Loading…

Maternally Administered Cyclic Glycine-Proline Increases Insulin-Like Growth Factor-1 Bioavailability and Novelty Recognition in Developing Offspring

Cyclic glycine-proline (cGP), a metabolite of IGF-1, is an endogenous neuropeptide that improves memory in adult rats. The presence and concentrations of endogenous cGP, and its association with IGF-1 and IGF binding protein-3 (IGFBP-3) in rat milk and plasma, were evaluated during postnatal develop...

Full description

Saved in:
Bibliographic Details
Published in:Endocrinology (Philadelphia) 2016-08, Vol.157 (8), p.3130-3139
Main Authors: Singh-Mallah, Gagandeep, Singh, Kuljeet, McMahon, Christopher D, Harris, Paul, Brimble, Margaret A, Thorstensen, Eric, Guan, Jian
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c536t-748685a66608349929011e29f659c6b6eeb58a50f548c2161e356b577fb4fd733
cites cdi_FETCH-LOGICAL-c536t-748685a66608349929011e29f659c6b6eeb58a50f548c2161e356b577fb4fd733
container_end_page 3139
container_issue 8
container_start_page 3130
container_title Endocrinology (Philadelphia)
container_volume 157
creator Singh-Mallah, Gagandeep
Singh, Kuljeet
McMahon, Christopher D
Harris, Paul
Brimble, Margaret A
Thorstensen, Eric
Guan, Jian
description Cyclic glycine-proline (cGP), a metabolite of IGF-1, is an endogenous neuropeptide that improves memory in adult rats. The presence and concentrations of endogenous cGP, and its association with IGF-1 and IGF binding protein-3 (IGFBP-3) in rat milk and plasma, were evaluated during postnatal development. Maternal-infantile transfer of cGP during lactation and its efficacy on the memory of developing offspring were also investigated. Dams were gavaged with either cGP (3 mg/kg) or saline daily from postnatal days 8–22. Concentrations of cGP were measured in dams' milk, and concentrations of cGP, IGF-1, and IGFBP-3 were measured in the plasma of dams, pups, and young adults. The recognition memory, locomotor function, and anxiety-like behavior of offspring were evaluated using behavioral tests. Endogenous cGP was detected in rat milk, and its concentration was higher during peak lactation compared with late lactation. Comparisons within control groups showed low endogenous IGF-1 and IGFBP-3 and high endogenous cGP concentrations in the plasma of male pups. The reduced IGFBP-3 and increased cGP may be a response to increase the bioavailability of IGF-1 during infancy. Exogenous cGP showed oral bioavailability and effective maternal-infantile transfer through milk. Maternally transferred cGP also led to improved recognition memory in the developing offspring, possibly through increased IGF-1 bioavailability, with no effect on locomotor activity and anxiety-like behavior. These results show that cGP is an essential endogenous peptide during early postnatal development as it improves the bioavailability of IGF-1 during infancy. Furthermore, maternal cGP supplementation offers an effective and natural route of administration for improving memory in the developing offspring.
doi_str_mv 10.1210/en.2016-1189
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1897391435</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1210/en.2016-1189</oup_id><sourcerecordid>1808387434</sourcerecordid><originalsourceid>FETCH-LOGICAL-c536t-748685a66608349929011e29f659c6b6eeb58a50f548c2161e356b577fb4fd733</originalsourceid><addsrcrecordid>eNqNkUtv1DAUhSMEotPCjjWyxAIWuNjxK1mWgQ6VBooQrCPHuSkuHju1k1b5IfxfHM0AEgKJ1X3o0_HxPUXxhJJTWlLyCvxpSajElFb1vWJFay6woorcL1aEUIZVWaqj4jil6zxyztnD4qhUTAhe01Xx_b0eIXrt3IzOup31NuUZOrSejbMGbdxsrAf8MQaXK7rwJoJOkHKXprzCW_sN0CaGu_ErOtdmDBFT9NoGfaut0611dpyR9h36EG7B5f4TmHDl7WiDR9ajN5DXYbD-Cl32fRpi7h4VD3rtEjw-1JPiy_nbz-t3eHu5uVifbbERTI5Y8UpWQkspScV4XZc1oRTKupeiNrKVAK2otCC94JUpqaTAhGyFUn3L-04xdlK82OsOMdxMkMZmZ5MB57SHMKUmn1SxmnIm_gPNHirFGc_osz_Q6zAtN04No4woygRd3n65p0wMKUXom_z1nY5zQ0mzJNuAb5ZkmyXZjD89iE7tDrpf8M8oM_B8D4Rp-JcUPkixPQm-CybfG4YIKf12-VcDPwCJbLuF</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3130713513</pqid></control><display><type>article</type><title>Maternally Administered Cyclic Glycine-Proline Increases Insulin-Like Growth Factor-1 Bioavailability and Novelty Recognition in Developing Offspring</title><source>Oxford Journals Online</source><creator>Singh-Mallah, Gagandeep ; Singh, Kuljeet ; McMahon, Christopher D ; Harris, Paul ; Brimble, Margaret A ; Thorstensen, Eric ; Guan, Jian</creator><creatorcontrib>Singh-Mallah, Gagandeep ; Singh, Kuljeet ; McMahon, Christopher D ; Harris, Paul ; Brimble, Margaret A ; Thorstensen, Eric ; Guan, Jian</creatorcontrib><description>Cyclic glycine-proline (cGP), a metabolite of IGF-1, is an endogenous neuropeptide that improves memory in adult rats. The presence and concentrations of endogenous cGP, and its association with IGF-1 and IGF binding protein-3 (IGFBP-3) in rat milk and plasma, were evaluated during postnatal development. Maternal-infantile transfer of cGP during lactation and its efficacy on the memory of developing offspring were also investigated. Dams were gavaged with either cGP (3 mg/kg) or saline daily from postnatal days 8–22. Concentrations of cGP were measured in dams' milk, and concentrations of cGP, IGF-1, and IGFBP-3 were measured in the plasma of dams, pups, and young adults. The recognition memory, locomotor function, and anxiety-like behavior of offspring were evaluated using behavioral tests. Endogenous cGP was detected in rat milk, and its concentration was higher during peak lactation compared with late lactation. Comparisons within control groups showed low endogenous IGF-1 and IGFBP-3 and high endogenous cGP concentrations in the plasma of male pups. The reduced IGFBP-3 and increased cGP may be a response to increase the bioavailability of IGF-1 during infancy. Exogenous cGP showed oral bioavailability and effective maternal-infantile transfer through milk. Maternally transferred cGP also led to improved recognition memory in the developing offspring, possibly through increased IGF-1 bioavailability, with no effect on locomotor activity and anxiety-like behavior. These results show that cGP is an essential endogenous peptide during early postnatal development as it improves the bioavailability of IGF-1 during infancy. Furthermore, maternal cGP supplementation offers an effective and natural route of administration for improving memory in the developing offspring.</description><identifier>ISSN: 0013-7227</identifier><identifier>EISSN: 1945-7170</identifier><identifier>DOI: 10.1210/en.2016-1189</identifier><identifier>PMID: 27355491</identifier><language>eng</language><publisher>United States: Endocrine Society</publisher><subject>Animals ; Anxiety ; Bioavailability ; Biological Availability ; Breastfeeding &amp; lactation ; Effectiveness ; Exploratory Behavior - drug effects ; Female ; Glycine ; Glycine - administration &amp; dosage ; Glycine - pharmacology ; Growth factors ; Insulin-like growth factor I ; Insulin-Like Growth Factor I - metabolism ; Insulin-Like Growth Factor I - pharmacokinetics ; Insulin-like growth factor-binding protein 3 ; Insulin-like growth factors ; Juveniles ; Lactation ; Locomotor activity ; Male ; Maternal Nutritional Physiological Phenomena ; Metabolites ; Milk ; Offspring ; Peptides, Cyclic - administration &amp; dosage ; Peptides, Cyclic - pharmacology ; Postpartum period ; Pregnancy ; Prenatal Exposure Delayed Effects - metabolism ; Prenatal Exposure Delayed Effects - psychology ; Proline ; Proline - administration &amp; dosage ; Proline - pharmacology ; Rats ; Rats, Sprague-Dawley ; Recognition ; Recognition (Psychology) - drug effects ; Young adults</subject><ispartof>Endocrinology (Philadelphia), 2016-08, Vol.157 (8), p.3130-3139</ispartof><rights>Copyright © 2016 by the Endocrine Society</rights><rights>Copyright © 2016 by the Endocrine Society 2016</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c536t-748685a66608349929011e29f659c6b6eeb58a50f548c2161e356b577fb4fd733</citedby><cites>FETCH-LOGICAL-c536t-748685a66608349929011e29f659c6b6eeb58a50f548c2161e356b577fb4fd733</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/27355491$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Singh-Mallah, Gagandeep</creatorcontrib><creatorcontrib>Singh, Kuljeet</creatorcontrib><creatorcontrib>McMahon, Christopher D</creatorcontrib><creatorcontrib>Harris, Paul</creatorcontrib><creatorcontrib>Brimble, Margaret A</creatorcontrib><creatorcontrib>Thorstensen, Eric</creatorcontrib><creatorcontrib>Guan, Jian</creatorcontrib><title>Maternally Administered Cyclic Glycine-Proline Increases Insulin-Like Growth Factor-1 Bioavailability and Novelty Recognition in Developing Offspring</title><title>Endocrinology (Philadelphia)</title><addtitle>Endocrinology</addtitle><description>Cyclic glycine-proline (cGP), a metabolite of IGF-1, is an endogenous neuropeptide that improves memory in adult rats. The presence and concentrations of endogenous cGP, and its association with IGF-1 and IGF binding protein-3 (IGFBP-3) in rat milk and plasma, were evaluated during postnatal development. Maternal-infantile transfer of cGP during lactation and its efficacy on the memory of developing offspring were also investigated. Dams were gavaged with either cGP (3 mg/kg) or saline daily from postnatal days 8–22. Concentrations of cGP were measured in dams' milk, and concentrations of cGP, IGF-1, and IGFBP-3 were measured in the plasma of dams, pups, and young adults. The recognition memory, locomotor function, and anxiety-like behavior of offspring were evaluated using behavioral tests. Endogenous cGP was detected in rat milk, and its concentration was higher during peak lactation compared with late lactation. Comparisons within control groups showed low endogenous IGF-1 and IGFBP-3 and high endogenous cGP concentrations in the plasma of male pups. The reduced IGFBP-3 and increased cGP may be a response to increase the bioavailability of IGF-1 during infancy. Exogenous cGP showed oral bioavailability and effective maternal-infantile transfer through milk. Maternally transferred cGP also led to improved recognition memory in the developing offspring, possibly through increased IGF-1 bioavailability, with no effect on locomotor activity and anxiety-like behavior. These results show that cGP is an essential endogenous peptide during early postnatal development as it improves the bioavailability of IGF-1 during infancy. Furthermore, maternal cGP supplementation offers an effective and natural route of administration for improving memory in the developing offspring.</description><subject>Animals</subject><subject>Anxiety</subject><subject>Bioavailability</subject><subject>Biological Availability</subject><subject>Breastfeeding &amp; lactation</subject><subject>Effectiveness</subject><subject>Exploratory Behavior - drug effects</subject><subject>Female</subject><subject>Glycine</subject><subject>Glycine - administration &amp; dosage</subject><subject>Glycine - pharmacology</subject><subject>Growth factors</subject><subject>Insulin-like growth factor I</subject><subject>Insulin-Like Growth Factor I - metabolism</subject><subject>Insulin-Like Growth Factor I - pharmacokinetics</subject><subject>Insulin-like growth factor-binding protein 3</subject><subject>Insulin-like growth factors</subject><subject>Juveniles</subject><subject>Lactation</subject><subject>Locomotor activity</subject><subject>Male</subject><subject>Maternal Nutritional Physiological Phenomena</subject><subject>Metabolites</subject><subject>Milk</subject><subject>Offspring</subject><subject>Peptides, Cyclic - administration &amp; dosage</subject><subject>Peptides, Cyclic - pharmacology</subject><subject>Postpartum period</subject><subject>Pregnancy</subject><subject>Prenatal Exposure Delayed Effects - metabolism</subject><subject>Prenatal Exposure Delayed Effects - psychology</subject><subject>Proline</subject><subject>Proline - administration &amp; dosage</subject><subject>Proline - pharmacology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Recognition</subject><subject>Recognition (Psychology) - drug effects</subject><subject>Young adults</subject><issn>0013-7227</issn><issn>1945-7170</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNkUtv1DAUhSMEotPCjjWyxAIWuNjxK1mWgQ6VBooQrCPHuSkuHju1k1b5IfxfHM0AEgKJ1X3o0_HxPUXxhJJTWlLyCvxpSajElFb1vWJFay6woorcL1aEUIZVWaqj4jil6zxyztnD4qhUTAhe01Xx_b0eIXrt3IzOup31NuUZOrSejbMGbdxsrAf8MQaXK7rwJoJOkHKXprzCW_sN0CaGu_ErOtdmDBFT9NoGfaut0611dpyR9h36EG7B5f4TmHDl7WiDR9ajN5DXYbD-Cl32fRpi7h4VD3rtEjw-1JPiy_nbz-t3eHu5uVifbbERTI5Y8UpWQkspScV4XZc1oRTKupeiNrKVAK2otCC94JUpqaTAhGyFUn3L-04xdlK82OsOMdxMkMZmZ5MB57SHMKUmn1SxmnIm_gPNHirFGc_osz_Q6zAtN04No4woygRd3n65p0wMKUXom_z1nY5zQ0mzJNuAb5ZkmyXZjD89iE7tDrpf8M8oM_B8D4Rp-JcUPkixPQm-CybfG4YIKf12-VcDPwCJbLuF</recordid><startdate>201608</startdate><enddate>201608</enddate><creator>Singh-Mallah, Gagandeep</creator><creator>Singh, Kuljeet</creator><creator>McMahon, Christopher D</creator><creator>Harris, Paul</creator><creator>Brimble, Margaret A</creator><creator>Thorstensen, Eric</creator><creator>Guan, Jian</creator><general>Endocrine Society</general><general>Oxford University Press</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>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7T5</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope></search><sort><creationdate>201608</creationdate><title>Maternally Administered Cyclic Glycine-Proline Increases Insulin-Like Growth Factor-1 Bioavailability and Novelty Recognition in Developing Offspring</title><author>Singh-Mallah, Gagandeep ; Singh, Kuljeet ; McMahon, Christopher D ; Harris, Paul ; Brimble, Margaret A ; Thorstensen, Eric ; Guan, Jian</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c536t-748685a66608349929011e29f659c6b6eeb58a50f548c2161e356b577fb4fd733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Animals</topic><topic>Anxiety</topic><topic>Bioavailability</topic><topic>Biological Availability</topic><topic>Breastfeeding &amp; lactation</topic><topic>Effectiveness</topic><topic>Exploratory Behavior - drug effects</topic><topic>Female</topic><topic>Glycine</topic><topic>Glycine - administration &amp; dosage</topic><topic>Glycine - pharmacology</topic><topic>Growth factors</topic><topic>Insulin-like growth factor I</topic><topic>Insulin-Like Growth Factor I - metabolism</topic><topic>Insulin-Like Growth Factor I - pharmacokinetics</topic><topic>Insulin-like growth factor-binding protein 3</topic><topic>Insulin-like growth factors</topic><topic>Juveniles</topic><topic>Lactation</topic><topic>Locomotor activity</topic><topic>Male</topic><topic>Maternal Nutritional Physiological Phenomena</topic><topic>Metabolites</topic><topic>Milk</topic><topic>Offspring</topic><topic>Peptides, Cyclic - administration &amp; dosage</topic><topic>Peptides, Cyclic - pharmacology</topic><topic>Postpartum period</topic><topic>Pregnancy</topic><topic>Prenatal Exposure Delayed Effects - metabolism</topic><topic>Prenatal Exposure Delayed Effects - psychology</topic><topic>Proline</topic><topic>Proline - administration &amp; dosage</topic><topic>Proline - pharmacology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Recognition</topic><topic>Recognition (Psychology) - drug effects</topic><topic>Young adults</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Singh-Mallah, Gagandeep</creatorcontrib><creatorcontrib>Singh, Kuljeet</creatorcontrib><creatorcontrib>McMahon, Christopher D</creatorcontrib><creatorcontrib>Harris, Paul</creatorcontrib><creatorcontrib>Brimble, Margaret A</creatorcontrib><creatorcontrib>Thorstensen, Eric</creatorcontrib><creatorcontrib>Guan, Jian</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Endocrinology (Philadelphia)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Singh-Mallah, Gagandeep</au><au>Singh, Kuljeet</au><au>McMahon, Christopher D</au><au>Harris, Paul</au><au>Brimble, Margaret A</au><au>Thorstensen, Eric</au><au>Guan, Jian</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Maternally Administered Cyclic Glycine-Proline Increases Insulin-Like Growth Factor-1 Bioavailability and Novelty Recognition in Developing Offspring</atitle><jtitle>Endocrinology (Philadelphia)</jtitle><addtitle>Endocrinology</addtitle><date>2016-08</date><risdate>2016</risdate><volume>157</volume><issue>8</issue><spage>3130</spage><epage>3139</epage><pages>3130-3139</pages><issn>0013-7227</issn><eissn>1945-7170</eissn><abstract>Cyclic glycine-proline (cGP), a metabolite of IGF-1, is an endogenous neuropeptide that improves memory in adult rats. The presence and concentrations of endogenous cGP, and its association with IGF-1 and IGF binding protein-3 (IGFBP-3) in rat milk and plasma, were evaluated during postnatal development. Maternal-infantile transfer of cGP during lactation and its efficacy on the memory of developing offspring were also investigated. Dams were gavaged with either cGP (3 mg/kg) or saline daily from postnatal days 8–22. Concentrations of cGP were measured in dams' milk, and concentrations of cGP, IGF-1, and IGFBP-3 were measured in the plasma of dams, pups, and young adults. The recognition memory, locomotor function, and anxiety-like behavior of offspring were evaluated using behavioral tests. Endogenous cGP was detected in rat milk, and its concentration was higher during peak lactation compared with late lactation. Comparisons within control groups showed low endogenous IGF-1 and IGFBP-3 and high endogenous cGP concentrations in the plasma of male pups. The reduced IGFBP-3 and increased cGP may be a response to increase the bioavailability of IGF-1 during infancy. Exogenous cGP showed oral bioavailability and effective maternal-infantile transfer through milk. Maternally transferred cGP also led to improved recognition memory in the developing offspring, possibly through increased IGF-1 bioavailability, with no effect on locomotor activity and anxiety-like behavior. These results show that cGP is an essential endogenous peptide during early postnatal development as it improves the bioavailability of IGF-1 during infancy. Furthermore, maternal cGP supplementation offers an effective and natural route of administration for improving memory in the developing offspring.</abstract><cop>United States</cop><pub>Endocrine Society</pub><pmid>27355491</pmid><doi>10.1210/en.2016-1189</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0013-7227
ispartof Endocrinology (Philadelphia), 2016-08, Vol.157 (8), p.3130-3139
issn 0013-7227
1945-7170
language eng
recordid cdi_proquest_miscellaneous_1897391435
source Oxford Journals Online
subjects Animals
Anxiety
Bioavailability
Biological Availability
Breastfeeding & lactation
Effectiveness
Exploratory Behavior - drug effects
Female
Glycine
Glycine - administration & dosage
Glycine - pharmacology
Growth factors
Insulin-like growth factor I
Insulin-Like Growth Factor I - metabolism
Insulin-Like Growth Factor I - pharmacokinetics
Insulin-like growth factor-binding protein 3
Insulin-like growth factors
Juveniles
Lactation
Locomotor activity
Male
Maternal Nutritional Physiological Phenomena
Metabolites
Milk
Offspring
Peptides, Cyclic - administration & dosage
Peptides, Cyclic - pharmacology
Postpartum period
Pregnancy
Prenatal Exposure Delayed Effects - metabolism
Prenatal Exposure Delayed Effects - psychology
Proline
Proline - administration & dosage
Proline - pharmacology
Rats
Rats, Sprague-Dawley
Recognition
Recognition (Psychology) - drug effects
Young adults
title Maternally Administered Cyclic Glycine-Proline Increases Insulin-Like Growth Factor-1 Bioavailability and Novelty Recognition in Developing Offspring
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-01T12%3A45%3A53IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Maternally%20Administered%20Cyclic%20Glycine-Proline%20Increases%20Insulin-Like%20Growth%20Factor-1%20Bioavailability%20and%20Novelty%20Recognition%20in%20Developing%20Offspring&rft.jtitle=Endocrinology%20(Philadelphia)&rft.au=Singh-Mallah,%20Gagandeep&rft.date=2016-08&rft.volume=157&rft.issue=8&rft.spage=3130&rft.epage=3139&rft.pages=3130-3139&rft.issn=0013-7227&rft.eissn=1945-7170&rft_id=info:doi/10.1210/en.2016-1189&rft_dat=%3Cproquest_cross%3E1808387434%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c536t-748685a66608349929011e29f659c6b6eeb58a50f548c2161e356b577fb4fd733%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=3130713513&rft_id=info:pmid/27355491&rft_oup_id=10.1210/en.2016-1189&rfr_iscdi=true