Influence of Remote Ischemic Preconditioning Reperfusion/Reocclusion Training and Physical Exercises on the Inflammatory, Angiogenic, Neurotrophic and Anti-tumor Potential of Human Serum in Vivio/in Vitro Studies - Role of Vitamin d and Iron Metabolism
试验速览
- 阶段
- 不适用
- 状态
- Enrolling By Invitation
- 发起方
- 入组人数
- 250
- 试验地点
- 4
- 主要终点
- Measurement of the inflammation blood markers using Magnetic Luminex Performance Assays
研究概览
简要总结
Both in sports and medicine, methods that can significantly contribute to improving the ability of tissues to perform their functions are constantly being searched. One of those methods that is increasingly used also in sports is remote ischemic preconditioning (RIPC). Mostly, this procedure involves repeated brief cycles of limb ischemia/reperfusion. This method is often referred as ischemic blood reperfusion and helps to increase the tolerance of treated tissues to the occurrence of possible ischemic episodes in the future. Numerous studies have shown that RIPC induces changes that lead to increased resistance to hypoxia and other stressors in organs (brain, heart, liver). In addition, it has been proven that induction of arterial occlusion in the area of selected limbs before performing physical exercises can affect the improvement of their function, and thus can translate into sports results. In addition, an adaptation of such fibres to damage is mostly associated with the secretion of many factors that influence body function. That's why we conclude that it may affect protein kinases (such like c-Jun N-terminal kinases (JNKs) or serine-threonine kinase = protein kinase B (AKTs)) whose main role is regulation of the activity of a wide spectrum of substrates, influencing cells proliferation, apoptosis, responses to cellular stress and inflammatory process in normal and cancer cells. Concluding that presented kinases activity is associated with cells differentiation and RIPC and physical activity may affect them and the inflammation process that may lead to cytotoxic activity against cancer cells (especially if the effects are combined together). The beneficial increase of anti-tumour activity of the blood serum against pathological isolated tumour cells of prostate cancer (cell lines - LNCaP and PC- 3) was confirmed in our pilot studies. We observed an increase in the anti-cancer properties of serum taken from people that attended RIPC training and performed physical activity. However, the exact mechanism and associated changes in the proteome of blood serum people attending in the RIPC training have not yet been determined. This knowledge would allow us to determine the exact mechanisms of the reperfusion/reocclusion training on the human body and its beneficial activity. Considering that the skeletal muscle is an organ capable of synthesis and release of a number of proteins, cytokines and low molecular weight compounds, especially during physical activity, it should be assumed that intermittent muscle ischemic episodes will lead to increased release of factors that will increase the resistance of muscles and other tissues to stress. At the same time, it was noticed that under conditions of muscular stress induced changes in iron metabolism occur. The binding of free iron through the ferritin protein at the cell level leads to its greater resistance to stressors. In the prism of the above considerations, the results of our preliminary studies showing that the upper limb RIPC procedures cause changes in iron metabolism in white blood cells and may suggest that the procedure of RIPC leads to changes that allow storing iron in a safe form in as ferritin. At the same time, with the increasing interest in iron metabolism, the role and function of amyloid precursor protein (APP) and hepcidin are increasing. It has been proven that APP is a protein that works with ferroportin, thus taking part in iron export from a cell. Moreover, it has been shown that the post-translational modification of APP leads to the formation of amyloid α (determines positive changes) and amyloid β (negative changes). Because there are some indications that sAPPα may be modified by iron changes and associated with cfDNA changes, which substantially increase during i.e. tissue damage, we would like to explore those correlations more deeply. The same decrease in the APP protein level will lead to the inhibition of iron export from the cell and an increase of its concentration in the cell. The nature of such changes in iron metabolism should be considered as adaptive to the ischemic stress on which muscle is exposed during the RIPC procedure. The increase in ferritin in the cell leads to a decrease in the concentration of free iron and thus a reduction in iron-dependent ROS formation. This project will have an impact on the development of the current state of knowledge of the mechanisms of biochemical response to the specific tissue-affecting method in form of remote ischemic preconditioning and will allow determining the role of sAPPα and Cathepsin C and other trophic factors and changes in iron metabolism in this process, taking into account the role of hepcidin and vitamin D. Moreover, the present project may contribute to the determination of the role of presented procedures on cells proliferation, as an example of anti-tumour proprieties, and changes of human serum proteomes.
详细描述
Both in sport and medicine, constantly new methods are being search that can significantly improve the ability of tissues to perform their functions. One of such methods, increasingly used also in sport an physical activity is the Remot Ischemic Preconditioning (RIPC). In most cases, this procedure involves repeated brief cycles of limb ischemia and reperfusion. And often is being said that it helps to increase the tolerance of treated tissues to the occurrence of possible ischemic episodes in the future. Numerous studies have shown that RIPC induces changes that lead to increased resistance to hypoxia and many other tissue stressors in numerus organs, such as brain, heart, liver, kidneys etc.
In addition, in case of skeletal muscles, it has been proven that induction of arterial occlusion in the part of selected limbs before performing physical exercises can affect its activity by causing the improvement of its function and performance, and thus can result in to a sports scores (results). In addition, a greater resistance of such fibers to damage induced by eccentric contractions was observed. The mechanism of this method, however, is not fully understood, and its character can be very complex and effects tissue on many stages of its activity.
On the other hand considering that the skeletal muscle is an endocrine organ capable to synthesis and release a number of proteins, cytokines and low molecular weight compounds, especially during physical activity, it should be assumed that that intermittent muscle ischemic episodes will lead to increased release of factors that will increase the resistance of muscles and other tissues to stress.
In addition, adaptation of such fibers i mostly associated with the secretion of many factors that influence whole body function.
One of such substances are protein kinases. They are responsible for regulation of many biological processes, as well as a molecularly targeted anti-cancer therapy due to the increased level it's activity in many cancers. These enzymes carry out the phosphorylation reaction of a specific molecules. Phosphorylation usually changes the conformation of the protein molecules and, consequently, changes its activity, and ability to bind to other proteins, or the movement of the molecule within the cell. Most research indicates that they play a key role in many fundamental cellular processes such as the cell cycle, cell division, differentiation and apoptosis. Deregulation of kinase activity as a result of chromosomal mutations, rearrangements and / or gene amplification is observed in many types of cancer cells. Therefore, such procedures like RIPC or intensive physical activity that could affects it's activity may be specific inhibitors of these enzymes, fulfilling the idea of molecularly targeted therapy. Therefore, we conclude that it may affect some specific protein kinases (such like c-Jun N-terminal kinases (JNKs) or serine-threonine kinase = protein kinase B (AKTs)), and may be associated with cancer cells life, especially if the effect is combined together (RIPC + physical activity). Therefore, in our pilot studies, we assessed the effect of the 10 days RIPC procedure on the anti-tumor potential of human serum in relation to the prostate tumor line LNCaP. We observed statistical significance increase of human serum antitumor potential which may be connected to the effect on protein kinase pathways. However, this requires further confirmation and analyzes of a larger population of people subjected to the RIPC procedure and physical activity. From this research it's seems advisable to assess whether the ischemic procedures affects antitumor properties of human serum by itself or is it connected to the impact of other factors such like physical activity.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 49 Years(Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Dependent on the studied population:
- •Population of not training grope age and morphologically appropriate participation will take part. Participants will be recruited basing on a voluntary letter of intent. All representatives of the analyzed group participating in the pre-qualification research will fill in the physical activity sheet - Global Health Activity Questionnaire - World Health Organization in Polish adaptation. This will allow to eliminate people who report high levels of physical activity (similar to the level of sport training individuals).
- •Aerobic sport training Population (long distance runners, marathon runners and other). Participants will be recruited basing on a voluntary letter of intent. All representatives of the analysed group participating in the pre-qualification research will fill in the physical activity sheet - Global Health Activity Questionnaire - World Health Organization in Polish adaptation. All participants have to declare minimum 5 marathon run history (similar to the level of sport results during the run).
排除标准
- •taking medicines during the study,
- •history of cardiovascular disorders,
- •history of autonomic nervous system disorders,
- •history of mental disorders,
- •history of cerebro-cranial traumas,
- •history of other diseases that may directly affect obtained results,
- •concurrent injuries,
- •drugs intake,
- •supplements consumption
结局指标
主要结局
Measurement of the inflammation blood markers using Magnetic Luminex Performance Assays
时间窗: Change from baseline at 24 hours after fatigue-induced exercise (before and after IPC protocol)
The intake will be performed in appropriate standardized BD Vacutainer tubes by qualified medical personnel: Serum and plasma will be separated from the samples, Each sample to obtain the serum will be centrifuged at 2500-3000 rpm for 10 minutes in 4° C and stored in 1.5 ml tubes at - 80° C until the assay (no longer than 6 months). The following secretory factors and markers of inflammation will be determined in serum or blood plasma (depending on the requirements of the method used) and then analysed in detail using immu: * high sensitive C-protein (hsCRP), * creatine kinas (CK), * lactic acid (LA), * interleukin 6 (IL6), * interleukin 10 (IL10), * interleukin 15 (IL15),
Measurement of the Iron metabolism blood markers using Magnetic Luminex Performance Assays and ELISA Assays
时间窗: Change from baseline at 24 hours after fatigue-induced exercise (before and after IPC protocol)
The intake will be performed in appropriate standardized BD Vacutainer tubes by qualified medical personnel: Serum and plasma will be separated from the samples, Each sample to obtain the serum will be centrifuged at 2500-3000 rpm for 10 minutes in 4° C and stored in 1.5 ml tubes at - 80° C until the assay (no longer than 6 months). The following secretory factors and markers will be messured: * free Iron * hepcidin, * transferrin, * ferritin, * EPO, * EFRE, * TIBC,
Measurement of neurotrophic, angiogenic blood markers using Automated Hematology Analyzers and Magnetic Luminex Performance Assays
时间窗: Change from baseline at 24 hours after fatigue-induced exercise (before and after IPC protocol)
The intake will be performed in appropriate standardized BD Vacutainer tubes by qualified medical personnel: Serum and plasma will be separated from the samples, Each sample to obtain the serum will be centrifuged at 2500-3000 rpm for 10 minutes in 4° C and stored in 1.5 ml tubes at - 80° C until the assay (no longer than 6 months). The following secretory factors and markers of inflammation will be determined: angiogenin (ANG), • insulin-like growth factor-1 (IGF-1), • Growth Differentiation Factor 15 (GDF15), • nerve growth factor (NGF), • Amyloid Precursor Protein- α (sAPPα), • angiopoietin (ANGP1), • brain-derived neurotrophic factor (BDNF) • growth differentiation factor 15 (GDF-15), • tumor necrosis factor α (TNFα).
The general assessment of the homoeostasis Automated Hematology Analyzers
时间窗: Before all procedures and before post-IPC testing
* blood morphology, * glycemia, * free iron, * activity of alanine aminotransferase (ALT), * aspartate aminotransferase (AST), * creatine kinase (CK), * lactate dehydrogenase (LDH), * concentration of insulin, * total cholesterole * creatinine,
次要结局
- Messurment of cfDNA changes(Before, and 5 min, 60 min after every WAnT performance)
- Body composition analyses using bioelectrical impedance analysis (BIA)(During the initial visit, and before and after every experimental phase (1-time; 10-times IPC procedures))
- Measurement of proteins involved in antioxidant defence using Western Blotting Techniques(Change from baseline at 24 hours after fatigue-induced exercise (before and after IPC protocol))
- Measurement of anaerobic power of the lower limbs (Wingate Anaerobic Test)(Before and after 1-time and 10-times IPC/SHAM procedures)
- Measurement of isolated serum cytotoxic activity(Up to 3 months post-experimental period)
