Age-related changes in the glutathione redox system
The effect of aging on the glutathione redox system was evaluated in this study. For this purpose, we determined reduced glutathione (GSH) and oxidized glutathione (GSSG) in whole blood, glutathione peroxidase (GPx) and glutathione reductase (GSSGR) in erythrocytes and selenium (Se) in plasma in 176...
Saved in:
Published in | Cell biochemistry and function Vol. 20; no. 1; pp. 61 - 66 |
---|---|
Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Chichester, UK
John Wiley & Sons, Ltd
01.03.2002
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | The effect of aging on the glutathione redox system was evaluated in this study. For this purpose, we determined reduced glutathione (GSH) and oxidized glutathione (GSSG) in whole blood, glutathione peroxidase (GPx) and glutathione reductase (GSSGR) in erythrocytes and selenium (Se) in plasma in 176 healthy individuals. We also calculated GSH/GSSG molar ratios. These subjects were divided into five groups: group 1 (n = 25; 0.2–1 years old); group 2 (n = 28; 2–11 years old); group 3 (n = 23; 12–24 years old); group 4 (n = 40; 25–40 years old); group 5 (n = 60; 41–69 years old). GSH levels in groups 1 and 5 were significantly lower than the other groups (p< 0.001). Conversely, GSSG levels were significantly high in these periods (p< 0.001). The GSH/GSSG molar ratio was found to be low both in the first year of life and in the oldest group (p< 0.001, respectively). GPx activity in group 5 was increased as compared to the other groups (p< 0.001). GSSGR activity was significantly lower in the oldest groups than in the other groups (p< 0.001). Se levels were found to be low in the oldest group (p< 0.001). Selenium levels of women in group 5 were significantly high as compared to the men (p< 0.01). We found negative correlations between age and GSH levels (r = 0.402; p< 0.001), selenium levels (r = 0.454; p< 0.001), GSH/GSSG molar ratio (r = 0.557; p< 0.001) and GSSGR activity (r = 0.556; p< 0.001). There were positive correlations between age and GPx (r = 0.538; p< 0.001) and GSSG level (r = 0.551; p< 0.001). In conclusion, our findings show that the glutathione redox system is affected by age. Oxidative stress increases during the aging process. There is no effect of aging on the glutathione redox system according to sex except for the Se level. Copyright © 2001 John Wiley & Sons, Ltd. |
---|---|
AbstractList | The effect of aging on the glutathione redox system was evaluated in this study. For this purpose, we determined reduced glutathione (GSH) and oxidized glutathione (GSSG) in whole blood, glutathione peroxidase (GPx) and glutathione reductase (GSSGR) in erythrocytes and selenium (Se) in plasma in 176 healthy individuals. We also calculated GSH/GSSG molar ratios. These subjects were divided into five groups: group 1 (
n
= 25; 0.2–1 years old); group 2 (
n
= 28; 2–11 years old); group 3 (
n
= 23; 12–24 years old); group 4 (
n
= 40; 25–40 years old); group 5 (
n
= 60; 41–69 years old). GSH levels in groups 1 and 5 were significantly lower than the other groups (
p
< 0.001). Conversely, GSSG levels were significantly high in these periods (
p
< 0.001). The GSH/GSSG molar ratio was found to be low both in the first year of life and in the oldest group (
p
< 0.001, respectively). GPx activity in group 5 was increased as compared to the other groups (
p
< 0.001). GSSGR activity was significantly lower in the oldest groups than in the other groups (
p
< 0.001). Se levels were found to be low in the oldest group (
p
< 0.001). Selenium levels of women in group 5 were significantly high as compared to the men (
p
< 0.01). We found negative correlations between age and GSH levels (
r
= 0.402;
p
< 0.001), selenium levels (
r
= 0.454;
p
< 0.001), GSH/GSSG molar ratio (
r
= 0.557;
p
< 0.001) and GSSGR activity (
r
= 0.556;
p
< 0.001). There were positive correlations between age and GPx (
r
= 0.538;
p
< 0.001) and GSSG level (
r
= 0.551;
p
< 0.001). In conclusion, our findings show that the glutathione redox system is affected by age. Oxidative stress increases during the aging process. There is no effect of aging on the glutathione redox system according to sex except for the Se level. Copyright © 2001 John Wiley & Sons, Ltd. The effect of aging on the glutathione redox system was evaluated in this study. For this purpose, we determined reduced glutathione (GSH) and oxidized glutathione (GSSG) in whole blood, glutathione peroxidase (GPx) and glutathione reductase (GSSGR) in erythrocytes and selenium (Se) in plasma in 176 healthy individuals. We also calculated GSH/GSSG molar ratios. These subjects were divided into five groups: group 1 (n=25; 0.2-1 years old); group 2 (n=28; 2-11 years old); group 3 (n=23; 12-24 years old); group 4 (n=40; 25-40 years old); group 5 (n=60; 41-69 years old). GSH levels in groups 1 and 5 were significantly lower than the other groups (p<0.001). Conversely, GSSG levels were significantly high in these periods (p<0.001). The GSH/GSSG molar ratio was found to be low both in the first year of life and in the oldest group (p<0.001, respectively). GPx activity in group 5 was increased as compared to the other groups (p<0.001). GSSGR activity was significantly lower in the oldest groups than in the other groups (p<0.001). Se levels were found to be low in the oldest group (p<0.001). Selenium levels of women in group 5 were significantly high as compared to the men (p<0.01). We found negative correlations between age and GSH levels (r=0.402; p<0.001), selenium levels (r=0.454; p<0.001), GSH/GSSG molar ratio (r=0.557; p<0.001) and GSSGR activity (r=0.556; p<0.001). There were positive correlations between age and GPx (r=0.538; p<0.001) and GSSG level (r=0.551; p<0.001). In conclusion, our findings show that the glutathione redox system is affected by age. Oxidative stress increases during the aging process. There is no effect of aging on the glutathione redox system according to sex except for the Se level.The effect of aging on the glutathione redox system was evaluated in this study. For this purpose, we determined reduced glutathione (GSH) and oxidized glutathione (GSSG) in whole blood, glutathione peroxidase (GPx) and glutathione reductase (GSSGR) in erythrocytes and selenium (Se) in plasma in 176 healthy individuals. We also calculated GSH/GSSG molar ratios. These subjects were divided into five groups: group 1 (n=25; 0.2-1 years old); group 2 (n=28; 2-11 years old); group 3 (n=23; 12-24 years old); group 4 (n=40; 25-40 years old); group 5 (n=60; 41-69 years old). GSH levels in groups 1 and 5 were significantly lower than the other groups (p<0.001). Conversely, GSSG levels were significantly high in these periods (p<0.001). The GSH/GSSG molar ratio was found to be low both in the first year of life and in the oldest group (p<0.001, respectively). GPx activity in group 5 was increased as compared to the other groups (p<0.001). GSSGR activity was significantly lower in the oldest groups than in the other groups (p<0.001). Se levels were found to be low in the oldest group (p<0.001). Selenium levels of women in group 5 were significantly high as compared to the men (p<0.01). We found negative correlations between age and GSH levels (r=0.402; p<0.001), selenium levels (r=0.454; p<0.001), GSH/GSSG molar ratio (r=0.557; p<0.001) and GSSGR activity (r=0.556; p<0.001). There were positive correlations between age and GPx (r=0.538; p<0.001) and GSSG level (r=0.551; p<0.001). In conclusion, our findings show that the glutathione redox system is affected by age. Oxidative stress increases during the aging process. There is no effect of aging on the glutathione redox system according to sex except for the Se level. The effect of aging on the glutathione redox system was evaluated in this study. For this purpose, we determined reduced glutathione (GSH) and oxidized glutathione (GSSG) in whole blood, glutathione peroxidase (GPx) and glutathione reductase (GSSGR) in erythrocytes and selenium (Se) in plasma in 176 healthy individuals. We also calculated GSH/GSSG molar ratios. These subjects were divided into five groups: group 1 (n = 25; 0.2–1 years old); group 2 (n = 28; 2–11 years old); group 3 (n = 23; 12–24 years old); group 4 (n = 40; 25–40 years old); group 5 (n = 60; 41–69 years old). GSH levels in groups 1 and 5 were significantly lower than the other groups (p< 0.001). Conversely, GSSG levels were significantly high in these periods (p< 0.001). The GSH/GSSG molar ratio was found to be low both in the first year of life and in the oldest group (p< 0.001, respectively). GPx activity in group 5 was increased as compared to the other groups (p< 0.001). GSSGR activity was significantly lower in the oldest groups than in the other groups (p< 0.001). Se levels were found to be low in the oldest group (p< 0.001). Selenium levels of women in group 5 were significantly high as compared to the men (p< 0.01). We found negative correlations between age and GSH levels (r = 0.402; p< 0.001), selenium levels (r = 0.454; p< 0.001), GSH/GSSG molar ratio (r = 0.557; p< 0.001) and GSSGR activity (r = 0.556; p< 0.001). There were positive correlations between age and GPx (r = 0.538; p< 0.001) and GSSG level (r = 0.551; p< 0.001). In conclusion, our findings show that the glutathione redox system is affected by age. Oxidative stress increases during the aging process. There is no effect of aging on the glutathione redox system according to sex except for the Se level. Copyright © 2001 John Wiley & Sons, Ltd. The effect of aging on the glutathione redox system was evaluated in this study. For this purpose, we determined reduced glutathione (GSH) and oxidized glutathione (GSSG) in whole blood, glutathione peroxidase (GPx) and glutathione reductase (GSSGR) in erythrocytes and selenium (Se) in plasma in 176 healthy individuals. We also calculated GSH/GSSG molar ratios. These subjects were divided into five groups: group 1 (n=25; 0.2-1 years old); group 2 (n=28; 2-11 years old); group 3 (n=23; 12-24 years old); group 4 (n=40; 25-40 years old); group 5 (n=60; 41-69 years old). GSH levels in groups 1 and 5 were significantly lower than the other groups (p<0.001). Conversely, GSSG levels were significantly high in these periods (p<0.001). The GSH/GSSG molar ratio was found to be low both in the first year of life and in the oldest group (p<0.001, respectively). GPx activity in group 5 was increased as compared to the other groups (p<0.001). GSSGR activity was significantly lower in the oldest groups than in the other groups (p<0.001). Se levels were found to be low in the oldest group (p<0.001). Selenium levels of women in group 5 were significantly high as compared to the men (p<0.01). We found negative correlations between age and GSH levels (r=0.402; p<0.001), selenium levels (r=0.454; p<0.001), GSH/GSSG molar ratio (r=0.557; p<0.001) and GSSGR activity (r=0.556; p<0.001). There were positive correlations between age and GPx (r=0.538; p<0.001) and GSSG level (r=0.551; p<0.001). In conclusion, our findings show that the glutathione redox system is affected by age. Oxidative stress increases during the aging process. There is no effect of aging on the glutathione redox system according to sex except for the Se level. |
Author | Erden-İnal, Mine Kanbak, Güngör Sunal, Emine |
Author_xml | – sequence: 1 givenname: Mine surname: Erden-İnal fullname: Erden-İnal, Mine email: minal@ogu.edu.tr organization: Osmangazi University, The Medical School, Department of Biochemistry Eskişehir, Turkey – sequence: 2 givenname: Emine surname: Sunal fullname: Sunal, Emine organization: Osmangazi University, The Medical School, Department of Biochemistry Eskişehir, Turkey – sequence: 3 givenname: Güngör surname: Kanbak fullname: Kanbak, Güngör organization: Osmangazi University, The Medical School, Department of Biochemistry Eskişehir, Turkey |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/11835271$$D View this record in MEDLINE/PubMed |
BookMark | eNp10M9LwzAUwPEgE_dD8T-QnvQgnUlf2rRHHW4KY6JMPIYkTbZq186kw-2_N7KpKHpKDh_e4327qFXVlUbomOA-wTi6UNL0M2B7qENwloU4pbSFOjhKIExoStuo69wzxjhLAB-gNiEpxBEjHQSXMx1aXYpG54Gai2qmXVBUQTPXwaxcNaKZF35VYHVerwO3cY1eHKJ9I0qnj3ZvDz0Or6eDm3B8N7odXI5DRQljocREyDQHBYQClbkBI6TJSYRxnkYK8thIkwqcEZVJJoDIhBoQ0v9iUBJDD51u5y5t_brSruGLwildlqLS9cpxRmgMzJ_SQyc7uJILnfOlLRbCbvjnmR6cbYGytXNWm2-C-UdA7gNyH9DL8JdUhY_gGzRWFOUf_nzr34pSb_4bywdXwx_TC99x_aWFfeEJAxbzp8mIT9g0SdOHMb-Hd5Mijhs |
CitedBy_id | crossref_primary_10_3390_antiox12081529 crossref_primary_10_1080_13547500600625828 crossref_primary_10_1515_CCLM_2005_131 crossref_primary_10_1292_jvms_17_0623 crossref_primary_10_3390_antiox9070618 crossref_primary_10_1177_1934578X19896676 crossref_primary_10_1016_j_redox_2016_09_010 crossref_primary_10_4236_jbm_2016_45001 crossref_primary_10_3390_antiox13091028 crossref_primary_10_1016_j_expneurol_2004_12_017 crossref_primary_10_1007_s12012_010_9096_5 crossref_primary_10_1016_j_jchromb_2015_12_035 crossref_primary_10_1139_apnm_2012_0219 crossref_primary_10_1152_ajpregu_00254_2005 crossref_primary_10_3174_ajnr_A6543 crossref_primary_10_5551_jat_56531 crossref_primary_10_1080_2314808X_2022_2065438 crossref_primary_10_1017_S0007114511002170 crossref_primary_10_3897_rrpharmacology_8_81358 crossref_primary_10_1080_13510002_2017_1324381 crossref_primary_10_1080_15287394_2010_484709 crossref_primary_10_1089_ars_2013_5728 crossref_primary_10_1016_j_jds_2013_11_002 crossref_primary_10_3389_fpsyt_2022_1035986 crossref_primary_10_1016_S0985_0562_02_00173_5 crossref_primary_10_1093_gerona_63_11_1168 crossref_primary_10_1093_jn_136_6_1694S crossref_primary_10_1089_rej_2011_1166 crossref_primary_10_1100_2012_982594 crossref_primary_10_1007_s12011_009_8346_5 crossref_primary_10_1016_j_archger_2004_04_065 crossref_primary_10_1186_s12014_017_9138_0 crossref_primary_10_3945_ajcn_114_096701 crossref_primary_10_4236_jep_2018_94023 crossref_primary_10_1196_annals_1395_041 crossref_primary_10_1007_s00134_005_2687_0 crossref_primary_10_1016_S0531_5565_02_00175_4 crossref_primary_10_3390_vaccines10111892 crossref_primary_10_3390_metabo14010076 crossref_primary_10_1177_1091581817721675 crossref_primary_10_1016_j_fct_2020_111327 crossref_primary_10_1021_acs_jafc_7b01929 crossref_primary_10_4162_nrp_2011_5_4_357 crossref_primary_10_1097_01_ijg_0000243480_67532_1b crossref_primary_10_1089_rej_2007_0652 crossref_primary_10_1517_17460441_2011_533653 crossref_primary_10_1016_j_mad_2013_02_008 crossref_primary_10_1016_j_clinbiochem_2008_10_026 crossref_primary_10_12968_jowc_2019_28_Sup7_S16 crossref_primary_10_3390_nu12113224 crossref_primary_10_1016_j_biopha_2010_09_010 crossref_primary_10_1038_sj_jhh_1001912 crossref_primary_10_1111_j_2042_7158_2012_01512_x crossref_primary_10_1016_j_exger_2012_06_011 crossref_primary_10_1016_j_exger_2011_11_015 crossref_primary_10_3892_etm_2023_12184 crossref_primary_10_1016_j_anpedi_2009_01_019 crossref_primary_10_1016_j_abb_2016_01_017 crossref_primary_10_1016_j_nut_2005_01_006 crossref_primary_10_1208_s12248_024_00890_1 crossref_primary_10_1007_s11064_012_0775_4 crossref_primary_10_1186_s13099_015_0054_4 crossref_primary_10_1016_j_toxlet_2004_03_009 crossref_primary_10_1098_rstb_2005_1770 crossref_primary_10_1194_jlr_M048223 crossref_primary_10_1371_journal_pone_0161548 crossref_primary_10_3390_biom11050714 crossref_primary_10_3390_brainsci10070437 crossref_primary_10_1002_bmc_954 crossref_primary_10_1155_2011_624156 crossref_primary_10_1016_j_smrv_2022_101616 crossref_primary_10_1007_s10522_022_09987_6 crossref_primary_10_1515_BC_2008_031 crossref_primary_10_3390_antiox9030201 crossref_primary_10_1089_ars_2010_3453 crossref_primary_10_1080_10715760600592962 crossref_primary_10_3390_antiox11051026 crossref_primary_10_1016_S0211_139X_08_71177_6 crossref_primary_10_1067_mlc_2002_129505 crossref_primary_10_2478_v10011_011_0008_4 crossref_primary_10_1089_10945450260195658 crossref_primary_10_1155_2017_6568501 crossref_primary_10_1016_j_freeradbiomed_2013_07_021 crossref_primary_10_1002_aur_2436 crossref_primary_10_1519_JSC_0b013e3181b339ac crossref_primary_10_1111_j_1582_4934_2008_00417_x crossref_primary_10_1016_j_nutres_2012_03_012 crossref_primary_10_3746_jkfn_2002_31_5_834 crossref_primary_10_5432_ijshs_4_515 crossref_primary_10_1177_14746514070070060201 crossref_primary_10_1007_s00394_014_0706_z crossref_primary_10_1016_j_pathophys_2006_05_007 crossref_primary_10_3945_ajcn_110_003483 crossref_primary_10_54005_geneltip_1005716 crossref_primary_10_1016_j_arr_2023_102066 crossref_primary_10_1016_j_redare_2015_07_001 crossref_primary_10_1016_j_jff_2013_12_017 crossref_primary_10_1155_2022_7911222 crossref_primary_10_1515_REVEH_2007_22_2_139 crossref_primary_10_1016_j_clnesp_2017_07_004 crossref_primary_10_1007_s00344_022_10800_4 crossref_primary_10_7314_APJCP_2014_15_18_7603 crossref_primary_10_1080_10715760600895191 crossref_primary_10_1186_s13568_019_0760_2 crossref_primary_10_1007_s12011_010_8840_9 crossref_primary_10_1007_s12035_019_01742_2 crossref_primary_10_1016_j_exger_2024_112593 crossref_primary_10_1016_j_jtemb_2021_126782 crossref_primary_10_1007_s00421_009_1004_y crossref_primary_10_1002_jmri_24970 crossref_primary_10_1007_s00726_003_0025_9 crossref_primary_10_1080_10715760600953859 crossref_primary_10_1179_174329211X13002357050897 crossref_primary_10_1016_j_redar_2015_01_015 crossref_primary_10_1152_japplphysiol_00412_2005 crossref_primary_10_1016_j_freeradbiomed_2013_08_002 crossref_primary_10_1016_j_jchromb_2016_02_015 crossref_primary_10_1016_S1532_0456_03_00151_0 crossref_primary_10_1016_j_biomag_2011_03_001 crossref_primary_10_1016_j_arr_2005_02_005 crossref_primary_10_1016_S1570_0232_03_00061_8 crossref_primary_10_1007_s11920_017_0799_1 crossref_primary_10_1097_FJC_0b013e31824cc31c crossref_primary_10_1016_j_jsbmb_2007_09_010 crossref_primary_10_1155_2016_3286365 crossref_primary_10_3390_nu10121989 crossref_primary_10_3390_antiox9070624 crossref_primary_10_7717_peerj_1055 |
Cites_doi | 10.1096/fasebj.6.9.1612291 10.1016/0305-0491(87)90097-6 10.1016/0047-6374(90)90033-C 10.1152/physrev.1994.74.1.139 10.1016/S0076-6879(55)02291-X 10.1093/geronj/11.3.298 10.1079/BJN19890022 10.1016/0163-7258(90)90073-B 10.1016/0006-2944(84)90026-7 10.1111/j.2042-7158.1987.tb07154.x 10.1016/0047-6374(92)90054-H 10.3177/jnsv.43.497 10.1016/S0009-9120(99)00041-7 10.1126/science.273.5271.59 10.3109/10715769309111598 10.1073/pnas.90.17.7915 10.1620/tjem.165.247 10.4327/jsnfs.44.357 10.1016/S0009-9120(97)00047-7 |
ContentType | Journal Article |
Copyright | Copyright © 2001 John Wiley & Sons, Ltd. Copyright 2001 John Wiley & Sons, Ltd. |
Copyright_xml | – notice: Copyright © 2001 John Wiley & Sons, Ltd. – notice: Copyright 2001 John Wiley & Sons, Ltd. |
DBID | BSCLL AAYXX CITATION CGR CUY CVF ECM EIF NPM 7X8 |
DOI | 10.1002/cbf.937 |
DatabaseName | Istex CrossRef Medline MEDLINE MEDLINE (Ovid) MEDLINE MEDLINE PubMed MEDLINE - Academic |
DatabaseTitle | CrossRef MEDLINE Medline Complete MEDLINE with Full Text PubMed MEDLINE (Ovid) MEDLINE - Academic |
DatabaseTitleList | CrossRef MEDLINE - Academic MEDLINE |
Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database – sequence: 2 dbid: EIF name: MEDLINE url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search sourceTypes: Index Database |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry Biology |
EISSN | 1099-0844 |
EndPage | 66 |
ExternalDocumentID | 11835271 10_1002_cbf_937 CBF937 ark_67375_WNG_N7T688RL_Q |
Genre | article Journal Article Comparative Study |
GroupedDBID | --- .3N .GA .Y3 05W 0R~ 10A 1L6 1OB 1OC 1ZS 29B 31~ 33P 3SF 3WU 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52R 52S 52T 52U 52V 52W 52X 53G 5GY 5VS 66C 6J9 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A01 A03 AAESR AAEVG AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABEML ABIJN ABPVW ABQWH ABXGK ACAHQ ACBWZ ACCFJ ACCZN ACGFO ACGFS ACGOF ACIWK ACMXC ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADBTR ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFFPM AFGKR AFPWT AFRAH AFZJQ AHBTC AIACR AIAGR AITYG AIURR AIWBW AJBDE ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ASPBG ATUGU AVWKF AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BLYAC BMXJE BROTX BRXPI BSCLL BY8 C45 CS3 D-6 D-7 D-E D-F DCZOG DPXWK DR1 DR2 DRFUL DRMAN DRSTM DU5 EBD EBS EJD EMOBN F00 F01 F04 F5P FEDTE FUBAC G-S G.N GNP GODZA H.X HF~ HGLYW HHY HHZ HVGLF HZ~ IX1 J0M JPC KBYEO KQQ LATKE LAW LC2 LC3 LEEKS LH4 LH6 LITHE LOXES LP6 LP7 LUTES LW6 LYRES MEWTI MK4 MRFUL MRMAN MRSTM MSFUL MSMAN MSSTM MXFUL MXMAN MXSTM N04 N05 N9A NDZJH NF~ O66 O9- OIG OVD P2P P2W P2X P2Z P4B P4D PALCI Q.N Q11 QB0 QRW R.K RBB RIWAO RJQFR ROL RWI RX1 RYL SAMSI SUPJJ SV3 TEORI UB1 V2E V8K W8V W99 WBKPD WH7 WIB WIH WIJ WIK WJL WNSPC WOHZO WQJ WRC WSB WXI WXSBR WYISQ XG1 XPP XV2 ZZTAW ~IA ~WT AAHQN AAIPD AAMNL AANHP AAYCA ACRPL ACYXJ ADNMO AFWVQ ALVPJ AAYXX AEYWJ AGHNM AGQPQ AGYGG CITATION CGR CUY CVF ECM EIF NPM 7X8 AAMMB AEFGJ AGXDD AIDQK AIDYY |
ID | FETCH-LOGICAL-c4177-b01ab8d3c31434bdf3fabfd1200d82c3d5fbf8a091c9b7a31b64f3aba3153cb03 |
IEDL.DBID | DR2 |
ISSN | 0263-6484 |
IngestDate | Thu Jul 10 20:52:01 EDT 2025 Wed Feb 19 01:31:12 EST 2025 Tue Jul 01 02:49:04 EDT 2025 Thu Apr 24 23:12:56 EDT 2025 Wed Jan 22 17:04:32 EST 2025 Wed Oct 30 09:54:07 EDT 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 1 |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor Copyright 2001 John Wiley & Sons, Ltd. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c4177-b01ab8d3c31434bdf3fabfd1200d82c3d5fbf8a091c9b7a31b64f3aba3153cb03 |
Notes | ark:/67375/WNG-N7T688RL-Q istex:EBCDF59FCF78C45C85088B38BB1454E302896E0A ArticleID:CBF937 ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
PMID | 11835271 |
PQID | 71453718 |
PQPubID | 23479 |
PageCount | 6 |
ParticipantIDs | proquest_miscellaneous_71453718 pubmed_primary_11835271 crossref_primary_10_1002_cbf_937 crossref_citationtrail_10_1002_cbf_937 wiley_primary_10_1002_cbf_937_CBF937 istex_primary_ark_67375_WNG_N7T688RL_Q |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | March 2002 |
PublicationDateYYYYMMDD | 2002-03-01 |
PublicationDate_xml | – month: 03 year: 2002 text: March 2002 |
PublicationDecade | 2000 |
PublicationPlace | Chichester, UK |
PublicationPlace_xml | – name: Chichester, UK – name: England |
PublicationTitle | Cell biochemistry and function |
PublicationTitleAlternate | Cell Biochem. Funct |
PublicationYear | 2002 |
Publisher | John Wiley & Sons, Ltd |
Publisher_xml | – name: John Wiley & Sons, Ltd |
References | Harris ED. Regulation of antioxidant enzymes. FASEB J 1992; 6: 2675-2683. Yoshida M. Factors associated with variations in blood and urinary selenium concentrations among male employees of companies in Osaka Prefecture. Jpn Soc Nutr Food Sci 1991; 44: 357-363. Alejendro DB, Martha SB, Nestor OB. Superoxide dismutase, catalase and glutathone peroxidase activities in human blood: Influence of sex, age and cigarette smoking. Clin Biochem 1997; 30: 449-453. Gutteridge JMC. Free radicals in disease processes: a compilation of cause and consequence. Free Rad Res Commun 1993; 19: 141-158. Irene CP, Jean MT, Annie T, Pierre MS, Marc T. Age-correlated modifications of copper-zinc superoxide dismutase and glutathione-related enzyme activities in human erythrocytes. Clin Chem 1992; 31: 66-70. Yu BP. Cellular defences against damage from reactive oxygen species. Physiol Rev 1994; 74: 139-162. Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 1967; 70: 158-168. Erden M, Bor NM. Changes of reduced glutahione,glutathione reductase, and glutathione peroxidase after radiation in guinea pigs. Biochem Med 1984; 31: 217-227. Ellman B, Robson MJ, Buttenweiser E. The glutathione instability of drug sensivity red cells. J Lab Clin Med 1957; 49: 84-95. Meister A. New aspects of glutathione biochemistry and transport. Selective alteration of glutathione metabolism. Fed Proc 1984; 43: 3031-3042. Matsubara LS, Machado PEA. Age-related changes of glutathione content, glutathione reductase and glutathione peroxidase activity of human erythrocytes. Brazil J Med Biol Res 1991; 24: 449-459. Farooqui YH, Day WW, Zamarano DM. Glutathione and lipid peroxidation in aging rat. Comp Biochem Physiol 1987; 88: 177-180. Deguchi Y, Ogata A. Relationship between serum selenium concentration and atherogenic index in Japanase adults. Tohoku J Exp Med 1991; 165: 247-251. Ames BN, Shigenaga MK, Hagen T. Oxidant, antioxidants, and degenerative diseases of aging. Proc Natl Acad Sci 1993; 90: 7915-7922. Al-Turk W, Sindey JS, Fatma HER, Sadeg O. Changes in glutathione and its metabolizing enzymes in human erythrocytes and lymphocytes with age. J Pharm Pharmacol 1987; 39: 13-16. Akihiko M, Mieko K, Yoshinori I. Selenium level and glutathione peroxidase activity in plasma, erythrocytes and platelets of healthy Japanase volunteers. J Nutr Sci Vitaminol 1997; 43: 497-504. Portakal O, İnal M. Effects of pentoxyfilline and coenzyme Q10 in hepatic ischemia/reperfusion injury. Clin Biochem 1999; 36: 461-466. Asensi M, Sastre J, Pallardo VF, Estrela MJ, Vina J. Methods in Enzymology vol 234. Academic Press: New York, 1994; 367-371. Harman D. Aging. A theory based on free radical and radiation chemistry. J Gerantol 1956; 11: 298-300. Compbell D, Bunker VW, Thomas AJ. Selenium and vitamin E status of healthy and institutionalized elderly subjects: analysis of plasma,erythrocytes and platelets. Br J Nutr 1989; 62: 221-227. Sohal RS, Weindruch R. Oxidative stress,caloric restriction, and aging. Science 1996; 273: 59-63. Güneral F, Sunguroğlu K. Fluorometric determination of selenium in plasma, erythrocytes and urine. Tr J Med Sci 1995; 23: 151-154. Burk RF. Protection against free radical injury by seleno-enzymes. Pharmac Ther 1990; 45: 383-385. Hall well B, Gutteridge JMC. Free Radicals in Biology and Medicine (2nd edn). Clarendon Press: Oxford, UK, 1989. Sastre J, Joaquin VR, Federico VP, et al. Effect of aging on metabolic zonation in rat liver. Acinar distribution of GSH metabolism. Mech Age Develop 1992; 62: 181-190. Govinda R, Erning X, Arlan R. Effect of age on the expression of antioxidant enzymes in male Fischer F344 rats. Mech Age Develop 1990; 53: 49-60. Masaaki K, Masatoshi S, Nihal SA. Antioxidant systems and erythrocyte life-span in mammals. Comp Biochem Physiol 1993; 106B: 477-487. 1989; 62 1990; 53 1997; 43 1984; 43 1956; 11 1994 1993; 90 1992; 31 1987; 39 1955 1992; 6 1991; 165 1987; 88 1984; 31 1967; 70 1993; 19 1990; 45 1993; 106B 1991; 24 1997; 30 1991; 44 1995; 23 1999; 36 1996; 273 1957; 49 1994; 74 1989 1992; 62 Irene CP (e_1_2_1_25_2) 1992; 31 Paglia DE (e_1_2_1_14_2) 1967; 70 Racker E (e_1_2_1_13_2) 1955 Asensi M (e_1_2_1_12_2) 1994 Meister A (e_1_2_1_24_2) 1984; 43 e_1_2_1_22_2 e_1_2_1_23_2 Hall well B (e_1_2_1_6_2) 1989 Güneral F (e_1_2_1_15_2) 1995; 23 e_1_2_1_26_2 e_1_2_1_27_2 Masaaki K (e_1_2_1_21_2) 1993; 106 e_1_2_1_28_2 e_1_2_1_29_2 Ellman B (e_1_2_1_11_2) 1957; 49 e_1_2_1_7_2 e_1_2_1_4_2 e_1_2_1_5_2 e_1_2_1_2_2 e_1_2_1_3_2 e_1_2_1_10_2 Matsubara LS (e_1_2_1_20_2) 1991; 24 e_1_2_1_16_2 e_1_2_1_19_2 e_1_2_1_8_2 e_1_2_1_17_2 e_1_2_1_9_2 e_1_2_1_18_2 |
References_xml | – reference: Farooqui YH, Day WW, Zamarano DM. Glutathione and lipid peroxidation in aging rat. Comp Biochem Physiol 1987; 88: 177-180. – reference: Paglia DE, Valentine WN. Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase. J Lab Clin Med 1967; 70: 158-168. – reference: Compbell D, Bunker VW, Thomas AJ. Selenium and vitamin E status of healthy and institutionalized elderly subjects: analysis of plasma,erythrocytes and platelets. Br J Nutr 1989; 62: 221-227. – reference: Güneral F, Sunguroğlu K. Fluorometric determination of selenium in plasma, erythrocytes and urine. Tr J Med Sci 1995; 23: 151-154. – reference: Meister A. New aspects of glutathione biochemistry and transport. Selective alteration of glutathione metabolism. Fed Proc 1984; 43: 3031-3042. – reference: Portakal O, İnal M. Effects of pentoxyfilline and coenzyme Q10 in hepatic ischemia/reperfusion injury. Clin Biochem 1999; 36: 461-466. – reference: Asensi M, Sastre J, Pallardo VF, Estrela MJ, Vina J. Methods in Enzymology vol 234. Academic Press: New York, 1994; 367-371. – reference: Hall well B, Gutteridge JMC. Free Radicals in Biology and Medicine (2nd edn). Clarendon Press: Oxford, UK, 1989. – reference: Al-Turk W, Sindey JS, Fatma HER, Sadeg O. Changes in glutathione and its metabolizing enzymes in human erythrocytes and lymphocytes with age. J Pharm Pharmacol 1987; 39: 13-16. – reference: Sastre J, Joaquin VR, Federico VP, et al. Effect of aging on metabolic zonation in rat liver. Acinar distribution of GSH metabolism. Mech Age Develop 1992; 62: 181-190. – reference: Gutteridge JMC. Free radicals in disease processes: a compilation of cause and consequence. Free Rad Res Commun 1993; 19: 141-158. – reference: Alejendro DB, Martha SB, Nestor OB. Superoxide dismutase, catalase and glutathone peroxidase activities in human blood: Influence of sex, age and cigarette smoking. Clin Biochem 1997; 30: 449-453. – reference: Harman D. Aging. A theory based on free radical and radiation chemistry. J Gerantol 1956; 11: 298-300. – reference: Matsubara LS, Machado PEA. Age-related changes of glutathione content, glutathione reductase and glutathione peroxidase activity of human erythrocytes. Brazil J Med Biol Res 1991; 24: 449-459. – reference: Govinda R, Erning X, Arlan R. Effect of age on the expression of antioxidant enzymes in male Fischer F344 rats. Mech Age Develop 1990; 53: 49-60. – reference: Masaaki K, Masatoshi S, Nihal SA. Antioxidant systems and erythrocyte life-span in mammals. Comp Biochem Physiol 1993; 106B: 477-487. – reference: Burk RF. Protection against free radical injury by seleno-enzymes. Pharmac Ther 1990; 45: 383-385. – reference: Yoshida M. Factors associated with variations in blood and urinary selenium concentrations among male employees of companies in Osaka Prefecture. Jpn Soc Nutr Food Sci 1991; 44: 357-363. – reference: Ames BN, Shigenaga MK, Hagen T. Oxidant, antioxidants, and degenerative diseases of aging. Proc Natl Acad Sci 1993; 90: 7915-7922. – reference: Ellman B, Robson MJ, Buttenweiser E. The glutathione instability of drug sensivity red cells. J Lab Clin Med 1957; 49: 84-95. – reference: Sohal RS, Weindruch R. Oxidative stress,caloric restriction, and aging. Science 1996; 273: 59-63. – reference: Irene CP, Jean MT, Annie T, Pierre MS, Marc T. Age-correlated modifications of copper-zinc superoxide dismutase and glutathione-related enzyme activities in human erythrocytes. Clin Chem 1992; 31: 66-70. – reference: Akihiko M, Mieko K, Yoshinori I. Selenium level and glutathione peroxidase activity in plasma, erythrocytes and platelets of healthy Japanase volunteers. J Nutr Sci Vitaminol 1997; 43: 497-504. – reference: Erden M, Bor NM. Changes of reduced glutahione,glutathione reductase, and glutathione peroxidase after radiation in guinea pigs. Biochem Med 1984; 31: 217-227. – reference: Yu BP. Cellular defences against damage from reactive oxygen species. Physiol Rev 1994; 74: 139-162. – reference: Harris ED. Regulation of antioxidant enzymes. FASEB J 1992; 6: 2675-2683. – reference: Deguchi Y, Ogata A. Relationship between serum selenium concentration and atherogenic index in Japanase adults. Tohoku J Exp Med 1991; 165: 247-251. – volume: 31 start-page: 217 year: 1984 end-page: 227 article-title: Changes of reduced glutahione,glutathione reductase, and glutathione peroxidase after radiation in guinea pigs publication-title: Biochem Med – start-page: 367 year: 1994 end-page: 371 – volume: 53 start-page: 49 year: 1990 end-page: 60 article-title: Effect of age on the expression of antioxidant enzymes in male Fischer F344 rats publication-title: Mech Age Develop – year: 1989 – volume: 23 start-page: 151 year: 1995 end-page: 154 article-title: Fluorometric determination of selenium in plasma, erythrocytes and urine publication-title: Tr J Med Sci – volume: 49 start-page: 84 year: 1957 end-page: 95 article-title: The glutathione instability of drug sensivity red cells publication-title: J Lab Clin Med – start-page: 722 year: 1955 end-page: 725 – volume: 19 start-page: 141 year: 1993 end-page: 158 article-title: Free radicals in disease processes: a compilation of cause and consequence publication-title: Free Rad Res Commun – volume: 273 start-page: 59 year: 1996 end-page: 63 article-title: Oxidative stress,caloric restriction, and aging publication-title: Science – volume: 44 start-page: 357 year: 1991 end-page: 363 article-title: Factors associated with variations in blood and urinary selenium concentrations among male employees of companies in Osaka Prefecture publication-title: Jpn Soc Nutr Food Sci – volume: 24 start-page: 449 year: 1991 end-page: 459 article-title: Age‐related changes of glutathione content, glutathione reductase and glutathione peroxidase activity of human erythrocytes publication-title: Brazil J Med Biol Res – volume: 36 start-page: 461 year: 1999 end-page: 466 article-title: Effects of pentoxyfilline and coenzyme Q in hepatic ischemia/reperfusion injury publication-title: Clin Biochem – volume: 11 start-page: 298 year: 1956 end-page: 300 article-title: Aging. A theory based on free radical and radiation chemistry publication-title: J Gerantol – volume: 106B start-page: 477 year: 1993 end-page: 487 article-title: Antioxidant systems and erythrocyte life‐span in mammals publication-title: Comp Biochem Physiol – volume: 45 start-page: 383 year: 1990 end-page: 385 article-title: Protection against free radical injury by seleno‐enzymes publication-title: Pharmac Ther – volume: 74 start-page: 139 year: 1994 end-page: 162 article-title: Cellular defences against damage from reactive oxygen species publication-title: Physiol Rev – volume: 88 start-page: 177 year: 1987 end-page: 180 article-title: Glutathione and lipid peroxidation in aging rat publication-title: Comp Biochem Physiol – volume: 165 start-page: 247 year: 1991 end-page: 251 article-title: Relationship between serum selenium concentration and atherogenic index in Japanase adults publication-title: Tohoku J Exp Med – volume: 62 start-page: 221 year: 1989 end-page: 227 article-title: Selenium and vitamin E status of healthy and institutionalized elderly subjects: analysis of plasma,erythrocytes and platelets publication-title: Br J Nutr – volume: 43 start-page: 497 year: 1997 end-page: 504 article-title: Selenium level and glutathione peroxidase activity in plasma, erythrocytes and platelets of healthy Japanase volunteers publication-title: J Nutr Sci Vitaminol – volume: 70 start-page: 158 year: 1967 end-page: 168 article-title: Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase publication-title: J Lab Clin Med – volume: 39 start-page: 13 year: 1987 end-page: 16 article-title: Changes in glutathione and its metabolizing enzymes in human erythrocytes and lymphocytes with age publication-title: J Pharm Pharmacol – volume: 6 start-page: 2675 year: 1992 end-page: 2683 article-title: Regulation of antioxidant enzymes publication-title: FASEB J – volume: 31 start-page: 66 year: 1992 end-page: 70 article-title: Age‐correlated modifications of copper‐zinc superoxide dismutase and glutathione‐related enzyme activities in human erythrocytes publication-title: Clin Chem – volume: 90 start-page: 7915 year: 1993 end-page: 7922 article-title: Oxidant, antioxidants, and degenerative diseases of aging publication-title: Proc Natl Acad Sci – volume: 62 start-page: 181 year: 1992 end-page: 190 article-title: Effect of aging on metabolic zonation in rat liver. Acinar distribution of GSH metabolism publication-title: Mech Age Develop – volume: 30 start-page: 449 year: 1997 end-page: 453 article-title: Superoxide dismutase, catalase and glutathone peroxidase activities in human blood: Influence of sex, age and cigarette smoking publication-title: Clin Biochem – volume: 43 start-page: 3031 year: 1984 end-page: 3042 article-title: New aspects of glutathione biochemistry and transport. Selective alteration of glutathione metabolism publication-title: Fed Proc – ident: e_1_2_1_9_2 doi: 10.1096/fasebj.6.9.1612291 – volume: 23 start-page: 151 year: 1995 ident: e_1_2_1_15_2 article-title: Fluorometric determination of selenium in plasma, erythrocytes and urine publication-title: Tr J Med Sci – volume: 49 start-page: 84 year: 1957 ident: e_1_2_1_11_2 article-title: The glutathione instability of drug sensivity red cells publication-title: J Lab Clin Med – ident: e_1_2_1_23_2 doi: 10.1016/0305-0491(87)90097-6 – volume-title: Free Radicals in Biology and Medicine year: 1989 ident: e_1_2_1_6_2 – ident: e_1_2_1_17_2 doi: 10.1016/0047-6374(90)90033-C – ident: e_1_2_1_5_2 doi: 10.1152/physrev.1994.74.1.139 – start-page: 367 volume-title: Methods in Enzymology vol 234 year: 1994 ident: e_1_2_1_12_2 – start-page: 722 volume-title: Methods in Enzymology vol. 2. I year: 1955 ident: e_1_2_1_13_2 doi: 10.1016/S0076-6879(55)02291-X – volume: 106 start-page: 477 year: 1993 ident: e_1_2_1_21_2 article-title: Antioxidant systems and erythrocyte life‐span in mammals publication-title: Comp Biochem Physiol – ident: e_1_2_1_2_2 doi: 10.1093/geronj/11.3.298 – ident: e_1_2_1_10_2 doi: 10.1079/BJN19890022 – ident: e_1_2_1_27_2 doi: 10.1016/0163-7258(90)90073-B – ident: e_1_2_1_7_2 doi: 10.1016/0006-2944(84)90026-7 – ident: e_1_2_1_22_2 doi: 10.1111/j.2042-7158.1987.tb07154.x – ident: e_1_2_1_16_2 doi: 10.1016/0047-6374(92)90054-H – ident: e_1_2_1_26_2 doi: 10.3177/jnsv.43.497 – ident: e_1_2_1_8_2 doi: 10.1016/S0009-9120(99)00041-7 – volume: 24 start-page: 449 year: 1991 ident: e_1_2_1_20_2 article-title: Age‐related changes of glutathione content, glutathione reductase and glutathione peroxidase activity of human erythrocytes publication-title: Brazil J Med Biol Res – ident: e_1_2_1_3_2 doi: 10.1126/science.273.5271.59 – volume: 43 start-page: 3031 year: 1984 ident: e_1_2_1_24_2 article-title: New aspects of glutathione biochemistry and transport. Selective alteration of glutathione metabolism publication-title: Fed Proc – ident: e_1_2_1_18_2 doi: 10.3109/10715769309111598 – ident: e_1_2_1_4_2 doi: 10.1073/pnas.90.17.7915 – ident: e_1_2_1_28_2 doi: 10.1620/tjem.165.247 – ident: e_1_2_1_29_2 doi: 10.4327/jsnfs.44.357 – volume: 70 start-page: 158 year: 1967 ident: e_1_2_1_14_2 article-title: Studies on the quantitative and qualitative characterization of erythrocyte glutathione peroxidase publication-title: J Lab Clin Med – ident: e_1_2_1_19_2 doi: 10.1016/S0009-9120(97)00047-7 – volume: 31 start-page: 66 year: 1992 ident: e_1_2_1_25_2 article-title: Age‐correlated modifications of copper‐zinc superoxide dismutase and glutathione‐related enzyme activities in human erythrocytes publication-title: Clin Chem |
SSID | ssj0009630 |
Score | 2.0193202 |
Snippet | The effect of aging on the glutathione redox system was evaluated in this study. For this purpose, we determined reduced glutathione (GSH) and oxidized... |
SourceID | proquest pubmed crossref wiley istex |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 61 |
SubjectTerms | Adolescent Adult Aged aging Aging - blood antioxidant enzymes Antioxidants - metabolism Child Child, Preschool Erythrocytes - enzymology Erythrocytes - metabolism Female glutathione Glutathione - blood Glutathione Peroxidase - metabolism Glutathione Reductase - metabolism Humans Infant Male Middle Aged Oxidation-Reduction Oxidative Stress selenium Selenium - blood |
Title | Age-related changes in the glutathione redox system |
URI | https://api.istex.fr/ark:/67375/WNG-N7T688RL-Q/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcbf.937 https://www.ncbi.nlm.nih.gov/pubmed/11835271 https://www.proquest.com/docview/71453718 |
Volume | 20 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LbxMxEB6hIgQXHuUVnj5UvW0ax3bWeywRoUIQiaoVFRfL40dVFW1Rk0iFEz-B38gvYWxvEspDQpx2pR3vemfGnm-9428AtqJs6Os_rbhTOKokD6pC34TKDQdN8I7HOqf8v52O9g7l6yN19FOpr8IPsVpwSyMjz9dpgFuc7axJQx3GPsVWmn1TplaCQ_tr4ihyq251RVQjqWXZLpta7nTtLsWhq0mlF38CmZcxaw46k1vwYdndkmty2l_Mse--_MLk-F_vcxtudlCU7RbfuQNXQrsJ10pxys-bcH28rAV3F9Tucfj-9Vve-BI8K7uFZ-ykZYQf2TF5b0piPGsDS_yjF6zwQ9-Dw8nLg_Fe1RVcqJzkdV3hgFvUXjhBKEqijyJajJ7TSPJ66IRXEaO2BDFcg7UVHEcyCot0poTDgbgPGy096yEw6a12IWplPUq0JOPiQKPSdMPQRN6D7aX6jevYyFNRjI-m8CgPDenDkD56wFaCnwoBx-8i29l-q-v2_DTlq9XKvJ--MtP6YKT1_hvzrgfPlwY2pMD0a8S24WwxMzWXSlCY7sGDYvf1s3jCqDV1eCtb72-dMOMXEzo8-jexx3Ajl5XJyWxPYGN-vghPCd3M8Vl25B-F4fee |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1LbxMxEB5BK9ReeBQogUJ9qHrbNI7trPdYooYAaSSqVFTiYPlZoVbbqk2kwomfwG_klzC2N4nKQ0KcdqUd73pnxjvj2ZlvAHYCr3D3HyPuaI4KTr0ojKt8YbudyjtLQ5lS_g_HveExf3ciTpqsylgLk_EhFgG3uDLS9zou8BiQ3luihloT2mhc78Jq7OedtlNHS-goVKwmvsKKHpc8F8zGoXvNwFuWaDUy9eZPbuZtrzWZncED-DSfcM42OWvPpqZtv_6C5fh_b_QQ7jfeKNnP6vMI7vh6A-7l_pRfNmCtP28H9xjE_qn_8e17qn3xjuSC4WvyuSboQpJTVOCYx3hRexIhSG9Ihoh-AseDg0l_WDQ9FwrLaVkWpkO1kY5Zho4UNy6woE1wFBeTk13LnAgmSI1ehq1MqRk1PR6YNngmmDUd9hRWanzWMyDcaWl9kEI7w41GGhs60giJN_RVoC3YnfNf2QaQPPbFOFcZSrmrkB8K-dECsiC8zBgcv5PsJgEuruurs5iyVgr1cfxGjctJT8qjkfrQgu25hBUyMP4d0bW_mF2rknLB0FK3YDMLfvksGt3UEie8k8T3t0mo_usBHp7_G9k2rA0nhyM1ejt-_wLWU5eZlNu2BSvTq5l_ic7O1LxKWv0T75r7uQ |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Lb9QwEB5BKx4XHuW1vOpD1Vu28dpOnGPZshQoK6haUXGx_KxQUVq1u1LhxE_gN_JLGNvZXcpDQpwSKePYmRlnvjjjbwDWAm_w6z-uuGM4Kjj1ojCu8YUdlI13loY6pfy_GVfb-_zVgTj4qdRX5oeYL7jFmZHe13GCn7iwsSANtSb0MbZehmVelTI69NbugjkK_apbXmFFxSXP-2Vj042u4YVAtBx1ev4nlHkRtKaoM7oJH2bjzckmR_3pxPTtl1-oHP_rgW7BjQ6Lks3sPLfhkm9X4EquTvl5Ba4NZ8Xg7oDYPPTfv35LO1-8I3m78Bn52BIEkOQQ3TdmMR63nkQC0nOSCaLvwv7o-d5wu-gqLhSW07ouTEm1kY5ZhjCKGxdY0CY4ilPJyYFlTgQTpEaMYRtTa0ZNxQPTBs8Es6Zk92Cpxb4eAOFOS-uDFNoZbjTK2FBKIyTe0DeB9mB9pn5lOzryWBXjk8pEygOF-lCojx6QueBJZuD4XWQ92W9-XZ8exYS1Wqj34xdqXO9VUu7uqHc9WJ0ZWKEC478R3frj6ZmqKRcM43QP7me7L_qiEaTWOOC1ZL2_DUINn43w8PDfxFbh6tutkdp5OX79CK6nEjMpse0xLE1Op_4JIp2JeZp8-gcnBvpx |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Age-related+changes+in+the+glutathione+redox+system&rft.jtitle=Cell+biochemistry+and+function&rft.au=Erden-%C4%B0nal%2C+Mine&rft.au=Sunal%2C+Emine&rft.au=Kanbak%2C+G%C3%BCng%C3%B6r&rft.date=2002-03-01&rft.pub=John+Wiley+%26+Sons%2C+Ltd&rft.issn=0263-6484&rft.eissn=1099-0844&rft.volume=20&rft.issue=1&rft.spage=61&rft.epage=66&rft_id=info:doi/10.1002%2Fcbf.937&rft.externalDBID=n%2Fa&rft.externalDocID=ark_67375_WNG_N7T688RL_Q |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0263-6484&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0263-6484&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0263-6484&client=summon |