Cargando…
Absence of a gestational diabetes phenotype in the LepRdb/+ mouse is independent of control strain, diet, misty allele, or parity
Treatment options for gestational diabetes (GDM) are limited. In order to better understand mechanisms and improve treatments, appropriate animal models of GDM are crucial. Heterozygous db mice (db/+) present with glucose intolerance, insulin resistance, and increased weight gain during, but not pri...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364537/ https://www.ncbi.nlm.nih.gov/pubmed/28338021 http://dx.doi.org/10.1038/srep45130 |
_version_ | 1782517339634270208 |
---|---|
author | Plows, Jasmine F. Yu, XinYang Broadhurst, Ric Vickers, Mark H. Tong, Chao Zhang, Hua Qi, HongBo Stanley, Joanna L. Baker, Philip N. |
author_facet | Plows, Jasmine F. Yu, XinYang Broadhurst, Ric Vickers, Mark H. Tong, Chao Zhang, Hua Qi, HongBo Stanley, Joanna L. Baker, Philip N. |
author_sort | Plows, Jasmine F. |
collection | PubMed |
description | Treatment options for gestational diabetes (GDM) are limited. In order to better understand mechanisms and improve treatments, appropriate animal models of GDM are crucial. Heterozygous db mice (db/+) present with glucose intolerance, insulin resistance, and increased weight gain during, but not prior to, pregnancy. This makes them an ideal model for GDM. However, several recent studies have reported an absence of GDM phenotype in their colony. We investigated several hypotheses for why the phenotype may be absent, with the aim of re-establishing it and preventing further resources being wasted on an ineffective model. Experiments were carried out across two laboratories in two countries (New Zealand and China), and were designed to assess type of control strain, diet, presence of the misty allele, and parity as potential contributors to the lost phenotype. While hyperleptinemia and pre-pregnancy weight gain were present in all db/+mice across the four studies, we found no consistent evidence of glucose intolerance or insulin resistance during pregnancy. In conclusion, we were unable to acquire the GDM phenotype in any of our experiments, and we recommend researchers do not use the db/+ mouse as a model of GDM unless they are certain the phenotype remains in their colony. |
format | Online Article Text |
id | pubmed-5364537 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53645372017-03-28 Absence of a gestational diabetes phenotype in the LepRdb/+ mouse is independent of control strain, diet, misty allele, or parity Plows, Jasmine F. Yu, XinYang Broadhurst, Ric Vickers, Mark H. Tong, Chao Zhang, Hua Qi, HongBo Stanley, Joanna L. Baker, Philip N. Sci Rep Article Treatment options for gestational diabetes (GDM) are limited. In order to better understand mechanisms and improve treatments, appropriate animal models of GDM are crucial. Heterozygous db mice (db/+) present with glucose intolerance, insulin resistance, and increased weight gain during, but not prior to, pregnancy. This makes them an ideal model for GDM. However, several recent studies have reported an absence of GDM phenotype in their colony. We investigated several hypotheses for why the phenotype may be absent, with the aim of re-establishing it and preventing further resources being wasted on an ineffective model. Experiments were carried out across two laboratories in two countries (New Zealand and China), and were designed to assess type of control strain, diet, presence of the misty allele, and parity as potential contributors to the lost phenotype. While hyperleptinemia and pre-pregnancy weight gain were present in all db/+mice across the four studies, we found no consistent evidence of glucose intolerance or insulin resistance during pregnancy. In conclusion, we were unable to acquire the GDM phenotype in any of our experiments, and we recommend researchers do not use the db/+ mouse as a model of GDM unless they are certain the phenotype remains in their colony. Nature Publishing Group 2017-03-24 /pmc/articles/PMC5364537/ /pubmed/28338021 http://dx.doi.org/10.1038/srep45130 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Plows, Jasmine F. Yu, XinYang Broadhurst, Ric Vickers, Mark H. Tong, Chao Zhang, Hua Qi, HongBo Stanley, Joanna L. Baker, Philip N. Absence of a gestational diabetes phenotype in the LepRdb/+ mouse is independent of control strain, diet, misty allele, or parity |
title | Absence of a gestational diabetes phenotype in the LepRdb/+ mouse is independent of control strain, diet, misty allele, or parity |
title_full | Absence of a gestational diabetes phenotype in the LepRdb/+ mouse is independent of control strain, diet, misty allele, or parity |
title_fullStr | Absence of a gestational diabetes phenotype in the LepRdb/+ mouse is independent of control strain, diet, misty allele, or parity |
title_full_unstemmed | Absence of a gestational diabetes phenotype in the LepRdb/+ mouse is independent of control strain, diet, misty allele, or parity |
title_short | Absence of a gestational diabetes phenotype in the LepRdb/+ mouse is independent of control strain, diet, misty allele, or parity |
title_sort | absence of a gestational diabetes phenotype in the leprdb/+ mouse is independent of control strain, diet, misty allele, or parity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5364537/ https://www.ncbi.nlm.nih.gov/pubmed/28338021 http://dx.doi.org/10.1038/srep45130 |
work_keys_str_mv | AT plowsjasminef absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity AT yuxinyang absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity AT broadhurstric absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity AT vickersmarkh absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity AT tongchao absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity AT zhanghua absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity AT qihongbo absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity AT stanleyjoannal absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity AT bakerphilipn absenceofagestationaldiabetesphenotypeintheleprdbmouseisindependentofcontrolstraindietmistyalleleorparity |