Obesity is associated with an increased risk of premature death and represents a fast growing worldwide health problem. Although it has been long recognized that obesity is associated with an impaired insulin sensitivity, significantly increases the risk of developing type 2 diabetes, dyslipidemia, fatty liver disease, hypertension, cardiovascular disease and certain types of cancers, a subgroup of obese individuals called metabolic healthy obese seems to be protected from metabolic and cardiovascular obesity comorbidities. This article focuses on potential mechanisms underlying the healthy obese phenotype (protection against development of hepatic steatosis, inflammation of visceral adipose tissue, ectopic fat deposition and adipose tissue dysfunction) and on clinical relevance of this interesting subgroup of obese individuals. Additionally, definition, epidemiology and stability of healthy obese phenotype are discussed.
{"title":"Metabolically healthy obese individuals -- mechanisms and clinical relevance.","authors":"T Hrasko, B Bendlová, V Hainer, M Haluzík","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Obesity is associated with an increased risk of premature death and represents a fast growing worldwide health problem. Although it has been long recognized that obesity is associated with an impaired insulin sensitivity, significantly increases the risk of developing type 2 diabetes, dyslipidemia, fatty liver disease, hypertension, cardiovascular disease and certain types of cancers, a subgroup of obese individuals called metabolic healthy obese seems to be protected from metabolic and cardiovascular obesity comorbidities. This article focuses on potential mechanisms underlying the healthy obese phenotype (protection against development of hepatic steatosis, inflammation of visceral adipose tissue, ectopic fat deposition and adipose tissue dysfunction) and on clinical relevance of this interesting subgroup of obese individuals. Additionally, definition, epidemiology and stability of healthy obese phenotype are discussed.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 1","pages":"38-46"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35869022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
P Makovický, F Caja, L Vodicková, P Makovický, M Cervinková, A Juhász, G Samasca, P Vodicka
The mismatch repair gene MLH1 is a gene encoding the mismatch repair protein MutL homolog 1 (MLH1), important for repairing mutations generated during DNA replication. MLH1 absence has been observed in human gastrointestinal tumours as well as tumours of the female reproductive tract. We describe the functions of MLH 1 in cell cycle regulation and DNA mismatch repair. In this sense we discuss foriegn knowledges, in which the canine colon adencarcinoma is less frequently diagnosed in Czech and Slovak regions. We briefly described a molecular mechanism of evolution of MSI+ and MSI- colorectal carcinomas in human, and this was confronted with the current opinion of canine colon adenocarcinomas. We suppose that canine colon adenocarcinomas may occur in higher frequency, but they are underdiagnosed in the clinical veterinary practice. At the end, we describe two cases of dogs diagnosed with colorectal adenocarcinoma. The authors propose the centralized collection of colon adenocarcinoma samples from dogs, in one reference veterinary histopathological laboratory, which would analyse mismatch repair proteins.
{"title":"MutL protein homologue 1(MLH1) in colon adenocarcinomas of the dog: minireview.","authors":"P Makovický, F Caja, L Vodicková, P Makovický, M Cervinková, A Juhász, G Samasca, P Vodicka","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The mismatch repair gene MLH1 is a gene encoding the mismatch repair protein MutL homolog 1 (MLH1), important for repairing mutations generated during DNA replication. MLH1 absence has been observed in human gastrointestinal tumours as well as tumours of the female reproductive tract. We describe the functions of MLH 1 in cell cycle regulation and DNA mismatch repair. In this sense we discuss foriegn knowledges, in which the canine colon adencarcinoma is less frequently diagnosed in Czech and Slovak regions. We briefly described a molecular mechanism of evolution of MSI+ and MSI- colorectal carcinomas in human, and this was confronted with the current opinion of canine colon adenocarcinomas. We suppose that canine colon adenocarcinomas may occur in higher frequency, but they are underdiagnosed in the clinical veterinary practice. At the end, we describe two cases of dogs diagnosed with colorectal adenocarcinoma. The authors propose the centralized collection of colon adenocarcinoma samples from dogs, in one reference veterinary histopathological laboratory, which would analyse mismatch repair proteins.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 2","pages":"88-93"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35869018","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Stem cells become an effective tool for treatment of a variety of defects and diseases. Recently, it appears that the therapeutic effect of stem cells lies not only in their integration and differentiation into cells of the tissue, but especially in their paracrine activity, i.e. the ability to secrete trophic and growth factors, cytokines and chemokines that have regenerative and anti-inflammatory effects. Conditioned medium (CM) containing secretory products of stem cells can thus be used in cell-free therapy which represents an alternative to the cell-based therapy, with advantage of lower risks, the possibility of allogenic administration and mass production. Preclinical studies confirm that the therapeutic effect of CM is comparable to the effect of the application of stem cells. The aim of this paper is to summarize the results of studies using CM from different types of stem cells in regenerative medicine and simultaneously develop an overview of the factors that can modify cellular secretion and the composition of CM.
{"title":"Stem cell conditioned medium for cell-free therapies.","authors":"I Vackovcá, S Kubinová","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Stem cells become an effective tool for treatment of a variety of defects and diseases. Recently, it appears that the therapeutic effect of stem cells lies not only in their integration and differentiation into cells of the tissue, but especially in their paracrine activity, i.e. the ability to secrete trophic and growth factors, cytokines and chemokines that have regenerative and anti-inflammatory effects. Conditioned medium (CM) containing secretory products of stem cells can thus be used in cell-free therapy which represents an alternative to the cell-based therapy, with advantage of lower risks, the possibility of allogenic administration and mass production. Preclinical studies confirm that the therapeutic effect of CM is comparable to the effect of the application of stem cells. The aim of this paper is to summarize the results of studies using CM from different types of stem cells in regenerative medicine and simultaneously develop an overview of the factors that can modify cellular secretion and the composition of CM.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 1","pages":"25-31"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35869020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Women, who abuse drugs during pregnancy, expose not just themselves but also their developing fetus to impairing effects, which can have potentially harmful and even long-term effects on the exposed children. For some years, methamphetamine (MA) has dominated the illicit drug market in the Czech Republic and Slovakia; additionally this drug is on the rise worldwide. It is one of the most accessible drugs, and in many cases the first choice drug for many drug-addicted pregnant women; in part due to its anorectic and stimulant effects. These women are rarely aware of the consequences of their behavior and their pregnancy is hardly ever a good enough reason for giving up drug use. These findings are supported by many experimental studies that show the damaging effects of maternal MA exposure on their offspring. There is growing evidence that exposure to MA in utero not only causes birth defects and delays in infant development, but also impairs the brain reward neural pathways of a developing offspring in such a way, that it could increase the predisposition for drug addiction later in life. Previously published animal studies have shown that offspring of mothers exposed to MA during pregnancy are more sensitive to MA when they encounter this drug later in adulthood. With respect to increased sensitivity, the term of sensitization has been introduced. It is defined as augmented psychomotor activity, which can be observed after drug re-administration following discontinuation of repeated drug exposure, and has been demonstrated to develop not only after repeated drug administration in adulthood, but also after chronic prenatal exposure. Results from our studies have shown that prenatal MA exposure can influence the sensitivity to the effects of some drugs, given as a challenge, in adulthood, specifically to those with a similar action mechanism. Our findings indicate that cross-sensitization between prenatal MA exposure and adult drug treatment cannot be simply termed as a general drug addiction, since it seems that the mechanism by which a drug impairs specific neurotransmitter systems plays an important role. The study findings show that although the offspring of MA-addicted mothers have altered sensitivity to certain drugs in adulthood, they do not display increased active drug-seeking behavior. Therefore, if we extrapolate the results to humans, it appears that there is a relatively little risk that a person, whose mother abused MA during pregnancy, will actively seek out drugs.
{"title":"Drug sensitization induced by prenatal methamphetamine exposure.","authors":"E Macúchová, R Slamberová","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Women, who abuse drugs during pregnancy, expose not just themselves but also their developing fetus to impairing effects, which can have potentially harmful and even long-term effects on the exposed children. For some years, methamphetamine (MA) has dominated the illicit drug market in the Czech Republic and Slovakia; additionally this drug is on the rise worldwide. It is one of the most accessible drugs, and in many cases the first choice drug for many drug-addicted pregnant women; in part due to its anorectic and stimulant effects. These women are rarely aware of the consequences of their behavior and their pregnancy is hardly ever a good enough reason for giving up drug use. These findings are supported by many experimental studies that show the damaging effects of maternal MA exposure on their offspring. There is growing evidence that exposure to MA in utero not only causes birth defects and delays in infant development, but also impairs the brain reward neural pathways of a developing offspring in such a way, that it could increase the predisposition for drug addiction later in life. Previously published animal studies have shown that offspring of mothers exposed to MA during pregnancy are more sensitive to MA when they encounter this drug later in adulthood. With respect to increased sensitivity, the term of sensitization has been introduced. It is defined as augmented psychomotor activity, which can be observed after drug re-administration following discontinuation of repeated drug exposure, and has been demonstrated to develop not only after repeated drug administration in adulthood, but also after chronic prenatal exposure. Results from our studies have shown that prenatal MA exposure can influence the sensitivity to the effects of some drugs, given as a challenge, in adulthood, specifically to those with a similar action mechanism. Our findings indicate that cross-sensitization between prenatal MA exposure and adult drug treatment cannot be simply termed as a general drug addiction, since it seems that the mechanism by which a drug impairs specific neurotransmitter systems plays an important role. The study findings show that although the offspring of MA-addicted mothers have altered sensitivity to certain drugs in adulthood, they do not display increased active drug-seeking behavior. Therefore, if we extrapolate the results to humans, it appears that there is a relatively little risk that a person, whose mother abused MA during pregnancy, will actively seek out drugs.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 1","pages":"32-37"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35869021","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chronic fatigue syndrome is a disease detected in recent 15 or 20 years. Overtrained athletes, people living in stress, the ones with disturbed immunity or people suffering from some of the infectious diseases are the most threatened ones. During ultra-long-distance run, human immune, physiological a biochemical parameters drift of their physiological ranges. The values could increase or decrease. The samples of serum of ultramarathon runners, who took part in the National Ultramarathon Mastership, were collected and measured before and after the race. The parameters include IgA, IgM, IgG and C3 part of complement. Statistically important increases in IgA and IgG concentrations after the race were observed. The changes of concentrations of IgM and C3 part of complement was not statistically important. IgG is responsible for the activation of complement, secondary immune reactions and the neutralization of bacterial toxins. IgA in the role of muckal imunoglobulin helps immune cells to swallow heterogenous particles, germs and toxins. Our immune syst6m is more threatened by heterogenous infectious diseases and even the chronic fatigue syndrome.
{"title":"[The influence of physical load on the propriate immune and physiological parameters.]","authors":"M Milicková, A Zákovská, D Chlíbková","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Chronic fatigue syndrome is a disease detected in recent 15 or 20 years. Overtrained athletes, people living in stress, the ones with disturbed immunity or people suffering from some of the infectious diseases are the most threatened ones. During ultra-long-distance run, human immune, physiological a biochemical parameters drift of their physiological ranges. The values could increase or decrease. The samples of serum of ultramarathon runners, who took part in the National Ultramarathon Mastership, were collected and measured before and after the race. The parameters include IgA, IgM, IgG and C3 part of complement. Statistically important increases in IgA and IgG concentrations after the race were observed. The changes of concentrations of IgM and C3 part of complement was not statistically important. IgG is responsible for the activation of complement, secondary immune reactions and the neutralization of bacterial toxins. IgA in the role of muckal imunoglobulin helps immune cells to swallow heterogenous particles, germs and toxins. Our immune syst6m is more threatened by heterogenous infectious diseases and even the chronic fatigue syndrome.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 2","pages":"84-87"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35870022","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Vincenc Alexandr Bohdálek (Vincenz Alexander Bochdalek) is known primarily as an anatomist and pathologist and entered into the history of anatomy by describing a number of anatomical structures. Unfortunately his findings in the field of neuroscience are, with few exceptions, almost unknown. Current reviewtherefore partially fills a gap in the evaluation of the contributions of Bohdálek and based on available archival sources provides an overview of his results in the field of the nervous system research, which accounts for almost half of his works. He studied in detailpredominantly the innervation of eye, upper jaw, hard palate,auditory system and meninges, and surprisingly also dealt with the tissue regeneration. Bohdálek's works also show that he tried to find a physiological explanation to the observed anatomical and pathological findings, therefore he could be considered as a pioneer of the field, which is now called as func- tional anatomy. Present overview of his neuroscience works, including his complete bibliography,partially fills a huge debt to Bohdálek. Key words: nerves, brain, Bohdálek, 19th century.
Vincenz Alexander Bohdálek (Vincenz Alexander Bochdalek)主要被称为解剖学家和病理学家,并通过描述一些解剖结构进入解剖学的历史。不幸的是,除了少数例外,他在神经科学领域的发现几乎无人知晓。因此,当前的评论部分填补了对Bohdálek贡献评估的空白,并基于现有的档案来源提供了他在神经系统研究领域的研究成果的概述,这几乎占他作品的一半。他主要研究了眼睛、上颌、硬腭、听觉系统和脑膜的神经支配,令人惊讶的是,他还研究了组织再生。Bohdálek的作品也表明,他试图找到一个生理的解释,以观察解剖和病理的发现,因此他可以被认为是一个领域的先驱,这是现在被称为功能解剖学。目前概述他的神经科学工作,包括他的完整的参考书目,部分填补了巨大的债务Bohdálek。关键词:神经,大脑,Bohdálek, 19世纪。
{"title":"Vincenc Alexandr Bohdálek (1801-1883) and his contributions in the field of neuroscience.","authors":"A Chvtal","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Vincenc Alexandr Bohdálek (Vincenz Alexander Bochdalek) is known primarily as an anatomist and pathologist and entered into the history of anatomy by describing a number of anatomical structures. Unfortunately his findings in the field of neuroscience are, with few exceptions, almost unknown. Current reviewtherefore partially fills a gap in the evaluation of the contributions of Bohdálek and based on available archival sources provides an overview of his results in the field of the nervous system research, which accounts for almost half of his works. He studied in detailpredominantly the innervation of eye, upper jaw, hard palate,auditory system and meninges, and surprisingly also dealt with the tissue regeneration. Bohdálek's works also show that he tried to find a physiological explanation to the observed anatomical and pathological findings, therefore he could be considered as a pioneer of the field, which is now called as func- tional anatomy. Present overview of his neuroscience works, including his complete bibliography,partially fills a huge debt to Bohdálek. Key words: nerves, brain, Bohdálek, 19th century.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 1","pages":"4-24"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35869019","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Chronic fatigue syndrome - CFS is a disease that lasts about 6 months in adults and in children three months. Other names are myalgia encephalomyelitis, postviral immune syndrome, chronic fatigue immune dysfunction syndrome. The reasons are biological, genetical, infectious or psychological. The paper discusses the history of chronic fatigue syndrome, epidemiology and its prevalence, clinical course, pathophysiology, diagnosis, therapy and prognosis, and also economics.
{"title":"[Chronic fatifue syndrome.]","authors":"V Holecek, R Rokyta","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Chronic fatigue syndrome - CFS is a disease that lasts about 6 months in adults and in children three months. Other names are myalgia encephalomyelitis, postviral immune syndrome, chronic fatigue immune dysfunction syndrome. The reasons are biological, genetical, infectious or psychological. The paper discusses the history of chronic fatigue syndrome, epidemiology and its prevalence, clinical course, pathophysiology, diagnosis, therapy and prognosis, and also economics.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 2","pages":"69-74"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35870017","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
The results obtained during the studies of the microscopic structure of animal and human tissues by the famous 19th century Czech scientist Jan Evangelista Purkynĕ are already sufficiently described in a variety of older and newer publications. The contents of the present paper are an overview of the microscopes and other tools and instruments that Purkynĕ and his assistants and pupils used for research of tissue histology and during teaching, and in whose development there were directly involved. A brief overview of the development of the cutting engines suggests that the first microtome, from which all modern sliding microtomes are derived, originated under the supervision of Purkynĕ at the Institute of Physiology in Wroclaw. Purkynĕ and his assistants thus not only obtained priority results in the field of the structure of animal and human tissues, but also substantially contributed to the development of instruments and equipment for their study, which is often forgotten today.
{"title":"[Jan Evangelista Purkynĕ and his instruments for microscopic research.]","authors":"A Chvtal","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The results obtained during the studies of the microscopic structure of animal and human tissues by the famous 19th century Czech scientist Jan Evangelista Purkynĕ are already sufficiently described in a variety of older and newer publications. The contents of the present paper are an overview of the microscopes and other tools and instruments that Purkynĕ and his assistants and pupils used for research of tissue histology and during teaching, and in whose development there were directly involved. A brief overview of the development of the cutting engines suggests that the first microtome, from which all modern sliding microtomes are derived, originated under the supervision of Purkynĕ at the Institute of Physiology in Wroclaw. Purkynĕ and his assistants thus not only obtained priority results in the field of the structure of animal and human tissues, but also substantially contributed to the development of instruments and equipment for their study, which is often forgotten today.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 2","pages":"56-68"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35870015","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Diabetes mellitus is a powerful risk factor for cardiovascular disease associated with high morbidity and mortality rates. Diabetic patients also have an increased incidence of heart failure which has been traditionally attributed to the presence of ischemic or hypertensive heart disease. However, the diabetic milieu is itself noxious to the heart, and cardiomyopathy can develop independent of elevated blood pressure, coronary artery disease or other risk factors with the potential to lead to a progressive development of heart failure. Diabetic car- diomyopathy is characterized by significant changes in function and structure of the heart. They have been studied in numerous diabetic experimental models in animals, mostly rodents. Revealing of potential underlying mechanisms of these pathophysiological alterations holds the promise to design new pharmacological strategies for diabetic patients. Our current review provides an update on functional and structural alterations in the diabetic heart and pathophysiological mechanisms of their development and progression.
{"title":"[Diabetic cardiomyopathy: pathophysiological mechanisms of structural and functional changes.]","authors":"J Slavíková, E Mistrová, M Dvoráková Chottová","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Diabetes mellitus is a powerful risk factor for cardiovascular disease associated with high morbidity and mortality rates. Diabetic patients also have an increased incidence of heart failure which has been traditionally attributed to the presence of ischemic or hypertensive heart disease. However, the diabetic milieu is itself noxious to the heart, and cardiomyopathy can develop independent of elevated blood pressure, coronary artery disease or other risk factors with the potential to lead to a progressive development of heart failure. Diabetic car- diomyopathy is characterized by significant changes in function and structure of the heart. They have been studied in numerous diabetic experimental models in animals, mostly rodents. Revealing of potential underlying mechanisms of these pathophysiological alterations holds the promise to design new pharmacological strategies for diabetic patients. Our current review provides an update on functional and structural alterations in the diabetic heart and pathophysiological mechanisms of their development and progression.</p>","PeriodicalId":75688,"journal":{"name":"Ceskoslovenska fysiologie","volume":"65 2","pages":"75-83"},"PeriodicalIF":0.0,"publicationDate":"2016-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"35870020","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}