The Fundamentals of Vitalism
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Gregoriy Shifrin
Professor Gregoriy Shifrin is an expert in the field of biology and vitalism.
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The Fundamentals of Vitalism - Gregoriy Shifrin
The Fundamentals
of Vitalism
by Prof. Gregoriy Shifrin
Contents
Title Page
Introduction
CHAPTER 1: Phenomen of Human Vitalism
1.1 Cellular response to stimulation and alteration
1.2. Energy- structural conjugation
1.3 Major Energy Recipients
1.4 Implementation Of Vitalism
1.5 Biological and Energy Quantums.
1.5 2. Energy Protective Quantum
1.6 Energy-Protective Theory
CHAPTER 2: Logic of Vitalism Concept
2.1 Auto regulation of adaptation
2.2 Stress – Response to Extreme Conditions
2.3. Adaptation Syndrome
2.4 Generic Categories of Energy-Structural Status
2.5 Energy Protective Reserves
2.6 Destabilisation of Autoregulation
2.7. Energy-Structural Status Properties
2.8. Vitalism Space
CHAPTER 3: Nozogenous Euvitalism
3.1 Autoregulation of Vitalism
3.2 Water–Electrolite Interaction
3.3 Regulation of Electrolyte Balance
3.4 Conjugation of Autoregulation Components
3.5 Natriyuretic Regulation
3.6 Restoration Of Structural Elements
CHAPTER 4: Energy Cellular Resuscitation in Vitalism Impairment
4.1 General Conditions Leading to Disorders
4.2. Nozogenic Activation of Pulmonary Vasoconstriction
4.3. Hypoxic Ischaemia Reperfusion Lung Injury
4.4 Capillary Permeability Impairment
4.5 Energy and Cellular Energy Resuscitation Impaired Energy Structural Coupling
4.6.1 Energy resuscitation scheme
4.6.2 Energy and Energy-Cellular Resuscitation in the Catabolic Impairment
4.7 Reparation Of Damaged Cells
CHAPTER 5: Status-Resuscitation in Vitalism Failure
5.1. Evolution of Nosogenous Implementation of Energy-Structural Interaction
5.2 Main Pathways of Status Correction
5.3 Energo-Protection in Acute Lung Injury/Acute Respiratory Distress Syndrome (ARDS)
5.4. The Role of Enteral Oxygenation (EO)
5.5. Microcirculation Component of Status-Correction
5.6 Status Resuscitation in Patho-Energy Biothy
5.7. Cell Mass Catabolic Destruction Status-Resuscitation
CHAPTER 6: Remodeling of Vitalism
6.1 Generic Disintegration of Energy-Structural Coupling
6.2 Splanchnic Ischaemia
6.3 Acute Kidney Injury
6.4 Uncontrolled Proteolysis
6.5 Symptomatic Therapy in Vitalism Imbalance
6.6 Methods of Detoxication
6.7 Circulation Drainage
6.8. Main Pathways of Vitalism Remodelling
6.9 Dyshydric Nature of Disintegration
6.10 Prosthesis of Histo-Hematic Exchange
6.11 Energy Efficiency of Vitalism Remodeling (Prosthesis)
CHAPTER 7: Medical Practice of Programmed Information System ‘Vitalism Audit’
7.1 Abstract, Primary and Refinement Data
7.2 Parameters of Audit
7.3 Audit of Perinosal Vitalism
7.4 Energystructural Reserves (ESR)
7.5 Autoregulation of Energyprotectivity
7.6 Energobioty and Energyprotectivity
7.7 Resume
Conclusion
Bibliography
Copyright
Vitalism is new conception of maintaining and restoration of human life forces in accordance with changing genome programs. Its methods of vital resistibility will expand the competence of physicians and help apply unique personalised approach to etiotropic treatment of diseases and injuries. Through the use of innovative technologies of optimisation intensity of energy structural capacity, the reliable elimination of energy structural disorders and restoration the biological integrity the bodies of patients will be achieved. This manual is intended for physicians of all specialties.
Introduction
The success of biology together with evolution laws opens up new opportunities in implementing the theory of body integrity in assessment patients clinical state and finding new ways of healing – to treat not a disease but the patient.
The evolutionary essence of living being predetermines the supremacy of energy-structural ideology of medicine, which defines the biological integrity of an organism or body (BIO) as the functional harmony of energy production and energy supply. The main component of BIO is called bio sustainability (BS) – which contemplates living strengths of a body necessary to provide self-resuscitation of cells’ DNA (deoxyribonucleic acid) and other organelles, initiate physiological regeneration as well as minimise or eliminate structural deficit.
Therefore, a power of BIO responsible for the energy production multiplied by body cell mass, which we call ‘vitalism’ is the calculated measure, unique for every single individual. This will set the difference between reliable energy consumption (in active healthy body) and minimum energy used dictated by hypoxic genes just to assure cells survival.
Finally, vitalism is a subject of study of an independent medical science: vitalology. This manual presents the nature of vitalism establishes a new model of healing.
CHAPTER 1
Phenomen of Human Vitalism
1.1 Cellular response to stimulation and alteration
Functioning living cells are the realisation of certain genetic programs in response to numerous external signals. In the same cell these extracellular signals might activate cell mitosis, movement, growth, proliferation or might cause cellular self-destruction or apoptosis. Final cell response (if it is any) depends on concentration of extracellular molecular stimulants, a number of cells receptors and its sensitivity.
By stimulating synthesis and proliferation intracellular organelles a cell or cells undergo adaptation either in a form of hypertrophy (increase in size) or hyperplasia (increase in a number of cells), if talking of a tissue or an organ alone.
Each cell energy production is strictly personalised and supported by genes. It varies with changing cells activity, and suffers from diminished nutrients (proteins, carbohydrates, fat), electrolytes (Na, K, Ca, Cl) and micro-circulation alteration.
Cell/organ function depends on intensity of cellular metabolism which is different at any given time. Therefore, the strength of life (‘vitality’ or ‘vitalism’ – a new term) describes a level of intensity of metabolism; or calculated amount of energy immediately produced in active single cell to facilitate effective response to ‘fight and flight’ mode.
Cell integrity is a minimum level of energy produced that is required for sufficient cell preservation. Plenty of conditions still need to be met for cells to retain its vitalism. If these are not maintained, the living cell is dying.
The conditions are:
Energy supply
Physicochemical state and membrane structure
Enzyme activity
Ion balance
Genetic factors
Energy structural conjugation (vitalism)
Fig 1.1 The implication of metabolism on an active cell
… Break in energy supply and therefore structural disorders trigger similar changers as an ischemia or re-perfusion syndrome. It affects all stages of energy production cascade:
a) ATF synthesis
b) ATF transportation to target cells
c) ATF utilisation
In tissue hypoxia – the disorders observed mainly on a stage of ATF production – it decreases in a two-phase fashion: initially sharply and then delayed, all due to the depression of glycolysis. Glycolysis alteration contributes to inadequate microcirculation, which in a chain reaction affects further transport and utilisation of ATF
Fig. 1.2 Vitalism disorders in ischemia and re-perfusion
If ischaemia lasts longer than 10 min the adequate energy delivery is preserved. This happens at the expense of further mitochondrial damage (see Pict 1.3)
Fig 1.3 Mitochondrial respiratory chain impairment
1.2. Energy- structural conjugation
Conjugation structure and energy determines that a transfer of electrons from carbon and hydrogen to oxygen in the utilisation of nutrients allows these atoms to reach stability. This makes this process energy beneficial. As one atom of oxygen takes two atoms of hydrogen to form a molecule of water, its calculated that each minute in body cells to transport around 2.86 x 10 electrons and will require in average 264 ml/min of oxygen. The chemical reactions also generate a current of 76A, which is produced and later consumed by an adult at a rate of around 85.88W per minute (G.A. Apanasenko, 1992). It is crucial that this ‘biological battery’ be able to generate 15-20 times more energy to secure body response to different stress conditions.
The structural basis of vitalism is determined by four groups of cells:
Cells in apoptosis or necrosis
Hibernating or stunned cells
Functional cells of a body, main providers of organs activity
Regenerated (proliferated cells).
Every minute 1 million cells die and the same number regenerates to maintain energy-structural balance.
The physiological state of a body is the main component of the body’s life source, necessary to cover basic body’s needs: growth, proliferation, regeneration, multiplication and finally death.
There is no central energy storage that can meet all cell requirements in the body. Therefore, each cell must allocate where the limited energy resources will be directed. As oxygen demand increases, cells can produce more energy; by speeding up metabolism and initiate regeneration process when the energy resources are depleted. While at rest this self-regulating process goes into hibernation.
Adenyl nucleotides such as ATP, ADP and cyclic AMP that play the leading role in metabolic bio cycles are also necessary for cells reparation and regeneration. A number of other organic compounds like diphosphate (pyrophosphate) play a part as an energy buffer in muscle cells, as an additional phosphate group to different biological compounds, and the raise sensitivity of numbers of metabolic cascades.
1.3 Major Energy Recipients
There are five main energy distribution pathways. All of these are design to various chemical body reactions, maintain osmotic cells and tissue integrity as well as contributing to a body’s movements or heat production.
ATP is a universal converter of preserved energy into one of processes as it shown below:
Graph 1.4. Mass body cell (MBC) potency
In addition, other tree phosphates such as guanosine triphosphate, uridine triphosphate and cytosine triphosphate are main ingredients for the synthesis of proteins, carbohydrate and phospholipids. Depending on availability, intracellular ATP, ADP, AMP, mitochondria, etc. can initiate different metabolic pathways.
For instance, in active mitochondria there will be enough substances for phosphorylation in a form of ATP, PK, NTP, and oxygen will be actively absorbed as phosphorylation cannot occur without oxidation. While in resting cell mitochondria in saving mode with oxygen and plenty components for an oxidation, but lack of ADP makes phosphorylation process impossible. In later cases, cell respiration rate decreased while the concentration of energy transporters like NADH increased. It is calculated that in cells a speed oxidative phosphorylation depends on the ATP/ADP ratio.
Increasing energy demand leads to mitochondria ‘awakening’ and thermodynamic regulation of cells respiration becomes kinetic. Under this condition, the equilibrium of a self-reparation dynamic system (SRDS) depends on