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A rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3D printing and further outcome assessments

A stable and reproducible rat injury model is not currently available to study central diabetes insipidus (CDI) and the neurohypophyseal system. In addition, a system is needed to assess the severity of CDI and measure the accompanying neurobiological alterations. In the present study, a 3D-printed...

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Autores principales: Feng, Zhanpeng, Ou, Yichao, Zhou, Mingfeng, Wu, Guangsen, Ma, Linzi, Bao, Yun, Qiu, Binghui, Qi, Songtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Association for Laboratory Animal Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083024/
https://www.ncbi.nlm.nih.gov/pubmed/29681579
http://dx.doi.org/10.1538/expanim.18-0014
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author Feng, Zhanpeng
Ou, Yichao
Zhou, Mingfeng
Wu, Guangsen
Ma, Linzi
Bao, Yun
Qiu, Binghui
Qi, Songtao
author_facet Feng, Zhanpeng
Ou, Yichao
Zhou, Mingfeng
Wu, Guangsen
Ma, Linzi
Bao, Yun
Qiu, Binghui
Qi, Songtao
author_sort Feng, Zhanpeng
collection PubMed
description A stable and reproducible rat injury model is not currently available to study central diabetes insipidus (CDI) and the neurohypophyseal system. In addition, a system is needed to assess the severity of CDI and measure the accompanying neurobiological alterations. In the present study, a 3D-printed lesion knife with a curved head was designed to fit into the stereotaxic instrument. The neuro-anatomical features of the brain injury were determined by in vivo magnetic resonance imaging (MRI) and arginine vasopressin (AVP) immunostaining on brain sections. Rats that underwent pituitary stalk electrical lesion (PEL) exhibited a tri-phasic pattern of CDI. MRI revealed that the hyperintenseT1-weighted signal of the pituitary stalk was interrupted, and the brain sections showed an enlarged end proximal to the injury site after PEL. In addition, the number of AVP-positive cells in supraoptic nucleus (SON) and paraventricular nucleus (PVN) decreased after PEL, which confirmed the success of the CDI model. Unlike hand-made tools, the 3D-printed lesion knives were stable and reproducible. Next, we used an ordinal clustering method for staging and the k-means’ clustering method to construct a CDI index to evaluate the severity and recovery of CDI that could be used in other multiple animals, even in clinical research. In conclusion, we established a standard PEL model with a 3D-printed knife tool and proposed a CDI index that will greatly facilitate further research on CDI.
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spelling pubmed-60830242018-08-13 A rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3D printing and further outcome assessments Feng, Zhanpeng Ou, Yichao Zhou, Mingfeng Wu, Guangsen Ma, Linzi Bao, Yun Qiu, Binghui Qi, Songtao Exp Anim Original A stable and reproducible rat injury model is not currently available to study central diabetes insipidus (CDI) and the neurohypophyseal system. In addition, a system is needed to assess the severity of CDI and measure the accompanying neurobiological alterations. In the present study, a 3D-printed lesion knife with a curved head was designed to fit into the stereotaxic instrument. The neuro-anatomical features of the brain injury were determined by in vivo magnetic resonance imaging (MRI) and arginine vasopressin (AVP) immunostaining on brain sections. Rats that underwent pituitary stalk electrical lesion (PEL) exhibited a tri-phasic pattern of CDI. MRI revealed that the hyperintenseT1-weighted signal of the pituitary stalk was interrupted, and the brain sections showed an enlarged end proximal to the injury site after PEL. In addition, the number of AVP-positive cells in supraoptic nucleus (SON) and paraventricular nucleus (PVN) decreased after PEL, which confirmed the success of the CDI model. Unlike hand-made tools, the 3D-printed lesion knives were stable and reproducible. Next, we used an ordinal clustering method for staging and the k-means’ clustering method to construct a CDI index to evaluate the severity and recovery of CDI that could be used in other multiple animals, even in clinical research. In conclusion, we established a standard PEL model with a 3D-printed knife tool and proposed a CDI index that will greatly facilitate further research on CDI. Japanese Association for Laboratory Animal Science 2018-04-20 2018 /pmc/articles/PMC6083024/ /pubmed/29681579 http://dx.doi.org/10.1538/expanim.18-0014 Text en ©2018 Japanese Association for Laboratory Animal Science This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (by-nc-nd) License. (CC-BY-NC-ND 4.0: https://creativecommons.org/licenses/by-nc-nd/4.0/)
spellingShingle Original
Feng, Zhanpeng
Ou, Yichao
Zhou, Mingfeng
Wu, Guangsen
Ma, Linzi
Bao, Yun
Qiu, Binghui
Qi, Songtao
A rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3D printing and further outcome assessments
title A rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3D printing and further outcome assessments
title_full A rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3D printing and further outcome assessments
title_fullStr A rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3D printing and further outcome assessments
title_full_unstemmed A rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3D printing and further outcome assessments
title_short A rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3D printing and further outcome assessments
title_sort rat model for pituitary stalk electric lesion-induced central diabetes insipidus: application of 3d printing and further outcome assessments
topic Original
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6083024/
https://www.ncbi.nlm.nih.gov/pubmed/29681579
http://dx.doi.org/10.1538/expanim.18-0014
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