Morphological signs of neurogenic inflammation in the heart of rats during aging

С помощью гистологических методов окраски толуидиновым синим, гематоксилином и эозином и иммуногистохимических реакций на белок PGP 9.5, тирозингидроксилазу (ТГ), белок Iba-1, изучены клеточные изменения в разных отделах сердца крыс линии Wistar в возрасте 18- 23 мес. В соединительной ткани основания сердца обнаружены очаговые воспалительные инфильтраты, внутри которых выявлены PGP 9.5 и ТГ сплетения, состоящие из парасимпатических и симпатических нервных волокон. В области клапанного аппарата, на границе фиброзного кольца и миокарда правого предсердия, обнаружены патологические изменения нервных структур - дегенерация нервных пучков и зернистый распад варикозных аксонов терминального сплетения. Установлены тесные взаимоотношения аксонов терминальной нервной сети с клетками воспалительных инфильтратов и кровеносными сосудами. Определены закономерности встречаемости в различных отделах миокарда у старых животных нейроклеточных воспалительных комплексов, состоящих из нервных волокон, кровеносных капилляров и клеток-участников местного воспалительного процесса (тучных клеток, макрофагов, фибробластов, плазмоцитов). Установлен хронический характер нейрогенного воспаления в сердце при старении. Using histological methods of staining with toluidine blue, hematoxylin-eosin and immunohistochemical reactions for the PGP 9,5 protein, tyrosine hydroxylase (TH), Iba-1 protein, cellular changes in different parts of the heart of Wistar rats at the age of 18-23 months were studied. In the connective tissue of the heart base, focal inflammatory infiltrates were found, near which PGP 9.5 and TH plexuses, consisting of parasympathetic and sympathetic nerve fibers, were detected. In the area of the valvular heart apparatus, at the border of the anneau fibreux and the myocardium of the right atrium, pathological changes in nerve structures were found: degeneration of nerve fibers and granular destruction varicose axons of the terminal plexus. A close relationship has been established between axons of the terminal nervous network and cells of inflammatory infiltrates and blood capillaries. The features of the localization of neurocellular inflammatory complexes consisting of nerve fibers, blood capillaries and cells participating in the local inflammatory process (mast cells, histiocytes, monocytes, fibroblasts, plasma cells) in various parts of the myocardium in old animals are described. The chronic nature of neurogenic inflammation in the heart during aging has been established.

The severity of pulmonary lesions in acquired heart defects

Acquired heart defects are a group of diseases (represented by stenosis, valve insufficiency, combined and concomitant defects), accompanied by a violation of the structure and functions of the valvular heart apparatus and leading to changes in the intracardiac circulation. Against the background of such violations, stagnation occurs not only in the small, but also in the great blood circulation circle, which is manifested by a chronic dry cough, often with an admixture of blood. Compensated heart defects can be hidden, while decompensated ones are manifested by shortness of breath, palpitations, fatigue, pain in the heart, and a tendency to fainting. In such conditions, there is an increase in pressure in the pulmonary artery, which ultimately can cause the development of pulmonary edema. Acquired heart defects are also a serious danger in terms of the development of heart failure, damage to internal organs (in particular, the liver and kidneys), the appearance of ascites, and if the course is unfavorable, the fatal outcome is possible.

CLINICAL FEATURES AND RISK FACTORS OF EMERGENCE AND DEVELOPMENT OF ATRIOVENTRICULAR VALVE DEGENERATION IN DOGS

The study of cardiovascular diseases in small domestic animals is an urgent problem of modern veterinary medi-cine. The research goal is to develop a science-based ap-proach to the clinical picture and risk factors of the emer-genceand development of atrioventricular valve degenera-tion in dogs. The study was conducted in the Department of Biology and Pathology of Small Domestic, Laboratory and Exotic Animals of the Moscow State Academy of Vet-erinary Medicine and Biotechnology named after K.I. Skryabin. The research targets were 162 dogs with myx-omatous degeneration of atriovetricular valves. Myxoma-tous degeneration of the valvular heart apparatus was more often found in dogs of the age of 7 to 10 years -61.7%. The cases were most often diagnosed in dogs of the breeds Chihuahua -29.63%, and Yorkshire Terrier-21%. Of the total number of animals, the disease was more common in males -69.14%. Clinical signs of myxomatous degeneration of the valvular heart apparatus in dogs were diverse. The objective diagnostic clinical signs of myxoma-tous degeneration of the mitral valve of the heart in dogs were the following: cough (53%), sudden lethargy (48%), dyspnea (26%); less frequently -weight loss (12%), loss of consciousness (2.21%) and ascites (0.74%). The main clinical signs of tricuspid valve damage were the following ones: cough (57.14%) and ascites (42.86%). Dyspnea and loss of consciousness were less common (14.29%). With a combined damage of the mitral and tricuspid valves, the clinical picture was more pronounced. The most common symptoms were cough (84.21%), dyspnea (73.68%), and sudden lethargy (63.16%). The clinical substantiation for the development of myxomatous degeneration of the valvu-lar heart apparatus in dogs is the following factors: age, breed and sex of the animal. The clinical signs and differ-ential diagnostic criteria were characterized by polymor-phism and differed in cases of mitral and tricuspid valve lesions and their joint degeneration.

The practicalities of establishing a porcine isolated heart model

Background: The isolated heart apparatus is over 100 years old, but remains a useful research tool today. While designs of many large animal systems have been described in the literature, trouble-shooting and refining such a model to yield a stable, workable system has not been previously described. This paper outlines the issues, in tabular form, that our group encountered in developing our own porcine isolated heart rig with the aim of assisting other workers in the field planning similar work. The paper also highlights some of the modern applications of the isolated heart apparatus. Methods Landrace pigs (50-80 kg) were used in a pilot project to develop the model. The model was then used in a study examining the effects of various cardioplegic solutions on function after reanimation of porcine hearts. During the two projects, non-protocol issues were documented as well as their solutions. These were aggregated in this paper. Results: Issues faced by the group without explicit literature solutions included pig size selection, animal acclimatisation, porcine transoesophageal echocardiography, cannulation and phlebotomy for cross-clamping, cardioplegia delivery, heart suspension and rig tuning. Conclusion: Prior recognition of issues and possible solutions faced by workers establishing a porcine isolated heart system will speed progress towards a useable system for research. The isolated heart apparatus remains applicable in transplant, ischaemia reperfusion, heart failure and organ preservation research.

A Novel Ex Vivo Heart Model for the Assessment of Cardiac Pacing Systems

Background: Advances in endocardial device design have been limited by the inability to visualize the device-tissue interface. The purpose of this study was to assess the validity of an isolated heart approach, which allows direct ex vivo intracardiac visualization, as a research tool for studying endocardial pacing systems. Method of approach: Endocardial pacing leads were implanted in the right atria and ventricles of intact swine (n=8) under fluoroscopic guidance. After collection of pacing and sensing performance parameters, the hearts were excised with the leads intact and reanimated on the isolated heart apparatus, and parameters again recorded. Results: Atrial ex vivo parameters significantly decreased compared with in vivo measurements: P-wave amplitudes by 39%, slew rates by 61%, and pacing impedances by 42% (p<0.05 for each). Similarly, several ventricular ex vivo parameters decreased: R-wave amplitudes by 39%, slew rates by 62%, and pacing impedances by 31%. In contrast, both atrial (4.4±2.8 vs 3.3±2.8V; p=ns) and ventricular thresholds increased (1.2±0.7 vs 0.6±0.1V; p<0.05 for all). Three distinct phenomena were observed at the lead-tissue interface. Normal implants (70%) demonstrated minimal tissue distortion and resulted in elevated impedance and threshold values. Three implants (13%) resulted in severe tissue distortion and/or tissue wrapping and were associated with highly elevated pacing parameters. Tissue coring occurred in four implants (17%) where the lead would spin freely in the tissue after overtorquing of the lead. Conclusions: The utility of the isolated heart approach was demonstrated as a tool for the design and assessment of the performance of endocardial pacing systems. Specifically, the ability to visualize device-heart interactions allows new insights into the impact of product design and clinical factors on lead performance and successful implantation.

Myocardial performance of STZ-diabetic DOCA-hypertensive rats

Myocardial performance of streptozotocin (STZ)-diabetic deoxycorticosterone acetate (DOCA)-hypertensive rats was examined using the isolated working heart apparatus at various time periods after induction of the experimental diseases. Blood pressure, pulse rate, and plasma levels of glucose, insulin, cholesterol, and triglycerides, as well as ventricular weight-to-body weight ratio, were also determined. In nondiabetic rats it was found that DOCA hypertension was associated with an increase in plasma cholesterol, a decrease in circulating insulin level, lower weight gain, and ventricular enlargement compared with control rats. Diabetic rats developed myocardial dysfunction in a time-dependent manner and exhibited hyperglycemia, hypoinsulinemia, bradycardia, and ventricular enlargement. Compared with the normotensive diabetic animals, STZ-diabetic DOCA-hypertensive rats showed a similar magnitude of myocardial dysfunction and a greater degree of ventricular enlargement, but significantly less severe hyperglycemia. It is concluded that DOCA-induced hypertension does not aggravate the severity of myocardial dysfunction developed in STZ-diabetic rats. It is also suggested that DOCA may have an action on glucose metabolism either directly or via an effect on insulin secretion.

Effects of systolic overload and swim training on cardiac mechanics and biochemistry in rats

We have previously shown that swim conditioning corrects the depressed mechanical function and myosin adenosinetriphosphatase (ATPase) activities associated with renovascular hypertension (HTN) in the rat. The present study was designed to assess the effects of swim conditioning on another form of systolic overload, subdiaphragmatic suprarenal aortic stenosis. Cardiac mechanics in an isolated working heart apparatus and myosin enzymology were studied in four groups of rats: controls (C), animals with chronic systolic overload secondary to aortic constriction (St), swim-conditioning animals (Sw), and animals exposed to a combined load (St-Sw). Heart weight was increased by 23% in St, 27% in Sw, and 36% in St-Sw. In contrast to HTN, cardiac pump and muscle function were not depressed in St. Sw was associated with improved cardiac output, stroke work, and velocity of circumferential fiber shortening. St-Sw showed improved mechanical cardiac performance relative to both C and St. The percent of ventricular myosin of the V1 type and Ca2+-activated myosin ATPase activity relative to C was unchanged in Sw but was depressed in St and St-Sw. These data demonstrate that the salutory mechanical effects of Sw can be superimposed on the systolic overload of St. However, the dissociation between mechanics and myosin enzymology suggests that factors in excitation-contraction coupling other than myosin isoenzyme shifts are responsible for this finding.