Cardiac Rhythm Variability: Approaches to Mechanisms

Physiological mechanisms of cardiac rhythm variability (CRV) are reviewed. The results of original experiments are discussed together with the history of the problem and data available from the literature. Special emphasis is placed on the spectral analysis of cardiac rhythm. Various mechanisms of the generation of periodic and aperiodic components of CRV are considered. Although the variability of cardiac rhythm has been studied for many years in many laboratories worldwide, fine mechanisms of CRV remain obscure. However, a number of specific features of CRV are presently widely recognized. Periodic CRV components isolated from short-term records in patients at rest are represented by high-frequency, low-frequency, and very low-frequency oscillations. Fourier-transform spectral analysis of cardiac rhythm is the most appropriate method of the detection of these oscillations. High-frequency components are associated with respiration and represent the effects of the parasympathetic nervous system on myocardium. Low-frequency components are due to the activity of the postganglionic sympathetic fibers and represent the processes of cardiac rhythm modulation by the sympathetic nervous system. Genesis of very low-frequency oscillations is still uncertain. Most probably, these oscillations are associated with the effects of suprasegmental (primarily, hypothalamic) centers of autonomic regulation. Aperiodic CRV components represent random events associated with the reflex regulation of the heart rate by external or internal factors. Because aperiodic components significantly modify the results of the CRV analysis, the effects of these factors should be eliminated. It is concluded that because many problems associated with cardiac rhythm variability remain to be solved, extensive research in this direction should be continued.     

Validation and development of an immunofluorescence method for isolating and identifying mycobacteria L forms

The complement fixation test and the immunofluorescence test have demonstrated that the L-forms of mycobacteria retain their species-specific and genus-specific determinants and possess serological activity. The L-variants obtained by different methods differ in size, depending on the degree of the destruction of their cell wall. Specific antisera to the L-forms of mycobacteria, suitable for use in the indirect immunofluorescence test, have been obtained. These antisera are highly specific and permit not only the rapid detection, but also identification of the L-forms.     

Immunoglobulin content in persons with a varying donor record]

The blood level of IgA, IgG Igm, and protein in male donors was studied in connection with the duration of the donor's activity. The content of the main blood immunoglobulin classes and proteins depended significantly on the duration of the donor's activity. Therefore it is not recommended to use donors as control group in determining the immunoglobulin level in the blood.     

ACTH inhibits the development of primary decompensation of the systemic and portal circulation in acute blood loss in rats]

Using the method of contact luminescent biomicroscopy of the liver and intestine coupled with the measurement of systemic blood pressure by micromanometer and ultrasonic registration of blood flow velocity in portal vein and hepatic artery it has been established that in rats with acute decompensatory hemorrhage fragments of ACTH (1-24) and (4-10) improve the state of portal macro- and microcirculation and increase the life span 2-3-fold. ACTH does not influence the dynamics of acute compensatory hemorrhage and the development of the posthemorrhagic microcirculatory disturbances (local microstases, microthromboses, erythrocyte aggregation).     

Hydrolase biosynthesis by morphological variants of Bacillus mesentericus as dependent on the storage conditions

A method used to prepare the inoculum (a strain of Bacillus mesentericus, a producer of a complex of hydrolytic enzymes) has been studied for its effect on the activity of proteinases and amylases under submerged cultivation in fermenters. Optimal conditions for the culture storage and inoculum cultivation are developed to obtain standard enzymic preparations.