The Effect of Perinatal Gadolinium-Based Contrast Agents on Adult Mice Behavior

OBJECTIVESThe aim of this study was to examine the effects of perinatal exposure to gadolinium (Gd)-based contrast agents (GBCAs) on the behavior of adulthood offspring. MATERIALS AND METHODSPregnant Balb/C mice (n = 5 per group) were intravenously injected with gadoterate meglumine (Magnescope, mac...

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Veröffentlicht in:Investigative radiology 2018-02, Vol.53 (2), p.110-118
Hauptverfasser: Khairinisa, Miski Aghnia, Takatsuru, Yusuke, Amano, Izuki, Erdene, Khongorzul, Nakajima, Takahito, Kameo, Satomi, Koyama, Hiroshi, Tsushima, Yoshito, Koibuchi, Noriyuki
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container_end_page 118
container_issue 2
container_start_page 110
container_title Investigative radiology
container_volume 53
creator Khairinisa, Miski Aghnia
Takatsuru, Yusuke
Amano, Izuki
Erdene, Khongorzul
Nakajima, Takahito
Kameo, Satomi
Koyama, Hiroshi
Tsushima, Yoshito
Koibuchi, Noriyuki
description OBJECTIVESThe aim of this study was to examine the effects of perinatal exposure to gadolinium (Gd)-based contrast agents (GBCAs) on the behavior of adulthood offspring. MATERIALS AND METHODSPregnant Balb/C mice (n = 5 per group) were intravenously injected with gadoterate meglumine (Magnescope, macrocyclic GBCA), gadodiamide (Omniscan, linear GBCA), or vehicle from pregnancy day 15 to 19, corresponding to embryonic day 15 to 19 of the fetus, at 2 mmol/kg body weight per day. Brain samples from dams and pups were collected on postpartum day 28. The total Gd concentration was quantified by inductively coupled plasma-mass spectrometry (dams, n = 3; gadoterate meglumine-treated pups group, n = 9; and gadodiamide-treated pups group, n = 10). Behavioral testing of offspring was started on postpartum day 70 (control group, n = 22; gadoterate meglumine-treated group, n = 23; and gadodiamide-treated group, n = 20). RESULTSHigher levels of Gd retention were observed in dams and pups in the gadodiamide-treated group. Perinatal exposure to GBCAs caused anxiety-like behavior, disrupted motor coordination, impaired memory function, stimulated tactile sensitivity, and decreased muscle strength, particularly in the gadodiamide-treated group. CONCLUSIONSIn the present study, we showed that Gd was transferred to pups and was retained in their brain during postnatal development. Gadolinium retention may lead to impaired brain development. These findings indicate that the use of GBCAs in pregnant women should be avoided because it may have adverse effects on the fetus, particularly on brain development.
doi_str_mv 10.1097/RLI.0000000000000417
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MATERIALS AND METHODSPregnant Balb/C mice (n = 5 per group) were intravenously injected with gadoterate meglumine (Magnescope, macrocyclic GBCA), gadodiamide (Omniscan, linear GBCA), or vehicle from pregnancy day 15 to 19, corresponding to embryonic day 15 to 19 of the fetus, at 2 mmol/kg body weight per day. Brain samples from dams and pups were collected on postpartum day 28. The total Gd concentration was quantified by inductively coupled plasma-mass spectrometry (dams, n = 3; gadoterate meglumine-treated pups group, n = 9; and gadodiamide-treated pups group, n = 10). Behavioral testing of offspring was started on postpartum day 70 (control group, n = 22; gadoterate meglumine-treated group, n = 23; and gadodiamide-treated group, n = 20). RESULTSHigher levels of Gd retention were observed in dams and pups in the gadodiamide-treated group. Perinatal exposure to GBCAs caused anxiety-like behavior, disrupted motor coordination, impaired memory function, stimulated tactile sensitivity, and decreased muscle strength, particularly in the gadodiamide-treated group. CONCLUSIONSIn the present study, we showed that Gd was transferred to pups and was retained in their brain during postnatal development. Gadolinium retention may lead to impaired brain development. These findings indicate that the use of GBCAs in pregnant women should be avoided because it may have adverse effects on the fetus, particularly on brain development.</description><identifier>ISSN: 0020-9996</identifier><identifier>EISSN: 1536-0210</identifier><identifier>DOI: 10.1097/RLI.0000000000000417</identifier><identifier>PMID: 28915162</identifier><language>eng</language><publisher>United States: Copyright Wolters Kluwer Health, Inc. All rights reserved</publisher><subject>Animals ; Behavior, Animal - drug effects ; Brain - drug effects ; Contrast Media - administration &amp; dosage ; Contrast Media - adverse effects ; Contrast Media - pharmacology ; Disease Models, Animal ; Female ; Gadolinium - adverse effects ; Gadolinium - pharmacology ; Gadolinium DTPA - adverse effects ; Gadolinium DTPA - pharmacology ; Humans ; Male ; Meglumine - adverse effects ; Meglumine - pharmacology ; Mice ; Mice, Inbred BALB C ; Organometallic Compounds - adverse effects ; Organometallic Compounds - pharmacology ; Pregnancy ; Prenatal Exposure Delayed Effects - chemically induced ; Spectrophotometry, Atomic</subject><ispartof>Investigative radiology, 2018-02, Vol.53 (2), p.110-118</ispartof><rights>Copyright © 2018 Wolters Kluwer Health, Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4227-375a69c81d518b1d8e7b3478e31a4bc42230bc263f2a36e4c6b58407f18bdc483</citedby><cites>FETCH-LOGICAL-c4227-375a69c81d518b1d8e7b3478e31a4bc42230bc263f2a36e4c6b58407f18bdc483</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28915162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Khairinisa, Miski Aghnia</creatorcontrib><creatorcontrib>Takatsuru, Yusuke</creatorcontrib><creatorcontrib>Amano, Izuki</creatorcontrib><creatorcontrib>Erdene, Khongorzul</creatorcontrib><creatorcontrib>Nakajima, Takahito</creatorcontrib><creatorcontrib>Kameo, Satomi</creatorcontrib><creatorcontrib>Koyama, Hiroshi</creatorcontrib><creatorcontrib>Tsushima, Yoshito</creatorcontrib><creatorcontrib>Koibuchi, Noriyuki</creatorcontrib><title>The Effect of Perinatal Gadolinium-Based Contrast Agents on Adult Mice Behavior</title><title>Investigative radiology</title><addtitle>Invest Radiol</addtitle><description>OBJECTIVESThe aim of this study was to examine the effects of perinatal exposure to gadolinium (Gd)-based contrast agents (GBCAs) on the behavior of adulthood offspring. MATERIALS AND METHODSPregnant Balb/C mice (n = 5 per group) were intravenously injected with gadoterate meglumine (Magnescope, macrocyclic GBCA), gadodiamide (Omniscan, linear GBCA), or vehicle from pregnancy day 15 to 19, corresponding to embryonic day 15 to 19 of the fetus, at 2 mmol/kg body weight per day. Brain samples from dams and pups were collected on postpartum day 28. The total Gd concentration was quantified by inductively coupled plasma-mass spectrometry (dams, n = 3; gadoterate meglumine-treated pups group, n = 9; and gadodiamide-treated pups group, n = 10). Behavioral testing of offspring was started on postpartum day 70 (control group, n = 22; gadoterate meglumine-treated group, n = 23; and gadodiamide-treated group, n = 20). RESULTSHigher levels of Gd retention were observed in dams and pups in the gadodiamide-treated group. Perinatal exposure to GBCAs caused anxiety-like behavior, disrupted motor coordination, impaired memory function, stimulated tactile sensitivity, and decreased muscle strength, particularly in the gadodiamide-treated group. CONCLUSIONSIn the present study, we showed that Gd was transferred to pups and was retained in their brain during postnatal development. Gadolinium retention may lead to impaired brain development. These findings indicate that the use of GBCAs in pregnant women should be avoided because it may have adverse effects on the fetus, particularly on brain development.</description><subject>Animals</subject><subject>Behavior, Animal - drug effects</subject><subject>Brain - drug effects</subject><subject>Contrast Media - administration &amp; dosage</subject><subject>Contrast Media - adverse effects</subject><subject>Contrast Media - pharmacology</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Gadolinium - adverse effects</subject><subject>Gadolinium - pharmacology</subject><subject>Gadolinium DTPA - adverse effects</subject><subject>Gadolinium DTPA - pharmacology</subject><subject>Humans</subject><subject>Male</subject><subject>Meglumine - adverse effects</subject><subject>Meglumine - pharmacology</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Organometallic Compounds - adverse effects</subject><subject>Organometallic Compounds - pharmacology</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects - chemically induced</subject><subject>Spectrophotometry, Atomic</subject><issn>0020-9996</issn><issn>1536-0210</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtLw0AUhQdRbK3-A5FZukmdV17LWmotVCpS12EyuTHRSabOTCz-e1NaRVx4N2fznXPhQ-iSkjElaXzztFyMye8TND5CQxryKCCMkmM0JISRIE3TaIDOnHvtGRYTfooGLElpSCM2RKt1BXhWlqA8NiV-BFu30kuN57Iwum7rrglupYMCT03rrXQeT16g9Q6bFk-KTnv8UCvAt1DJj9rYc3RSSu3g4pAj9Hw3W0_vg-VqvphOloESjMUBj0MZpSqhRUiTnBYJxDkXcQKcSpHvGE5yxSJeMskjECrKw0SQuOzpQomEj9D1fndjzXsHzmdN7RRoLVswnctoKggJRZTSHhV7VFnjnIUy29i6kfYzoyTbqcx6ldlflX3t6vChyxsofkrf7nog2QNboz1Y96a7LdisAql99f_2FytxfeA</recordid><startdate>201802</startdate><enddate>201802</enddate><creator>Khairinisa, Miski Aghnia</creator><creator>Takatsuru, Yusuke</creator><creator>Amano, Izuki</creator><creator>Erdene, Khongorzul</creator><creator>Nakajima, Takahito</creator><creator>Kameo, Satomi</creator><creator>Koyama, Hiroshi</creator><creator>Tsushima, Yoshito</creator><creator>Koibuchi, Noriyuki</creator><general>Copyright Wolters Kluwer Health, Inc. All rights reserved</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>201802</creationdate><title>The Effect of Perinatal Gadolinium-Based Contrast Agents on Adult Mice Behavior</title><author>Khairinisa, Miski Aghnia ; Takatsuru, Yusuke ; Amano, Izuki ; Erdene, Khongorzul ; Nakajima, Takahito ; Kameo, Satomi ; Koyama, Hiroshi ; Tsushima, Yoshito ; Koibuchi, Noriyuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4227-375a69c81d518b1d8e7b3478e31a4bc42230bc263f2a36e4c6b58407f18bdc483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Behavior, Animal - drug effects</topic><topic>Brain - drug effects</topic><topic>Contrast Media - administration &amp; dosage</topic><topic>Contrast Media - adverse effects</topic><topic>Contrast Media - pharmacology</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Gadolinium - adverse effects</topic><topic>Gadolinium - pharmacology</topic><topic>Gadolinium DTPA - adverse effects</topic><topic>Gadolinium DTPA - pharmacology</topic><topic>Humans</topic><topic>Male</topic><topic>Meglumine - adverse effects</topic><topic>Meglumine - pharmacology</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Organometallic Compounds - adverse effects</topic><topic>Organometallic Compounds - pharmacology</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects - chemically induced</topic><topic>Spectrophotometry, Atomic</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Khairinisa, Miski Aghnia</creatorcontrib><creatorcontrib>Takatsuru, Yusuke</creatorcontrib><creatorcontrib>Amano, Izuki</creatorcontrib><creatorcontrib>Erdene, Khongorzul</creatorcontrib><creatorcontrib>Nakajima, Takahito</creatorcontrib><creatorcontrib>Kameo, Satomi</creatorcontrib><creatorcontrib>Koyama, Hiroshi</creatorcontrib><creatorcontrib>Tsushima, Yoshito</creatorcontrib><creatorcontrib>Koibuchi, Noriyuki</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Investigative radiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Khairinisa, Miski Aghnia</au><au>Takatsuru, Yusuke</au><au>Amano, Izuki</au><au>Erdene, Khongorzul</au><au>Nakajima, Takahito</au><au>Kameo, Satomi</au><au>Koyama, Hiroshi</au><au>Tsushima, Yoshito</au><au>Koibuchi, Noriyuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Effect of Perinatal Gadolinium-Based Contrast Agents on Adult Mice Behavior</atitle><jtitle>Investigative radiology</jtitle><addtitle>Invest Radiol</addtitle><date>2018-02</date><risdate>2018</risdate><volume>53</volume><issue>2</issue><spage>110</spage><epage>118</epage><pages>110-118</pages><issn>0020-9996</issn><eissn>1536-0210</eissn><abstract>OBJECTIVESThe aim of this study was to examine the effects of perinatal exposure to gadolinium (Gd)-based contrast agents (GBCAs) on the behavior of adulthood offspring. MATERIALS AND METHODSPregnant Balb/C mice (n = 5 per group) were intravenously injected with gadoterate meglumine (Magnescope, macrocyclic GBCA), gadodiamide (Omniscan, linear GBCA), or vehicle from pregnancy day 15 to 19, corresponding to embryonic day 15 to 19 of the fetus, at 2 mmol/kg body weight per day. Brain samples from dams and pups were collected on postpartum day 28. The total Gd concentration was quantified by inductively coupled plasma-mass spectrometry (dams, n = 3; gadoterate meglumine-treated pups group, n = 9; and gadodiamide-treated pups group, n = 10). Behavioral testing of offspring was started on postpartum day 70 (control group, n = 22; gadoterate meglumine-treated group, n = 23; and gadodiamide-treated group, n = 20). RESULTSHigher levels of Gd retention were observed in dams and pups in the gadodiamide-treated group. Perinatal exposure to GBCAs caused anxiety-like behavior, disrupted motor coordination, impaired memory function, stimulated tactile sensitivity, and decreased muscle strength, particularly in the gadodiamide-treated group. CONCLUSIONSIn the present study, we showed that Gd was transferred to pups and was retained in their brain during postnatal development. Gadolinium retention may lead to impaired brain development. These findings indicate that the use of GBCAs in pregnant women should be avoided because it may have adverse effects on the fetus, particularly on brain development.</abstract><cop>United States</cop><pub>Copyright Wolters Kluwer Health, Inc. All rights reserved</pub><pmid>28915162</pmid><doi>10.1097/RLI.0000000000000417</doi><tpages>9</tpages></addata></record>
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subjects Animals
Behavior, Animal - drug effects
Brain - drug effects
Contrast Media - administration & dosage
Contrast Media - adverse effects
Contrast Media - pharmacology
Disease Models, Animal
Female
Gadolinium - adverse effects
Gadolinium - pharmacology
Gadolinium DTPA - adverse effects
Gadolinium DTPA - pharmacology
Humans
Male
Meglumine - adverse effects
Meglumine - pharmacology
Mice
Mice, Inbred BALB C
Organometallic Compounds - adverse effects
Organometallic Compounds - pharmacology
Pregnancy
Prenatal Exposure Delayed Effects - chemically induced
Spectrophotometry, Atomic
title The Effect of Perinatal Gadolinium-Based Contrast Agents on Adult Mice Behavior
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