The expression of orexigenic and anorexigenic factors in middle-aged female rats that had been subjected to prenatal undernutrition
•The effects of prenatal undernutrition on the adult response to fasting was examined.•Fasting-induced decrease of leptin was enhanced by prenatal undernutrition.•Fasting-induced increase of hypothalamic NPY was enhanced by prenatal undernutrition.•Response of orexigenic functions were increased by...
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creator | Tungalagsuvd, Altankhuu Matsuzaki, Toshiya Iwasa, Takeshi Munkhzaya, Munkhsaikhan Yiliyasi, Mayila Kawami, Takako Kato, Takeshi Kuwahara, Akira Irahara, Minoru |
description | •The effects of prenatal undernutrition on the adult response to fasting was examined.•Fasting-induced decrease of leptin was enhanced by prenatal undernutrition.•Fasting-induced increase of hypothalamic NPY was enhanced by prenatal undernutrition.•Response of orexigenic functions were increased by prenatal undernutrition.
Fetal growth retardation, which affects short- and long-term fetal brain development, is associated with metabolic, hematological, and thermal disturbances, which can increase the risk of metabolic syndrome later in life. Orexigenic and anorexigenic factors regulate food intake and energy expenditure. We studied how the expression of these factors was affected by food deprivation (FD) in middle-aged female rats that had been subjected to prenatal undernutrition. Eight pregnant rats were divided into two groups, the normal nutrition (NN) (n=4) group and the undernutrition (UN) (n=4) group, which received 50% (approximately 11g) of the daily food intake of the normal nutrition rats from day 13 of pregnancy to delivery. The pups from these dams were defined as the maternal NN (mNN) and maternal UN (mUN) groups, respectively. After weaning, all of the pups were housed and allowed ad libitum access to food and water. At the age of 6 months, both groups of pups were sub-divided into three groups. One group was allowed to consume normal amounts of food (Fed), and the other two groups were subjected to 24h or 48h FD (n=7–8 per group). The rats’ serum leptin levels and hypothalamic mRNA expression levels of various orexigenic or anorexigenic factors were measured. In both the mNN and mUN rats, the serum leptin levels of the 24h and 48h FD groups tended to be lower than those of the Fed group, and the serum leptin levels of the 24h FD mUN rats and the Fed mUN rats differed significantly. The hypothalamic neuropeptide Y (NPY) mRNA expression levels of the 24h and 48h FD groups were significantly higher in the mUN rats than in the mNN rats. In addition, among the mUN rats the hypothalamic NPY mRNA expression levels of the 48h FD group were significantly higher than those of the Fed group. In both the mNN and mUN rats, prepro-orexin mRNA expression was lower in the 48h FD group than in the corresponding Fed group. Among the mUN rats, the 48h FD group exhibited significantly lower hypothalamic proopiomelanocortin (POMC) mRNA expression than the Fed group, and a similar tendency was seen among the mNN rats. Among the mNN rats, the 24h FD group displaye |
doi_str_mv | 10.1016/j.ijdevneu.2015.12.002 |
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Fetal growth retardation, which affects short- and long-term fetal brain development, is associated with metabolic, hematological, and thermal disturbances, which can increase the risk of metabolic syndrome later in life. Orexigenic and anorexigenic factors regulate food intake and energy expenditure. We studied how the expression of these factors was affected by food deprivation (FD) in middle-aged female rats that had been subjected to prenatal undernutrition. Eight pregnant rats were divided into two groups, the normal nutrition (NN) (n=4) group and the undernutrition (UN) (n=4) group, which received 50% (approximately 11g) of the daily food intake of the normal nutrition rats from day 13 of pregnancy to delivery. The pups from these dams were defined as the maternal NN (mNN) and maternal UN (mUN) groups, respectively. After weaning, all of the pups were housed and allowed ad libitum access to food and water. At the age of 6 months, both groups of pups were sub-divided into three groups. One group was allowed to consume normal amounts of food (Fed), and the other two groups were subjected to 24h or 48h FD (n=7–8 per group). The rats’ serum leptin levels and hypothalamic mRNA expression levels of various orexigenic or anorexigenic factors were measured. In both the mNN and mUN rats, the serum leptin levels of the 24h and 48h FD groups tended to be lower than those of the Fed group, and the serum leptin levels of the 24h FD mUN rats and the Fed mUN rats differed significantly. The hypothalamic neuropeptide Y (NPY) mRNA expression levels of the 24h and 48h FD groups were significantly higher in the mUN rats than in the mNN rats. In addition, among the mUN rats the hypothalamic NPY mRNA expression levels of the 48h FD group were significantly higher than those of the Fed group. In both the mNN and mUN rats, prepro-orexin mRNA expression was lower in the 48h FD group than in the corresponding Fed group. Among the mUN rats, the 48h FD group exhibited significantly lower hypothalamic proopiomelanocortin (POMC) mRNA expression than the Fed group, and a similar tendency was seen among the mNN rats. Among the mNN rats, the 24h FD group displayed significantly higher hypothalamic leptin receptor (OBRb) mRNA levels than the Fed group. However, no such differences were seen among the mUN rats. As a result, the hypothalamic OBRb mRNA expression levels of the mUN rats in the 24h and 48h FD groups were lower than those of the corresponding mNN rat groups. These findings indicate that rats that are subjected to prenatal undernutrition exhibit upregulated expression of orexigenic factors and are more sensitive to FD in middle age, which might increase their risk of developing metabolic disorders in later life.</description><identifier>ISSN: 0736-5748</identifier><identifier>EISSN: 1873-474X</identifier><identifier>DOI: 10.1016/j.ijdevneu.2015.12.002</identifier><identifier>PMID: 26702900</identifier><language>eng</language><publisher>United States: Elsevier Ltd</publisher><subject>Analysis of Variance ; Animals ; Anorexigenic factor ; Body Weight - physiology ; DOHaD ; Female ; FGR ; Food Deprivation - physiology ; Gene Expression Regulation - physiology ; Hypothalamus - metabolism ; Leptin - blood ; Malnutrition - blood ; Malnutrition - pathology ; Neuropeptide Y - genetics ; Neuropeptide Y - metabolism ; NPY ; Orexigenic factor ; Pregnancy ; Prenatal Nutritional Physiological Phenomena ; Pro-Opiomelanocortin - genetics ; Pro-Opiomelanocortin - metabolism ; Rats ; Rats, Sprague-Dawley ; Receptors, Leptin - genetics ; Receptors, Leptin - metabolism ; RNA, Messenger - metabolism ; Time Factors</subject><ispartof>International journal of developmental neuroscience, 2016-04, Vol.49 (1), p.1-5</ispartof><rights>2015 Elsevier Ltd</rights><rights>2016 ISDN</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5512-b1042f7ffa75406ef5caa069278cead61cc76b45f7f5746206cc527c074f5e5d3</citedby><cites>FETCH-LOGICAL-c5512-b1042f7ffa75406ef5caa069278cead61cc76b45f7f5746206cc527c074f5e5d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1016%2Fj.ijdevneu.2015.12.002$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1016%2Fj.ijdevneu.2015.12.002$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26702900$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Tungalagsuvd, Altankhuu</creatorcontrib><creatorcontrib>Matsuzaki, Toshiya</creatorcontrib><creatorcontrib>Iwasa, Takeshi</creatorcontrib><creatorcontrib>Munkhzaya, Munkhsaikhan</creatorcontrib><creatorcontrib>Yiliyasi, Mayila</creatorcontrib><creatorcontrib>Kawami, Takako</creatorcontrib><creatorcontrib>Kato, Takeshi</creatorcontrib><creatorcontrib>Kuwahara, Akira</creatorcontrib><creatorcontrib>Irahara, Minoru</creatorcontrib><title>The expression of orexigenic and anorexigenic factors in middle-aged female rats that had been subjected to prenatal undernutrition</title><title>International journal of developmental neuroscience</title><addtitle>Int J Dev Neurosci</addtitle><description>•The effects of prenatal undernutrition on the adult response to fasting was examined.•Fasting-induced decrease of leptin was enhanced by prenatal undernutrition.•Fasting-induced increase of hypothalamic NPY was enhanced by prenatal undernutrition.•Response of orexigenic functions were increased by prenatal undernutrition.
Fetal growth retardation, which affects short- and long-term fetal brain development, is associated with metabolic, hematological, and thermal disturbances, which can increase the risk of metabolic syndrome later in life. Orexigenic and anorexigenic factors regulate food intake and energy expenditure. We studied how the expression of these factors was affected by food deprivation (FD) in middle-aged female rats that had been subjected to prenatal undernutrition. Eight pregnant rats were divided into two groups, the normal nutrition (NN) (n=4) group and the undernutrition (UN) (n=4) group, which received 50% (approximately 11g) of the daily food intake of the normal nutrition rats from day 13 of pregnancy to delivery. The pups from these dams were defined as the maternal NN (mNN) and maternal UN (mUN) groups, respectively. After weaning, all of the pups were housed and allowed ad libitum access to food and water. At the age of 6 months, both groups of pups were sub-divided into three groups. One group was allowed to consume normal amounts of food (Fed), and the other two groups were subjected to 24h or 48h FD (n=7–8 per group). The rats’ serum leptin levels and hypothalamic mRNA expression levels of various orexigenic or anorexigenic factors were measured. In both the mNN and mUN rats, the serum leptin levels of the 24h and 48h FD groups tended to be lower than those of the Fed group, and the serum leptin levels of the 24h FD mUN rats and the Fed mUN rats differed significantly. The hypothalamic neuropeptide Y (NPY) mRNA expression levels of the 24h and 48h FD groups were significantly higher in the mUN rats than in the mNN rats. In addition, among the mUN rats the hypothalamic NPY mRNA expression levels of the 48h FD group were significantly higher than those of the Fed group. In both the mNN and mUN rats, prepro-orexin mRNA expression was lower in the 48h FD group than in the corresponding Fed group. Among the mUN rats, the 48h FD group exhibited significantly lower hypothalamic proopiomelanocortin (POMC) mRNA expression than the Fed group, and a similar tendency was seen among the mNN rats. Among the mNN rats, the 24h FD group displayed significantly higher hypothalamic leptin receptor (OBRb) mRNA levels than the Fed group. However, no such differences were seen among the mUN rats. As a result, the hypothalamic OBRb mRNA expression levels of the mUN rats in the 24h and 48h FD groups were lower than those of the corresponding mNN rat groups. These findings indicate that rats that are subjected to prenatal undernutrition exhibit upregulated expression of orexigenic factors and are more sensitive to FD in middle age, which might increase their risk of developing metabolic disorders in later life.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Anorexigenic factor</subject><subject>Body Weight - physiology</subject><subject>DOHaD</subject><subject>Female</subject><subject>FGR</subject><subject>Food Deprivation - physiology</subject><subject>Gene Expression Regulation - physiology</subject><subject>Hypothalamus - metabolism</subject><subject>Leptin - blood</subject><subject>Malnutrition - blood</subject><subject>Malnutrition - pathology</subject><subject>Neuropeptide Y - genetics</subject><subject>Neuropeptide Y - metabolism</subject><subject>NPY</subject><subject>Orexigenic factor</subject><subject>Pregnancy</subject><subject>Prenatal Nutritional Physiological Phenomena</subject><subject>Pro-Opiomelanocortin - genetics</subject><subject>Pro-Opiomelanocortin - metabolism</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Receptors, Leptin - genetics</subject><subject>Receptors, Leptin - metabolism</subject><subject>RNA, Messenger - metabolism</subject><subject>Time Factors</subject><issn>0736-5748</issn><issn>1873-474X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkUFvFCEUx4nR2LX6FRqOXmYEdoDZm6ZddTdNvbTGG2Hg0WUyy6zA1PbsF5fNtMZbPRCSl997f3g_hM4oqSmh4kNf-97CXYCpZoTymrKaEPYCLWgrl1Ujmx8v0YLIpai4bNoT9CalnhDCOWleoxMmJGErQhbo9_UOMNwfIqTkx4BHh8cI9_4WgjdYB1vOPwWnTR5jwj7gvbd2gErfgsUO9noAHHVOOO90xjttcQcQcJq6HkwuTB5xSQk66wFPwUIMU44-l9C36JXTQ4J3j_cpuvm8vj7_Wl1--7I5_3RZGc4pqzpKGuakc1ryhghw3GhNxIrJ1oC2ghojRdfwgpQ_C0aEMZxJQ2TjOHC7PEXv57mHOP6cIGW198nAMOgA45QUbUkrmtVSsOdRKVp-3CwvqJhRE8eUIjh1iH6v44OiRB1dqV49uVJHV4oyVVyVxrPHjKnbg_3b9iSnAJsZ-OUHePjPsWp7cbXdbC_W36_WN8c6ZXPYx3kWlAXfeYgqGQ_BgPWx-FF29M-99w8hvsGr</recordid><startdate>201604</startdate><enddate>201604</enddate><creator>Tungalagsuvd, Altankhuu</creator><creator>Matsuzaki, Toshiya</creator><creator>Iwasa, Takeshi</creator><creator>Munkhzaya, Munkhsaikhan</creator><creator>Yiliyasi, Mayila</creator><creator>Kawami, Takako</creator><creator>Kato, Takeshi</creator><creator>Kuwahara, Akira</creator><creator>Irahara, Minoru</creator><general>Elsevier Ltd</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><scope>7TK</scope></search><sort><creationdate>201604</creationdate><title>The expression of orexigenic and anorexigenic factors in middle-aged female rats that had been subjected to prenatal undernutrition</title><author>Tungalagsuvd, Altankhuu ; Matsuzaki, Toshiya ; Iwasa, Takeshi ; Munkhzaya, Munkhsaikhan ; Yiliyasi, Mayila ; Kawami, Takako ; Kato, Takeshi ; Kuwahara, Akira ; Irahara, Minoru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5512-b1042f7ffa75406ef5caa069278cead61cc76b45f7f5746206cc527c074f5e5d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Anorexigenic factor</topic><topic>Body Weight - physiology</topic><topic>DOHaD</topic><topic>Female</topic><topic>FGR</topic><topic>Food Deprivation - physiology</topic><topic>Gene Expression Regulation - physiology</topic><topic>Hypothalamus - metabolism</topic><topic>Leptin - blood</topic><topic>Malnutrition - blood</topic><topic>Malnutrition - pathology</topic><topic>Neuropeptide Y - genetics</topic><topic>Neuropeptide Y - metabolism</topic><topic>NPY</topic><topic>Orexigenic factor</topic><topic>Pregnancy</topic><topic>Prenatal Nutritional Physiological Phenomena</topic><topic>Pro-Opiomelanocortin - genetics</topic><topic>Pro-Opiomelanocortin - metabolism</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Receptors, Leptin - genetics</topic><topic>Receptors, Leptin - metabolism</topic><topic>RNA, Messenger - metabolism</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Tungalagsuvd, Altankhuu</creatorcontrib><creatorcontrib>Matsuzaki, Toshiya</creatorcontrib><creatorcontrib>Iwasa, Takeshi</creatorcontrib><creatorcontrib>Munkhzaya, Munkhsaikhan</creatorcontrib><creatorcontrib>Yiliyasi, Mayila</creatorcontrib><creatorcontrib>Kawami, Takako</creatorcontrib><creatorcontrib>Kato, Takeshi</creatorcontrib><creatorcontrib>Kuwahara, Akira</creatorcontrib><creatorcontrib>Irahara, Minoru</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><collection>Neurosciences Abstracts</collection><jtitle>International journal of developmental neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Tungalagsuvd, Altankhuu</au><au>Matsuzaki, Toshiya</au><au>Iwasa, Takeshi</au><au>Munkhzaya, Munkhsaikhan</au><au>Yiliyasi, Mayila</au><au>Kawami, Takako</au><au>Kato, Takeshi</au><au>Kuwahara, Akira</au><au>Irahara, Minoru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The expression of orexigenic and anorexigenic factors in middle-aged female rats that had been subjected to prenatal undernutrition</atitle><jtitle>International journal of developmental neuroscience</jtitle><addtitle>Int J Dev Neurosci</addtitle><date>2016-04</date><risdate>2016</risdate><volume>49</volume><issue>1</issue><spage>1</spage><epage>5</epage><pages>1-5</pages><issn>0736-5748</issn><eissn>1873-474X</eissn><abstract>•The effects of prenatal undernutrition on the adult response to fasting was examined.•Fasting-induced decrease of leptin was enhanced by prenatal undernutrition.•Fasting-induced increase of hypothalamic NPY was enhanced by prenatal undernutrition.•Response of orexigenic functions were increased by prenatal undernutrition.
Fetal growth retardation, which affects short- and long-term fetal brain development, is associated with metabolic, hematological, and thermal disturbances, which can increase the risk of metabolic syndrome later in life. Orexigenic and anorexigenic factors regulate food intake and energy expenditure. We studied how the expression of these factors was affected by food deprivation (FD) in middle-aged female rats that had been subjected to prenatal undernutrition. Eight pregnant rats were divided into two groups, the normal nutrition (NN) (n=4) group and the undernutrition (UN) (n=4) group, which received 50% (approximately 11g) of the daily food intake of the normal nutrition rats from day 13 of pregnancy to delivery. The pups from these dams were defined as the maternal NN (mNN) and maternal UN (mUN) groups, respectively. After weaning, all of the pups were housed and allowed ad libitum access to food and water. At the age of 6 months, both groups of pups were sub-divided into three groups. One group was allowed to consume normal amounts of food (Fed), and the other two groups were subjected to 24h or 48h FD (n=7–8 per group). The rats’ serum leptin levels and hypothalamic mRNA expression levels of various orexigenic or anorexigenic factors were measured. In both the mNN and mUN rats, the serum leptin levels of the 24h and 48h FD groups tended to be lower than those of the Fed group, and the serum leptin levels of the 24h FD mUN rats and the Fed mUN rats differed significantly. The hypothalamic neuropeptide Y (NPY) mRNA expression levels of the 24h and 48h FD groups were significantly higher in the mUN rats than in the mNN rats. In addition, among the mUN rats the hypothalamic NPY mRNA expression levels of the 48h FD group were significantly higher than those of the Fed group. In both the mNN and mUN rats, prepro-orexin mRNA expression was lower in the 48h FD group than in the corresponding Fed group. Among the mUN rats, the 48h FD group exhibited significantly lower hypothalamic proopiomelanocortin (POMC) mRNA expression than the Fed group, and a similar tendency was seen among the mNN rats. Among the mNN rats, the 24h FD group displayed significantly higher hypothalamic leptin receptor (OBRb) mRNA levels than the Fed group. However, no such differences were seen among the mUN rats. As a result, the hypothalamic OBRb mRNA expression levels of the mUN rats in the 24h and 48h FD groups were lower than those of the corresponding mNN rat groups. These findings indicate that rats that are subjected to prenatal undernutrition exhibit upregulated expression of orexigenic factors and are more sensitive to FD in middle age, which might increase their risk of developing metabolic disorders in later life.</abstract><cop>United States</cop><pub>Elsevier Ltd</pub><pmid>26702900</pmid><doi>10.1016/j.ijdevneu.2015.12.002</doi><tpages>5</tpages></addata></record> |
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subjects | Analysis of Variance Animals Anorexigenic factor Body Weight - physiology DOHaD Female FGR Food Deprivation - physiology Gene Expression Regulation - physiology Hypothalamus - metabolism Leptin - blood Malnutrition - blood Malnutrition - pathology Neuropeptide Y - genetics Neuropeptide Y - metabolism NPY Orexigenic factor Pregnancy Prenatal Nutritional Physiological Phenomena Pro-Opiomelanocortin - genetics Pro-Opiomelanocortin - metabolism Rats Rats, Sprague-Dawley Receptors, Leptin - genetics Receptors, Leptin - metabolism RNA, Messenger - metabolism Time Factors |
title | The expression of orexigenic and anorexigenic factors in middle-aged female rats that had been subjected to prenatal undernutrition |
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