Arsenic Exposure and Glucose Intolerance/Insulin Resistance in Estrogen-Deficient Female Mice

Epidemiological studies have reported that the prevalence of diabetes in women > 40 years of age, especially those in the postmenopausal phase, was higher than in men in areas with high levels of arsenic in drinking water. The detailed effect of arsenic on glucose metabolism/homeostasis in the po...

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Published inEnvironmental health perspectives Vol. 123; no. 11; pp. 1138 - 1144
Main Authors Huang, Chun-Fa, Yang, Ching-Yao, Chan, Ding-Cheng, Wang, Ching-Chia, Huang, Kuo-How, Wu, Chin-Ching, Tsai, Keh-Sung, Yang, Rong-Sen, Liu, Shing-Hwa
Format Journal Article
LanguageEnglish
Published United States National Institute of Environmental Health Sciences 01.11.2015
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Abstract Epidemiological studies have reported that the prevalence of diabetes in women > 40 years of age, especially those in the postmenopausal phase, was higher than in men in areas with high levels of arsenic in drinking water. The detailed effect of arsenic on glucose metabolism/homeostasis in the postmenopausal condition is still unclear. We investigated the effects of arsenic at doses relevant to human exposure from drinking water on blood glucose regulation in estrogen-deficient female mice. Adult female mice who underwent ovariectomy or sham surgery were exposed to drinking water contaminated with arsenic trioxide (0.05 or 0.5 ppm) in the presence or absence of 17β-estradiol supplementation for 2-6 weeks. Assays related to glucose metabolism were performed. Exposure of sham mice to arsenic significantly increased blood glucose, decreased plasma insulin, and impaired glucose tolerance, but did not induce insulin resistance. Blood glucose and insulin were higher, and glucose intolerance, insulin intolerance, and insulin resistance were increased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Furthermore, liver phosphoenolpyruvate carboxykinase (PEPCK) mRNA expression was increased and liver glycogen content was decreased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Glucose-stimulated insulin secretion in islets isolated from arsenic-treated ovariectomized mice was also significantly decreased. Arsenic treatment significantly decreased plasma adiponectin levels in sham and ovariectomized mice. Altered glucose metabolism/homeostasis in arsenic-treated ovariectomized mice was reversed by 17β-estradiol supplementation. Our findings suggest that estrogen deficiency plays an important role in arsenic-altered glucose metabolism/homeostasis in females. Huang CF, Yang CY, Chan DC, Wang CC, Huang KH, Wu CC, Tsai KS, Yang RS, Liu SH. 2015. Arsenic exposure and glucose intolerance/insulin resistance in estrogen-deficient female mice. Environ Health Perspect 123:1138-1144; http://dx.doi.org/10.1289/ehp.1408663.
AbstractList BACKGROUND: Epidemiological studies have reported that the prevalence of diabetes in women > 40 years of age, especially those in the postmenopausal phase, was higher than in men in areas with high levels of arsenic in drinking water. The detailed effect of arsenic on glucose metabolism/ homeostasis in the postmenopausal condition is still unclear. OBJECTIVES: We investigated the effects of arsenic at doses relevant to human exposure from drinking water on blood glucose regulation in estrogen-deficient female mice. METHODS: Adult female mice who underwent ovariectomy or sham surgery were exposed to drinking water contaminated with arsenic trioxide (0.05 or 0.5 ppm) in the presence or absence of 17β-estradiol supplementation for 2-6 weeks. Assays related to glucose metabolism were performed. RESULTS: Exposure of sham mice to arsenic significantly increased blood glucose, decreased plasma insulin, and impaired glucose tolerance, but did not induce insulin resistance. Blood glucose and insulin were higher, and glucose intolerance, insulin intolerance, and insulin resistance were increased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Furthermore, liver phosphoenolpyruvate carboxykinase (PEPCK) mRNA expression was increased and liver glycogen content was decreased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Glucose-stimulated insulin secretion in islets isolated from arsenic-treated ovariectomized mice was also significantly decreased. Arsenic treatment significantly decreased plasma adiponectin levels in sham and ovariectomized mice. Altered glucose metabolism/ homeostasis in arsenic-treated ovariectomized mice was reversed by 17β-estradiol supplementation. CONCLUSIONS: Our findings suggest that estrogen deficiency plays an important role in arsenicaltered glucose metabolism/homeostasis in females.
Epidemiological studies have reported that the prevalence of diabetes in women > 40 years of age, especially those in the postmenopausal phase, was higher than in men in areas with high levels of arsenic in drinking water. The detailed effect of arsenic on glucose metabolism/homeostasis in the postmenopausal condition is still unclear. We investigated the effects of arsenic at doses relevant to human exposure from drinking water on blood glucose regulation in estrogen-deficient female mice. Adult female mice who underwent ovariectomy or sham surgery were exposed to drinking water contaminated with arsenic trioxide (0.05 or 0.5 ppm) in the presence or absence of 17β-estradiol supplementation for 2-6 weeks. Assays related to glucose metabolism were performed. Exposure of sham mice to arsenic significantly increased blood glucose, decreased plasma insulin, and impaired glucose tolerance, but did not induce insulin resistance. Blood glucose and insulin were higher, and glucose intolerance, insulin intolerance, and insulin resistance were increased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Furthermore, liver phosphoenolpyruvate carboxykinase (PEPCK) mRNA expression was increased and liver glycogen content was decreased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Glucose-stimulated insulin secretion in islets isolated from arsenic-treated ovariectomized mice was also significantly decreased. Arsenic treatment significantly decreased plasma adiponectin levels in sham and ovariectomized mice. Altered glucose metabolism/homeostasis in arsenic-treated ovariectomized mice was reversed by 17β-estradiol supplementation. Our findings suggest that estrogen deficiency plays an important role in arsenic-altered glucose metabolism/homeostasis in females. Huang CF, Yang CY, Chan DC, Wang CC, Huang KH, Wu CC, Tsai KS, Yang RS, Liu SH. 2015. Arsenic exposure and glucose intolerance/insulin resistance in estrogen-deficient female mice. Environ Health Perspect 123:1138-1144; http://dx.doi.org/10.1289/ehp.1408663.
Epidemiological studies have reported that the prevalence of diabetes in women > 40 years of age, especially those in the postmenopausal phase, was higher than in men in areas with high levels of arsenic in drinking water. The detailed effect of arsenic on glucose metabolism/homeostasis in the postmenopausal condition is still unclear.BACKGROUNDEpidemiological studies have reported that the prevalence of diabetes in women > 40 years of age, especially those in the postmenopausal phase, was higher than in men in areas with high levels of arsenic in drinking water. The detailed effect of arsenic on glucose metabolism/homeostasis in the postmenopausal condition is still unclear.We investigated the effects of arsenic at doses relevant to human exposure from drinking water on blood glucose regulation in estrogen-deficient female mice.OBJECTIVESWe investigated the effects of arsenic at doses relevant to human exposure from drinking water on blood glucose regulation in estrogen-deficient female mice.Adult female mice who underwent ovariectomy or sham surgery were exposed to drinking water contaminated with arsenic trioxide (0.05 or 0.5 ppm) in the presence or absence of 17β-estradiol supplementation for 2-6 weeks. Assays related to glucose metabolism were performed.METHODSAdult female mice who underwent ovariectomy or sham surgery were exposed to drinking water contaminated with arsenic trioxide (0.05 or 0.5 ppm) in the presence or absence of 17β-estradiol supplementation for 2-6 weeks. Assays related to glucose metabolism were performed.Exposure of sham mice to arsenic significantly increased blood glucose, decreased plasma insulin, and impaired glucose tolerance, but did not induce insulin resistance. Blood glucose and insulin were higher, and glucose intolerance, insulin intolerance, and insulin resistance were increased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Furthermore, liver phosphoenolpyruvate carboxykinase (PEPCK) mRNA expression was increased and liver glycogen content was decreased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Glucose-stimulated insulin secretion in islets isolated from arsenic-treated ovariectomized mice was also significantly decreased. Arsenic treatment significantly decreased plasma adiponectin levels in sham and ovariectomized mice. Altered glucose metabolism/homeostasis in arsenic-treated ovariectomized mice was reversed by 17β-estradiol supplementation.RESULTSExposure of sham mice to arsenic significantly increased blood glucose, decreased plasma insulin, and impaired glucose tolerance, but did not induce insulin resistance. Blood glucose and insulin were higher, and glucose intolerance, insulin intolerance, and insulin resistance were increased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Furthermore, liver phosphoenolpyruvate carboxykinase (PEPCK) mRNA expression was increased and liver glycogen content was decreased in arsenic-treated ovariectomized mice compared with arsenic-treated sham mice. Glucose-stimulated insulin secretion in islets isolated from arsenic-treated ovariectomized mice was also significantly decreased. Arsenic treatment significantly decreased plasma adiponectin levels in sham and ovariectomized mice. Altered glucose metabolism/homeostasis in arsenic-treated ovariectomized mice was reversed by 17β-estradiol supplementation.Our findings suggest that estrogen deficiency plays an important role in arsenic-altered glucose metabolism/homeostasis in females.CONCLUSIONSOur findings suggest that estrogen deficiency plays an important role in arsenic-altered glucose metabolism/homeostasis in females.Huang CF, Yang CY, Chan DC, Wang CC, Huang KH, Wu CC, Tsai KS, Yang RS, Liu SH. 2015. Arsenic exposure and glucose intolerance/insulin resistance in estrogen-deficient female mice. Environ Health Perspect 123:1138-1144; http://dx.doi.org/10.1289/ehp.1408663.CITATIONHuang CF, Yang CY, Chan DC, Wang CC, Huang KH, Wu CC, Tsai KS, Yang RS, Liu SH. 2015. Arsenic exposure and glucose intolerance/insulin resistance in estrogen-deficient female mice. Environ Health Perspect 123:1138-1144; http://dx.doi.org/10.1289/ehp.1408663.
Audience Academic
Author Huang, Chun-Fa
Wang, Ching-Chia
Wu, Chin-Ching
Chan, Ding-Cheng
Tsai, Keh-Sung
Liu, Shing-Hwa
Yang, Rong-Sen
Yang, Ching-Yao
Huang, Kuo-How
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  surname: Huang
  fullname: Huang, Chun-Fa
  organization: School of Chinese Medicine, College of Chinese Medicine, China Medical University, Taichung, Taiwan
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  givenname: Ching-Yao
  surname: Yang
  fullname: Yang, Ching-Yao
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  surname: Chan
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  givenname: Ching-Chia
  surname: Wang
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  organization: Department of Pediatrics, and
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  givenname: Kuo-How
  surname: Huang
  fullname: Huang, Kuo-How
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  givenname: Chin-Ching
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  surname: Liu
  fullname: Liu, Shing-Hwa
  organization: Department of Pediatrics, and, Department of Medical Research, China Medical University Hospital, China Medical University, Taichung, Taiwan, Institute of Toxicology, College of Medicine, National Taiwan University, Taipei, Taiwan
BackLink https://www.ncbi.nlm.nih.gov/pubmed/25859628$$D View this record in MEDLINE/PubMed
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Cites_doi 10.1093/toxsci/kfn172
10.1242/dmm.006239
10.1097/01.jom.0000184854.75053.03
10.1016/S0378-4274(02)00085-1
10.2337/diabetes.52.6.1333
10.1172/JCI29126
10.1001/jama.2009.976
10.1530/JOE-11-0044
10.1258/la.2008.007075
10.2113/gselements.2.2.77
10.1093/aje/kws153
10.3181/00379727-104-25975
10.1016/j.envres.2013.02.005
10.1093/oxfordjournals.aje.a117031
10.1016/j.yfrne.2013.08.001
10.1093/aje/kws329
10.1289/ehp.8551
10.1289/ehp.98106s41005
10.2337/db06-0029
10.1093/oxfordjournals.aje.a009624
10.1007/s00125-007-0785-y
10.1073/pnas.0602956103
10.4103/0976-500X.72350
10.1016/j.bbrc.2010.09.018
10.1289/ehp.0901608
10.2337/diabetes.54.7.1942
10.1016/j.taap.2012.12.007
10.1016/j.envres.2007.08.011
10.1016/j.freeradbiomed.2014.06.012
10.1016/S0021-9258(18)31478-9
10.1021/es00054a019
10.1385/ENDO:30:2:217
10.1007/BF00798356
10.1016/0378-8741(88)90229-2
10.1001/jama.300.7.814
10.1289/ehp.9058
10.2337/diabetes.55.02.06.db05-0686
10.1258/1362180053654475
10.1289/ehp.1003324
10.1136/jech-2013-203114
10.2337/db12-0585
10.1172/JCI117823
10.1007/s00125-009-1456-y
10.1289/ehp.1104579
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References e_1_3_2_28_1
e_1_3_2_49_1
e_1_3_2_20_1
e_1_3_2_41_1
e_1_3_2_22_1
e_1_3_2_43_1
e_1_3_2_24_1
e_1_3_2_45_1
e_1_3_2_26_1
e_1_3_2_47_1
Shirasaki Y (e_1_3_2_48_1) 2012; 51
Friedman JE (e_1_3_2_19_1) 1993; 268
e_1_3_2_16_1
e_1_3_2_39_1
e_1_3_2_9_1
e_1_3_2_18_1
e_1_3_2_7_1
e_1_3_2_31_1
e_1_3_2_10_1
e_1_3_2_33_1
e_1_3_2_12_1
e_1_3_2_5_1
e_1_3_2_14_1
e_1_3_2_37_1
e_1_3_2_3_1
e_1_3_2_50_1
e_1_3_2_27_1
e_1_3_2_29_1
e_1_3_2_42_1
e_1_3_2_21_1
e_1_3_2_44_1
e_1_3_2_23_1
e_1_3_2_46_1
e_1_3_2_25_1
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Mahram M (e_1_3_2_35_1) 2013; 18
17900557 - Environ Res. 2008 Jan;106(1):110-20
7685354 - J Biol Chem. 1993 Jun 15;268(17):12952-7
18714061 - JAMA. 2008 Aug 20;300(7):814-22
22191829 - Environ Sci Technol. 1994 May 1;28(5):877-81
19584347 - JAMA. 2009 Jul 8;302(2):179-88
17107869 - Environ Health Perspect. 2006 Nov;114(11):1790-6
23504692 - Am J Epidemiol. 2013 May 1;177(9):962-9
9676702 - Am J Epidemiol. 1998 Jul 15;148(2):198-203
16404211 - J Occup Environ Med. 2006 Jan;48(1):63-7
16823476 - J Clin Invest. 2006 Jul;116(7):1784-92
23261974 - Toxicol Appl Pharmacol. 2013 Feb 15;267(1):11-5
23069626 - Diabetes. 2013 Feb;62(2):628-38
23097256 - Am J Epidemiol. 2012 Nov 15;176(10):865-74
19629429 - Diabetologia. 2009 Oct;52(10):2092-100
24174947 - J Res Med Sci. 2013 May;18(5):408-12
15814056 - J Br Menopause Soc. 2005 Mar;11(1):6-11
12076511 - Toxicol Lett. 2002 Jul 7;133(1):69-76
24133074 - J Epidemiol Community Health. 2014 Feb;68(2):176-84
12765941 - Diabetes. 2003 Jun;52(6):1333-9
16731823 - Diabetes. 2006 Jun;55(6):1614-24
24960579 - Free Radic Biol Med. 2014 Sep;74:64-73
15983193 - Diabetes. 2005 Jul;54(7):1942-8
21592922 - Environ Health Perspect. 2011 Aug;119(8):1104-9
17701157 - Diabetologia. 2007 Oct;50(10):2076-84
22776193 - J Am Assoc Lab Anim Sci. 2012 May;51(3):345-51
9703486 - Environ Health Perspect. 1998 Aug;106 Suppl 4:1005-15
8154472 - Am J Epidemiol. 1994 Mar 1;139(5):484-92
21511884 - J Endocrinol. 2012 Jan;212(1):3-12
17322583 - Endocrine. 2006 Oct;30(2):217-21
20713647 - Dis Model Mech. 2010 Sep-Oct;3(9-10):525-34
16675414 - Environ Health Perspect. 2006 May;114(5):641-8
20833131 - Biochem Biophys Res Commun. 2010 Oct 8;401(1):104-11
16443772 - Diabetes. 2006 Feb;55(2):390-7
18713764 - Toxicol Sci. 2008 Nov;106(1):1-4
16754860 - Proc Natl Acad Sci U S A. 2006 Jun 13;103(24):9232-7
13741689 - Proc Soc Exp Biol Med. 1960 Aug-Sep;104:751-4
21350616 - J Pharmacol Pharmacother. 2010 Jul;1(2):87-93
23507312 - Environ Res. 2013 May;123:33-8
19001062 - Lab Anim. 2009 Jan;43(1):65-71
22889723 - Environ Health Perspect. 2012 Dec;120(12):1658-70
20100676 - Environ Health Perspect. 2010 Jun;118(6):864-70
23994581 - Front Neuroendocrinol. 2014 Jan;35(1):8-30
7706456 - J Clin Invest. 1995 Apr;95(4):1512-8
3352284 - J Ethnopharmacol. 1988 Jan;22(1):45-9
References_xml – ident: e_1_3_2_38_1
  doi: 10.1093/toxsci/kfn172
– ident: e_1_3_2_7_1
  doi: 10.1242/dmm.006239
– ident: e_1_3_2_12_1
  doi: 10.1097/01.jom.0000184854.75053.03
– ident: e_1_3_2_49_1
  doi: 10.1016/S0378-4274(02)00085-1
– ident: e_1_3_2_3_1
  doi: 10.2337/diabetes.52.6.1333
– ident: e_1_3_2_28_1
  doi: 10.1172/JCI29126
– ident: e_1_3_2_33_1
  doi: 10.1001/jama.2009.976
– ident: e_1_3_2_18_1
  doi: 10.1530/JOE-11-0044
– ident: e_1_3_2_13_1
  doi: 10.1258/la.2008.007075
– ident: e_1_3_2_42_1
  doi: 10.2113/gselements.2.2.77
– ident: e_1_3_2_22_1
  doi: 10.1093/aje/kws153
– ident: e_1_3_2_47_1
  doi: 10.3181/00379727-104-25975
– ident: e_1_3_2_27_1
  doi: 10.1016/j.envres.2013.02.005
– ident: e_1_3_2_31_1
  doi: 10.1093/oxfordjournals.aje.a117031
– ident: e_1_3_2_46_1
  doi: 10.1016/j.yfrne.2013.08.001
– ident: e_1_3_2_30_1
  doi: 10.1093/aje/kws329
– ident: e_1_3_2_9_1
– ident: e_1_3_2_40_1
  doi: 10.1289/ehp.8551
– ident: e_1_3_2_24_1
  doi: 10.1289/ehp.98106s41005
– ident: e_1_3_2_11_1
  doi: 10.2337/db06-0029
– ident: e_1_3_2_45_1
  doi: 10.1093/oxfordjournals.aje.a009624
– ident: e_1_3_2_15_1
  doi: 10.1007/s00125-007-0785-y
– ident: e_1_3_2_32_1
  doi: 10.1073/pnas.0602956103
– ident: e_1_3_2_43_1
  doi: 10.4103/0976-500X.72350
– ident: e_1_3_2_2_1
  doi: 10.1016/j.bbrc.2010.09.018
– ident: e_1_3_2_20_1
  doi: 10.1289/ehp.0901608
– ident: e_1_3_2_8_1
  doi: 10.2337/diabetes.54.7.1942
– ident: e_1_3_2_16_1
  doi: 10.1016/j.taap.2012.12.007
– ident: e_1_3_2_34_1
  doi: 10.1016/j.envres.2007.08.011
– ident: e_1_3_2_17_1
– volume: 18
  start-page: 408
  issue: 5
  year: 2013
  ident: e_1_3_2_35_1
  article-title: Comparison of hypertension and diabetes mellitus prevalence in areas with and without water arsenic contamination.
  publication-title: J Res Med Sci
– ident: e_1_3_2_5_1
  doi: 10.1016/j.freeradbiomed.2014.06.012
– volume: 268
  start-page: 12952
  year: 1993
  ident: e_1_3_2_19_1
  article-title: Glucocorticoids regulate the induction of phosphoenolpyruvate carboxykinase (GTP) gene transcription during diabetes.
  publication-title: J Biol Chem
  doi: 10.1016/S0021-9258(18)31478-9
– ident: e_1_3_2_41_1
– ident: e_1_3_2_10_1
  doi: 10.1021/es00054a019
– ident: e_1_3_2_23_1
  doi: 10.1385/ENDO:30:2:217
– ident: e_1_3_2_36_1
  doi: 10.1007/BF00798356
– ident: e_1_3_2_4_1
  doi: 10.1016/0378-8741(88)90229-2
– ident: e_1_3_2_39_1
  doi: 10.1001/jama.300.7.814
– ident: e_1_3_2_26_1
  doi: 10.1289/ehp.9058
– ident: e_1_3_2_6_1
  doi: 10.2337/diabetes.55.02.06.db05-0686
– ident: e_1_3_2_29_1
  doi: 10.1258/1362180053654475
– ident: e_1_3_2_44_1
  doi: 10.1289/ehp.1003324
– ident: e_1_3_2_50_1
  doi: 10.1136/jech-2013-203114
– volume: 51
  start-page: 345
  issue: 3
  year: 2012
  ident: e_1_3_2_48_1
  article-title: Validation studies on blood collection from the jugular vein of conscious mice.
  publication-title: J Am Assoc Lab Anim Sci
– ident: e_1_3_2_51_1
– ident: e_1_3_2_25_1
  doi: 10.2337/db12-0585
– ident: e_1_3_2_21_1
  doi: 10.1172/JCI117823
– ident: e_1_3_2_14_1
  doi: 10.1007/s00125-009-1456-y
– ident: e_1_3_2_37_1
  doi: 10.1289/ehp.1104579
– reference: 23504692 - Am J Epidemiol. 2013 May 1;177(9):962-9
– reference: 17900557 - Environ Res. 2008 Jan;106(1):110-20
– reference: 12076511 - Toxicol Lett. 2002 Jul 7;133(1):69-76
– reference: 19629429 - Diabetologia. 2009 Oct;52(10):2092-100
– reference: 15814056 - J Br Menopause Soc. 2005 Mar;11(1):6-11
– reference: 15983193 - Diabetes. 2005 Jul;54(7):1942-8
– reference: 23994581 - Front Neuroendocrinol. 2014 Jan;35(1):8-30
– reference: 20100676 - Environ Health Perspect. 2010 Jun;118(6):864-70
– reference: 17701157 - Diabetologia. 2007 Oct;50(10):2076-84
– reference: 22776193 - J Am Assoc Lab Anim Sci. 2012 May;51(3):345-51
– reference: 20713647 - Dis Model Mech. 2010 Sep-Oct;3(9-10):525-34
– reference: 23507312 - Environ Res. 2013 May;123:33-8
– reference: 16675414 - Environ Health Perspect. 2006 May;114(5):641-8
– reference: 3352284 - J Ethnopharmacol. 1988 Jan;22(1):45-9
– reference: 24960579 - Free Radic Biol Med. 2014 Sep;74:64-73
– reference: 23261974 - Toxicol Appl Pharmacol. 2013 Feb 15;267(1):11-5
– reference: 9676702 - Am J Epidemiol. 1998 Jul 15;148(2):198-203
– reference: 23069626 - Diabetes. 2013 Feb;62(2):628-38
– reference: 20833131 - Biochem Biophys Res Commun. 2010 Oct 8;401(1):104-11
– reference: 18713764 - Toxicol Sci. 2008 Nov;106(1):1-4
– reference: 21592922 - Environ Health Perspect. 2011 Aug;119(8):1104-9
– reference: 24133074 - J Epidemiol Community Health. 2014 Feb;68(2):176-84
– reference: 16823476 - J Clin Invest. 2006 Jul;116(7):1784-92
– reference: 17322583 - Endocrine. 2006 Oct;30(2):217-21
– reference: 16731823 - Diabetes. 2006 Jun;55(6):1614-24
– reference: 9703486 - Environ Health Perspect. 1998 Aug;106 Suppl 4:1005-15
– reference: 22889723 - Environ Health Perspect. 2012 Dec;120(12):1658-70
– reference: 17107869 - Environ Health Perspect. 2006 Nov;114(11):1790-6
– reference: 16443772 - Diabetes. 2006 Feb;55(2):390-7
– reference: 22191829 - Environ Sci Technol. 1994 May 1;28(5):877-81
– reference: 19001062 - Lab Anim. 2009 Jan;43(1):65-71
– reference: 7706456 - J Clin Invest. 1995 Apr;95(4):1512-8
– reference: 19584347 - JAMA. 2009 Jul 8;302(2):179-88
– reference: 8154472 - Am J Epidemiol. 1994 Mar 1;139(5):484-92
– reference: 24174947 - J Res Med Sci. 2013 May;18(5):408-12
– reference: 12765941 - Diabetes. 2003 Jun;52(6):1333-9
– reference: 18714061 - JAMA. 2008 Aug 20;300(7):814-22
– reference: 7685354 - J Biol Chem. 1993 Jun 15;268(17):12952-7
– reference: 21511884 - J Endocrinol. 2012 Jan;212(1):3-12
– reference: 21350616 - J Pharmacol Pharmacother. 2010 Jul;1(2):87-93
– reference: 16404211 - J Occup Environ Med. 2006 Jan;48(1):63-7
– reference: 13741689 - Proc Soc Exp Biol Med. 1960 Aug-Sep;104:751-4
– reference: 23097256 - Am J Epidemiol. 2012 Nov 15;176(10):865-74
– reference: 16754860 - Proc Natl Acad Sci U S A. 2006 Jun 13;103(24):9232-7
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Snippet Epidemiological studies have reported that the prevalence of diabetes in women > 40 years of age, especially those in the postmenopausal phase, was higher than...
BACKGROUND: Epidemiological studies have reported that the prevalence of diabetes in women > 40 years of age, especially those in the postmenopausal phase, was...
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SubjectTerms Adiponectin - blood
Animals
Arsenic
Arsenic - toxicity
Blood Glucose - drug effects
Estradiol - pharmacology
Estrogen
Estrogens - deficiency
Female
Glucose intolerance
Glucose Intolerance - chemically induced
Health aspects
Insulin - blood
Insulin Resistance
Liver - metabolism
Mice
Ovariectomy
Physiological aspects
Title Arsenic Exposure and Glucose Intolerance/Insulin Resistance in Estrogen-Deficient Female Mice
URI https://www.ncbi.nlm.nih.gov/pubmed/25859628
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https://pubmed.ncbi.nlm.nih.gov/PMC4629734
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