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Modern methods of studying the nervous system. Methods for studying the functions of the central nervous system |
The study of the central nervous system includes a group of experimental and clinical methods. Experimental methods include cutting, extirpation, destruction of brain structures, as well as electrical stimulation and electrical coagulation. Clinical methods include electroencephalography, evoked potentials, tomography, etc. Experimental methods 1. Cut and cut method. The method of cutting and switching off various parts of the central nervous system is done in various ways. Using this method, you can observe changes in conditioned reflex behavior. 2. Methods of cold switching off brain structures make it possible to visualize the spatio-temporal mosaic of electrical processes in the brain during the formation of a conditioned reflex in different functional states. 3. Methods of molecular biology are aimed at studying the role of DNA, RNA molecules and other biologically active substances in the formation of a conditioned reflex. 4. The stereotactic method is that an electrode is introduced into the animal’s subcortical structures, with which one can irritate, destroy, or introduce chemical substances. Thus, the animal is prepared for a chronic experiment. After the animal recovers, the conditioned reflex method is used. Clinical methods Clinical methods make it possible to objectively assess the sensory functions of the brain, the state of the pathways, the brain’s ability to perceive and analyze stimuli, as well as identify pathological signs of disruption of the higher functions of the cerebral cortex. Electroencephalography Electroencephalography is one of the most common electrophysiological methods for studying the central nervous system. Its essence lies in recording rhythmic changes in the potentials of certain areas of the cortex big brain between two active electrodes (bipolar method) or an active electrode in a certain area of the cortex and a passive one, superimposed on an area remote from the brain. An electroencephalogram is a recording curve of the total potential of the constantly changing bioelectrical activity of a significant group of nerve cells. This amount includes synaptic potentials and partly action potentials of neurons and nerve fibers. Total bioelectrical activity is recorded in the range from 1 to 50 Hz from electrodes located on the scalp. The same activity from the electrodes, but on the surface of the cerebral cortex is called an electrocorticogram. When analyzing EEG, the frequency, amplitude, shape of individual waves and the repeatability of certain groups of waves are taken into account. Amplitude is measured as the distance from the baseline to the peak of the wave. In practice, due to the difficulty of determining the baseline, peak-to-peak amplitude measurements are used. Frequency refers to the number of complete cycles completed by a wave in 1 second. This indicator is measured in hertz. The reciprocal of the frequency is called the period of the wave. The EEG records 4 main physiological rhythms: ά -, β -, θ -. and δ – rhythms. α - rhythm has a frequency of 8-12 Hz, amplitude from 50 to 70 μV. It predominates in 85-95% of healthy people over nine years of age (except for those born blind) in a state of quiet wakefulness with eyes closed and is observed mainly in the occipital and parietal regions. If it dominates, then the EEG is considered synchronized. The synchronization reaction is an increase in amplitude and a decrease in EEG frequency. The EEG synchronization mechanism is associated with the activity of the output nuclei of the thalamus. A variant of the ά-rhythm are “sleep spindles” lasting 2-8 seconds, which are observed when falling asleep and represent regular alternations of increasing and decreasing amplitude of waves in the frequencies of the ά-rhythm. Rhythms of the same frequency are: μ – rhythm recorded in the Rolandic sulcus, having an arched or comb-shaped waveform with a frequency of 7-11 Hz and an amplitude of less than 50 μV; κ - rhythm noted when applying electrodes in the temporal lead, having a frequency of 8-12 Hz and an amplitude of about 45 μV. β - rhythm has a frequency from 14 to 30 Hz and a low amplitude - from 25 to 30 μV. It replaces the ά rhythm during sensory stimulation and emotional arousal. The β rhythm is most pronounced in the precentral and frontal areas and reflects a high level of functional activity of the brain. The change from ά - rhythm (slow activity) to β - rhythm (fast low-amplitude activity) is called EEG desynchronization and is explained by the activating influence on the cerebral cortex of the reticular formation of the brainstem and the limbic system. θ – rhythm has a frequency from 3.5 to 7.5 Hz, amplitude from 5 to 200 μV. In a waking person, the θ rhythm is usually recorded in the anterior regions of the brain during prolonged emotional stress and is almost always recorded during the development of the phases of slow-wave sleep. It is clearly registered in children who are in a state of displeasure. The origin of the θ rhythm is associated with the activity of the bridge synchronizing system. δ - rhythm has a frequency of 0.5-3.5 Hz, amplitude from 20 to 300 μV. Occasionally recorded in all areas of the brain. The appearance of this rhythm in a awake person indicates a decrease in the functional activity of the brain. Stably fixed during deep slow-wave sleep. The origin of the δ - EEG rhythm is associated with the activity of the bulbar synchronizing system. γ - waves have a frequency of more than 30 Hz and an amplitude of about 2 μV. Localized in the precentral, frontal, temporal, parietal areas of the brain. When visually analyzing the EEG, two indicators are usually determined: the duration of the ά-rhythm and the blockade of the ά-rhythm, which is recorded when a particular stimulus is presented to the subject. In addition, the EEG has special waves that differ from the background ones. These include: K-complex, λ - waves, μ - rhythm, spike, sharp wave. The K complex is a combination of a slow wave with a sharp wave, followed by waves with a frequency of about 14 Hz. The K-complex occurs during sleep or spontaneously in a waking person. The maximum amplitude is observed in the vertex and usually does not exceed 200 μV. Λ waves are monophasic positive sharp waves arising in the occipital area associated with eye movements. Their amplitude is less than 50 μV, frequency is 12-14 Hz. Μ – rhythm – a group of arched and comb-shaped waves with a frequency of 7-11 Hz and an amplitude of less than 50 μV. They are registered in the central areas of the cortex (Roland's sulcus) and are blocked by tactile stimulation or motor activity. A spike is a wave that clearly differs from background activity, with a pronounced peak lasting from 20 to 70 ms. Its primary component is usually negative. Spike-slow wave is a sequence of superficially negative slow waves with a frequency of 2.5-3.5 Hz, each of which is associated with a spike. A sharp wave is a wave that differs from background activity with an emphasized peak lasting 70-200 ms. At the slightest attraction of attention to a stimulus, desynchronization of the EEG develops, that is, a reaction of ά-rhythm blockade develops. A well-defined ά-rhythm is an indicator of the body’s rest. A stronger activation reaction is expressed not only in the blockade of the ά - rhythm, but also in the strengthening of high-frequency components of the EEG: β - and γ - activity. A decrease in the level of functional state is expressed in a decrease in the proportion of high-frequency components and an increase in the amplitude of slower rhythms - θ- and δ-oscillations. Method for recording impulse activity of nerve cells The impulse activity of individual neurons or a group of neurons can be assessed only in animals and, in some cases, in humans during brain surgery. To record neural impulse activity of the human brain, microelectrodes with tip diameters of 0.5-10 microns are used. They can be made of stainless steel, tungsten, platinum-iridium alloys or gold. The electrodes are inserted into the brain using special micromanipulators, which allow the electrode to be precisely positioned to the desired location. The electrical activity of an individual neuron has a certain rhythm, which naturally changes under different functional states. The electrical activity of a group of neurons has a complex structure and on a neurogram looks like the total activity of many neurons, excited at different times, differing in amplitude, frequency and phase. The received data is processed automatically using special programs. Evoked potential method The specific activity associated with a stimulus is called an evoked potential. In humans, this is the registration of fluctuations in electrical activity that appear on the EEG with a single stimulation of peripheral receptors (visual, auditory, tactile). In animals, afferent pathways and switching centers of afferent impulses are also irritated. Their amplitude is usually small, therefore, to effectively isolate evoked potentials, the technique of computer summation and averaging of EEG sections that was recorded during repeated presentation of the stimulus is used. The evoked potential consists of a sequence of negative and positive deviations from the baseline and lasts about 300 ms after the end of the stimulus. The amplitude and latency period of the evoked potential are determined. Some of the components of the evoked potential, which reflect the entry of afferent excitations into the cortex through specific nuclei of the thalamus, and have a short latent period, are called the primary response. They are registered in the cortical projection zones of certain peripheral receptor zones. Later components that enter the cortex through the brainstem reticular formation, nonspecific nuclei of the thalamus and limbic system and have a longer latency period are called secondary responses. Secondary responses, unlike primary ones, are recorded not only in the primary projection zones, but also in other areas of the brain, connected by horizontal and vertical nerve pathways. The same evoked potential can be caused by many psychological processes, and the same mental processes can be associated with different evoked potentials. Tomographic methods Tomography is based on obtaining images of brain slices using special techniques. The idea of this method was proposed by J. Rawdon in 1927, who showed that the structure of an object can be reconstructed from the totality of its projections, and the object itself can be described by many of its projections. Computed tomography is a modern method that allows you to visualize the structural features of the human brain using a computer and an X-ray machine. In a CT scan, a thin beam of X-rays is passed through the brain, the source of which rotates around the head in a given plane; The radiation passing through the skull is measured by a scintillation counter. In this way, X-ray images of each part of the brain are obtained from different points. Then, using a computer program, these data are used to calculate the radiation density of the tissue at each point of the plane under study. The result is a high-contrast image of a brain slice in a given plane. Positron emission tomography is a method that allows you to evaluate metabolic activity in various parts of the brain. The test subject ingests a radioactive compound, which makes it possible to trace changes in blood flow in a particular part of the brain, which indirectly indicates the level of metabolic activity in it. The essence of the method is that each positron emitted by a radioactive compound collides with an electron; in this case, both particles mutually annihilate with the emission of two γ-rays at an angle of 180°. These are detected by photodetectors located around the head, and their registration occurs only when two detectors located opposite each other are excited simultaneously. Based on the data obtained, an image is constructed in the appropriate plane, which reflects the radioactivity of different parts of the studied volume of brain tissue. The nuclear magnetic resonance (NMR) method allows you to visualize the structure of the brain without the use of X-rays and radioactive compounds. A very strong magnetic field is created around the subject's head, which affects the nuclei of hydrogen atoms, which have internal rotation. Under normal conditions, the rotation axes of each core have a random direction. In a magnetic field, they change orientation in accordance with the lines of force of this field. Turning off the field leads to the fact that the atoms lose the uniform direction of the axes of rotation and, as a result, emit energy. This energy is recorded by a sensor, and the information is transmitted to a computer. Impact Cycle magnetic field is repeated many times and as a result, a layer-by-layer image of the subject’s brain is created on the computer. Rheoencephalography Rheoencephalography is a method for studying the blood circulation of the human brain, based on recording changes in the resistance of brain tissue to high-frequency alternating current depending on the blood supply and allows one to indirectly judge the amount of total blood supply to the brain, the tone, elasticity of its vessels and the state of venous outflow. Echoencephalography The method is based on the property of ultrasound to be reflected differently from brain structures, cerebrospinal fluid, skull bones, and pathological formations. In addition to determining the size of the localization of certain brain formations, this method allows you to estimate the speed and direction of blood flow. Study of the functional state of the vegetative nervous system person The study of the functional state of the ANS is of great diagnostic importance in clinical practice. The tone of the ANS is judged by the state of reflexes, as well as by the results of a number of special functional tests. Methods for clinical research of VNS are conditionally divided into the following groups: Patient interview; Study of dermographism (white, red, elevated, reflex); Study of vegetative pain points; Cardiovascular tests (capillaroscopy, adrenaline and histamine skin tests, oscillography, plethysmography, determination of skin temperature, etc.); Electrophysiological tests – study of electro-skin resistance using a direct current apparatus; Determination of the content of biologically active substances, for example catecholamines in urine and blood, determination of blood cholinesterase activity. There are the following methods for studying the functions of the central nervous system: 1. Method of cutting the brain stem at various levels. For example, between the medulla oblongata and the spinal cord. 2. Method of extirpation (removal) or destruction of parts of the brain. 3. Method of irritating various parts and centers of the brain. 4. Anatomical and clinical method. Clinical observations of changes in the functions of the central nervous system when any of its parts are affected, followed by a pathological examination. 5. Electrophysiological methods: A. electroencephalography - registration of brain biopotentials from the surface of the scalp. The technique was developed and introduced into the clinic by G. Berger. b. registration of biopotentials of various nerve centers; used in conjunction with stereotactic technique, in which electrodes are inserted into a strictly defined nucleus using micromanipulators. V. evoked potential method, recording the electrical activity of brain areas during electrical stimulation of peripheral receptors or other areas; 6. method of intracerebral administration of substances using microinophoresis; 7. chronoreflexometry - determination of reflex time. End of work - This topic belongs to the section: Lectures on human physiologyLectures.. ON HUMAN PHYSIOLOGY.. Physiology as a science Subject matter methods history of physiology Based on.. If you need additional material on this topic, or you did not find what you were looking for, we recommend using the search in our database of works: What will we do with the received material:If this material was useful to you, you can save it to your page on social networks:
All topics in this section:Physiology as a science. Subject, tasks, methods, history of physiology Humoral and nervous regulation. Reflex. Reflex arc. Basic principles of reflex theory Biological and functional systems And homeokinesis And neurohumoral regulation Laws of irritation. Excitability parameters The effect of direct current on excitable tissues Structure and functions of the cytoplasmic membrane of cells Mechanisms of cell excitability. Membrane ion channels And action potentials Relationship between action potential and excitability phases Ultrastructure of skeletal muscle fiber Mechanisms of muscle contraction Energy of muscle contraction Single contraction, summation, tetanus The influence of frequency and strength of stimulation on the amplitude of contraction Reduction modes. Strength and muscle function Muscle fatigue Motor units Smooth muscle physiology Conducting stimulation along nerves Postsynaptic potentials Properties of nerve centers Braking in C.N.S Inhibitions in nerve centers Reflex coordination mechanisms Functions of the spinal cord Functions of the medulla oblongata Functions of the pons and midbrain Functions of the diencephalon Functions of the reticular formation of the brainstem Functions of the cerebellum Functions of the basal ganglia General principles of movement organization Limbic system Functions of the cerebral cortex Functional asymmetry of the hemispheres Cortical plasticity Electroencephalography. Its significance for experimental research and clinical practice Autonomic nervous system Mechanisms of synaptic transmission in the autonomic nervous system Functions of blood Blood composition. Basic physiological blood constants Composition, properties and significance of plasma components Mechanisms for maintaining acid-base balance in the blood Structure and functions of erythrocytes. Hemolysis Hemoglobin. Its varieties and functions Erythrocyte sedimentation reaction Functions of leukocytes Structure and function of platelets Regulation of erythro- and leukopoiesis Mechanisms to stop bleeding. Blood clotting process Fibrinolysis Anticoagulant system Factors influencing blood clotting Blood groups. Rh factor. Blood transfusion Protective function of blood. Immunity. Regulation of the immune response General plan of the structure of the circulatory system In different phases of cardiac activity Automaticity of the heart Mechanisms of excitability, automation and contractions of cardiomyocytes The relationship between excitation, excitability and contraction of the heart. Disorders of the rhythm and functions of the cardiac conduction system Mechanisms of regulation of cardiac activity Reflex and humoral regulation of heart activity Mechanical and acoustic manifestations Electrocardiography Factors ensuring blood movement Blood flow speed Blood pressure Arterial and venous pulse Mechanisms of regulation of vascular tone Vasomotor centers Reflex regulation of systemic arterial blood flow Physiology of the microvasculature Regulation of organ circulation Mechanisms of external respiration Pulmonary ventilation indicators Functions of the airways. Protective breathing reflexes. Dead space Exchange of gases in the lungs Transport of gases by blood Exchange of respiratory gases in tissues Regulation of breathing. Respiratory center Reflex regulation of breathing Humoral regulation of respiration Breathing at low atmospheric pressure. Hypoxia Breathing at elevated atmospheric pressure. Caisson disease Hyperbaric oxygenation The meaning of digestion and its types. Functions of the digestive tract Composition and physiological significance of saliva Mechanisms of saliva formation and regulation of salivation Chewing Swallowing Composition and properties of gastric juice. The meaning of its components Regulation of gastric secretion The role of the pancreas in digestion Mechanisms of production and regulation of pancreatic juice secretion Liver functions. The role of the liver in digestion The importance of the small intestine. Composition and properties of intestinal juice Cavity and parietal digestion Functions of the large intestine Motor function of the small and large intestines Mechanisms of absorption of substances in the digestive canal Food motivation Nutrients Methods for measuring the body's energy balance BX Physiological basis of nutrition. Power modes Exchange of water and minerals Regulation of metabolism and energy Thermoregulation Kidney functions. Mechanisms of urine formation Regulation of urine formation Non-excretory functions of the kidneys Urinary excretion Skin functions Types V.N.D Speech functions of the hemispheres Congenital forms of behavior. Unconditioned reflexes Conditioned reflexes, mechanisms of formation, meaning Unconditioned and conditioned inhibition Dynamic stereotype Structure of a behavioral act Memory and its importance in the formation of adaptive reactions Physiology of emotions Stress, its physiological significance Dream theories Theories of sleep mechanisms Types V.N.D Functions of the hemispheres Thinking and consciousness Unconditioned reflex, conditioned reflex, humoral mechanisms of regulation of sexual functions Adaptation, its types and periods Physiological basis of labor activity Biorhythms Periods of human ontogenesis Development of the neuromuscular system of children Indicators of strength, work and endurance of muscles during development Physicochemical properties of children's blood Changes in the cellular composition of blood during postnatal ontogenesis Features of cardiac activity in children Functional properties of the vascular system in children Cardiac activity and vascular tone Age-related features of external respiration functions Gas exchange in the lungs and tissues, gas transport in the blood Features of breathing regulation General patterns of nutritional development in ontogenesis Features of the functions of the digestive organs in infancy Functions of the digestive organs in definitive nutrition Metabolism and energy in childhood Development of thermoregulation mechanisms Age-related features of kidney function Child's brain Higher nervous activity of a child There are the following methods for studying the functions of the central nervous system: 1. Method of cutting the brain stem at various levels. For example, between the medulla oblongata and the spinal cord. 2. Method of extirpation (removal) or destruction of parts of the brain. 3. Method of irritating various parts and centers of the brain. 4. Anatomical and clinical method. Clinical observations of changes in the functions of the central nervous system when any of its parts are affected, followed by a pathological examination. 5. Electrophysiological methods: A. electroencephalography - registration of brain biopotentials from the surface of the scalp. The technique was developed and introduced into the clinic by G. Berger. b. registration of biopotentials of various nerve centers; used in conjunction with stereotactic technique, in which electrodes are inserted into a strictly defined nucleus using micromanipulators. V. evoked potential method, recording the electrical activity of brain areas during electrical stimulation of peripheral receptors or other areas; 6. method of intracerebral administration of substances using microinophoresis; 7. chronoreflexometry - determination of reflex time. Properties of nerve centers The nerve center (NC) is a collection of neurons in various parts of the central nervous system that provide regulation of any function of the body. For example, the bulbar respiratory center. For the conduction of excitation through nerve centers, they are characterized by following features: 1. Unilateral conduction. It goes from the afferent, through the intercalary to the efferent neuron. This is due to the presence of interneuron synapses. 2. Central delay in the conduction of excitation. Those. Excitation along the NC is much slower than along the nerve fiber. This is explained by synaptic delay. Since there are most synapses in the central link of the reflex arc, the conduction speed there is the lowest. Based on this, reflex time is the time from the onset of exposure to the stimulus to the appearance of the response. The longer the central delay, the longer the reflex time. However, it depends on the strength of the stimulus. The larger it is, the shorter the reflex time and vice versa. This is explained by the phenomenon of summation of excitations in synapses. In addition, it is determined by the functional state of the central nervous system. For example, when the NC is tired, the duration of the reflex reaction increases. 3. Spatial and temporal summation. Temporal summation occurs, as in synapses, due to the fact that the more nerve impulses arrive, the more neurotransmitter is released in them, the higher the EPSP amplitude. Therefore, a reflex reaction can occur to several successive subthreshold stimuli. Spatial summation is observed when impulses from several neuron receptors go to the nerve center. When subthreshold stimuli act on them, the resulting postsynaptic potentials are summed up and a propagating AP is generated in the neuron membrane. 4. Transformation of the rhythm of excitation - a change in the frequency of nerve impulses when passing through the nerve center. The frequency may decrease or increase. For example, increasing transformation (increase in frequency) is due to the dispersion and multiplication of excitation in neurons. The first phenomenon occurs as a result of the division of nerve impulses into several neurons, the axons of which then form synapses on one neuron (Figure). Second, the generation of several nerve impulses during the development of an excitatory postsynaptic potential on the membrane of one neuron. The downward transformation is explained by the summation of several EPSPs and the appearance of one AP in the neuron. 5. Post-tetanic potentiation is an increase in the reflex response as a result of prolonged excitation of the neurons of the center. Under the influence of many series of nerve impulses passing at high frequency through synapses. A large amount of neurotransmitter is released at interneuron synapses. This leads to a progressive increase in the amplitude of the excitatory postsynaptic potential and long-term (several hours) excitation of neurons. 6. Aftereffect is a delay in the end of the reflex response after the cessation of the stimulus. Associated with the circulation of nerve impulses along closed circuits of neurons. 7. The tone of the nerve centers is a state of constant increased activity. It is caused by the constant supply of nerve impulses to the NC from peripheral receptors, the stimulating influence of metabolic products and other humoral factors on neurons. For example, a manifestation of the tone of the corresponding centers is the tone of a certain muscle group. 8. Automaticity or spontaneous activity of nerve centers. Periodic or constant generation of nerve impulses by neurons that arise spontaneously in them, i.e. in the absence of signals from other neurons or receptors. It is caused by fluctuations in metabolic processes in neurons and the effect of humoral factors on them. 9. Plasticity of nerve centers. This is their ability to change functional properties. In this case, the center acquires the ability to perform new functions or restore old ones after damage. The basis of plasticity N.Ts. lies the plasticity of synapses and membranes of neurons, which can change their molecular structure. 10. Low physiological lability and fatigue. N.Ts. can conduct pulses of only a limited frequency. Their fatigue is explained by fatigue of synapses and deterioration of neuronal metabolism. Inhibition in the central nervous system The phenomenon of central inhibition was discovered by I.M. Sechenov in 1862. He removed the frog's brain hemispheres and determined the time of the spinal reflex to irritation of the paw with sulfuric acid. Then to the thalamus, i.e. visual tubercles applied a crystal of table salt and found that the reflex time increased significantly. This indicated inhibition of the reflex. Sechenov concluded that the overlying N.Ts. when excited, they inhibit the underlying ones. Inhibition in the central nervous system prevents the development of excitation or weakens ongoing excitation. An example of inhibition could be the cessation of a reflex reaction against the background of the action of another, stronger stimulus. Initially, a unitary-chemical theory of inhibition was proposed. It was based on Dale's principle: one neuron - one transmitter. According to it, inhibition is provided by the same neurons and synapses as excitation. Subsequently, the correctness of the binary chemical theory was proven. In accordance with the latter, inhibition is provided by special inhibitory neurons, which are intercalary. These are Renshaw cells of the spinal cord and Purkinje neurons. Inhibition in the central nervous system is necessary for the integration of neurons into a single nerve center. The following inhibitory mechanisms are distinguished in the central nervous system: 1. Postsynaptic. It arises in the postsynaptic membrane of the soma and dendrites of neurons. Those. after the transmitting synapse. In these areas, specialized inhibitory neurons form axo-dendritic or axo-somatic synapses (Fig.). These synapses are glycinergic. As a result of the effect of GLI on glycine chemoreceptors of the postsynaptic membrane, its potassium and chloride channels open. Potassium and chloride ions enter the neuron, and IPSP develops. The role of chlorine ions in the development of IPSP is small. As a result of the resulting hyperpolarization, the excitability of the neuron decreases. The conduction of nerve impulses through it stops. The alkaloid strychnine can bind to glycine receptors on the postsynaptic membrane and turn off inhibitory synapses. This is used to demonstrate the role of inhibition. After the administration of strychnine, the animal develops cramps in all muscles. 2. Presynaptic inhibition. In this case, the inhibitory neuron forms a synapse on the axon of the neuron that approaches the transmitting synapse. Those. such a synapse is axo-axonal (Fig.). The mediator of these synapses is GABA. Under the influence of GABA, chloride channels of the postsynaptic membrane are activated. But in this case, chlorine ions begin to leave the axon. This leads to a small local but long-lasting depolarization of its membrane. A significant part of the sodium channels of the membrane is inactivated, which blocks the conduction of nerve impulses along the axon, and consequently the release of the neurotransmitter at the transmitting synapse. The closer the inhibitory synapse is located to the axon hillock, the stronger its inhibitory effect. Presynaptic inhibition is most effective in information processing, since the conduction of excitation is not blocked in the entire neuron, but only at its one input. Other synapses located on the neuron continue to function. 3. Pessimal inhibition. Discovered by N.E. Vvedensky. Occurs at a very high frequency of nerve impulses. A persistent, long-term depolarization of the entire neuron membrane and inactivation of its sodium channels develops. The neuron becomes unexcitable. Both inhibitory and excitatory postsynaptic potentials can simultaneously arise in a neuron. Due to this, the necessary signals are isolated. Related information. There are the following methods for studying the functions of the central nervous system: 1. method cutting brain stem at various levels. For example, between the medulla oblongata and the spinal cord; 2. method extirpation(deletion) or destruction areas of the brain; 3. method irritation various parts and centers of the brain; 4. anatomical-clinical method. Clinical observations of changes in the functions of the central nervous system when any of its parts are damaged, followed by a pathological examination; 5. electrophysiological methods: A. electroencephalography– registration of brain biopotentials from the surface of the scalp. The technique was developed and introduced into the clinic by G. Berger; b. registration biopotentials various nerve centers; used in conjunction with the stereotactic technique, in which electrodes are inserted into a strictly defined nucleus using micromanipulators; V. method evoked potentials, recording the electrical activity of areas of the brain during electrical stimulation of peripheral receptors or other areas. 6. method of intracerebral administration of substances using microinophoresis; 7. chronoreflexometry– determination of reflex time. Properties of nerve centers Nerve center(NC) is a collection of neurons in various parts of the central nervous system that provide regulation of any function of the body. For example, the bulbar respiratory center. The following features are characteristic for the conduction of excitation through nerve centers: 1. Unilateral conduction. It goes from the afferent, through the intercalary, to the efferent neuron. This is due to the presence of interneuron synapses. 2. Central delay carrying out excitation. Those. Excitation along the NC is much slower than along the nerve fiber. This is explained by synaptic delay. Since there are most synapses in the central link of the reflex arc, the conduction speed there is the lowest. Based on this, reflex time – This is the time from the onset of exposure to a stimulus to the appearance of a response. The longer the central delay, the longer the reflex time. However, it depends on the strength of the stimulus. The larger it is, the shorter the reflex time and vice versa. This is explained by the phenomenon of summation of excitations in synapses. In addition, it is determined by the functional state of the central nervous system. For example, when the NC is tired, the duration of the reflex reaction increases. 3. Spatial and temporal summation. Time summation arises, as in synapses, due to the fact that the more nerve impulses are received, the more neurotransmitter is released in them, the higher the amplitude of excitation of postsynaptic potentials (EPSP). Therefore, a reflex reaction can occur to several successive subthreshold stimuli. Spatial summation observed when impulses from several receptor neurons go to the nerve center. When subthreshold stimuli act on them, the resulting postsynaptic potentials are summed up and a propagating AP is generated in the neuron membrane. 4. Rhythm transformation excitation - a change in the frequency of nerve impulses as they pass through the nerve center. The frequency may decrease or increase. For example, enhancing transformation(increase in frequency) due to dispersion And animation excitations in neurons. The first phenomenon occurs as a result of the division of nerve impulses into several neurons, the axons of which then form synapses on one neuron. The second is the generation of several nerve impulses during the development of an excitatory postsynaptic potential on the membrane of one neuron. Downward Transformation is explained by the summation of several EPSPs and the occurrence of one AP in the neuron. 5. Postetanic potentiation– this is an increase in the reflex reaction as a result of prolonged excitation of the neurons of the center. Under the influence of many series of nerve impulses passing at high frequency through synapses, a large amount of neurotransmitter is released at interneuron synapses. This leads to a progressive increase in the amplitude of the excitatory postsynaptic potential and long-term (several hours) excitation of neurons. 6. Aftereffect- this is a delay in the end of the reflex response after the cessation of the stimulus. Associated with the circulation of nerve impulses along closed circuits of neurons. 7. Tone of nerve centers– a state of constant increased activity. It is caused by the constant supply of nerve impulses to the NC from peripheral receptors, the stimulating influence of metabolic products and other humoral factors on neurons. For example, the manifestation of the tone of the corresponding centers is the tone of a certain muscle group. 8. Automatic(spontaneous activity) of nerve centers. Periodic or constant generation of nerve impulses by neurons that arise spontaneously in them, i.e. in the absence of signals from other neurons or receptors. It is caused by fluctuations in metabolic processes in neurons and the effect of humoral factors on them. 9. Plastic nerve centers. This is their ability to change functional properties. In this case, the center acquires the ability to perform new functions or restore old ones after damage. The plasticity of NCs is based on the plasticity of synapses and membranes of neurons, which can change their molecular structure. 10. Low physiological lability And fast fatiguability. NCs can conduct pulses of only a limited frequency. Their fatigue is explained by fatigue of synapses and deterioration of neuronal metabolism. Inhibition in the central nervous system Phenomenon central braking discovered by I.M. Sechenov in 1862. He removed the frog's brain hemispheres and determined the time of the spinal reflex to irritation of the paw with sulfuric acid. Then a crystal of table salt was placed on the thalamus (visual tubercles) and found that the reflex time increased significantly. This indicated inhibition of the reflex. Sechenov concluded that the overlying NCs, when excited, inhibit the underlying ones. Inhibition in the central nervous system prevents the development of excitation or weakens ongoing excitation. An example of inhibition could be the cessation of a reflex reaction against the background of the action of another, stronger stimulus. Was originally proposed unitary chemical theory of inhibition. It was based on Dale's principle: one neuron - one transmitter. According to it, inhibition is provided by the same neurons and synapses as excitation. It was subsequently proven correct binary chemical theory. In accordance with the latter, inhibition is provided by special inhibitory neurons, which are intercalary. These are Renshaw cells of the spinal cord and Purkinje neurons. Inhibition in the central nervous system is necessary for the integration of neurons into a single nerve center. The following are distinguished in the central nervous system: braking mechanisms: 1. Postsynaptic. It occurs in the postsynaptic membrane of the soma and dendrites of neurons, i.e. after the transmitting synapse. In these areas, specialized inhibitory neurons form axo-dendritic or axo-somatic synapses. These synapses are glycinergic. As a result of the effect of glycine on glycine chemoreceptors of the postsynaptic membrane, its potassium and chloride channels open. Potassium and chloride ions enter the neuron, and inhibition of postsynaptic potentials (IPSPs) develops. The role of chlorine ions in the development of IPSP is small. As a result of the resulting hyperpolarization, the excitability of the neuron decreases. The conduction of nerve impulses through it stops. Alkaloid strychnine can bind to glycine receptors on the postsynaptic membrane and turn off inhibitory synapses. This is used to demonstrate the role of inhibition. After the administration of strychnine, the animal develops cramps in all muscles. 2. Presynaptic braking. In this case, the inhibitory neuron forms a synapse on the axon of the neuron that approaches the transmitting synapse. Those. such a synapse is axo-axonal. The mediator of these synapses is GABA. Under the influence of GABA, chloride channels of the postsynaptic membrane are activated. But in this case, chlorine ions begin to leave the axon. This leads to a small local but long-lasting depolarization of its membrane. A significant part of the sodium channels of the membrane is inactivated, which blocks the conduction of nerve impulses along the axon, and consequently the release of the neurotransmitter at the transmitting synapse. The closer the inhibitory synapse is located to the axon hillock, the stronger its inhibitory effect. Presynaptic inhibition is most effective in information processing, since the conduction of excitation is not blocked in the entire neuron, but only at its one input. Other synapses located on the neuron continue to function. 3. Pessimal braking. Discovered by N.E. Vvedensky. Occurs at a very high frequency of nerve impulses. A persistent, long-term depolarization of the entire neuron membrane and inactivation of its sodium channels develops. The neuron becomes unexcitable. Both inhibitory and excitatory postsynaptic potentials can simultaneously arise in a neuron. Due to this, the necessary signals are isolated. The study of the central nervous system includes a group of experimental and clinical methods. Experimental methods include cutting, extirpation, destruction of brain structures, as well as electrical stimulation and electrical coagulation. Clinical methods include electroencephalography, evoked potentials, tomography, etc. Experimental methods1. Cut and cut method. The method of cutting and switching off various parts of the central nervous system is done in various ways. Using this method, you can observe changes in conditioned reflex behavior. 2. Methods of cold switching off brain structures make it possible to visualize the spatio-temporal mosaic of electrical processes in the brain during the formation of a conditioned reflex in different functional states. 3. Methods of molecular biology are aimed at studying the role of DNA, RNA molecules and other biologically active substances in the formation of a conditioned reflex. 4. The stereotactic method consists in introducing an electrode into the animal’s subcortical structures, with which one can irritate, destroy, or inject chemicals. Thus, the animal is prepared for a chronic experiment. After the animal recovers, the conditioned reflex method is used. Clinical methodsClinical methods make it possible to objectively assess the sensory functions of the brain, the state of the pathways, the brain’s ability to perceive and analyze stimuli, as well as identify pathological signs of disruption of the higher functions of the cerebral cortex. ElectroencephalographyElectroencephalography is one of the most common electrophysiological methods for studying the central nervous system. Its essence lies in recording rhythmic changes in the potentials of certain areas of the cerebral cortex between two active electrodes (bipolar method) or an active electrode in a certain zone of the cortex and a passive electrode superimposed on an area remote from the brain. Electroencephalogram is a recording curve of the total potential of the constantly changing bioelectrical activity of a significant group of nerve cells. This amount includes synaptic potentials and partly action potentials of neurons and nerve fibers. Total bioelectrical activity is recorded in the range from 1 to 50 Hz from electrodes located on the scalp. The same activity from the electrodes, but on the surface of the cerebral cortex is called electrocorticogram. When analyzing EEG, the frequency, amplitude, shape of individual waves and the repeatability of certain groups of waves are taken into account. Amplitude measured as the distance from the baseline to the peak of the wave. In practice, due to the difficulty of determining the baseline, peak-to-peak amplitude measurements are used. Under frequency refers to the number of complete cycles completed by a wave in 1 second. This indicator is measured in hertz. The reciprocal of the frequency is called period waves. The EEG records 4 main physiological rhythms: ά -, β -, θ -. and δ – rhythms. α – rhythm has a frequency of 8-12 Hz, amplitude from 50 to 70 μV. It predominates in 85-95% of healthy people over nine years of age (except for those born blind) in a state of quiet wakefulness with eyes closed and is observed mainly in the occipital and parietal regions. If it dominates, then the EEG is considered as synchronized. Synchronization reaction called an increase in amplitude and a decrease in frequency of the EEG. The EEG synchronization mechanism is associated with the activity of the output nuclei of the thalamus. A variant of the ά-rhythm are “sleep spindles” lasting 2-8 seconds, which are observed when falling asleep and represent regular alternations of increasing and decreasing amplitude of waves in the frequencies of the ά-rhythm. Rhythms of the same frequency are: μ – rhythm, recorded in the Rolandic sulcus, having an arched or comb-shaped waveform with a frequency of 7-11 Hz and an amplitude of less than 50 μV; κ - rhythm, noted when applying electrodes in the temporal lead, having a frequency of 8-12 Hz and an amplitude of about 45 μV. β - rhythm has a frequency from 14 to 30 Hz and a low amplitude - from 25 to 30 μV. It replaces the ά rhythm during sensory stimulation and emotional arousal. β- rhythm is most pronounced in the precentral and frontal areas and reflects high level functional activity of the brain. The change from ά - rhythm (slow activity) to β - rhythm (fast low-amplitude activity) is called desynchronization EEG is explained by the activating influence on the cerebral cortex of the reticular formation of the brainstem and the limbic system. θ – rhythm has a frequency from 3.5 to 7.5 Hz, amplitude from 5 to 200 μV. In a waking person, the θ rhythm is usually recorded in the anterior regions of the brain during prolonged emotional stress and is almost always recorded during the development of the phases of slow-wave sleep. It is clearly registered in children who are in a state of displeasure. The origin of the θ rhythm is associated with the activity of the bridge synchronizing system. δ – rhythm has a frequency of 0.5-3.5 Hz, amplitude from 20 to 300 μV. Occasionally recorded in all areas of the brain. The appearance of this rhythm in a awake person indicates a decrease in the functional activity of the brain. Stably fixed during deep slow-wave sleep. The origin of the δ - EEG rhythm is associated with the activity of the bulbar synchronizing system. γ – waves have a frequency of more than 30 Hz and an amplitude of about 2 μV. Localized in the precentral, frontal, temporal, parietal areas of the brain. When visually analyzing the EEG, two indicators are usually determined: the duration of the ά-rhythm and the blockade of the ά-rhythm, which is recorded when a particular stimulus is presented to the subject. In addition, the EEG has special waves that differ from the background ones. These include: K-complex, λ - waves, μ - rhythm, spike, sharp wave. K - complex- This is a combination of a slow wave with a sharp wave, followed by waves with a frequency of about 14 Hz. The K-complex occurs during sleep or spontaneously in a waking person. The maximum amplitude is observed in the vertex and usually does not exceed 200 μV. Λ – waves- monophasic positive sharp waves arising in the occipital area associated with eye movements. Their amplitude is less than 50 μV, frequency is 12-14 Hz. M – rhythm– a group of arc-shaped and comb-shaped waves with a frequency of 7-11 Hz and an amplitude of less than 50 μV. They are registered in the central areas of the cortex (Roland's sulcus) and are blocked by tactile stimulation or motor activity. Spike– a wave clearly different from background activity, with a pronounced peak lasting from 20 to 70 ms. Its primary component is usually negative. Spike-slow wave is a sequence of superficially negative slow waves with a frequency of 2.5-3.5 Hz, each of which is associated with a spike. sharp wave– a wave that differs from background activity with an emphasized peak lasting 70-200 ms. At the slightest attraction of attention to a stimulus, desynchronization of the EEG develops, that is, a reaction of ά-rhythm blockade develops. A well-defined ά-rhythm is an indicator of the body’s rest. A stronger activation reaction is expressed not only in the blockade of the ά - rhythm, but also in the strengthening of high-frequency components of the EEG: β - and γ - activity. A decrease in the level of functional state is expressed in a decrease in the proportion of high-frequency components and an increase in the amplitude of slower rhythms - θ- and δ-oscillations. Method for recording impulse activity of nerve cells The impulse activity of individual neurons or a group of neurons can be assessed only in animals and, in some cases, in humans during brain surgery. To record neural impulse activity of the human brain, microelectrodes with tip diameters of 0.5-10 microns are used. They can be made of stainless steel, tungsten, platinum-iridium alloys or gold. The electrodes are inserted into the brain using special micromanipulators, which allow the electrode to be precisely positioned to the desired location. The electrical activity of an individual neuron has a certain rhythm, which naturally changes under different functional states. The electrical activity of a group of neurons has a complex structure and on a neurogram looks like the total activity of many neurons, excited at different times, differing in amplitude, frequency and phase. The received data is processed automatically using special programs. Evoked potential method The specific activity associated with a stimulus is called an evoked potential. In humans, this is the registration of fluctuations in electrical activity that appear on the EEG with a single stimulation of peripheral receptors (visual, auditory, tactile). In animals, afferent pathways and switching centers of afferent impulses are also irritated. Their amplitude is usually small, therefore, to effectively isolate evoked potentials, the technique of computer summation and averaging of EEG sections that was recorded during repeated presentation of the stimulus is used. The evoked potential consists of a sequence of negative and positive deviations from the baseline and lasts about 300 ms after the end of the stimulus. The amplitude and latency period of the evoked potential are determined. Some of the components of the evoked potential, which reflect the entry of afferent excitations into the cortex through specific nuclei of the thalamus, and have a short latent period, are called primary response. They are registered in the cortical projection zones of certain peripheral receptor zones. Later components that enter the cortex through the reticular formation of the brainstem, nonspecific nuclei of the thalamus and limbic system and have a longer latent period are called secondary responses. Secondary responses, unlike primary ones, are recorded not only in the primary projection zones, but also in other areas of the brain, connected by horizontal and vertical nerve pathways. The same evoked potential can be caused by many psychological processes, and the same mental processes may be associated with different evoked potentials. Tomographic methods Tomography– is based on obtaining images of brain slices using special techniques. The idea of this method was proposed by J. Rawdon in 1927, who showed that the structure of an object can be reconstructed from the totality of its projections, and the object itself can be described by many of its projections. CT scan is a modern method that allows you to visualize the structural features of the human brain using a computer and an X-ray machine. In a CT scan, a thin beam of X-rays is passed through the brain, the source of which rotates around the head in a given plane; The radiation passing through the skull is measured by a scintillation counter. In this way, X-ray images of each part of the brain are obtained from different points. Then, using a computer program, these data are used to calculate the radiation density of the tissue at each point of the plane under study. The result is a high-contrast image of a brain slice in a given plane. Positron emission tomography– a method that allows you to assess metabolic activity in different parts of the brain. The test subject ingests a radioactive compound, which makes it possible to trace changes in blood flow in a particular part of the brain, which indirectly indicates the level of metabolic activity in it. The essence of the method is that each positron emitted by a radioactive compound collides with an electron; in this case, both particles mutually annihilate with the emission of two γ-rays at an angle of 180°. These are detected by photodetectors located around the head, and their registration occurs only when two detectors located opposite each other are excited simultaneously. Based on the data obtained, an image is constructed in the appropriate plane, which reflects the radioactivity of different parts of the studied volume of brain tissue. Nuclear magnetic resonance method(NMR imaging) allows you to visualize the structure of the brain without the use of X-rays and radioactive compounds. A very strong magnetic field is created around the subject's head, which affects the nuclei of hydrogen atoms, which have internal rotation. Under normal conditions, the rotation axes of each core have a random direction. In a magnetic field, they change orientation in accordance with the lines of force of this field. Turning off the field leads to the fact that the atoms lose the uniform direction of the axes of rotation and, as a result, emit energy. This energy is recorded by a sensor, and the information is transmitted to a computer. The cycle of exposure to the magnetic field is repeated many times and as a result, a layer-by-layer image of the subject’s brain is created on the computer. Rheoencephalography Rheoencephalography is a method for studying the blood circulation of the human brain, based on recording changes in the resistance of brain tissue to high-frequency alternating current depending on the blood supply and allows one to indirectly judge the amount of total blood supply to the brain, the tone, elasticity of its vessels and the state of venous outflow. Echoencephalography The method is based on the property of ultrasound to be reflected differently from brain structures, cerebrospinal fluid, skull bones, and pathological formations. In addition to determining the size of the localization of certain brain formations, this method allows you to estimate the speed and direction of blood flow. Study of the functional state of the human autonomic nervous systemThe study of the functional state of the ANS is of great diagnostic importance in clinical practice. The tone of the ANS is judged by the state of reflexes, as well as by the results of a number of special functional tests. Methods for clinical research of VNS are conditionally divided into the following groups:
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