首页 > 最新文献

Anti-Aging Eastern Europe最新文献

英文 中文
REGENERATIVE EFFECTS OF MOUSE ADIPOSE-DERIVED MULTIPOTENT STROMAL CELLS IN A MICROMASS GRAFT FOR THE TREATMENT OF BONE INJURY MODEL 小鼠脂肪源性多能基质细胞微块移植治疗骨损伤模型的再生效果
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.11
Vitalii Kyryk, O. Kuchuk, P. Klymenko
Background. Adipose-derived stem cells (ADSCs) are a promising source for the regeneration of bone tissue injuries. At the same time, three-dimensional cultures provide spatial organization of stem cells for optimal intercellular signaling, contact interaction and increase the efficiency of directed osteogenic differentiation prior to further transplantation. The aim of the study was to establish the regenerative potential of mouse adipose-derived stem cells in micromass grafts differentiated into the osteogenic direction to restore the bone injury in mice. Methods. Three-dimensional micromass cultures of murine ADSCs with further differentiation into osteogenic direction were obtained. The migration potential of cells from micromass in vitro and the effectiveness of differentiation by staining for alkaline phosphatase were evaluated. Mice with the model of femoral bone injury were transplanted with ADSCs micromass grafts and 21 days later the lesion site was examined by histological and morphometric methods. Results. The protocols for the cultivation and directed osteogenic differentiation of ADSCs in the three-dimensional micromass culture have been developed. Alkaline phosphatase production was demonstrated in cells that migrated from micromass, confirming the effectiveness of differentiation. In macroscopic examination 21 days after graft transplantation, the defect sites in femur were filled with dense tissue, while in control bones without the use of transplants, the size of the defect by 80 ± 6 % corresponded to the initial diameter and depth of injury. Histological examination of femoral bone lesions in the area of transplantation of micromass grafts revealed the formation of granulation tissue followed by the replacement of defects with newly formed bone tissue with thickening of periosteum and compact bone substance, similar to callus in fracture regeneration. In animals that underwent transplantation of micromass without prior osteogenic differentiation, the diameter of the zone of active regeneration of the diaphysis at the site of injury was 1.3 ± 0.2 mm while in the group with transplantation of directed differentiated graft it was significantly lower (0.37 ± 0.12 mm, p ≤ 0.05). Conclusions. Three-dimensional grafts of adipose-derived multipotent mesenchymal stromal cells cultured in micromass are able to improve bone tissue regeneration in a model of bone injury in mice. In this case, the grafts differentiated into osteogenic direction, provide better morphological indicators of bone recovery, compared with the micromass without prior differentiation.
背景。脂肪源性干细胞(ADSCs)是骨组织损伤再生的一个有前景的来源。同时,三维培养为干细胞提供了最佳的细胞间信号传导和接触相互作用的空间组织,并在进一步移植之前提高了定向成骨分化的效率。本研究的目的是建立小鼠脂肪源性干细胞在成骨方向分化的微块移植物中的再生潜能,以恢复小鼠骨损伤。方法。获得小鼠ADSCs的三维微块培养,并进一步向成骨方向分化。用碱性磷酸酶染色法评价微团细胞在体外的迁移潜力和分化效果。用ADSCs微块移植股骨骨损伤模型小鼠,21 d后用组织学和形态计量学方法观察损伤部位。结果。建立了三维微块培养中ADSCs的定向成骨分化方法。碱性磷酸酶在从微团迁移的细胞中产生,证实了分化的有效性。在移植21天后的宏观检查中,股骨缺损部位充满了致密的组织,而在未使用移植的对照骨中,缺损的大小为80±6%,与损伤的初始直径和深度相对应。微块移植物移植区股骨病变组织学检查显示,肉芽组织形成,缺损被新形成的骨组织取代,骨膜增厚,骨物质致密,类似骨折再生中的骨痂。未进行成骨分化的小块移植组损伤部位骨干主动再生区直径为1.3±0.2 mm,而定向分化移植组损伤部位骨干主动再生区直径明显低于对照组(0.37±0.12 mm, p≤0.05)。结论。脂肪来源的多能间充质间质细胞微团培养的三维移植物能够改善小鼠骨损伤模型中的骨组织再生。在这种情况下,移植物向成骨方向分化,与未分化的微块相比,提供了更好的骨恢复形态学指标。
{"title":"REGENERATIVE EFFECTS OF MOUSE ADIPOSE-DERIVED MULTIPOTENT STROMAL CELLS IN A MICROMASS GRAFT FOR THE TREATMENT OF BONE INJURY MODEL","authors":"Vitalii Kyryk, O. Kuchuk, P. Klymenko","doi":"10.56543/aaeeu.2022.1.1.11","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.11","url":null,"abstract":"Background. Adipose-derived stem cells (ADSCs) are a promising source for the regeneration of bone tissue injuries. At the same time, three-dimensional cultures provide spatial organization of stem cells for optimal intercellular signaling, contact interaction and increase the efficiency of directed osteogenic differentiation prior to further transplantation. \u0000The aim of the study was to establish the regenerative potential of mouse adipose-derived stem cells in micromass grafts differentiated into the osteogenic direction to restore the bone injury in mice. \u0000Methods. Three-dimensional micromass cultures of murine ADSCs with further differentiation into osteogenic direction were obtained. The migration potential of cells from micromass in vitro and the effectiveness of differentiation by staining for alkaline phosphatase were evaluated. Mice with the model of femoral bone injury were transplanted with ADSCs micromass grafts and 21 days later the lesion site was examined by histological and morphometric methods. \u0000Results. The protocols for the cultivation and directed osteogenic differentiation of ADSCs in the three-dimensional micromass culture have been developed. Alkaline phosphatase production was demonstrated in cells that migrated from micromass, confirming the effectiveness of differentiation. In macroscopic examination 21 days after graft transplantation, the defect sites in femur were filled with dense tissue, while in control bones without the use of transplants, the size of the defect by 80 ± 6 % corresponded to the initial diameter and depth of injury. Histological examination of femoral bone lesions in the area of transplantation of micromass grafts revealed the formation of granulation tissue followed by the replacement of defects with newly formed bone tissue with thickening of periosteum and compact bone substance, similar to callus in fracture regeneration. In animals that underwent transplantation of micromass without prior osteogenic differentiation, the diameter of the zone of active regeneration of the diaphysis at the site of injury was 1.3 ± 0.2 mm while in the group with transplantation of directed differentiated graft it was significantly lower (0.37 ± 0.12 mm, p ≤ 0.05). \u0000Conclusions. Three-dimensional grafts of adipose-derived multipotent mesenchymal stromal cells cultured in micromass are able to improve bone tissue regeneration in a model of bone injury in mice. In this case, the grafts differentiated into osteogenic direction, provide better morphological indicators of bone recovery, compared with the micromass without prior differentiation.","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"66 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124616415","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}
引用次数: 1
INFLAMMAGING IN MUSCLE: THE MISSING LINK BETWEEN SARCOPENIA AND IDIOPATHIC INFLAMMATORY MYOPATHIES 肌肉炎症:肌肉减少症和特发性炎性肌病之间缺失的联系
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.10
K. Jagtap, L. Hoff, E. Conticini, R. Naveen, Latika Gupta
Ageing is associated with a progressive decline in muscle mass and quality. Inflammaging, chronic low-grade inflammation is a major causative as well as maintenance factor in age-related disorders. Idiopathic inflammatory myopathies or myositis also exhibit a chronic stage of inflammation caused by various immune and non-immune-mediated processes. This review draws parallels between the mechanisms of inflammaging, sarcopenia, and myositis, and their possible interconnection. We searched literature on information about myositis, sarcopenia, ageing, inflammaging, and senescence to draw parallels between the mechanisms linking myositis, sarcopenia, and inflammaging. Further, we discuss the evidence base to support that the process of senescence is hastened in an inflamed muscle [1].
衰老与肌肉量和质量的逐渐下降有关。炎症,慢性低度炎症是年龄相关疾病的主要病因和维持因素。特发性炎症性肌病或肌炎也表现出由各种免疫和非免疫介导的过程引起的慢性炎症。本文综述了炎症、肌肉减少症和肌炎的机制,以及它们之间可能的联系。我们检索了有关肌炎、肌肉减少症、衰老、炎症和衰老的文献,以找出肌炎、肌肉减少症和炎症之间的相似机制。此外,我们讨论了支持炎症肌肉加速衰老过程的证据基础[1]。
{"title":"INFLAMMAGING IN MUSCLE: THE MISSING LINK BETWEEN SARCOPENIA AND IDIOPATHIC INFLAMMATORY MYOPATHIES","authors":"K. Jagtap, L. Hoff, E. Conticini, R. Naveen, Latika Gupta","doi":"10.56543/aaeeu.2022.1.1.10","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.10","url":null,"abstract":"Ageing is associated with a progressive decline in muscle mass and quality. Inflammaging, chronic low-grade inflammation is a major causative as well as maintenance factor in age-related disorders. Idiopathic inflammatory myopathies or myositis also exhibit a chronic stage of inflammation caused by various immune and non-immune-mediated processes. This review draws parallels between the mechanisms of inflammaging, sarcopenia, and myositis, and their possible interconnection. \u0000We searched literature on information about myositis, sarcopenia, ageing, inflammaging, and senescence to draw parallels between the mechanisms linking myositis, sarcopenia, and inflammaging. Further, we discuss the evidence base to support that the process of senescence is hastened in an inflamed muscle [1].","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"207 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"114364728","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}
引用次数: 1
AGING AND ANTI-AGING RESEARCH AND PUBLISHING PRIORITIES 衰老和抗衰老的研究和出版重点
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.01
Oleksii Bashkirtsev, O. Zimba
AGING AND ANTI-AGING RESEARCH AND PUBLISHING PRIORITIES
衰老和抗衰老的研究和出版重点
{"title":"AGING AND ANTI-AGING RESEARCH AND PUBLISHING PRIORITIES","authors":"Oleksii Bashkirtsev, O. Zimba","doi":"10.56543/aaeeu.2022.1.1.01","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.01","url":null,"abstract":"AGING AND ANTI-AGING RESEARCH AND PUBLISHING PRIORITIES","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"8 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"134332729","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}
引用次数: 1
POLYPHARMACY AS A THREAT TO AGING POPULATION 多重药房是人口老龄化的威胁
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.12
I. Benlidayı
POLYPHARMACY AS A THREAT TO AGING POPULATION
多重药房是人口老龄化的威胁
{"title":"POLYPHARMACY AS A THREAT TO AGING POPULATION","authors":"I. Benlidayı","doi":"10.56543/aaeeu.2022.1.1.12","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.12","url":null,"abstract":"POLYPHARMACY AS A THREAT TO AGING POPULATION","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"51 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116772306","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}
引用次数: 0
THE ROLE OF PHYSICAL MEDICINE AND REHABILITATION IN LONG COVID-19 MANAGEMENT 物理医学和康复在COVID-19长期管理中的作用
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.02
B. Koçyiğit
COVID-19 is an infectious disease that can have a multi-system involvement, most notably, the respiratory tract. After acute infection, a considerable proportion of patients suffer from persistent symptoms and signs, defined as long COVID-19. Depending on the affected systems and organs, patients can experience  various clinic pictures. Rehabilitation approaches serve a crucial role in providing functional recovery and improving quality of life for COVID-19 survivors. As a result of the wideness of the clinical spectrum of the long COVID-19, rehabilitation practices differ according to the affected systems. Therefore, the formation of multidisciplinary rehabilitation teams is an inevitable necessity. The establishment of specific centers for long COVID-19 rehabilitation will be beneficial. If it is not possible, existing rehabilitation centers should be strengthened for this purpose. Since the pulmonary system and respiratory tract are the most affected structures, one of the main issues to be considered in long COVID-19 cases is cardiopulmonary rehabilitation. Patients experience musculoskeletal disorders such as atrophy, sarcopenia, poor physical performance and contracture due to long-term hospitalization, intensive care treatment, quarantine practices and immobilization. Rehabilitation practices also focus on these disorders. All rehabilitation practices in long COVID-19 patients should start with low intensity, and parameters such as intensity and frequency should be increased as the patient's tolerance improves. In high-risk cases, parameters including oxygen saturation, blood pressure, and heart rhythm should be monitored. Health-care authorities should prioritize the rehabilitation of the long COVID-19 syndrome and invest in this area. Authorities, physicians and patients should collaborate to facilitate long COVID-19 rehabilitation and to establish a self-contained system.
COVID-19是一种传染病,可涉及多系统,最明显的是呼吸道。急性感染后,相当一部分患者出现持续症状和体征,定义为长时间COVID-19。根据受影响的系统和器官,患者可以体验到不同的临床图像。康复方法在为COVID-19幸存者提供功能恢复和改善生活质量方面发挥着至关重要的作用。由于COVID-19的临床范围很广,康复做法因受影响的系统而异。因此,组建多学科康复团队是必然的需要。建立专门的COVID-19长期康复中心将是有益的。如果不可能,应为此目的加强现有的康复中心。由于肺系统和呼吸道是受影响最大的结构,因此在长期COVID-19病例中需要考虑的主要问题之一是心肺康复。由于长期住院、重症监护治疗、隔离措施和固定,患者会出现肌肉骨骼疾病,如萎缩、肌肉减少、体能差和挛缩。康复实践也侧重于这些疾病。COVID-19长期患者的所有康复实践都应从低强度开始,并随着患者耐受性的提高而增加强度和频率等参数。在高危病例中,应监测血氧饱和度、血压和心律等参数。卫生保健当局应优先考虑COVID-19长期综合征的康复,并在这一领域进行投资。当局、医生和患者应通力合作,促进COVID-19的长期康复,并建立一个独立的系统。
{"title":"THE ROLE OF PHYSICAL MEDICINE AND REHABILITATION IN LONG COVID-19 MANAGEMENT","authors":"B. Koçyiğit","doi":"10.56543/aaeeu.2022.1.1.02","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.02","url":null,"abstract":"COVID-19 is an infectious disease that can have a multi-system involvement, most notably, the respiratory tract. After acute infection, a considerable proportion of patients suffer from persistent symptoms and signs, defined as long COVID-19. Depending on the affected systems and organs, patients can experience  various clinic pictures. Rehabilitation approaches serve a crucial role in providing functional recovery and improving quality of life for COVID-19 survivors. As a result of the wideness of the clinical spectrum of the long COVID-19, rehabilitation practices differ according to the affected systems. Therefore, the formation of multidisciplinary rehabilitation teams is an inevitable necessity. The establishment of specific centers for long COVID-19 rehabilitation will be beneficial. If it is not possible, existing rehabilitation centers should be strengthened for this purpose. Since the pulmonary system and respiratory tract are the most affected structures, one of the main issues to be considered in long COVID-19 cases is cardiopulmonary rehabilitation. Patients experience musculoskeletal disorders such as atrophy, sarcopenia, poor physical performance and contracture due to long-term hospitalization, intensive care treatment, quarantine practices and immobilization. Rehabilitation practices also focus on these disorders. All rehabilitation practices in long COVID-19 patients should start with low intensity, and parameters such as intensity and frequency should be increased as the patient's tolerance improves. In high-risk cases, parameters including oxygen saturation, blood pressure, and heart rhythm should be monitored. Health-care authorities should prioritize the rehabilitation of the long COVID-19 syndrome and invest in this area. Authorities, physicians and patients should collaborate to facilitate long COVID-19 rehabilitation and to establish a self-contained system.","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"35 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125815958","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}
引用次数: 1
INFLAMM-AGING: A MECHANISM OF AGING THAT CONTRIBUTES TO THE CHARACTERISTICS OF SKIN INVOLVEMENT IN SYSTEMIC SCLEROSIS 炎症老化:一种老化机制,有助于皮肤参与系统性硬化症的特征
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.07
N. Gokcen
Aging is associated with deterioration of the immune function. Two contributory mechanisms are inflamm-aging, which is a chronic, low-grade systemic inflammation, and immunosenescence, an impairment of adaptive immune function that may also contribute to the development of inflamm-aging. This age-related inflammatory event is associated with alteration to the balance of pro-inflammatory and anti-inflammatory cytokines. The effect of inflamm-aging on skin aging in healthy people is accepted; however, its effect on normal skin aging and/or skin characteristics in systemic sclerosis is unknown. The hypothesis presented herein suggests that inflamm-aging may contribute to the evolution of the skin phases in systemic sclerosis, which progress from edematous, fibrotic, and indurative phases to the atrophic phase.
衰老与免疫功能的退化有关。两种促进机制是炎症老化和免疫衰老,前者是一种慢性、低度的全身性炎症,后者是适应性免疫功能的损害,也可能促进炎症老化的发展。这种与年龄相关的炎症事件与促炎和抗炎细胞因子平衡的改变有关。炎症老化对健康人皮肤老化的影响是公认的;然而,它对正常皮肤老化和/或系统性硬化症皮肤特征的影响尚不清楚。本文提出的假设表明,炎症老化可能有助于系统性硬化症皮肤阶段的演变,从水肿、纤维化和硬化阶段发展到萎缩阶段。
{"title":"INFLAMM-AGING: A MECHANISM OF AGING THAT CONTRIBUTES TO THE CHARACTERISTICS OF SKIN INVOLVEMENT IN SYSTEMIC SCLEROSIS","authors":"N. Gokcen","doi":"10.56543/aaeeu.2022.1.1.07","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.07","url":null,"abstract":"Aging is associated with deterioration of the immune function. Two contributory mechanisms are inflamm-aging, which is a chronic, low-grade systemic inflammation, and immunosenescence, an impairment of adaptive immune function that may also contribute to the development of inflamm-aging. This age-related inflammatory event is associated with alteration to the balance of pro-inflammatory and anti-inflammatory cytokines. The effect of inflamm-aging on skin aging in healthy people is accepted; however, its effect on normal skin aging and/or skin characteristics in systemic sclerosis is unknown. The hypothesis presented herein suggests that inflamm-aging may contribute to the evolution of the skin phases in systemic sclerosis, which progress from edematous, fibrotic, and indurative phases to the atrophic phase.","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126970485","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}
引用次数: 1
VITAMIN D AND AGING: AN INTERPLAY OF MULTIPLE MECHANISMS 维生素d与衰老:多种机制的相互作用
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.08
M. Goyal, Arun Kumar Kedia
Vitamin D has anti-inflammatory and pro-autophagy actions and influences the genetic and epigenetic landscape to promote healthy aging. A deficiency of this vitamin leads to accelerated aging. Deficiency of vitamin D causes sarcopenia, osteoporosis, frailty and a high risk of fractures and consequently high morbidity. To complicate matters, in the elderly, various factors like reduced dietary intake, reduced mobility and sun exposure, decreased production and activation of vitamin D, reduction in the population of vitamin D receptors and diminished responsiveness of tissues to vitamin D cause reduced vitamin D levels and function. The above factors indicate that a special considered approach be adopted for the prevention and treatment of vitamin D deficiency in the elderly.
维生素D具有抗炎和促自噬作用,影响遗传和表观遗传景观,促进健康衰老。缺乏这种维生素会加速衰老。缺乏维生素D会导致肌肉减少症、骨质疏松症、虚弱和骨折的高风险,从而导致高发病率。更复杂的是,在老年人中,各种因素,如减少饮食摄入量,减少流动性和阳光照射,维生素D的产生和激活减少,维生素D受体数量减少,组织对维生素D的反应性降低,导致维生素D水平和功能下降。上述因素表明,预防和治疗老年人维生素D缺乏症需要采取一种特殊的考虑方法。
{"title":"VITAMIN D AND AGING: AN INTERPLAY OF MULTIPLE MECHANISMS","authors":"M. Goyal, Arun Kumar Kedia","doi":"10.56543/aaeeu.2022.1.1.08","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.08","url":null,"abstract":"Vitamin D has anti-inflammatory and pro-autophagy actions and influences the genetic and epigenetic landscape to promote healthy aging. A deficiency of this vitamin leads to accelerated aging. Deficiency of vitamin D causes sarcopenia, osteoporosis, frailty and a high risk of fractures and consequently high morbidity. To complicate matters, in the elderly, various factors like reduced dietary intake, reduced mobility and sun exposure, decreased production and activation of vitamin D, reduction in the population of vitamin D receptors and diminished responsiveness of tissues to vitamin D cause reduced vitamin D levels and function. The above factors indicate that a special considered approach be adopted for the prevention and treatment of vitamin D deficiency in the elderly.","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"13 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"126957247","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}
引用次数: 0
IMMUNOSENESCENCE AND LATE-ONSET FAMILIAL MEDITERRANEAN FEVER 免疫衰老和晚发性家族性地中海热
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.05
D. Cansu, C. Korkmaz
Familial Mediterranean fever (FMF) is an autoinflammatory disease that causes recurrent fever and serositis. FMF often begins in childhood and is diagnosed at an early age. Although it is uncommon for the disease to occur after the age of 40, late-onset patient series have been published and compared to early-onset patient series in recent years. Although it is a genetically inherited disease, the reason why clinical symptoms appear at such a late age in some patients is unknown. The frequency of pathogenic mutations is lower in these patients than in early-onset FMF patients, and the disease has a milder course. Whether or not this clinical presentation is related to immune system changes associated with aging is an open question. Age-related immune system changes, such as an increase in senescence cells, the development of senescence-associated secretory phenotype, and a decline in autophagy with age, can trigger the inflammasome activation. In this regard, understanding the cause of the late-onset of FMF attacks may open up new avenues for research into pathogenesis. In this review, we will first compare the clinical features of the early and late-onset FMF series. We will then consider hypothetical causes of late-onset FMF attacks by reviewing age-related changes in the innate immune system.
家族性地中海热(FMF)是一种引起反复发热和血清炎的自身炎症性疾病。FMF通常开始于儿童时期,并在早期被诊断出来。虽然该病在40岁以后发生并不常见,但近年来已发表了晚发性患者系列,并与早发性患者系列进行了比较。虽然这是一种遗传性疾病,但一些患者在如此晚的年龄才出现临床症状的原因尚不清楚。与早发性FMF患者相比,这些患者致病性突变的频率较低,病程较轻。这种临床表现是否与与衰老相关的免疫系统变化有关是一个悬而未决的问题。与年龄相关的免疫系统变化,如衰老细胞的增加、衰老相关分泌表型的发展以及自噬随着年龄的增长而下降,都可以触发炎性体的激活。在这方面,了解迟发性FMF发作的原因可能为研究发病机制开辟新的途径。在这篇综述中,我们将首先比较早发性和晚发性FMF系列的临床特征。然后,我们将通过回顾先天免疫系统中与年龄相关的变化来考虑迟发性FMF发作的假设原因。
{"title":"IMMUNOSENESCENCE AND LATE-ONSET FAMILIAL MEDITERRANEAN FEVER","authors":"D. Cansu, C. Korkmaz","doi":"10.56543/aaeeu.2022.1.1.05","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.05","url":null,"abstract":"Familial Mediterranean fever (FMF) is an autoinflammatory disease that causes recurrent fever and serositis. FMF often begins in childhood and is diagnosed at an early age. Although it is uncommon for the disease to occur after the age of 40, late-onset patient series have been published and compared to early-onset patient series in recent years. Although it is a genetically inherited disease, the reason why clinical symptoms appear at such a late age in some patients is unknown. The frequency of pathogenic mutations is lower in these patients than in early-onset FMF patients, and the disease has a milder course. Whether or not this clinical presentation is related to immune system changes associated with aging is an open question. Age-related immune system changes, such as an increase in senescence cells, the development of senescence-associated secretory phenotype, and a decline in autophagy with age, can trigger the inflammasome activation. In this regard, understanding the cause of the late-onset of FMF attacks may open up new avenues for research into pathogenesis. In this review, we will first compare the clinical features of the early and late-onset FMF series. We will then consider hypothetical causes of late-onset FMF attacks by reviewing age-related changes in the innate immune system.","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"28 9 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"116292634","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}
引用次数: 1
CIRCADIAN RHYTHMS AND PERSONALIZED STRATEGIES FOR ANTI-AGING THERAPIES 抗衰老疗法的昼夜节律和个性化策略
Pub Date : 2022-06-28 DOI: 10.56543/aaeeu.2022.1.1.03
O. Kalmukova, Vitalii Kyryk, M. Dzerzhynsky
Background. Nowadays personalized medicine is actively developing and consists of individual approaches during patients' treatment, diagnoses and prognoses. Since the first use of DNA sequence analysis in 2009, many other directions and methods for precision medicine have been proposed, including metabolome, transcriptome, proteome, microbiome analysis etc., which reflect internal factors of organisms. Moreover, to take into account environmental influence on organisms including day/night activity, feeding and physical training regime, it was proposed to apply the descriptions of circadian system rhythmicity of each patient. Also, with organism aging, the sensitivity to external factors is raised that emphasizes the importance of the chronobiological approach in anti-aging concept. In this review we discussed available ways of the application of circadian system parameters to analyze human metabolic state. Methods. Search strategy: PubMed, Scopus, DOAJ (Directory of Open Access Journals) and Google Scholar were used to search for original research and articles review; no abstracts from meeting reports have been cited. ClinicalTrials.gov was used to search for clinical studies. Search terms included “chronotherapy”, “circadian system”, and “chronobiology”. Results. According to personalized medicine, the analysis of circadian system in the case of each patient is necessary as circadian rhythmicity varies in every person. Taking into account the peculiarities of patient’s circadian system it will be easy to choose the best time for drug administration resulting in high efficacy and low side effects. The analysis of circadian system can be performed on molecular, physiological and systemic (general, metabolic and inflammation markers) levels. There was shown the increase in the number of clinical trials which are based on the use of chronobiological approach during the treatment of different pathologies that increase with aging: depression, insomnia, metabolic and cardiovascular disease, cancer. More than 1,000 clinical trials involving circadian interventions and chronobiology have been registered worldwide. Conclusion. Chronobiological approach can be used as an additional measure to anti-aging therapy to diagnose metabolic state, to choose more effective treatment time as well as in preventive healthcare in terms of personalized medicine.
背景。目前,个性化医疗正在积极发展,包括患者治疗、诊断和预后的个性化方法。自2009年首次使用DNA序列分析以来,人们提出了许多其他精准医学的方向和方法,包括代谢组学、转录组学、蛋白质组学、微生物组学等,这些分析反映了生物体的内部因素。此外,考虑到环境对生物体的影响,包括昼/夜活动、喂养和身体训练制度,建议应用每个患者的昼夜节律系统节律描述。此外,随着机体衰老,对外界因素的敏感性提高,强调了时间生物学方法在抗衰老概念中的重要性。本文综述了应用昼夜节律系统参数分析人体代谢状态的可行方法。方法。搜索策略:使用PubMed、Scopus、DOAJ (Open Access Journals Directory)和Google Scholar搜索原创性研究和文章综述;没有引用会议报告的摘要。ClinicalTrials.gov被用来搜索临床研究。搜索词包括“时间疗法”、“昼夜节律系统”和“时间生物学”。结果。根据个性化医学,分析每个病人的昼夜节律系统是必要的,因为每个人的昼夜节律是不同的。考虑到患者昼夜节律系统的特殊性,可以很容易地选择最佳给药时间,从而达到高效、低副作用的目的。昼夜节律系统的分析可以在分子、生理和系统(一般、代谢和炎症标志物)水平上进行。有证据表明,临床试验的数量有所增加,这些试验是基于在治疗随着年龄增长而增加的不同病理时使用时间生物学方法的:抑郁症、失眠、代谢和心血管疾病、癌症。在世界范围内,已经注册了1000多项涉及昼夜节律干预和时间生物学的临床试验。结论。时间生物学方法可以作为抗衰老治疗的附加手段来诊断代谢状态,选择更有效的治疗时间,以及在个性化医疗方面的预防保健。
{"title":"CIRCADIAN RHYTHMS AND PERSONALIZED STRATEGIES FOR ANTI-AGING THERAPIES","authors":"O. Kalmukova, Vitalii Kyryk, M. Dzerzhynsky","doi":"10.56543/aaeeu.2022.1.1.03","DOIUrl":"https://doi.org/10.56543/aaeeu.2022.1.1.03","url":null,"abstract":"Background. Nowadays personalized medicine is actively developing and consists of individual approaches during patients' treatment, diagnoses and prognoses. Since the first use of DNA sequence analysis in 2009, many other directions and methods for precision medicine have been proposed, including metabolome, transcriptome, proteome, microbiome analysis etc., which reflect internal factors of organisms. Moreover, to take into account environmental influence on organisms including day/night activity, feeding and physical training regime, it was proposed to apply the descriptions of circadian system rhythmicity of each patient. Also, with organism aging, the sensitivity to external factors is raised that emphasizes the importance of the chronobiological approach in anti-aging concept. In this review we discussed available ways of the application of circadian system parameters to analyze human metabolic state. \u0000Methods. Search strategy: PubMed, Scopus, DOAJ (Directory of Open Access Journals) and Google Scholar were used to search for original research and articles review; no abstracts from meeting reports have been cited. ClinicalTrials.gov was used to search for clinical studies. Search terms included “chronotherapy”, “circadian system”, and “chronobiology”. \u0000Results. According to personalized medicine, the analysis of circadian system in the case of each patient is necessary as circadian rhythmicity varies in every person. Taking into account the peculiarities of patient’s circadian system it will be easy to choose the best time for drug administration resulting in high efficacy and low side effects. The analysis of circadian system can be performed on molecular, physiological and systemic (general, metabolic and inflammation markers) levels. There was shown the increase in the number of clinical trials which are based on the use of chronobiological approach during the treatment of different pathologies that increase with aging: depression, insomnia, metabolic and cardiovascular disease, cancer. More than 1,000 clinical trials involving circadian interventions and chronobiology have been registered worldwide. \u0000Conclusion. Chronobiological approach can be used as an additional measure to anti-aging therapy to diagnose metabolic state, to choose more effective treatment time as well as in preventive healthcare in terms of personalized medicine.","PeriodicalId":437966,"journal":{"name":"Anti-Aging Eastern Europe","volume":"6 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-06-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"124302346","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}
引用次数: 0
期刊
Anti-Aging Eastern Europe
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1