Effects of moderate exercise over different phases on age-related physiological dysfunction in testes of SAMP8 mice

Oxidative stress and chronic inflammation have been implicated in the testicular aging process. Different types and moderate-intensity of regular exercise may reduce age-related physiological dysfunction associated with inflammation and oxidative stress, but such effects of moderate-intensity of exe...

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Veröffentlicht in:Experimental gerontology 2013-09, Vol.48 (9), p.869-880
Hauptverfasser: Zhao, Xiujun, Bian, Yanqing, Sun, Yichong, Li, Li, Wang, Lixuan, Zhao, Chunfang, Shen, Yongqing, Song, Qingliang, Qu, Yine, Niu, Siyun, Wu, Wenshuang, Gao, Fulu
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container_end_page 880
container_issue 9
container_start_page 869
container_title Experimental gerontology
container_volume 48
creator Zhao, Xiujun
Bian, Yanqing
Sun, Yichong
Li, Li
Wang, Lixuan
Zhao, Chunfang
Shen, Yongqing
Song, Qingliang
Qu, Yine
Niu, Siyun
Wu, Wenshuang
Gao, Fulu
description Oxidative stress and chronic inflammation have been implicated in the testicular aging process. Different types and moderate-intensity of regular exercise may reduce age-related physiological dysfunction associated with inflammation and oxidative stress, but such effects of moderate-intensity of exercise over different phases of life in testes have not been reported. In this study, male SAMP8 mice, a senescence-accelerated strain, were maintained as sedentary (sed) or subjected to daily 15-min periods of swimming exercise between ages of 2–7months (lifelong), 2–4months (earlier) or 5–7months (late). Age-related changes, including serum testosterone levels and biomarkers of inflammation and oxidative stress were analyzed at the end of the experiment. All exercise groups showed significantly greater serum testosterone levels and decreased age-related inflammation and oxidative stress compared with the sedentary group. Exercise also increased expression and activity of the nuclear factor erythroid 2-related factor (Nrf2), a transcriptional regulator of the cellular anti-oxidant system, and decreased expression and activity of nuclear factor kappa beta (NF-κB), a mediator of inflammatory molecules, in the nucleus of testicular cells. However, lifelong and earlier groups generally showed significantly better protective effects than the late group against age-related physiological dysfunction in testes. Thus, lifelong exercise and earlier phase exercise were most effective in counteracting oxidative stress and inflammation and in preserving testes function through regulation of Nrf2 and NF-κB. These results advocate the benefits of lifelong exercise and emphasize a greater protection against male aging by instituting exercise earlier rather than late in life. •Lifelong or earlier exercise may be more beneficial to counteract testes aging.•The responses of Nrf2 to exercise may lower age-associated oxidative stress.•NF-κB may be involved into exercises counteracting age-related inflammation.
doi_str_mv 10.1016/j.exger.2013.05.063
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Different types and moderate-intensity of regular exercise may reduce age-related physiological dysfunction associated with inflammation and oxidative stress, but such effects of moderate-intensity of exercise over different phases of life in testes have not been reported. In this study, male SAMP8 mice, a senescence-accelerated strain, were maintained as sedentary (sed) or subjected to daily 15-min periods of swimming exercise between ages of 2–7months (lifelong), 2–4months (earlier) or 5–7months (late). Age-related changes, including serum testosterone levels and biomarkers of inflammation and oxidative stress were analyzed at the end of the experiment. All exercise groups showed significantly greater serum testosterone levels and decreased age-related inflammation and oxidative stress compared with the sedentary group. Exercise also increased expression and activity of the nuclear factor erythroid 2-related factor (Nrf2), a transcriptional regulator of the cellular anti-oxidant system, and decreased expression and activity of nuclear factor kappa beta (NF-κB), a mediator of inflammatory molecules, in the nucleus of testicular cells. However, lifelong and earlier groups generally showed significantly better protective effects than the late group against age-related physiological dysfunction in testes. Thus, lifelong exercise and earlier phase exercise were most effective in counteracting oxidative stress and inflammation and in preserving testes function through regulation of Nrf2 and NF-κB. 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Different types and moderate-intensity of regular exercise may reduce age-related physiological dysfunction associated with inflammation and oxidative stress, but such effects of moderate-intensity of exercise over different phases of life in testes have not been reported. In this study, male SAMP8 mice, a senescence-accelerated strain, were maintained as sedentary (sed) or subjected to daily 15-min periods of swimming exercise between ages of 2–7months (lifelong), 2–4months (earlier) or 5–7months (late). Age-related changes, including serum testosterone levels and biomarkers of inflammation and oxidative stress were analyzed at the end of the experiment. All exercise groups showed significantly greater serum testosterone levels and decreased age-related inflammation and oxidative stress compared with the sedentary group. Exercise also increased expression and activity of the nuclear factor erythroid 2-related factor (Nrf2), a transcriptional regulator of the cellular anti-oxidant system, and decreased expression and activity of nuclear factor kappa beta (NF-κB), a mediator of inflammatory molecules, in the nucleus of testicular cells. However, lifelong and earlier groups generally showed significantly better protective effects than the late group against age-related physiological dysfunction in testes. Thus, lifelong exercise and earlier phase exercise were most effective in counteracting oxidative stress and inflammation and in preserving testes function through regulation of Nrf2 and NF-κB. These results advocate the benefits of lifelong exercise and emphasize a greater protection against male aging by instituting exercise earlier rather than late in life. •Lifelong or earlier exercise may be more beneficial to counteract testes aging.•The responses of Nrf2 to exercise may lower age-associated oxidative stress.•NF-κB may be involved into exercises counteracting age-related inflammation.</description><subject>Aging</subject><subject>Aging, Premature - metabolism</subject><subject>Aging, Premature - physiopathology</subject><subject>Animals</subject><subject>Antioxidants - metabolism</subject><subject>Cyclooxygenase 2 - metabolism</subject><subject>Cytokines - biosynthesis</subject><subject>Exercise</subject><subject>Inflammation</subject><subject>Inflammation Mediators - metabolism</subject><subject>Macrophages - pathology</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Mutant Strains</subject><subject>NF-E2-Related Factor 2 - biosynthesis</subject><subject>NF-kappa B - metabolism</subject><subject>Orchitis - metabolism</subject><subject>Orchitis - physiopathology</subject><subject>Oxidative stress</subject><subject>Oxidative Stress - physiology</subject><subject>Phosphoproteins - metabolism</subject><subject>Physical Conditioning, Animal</subject><subject>Testis - enzymology</subject><subject>Testis - pathology</subject><subject>Testis - physiopathology</subject><subject>Testosterone</subject><subject>Testosterone - blood</subject><issn>0531-5565</issn><issn>1873-6815</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1vEzEQhi0EoqHwC5CQj1x2GX9vDhyqqkClIpCAs-XY4-Bodx3sTdX8e9ym9MhppNHzzsdDyFsGPQOmP-x6vNti6Tkw0YPqQYtnZMUGIzo9MPWcrEAJ1iml1Rl5VesOADQX7CU548IoJsGsSL2KEf1SaY50ygGLW5DiHRafKtJ8i4WG1JCC80L3v13Fhs7UbbErODY4tO6xpjzmbfJupOFY42H2S2pUmumCdcGH6T8uvn4f6JQ8viYvohsrvnms5-TXp6ufl1-6m2-fry8vbjov1HrphIcotRMalUFtdJDcRS-Bbzg6rkBxOUQjho0fhDYOhfRCDgPGuJZhvWHinLw_zd2X_OfQDrFTqh7H0c2YD9UyyQ2AMUw3VJxQX3KtBaPdlzS5crQM7L1tu7MPtu29bQvKNtst9e5xwWEzYXjK_NPbgI8nANubt6nFq084ewypNOs25PTfBX8BVPiSog</recordid><startdate>201309</startdate><enddate>201309</enddate><creator>Zhao, Xiujun</creator><creator>Bian, Yanqing</creator><creator>Sun, Yichong</creator><creator>Li, Li</creator><creator>Wang, Lixuan</creator><creator>Zhao, Chunfang</creator><creator>Shen, Yongqing</creator><creator>Song, Qingliang</creator><creator>Qu, Yine</creator><creator>Niu, Siyun</creator><creator>Wu, Wenshuang</creator><creator>Gao, Fulu</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>201309</creationdate><title>Effects of moderate exercise over different phases on age-related physiological dysfunction in testes of SAMP8 mice</title><author>Zhao, Xiujun ; 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Different types and moderate-intensity of regular exercise may reduce age-related physiological dysfunction associated with inflammation and oxidative stress, but such effects of moderate-intensity of exercise over different phases of life in testes have not been reported. In this study, male SAMP8 mice, a senescence-accelerated strain, were maintained as sedentary (sed) or subjected to daily 15-min periods of swimming exercise between ages of 2–7months (lifelong), 2–4months (earlier) or 5–7months (late). Age-related changes, including serum testosterone levels and biomarkers of inflammation and oxidative stress were analyzed at the end of the experiment. All exercise groups showed significantly greater serum testosterone levels and decreased age-related inflammation and oxidative stress compared with the sedentary group. Exercise also increased expression and activity of the nuclear factor erythroid 2-related factor (Nrf2), a transcriptional regulator of the cellular anti-oxidant system, and decreased expression and activity of nuclear factor kappa beta (NF-κB), a mediator of inflammatory molecules, in the nucleus of testicular cells. However, lifelong and earlier groups generally showed significantly better protective effects than the late group against age-related physiological dysfunction in testes. Thus, lifelong exercise and earlier phase exercise were most effective in counteracting oxidative stress and inflammation and in preserving testes function through regulation of Nrf2 and NF-κB. These results advocate the benefits of lifelong exercise and emphasize a greater protection against male aging by instituting exercise earlier rather than late in life. •Lifelong or earlier exercise may be more beneficial to counteract testes aging.•The responses of Nrf2 to exercise may lower age-associated oxidative stress.•NF-κB may be involved into exercises counteracting age-related inflammation.</abstract><cop>England</cop><pub>Elsevier Inc</pub><pmid>23751407</pmid><doi>10.1016/j.exger.2013.05.063</doi><tpages>12</tpages></addata></record>
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subjects Aging
Aging, Premature - metabolism
Aging, Premature - physiopathology
Animals
Antioxidants - metabolism
Cyclooxygenase 2 - metabolism
Cytokines - biosynthesis
Exercise
Inflammation
Inflammation Mediators - metabolism
Macrophages - pathology
Male
Mice
Mice, Mutant Strains
NF-E2-Related Factor 2 - biosynthesis
NF-kappa B - metabolism
Orchitis - metabolism
Orchitis - physiopathology
Oxidative stress
Oxidative Stress - physiology
Phosphoproteins - metabolism
Physical Conditioning, Animal
Testis - enzymology
Testis - pathology
Testis - physiopathology
Testosterone
Testosterone - blood
title Effects of moderate exercise over different phases on age-related physiological dysfunction in testes of SAMP8 mice
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