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 |
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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 |
format | Article |
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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 & 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 & 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 & 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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