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A New Spontaneously Diabetic Non-obese Torii Rat Strain With Severe Ocular Complications

A new spontaneously diabetic strain of the Sprague-Dawley rat was established in 1997 and named the SDT (Spontaneously Diabetic Torii) rat. In this research, we investigated the characteristics of the disease condition in the SDT rats. The time of onset of glucosuria was different between male and f...

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Autores principales: Shinohara, Masami, Masuyama, Taku, Shoda, Toshiyuki, Takahashi, Tadakazu, Katsuda, Yoshiaki, Komeda, Kajuro, Kuroki, Masatoshi, Kakehashi, Akihiro, Kanazaw, Yasunori
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2000
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2477755/
https://www.ncbi.nlm.nih.gov/pubmed/11469401
http://dx.doi.org/10.1155/EDR.2000.89
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author Shinohara, Masami
Masuyama, Taku
Shoda, Toshiyuki
Takahashi, Tadakazu
Katsuda, Yoshiaki
Komeda, Kajuro
Kuroki, Masatoshi
Kakehashi, Akihiro
Kanazaw, Yasunori
author_facet Shinohara, Masami
Masuyama, Taku
Shoda, Toshiyuki
Takahashi, Tadakazu
Katsuda, Yoshiaki
Komeda, Kajuro
Kuroki, Masatoshi
Kakehashi, Akihiro
Kanazaw, Yasunori
author_sort Shinohara, Masami
collection PubMed
description A new spontaneously diabetic strain of the Sprague-Dawley rat was established in 1997 and named the SDT (Spontaneously Diabetic Torii) rat. In this research, we investigated the characteristics of the disease condition in the SDT rats. The time of onset of glucosuria was different between male and female SDT rats; glucosuria appeared at approximately 20 weeks of age in male rats and at approximately 45 weeks of age in female rats. A cumulative incidence of diabetes of 100% was noted by 40 weeks of age in male rats, while it was only 33.3% even by 65 weeks of age in female rats. The survival rate up to 65 weeks of age was 92.9% in male rats and 97.4% in female rats. Glucose intolerance was observed in male rats from 16 weeks of age. The clinical characteristics of the male SDT rats were (1) hyperglycemia and hypoinsulinemia (from 25 weeks of age); (2) long-term survival without insulin treatment; (3) hypertriglyceridemia (by 35 weeks of age); however, no obesity was noted in any of the male rats. The histopathological characteristics of the male rats with diabetes mellitus (DM) were (1) fibrosis of the pancreatic islets (by 25 weeks of age); (2) cataract (by 40 weeks of age); (3) tractional retinal detachment with fibrous proliferation (by 70 weeks of age) and (4) massive hemorrhaging in the anterior chamber (by 77 weeks of age). These clinical and histopathological characteristics of the disease in SDT rats resemble those of human Type 2 diabetes with insulin hyposecretion. In conclusion, SDT rat is considered to be a potentially useful model for studies of diabetic retinopathy encountered in humans.
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spelling pubmed-24777552008-08-18 A New Spontaneously Diabetic Non-obese Torii Rat Strain With Severe Ocular Complications Shinohara, Masami Masuyama, Taku Shoda, Toshiyuki Takahashi, Tadakazu Katsuda, Yoshiaki Komeda, Kajuro Kuroki, Masatoshi Kakehashi, Akihiro Kanazaw, Yasunori Int J Exp Diabetes Res Research Article A new spontaneously diabetic strain of the Sprague-Dawley rat was established in 1997 and named the SDT (Spontaneously Diabetic Torii) rat. In this research, we investigated the characteristics of the disease condition in the SDT rats. The time of onset of glucosuria was different between male and female SDT rats; glucosuria appeared at approximately 20 weeks of age in male rats and at approximately 45 weeks of age in female rats. A cumulative incidence of diabetes of 100% was noted by 40 weeks of age in male rats, while it was only 33.3% even by 65 weeks of age in female rats. The survival rate up to 65 weeks of age was 92.9% in male rats and 97.4% in female rats. Glucose intolerance was observed in male rats from 16 weeks of age. The clinical characteristics of the male SDT rats were (1) hyperglycemia and hypoinsulinemia (from 25 weeks of age); (2) long-term survival without insulin treatment; (3) hypertriglyceridemia (by 35 weeks of age); however, no obesity was noted in any of the male rats. The histopathological characteristics of the male rats with diabetes mellitus (DM) were (1) fibrosis of the pancreatic islets (by 25 weeks of age); (2) cataract (by 40 weeks of age); (3) tractional retinal detachment with fibrous proliferation (by 70 weeks of age) and (4) massive hemorrhaging in the anterior chamber (by 77 weeks of age). These clinical and histopathological characteristics of the disease in SDT rats resemble those of human Type 2 diabetes with insulin hyposecretion. In conclusion, SDT rat is considered to be a potentially useful model for studies of diabetic retinopathy encountered in humans. Hindawi Publishing Corporation 2000 /pmc/articles/PMC2477755/ /pubmed/11469401 http://dx.doi.org/10.1155/EDR.2000.89 Text en Copyright © 2000 Hindawi Publishing Corporation. http://creativecommons.org/licenses/by/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Shinohara, Masami
Masuyama, Taku
Shoda, Toshiyuki
Takahashi, Tadakazu
Katsuda, Yoshiaki
Komeda, Kajuro
Kuroki, Masatoshi
Kakehashi, Akihiro
Kanazaw, Yasunori
A New Spontaneously Diabetic Non-obese Torii Rat Strain With Severe Ocular Complications
title A New Spontaneously Diabetic Non-obese Torii Rat Strain With Severe Ocular Complications
title_full A New Spontaneously Diabetic Non-obese Torii Rat Strain With Severe Ocular Complications
title_fullStr A New Spontaneously Diabetic Non-obese Torii Rat Strain With Severe Ocular Complications
title_full_unstemmed A New Spontaneously Diabetic Non-obese Torii Rat Strain With Severe Ocular Complications
title_short A New Spontaneously Diabetic Non-obese Torii Rat Strain With Severe Ocular Complications
title_sort new spontaneously diabetic non-obese torii rat strain with severe ocular complications
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2477755/
https://www.ncbi.nlm.nih.gov/pubmed/11469401
http://dx.doi.org/10.1155/EDR.2000.89
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