulation; Hormones; Humans; Male; Mammals; Sexual Behavior, Animal
PubMed: 15749804
DOI: 10.1677/joe.1.05897