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Since Cannon, inspired by Bernard’s discussion of the conditions required for free and independent life, introduced the term homeostasis, many have embraced it as the main theoretical principle guiding physiology and medicine. Nonetheless, critics have argued that homeostasis is too limiting and have advanced a variety of alternative concepts such as heterostasis, rheostasis, and allostasis. We argue that the critics target a much narrower understanding of homeostasis put forward by the cyberneticists and that Bernard and Cannon embraced a far broader understanding that can accommodate the alternatives advanced by the critics and provide an integrated theoretical framework for physiology.
Enhanced dietary Ca intake linearly increases intestinal Ca absorption in pigs, but not in broilers, suggesting potential differences in whole body Ca homeostasis. To determine the role of kidney in Ca homeostasis in these species, we varied in growing pigs in experiment (Exp) 1, the dietary Ca content 2·0 v. 9·6 g/kg and phytase 0 v. 500 FTU/kg, in broilers, in Exp 2 the dietary Ca/retainable P from 1·3 to 2·8 and phytase 0 v. 1000 FTU/kg, and in Exp 3 dietary Ca/P from 0·50 to 1·75. Increasing dietary Ca reduced renal mRNA expression of Ca-related transporters (TRPV5, TRPV6, CaBP-D28k and NCX1) and tight junctions (CLDN-12 and −16) in pigs, indicating Ca reabsorption was reduced to maintain Ca homeostasis. In broilers (Exp 2), high dietary Ca increased renal TRPV6, CaBP-D28k and CLDN-2 mRNA, indicating an increased capacity for Ca reabsorption. Moreover, the effect of dietary Ca was enhanced by inclusion of dietary phytase in pigs but reduced in broilers. Furthermore, increasing dietary Ca upregulated inorganic phosphate transporter 1 (PiT-1), while phytase downregulated xenotropic and polytropic retrovirus receptor 1 (XPR1) mRNA expression in pigs; in broilers, dietary Ca downregulated renal mRNA expression of Na-dependent phosphate transporter IIa (NaPi-IIa), PiT-1, PiT-2 and XPR1, while phytase downregulated NaPi-IIa but upregulated PiT-2 and XPR1 mRNA expression. In Exp 3, Ca/P effect on transporter mRNA expression was largely consistent with Exp 2. In conclusion of this study, together with previously measured data about Ca and P homeostasis, in pigs the kidneys play a more regulatory role in Ca homeostasis than in broilers where the intestine is more important for regulation.
Ion homeostasis is a crucial process in plants that is closely linked to the efficiency of nutrient uptake, stress tolerance and overall plant growth and development. Nevertheless, our understanding of the fundamental processes of ion homeostasis is still incomplete and highly fragmented. Especially at the mechanistic level, we are still in the process of dissecting physiological systems to analyse the different parts in isolation. However, modelling approaches have shown that it is not individual transporters but rather transporter networks (homeostats) that control membrane transport and associated homeostatic processes in plant cells. To facilitate access to such theoretical approaches, the modelling of the potassium homeostat is explained here in detail to serve as a blueprint for other homeostats. The unbiased approach provided strong arguments for the abundant existence of electroneutral H+/K+ antiporters in plants.
Stress causes brain damage. Unrelenting stress is an essential feature of legal education and legal practice, and chronic stress hurts the brain. Lawyers suffer from higher rates of anxiety and depression than the rest of the population and they rank fourth in professions with the highest number of suicides. Lawyers’ anxiety, depression, and suicide rates are likely linked to overwork and exposure to toxic chronic stress. Anxiety and depression can cause changes in the brain that are related to an overactive fight-or-flight stress response system. Lawyer languishing, a state of incomplete mental health, may be a precursor to lawyer’s anxiety or depression. The rat-fumbling researcher Hans Seyle noticed that the discomfort his lab rats suffered made them sick. He used the term stress to describe the general unpleasantness his rats experienced when he routinely dropped, chased, and recaptured them during his experiments. The culture of his lab was making his rats sick. When law school or legal practice cultures subject students or lawyers to a broad array of incessant stressors; the general unpleasantness is prone to make them physically and emotionally sick; and it damages their brain.
This chapter introduces our stress response system and how it works in the sprints of life. Under the best of circumstances and when we are in the pink of health, our stress response system functions like a finely conducted orchestra, and we hardly notice what a marvel of orchestration we live by. Herbert Benson’s studies in the 1970’s of the physiology of transcendental meditation paved the way for the Mind Body Institute and others to practice approaches retraining dysregulated stress responses. A discussion of the distinguishing features of our stress response system leads the concept of allostasis or the cumulative burden of stressors across a lifetime—a measure of the wear and tear of life.
This chapter discusses the direct effects of racial discrimination on Black Americans’ health. It begins by documenting that daily exposure to the various forms of racial discrimination is a common experience for Black people living in the United States. Encountering racial discrimination creates stress, which activates physiological stress responses – bodily systems that normally provide person with the energy needed to rapidly reduce the stress. However, the stress created by racial discrimination is usually chronic because many Black Americans repeatedly experience racial discrimination over a prolonged period of time. When the bodily systems activated by stress response remain active, it creates a harmful physical condition – allostatic overload. Allostatic overload is responsible for a host of physical illnesses, including heart diseases, diabetes, and immune disorders. It is also associated with poorer mental health, as well as alterations in epigenetics, such as premature aging. Chronic stress can also cause people to engage in behaviors that may provide short-term emotional relief from discrimination-related stress but are unhealthy, such as drug use or eating certain unhealthy “comfort” foods. In sum, prolonged exposure to racial discrimination is a chronic stressor that threatens the health of Black Americans.
The introduction briefly summarizes the contrasts between traditional views about mind and communication, including the computer and code metaphors.It summarizes the central perspective of the book, that human communication is embodied in a biological sense, as well as in a social and cultural sense, and briefly explains the meaning of these terms. It presents a case for conceptual clarity as a basis for critiquing conventional terminology based on computer and code metaphors, and proposes a more direct and accurate set of terms.
Chapter 2 introduces and explains the concept of homeostasis, and other concepts central to the evolution of the neural system, brain, and signaling.It describes key communication-related features of the evolving brain and contrasts them with digital computers as a basis for criticizing the computer metaphor and associated terminology.It introduces crucial concepts, including theory of mind, identity, and consciousness.
The way the brain, body, and mind interact with social structure to shape communication has so far not received the attention it deserves. This book addresses this gap by providing a novel account of communication as a social, biological and neurological force. Combining theories from communication studies and psycholinguistics, and drawing on biological and evolutionary perspectives, it shows how communication is inherently both biological and social, and that language and the neural systems that support it have evolved in response to a complex social environment. It introduces a clear set of terms based on current research, and illustrates key concepts using real-life examples from everyday conversation - speaking to a number of current debates around the evolutionary and biological basis of language, and the relationship between language, cognition, and environment. Thought provoking and engaging, it will change the way we think about the relationship between communication and cognition.
The anticonvulsant m-Cl-BHM is promising for the pathogenetically directed thrapy does not cause negative effects.
Objectives
Investigation of the effect of m-Сl-BHM on “immunochemical homeostasis” in rats with experimental alcoholism.
Methods
m-Cl-BHM was injected at a dose of 100 mg/kg (1/20 LD50) for 5 and 30 days into the stomach of male Wistar rats who preferred alcohol according to the screening conditions and kept for 10 months. in free access to a 15% ethanol solution, which made up the group of “heavy drinkers” (HD). Phenobarbital was administered at a dose of 25 mg/kg (1/20 LD50).
Results
The features of the monooxygenase system of cytochrome P450 of the liver and ECT in the lymphoid organs of rats were studied at different periods of administration of m-CL-BHM -5 and 30 days. to HD rats. m-CL-BHM has an inducing effect on the monooxygenase system of the liver, causes phase changes in the lymphoid organs and ECT. Long-term administration of m-CL-BHM caused a depletion of the cellular composition of lymphoid organs, a decrease in ECT of spleen cells and peritoneal exudate, these changes were less pronounced compared with phenobarbital. The activation of the immune system inversely regulates the production of enzymes of the cytochrome system, since the concentration of low molecular weight targets is sharply reduced with the help of antibodies. m-Cl-BHM metabolites conjugated to endogenous macromolecules form a full-fledged stimulus for the immune system.
Conclusions
Neuroimmune response to the introduction of m-CL-BHM is significant in behavioral disorders associated with alcoholism and the correction of this condition.
The correspondence commences in the summer of 1970, when a still untenured Margulis sends Lovelock a request for information along with offprints of her own work. The scientific collaboration of Lovelock and Margulis launched in earnest in January 1972, a year and a half after their first exchange of letters. The opening chapters of their correspondence document Margulis’s importance for both the construction and the communication of Gaian ideas. Their collaboration develops precisely as a writing partnership, with Margulis in the de facto role of in-house editor as well as co-author of their early papers. The letters exchanged in 1972 show them meticulously working through the host of technical matters intrinsic to their bold project until an initial manuscript is ready for submission. These early letters are also the most minutely specialized, as they are both still teaching the other what they need to learn in order to bring their respective specializations together.
The following chapter will address electrolyte abnormalities commonly encountered in the intensive care unit. Table 3.11.1.1 provides a general overview of the homeostatic mechanisms and the metabolism of the cations sodium, potassium, calcium and magnesium, as well as the anion phosphate. Table 3.11.1.2 provides a summary of the ECG changes that occur with various electrolyte abnormalities.
The development of original drugs - new generation GABAA receptor modulators (GABAAR), with an anti-alcohol orientation, non-addictive and stimulating detoxification processes, makes it possible to increase the effectiveness of therapy and reduce the cost of treatment.
Objectives
Study the mechanism of interaction between m-Cl-BHU and GABAA - receptor
Methods
Molecular docking was performed to study the molecular docking of m-Cl-BHU with at the binding site of the target protein GABAAR.Radioreceptor studies were carried out using [3H] flunitrazepam binding with synaptosomal receptors in the cerebral cortex of Wistar rats in experimental alcoholism under the influence of therapy with m-CL-BHU. Kinetic parameters (T1/2, Clt, MRT, MET, AUC) of a model substrate - antipyrine were determined in the saliva of healthy volunteers and alcoholic patients.
Results
IResults of molecular docking (Schrödinger program (Glide) showed: m-CL-BHU (meta-chlorobenzhydryl urea) is complementary to the benzodiazepine GABAAR. Binding energy is low) (scoring (GScore) -11.14 kKal/mol); m-CL-BHU interacts with key amino acids at the α1γ2 interface: Tyr159, Tyr209, H101 Phe77 and is characterized by a high degree of model fit - dG insert: 0.741 Binding of [3H] flunitrazepam to the benzodiazepine site of GABAAR in rat brain in experimental alcoholism, who received 14 days of m-CL-BHU at 100 mg/kg /day, increased in receptor affinity. Changes in the kinetic parameters (T1/2, Clt, MRT, MET, AUC) of a model substrate - antipyrine in the saliva of healthy volunteers and alcoholic patients using Galodif (m-CL-BHU) at 300 mg/day 21 days
Conclusions
m-CL-BHU - GABAA receptor modulator with an alternative mechanism of action
Without brain systems that modulate arousal, we would not be able to have daily sleep-wake cycles, focus attention when needed, experience emotional responses, or even maintain consciousness. Thus, it is not surprising that there are multiple overlapping neurotransmitter systems that control arousal. In aging, most of these systems show decline in basic features such as number of receptors and transporters, and sometimes even in neuron count. These declines have the potential to disrupt basic arousal functions. Compensatory increases in activity in some of these systems allow for maintained levels of circulating neurotransmitters in those systems – but at the cost of reduced dynamic range in arousal responses.
The topic of marijuana addiction is emotionally charged. The two aspects of addiction—withdrawal symptoms unique to marijuana and alterations in the brain’s reward mechanism common to all addictive drugs—must be approached separately. THC’s stimulation of CB1 receptors causes a homeostatic reduction of receptor density, called downregulation. When THC stimulation wanes, the resultant relative lack of receptors leads to a transient deficiency of endocannabinoid activity. Hirnoven found a 20% reduction in endocannabinoid receptors in the cortex of individuals regularly using marijuana requiring 4 weeks of abstinence to be reversed. The effects of cannabinoid deficiency outlined by Budney include withdrawal symptoms of restlessness, anxiety, insomnia, boredom and irritability. Relapse to marijuana use often occurs to abort withdrawal symptoms. The influx of dopamine in the reward center (nucleus accumbens) caused by excessive cannabinoid stimulation is the sine qua non for addiction and leads to a neurologically based increase in the salience of marijuana. Modification of reward mechanisms increases the motivation to use marijuana to the point that cognitive rationality is clouded and denial is produced.
Studying humankind’s relationship to the earth involves broad and deep questions for students as today’s educators explore changing teaching methods. This article highlights benefits of a multidisciplinary approach to environmental education, drawing upon ancient natural philosophy as a coherent conceptual resource. The Greek philosopher Plotinus is introduced to show the application of ancient natural philosophy across all fields and on all levels of knowledge under a common banner. The significance of ancient natural philosophy is its conception of overall unity. This is the key. Unity is implicit in interrelationships between parts to whole on all levels of existence. From such a perspective, all life forms and other entities in the natural world can be understood as interrelated — just as James Lovelock demonstrated in describing the homeostatic state of natural processes on earth. On a similar reasoning, the diversity in people, societies and places can be appreciated physically and sociologically as belonging to one world. Several studies are cited to explore this overlap between ancient natural philosophy and honouring the connection and dependence of humanity on the fragility of the earth’s ecosystem.
Balanced vegetarian diets are popular, although they are nearly absent in creatine and carnosine and contain considerably less carnitine than non-vegetarian diets. Few longitudinal intervention studies investigating the effect of a vegetarian diet on the availability of these compounds currently exist. We aimed to investigate the effect of transiently switching omnivores onto a vegetarian diet for 6 months on muscle and plasma creatine, carnitine and carnosine homeostasis. In a 6-month intervention, forty omnivorous women were ascribed to three groups: continued omnivorous diet (control, n 10), vegetarian diet without supplementation (Veg+Pla, n 15) and vegetarian diet combined with daily β-alanine (0·8–0·4 g/d) and creatine supplementation (1 g creatine monohydrate/d) (Veg+Suppl, n 15). Before (0 months; 0M), after 3 months (3M) and 6 months (6M), a fasted venous blood sample and 24-h urine was collected, and muscle carnosine content was determined by proton magnetic resonance spectroscopy (1H-MRS). Muscle biopsies were obtained at 0M and 3M. Plasma creatine and muscle total creatine content declined from 0M to 3M in Veg+Pla (P=0·013 and P=0·009, respectively), whereas plasma creatine increased from 0M in Veg+Suppl (P=0·004). None of the carnitine-related compounds in plasma or muscle showed a significant time×group interaction effect. 1H-MRS-determined muscle carnosine content was unchanged over 6M in control and Veg+Pla, but increased in Veg+Suppl in soleus (P<0·001) and gastrocnemius (P=0·001) muscle. To conclude, the body creatine pool declined over a 3-month vegetarian diet in omnivorous women, which was ameliorated when accompanied by low-dose dietary creatine supplementation. Carnitine and carnosine homeostasis was unaffected by a 3- or 6-month vegetarian diet, respectively.
A well-developed theory of evolutionary biology requires understanding of the origins of life on Earth. However, the initial conditions (ontology) and causal (epistemology) bases on which physiology proceeded have more recently been called into question, given the teleologic nature of Darwinian evolutionary thinking. When evolutionary development is focused on cellular communication, a distinctly different perspective unfolds. The cellular communicative-molecular approach affords a logical progression for the evolutionary narrative based on the basic physiologic properties of the cell.
Critical to this appraisal is recognition of the cell as a fundamental reiterative unit of reciprocating communication that receives information from and reacts to epiphenomena to solve problems. Following the course of vertebrate physiology from its unicellular origins instead of its overt phenotypic appearances and functional associations provides a robust, predictive picture for the means by which complex physiology evolved from unicellular organisms. With this foreknowledge of physiologic principles, we can determine the fundamentals of Physiology based on cellular first principles using a logical, predictable method. Thus, evolutionary creativity on our planet can be viewed as a paradoxical product of boundary conditions that permit homeostatic moments of varying length and amplitude that can productively absorb a variety of epigenetic impacts to meet environmental challenges.
The analysis of motivational systems underlying temporal organisation in animal behaviour has relied primarily on two conceptual functional frameworks: Homeostasis and biological clocks. Homeostasis is one of the most general and influential concepts in physiology. Walter Cannon introduced homeostasis as a universal regulatory principle which animals employ to maintain constancy of their ‘internal milieu’ in the face of challenges and perturbations from the external environment. Cannon spoke of “The Wisdom of the Body”, the collective of responses designed to defend the ideal internal state against those perturbations.
The adult human typically exhibits a monophasic sleep-wake cycle, i.e., remains awake and alert for approximately 16 hours and then sleeps for 8 hours. Recent experiments have provided new insights in the role of the endogenous circadian pacemaker in this consolidation of sleep and wakefulness.
Sleep deprivation studies had shown previously that sleepiness and alertness are co-determined by a process which keeps track of the history of sleep and wakefulness and the circadian pacemaker, which keeps track of time. During every day life and during sleep deprivation both processes change simultaneously and their relative contribution to alertness and sleep propensity cannot be assessed under these conditions.