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卷 28, 编号 13 (2021)

Articles

News of medicine

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Pharmateca. 2021;28(13):6-8
pages 6-8 views

Drug-alcohol interactions: focus on central-acting drugs and analgesics

Pereverzev A., Ostroumova O., Sychev D.

摘要

It is known that alcohol abuse is a risk factor of many socially significant diseases like cardiovascular diseases, cirrhosis of the liver, acute pancreatitis, gastrointestinal bleeding, metabolic complications, malignant neoplasms and mental disorders. However, a negative prognosis in patients who regularly abuse alcohol is not only because of a large number of pathological conditions, but also due to complications of pharmacotherapy, drug-drug interactions, insufficient effectiveness against the background of drug-alcohol interaction. For example, there are literature evidence of an increase in the pharmacodynamic effect of amitriptilline, trazodone, gabapentin and other central-acting drugs. Also, a number of publications describe 20% increase in AUC12 after taking a single dose of carbamazepine 400 mg on the first day was noted than AUC after taking carbamazepine for 9 days after ethanol withdrawal in 7 chronic ethanol consumers; an increase in Cmax and AUC of esogabin by 23 and 36%, respectively, in 17 healthy men and women who reported moderate alcohol consumption; an increase in the Cmax and AUC of clobazam by an average of 59 and 54%, respectively, in 8 healthy male subjects who received clobazam (20 mg orally) together with ethanol (as a combination of beer and brandy). Thus, the simultaneous use of alcohol and drugs can potentially be associated with increased risks of ADRs. Healthcare practitioners should take into account the potential pharmacodynamic and pharmacokinetic interactions of alcohol and drugs when prescribing pharmacotherapy, but it is still much better to avoid the simultaneous use of alcohol and drugs.
Pharmateca. 2021;28(13):9-15
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Interactions between alcohol and drugs: focus on drugs used to treat diseases of the cardiovascular system, gastrointestinal tract, antimicrobial drugs

Pereverzev A., Ostroumova O., Sychev D.

摘要

According to the 2019 National Survey on Drug Use and Health, 85.6 percent of people ages 18 and older reported driank alcohol at some point in their lives, 69.5 percent reported. that they drank alcohol in the last year and 54.9 percent reported that they drank alcohol in the last month. Also, in the US in 2015-2016, 45.8% of the population used at least one prescription drug in the past 30 days, most of which belonged to the drugs used for the treatment of cardiovascular diseases and antibiotics. Potentially, these drugs can enter into pharmacodynamic or pharmacokinetic interactions. For example, a suppression of activity of alcohol dehydrogenase in the stomach due to consumption of acetylsalicylic acid, that can lead to an increase in Cmax and average AUC of ethanol, and therefore- to increase its toxicity! Another example of an interaction is a decrease in the serum concentration of amiodarone and a decrease in its effectiveness due to the consumption of a large doses or long-term use of ethanol. Alcohol can also affect the effectiveness of antibiotic therapy. For example, ethanol can change the rate, but not the degree of absorption of amoxicillin; reduce Cmax and AUC of erythromycin; increase the bioavailability of tetracycline. Thus, the risks of complications or insufficient effectiveness are extremely high in patients taking alcohol and drugs at the same time for the treatment of diseases of the cardiovascular system, gastrointestinal tract or infectious diseases. To reduce the risks of complications, the potential interactions of alcohol and drugs should be taken into account when choosing drug therapy, but it is still more effective strategies to exclude the combined use of alcohol and drugs.
Pharmateca. 2021;28(13):16-22
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On the question of systemic manifestations of early-onset rheumatoid arthritis

Bestaev D., Konushkaliev A.

摘要

Rheumatoid arthritis (RA) is an immune-inflammatory (autoimmune) rheumatic disease of unknown etiology, characterized by chronic erosive arthritis and systemic damage to internal organs. Many clinicians call RA rheumatoid disease, emphasizing the systemic nature of the pathological process. RA with systemic manifestations (SM) is a generalized form of the disease, usually found in seropositive patients. Recently, special attention has been paid to the issues of early-onset RA; the evolution of «undifferentiated» arthritis into typical RA is still not fully understood, therefore this stage of the disease is most interesting from the point of view of studying the features of SM as factors in predicting early-onset RA. Thus, early-onset RA has a number of features, and their understanding will make it possible to diagnose the disease in a timely manner. This also applies to the SM of early-onset RA. The review presents data on systemic diseases in patients with early-onset RA.
Pharmateca. 2021;28(13):23-30
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Facet syndrome in the clinical picture of dorsopathies

Tkachev A., Gordeeva I., Epifanov A., Akarachkova E., Zhurbenko V., Smirnova A.

摘要

Facet syndrome (FS) is the main cause of pain in 10-15% of young adult patients with chronic low back pain and much more often in older populations (according to various sources, from 40 to 85-90%). Each spine segment consists of the intervertebral disc, vertebral bodies, and posterior paired synovial joints, which make up a «three-component complex», where each component affects the other two, allowing a variety of movements, and the spine is a flexible mobile structure. Many authors have demonstrated pathological degenerative changes in these joints over time, as well as the associated inflammatory changes. The most common cause of facet joint disease is degenerative changes in the spine. FS is characterized by a relapsing course, gradual development, slow regression of each painful episode, a tendency to lengthening and aggravation of each subsequent exacerbation. A clinical case of a patient with chronic low back pain is presented. After examination and appropriate treatment, the patient noted an improvement. Conclusion. The clinical assessment of patients with suspected FS is based on the features of the clinical picture, «pain pattern», special tests that allow correct differential diagnosis with similar nosological forms and prescribe an optimal treatment.
Pharmateca. 2021;28(13):31-43
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The place and role of a therapist and general practitioner in the management of comorbid patients during the pandemic of the new coronavirus infection (COVID-19): an emphasis on the rehabilitation stage

Trukhan D., Davydov E.

摘要

The National Consensus 2020 «Features of management of comorbid patients during the pandemic of the new coronavirus infection (COVID-19)» notes that the problem of managing comorbid patients in a pandemic requires an integrated approach aimed at both optimal management of comorbid patients who are in self-isolation with forced restrictions on visits to medical institutions, and at the management of comorbid patients with COVID-19 aimed at both the optimal management comorbid patients who are in self-isolation, forced restrictions on visits to medical institutions, and at the management of comorbid patients with COVID-19. The global clinical experience in the management of comorbid patients with a new coronavirus infection gained over the past year makes it possible to highlight a number of other pressing problems. First of all, these are issues of specific and non-specific prevention, as well as follow-up of patients during the rehabilitation period, especially in the framework of post-COVID-19 syndrome. This review provides data on the potentials of nutraceuticals (vitamins and minerals) for the treatment of patients with COVID-19. The possible involvement of a therapist and general practitioner in the rehabilitation stage of the treatment of patients with COVID-19 and in the treatment of post-COVID-19 syndrome is being discussed.
Pharmateca. 2021;28(13):44-53
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Possibilities of using trimetazidine in the treatment of patients with ischemic heart disease and chronic heart failure

Polyakova O., Chochua A., Golovina O., Mironova E., Ostroumova O.

摘要

Ischemic heart disease (IHD) is the leading cause of death and disability worldwide. The high mortality rate in patients with IHD is primarily due to the presence of comorbid conditions that can mutually aggravate each other’s course and significantly worsen the prognosis. The most common concomitant pathology in patients with IHD is considered to be chronic heart failure (CHF). The combination of IHD and CHF reduces the quality of life of patients and increases the risk of death. In this regard, drug therapy in this clinical situation should be not only optimal in terms of safety, but also effective. However, the existing approaches to the treatment of IHD, including in the presence of CHF, do not demonstrate the desired results in reducing mortality and the incidence of cardiovascular events, therefore, there is a need to improve the tactics of managing patients with IHD and CHF. Currently, there is convincing evidence that metabolic disorders in the myocardium, including mitochondrial dysfunction, play an important role in the development and progression of IHD and CHF. In this regard, metabolic therapy aimed at increasing the energy efficiency of the myocardium is of particular interest in the treatment of patients of this category. One of the most studied metabolic drugs is trimetazidine. The aim of this review was to study the literature data on the possibility of using trimetazidine in the treatment of patients with a combination of IHD and CHF.
Pharmateca. 2021;28(13):54-62
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The role of magnesium deficiency in the pathogenesis of undifferentiated connective tissue dysplasia

Izmozherova N., Shambatov M., Bakhtin V., Popov A.

摘要

Magnesium is the second most common intracellular cation and plays an essential role in the implementation of cellular functions. Increasing importance is attached to the effect of magnesium deficiency on the structure and mechanical homeostasis of connective tissue (CT). Magnesium deficiency causes the development of a number of conditions, and undifferentiated CT dysplasia is one of the most common. This review highlights modern approaches to assessing the relationship between magnesium deficiency and the development of CT pathology. Mg2+ ions participate in the stabilization of the secondary and tertiary structures of nucleic acids, forming cationic bridges between anionic phosphate groups. Magnesium is involved in the regulation of the balance of formation, degradation of fibrillar and non-fibrillar components of the extracellular matrix by decreasing the expression of matrix metalloproteinase genes and stimulating collagen and aggrecan synthesis. Magnesium enhances the mitotic activity of CT cells by increasing the processes of protein synthesis and triggering signaling pathways associated with the mammalian target of rapamycin. Mg2+ ions promote the conversion of fibroblast integrins into a high-affinity form, allowing them to bind to collagen, thereby increasing tissue stability and integrity. Magnesium deficiency is associated with an increase in the activity of matrix metalloproteinases, which is a key factor in CT degradation. A lack of magnesium leads to the accumulation of defective collagen, a decrease in the synthesis of structural and signal proteins, nucleic acids, and suppression of the mitotic activity of cells. A decrease in the affinity of fibroblast integrins for collagen arising under conditions of magnesium deficiency leads to tissue disorganization. Thus, magnesium deficiency is associated with impaired cell functioning and the integrity of the CT extracellular matrix.
Pharmateca. 2021;28(13):63-68
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Antiarrhythmic therapy for atrial fibrillation in patients with the novel SARS-CoV-2 coronavirus infection: how to make the right choice?

Tarzimanova A., Bykova E.

摘要

The novel SARS-CoV-2 coronavirus infection (COVID-19) has become one of the global problems of the modern world community. An analysis of the factors associated with the severe course and poor prognosis of COVID-19 indicates an important role for comorbid pathology. Cardiac arrhythmias are one of the most common cardiovascular complications of coronavirus infection, and both supraventricular and ventricular arrhythmias can be diagnosed on an ECG. The most common arrhythmia in COVID-19 is atrial fibrillation (AF); in some patients, newly diagnosed AF cases occur during the acute course of coronavirus infection or in the first months after hospital discharge. It has been shown that the prevalence of AF among patients with coronavirus infection is approximately 2 times higher than in the general population, and reaches 8%. The onset of AF leads to an increase in thromboembolic complications and worsens the prognosis of patients with COVID-19. At the same time, the severity of coronavirus infection directly affects the incidence of AF. The administration of anticoagulant therapy is one of the most important directions in the treatment of patients with novel SARS-CoV-2 coronavirus infection. Anticoagulant therapy is indicated for all COVID-19 patients with newly diagnosed AF or a history of AF without exception. The drugs of IC and III classes are recommended to restore sinus rhythm in AF paroxysm in patients with stable hemodynamics. The choice of an antiarrhythmic drug for the relief and prevention of AF in patients with SARS-CoV-2 coronavirus infection should be based on an assessment of the severity of damage to the cardiovascular system.
Pharmateca. 2021;28(13):69-73
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Comparison of the effect of nebivolol and sotalol on the functional state of patients with paroxysmal supraventricular tachycardia

Tregubov V., Shubitidze I., Nazhalkina N.

摘要

Background. Paroxysmal supraventricular tachycardia (SVT) is subjectively poorly tolerated by patients and may be a predictor of a negative prognosis. The issue of optimizing its drug therapy remains relevant. Taking into account the multidirectional effects of antiarrhythmic drugs on the functional state of the body, a stepwise integrated approach to determine the effectiveness of treatment of patients with paroxysmal SVT is required. Objective. Determination of the effect of therapy with nebivolol or sotalol on the functional state of patients with paroxysmal SVT. Methods. The study involved 60 patients with paroxysmal SVT associated with stage II - III arterial hypertension (AH) and/or coronary artery disease (CAD), randomized into two groups for treatment with nebivolol (6.5±2.1 mg/day, n=30) or sotalol (164.3±46.8 mg/ day, n=30). As part of the combination therapy, lisinopril was prescribed (13.8±4.5 and 14.4±4.9 mg day), and if indicated, atorvastatin (12.9±4.3mg/day, n=14 and 14.2±4.6mg/day, n=15) andacetylsalicylicacid(95.8±14.4 mg/day, n=16and94.8±15.8mg/day, n=18), or rivaroxaban (Xarelto, Bayer, Germany) - 20 mg/day (n=2 and n=2, respectively). At baseline and 24 weeks after therapy, a quantitative assessment of the regulatory-adaptive status (RAS), echocardiography, treadmill test, 6-minute walk test, 24-hour Holter monitoring, and subjective assessment of the quality of life were performed. Results. Both schemes of combined pharmacotherapy significantly improved the structural and functional state of the heart, effectively suppressed SVT paroxysms, and improved the quality of life. At the same time, nebivolol had a positive effect on RAS and increased exercise tolerance to a greater extent. Conclusion. In patients with paroxysmal SVT associated with stage II-III arterial hypertension and/or coronary artery disease, the use of nebivolol compared to sotalol as part of a combination therapy may be preferable due to the positive effect on functional status.
Pharmateca. 2021;28(13):74-78
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Remodeling of the cardiovascular system in patients with essential arterial hypertension associated with primary subclinical hyperparathyroidism

Iskenderov B., Berenshtein N., Mozhzhukhina I.

摘要

Background. One of the pathogenetic mechanisms of essential arterial hypertension (AH) is a genetically determined violation of the transmembrane transport of calcium ions in smooth muscle cells of resistance vessels. It is known that the parathyroid glands are among the main regulators of calcium metabolism in the body. Objective. Assessment of the structural and functional remodeling of the heart and blood vessels in the presence of primary subclinical hyperparathyroidism in patients with essential AH. Methods. A cross-sectional clinical study included 88 patients (51 men and 37 women) with uncomplicated/asymptomatic AH I-II degree. In the examined subjects, the blood parathyroid hormone (PTH) levels were in the reference range for age and ranged from 5 to 78 pg/mL. The patients were divided into 3 groups: in group 1 (28 patients) PTH levels ranged from 0 to 20 pg/mL, in group 2 (37 patients) - from 21 to 55 pg/mL, and in group 3 (23 patients) - from 56 pg/mL to the upper reference value. All patients underwent echocardiography and 24-hour blood pressure monitoring, and also determination of the flow-mediated vasodilation of the brachial artery and the daily calciuresis. Results. The detection rate of left ventricular (LV) hypertrophy in group 3 compared to group 1 was significantly higher: 65.2 versus 39.3% (p=0.036). In addition, the value of daily calciuresis, total and free blood calcium in the group 3 was significantly higher than in the group 1. The parameters of the LV myocardial mass index, the interventricular septum thickness and the LV posterior wall thickness in the group 3 significantly (p<0.05) exceeded those in the group 1. In the group 2 and 3, the most pronounced LV diastolic dysfunction was revealed. It was shown that the PTH level directly correlates with the thickness of the intima-media complex of the carotid artery (R=0.57; p<0.001) and the LV myocardial mass index (R=0.29; p=0.006), inversely - with the value of the endothelium-dependent vasodilation (R= -0.33; p=0.002). Conclusion. It was revealed that the blood PTH level, which is the 90th percentile of the reference range, correlates with signs of cardiac and vascular remodeling in patients with uncomplicated/asymptomatic essential AH.
Pharmateca. 2021;28(13):79-85
pages 79-85 views

Effect of CYP2C9 gene polymorphism on losartan dosage regimen in patients with I-II degree arterial hypertension

Sinitsina I., Boyarko A., Temirbulatov I., Sychev D.

摘要

Background. Arterial hypertension (AH) occupies a leading position among cardiovascular diseases, determining the prognosis of morbidity and mortality among the population in the Russian Federation. Losartan is the first drug from the group of angiotensin II receptor antagonists, still frequently prescribed in the treatment of AH, often as monotherapy, which often determines the low efficacy of pharmacotherapy for AH. On the one hand, this is attributable to the losartan pharmacodynamics, on the other, from the point of view of pharmacogenetics, the efficacy of losartan can be influenced by the CYP2C9 gene polymorphisms, which affect the activity of the cytochrome P-450 isoenzyme 2C9 (CYP2C9), predetermining the pharmacological response. Objective. Evaluation of the effect of CYP2C9 gene polymorphism on the losartan dosage regimen in patients with I-II degree AH. Methods. The study included 81 patients - 46 (56.8%) men and 35 (43.2%) women with I - II degree AH aged 24 to 74 years, the mean age was 48.83±11.76 years. The study was conducted over a period of 12 weeks. At the first stage, 24-hour blood pressure monitoring and genotyping for CYP2C9*2 (rs1799853) and CYP2C9*3 (rs1057910) allelic variants were performed by PCR-RFLP. Depending on the results of CYP2C9 genotyping, the patients were divided into two groups, compared with each other; the first group (n=55 [67.9%]) - carriers of the «wild» type CYP2C9*1/*1 and the second - (n=26 [32.1%]) - homo- and heterozygous carriers of CYP2C9*2 and CYP2C9*3 allelic variants. Then a course of losartan at a dose of25-50 mg/day was prescribed. At sche-duled visits (2, 4 and 8 weeks), blood pressure was monitored and, if necessary, therapy was corrected. At the second stage, after 12 weeks of follow-up, the effectiveness of therapy as well as the dose of losartan, was assessed in groups with different CYP2C9 genotypes. Results. Comparative analysis of losartan doses showed that carriage of CYP2C9*2 and CYP2C9*3 polymorphic alleles is associated with an increased chance of increasing the dose of losartan: OR=7.00 (95% CI: 2.225-22.018), P=0.001. It should be noted that the dose of losartan at the beginning of the study was significantly higher in individuals with the CYP2C9*1/*1 genotype (P=0.001); however, at the end of the study, no significant difference in doses between patients with different genotypes was found (P=0.414). Conclusion. Carriage of CYP2C9*2 and CYP2C9*3 polymorphic alleles («slow» alleles) is associated with an increase in the dose of losartan, in contrast to that in patients with the CYP2C9*1 /*1 genotype.
Pharmateca. 2021;28(13):86-90
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About the trends in the change in indicators of occupational morbidity of healthcare practitioners in the Samara region

Babanov S., Azovskova T., Lavrentieva N.

摘要

Background. Healthcare practitioners represent one of the most significant professional groups, the number of which in Russia is more than 3 million people. The work of healthcare practitioners is associated with the impact of a variety of unfavorable factors of the working environment. The first place in the structure of occupational pathology of healthcare practitioners is consistently occupied by infectious diseases, accounting for 80.2% on average in Russia. Until now, among the infectious diseases of healthcare practitioners, tuberculosis and viral hepatitis prevailed. Healthcare practitioners are a group at increased risk of infection with the SARS-CoV-2 virus during the provision of medical care in modern conditions. A novel coronavirus infection in healthcare practitioners can be considered an occupational disease if the introduction of infection occurred during the course of their professional duties. In 2020, in the group of occupational diseases caused by the influence of biological factors, the first place is occupied by diseases caused by a novel coronavirus infection. The presence of severe complications and disability determine the relevance of the analysis of the features of occupational diseases in healthcare practitioners in order to improve their diagnosis, prevention, treatment and rehabilitation. Objective. Evaluation of the state of occupational morbidity of healthcare practitioners in the Samara region over the past 3 years (2018-2020) to determine the main trends in its dynamics, to analyze the structure, taking into account nosological forms, professions, and their features in the context of a pandemic of the novel coronavirus infection COVID-19 in 2020-2021. Methods. The analysis of the state of occupational morbidity of healthcare practitioners in the Samara region was carried out according to the data of the Samara Regional Center for Occupational Pathology for the period 2018-2020 based on expert, reporting and statistical methods. Results. Occupational morbidity in the Samara region remains at a high level and exceeds the national average ones. In 2018-2019, overexertion-caused diseases (45.6%) occupied a leading position among the nosological forms of occupational diseases of healthcare practitioners in the Samara region. Allergic pathology was in second place during this period (32.25%); diseases associated with exposure to biological factors accounted for 16.12% (tuberculosis - 60% and viral hepatitis - 40%). In 2020, the ratio of acute and chronic occupational morbidity changed due to the COVID-19 pandemic. In the structure of nosological forms of occupational diseases, the first place was taken by diseases associated with the influence of biological factors - 51.21%, with leading position of diseases caused by a novel coronavirus infection (92.3%). In the period from 2020 to October 2021, medical workers in the Samara region were diagnosed with 152 cases of acute occupational disease, a novel coronavirus infection COVID-19 (74 cases with temporary disability, 78 fatal) and 5 cases of chronic occupational diseases, associated with the coronavirus infection, which determined the permanent disability. Conclusion. Currently, the working environment of healthcare practitioners does not exclude a further increase in occupational morbidity. In the context of the spread of the novel coronavirus infection around the world, it is necessary to direct more efforts to increase knowledge and study of COVID-19 from the perspective of occupational medicine in order to preserve the health of healthcare practitioners as a socially significant category of citizens that ensures the maintenance and improvement of public health.
Pharmateca. 2021;28(13):91-96
pages 91-96 views

About the mechanism of development of acquired tethered cord syndrome in patients with lumbar osteochondrosis

Bektoshev O., Bektoshev R., Babazhanov A., Akhmedov A., Nizamova Y., Bektoshev S.

摘要

Background. Tethered cord syndrome includes a group of diseases that are heterogeneous in origin, but similar in pathogenesis; they are clinically manifested by neurological deficits of varying degrees of intensity, and have such feature as combination of loss of functions of the caudal spinal cord and cauda equina roots. Tethered cord syndrome can be either congenital or acquired. The study of the acquired form of tethered cord syndrome, which develops in various diseases of the lumbar spine and spinal cord, remains an urgent problem in scientific medicine. Objective. Evaluation of the mechanisms of the development of tethered cord syndrome in patients with lumbar osteochondrosis. Methods. A study included 112 (71 men, 61 women) patients who underwent surgery for lumbar osteochondrosis with lumbar ischialgic syndrome. To determine the pathomorphological elements of lumbar osteochondrosis, leading to the development of tethered cord syndrome, a detailed clinical and neurological examination was carried out: spondylographic computed tomography (CT) and magnetic resonance imaging (MRI) of the lumbar spine. Results. All patients had high intensity (unilateral) pain syndrome, accompanied by stretch symptoms. Functional spondylography did not reveal pathological mobility. CT scan showed general pathomorphological changes characteristic of osteochondrosis. On MRI, in 49 (44%) patients, fibrosis of the terminal cistern of the spinal cord was combined with a fibrosing arachnoid cyst. In 11 (10%) patients, fibrosis was combined with a herniated disc. The rest of the patients had fibrosis in the terminal cistern of the spinal cord, which became the main cause of the development of tethered cord syndrome. Conclusion. The good efficiency of meningoradiculolysis once again confirms that tethered cord syndrome is one of the main pathogenetic elements of the development of a resistant form of pain syndrome in patients with lumbar osteochondrosis.
Pharmateca. 2021;28(13):97-101
pages 97-101 views

The effectiveness of the new blood substitute rheoambrasol in experimental toxic hypoxia

Khuzhakhmedov Z., Shevchenko L., Karimov K., Alimov T.

摘要

Objective. Assessment of the effect of the new blood substitute rheoambrasol on the hypoxia-inducible factor (HIF-1a) level, lipid peroxidation (LPO) and the antioxidant system in toxic hypoxia. Methods. The model of toxic hypoxia was performed in outbred male rats. In the blood of experimental animals, the HIF-1α level, biochemical parameters using HUMAN test systems (HUMAN Gmbh, Germany), the intensity of lipid peroxidation by the level of malondial-dehyde, the activity of enzymes of the antioxidant system (AOS): catalase, superoxide dismutase, glutathione reductase and glutathione peroxidase were determined. Results. The action of rheoambrasol was clearly manifested and showed that the new blood substitute restores biochemical parameters and reduces the HIF-1α level and the balance of the LPO/AOS system in toxic hypoxia more effectively than rheopolyglucin. The biologically active composition, including a polysaccharide and a bioenergetic substrate, has good antihypoxic, antioxidant, detoxifying, membrane protective effects, which makes it possible to recommend it for various hypoxic toxic conditions. Conclusion. The created new blood substitute rheoambrasol, containing a polysaccharide and a bioenergetic substrate, restored the structural and functional parameters of the liver, which was manifested by a slowdown in the process of cytolysis, cholestasis in toxic hypoxia. The new blood substitute has an antihypoxic effect, reducing the level of hypoxia-inducible factor HIF-1α by 4.5 times (pi<0.05). Rheoambrasol has an antioxidant effect, reduces the intensity of LPO processes and restores the activity of AOS enzymes.
Pharmateca. 2021;28(13):102-106
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Effect of dopaminergic therapy on cognitive function in patients with Parkinson’s disease

Khabarova Y., Tappakhov A., Popova T.

摘要

Parkinson’s disease (PD) is a neurodegenerative disease with a chronic progressive course, which is caused by irreversible degenerative changes in dopaminergic neurons in the substantia nigra with a decrease in dopamine levels in the basal ganglia. Until now, PD remains an incurable disease, but the available therapeutic arsenal significantly alleviates the symptoms of the disease. The emergence of certain difficulties in identifying PD at the early stages of the disease leads to a decrease in the effectiveness of treatment, and, on the contrary, the positive effectiveness of PD treatment will depend on the timely and correct diagnosis. Severity of the condition, age criteria and individual characteristics should be taken into account in the therapeutic approach for PD. In PD motor and autonomic symptoms dominate, but neurocognitive impairments such as information acquisition, processing and analysis are also significant. According to some researchers, at the initial stage of PD in patients under 70 years of age, dementia was detected in 17%, and after 70 years - in 83% of cases. When patients perform neuropsychological tests, the cognitive status improves due to the replenishment of dopamine deficiency in the striatum, activation of dopamine receptors through the restoration of the functioning of the fronto-striatal circles, which leads to a decrease in dysfunction of the frontal lobes.
Pharmateca. 2021;28(13):107-111
pages 107-111 views
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