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dc.contributor.author |
Belkacemi, Louiza |
|
dc.contributor.author |
Selselet-Attou, Ghalem |
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dc.contributor.author |
Hupkens, Emeline |
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dc.contributor.author |
Nguidjoe, Evrard |
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dc.contributor.author |
Louchami, Karim |
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dc.contributor.author |
Sener, Abdullah |
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dc.contributor.author |
Malaisse, Willy J. |
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dc.date.accessioned |
2018-09-15T08:47:33Z |
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dc.date.available |
2018-09-15T08:47:33Z |
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dc.date.issued |
2012 |
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dc.identifier.uri |
http://hdl.handle.net/123456789/748 |
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dc.description.abstract |
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. |
en_US |
dc.language.iso |
en |
en_US |
dc.publisher |
International Journal of Endocrinology |
en_US |
dc.relation.ispartofseries |
Volume 2012, Article ID 962012; |
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dc.subject |
Intermittent Fasting, treptozotocin- diabetci rats, apoptosis, β-Cell Mass |
en_US |
dc.title |
Intermittent Fasting Modulation of the Diabetic Syndrome in Streptozotocin-Injected Rats |
en_US |
dc.type |
Article |
en_US |
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