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Sex Differences in Shotgun Proteome Analyses for Chronic Oral Intake of Cadmium in Mice

Environmental diseases related to cadmium exposure primarily develop owing to industrial wastewater pollution and/or contaminated food. In regions with high cadmium exposure in Japan, cadmium accumulation occurs primarily in the kidneys of individuals who are exposed to the metal. In contrast, in th...

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Autores principales: Yamanobe, Yoshiharu, Nagahara, Noriyuki, Matsukawa, Takehisa, Ito, Takaaki, Niimori-Kita, Kanako, Chiba, Momoko, Yokoyama, Kazuhito, Takizawa, Toshihiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368563/
https://www.ncbi.nlm.nih.gov/pubmed/25793409
http://dx.doi.org/10.1371/journal.pone.0121819
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author Yamanobe, Yoshiharu
Nagahara, Noriyuki
Matsukawa, Takehisa
Ito, Takaaki
Niimori-Kita, Kanako
Chiba, Momoko
Yokoyama, Kazuhito
Takizawa, Toshihiro
author_facet Yamanobe, Yoshiharu
Nagahara, Noriyuki
Matsukawa, Takehisa
Ito, Takaaki
Niimori-Kita, Kanako
Chiba, Momoko
Yokoyama, Kazuhito
Takizawa, Toshihiro
author_sort Yamanobe, Yoshiharu
collection PubMed
description Environmental diseases related to cadmium exposure primarily develop owing to industrial wastewater pollution and/or contaminated food. In regions with high cadmium exposure in Japan, cadmium accumulation occurs primarily in the kidneys of individuals who are exposed to the metal. In contrast, in the itai-itai disease outbreak that occurred in the Jinzu River basin in Toyama Prefecture in Japan, cadmium primarily accumulated in the liver. On the other hand, high concentration of cadmium caused renal tubular disorder and osteomalacia (multiple bone fracture), probably resulting from the renal tubular dysfunction and additional pathology. In this study, we aimed to establish a mouse model of chronic cadmium intake. We administered cadmium-containing drinking water (32 mg/l) to female and male mice ad libitum for 11 weeks. Metal analysis using inductively coupled plasma mass spectrometry revealed that cadmium accumulated in the kidneys (927 x 10 + 185 ng/g in females and 661 x 10 + 101 ng/g in males), liver (397 x 10 + 199 ng/g in females and 238 x 10 + 652 ng/g in males), and thyroid gland (293 + 93.7 ng/g in females and 129 + 72.7 ng/g in males) of mice. Female mice showed higher cadmium accumulation in the kidney, liver, and thyroid gland than males did (p = 0.00345, p = 0.00213, and p = 0.0331, respectively). Shotgun proteome analyses after chronic oral administration of cadmium revealed that protein levels of glutathione S-transferase Mu2, Mu4, and Mu7 decreased in the liver, and those of A1 and A2 decreased in the kidneys in both female and male mice.
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spelling pubmed-43685632015-03-27 Sex Differences in Shotgun Proteome Analyses for Chronic Oral Intake of Cadmium in Mice Yamanobe, Yoshiharu Nagahara, Noriyuki Matsukawa, Takehisa Ito, Takaaki Niimori-Kita, Kanako Chiba, Momoko Yokoyama, Kazuhito Takizawa, Toshihiro PLoS One Research Article Environmental diseases related to cadmium exposure primarily develop owing to industrial wastewater pollution and/or contaminated food. In regions with high cadmium exposure in Japan, cadmium accumulation occurs primarily in the kidneys of individuals who are exposed to the metal. In contrast, in the itai-itai disease outbreak that occurred in the Jinzu River basin in Toyama Prefecture in Japan, cadmium primarily accumulated in the liver. On the other hand, high concentration of cadmium caused renal tubular disorder and osteomalacia (multiple bone fracture), probably resulting from the renal tubular dysfunction and additional pathology. In this study, we aimed to establish a mouse model of chronic cadmium intake. We administered cadmium-containing drinking water (32 mg/l) to female and male mice ad libitum for 11 weeks. Metal analysis using inductively coupled plasma mass spectrometry revealed that cadmium accumulated in the kidneys (927 x 10 + 185 ng/g in females and 661 x 10 + 101 ng/g in males), liver (397 x 10 + 199 ng/g in females and 238 x 10 + 652 ng/g in males), and thyroid gland (293 + 93.7 ng/g in females and 129 + 72.7 ng/g in males) of mice. Female mice showed higher cadmium accumulation in the kidney, liver, and thyroid gland than males did (p = 0.00345, p = 0.00213, and p = 0.0331, respectively). Shotgun proteome analyses after chronic oral administration of cadmium revealed that protein levels of glutathione S-transferase Mu2, Mu4, and Mu7 decreased in the liver, and those of A1 and A2 decreased in the kidneys in both female and male mice. Public Library of Science 2015-03-20 /pmc/articles/PMC4368563/ /pubmed/25793409 http://dx.doi.org/10.1371/journal.pone.0121819 Text en © 2015 Yamanobe et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yamanobe, Yoshiharu
Nagahara, Noriyuki
Matsukawa, Takehisa
Ito, Takaaki
Niimori-Kita, Kanako
Chiba, Momoko
Yokoyama, Kazuhito
Takizawa, Toshihiro
Sex Differences in Shotgun Proteome Analyses for Chronic Oral Intake of Cadmium in Mice
title Sex Differences in Shotgun Proteome Analyses for Chronic Oral Intake of Cadmium in Mice
title_full Sex Differences in Shotgun Proteome Analyses for Chronic Oral Intake of Cadmium in Mice
title_fullStr Sex Differences in Shotgun Proteome Analyses for Chronic Oral Intake of Cadmium in Mice
title_full_unstemmed Sex Differences in Shotgun Proteome Analyses for Chronic Oral Intake of Cadmium in Mice
title_short Sex Differences in Shotgun Proteome Analyses for Chronic Oral Intake of Cadmium in Mice
title_sort sex differences in shotgun proteome analyses for chronic oral intake of cadmium in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4368563/
https://www.ncbi.nlm.nih.gov/pubmed/25793409
http://dx.doi.org/10.1371/journal.pone.0121819
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