- •Contents:
- •Introduction
- •Structure, functions and methods of research of biological membranes The general structure of cell
- •Ultrastrucrure and function of function of biological membrane
- •Kinds of passive transport
- •Methods of research of structure and functions of biological membranes
- •Method of a dark field.
- •Phase - contrast method.
- •Electronic microscopy.
- •Method of diffraction of X-rays radiation.
- •Ultramicroscopy.
- •Luminescent methods of research of membranes.
- •Method of ultrachemistry.
- •Nuclear magnetic resonance research and electronic paramagnetic resonance research.
- •Research of forces of a superficial tension Properties of liquids
- •Superficial tension.
- •Physical properties of biological membranes.
- •Molecular mechanisms of electrochemical potentials of membranes and distribution of a nervous impulse along excitability fibre.
- •Principles of transformation of biological and not electric signals in electric. Designs of sensors and electrodes, their basic characteristics
- •Application of sensors
- •Analog registering devices
- •Rhythm of heart. Parameters of cardiac activity.
- •External displays of activity of heart.
- •Activity of heart
- •Electric activity of cells of a myocardium
- •Functions of conductive system of heart
- •The electrocardiogram
- •Change of a rhythm of cardiac activity.
- •The device and main principles of work of electrocardiograph
- •Imposing of electrodes
- •The device, a principle of work of electroencephalograph. Basic rhythms of eeg. Registration of eeg and principles of the analysis
- •Introduction
- •Essence of a method
- •Technique of record of electroencephalogram.
- •Principles of analyses of electroencephalogram
- •Definition of a photoeffect
- •Types of photoeffects.
- •Einstein equation
- •Application of a photo effect in medicine.
- •The device, principle of work spectrophotometer. Application spectrophometrical methods of research for definition of concentration of substances in biological liquids
- •Method of the calibre graph.
- •Method of comparison.
- •Polarization of light by biosystems. Polarimeter. Light natural and polarized. Polaroids.
- •Research of microstructures in polarizing light
- •Rotation of a plane of fluctuations of polarized light. Saccharimetry.
- •Design of the device
- •Principle of action
- •Special receptions of microscopy of biological objects Special methods of light microscopy (illumination and supervision). Method of a dark field.
- •Method of ultramicroscopy
- •Method of a light field and its version
- •Method of phase contrast
- •Polarizing microscopy
- •The method interference contrast
- •Method of research in a view of a luminescence
- •Device of a microscope. Measurement of value of microscoping object.
- •Model of sliding strings. Biomechanics of a muscle. The equation of Hill. Modeling of muscular reduction Biophysics of muscular reduction
- •Structure of a cross-section-striped muscle. Model of sliding strands.
- •Biomechanics of a muscle
- •The equation of Hill. Power of single reduction.
- •Modelling of muscular reduction
- •Electromechanical interface in muscles
- •Devices for measurement of function of external breath. The device and a principle of work. Registration and the analysis of the given functional researches
- •Change of saturation by gases of an organism at differences of external pressure.
- •Biomechanics of external breath
- •Devices for measurement of function of external breath
- •Viscosity of a liquid
- •Current of a liquid on a horizontal pipe. Puazal’s law.
- •Current of a liquid on a pipe of variable section and branched out
- •Definition of speed of blood-groove
- •Full resistance (impedance) of tissues of the organism Physical bases of rheography
- •Measurement of factor of viscosity.
- •Physical bases of hemodynamic. Laws of movement of blood in an arterial and venous channel
- •Measurement of pressure of blood
- •Systolic and minute volume of a blood-groove
- •Change of minute volume of a blood-groove at work.
- •Biophysical features of an aorta.
- •Biophysical features of arterioles of the big circle of blood circulation.
- •Tomographic methods
- •Classification of kinds of a tomography.
- •Interposition of a source of probing radiation, bject and the detector.
- •Echosounding
- •Computer tomograph.
- •Magnetic-resonant tomography.
- •Three-dimensional ultrasonic
- •ElastoScan-flexography
- •Modes of an acoustic transparency of three-dimensional ultrasonic.
- •Methods of physiotherapeutic influence
- •The therapeutic techniques based on application of a direct current. Electrophoresis and galvanizing in a medical practice. Mobility of ions.
- •Medicinal electrophoresis.
- •Galvanizing.
- •Electrosecurity
- •The basic requirements to an electrosecurity of electromedical devices and devices.
- •Modelling of biophysical processes.
- •The basic stages of modelling
- •The basic stages of modelling
- •4. Creation of model, its research.
- •Classification of models:
- •Mathematical models of growth of number of a population.
- •Pharmacokinetic model.
- •Sources of X-ray radiation.
- •Artificial sources of radiation.
- •Interaction of X-ray radiation with substance.
- •1. Coherent dispersion;
- •2. Photoeffect
- •3. Kompton - effect
- •Radioactivity radiation Radioactive disintegration Structure of a nucleus
- •A radioactive disintegration. Kinds of radioactive radiation
- •It is thrown out and a nucleus has more stability complex of nucleons. Positron β-disintegration is described by the equation:
- •The basic law of radioactive disintegration in the differential form. A constant of disintegration.
- •The basic law of radioactive disintegration in the differential form.
- •A half-life period.
- •Activity. A unit of measure.
- •Radioactive elements in the nature.
- •Ionizing radioactive radiation and its biological action.
- •The absorbed and exposition doze. Power of a doze. Units of measure.
- •Relative biological efficiency.
- •Mehanisms of action of laser radiation on biological tissues.
- •Mechanisms of action of laser radiation on biological tissues
- •Список использованной литературы :
- •Educational handout on medical biophysics kovaleva larissa valentinovna
Functions of conductive system of heart
Spontaneous generation of rhythmic impulses is result of the harmonious activity of many cells of sinoatrial node which is provided with close contacts (nexuses) and electrotonic interaction of these cells. Excitation extends on conductive system on retractive a myocardium.
Feature of conductive system of heart is ability of each cell independently to generate excitation. There is a gradient of automatism, expressed in decreasing ability to automatism various sites of conductive systems.
In usual conditions automatism of all parts of conductive system is suppressed with more frequent impulses acting from sinoatrial node. Impulses will arise with frequency 40-50 in a minute.
Distinctive feature of conductive system of heart is presence in its cells of a plenty of intercellular contacts - nexuses. These contacts are a place of transition of excitation from one cell on another. The same contacts are available and between cells of conductive system and a working myocardium. Owing to presence of contacts the myocardium consisting of separate cells, works as a unit. Existence of a plenty of intercellular contacts increases reliability of carrying out of excitation in a myocardium.
Excitation extends on auricles, reaching atrioventricular node. In sinoatrial node there is some delay of carrying out of excitation. Owing to a delay excitation reaches up to sinoatrial bunch and cardiac conductive myocyte after the muscles of auricles have time to be reduced and pump over blood from auricles in ventricle.
Hence, atrioventricular delay provides necessary sequence (coordination) of reductions of auricles and ventricles.
Speed of distribution of excitation in sinoatrial bunch and in cardiac conductive myocytes reaches 4,5-5 m/sec, that in 5 times more speed of distribution of excitation on a working myocardium. Owing to it cells of a myocardium of ventricles are reduced almost at once or synchronously. Synchronism of reduction of cells raises capacity of a myocardium and efficiency force functions of ventricles.
Presence of conductive system provides a number of the important physiological features of heart: 1) rhythmic generation of impulses (potentials of action); 2) necessary consecution, (coordination) of reductions of auricles and ventricles; 3) synchronous involving in process of reduction of cells of a myocardium of ventricles (that increases efficiency of a systole).
The electrocardiogram
C
overage
by excitation of huge quantity of cells of the worker myocardium
causes occurrence of a negative charge on a surface of these cells.
Heart becomes the powerful electrogenerator. Tissues of a body,
possessing rather high electroconductivity, allow registering
electric potentials of heart from surface of bodies. Such technique
of research of electric activity of the heart, is entered into
practice by V. Enthoven, A.F. Samoilov, T. Lewis, V.F. Zelenin, is
called electrocardiography,
and the curve registered with its help is called the
electrocardiogram.
Electrocardiography is wide applied in medicine as the diagnostic
method, allowing to estimate dynamics of distribution of excitation
in heart and to judge infringements of cardiac activity at changes of
an electrocardiogram.
Now special device - electrocardiograph is used. Record of curves is made on a moving paper tape.
Fig. 3. Imposing of electrodes at standard assignments of the electrocardiogram (I-III) and forms of the electrocardiograms received at these assignments.
Owing to the certain position of heart in a thorax and the original form of a body of the person the electric power lines arising between raised (-) and not raised (+) sites of heart, are distributed on a surface of a body irregularly. For this reason depending upon a place of the location of electrodes the form of an electrocardiogram and amplitude of it peaks will be various. For registration of an electrocardiogram it is necessary to make tap of potentials from extremities and surfaces of a thorax.
Usually use three so-called standard taps from extremities: I tap: the right hand - the left hand; II tap: the right hand - the left leg; III tap: the left hand - the left leg (fig. 3). Three unipolar strengthened Goldberg’s taps on are registered: aVR; aVL; aVF. At registration of the strengthened tap two electrodes used for registration of standard taps, are united in one and the potential difference between the incorporated and active electrodes is registered. So, at aVR the electrode imposed on the right hand is active, at aVL - on the left hand, at aVF - on the left leg. Wilson offers registration of six thorax taps.
The mutual relation of size of peaks in three standard taps has been established by Enthoven. He has found, that electromotive force of heart registered in II standard tap, is equal to the sum of electromotive forces in I and III taps. Expression of electromotive power is the height of peaks, therefore peaks of II tap on the size are equal to the algebraic sum of peaks of I and III taps.
For tap of potentials from a thorax it is necessary to put the first electrode to one of six points shown on figure 4.
F
ig.
4. Places of imposing of electrodes at thorax
taps
of the electrocardiogram (1-6) and forms of the electrocardiograms
received at these taps. I-IV- intercostal intervals.
As the second electrode three electrodes connected together, imposed on both hands and the left leg serve. In this case the form of an electrocardiogram reflects electric changes only in a site of the part of the thorax electrode. The incorporated electrode, appurtenant to three extremities, is indifferent, or «zero» as its potential does not change during all cardiac cycle. Such taps are called unipolar, or unidirectional. These taps are designated by Latin letter V (V1, V2).
The normal electrocardiogram of the person received in II standard tap, is shown on fig. 5. At the analysis of electrocardiogram amplitude of peaks in mV is defined, time of their course in seconds, duration of segments - sites of isopotential lines between next peaks.
Formation of an electrocardiogram (it peaks and intervals) is caused by distribution of excitation in heart and displays this process. Peaks arise and develop, when between sites of excitable systems there is a potential difference. Any part of system is captured by excitation, and another is not captured by excitation. Isopotential line arises when within the limits of excitable systems are not present a potential difference. All system is not raised or, on the contrary, is captured by excitation. The registered electrocardiogram reflects consecutive coverage by excitation retractive myocardium of auricles and ventricle.
Fig. 5.
Peak Р (see fig. 5) displays coverage by excitation of auricles and is called atrial. Further excitation distributes on sinoatrial node also moves on conductive system of ventricle. At this time electrocardiograph registers isopotential line (both auricles are completely raised, both ventricles are not raised yet, and movement of excitation on conductive system of ventricles is not register by electro-cardiograph - segment PQ on an electro-cardiogram). In auricles excitation extends mainly on retractive myocardium avalanchely.
Coverage by excitation of ventricles is carried out by means of transfer of excitation from elements of conductive systems on retractive myocardium that causes complex character of complex QRS reflecting coverage by excitation of ventricles. Thus peak Q is caused by excitation of a top of heart, and internal surface of ventricles, peak R - excitation of the basis of heart and an external surface of ventricles. Process of full coverage by excitation of myocardium of ventricles will complete to the end of formation of peak S. Now both ventricles are raised, and segment ST is on isopotential line, owing to absence of a potential difference in excitable system of ventricles.
Peak Т reflects processes of repolarization, or restoration of normal membrane potential of cells of a myocardium. These processes in various cells arise not strictly synchronously. Therefore there is a potential difference between even depolarize sites of a myocardium (possessing negative charge) and the sites of the myocardium which as restored the positive charge. The specified potential difference is registered in the form of peak T. This peak is the most changeable part of an electrocardiogram. Between peak Т and the subsequent peak Р the isopotential line is registered, because in this time in a myocardium of ventricles and in a myocardium of auricles there is no potential difference. Visible reflection of peak, corresponding repolarization of auricle, is not present on an electrocardiogram, because it coincides with powerful complex QRS on time.
The general duration of an electric systole of ventricles (Q-T) almost coincides with duration of a mechanical systole (the mechanical systole begins a little bit later, than electric).
The electrocardiogram allows estimating character of violation of carrying out of excitation in heart. So, on size of interval Р-Q (from the beginning peak Р and to the beginning peak Q) it is possible to judge about, whether carrying out of excitation from an auricle to ventricle with normal speed is made. This time is equal to 0,12-0,2 sec in norm. The general duration of complex QRS reflects speed of coverage by excitation of conductive myocardium of ventricles and is equal to 0,06-0,1 (see fig. 5).
Processes of depolarization and repolarization arise in different sites of a myocardium non-simultaneously, therefore the size of a potential difference between various sites of a cardiac muscle during a cardiac cycle changes. A conditional line, connected two points, possessing the greatest potential difference, in each moment is called electric axis heart. During each given moment an electric axis of heart characterized by in the certain size and a direction, possesses properties of vector size. Owing to non-simultaneity of coverage by excitation of various departments of a myocardium this vector changes the direction. Simultaneous record of changes of size of a potential difference and a direction of an electric axis is called vectorcardiogram (VCG).
