Maternal periconceptional inflammation transgenerationally alters metabolic and behavioral phenotypes in offspring
Evidence is accumulating that maternal inflammation induces phenotypic changes in the next generation. However, whether maternal preconceptional inflammation alters metabolic and behavioral phenotypes in offspring remains poorly understood. Female mice were injected with either lipopolysaccharide or...
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creator | Xin, Yining Sun, Xiaoxiao Ren, Li Chen, Guo Chen, Yingqi Ni, Yingdong He, Bin |
description | Evidence is accumulating that maternal inflammation induces phenotypic changes in the next generation. However, whether maternal preconceptional inflammation alters metabolic and behavioral phenotypes in offspring remains poorly understood. Female mice were injected with either lipopolysaccharide or saline to establish the inflammatory model and then allowed to mate with normal males. Offspring from both control and inflammatory dams were subsequently given chow diet and water ad libitum, without any challenge, for metabolic and behavioral tests. Male offspring derived from inflammatory mothers (Inf-F1) maintained on the chow diet developed impaired glucose tolerance and hepatic ectopic fat deposition. Hepatic transcriptome sequencing showed the largest gene changes related to the metabolic pathway. Moreover, Inf-F1 mice exhibited anxiety- and depressive-like behaviors and were accompanied by higher serum corticosterone concentration and lower glucocorticoid receptor abundance in the hippocampus. The results expand the current knowledge of developmental programming of health and disease to include maternal preconceptional health and provide a basis for understanding metabolic and behavioral alterations in offspring linked to maternal inflammation. |
doi_str_mv | 10.1016/j.lfs.2023.121577 |
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However, whether maternal preconceptional inflammation alters metabolic and behavioral phenotypes in offspring remains poorly understood. Female mice were injected with either lipopolysaccharide or saline to establish the inflammatory model and then allowed to mate with normal males. Offspring from both control and inflammatory dams were subsequently given chow diet and water ad libitum, without any challenge, for metabolic and behavioral tests. Male offspring derived from inflammatory mothers (Inf-F1) maintained on the chow diet developed impaired glucose tolerance and hepatic ectopic fat deposition. Hepatic transcriptome sequencing showed the largest gene changes related to the metabolic pathway. Moreover, Inf-F1 mice exhibited anxiety- and depressive-like behaviors and were accompanied by higher serum corticosterone concentration and lower glucocorticoid receptor abundance in the hippocampus. 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However, whether maternal preconceptional inflammation alters metabolic and behavioral phenotypes in offspring remains poorly understood. Female mice were injected with either lipopolysaccharide or saline to establish the inflammatory model and then allowed to mate with normal males. Offspring from both control and inflammatory dams were subsequently given chow diet and water ad libitum, without any challenge, for metabolic and behavioral tests. Male offspring derived from inflammatory mothers (Inf-F1) maintained on the chow diet developed impaired glucose tolerance and hepatic ectopic fat deposition. Hepatic transcriptome sequencing showed the largest gene changes related to the metabolic pathway. Moreover, Inf-F1 mice exhibited anxiety- and depressive-like behaviors and were accompanied by higher serum corticosterone concentration and lower glucocorticoid receptor abundance in the hippocampus. The results expand the current knowledge of developmental programming of health and disease to include maternal preconceptional health and provide a basis for understanding metabolic and behavioral alterations in offspring linked to maternal inflammation.</description><subject>biochemical pathways</subject><subject>blood serum</subject><subject>corticosterone</subject><subject>diet</subject><subject>females</subject><subject>genes</subject><subject>glucocorticoid receptors</subject><subject>glucose tolerance</subject><subject>hippocampus</subject><subject>inflammation</subject><subject>lipopolysaccharides</subject><subject>males</subject><subject>phenotype</subject><subject>progeny</subject><subject>transcriptome</subject><issn>0024-3205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNqVjM9OAjEQxnvQRBQfgFuPXlinLcvCmWi8ePNOhmUKJd1p7RQT3h42-gKevnz_fkrNDDQGzPL11EQvjQXrGmNN23V3agJgF3NnoX1QjyInAGjbzk1U-cRKhTHqTCX0iXvKNaQxCOwjDgOOVteCLAdiKvhbx4vGeLuKHqjiLsXQa-S93tERf0IqI_FInOolk9xYOnkvuQQ-TNW9xyj0_KdP6uX97WvzMc8lfZ9J6nYI0lOMyJTOsrUrt7AA6_XK_WN6BXxMV0A</recordid><startdate>20230316</startdate><enddate>20230316</enddate><creator>Xin, Yining</creator><creator>Sun, Xiaoxiao</creator><creator>Ren, Li</creator><creator>Chen, Guo</creator><creator>Chen, Yingqi</creator><creator>Ni, Yingdong</creator><creator>He, Bin</creator><scope>7S9</scope><scope>L.6</scope></search><sort><creationdate>20230316</creationdate><title>Maternal periconceptional inflammation transgenerationally alters metabolic and behavioral phenotypes in offspring</title><author>Xin, Yining ; Sun, Xiaoxiao ; Ren, Li ; Chen, Guo ; Chen, Yingqi ; Ni, Yingdong ; He, Bin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_28342009983</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>biochemical pathways</topic><topic>blood serum</topic><topic>corticosterone</topic><topic>diet</topic><topic>females</topic><topic>genes</topic><topic>glucocorticoid receptors</topic><topic>glucose tolerance</topic><topic>hippocampus</topic><topic>inflammation</topic><topic>lipopolysaccharides</topic><topic>males</topic><topic>phenotype</topic><topic>progeny</topic><topic>transcriptome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Xin, Yining</creatorcontrib><creatorcontrib>Sun, Xiaoxiao</creatorcontrib><creatorcontrib>Ren, Li</creatorcontrib><creatorcontrib>Chen, Guo</creatorcontrib><creatorcontrib>Chen, Yingqi</creatorcontrib><creatorcontrib>Ni, Yingdong</creatorcontrib><creatorcontrib>He, Bin</creatorcontrib><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><jtitle>Life sciences (1973)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Xin, Yining</au><au>Sun, Xiaoxiao</au><au>Ren, Li</au><au>Chen, Guo</au><au>Chen, Yingqi</au><au>Ni, Yingdong</au><au>He, Bin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maternal periconceptional inflammation transgenerationally alters metabolic and behavioral phenotypes in offspring</atitle><jtitle>Life sciences (1973)</jtitle><date>2023-03-16</date><risdate>2023</risdate><issn>0024-3205</issn><abstract>Evidence is accumulating that maternal inflammation induces phenotypic changes in the next generation. However, whether maternal preconceptional inflammation alters metabolic and behavioral phenotypes in offspring remains poorly understood. Female mice were injected with either lipopolysaccharide or saline to establish the inflammatory model and then allowed to mate with normal males. Offspring from both control and inflammatory dams were subsequently given chow diet and water ad libitum, without any challenge, for metabolic and behavioral tests. Male offspring derived from inflammatory mothers (Inf-F1) maintained on the chow diet developed impaired glucose tolerance and hepatic ectopic fat deposition. Hepatic transcriptome sequencing showed the largest gene changes related to the metabolic pathway. Moreover, Inf-F1 mice exhibited anxiety- and depressive-like behaviors and were accompanied by higher serum corticosterone concentration and lower glucocorticoid receptor abundance in the hippocampus. The results expand the current knowledge of developmental programming of health and disease to include maternal preconceptional health and provide a basis for understanding metabolic and behavioral alterations in offspring linked to maternal inflammation.</abstract><doi>10.1016/j.lfs.2023.121577</doi></addata></record> |
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subjects | biochemical pathways blood serum corticosterone diet females genes glucocorticoid receptors glucose tolerance hippocampus inflammation lipopolysaccharides males phenotype progeny transcriptome |
title | Maternal periconceptional inflammation transgenerationally alters metabolic and behavioral phenotypes in offspring |
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