Analysis of the relationship between age-related erythrocyte dysfunction and fatigue

被引:0
作者
Ogata, Yuichiro [1 ]
Yamada, Takaaki [1 ]
Fujimura, Masahiro [1 ]
Igarashi, Toshio [1 ]
Hasegawa, Seiji [1 ,2 ]
机构
[1] Nippon Menard Cosmet Co Ltd, Res Labs, 2-7 Torimi-cho,Nishi-ku, Nagoya, Aichi, Japan
[2] Nagoya Univ, Grad Sch Med, MENARD Collaborat Chair, 65 Tsurumaicho,Showa-ku, Nagoya, Aichi, Japan
关键词
Erythrocyte; Fatigue; Hematopoietic stem cell; IL-1; alpha; Aging; Inflammation; SENESCENT CELLS; CLEARANCE; ANEMIA;
D O I
10.1007/s10522-024-10106-w
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
With the declining birth rates and aging societies in developed countries, the average age of the working population is increasing. Older people tend to get tired more easily, so prevention of fatigue is important to improve the quality of life for older workers. This study aimed to assess the mechanism of fatigue in older people, especially focused on relation between dysfunction of erythrocyte and fatigue. Total power (TP), which is the value of autonomic nerve activity, was measured as a value of fatigue and significantly decreased in workers with aging. As properties of senescent erythrocytes, the erythrocyte sedimentation rate and damaged erythrocytes population increased with aging and correlated with TP. These results suggested that the accumulation of damaged erythrocytes contributes to fatigue. Recent studies revealed that senescence-associated secretory phenotype (SASP), a phenomenon in which senescent cells secrete a variety of cytokines, affected hematopoiesis in bone marrow. We analyzed the effects of SASP factors on erythropoiesis and found that Interleukin -1 alpha (IL-1 alpha) suppressed erythrocyte differentiation of hematopoietic stem cells in vitro. We also showed that IL-1 alpha levels in human blood and saliva increase with aging, suggesting the possibility that IL-1 alpha level in saliva can be used to predict the decline in hematopoietic function.
引用
收藏
页码:809 / 817
页数:9
相关论文
共 50 条
[21]   Modulation of NOS activity in age-related cardiac dysfunction [J].
Yang, B ;
Larson, DF ;
Watson, RR .
LIFE SCIENCES, 2004, 75 (06) :655-667
[22]   Targeting Mitochondria to Counteract Age-Related Cellular Dysfunction [J].
Madreiter-Sokolowski, Corina T. ;
Sokolowski, Armin A. ;
Waldeck-Weiermair, Markus ;
Malli, Roland ;
Graier, Wolfgang F. .
GENES, 2018, 9 (03)
[23]   Promise of metformin for preventing age-related cognitive dysfunction [J].
Leelavathi N.Madhu ;
Maheedhar Kodali ;
Ashok K.Shetty .
Neural Regeneration Research, 2022, 17 (03) :503-507
[24]   Proteolysis dysfunction in the process of aging and age-related diseases [J].
Frankowska, Natalia ;
Lisowska, Katarzyna ;
Witkowski, Jacek M. .
FRONTIERS IN AGING, 2022, 3
[25]   Vitamin C improves age-related endothelial dysfunction [J].
Virdis, A ;
Ghiadoni, L ;
Salvetti, G ;
Taddei, S ;
Sudano, I ;
Salvetti, A .
AMERICAN JOURNAL OF HYPERTENSION, 1999, 12 (04) :57A-57A
[26]   Age-related slowing of movement as basal ganglia dysfunction [J].
Saling, L. L. ;
Phillips, J. G. .
EUROPEAN REVIEW OF AGING AND PHYSICAL ACTIVITY, 2008, 5 (02) :69-77
[27]   Association between dietary glycernic index and age-related macular degeneration in nondiabetic participants in the Age-Related Eye Disease Study [J].
Chiu, Chung-Jung ;
Milton, Roy C. ;
Gensler, Gary ;
Taylor, Allen .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2007, 86 (01) :180-188
[28]   Age-related dysfunction of mitochondria-Cause and therapeutic target of cardiovascular diseases [J].
Dihlmann, Susanne ;
Boeckler, Dittmar ;
Peters, Andreas S. .
GEFASSCHIRURGIE, 2022, 27 (04) :253-260
[29]   Effects of zinc status on age-related T cell dysfunction and chronic inflammation [J].
Carmen P. Wong ;
Kathy R. Magnusson ;
Thomas J. Sharpton ;
Emily Ho .
BioMetals, 2021, 34 :291-301
[30]   Effects of zinc status on age-related T cell dysfunction and chronic inflammation [J].
Wong, Carmen P. ;
Magnusson, Kathy R. ;
Sharpton, Thomas J. ;
Ho, Emily .
BIOMETALS, 2021, 34 (02) :291-301