- •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
Activity of heart
R
eductions
of heart occur owing to periodically arising
in
a cardiac muscle of processes of excitation.
Excitation in heart arises periodically under influence of the processes proceeding in it. This phenomenon is called automatism. Definite sites of a myocardium consisting from specific (atypical) of muscular tissues, poor by myofibrilla, rich sarcoplasmic have ability of automatism. The specific muscles form in heart the conductive system consisting from sinoatrial node – driver of a rhythm of the heart located in a wall of an auricle (Fig. 1).
Fig. 1. A structure of conductive system of heart and
Distribution of excitation. SA - sinoatrial node, AV - atrioventricular node. Figures designate scope by excitation of departments of heart in seconds from the moment of origin of an impulse in sinoatrial node.
Electric activity of cells of a myocardium
In natural conditions of a cell of a myocardium are in a condition of rhythmic activity (excitation), therefore it is possible to speak about their potential of rest only conditionally. Majority of cells have potential of rest nearby 90 mV and is defined by a concentration gradient of ions К+.
Potentials of action (PA), registered in different parts of heart by means of endocellular microelectrodes, differ under the form, amplitude and duration (fig. 2.A).
Fig. 2. Various types of potentials of action of the cardiac cells, correlated with a time course of an electrocardiogram.
A - a configuration of potentials of action of myocytes in various departments of heart;
C-A - sinoatrial node.
П - an auricle; A-B - atrioventricular node:
ПЖ - bunch of Ges; ПП and ЛП - the right and left legs of a bunch; Ж -ventricles. 1-6 - potentials of action of cells of a myocardium; 7 - an electrocardiogram; - potential of action of a single cell of a myocardium; a – PA of ventricle. By arrows prevailing streams of ions Na+, Са2+, K+, responsible for various phases (1-4) PA are shown; - autorhythmic activity of sinoatrial node. By arrows it is shown slow diastolic depolarization.
On fig. 2 PA of a single cell of a myocardium of ventricle is schematically shown. For occurrence of this potential it was required to depolarize a membrane on 30 mV.
It is possible to distinguish in PA following phases: fast initial depolarization - a phase 1; slow repolarization, a so-called plateau - a phase 2; fast repolarization - a phase 3; a phase of rest - a phase 4. The phase 1 in cells of a myocardium of auricles, cardiac conductive myocytes and a myocardium of ventricles has the same nature, as ascending phase PA nervous and skeletal muscular fibers - it is caused by increase of sodium permeability or activation fast sodium channels of a cellular membrane. During peak of PA there is a change of a sign membrane potential (with-90 up to +30 mV).
Depolarization of membranes causes activation of slow sodium - calcium channels. The stream of ions Са2 + inside of a cell on these channels leads to development of plateau of PA (a phase 2). During a plateau sodium channels is inactivated and the cell passes in a condition of absolute refractory period. Simultaneously there is an activation potassium channels. The stream of ions leaving a cell K+ provides fast depolarization of membranes (a phase 3) during which calcium channels are closed, that accelerates process of repolarization (as falls entering calcium current, depolarized of a membrane). Repolarization of membranes is caused gradual closing of potassium channels and reactivation of sodium channels. As a result excitability of myocardium cells is restored-it the period so-called relative refractory period.
In cells of a working myocardium (an auricle, ventricle) membrane potential (in intervals between the following one after another PA) is supported on constant level. However in cells of sinoatrial node which is carrying out a role of the driver of a rhythm of heart, it is observed spontaneous diastolic depolarization (a phase 4). Autorhythmic activity is based on this mechanism of specified cardiac cells. Biological activity of these cells has also other important features: 1) a small steepness of rise of PA; 2) slow repolarization (a phase 2), smoothly passing in a phase fast repolarization (a phase 3) during which membrane potential reaches a level - 60 mV (instead of 90 mV in a working myocardium) then the phase slow diastolic depolarization again begins. Similar features electric activity of cells of sinoatrial node, however has speed spontaneous diastolic depolarization at them considerably below, than at cells of sinoatrial node, accordingly the rhythm of their potential automatic activity is less.
Ionic mechanisms of generation of electric potentials in cells of the driver of a rhythm completely are not deciphered. It is established, that in development slow diastolic depolarization and slow ascending phase of PA of cells of sinoatrial node the leading part play calcium channels. They are penetrated not only for ions Са2+, but also for ions Na+. Fast sodium channels do not accept participation in generation of PA of these cells. Speed of development slow diastolic depolarization is regulated b y independent (vegetative) nervous system.
Ability of cells of a myocardium during human life be in a condition of continuous rhythmic activity is provided by effective work of ionic pumps of these cells. During diastole ions Na+ are deduced from a cell, and ions K+ come back in a cell. Ions Са2+, from cytoplasm, are absorbed by endoplasmic reticulum. Deterioration of blood supply of a myocardium (ischemia) conducts to pauperization of stocks ATP; work of pumps is broken, owing to what electric and mechanical activity myocardium cells decreases.
