Skip to main content
Top
Published in: Environmental Health and Preventive Medicine 1/2021

Open Access 01-12-2021 | Research article

Effects of maternal exposure to arsenic on social behavior and related gene expression in F2 male mice

Authors: Soe-Minn Htway, Takehiro Suzuki, Sanda Kyaw, Keiko Nohara, Tin-Tin Win-Shwe

Published in: Environmental Health and Preventive Medicine | Issue 1/2021

Login to get access

Abstract

Background

Arsenic is a developmental neurotoxicant. It means that its neurotoxic effect could occur in offspring by maternal arsenic exposure. Our previous study showed that developmental arsenic exposure impaired social behavior and serotonergic system in C3H adult male mice. These effects might affect the next generation with no direct exposure to arsenic. This study aimed to detect the social behavior and related gene expression changes in F2 male mice born to gestationally arsenite-exposed F1 mice.

Methods

Pregnant C3H/HeN mice (F0) were given free access to tap water (control mice) or tap water containing 85 ppm sodium arsenite from days 8 to 18 of gestation. Arsenite was not given to F1 or F2 mice. The F2 mice were generated by mating among control F1 males and females, and arsenite-F1 males and females at the age of 10 weeks. At 41 weeks and 74 weeks of age respectively, F2 males were used for the assessment of social behavior by a three-chamber social behavior apparatus. Histological features of the prefrontal cortex were studied by ordinary light microscope. Social behavior-related gene expressions were determined in the prefrontal cortex by real time RT-PCR method.

Results

The arsenite-F2 male mice showed significantly poor sociability and social novelty preference in both 41-week-old group and 74-week-old group. There was no significant histological difference between the control mice and the arsenite-F2 mice. Regarding gene expression, serotonin receptor 5B (5-HT 5B) mRNA expression was significantly decreased (p < 0.05) in the arsenite-F2 male mice compared to the control F2 male mice in both groups. Brain-derived neurotrophic factor (BDNF) and dopamine receptor D1a (Drd1a) gene expressions were significantly decreased (p < 0.05) only in the arsenite-F2 male mice of the 74-week-old group. Heme oxygenase-1 (HO-1) gene expression was significantly increased (p < 0.001) in the arsenite-F2 male mice of both groups, but plasma 8-hydroxy-2′-deoxyguanosine (8-OHdG) and cyclooxygenase-2 (COX-2) gene expression were not significantly different. Interleukin-1β (IL-1β) mRNA expression was significantly increased only in 41-week-old arsenite-F2 mice.

Conclusions

These findings suggest that maternal arsenic exposure affects social behavior in F2 male mice via serotonergic system in the prefrontal cortex. In this study, COX-2 were not increased although oxidative stress marker (HO-1) was increased significantly in arsnite-F2 male mice.
Literature
1.
go back to reference Saha JC, Dikshit AK, Bandyopadhyay M, Saha KC. A review of arsenic poisoning and its effects on human health. Crit Rev Environ Sci Technol. 1999;29(3):281–313.CrossRef Saha JC, Dikshit AK, Bandyopadhyay M, Saha KC. A review of arsenic poisoning and its effects on human health. Crit Rev Environ Sci Technol. 1999;29(3):281–313.CrossRef
3.
go back to reference Jin Y, Xi S, Li X, Lu C, Li G, Xu Y, Qu C, Niu Y, Sun G. Arsenic speciation transported through the placenta from mother mice to their newborn pups. Environ Res. 2006;101(3):349–55.CrossRef Jin Y, Xi S, Li X, Lu C, Li G, Xu Y, Qu C, Niu Y, Sun G. Arsenic speciation transported through the placenta from mother mice to their newborn pups. Environ Res. 2006;101(3):349–55.CrossRef
4.
go back to reference Brender JD, Suarez L, Felkner M, Gilani Z, Stinchcomb D, Moody K, Henry J, Hendricks K. Maternal exposure to arsenic, cadmium, lead, and mercury and neural tube defects in offspring. Environ Res. 2006;101(1):132–9.CrossRef Brender JD, Suarez L, Felkner M, Gilani Z, Stinchcomb D, Moody K, Henry J, Hendricks K. Maternal exposure to arsenic, cadmium, lead, and mercury and neural tube defects in offspring. Environ Res. 2006;101(1):132–9.CrossRef
5.
go back to reference Prakash C, Soni M, Kumar V. Mitochondrial oxidative stress and dysfunction in arsenic neurotoxicity: a review. J Appl Toxicol. 2016;36(2):179–88.CrossRef Prakash C, Soni M, Kumar V. Mitochondrial oxidative stress and dysfunction in arsenic neurotoxicity: a review. J Appl Toxicol. 2016;36(2):179–88.CrossRef
6.
go back to reference Sánchez-Peña LC, Petrosyan P, Morales M, González NB, Gutiérrez-Ospina G, Del Razo LM, Gonsebatt ME. Arsenic species, AS3MT amount, and AS3MT gene expression in different brain regions of mouse exposed to arsenite. Environ Res. 2010;110(5):428–34.CrossRef Sánchez-Peña LC, Petrosyan P, Morales M, González NB, Gutiérrez-Ospina G, Del Razo LM, Gonsebatt ME. Arsenic species, AS3MT amount, and AS3MT gene expression in different brain regions of mouse exposed to arsenite. Environ Res. 2010;110(5):428–34.CrossRef
7.
go back to reference Tyler CR, Allan AM. The effects of arsenic exposure on neurological and cognitive dysfunction in human and rodent studies: a review. Curr Environ Health Rep. 2014;1(2):132–47.CrossRef Tyler CR, Allan AM. The effects of arsenic exposure on neurological and cognitive dysfunction in human and rodent studies: a review. Curr Environ Health Rep. 2014;1(2):132–47.CrossRef
8.
go back to reference Htway SM, Sein MT, Nohara K, Win-Shwe TT. Effects of developmental arsenic exposure on the social behavior and related gene expression in C3H adult male mice. Int J Environ Res Public Health. 2019;16(2):174.CrossRef Htway SM, Sein MT, Nohara K, Win-Shwe TT. Effects of developmental arsenic exposure on the social behavior and related gene expression in C3H adult male mice. Int J Environ Res Public Health. 2019;16(2):174.CrossRef
9.
go back to reference Nohara K, Suzuki T, Okamura K, Matsushita J, Takumi S. Tumor-augmenting effects of gestational arsenic exposure on F1 and F2 in mice. Genes Environ. 2017;39:3.CrossRef Nohara K, Suzuki T, Okamura K, Matsushita J, Takumi S. Tumor-augmenting effects of gestational arsenic exposure on F1 and F2 in mice. Genes Environ. 2017;39:3.CrossRef
10.
go back to reference Nohara K, Tateishi Y, Suzuki T, Okamura K, Murai H, Takumi S, Maekawa F, Nishimura N, Kobori M, Ito T. Late-onset increases in oxidative stress and other tumorigenic activities and tumors with a Ha-ras mutation in the liver of adult male C3H mice gestationally exposed to arsenic. Toxicol Sci. 2012;129:293–304.CrossRef Nohara K, Tateishi Y, Suzuki T, Okamura K, Murai H, Takumi S, Maekawa F, Nishimura N, Kobori M, Ito T. Late-onset increases in oxidative stress and other tumorigenic activities and tumors with a Ha-ras mutation in the liver of adult male C3H mice gestationally exposed to arsenic. Toxicol Sci. 2012;129:293–304.CrossRef
11.
go back to reference Win-Shwe TT, Nway NC, Imai M, Lwin TT, Mar O, Watanabe H. Social behavior, neuroimmune markers and glutamic acid decarboxylase levels in a rat model of valproic acid-induced autism. J Toxicol Sci. 2018;43:631–43.CrossRef Win-Shwe TT, Nway NC, Imai M, Lwin TT, Mar O, Watanabe H. Social behavior, neuroimmune markers and glutamic acid decarboxylase levels in a rat model of valproic acid-induced autism. J Toxicol Sci. 2018;43:631–43.CrossRef
12.
go back to reference Flora SJ, Mittal M, Pachauri V, Dwivedi N. A possible mechanism for combined arsenic and fluoride induced cellular and DNA damage in mice. Metallomics. 2012;4(1):78–90.CrossRef Flora SJ, Mittal M, Pachauri V, Dwivedi N. A possible mechanism for combined arsenic and fluoride induced cellular and DNA damage in mice. Metallomics. 2012;4(1):78–90.CrossRef
13.
go back to reference Win-Shwe TT, Tsukahara S, Ahmed S, Fukushima A, Yamamoto S, Kakeyama M, Nakajima D, Goto S, Kobayashi T, Fujimaki H. Athymic nude mice are insensitive to low-level toluene-induced up-regulation of memory-related gene expressions in the hippocampus. Neurotoxicology. 2007;28:957–64.CrossRef Win-Shwe TT, Tsukahara S, Ahmed S, Fukushima A, Yamamoto S, Kakeyama M, Nakajima D, Goto S, Kobayashi T, Fujimaki H. Athymic nude mice are insensitive to low-level toluene-induced up-regulation of memory-related gene expressions in the hippocampus. Neurotoxicology. 2007;28:957–64.CrossRef
14.
go back to reference Valles S, Hernández-Sánchez J, Dipp VR, Huerta-González D, Olivares-Bañuelos TN, González-Fraga J, Bardullas U. Exposure to low doses of inorganic arsenic induces transgenerational changes on behavioral and epigenetic markers in zebrafish (Danio rerio). Toxicol Appl Pharmacol. 2020;396:115002.CrossRef Valles S, Hernández-Sánchez J, Dipp VR, Huerta-González D, Olivares-Bañuelos TN, González-Fraga J, Bardullas U. Exposure to low doses of inorganic arsenic induces transgenerational changes on behavioral and epigenetic markers in zebrafish (Danio rerio). Toxicol Appl Pharmacol. 2020;396:115002.CrossRef
15.
go back to reference Cases O, Seif I, Grimsby J, Gaspar P, Chen K, Pournin S, Muller U, Aguet M, Babinet C, Shih JC. Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA. Science. 1995;268(5218):1763–6.CrossRef Cases O, Seif I, Grimsby J, Gaspar P, Chen K, Pournin S, Muller U, Aguet M, Babinet C, Shih JC. Aggressive behavior and altered amounts of brain serotonin and norepinephrine in mice lacking MAOA. Science. 1995;268(5218):1763–6.CrossRef
16.
go back to reference Aung KH, Kyi-Tha-Thu C, Sano K, Nakamura K, Tanoue A, Nohara K, Kakeyama M, Tohyama C, Tsukahara S, Maekawa F. Prenatal exposure to arsenic impairs behavioral flexibility and cortical structure in mice. Front Neurosci. 2016;10:137.CrossRef Aung KH, Kyi-Tha-Thu C, Sano K, Nakamura K, Tanoue A, Nohara K, Kakeyama M, Tohyama C, Tsukahara S, Maekawa F. Prenatal exposure to arsenic impairs behavioral flexibility and cortical structure in mice. Front Neurosci. 2016;10:137.CrossRef
17.
go back to reference Rodriguez VM, Carrizales L, Mendoza MS, Fajardo OR, Giordano M. Effects of sodium arsenite exposure on development and behavior in the rat. Neurotoxicol Teratol. 2002;24:743–50.CrossRef Rodriguez VM, Carrizales L, Mendoza MS, Fajardo OR, Giordano M. Effects of sodium arsenite exposure on development and behavior in the rat. Neurotoxicol Teratol. 2002;24:743–50.CrossRef
18.
go back to reference Almeida RD, Manadas BJ, Melo CV, Gomes JR, Mendes CS, Graos MM, Carvalho RF, Carvalho AP, Duarte CB. Neuroprotection by BDNF against glutamate-induced apoptotic cell death is mediated by ERK and PI3-kinase pathways. Cell Death Differ. 2005;12(10):1329–43.CrossRef Almeida RD, Manadas BJ, Melo CV, Gomes JR, Mendes CS, Graos MM, Carvalho RF, Carvalho AP, Duarte CB. Neuroprotection by BDNF against glutamate-induced apoptotic cell death is mediated by ERK and PI3-kinase pathways. Cell Death Differ. 2005;12(10):1329–43.CrossRef
19.
go back to reference Karim Y, Siddique AE, Hossen F, Rahman M, Mondal V, Banna HU, Hasibuzzaman MM, Hosen Z, Islam MS, Sarker MK, Nikkon F. Dose-dependent relationships between chronic arsenic exposure and cognitive impairment and serum brain-derived neurotrophic factor. Environ Int. 2019;131:105029.CrossRef Karim Y, Siddique AE, Hossen F, Rahman M, Mondal V, Banna HU, Hasibuzzaman MM, Hosen Z, Islam MS, Sarker MK, Nikkon F. Dose-dependent relationships between chronic arsenic exposure and cognitive impairment and serum brain-derived neurotrophic factor. Environ Int. 2019;131:105029.CrossRef
20.
go back to reference Homberg JR, Olivier JD, VandenBroeke M, Youn J, Ellenbroek AK, Karel P, Shan L, van Boxtel R, Ooms S, Balemans M, Langedijk J, Muller M, Vriend G, Cools AR, Cuppen E, Ellenbroek BA. The role of the dopamine D1 receptor in social cognition: studies using a novel genetic rat model. Dis Model Mech. 2016;9(10):1147–58.CrossRef Homberg JR, Olivier JD, VandenBroeke M, Youn J, Ellenbroek AK, Karel P, Shan L, van Boxtel R, Ooms S, Balemans M, Langedijk J, Muller M, Vriend G, Cools AR, Cuppen E, Ellenbroek BA. The role of the dopamine D1 receptor in social cognition: studies using a novel genetic rat model. Dis Model Mech. 2016;9(10):1147–58.CrossRef
21.
go back to reference Liu ZM, Chen GG, Ng EK, Leung WK, Sung JJ, Chung SS. Upregulation of heme oxygenase-1 and p21 confers resistance to apoptosis in human gastric cancer cells. Oncogene. 2004;23(2):503–13.CrossRef Liu ZM, Chen GG, Ng EK, Leung WK, Sung JJ, Chung SS. Upregulation of heme oxygenase-1 and p21 confers resistance to apoptosis in human gastric cancer cells. Oncogene. 2004;23(2):503–13.CrossRef
22.
go back to reference Kim JY, Mukherjee S, Ngo LC, Christiani DC. Urinary 8-hydroxy-2′-deoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to fine particulates. Environ Health Perspect. 2004;112:666–71.CrossRef Kim JY, Mukherjee S, Ngo LC, Christiani DC. Urinary 8-hydroxy-2′-deoxyguanosine as a biomarker of oxidative DNA damage in workers exposed to fine particulates. Environ Health Perspect. 2004;112:666–71.CrossRef
23.
go back to reference Eskan MA, Benakanakere MR, Rose BG, Zhang P, Zhao J, Stathopoulou P, Fujioka D, Kinane DF. Interleukin-1β modulates proinflammatory cytokine production in human epithelial cells. Infect Immun. 2008;76(5):2080–9.CrossRef Eskan MA, Benakanakere MR, Rose BG, Zhang P, Zhao J, Stathopoulou P, Fujioka D, Kinane DF. Interleukin-1β modulates proinflammatory cytokine production in human epithelial cells. Infect Immun. 2008;76(5):2080–9.CrossRef
24.
go back to reference Crofford LJ. COX-1 and COX-2 tissue expression: implications and predictions. J Rheumatol Suppl. 1997;49:15–9.PubMed Crofford LJ. COX-1 and COX-2 tissue expression: implications and predictions. J Rheumatol Suppl. 1997;49:15–9.PubMed
25.
go back to reference Araujo JA, Zhang M, Yin F. Heme oxygenase-1, oxidation, inflammation, and atherosclerosis. Front Pharmacol. 2012;3:119.CrossRef Araujo JA, Zhang M, Yin F. Heme oxygenase-1, oxidation, inflammation, and atherosclerosis. Front Pharmacol. 2012;3:119.CrossRef
26.
go back to reference Shih RH, Yang CM. Induction of heme oxygenase-1 attenuates lipopolysaccharide-induced cyclooxygenase-2 expression in mouse brain endothelial cells. J Neuroinflammation. 2010;7(1):86.CrossRef Shih RH, Yang CM. Induction of heme oxygenase-1 attenuates lipopolysaccharide-induced cyclooxygenase-2 expression in mouse brain endothelial cells. J Neuroinflammation. 2010;7(1):86.CrossRef
Metadata
Title
Effects of maternal exposure to arsenic on social behavior and related gene expression in F2 male mice
Authors
Soe-Minn Htway
Takehiro Suzuki
Sanda Kyaw
Keiko Nohara
Tin-Tin Win-Shwe
Publication date
01-12-2021
Publisher
BioMed Central
Published in
Environmental Health and Preventive Medicine / Issue 1/2021
Print ISSN: 1342-078X
Electronic ISSN: 1347-4715
DOI
https://doi.org/10.1186/s12199-021-00956-y

Other articles of this Issue 1/2021

Environmental Health and Preventive Medicine 1/2021 Go to the issue