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The chapter provides a novel account of perceptual discrimination (krinein) in Aristotle. Against the widespread view that the most basic perceptual acts consist in noticing differences between two or more perceived qualities, I argue that discrimination is for Aristotle more like sifting, winnowing on a sieve: it consists in identifying – with an ultimate authority – the quality of an external object as distinct from any other quality of the given range that the object could have. The chapter further explores how the notion of discrimination is embedded by Aristotle within his causal assimilation model of perception. I argue that the central notion of a discriminative mean (mesotēs), introduced in An. 2.11, is intended to capture the role of the perceptive soul as the controlling factor of a homeostatic mechanism underlying perception. As such the notion lays the groundwork for resolving the apparent conflict between the passivity of perception and the impassivity of the soul (as analysed in Chapter 5). The prospect is further explored in Chapter 7. The present chapter concludes by arguing that Aristotle conceives perceptual discrimination as a holistic assessment of the external object acting on the perceiver, including those of its features which are not causally efficacious.
The chapter spells out the homeostatic model of how the soul is involved in perception introduced in Chapter 6, while addressing two main challenges for it. First, I argue that while the physiological details are not easy to tease out, there is no principal reason against Aristotle’s extension of the model from touch to other sense modalities. More importantly, I argue that we can understand the role of the perceptive soul as an extension of the model developed for the nutritive soul in An. 2.4 and based on Aristotle’s art analogy (from Phys. 2 and elsewhere). The upshot is that the basic perceptual acts are underlaid by bodily processes non-cognitively controlled by the soul. But while homeostasis is the aim of nutrition, in perception it only becomes a means for achieving something else, namely discrimination. The chapter closes by showing how the interpretation developed in this book pays off when it comes to understanding Aristotle’s two notoriously difficult concluding accounts: the account of perception as a reception of forms without the matter in An. 2.12 and the summarizing account of the cognitive soul in An. 3.8.
The addiction syndrome is quite similar across different addictive drug types, reflecting a shared pathway of pathological changes within motivational circuits that increasingly prioritize drug acquisition and use. This neurobiology, and drug addiction symptomatology, overlaps considerably with behavioral addictions (e.g., gambling disorder). However, addiction is distinct from symptoms and mechanisms underpinning intoxication and withdrawal, which are diverse and unique to each drug class. The intoxication phase is followed by some degree of withdrawal, manifesting clinically as opposite to intoxication, reflecting a homeostatic response to it. Withdrawal has a quality, duration, and dangerousness that depends on the individual, the drug type, and drug use history. Heavy/chronic patterns of use in addiction can produce longer, more severe withdrawal phases, but addiction and withdrawal can exist separately. How a drug acts upon different receptors and other downstream brain systems (pharmacodynamics) impacts the strength of its psychoactive (intoxicating) and motivational (addictive effects). Meanwhile, the route and rate of drug intake and its breakdown and elimination (pharmacokinetics) can also impact intoxication, withdrawal, and addiction risk. With addiction, the patient becomes tolerant (insensitive) to the intoxicating profiles of drugs they like, whereas their motivation, craving, and wanting to use the drug sensitizes (grows pathologically).
Homeostats are important to control homeostatic conditions. Here, we have analyzed the theoretical basis of their dynamic properties by bringing the K homeostat out of steady state (i) by an electrical stimulus, (ii) by an external imbalance in the K+ or H+ gradient or (iii) by a readjustment of transporter activities. The reactions to such changes can be divided into (i) a short-term response (tens of milliseconds), where the membrane voltage changed along with the concentrations of ions that are not very abundant in the cytosol (H+ and Ca2+), and (ii) a long-term response (minutes and longer) caused by the slow changes in K+ concentrations. The mechanistic insights into its dynamics are not limited to the K homeostat but can be generalized, providing a new perspective on electrical, chemical, hydraulic, pH and Ca2+ signaling in plants. The results presented here also provide a theoretical background for optogenetic experiments in plants.
Edited by
Dharti Patel, Mount Sinai West and Morningside Hospitals, New York,Sang J. Kim, Hospital for Special Surgery, New York,Himani V. Bhatt, Mount Sinai West and Morningside Hospitals, New York,Alopi M. Patel, Rutgers Robert Wood Johnson Medical School, New Jersey
Renal function plays a key role in the body homeostasis as well as perioperative management of fluids. This chapter discusses the renal system anatomy and physiology as well as various metabolic disturbances of electrolytes including potassium, sodium, calcium, and magnesium.
The brain does not passively register sensory input but actively predicts it. The activity of the sensory input is ‘explained away’ and only activity that was not predicted remains. This remaining activity is treated as an error signal that is used to update the predictive coding system. Learning is predictive coding.
Calcium ions (Ca2+) play pivotal roles in a host of cellular signalling processes. The requirement to maintain resting cytosolic Ca2+ levels in the 100–200 nM range provides a baseline for dynamic excursions from resting levels that determine the nature of many physiological responses to external stimuli and developmental processes. This review provides an overview of the key components of the Ca2+ homeostatic machinery, including known channel-mediated Ca2+ entry pathways along with transporters that act to shape the cytosolic Ca2+ signature. The relative roles of the vacuole and endoplasmic reticulum as sources or sinks for cytosolic Ca2+ are considered, highlighting significant gaps in our understanding. The components contributing to mitochondrial, chloroplast and nuclear Ca2+ homeostasis and organellar Ca2+ signals are also considered. Taken together, a complex picture of the cellular Ca2+ homeostatic machinery emerges with some clear differences from mechanisms operating in many animal cells.
Silicon (Si), the most abundant mineral element in soil, functions as a beneficial element for plant growth. Higher Si accumulation in the shoots is required for high and stable production of rice, a typical Si-accumulating plant species. During the last two decades, great progresses has been made in the identification of Si transporters involved in uptake, xylem loading and unloading as well as preferential distribution and deposition of Si in rice. In addition to these transporters, simulation by mathematical models revealed several other key factors required for efficient uptake and distribution of Si. The expression of Lsi1, Lsi2 and Lsi3 genes is down-regulated by Si deposition in the shoots rather than in the roots, but the exact mechanisms underlying this down-regulation are still unknown. In this short review, we focus on Si transporters identified in rice and discuss how rice optimizes Si accumulation (“homeostasis”) through regulating Si transporters in response to the fluctuations of this element in the soil solution.
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