Three pulmonary surthctant preparations: from human amniotic fluid, from bronchoalveolar lavage fluid, and from cattle lung tissue homogenate were tested in preclinical studies. The preparations are nontoxic, possess no mutagenic, teratogenic, and allergic activities and do not modify visceral morphology after repeated injections. After a single intratracheal administration the drugs normalize arterial blood oxygenation in 15-30 rain and arrest the respiratory distress syndrome in dogs, which is confirmed roentgenologically and clinically. Key Words: respiratory distress syndrome; surfactant; pharmacological properties; therapeutic activityThe respiratory distress syndrome (RDS) is one of the major causes of neonatal and adult mortality [3,5]. About 30,000 babies with RDS are annually born in Rnssia; in the USA 150,000 RDS cases are recorded annually in adults. In RDS 15-30% newborns and 50-70% adults die [3,5,7]. In preterm newborns RDS is caused by immaturity of type 2 alveolocytes and the resultant primary deficiency of puhnonary surthctant (PS) [2]. In RDS of adults, PS deficiency is secondary, developing as a result of structural and functional disorders in the airblood barrier. It often develops after multiple injury, sepsis, shock lung, radiation injury, etc. Natural and synthetic PS preparations have been widely used all over the world: smwana (USA), surfactant-TA (Japan), curosurf (Italy), alveofact (Germany), exosurf (UK) [8].We developed a technologically inexpensive method for preparing natural PS and chalacterized their physicochemical properties. Three preparations were studied: human PS isolated from parturients' amniotic fluid, PS from bronchoalveolar iavage fluid (PS-BLF), and PS prepared by water-salt extraction of finely dispersed cattle lung (PS-WSE).The pharmacological and therapeutic properties of these PS preparations are studied.
In recent years, the application of mesenchymal stem cells (MSCs) has been recognized as a promising method for treatment of different diseases associated with inflammation and sclerosis, which include nephrotuberculosis. The aim of our study is to investigate the effectiveness of MSCs in the complex therapy of experimental rabbit kidney tuberculosis and to evaluate the effect of cell therapy on the reparative processes. Methods: To simulate kidney tuberculosis, a suspension of the standard strain Mycobacterium tuberculosis H37Rv (106 CFU) was used, which was injected into the cortical layer of the lower pole parenchyma of the left kidney under ultrasound control in rabbits. Anti-tuberculosis therapy (aTBT) was started on the 18th day after infection. MSCs (5 × 107 cells) were transplanted intravenously after the start of aTBT. Results: 2.5 months after infection, all animals showed renal failure. Conducted aTBT significantly reduced the level of albumin, ceruloplasmin, elastase and the severity of disorders in the proteinase/inhibitor system and increased the productive nature of inflammation. A month after MSC transplantation, the level of inflammatory reaction activity proteins decreased, the area of specific and destructive inflammation in kidneys decreased and the formation of mature connective tissue was noted, which indicates the reparative reaction activation.
BACKGROUND: Biological systems of all levels of organization are characterized by the rhythm of functioning processes, which are one of the fundamental properties of living matter. The complex of circadian rhythms of mammals, being genetically determined, is quite plastically modulated by the action of periodic factors of the external and internal environment. Significant factors in the disorganization of biorhythms in the modern world include a violation of the light-dark regime, so-called light pollution. Alcohol abuse remains one of the most important medical and social problems of modern society. One of the important effects of alcohol is its destructive effect on the circadian rhythms of many physiological processes. AIM: The aim of the research was to study the influence of constant lighting, chronic alcohol intoxication and joint effect of these factors on the diurnal dynamics of several biochemical parameters in Wistar rats of both sexes. MATERIALS AND METHODS: The study was conducted on 200 and 160 female outbred Wistar rats at the age of 6 months, weighing 350 15 g. Rats were divided into 8 groups. 1st group (control ♂) is kept at fixed light regime (light/dark 10:14 hours with lights on at 8:00 and off at 18:00). 2nd group, males (n = 50) is kept under the same conditions as the control, but receives a 15 % aqueous solution of ethanol ad libitum as a drink instead of water, i.e. is subjected to chronic alcohol intoxication. Group 3, males (n = 50) are kept under constant light. The 4th group, males (n = 50) are also kept under constant illumination and receive 15 % aqueous ethanol solution ad libitum as a drink. Group 5 (control ♀) females (n = 40), are kept at a fixed light regime (light/dark 10:14 am with lights on at 8:00 and off at 18:00). The 6th group, females (n = 40) are kept under the same conditions as the control, but receive 15 % aqueous ethanol solution ad libitum instead of water as a drink, i.e. subjected to chronic alcohol intoxication. Group 7, females (n = 40) are kept under constant light. The 8th group, females (n = 40) are also kept under constant light and receive 15 % aqueous ethanol solution ad libitum as a drink. In the blood samples taken at 9:00, 15:00, 21:00 and 3:00 hours the content of AST, ALT, glucose, total protein, albumin, total and direct bilirubin was measured. The reliability of circadian rhythmicity of studied parameters was assessed with use of cosinor analysis. RESULTS: It is established that the chronic alcohol intoxication, constant illumination and joint action of this factors lead to similar changes in biochemical parameters in rats of both sexes, but in female rats the level of AST, total and direct bilirubin changes as a result of three weeks of intoxication, which is not observed in males. In turn, both individual and joint effects of chronic alcohol intoxication and dark deprivation lead to significant changes in rhythmostasis in rats, however, circadian rhythms of total protein, as well as both types of bilirubin, are more resistant to dark deprivation in females than in males. CONCLUSIONS: The conducted study testifies that a three-week chronic alcohol intoxication causes more significant changes in the biochemical profile in female rats compared to males. At the same time, the studied circadian rhythms of the biochemical parameters of the organism of females turn out to be more resistant to dark deprivation than those of males, being destroyed only under the combined action of chronic alcohol intoxication and constant illumination.
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