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Assessment of Pharmacological Responses to an Anti-diabetic Drug in a New Obese Type 2 Diabetic Rat Model

INTRODUCTION: The number of diabetic patients has recently been increasing worldwide, and numerous anti-diabetic drugs have been developed to induce good glycemic control. In particular, metformin, which exhibits glucose-lowering effects by suppressing gluconeogenesis in the liver, is widely used as...

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Autores principales: Murai, Yasutaka, Ohta, Takeshi, Tadaki, Hironobu, Miyajima, Katsuhiro, Shinohara, Masami, Fatchiyah, Fatchiyah, Yamada, Takahisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Academy of Medical Sciences of Bosnia and Herzegovina 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764610/
https://www.ncbi.nlm.nih.gov/pubmed/29416195
http://dx.doi.org/10.5455/medarh.2017.71.380-384
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author Murai, Yasutaka
Ohta, Takeshi
Tadaki, Hironobu
Miyajima, Katsuhiro
Shinohara, Masami
Fatchiyah, Fatchiyah
Yamada, Takahisa
author_facet Murai, Yasutaka
Ohta, Takeshi
Tadaki, Hironobu
Miyajima, Katsuhiro
Shinohara, Masami
Fatchiyah, Fatchiyah
Yamada, Takahisa
author_sort Murai, Yasutaka
collection PubMed
description INTRODUCTION: The number of diabetic patients has recently been increasing worldwide, and numerous anti-diabetic drugs have been developed to induce good glycemic control. In particular, metformin, which exhibits glucose-lowering effects by suppressing gluconeogenesis in the liver, is widely used as a first line oral anti-diabetic drug for type 2 diabetes mellitus. MATERIAL AND METHODS: In this study, the pharmacological effects of metformin were investigated using female and male Spontaneously Diabetic Torii (SDT) fatty rats, a new obese type 2 diabetic model. RESULTS: Two experiments were performed: an assessment of repeated treatment with metformin in female SDT fatty rats 5 to 13 weeks of age (experiment 1), and an assessment of repeated treatment with metformin in male SDT fatty rats 6 to 10 weeks of age (experiment 2). In female SDT fatty rats, metformin treatment led to good glycemic control, increases in sensory nerve conduction velocity, and improvements in pancreatic abnormalities such as irregular boundaries and vacuole form of islets. In male SDT fatty rats, metformin decreased blood glucose levels 4 weeks after treatment. CONCLUSION: Metformin treatment led to maintained good glycemic control and improved neuropathy and pancreatic lesions in female SDT fatty rats. The SDT fatty rat is useful for the development of novel anti-diabetic agents that show potential to improve glucose metabolic disorders in the liver.
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spelling pubmed-57646102018-02-07 Assessment of Pharmacological Responses to an Anti-diabetic Drug in a New Obese Type 2 Diabetic Rat Model Murai, Yasutaka Ohta, Takeshi Tadaki, Hironobu Miyajima, Katsuhiro Shinohara, Masami Fatchiyah, Fatchiyah Yamada, Takahisa Med Arch Original Paper INTRODUCTION: The number of diabetic patients has recently been increasing worldwide, and numerous anti-diabetic drugs have been developed to induce good glycemic control. In particular, metformin, which exhibits glucose-lowering effects by suppressing gluconeogenesis in the liver, is widely used as a first line oral anti-diabetic drug for type 2 diabetes mellitus. MATERIAL AND METHODS: In this study, the pharmacological effects of metformin were investigated using female and male Spontaneously Diabetic Torii (SDT) fatty rats, a new obese type 2 diabetic model. RESULTS: Two experiments were performed: an assessment of repeated treatment with metformin in female SDT fatty rats 5 to 13 weeks of age (experiment 1), and an assessment of repeated treatment with metformin in male SDT fatty rats 6 to 10 weeks of age (experiment 2). In female SDT fatty rats, metformin treatment led to good glycemic control, increases in sensory nerve conduction velocity, and improvements in pancreatic abnormalities such as irregular boundaries and vacuole form of islets. In male SDT fatty rats, metformin decreased blood glucose levels 4 weeks after treatment. CONCLUSION: Metformin treatment led to maintained good glycemic control and improved neuropathy and pancreatic lesions in female SDT fatty rats. The SDT fatty rat is useful for the development of novel anti-diabetic agents that show potential to improve glucose metabolic disorders in the liver. Academy of Medical Sciences of Bosnia and Herzegovina 2017-12 /pmc/articles/PMC5764610/ /pubmed/29416195 http://dx.doi.org/10.5455/medarh.2017.71.380-384 Text en © 2017 Yasutaka Murai, Takeshi Ohta, Hironobu Tadaki, Katsuhiro Miyajima, Masami Shinohara, Fatchiyah Fatchiyah, Takahisa Yamada http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Murai, Yasutaka
Ohta, Takeshi
Tadaki, Hironobu
Miyajima, Katsuhiro
Shinohara, Masami
Fatchiyah, Fatchiyah
Yamada, Takahisa
Assessment of Pharmacological Responses to an Anti-diabetic Drug in a New Obese Type 2 Diabetic Rat Model
title Assessment of Pharmacological Responses to an Anti-diabetic Drug in a New Obese Type 2 Diabetic Rat Model
title_full Assessment of Pharmacological Responses to an Anti-diabetic Drug in a New Obese Type 2 Diabetic Rat Model
title_fullStr Assessment of Pharmacological Responses to an Anti-diabetic Drug in a New Obese Type 2 Diabetic Rat Model
title_full_unstemmed Assessment of Pharmacological Responses to an Anti-diabetic Drug in a New Obese Type 2 Diabetic Rat Model
title_short Assessment of Pharmacological Responses to an Anti-diabetic Drug in a New Obese Type 2 Diabetic Rat Model
title_sort assessment of pharmacological responses to an anti-diabetic drug in a new obese type 2 diabetic rat model
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5764610/
https://www.ncbi.nlm.nih.gov/pubmed/29416195
http://dx.doi.org/10.5455/medarh.2017.71.380-384
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