Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected Rats

This study investigates the effects of intermittent overnight fasting in streptozotocin-induced diabetic rats (STZ rats). Over 30 days, groups of 5-6 control or STZ rats were allowed free food access, starved overnight, or exposed to a restricted food supply comparable to that ingested by the interm...

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Main Authors: Louiza Belkacemi, Ghalem Selselet-Attou, Emeline Hupkens, Evrard Nguidjoe, Karim Louchami, Abdullah Sener, Willy J. Malaisse
Format: Article
Language:English
Published: Wiley 2012-01-01
Series:International Journal of Endocrinology
Online Access:http://dx.doi.org/10.1155/2012/962012
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author Louiza Belkacemi
Ghalem Selselet-Attou
Emeline Hupkens
Evrard Nguidjoe
Karim Louchami
Abdullah Sener
Willy J. Malaisse
author_facet Louiza Belkacemi
Ghalem Selselet-Attou
Emeline Hupkens
Evrard Nguidjoe
Karim Louchami
Abdullah Sener
Willy J. Malaisse
author_sort Louiza Belkacemi
collection DOAJ
description This study investigates the effects of intermittent overnight fasting in streptozotocin-induced diabetic rats (STZ rats). Over 30 days, groups of 5-6 control or STZ rats were allowed free food access, starved overnight, or exposed to a restricted food supply comparable to that ingested by the intermittently fasting animals. Intermittent fasting improved glucose tolerance, increased plasma insulin, and lowered Homeostatis Model Assessment index. Caloric restriction failed to cause such beneficial effects. The β-cell mass, as well as individual β-cell and islet area, was higher in intermittently fasting than in nonfasting STZ rats, whilst the percentage of apoptotic β-cells appeared lower in the former than latter STZ rats. In the calorie-restricted STZ rats, comparable findings were restricted to individual islet area and percentage of apoptotic cells. Hence, it is proposed that intermittent fasting could represent a possible approach to prevent or minimize disturbances of glucose homeostasis in human subjects.
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language English
publishDate 2012-01-01
publisher Wiley
record_format Article
series International Journal of Endocrinology
spelling doaj-art-b87e352cb9ed4c4fb4977145f5aebc502025-02-03T01:12:00ZengWileyInternational Journal of Endocrinology1687-83371687-83452012-01-01201210.1155/2012/962012962012Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected RatsLouiza Belkacemi0Ghalem Selselet-Attou1Emeline Hupkens2Evrard Nguidjoe3Karim Louchami4Abdullah Sener5Willy J. Malaisse6Laboratoire de Technologie Alimentaire et Nutrition, Université de Mostaganem, 1070 Mostaganem, AlgeriaLaboratoire de Technologie Alimentaire et Nutrition, Université de Mostaganem, 1070 Mostaganem, AlgeriaLaboratory of Experimental Hormonology, Université Libre de Bruxelles, 808 Route de Lennik, 1070 Brussels, BelgiumLaboratory of Pharmacology, Université Libre de Bruxelles, 808 Route de Lennik, 1070 Brussels, BelgiumLaboratory of Experimental Hormonology, Université Libre de Bruxelles, 808 Route de Lennik, 1070 Brussels, BelgiumLaboratory of Experimental Hormonology, Université Libre de Bruxelles, 808 Route de Lennik, 1070 Brussels, BelgiumLaboratory of Experimental Hormonology, Université Libre de Bruxelles, 808 Route de Lennik, 1070 Brussels, BelgiumThis study investigates the effects of intermittent overnight fasting in streptozotocin-induced diabetic rats (STZ rats). Over 30 days, groups of 5-6 control or STZ rats were allowed free food access, starved overnight, or exposed to a restricted food supply comparable to that ingested by the intermittently fasting animals. Intermittent fasting improved glucose tolerance, increased plasma insulin, and lowered Homeostatis Model Assessment index. Caloric restriction failed to cause such beneficial effects. The β-cell mass, as well as individual β-cell and islet area, was higher in intermittently fasting than in nonfasting STZ rats, whilst the percentage of apoptotic β-cells appeared lower in the former than latter STZ rats. In the calorie-restricted STZ rats, comparable findings were restricted to individual islet area and percentage of apoptotic cells. Hence, it is proposed that intermittent fasting could represent a possible approach to prevent or minimize disturbances of glucose homeostasis in human subjects.http://dx.doi.org/10.1155/2012/962012
spellingShingle Louiza Belkacemi
Ghalem Selselet-Attou
Emeline Hupkens
Evrard Nguidjoe
Karim Louchami
Abdullah Sener
Willy J. Malaisse
Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected Rats
International Journal of Endocrinology
title Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected Rats
title_full Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected Rats
title_fullStr Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected Rats
title_full_unstemmed Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected Rats
title_short Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected Rats
title_sort intermittent fasting modulation of the diabetic syndrome in streptozotocin injected rats
url http://dx.doi.org/10.1155/2012/962012
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