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1.
Bull Exp Biol Med ; 171(6): 707-712, 2021 Oct.
Article in English | MEDLINE | ID: mdl-34705170

ABSTRACT

The viscosity of plasma and mitochondrial membranes of hepatocytes was studied in young (3-month-old) and old (9-month-old) male Wistar rats. It was shown that viscosity of hepatocyte plasma and mitochondrial membranes in young rats under optimal vital functions in the area of protein-lipid membrane contacts was significantly lower than in old rats. No age-related differences in the viscosity of lipid-lipid membrane contacts and in the polarity of protein-lipid contacts and lipid layers were found. Liver cirrhosis induced by carbon tetrachloride and ethanol administration was associated with increased fluidity of the plasma and mitochondrial membranes of hepatocytes in rats of both age groups. The decrease in membrane viscosity in young rats occurred due to a decrease of the viscosity in the area of protein-lipid and lipid-lipid contacts, while in old rats in the area of protein-lipid contacts. Carbon tetrachloride and ethanol did not affect the polarity of lipid contacts and lipid layers.


Subject(s)
Carbon Tetrachloride/toxicity , Ethanol/toxicity , Hepatocytes/drug effects , Liver Cirrhosis, Experimental/metabolism , Liver/drug effects , Age Factors , Animals , Cell Membrane/chemistry , Cell Membrane/drug effects , Hepatocytes/metabolism , Hepatocytes/pathology , Liver/metabolism , Liver/pathology , Liver Cirrhosis, Experimental/chemically induced , Liver Cirrhosis, Experimental/pathology , Male , Mitochondria/chemistry , Mitochondria/drug effects , Mitochondrial Membranes/chemistry , Mitochondrial Membranes/drug effects , Rats , Rats, Wistar , Viscosity/drug effects
2.
Bull Exp Biol Med ; 171(1): 127-133, 2021 May.
Article in English | MEDLINE | ID: mdl-34046793

ABSTRACT

We studied the age-related characteristics of the response of stem cells and liver in male Wistar rats to administration of carbon tetrachloride (CCl4) and ethanol. It was shown that modeling of liver cirrhosis caused inflammation, fibrosis, damage to sinusoidal capillaries, necrosis, and disturbances in the functional activity of hepatocytes in young rats. These processes were accompanied by mobilization of profibrotic mesenchymal stem cells (MSC), proinflammatory hematopoietic stem cells (HSC) and lymphocytes (CD45hiCD133+) from the bone marrow into the blood and migration to the liver. On the other hand, the number of hepatocyte precursors expressing Sox9 (cells of Hering's canal), immature cholangiocytes, Ito cells, oval cells, and endothelial cells of the liver sinusoids) sharply increased in the liver. In young rats, mobilization and migration of MSC, HSC, and hepatocyte precursors against the background of liver cirrhosis were more intensive than in old animals. The higher resistance of old rats to exposure is associated with age-related changes in the niches as well as in mobilization and migration of cells.


Subject(s)
Mesenchymal Stem Cell Transplantation , Mesenchymal Stem Cells , Animals , Carbon Tetrachloride/toxicity , Endothelial Cells , Hepatocytes/pathology , Liver/metabolism , Liver Cirrhosis/metabolism , Male , Rats , Rats, Wistar
3.
Bull Exp Biol Med ; 170(3): 326-331, 2021 Jan.
Article in English | MEDLINE | ID: mdl-33452984

ABSTRACT

We studied the formation of injuries in lung endothelium and the response of angiogenesis cells during modeling of pulmonary emphysema in male and female C57BL/6 mice with metabolic disorders. Hemodynamic disturbances and reduction in the area of the microvasculature caused by combined pathology in male mice were more pronounced than in females. Mobilization and migration of angiogenic precursors were impaired in both male and female mice. In males, activity of recruiting endothelial progenitor cells, vascular smooth muscle cells, luminal cells of nascent vessels and pericytes into the lungs was additionally reduced. In females, accumulation of endothelial progenitor cells (CD45-CD31+CD34+), vascular smooth muscle cells, and pericytes in the lungs was observed, which indicated activation of endothelial regeneration. Sex differences in the reaction of the lung endothelium and angiogenesis cells can be explained by genetic factors of lipid and glucose metabolism.


Subject(s)
Endothelium/metabolism , Endothelium/pathology , Lung/metabolism , Lung/pathology , Pulmonary Emphysema/metabolism , Pulmonary Emphysema/pathology , Animals , Antigens, CD34/metabolism , Dyslipidemias/metabolism , Dyslipidemias/pathology , Female , Hyperglycemia/metabolism , Hyperglycemia/pathology , Leukocyte Common Antigens/metabolism , Male , Mice , Mice, Inbred C57BL , Platelet Endothelial Cell Adhesion Molecule-1/metabolism , Sex Characteristics
4.
Bull Exp Biol Med ; 168(3): 334-340, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31940128

ABSTRACT

The changes in endothelial progenitor cells and progenitor cells of angiogenesis, pericytes and smooth muscle cells, were studied in female C57BL/6 mice with a combination of metabolic impairments induced by injections of sodium glutamate and lung emphysema modeled by the administration of cigarette smoke extract. It was observed that sodium glutamate significantly enhances pathological changes in the lungs (inflammation and lung emphysema) induced by the administration of cigarette smoke extract. Recruiting of endothelial progenitor cells (CD45-CD31+CD34+ and CD31+CD34+CD146-) and progenitor cells of angiogenesis (CD45-CD117+CD309+) was registered in the injured lungs. Angiogenesis impairment induced by combined exposure is related to altered migration of pericytes (CD31-CD34-CD146+) and smooth muscle cells (CD31-CD34+CD146+) in emphysema-like enlarged lung tissue.


Subject(s)
Myocytes, Smooth Muscle/cytology , Myocytes, Smooth Muscle/metabolism , Pericytes/cytology , Pericytes/metabolism , Pulmonary Emphysema/metabolism , Pulmonary Emphysema/pathology , Animals , Antigens, CD34/metabolism , CD146 Antigen/metabolism , Cigarette Smoking/adverse effects , Endothelial Progenitor Cells/cytology , Endothelial Progenitor Cells/drug effects , Endothelial Progenitor Cells/metabolism , Female , Leukocyte Common Antigens/metabolism , Mice , Mice, Inbred C57BL , Myocytes, Smooth Muscle/drug effects , Platelet Endothelial Cell Adhesion Molecule-1/metabolism , Proto-Oncogene Proteins c-kit/metabolism
5.
Adv Gerontol ; 27(3): 457-62, 2014.
Article in Russian | MEDLINE | ID: mdl-25826991

ABSTRACT

We examined the ratios microviscosity in the area of integral and annularly lipid membranes of erythrocytes of peripheral blood in patients of 35-50 and 60-75 years with chronic ischemic heart disease, as well as age-matched healthy controls. In healthy donors coefficients microviscosity in the area of integral and annularly lipids proved to be significantly higher in the older age group (60-75 years). In CHD, regardless of the age of the patients, erythrocyte membranes can be characterized as raising and lowering the parameters microviscosity of lipid-lipid interactions. In the protein-lipid contacts for patients aged 35-50 years an increase is typical, while for patients of 60-75 years, on the contrary, a decrease of the coefficient of microviscosity. It is concluded that the values of the microviscosity of erythrocyte membranes in patients of different age groups in the development of chronic ischemic heart disease, reflect both the implementation of the general mechanisms of adaptive changes of cell membranes, and the specifics of an individual, determined by their lipid and protein composition.


Subject(s)
Aging/blood , Blood Viscosity , Erythrocyte Membrane/metabolism , Myocardial Infarction/blood , Myocardial Ischemia/blood , Adult , Aged , Case-Control Studies , Chemical Phenomena , Chronic Disease , Erythrocyte Membrane/chemistry , Female , Hemorheology , Humans , Lipid Metabolism , Male , Membrane Lipids/metabolism , Middle Aged , Myocardial Infarction/complications , Myocardial Ischemia/complications
6.
Adv Gerontol ; 25(4): 644-7, 2012.
Article in Russian | MEDLINE | ID: mdl-23734510

ABSTRACT

The age-related changes in the coefficient of microviscosity and polarity in the area of lipid-lipid and protein-lipid contacts of erythrocyte membranes in 4 months old (group I, n = 20) and 12 months old (group II, n = 20) rats by the method of lateral diffusion of the pyrene probe were investigated. Each age group consisted of 10 intact animals and animals after postinfarction cardiac remodeling (PICS). An increase of microviscosity and polarity of the annular and total lipids of erythrocyte membranes in 12-month animals was found. When modeling PICS in 4-month animals is pronounced increase the polarity and microviscosity of erythrocyte membranes in the annular and total lipids. The 12-month animals after PICS demonstrate a decrease of microviscosity in a lipid bilayer, and its increase in the area of annular lipids for consistently high-polarity lipids.


Subject(s)
Aging/blood , Cell Membrane/pathology , Erythrocyte Membrane/pathology , Myocardial Infarction/blood , Aging/pathology , Animals , Disease Models, Animal , Male , Membrane Fluidity/physiology , Membrane Lipids/metabolism , Myocardial Infarction/pathology , Rats , Rats, Wistar , Sclerosis , Ventricular Remodeling/physiology , Viscosity
7.
Adv Gerontol ; 23(1): 59-63, 2010.
Article in Russian | MEDLINE | ID: mdl-20586250

ABSTRACT

Research results of features of an intracellular calcium homeostasis in 4 and 12-month's rat cardiomyocites at postinfarction cardiosclerosis are presented. It is shown that the myocardium of animals in the old rats group is more susceptible to extrasystolic impacts. In the pathology conditions additional extrasystolic influences also had the expressed age specificity of inotropic response. The data testifying to almost identical dynamics of postextrasystolic cycles of intact myocardium in animals of investigated age groups has been obtained. The different postextrasystolic potentiation in the remodeled myocardium in old and young rats testified to different of sarcoplasmic reticulum ability to accumulate additional calcium ions. The conclusion was made that the myocardium of animals in the old rats group has more chance for development of hemodynamic significant disturbance of cardiac rhythm as a consequence of age-related changes processes of the electromechanical coupling in cardiomyocites.


Subject(s)
Aging/metabolism , Calcium/metabolism , Homeostasis , Myocardial Infarction/metabolism , Myocytes, Cardiac/metabolism , Ventricular Remodeling , Aging/pathology , Animals , Disease Models, Animal , Male , Myocardial Infarction/pathology , Myocardial Infarction/physiopathology , Rats , Rats, Wistar
8.
Eksp Klin Farmakol ; 73(2): 14-7, 2010 Feb.
Article in Russian | MEDLINE | ID: mdl-20369595

ABSTRACT

Features of the extrasystolic and postextrasystolic contractility of myocardium isolated from rats aged 4 months (group I, n = 30) and 12 months (group II, n = 30) after postinfarction remodeling of the heart (PIRH) and long-term treatment with carvedilol have been studied. Each age group included in 10 intact control animals, 10 animals with postinfarction cardiosclerosis (PICS), and 10 rats with PICS treated with carvedilol (2.1 mg/kg) during 28 days, beginning with the 45th day after coronary occlusion. The isometric contractility of myocardium was monitored at an electric stimulation frequency of 0.5 Hz. The extrasystolic effect was produced by an electric pulse applied within 0.2 - 5 s interval after the basic stimulation. It is established that the inotropic response of myocardium to the extrasystolic impulse exhibits age-dependent features both the intact rats and in the rats with PICS. The differences can be related to the age-dependent involvement of the ion-transport systems of sarcolemma and sarcoplasmic reticulum into the modulation of excitation--contractility coupling during PIRH. The long-term treatment with carvedilol led to restoration of the Ca(2+)-accumulation reserve of sarcoplasmic reticulum to the age-normal level in young animalsand decreased the risk of development of hemodynamically significant heart rate disturbances in old rats.


Subject(s)
Adrenergic beta-Antagonists/pharmacology , Carbazoles/pharmacology , Myocardial Contraction/drug effects , Myocardial Infarction/physiopathology , Myocardium/metabolism , Propanolamines/pharmacology , Age Factors , Animals , Calcium/metabolism , Carvedilol , Electric Stimulation , Intracellular Space/metabolism , Male , Myocardial Infarction/metabolism , Myocytes, Cardiac/drug effects , Myocytes, Cardiac/metabolism , Rats , Rats, Wistar , Ventricular Remodeling/drug effects
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