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spelling paper:paper_09538194_v16_n8_p704_Saravia2023-06-08T15:55:32Z Oestradiol restores cell proliferation in dentate gyrus and subventricular zone of streptozotocin-diabetic mice Adult neurogenesis Bromodeoxyuridine Hippocampus Oestrogens Type 1 diabetes broxuridine estradiol animal model animal tissue article brain region brain tissue cell cycle S phase cell labeling cell proliferation controlled study diabetes mellitus diabetic neuropathy drug mechanism estrogen therapy hippocampus hormone action hyperglycemia insulin dependent diabetes mellitus male mouse nerve cell plasticity nervous system development neuroprotection nonhuman priority journal streptozocin diabetes Animals Blood Glucose Bromodeoxyuridine Cell Division Dentate Gyrus Diabetes Mellitus, Experimental Estradiol Immunohistochemistry Lateral Ventricles Male Mice Mice, Inbred C57BL Neurons Stem Cells Type 1 diabetes mellitus correlates with several brain disturbances, including hypersensitivity to stress, cognitive impairment, increased risk of stroke and dementia. Within the central nervous system, the hippocampus is considered a special target for alterations associated with diabetes. Neurogenesis is a plastic event restricted to few adult brain areas: the subgranular zone of the dentate gyrus and the subventricular zone (SVZ). First, we studied the ability for neurogenesis in the dentate gyrus and SVZ of chronic diabetic mice induced by streptozotocin (STZ). Using bromodeoxyuridine (BrdU) labelling of cells in the S-phase, we observed a strong reduction in cell proliferation rate in both brain regions of diabetic mice killed 20 days after STZ administration. Second, because oestrogens are active neuroprotective agents, we investigated whether 17β-oestradiol (200 μg pellet implant in cholesterol during 10 days) restored brain cell proliferation in the diabetic mouse brain. Our results demonstrated a complete reversibility of dentate gyrus cell proliferation in oestrogen-treated diabetic mice. This plasticity change was not exclusive to the hippocampus because oestrogen treatment restored BrdU incorporation into newborn cells of the SVZ region of diabetic animals. Oestrogen treatment did not alter the hyperglycemic status of STZ-diabetic mice. Moreover, oestrogen did not modify BrdU incorporation in control animals. These data show that oestrogen treatment strongly stimulates brain neurogenesis of diabetic mice and open up new venues for understanding the potential neuroprotective role of steroid hormones in diabetic encephalopathy. © 2004 Blackwell Publishing Ltd. 2004 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09538194_v16_n8_p704_Saravia http://hdl.handle.net/20.500.12110/paper_09538194_v16_n8_p704_Saravia
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Adult neurogenesis
Bromodeoxyuridine
Hippocampus
Oestrogens
Type 1 diabetes
broxuridine
estradiol
animal model
animal tissue
article
brain region
brain tissue
cell cycle S phase
cell labeling
cell proliferation
controlled study
diabetes mellitus
diabetic neuropathy
drug mechanism
estrogen therapy
hippocampus
hormone action
hyperglycemia
insulin dependent diabetes mellitus
male
mouse
nerve cell plasticity
nervous system development
neuroprotection
nonhuman
priority journal
streptozocin diabetes
Animals
Blood Glucose
Bromodeoxyuridine
Cell Division
Dentate Gyrus
Diabetes Mellitus, Experimental
Estradiol
Immunohistochemistry
Lateral Ventricles
Male
Mice
Mice, Inbred C57BL
Neurons
Stem Cells
spellingShingle Adult neurogenesis
Bromodeoxyuridine
Hippocampus
Oestrogens
Type 1 diabetes
broxuridine
estradiol
animal model
animal tissue
article
brain region
brain tissue
cell cycle S phase
cell labeling
cell proliferation
controlled study
diabetes mellitus
diabetic neuropathy
drug mechanism
estrogen therapy
hippocampus
hormone action
hyperglycemia
insulin dependent diabetes mellitus
male
mouse
nerve cell plasticity
nervous system development
neuroprotection
nonhuman
priority journal
streptozocin diabetes
Animals
Blood Glucose
Bromodeoxyuridine
Cell Division
Dentate Gyrus
Diabetes Mellitus, Experimental
Estradiol
Immunohistochemistry
Lateral Ventricles
Male
Mice
Mice, Inbred C57BL
Neurons
Stem Cells
Oestradiol restores cell proliferation in dentate gyrus and subventricular zone of streptozotocin-diabetic mice
topic_facet Adult neurogenesis
Bromodeoxyuridine
Hippocampus
Oestrogens
Type 1 diabetes
broxuridine
estradiol
animal model
animal tissue
article
brain region
brain tissue
cell cycle S phase
cell labeling
cell proliferation
controlled study
diabetes mellitus
diabetic neuropathy
drug mechanism
estrogen therapy
hippocampus
hormone action
hyperglycemia
insulin dependent diabetes mellitus
male
mouse
nerve cell plasticity
nervous system development
neuroprotection
nonhuman
priority journal
streptozocin diabetes
Animals
Blood Glucose
Bromodeoxyuridine
Cell Division
Dentate Gyrus
Diabetes Mellitus, Experimental
Estradiol
Immunohistochemistry
Lateral Ventricles
Male
Mice
Mice, Inbred C57BL
Neurons
Stem Cells
description Type 1 diabetes mellitus correlates with several brain disturbances, including hypersensitivity to stress, cognitive impairment, increased risk of stroke and dementia. Within the central nervous system, the hippocampus is considered a special target for alterations associated with diabetes. Neurogenesis is a plastic event restricted to few adult brain areas: the subgranular zone of the dentate gyrus and the subventricular zone (SVZ). First, we studied the ability for neurogenesis in the dentate gyrus and SVZ of chronic diabetic mice induced by streptozotocin (STZ). Using bromodeoxyuridine (BrdU) labelling of cells in the S-phase, we observed a strong reduction in cell proliferation rate in both brain regions of diabetic mice killed 20 days after STZ administration. Second, because oestrogens are active neuroprotective agents, we investigated whether 17β-oestradiol (200 μg pellet implant in cholesterol during 10 days) restored brain cell proliferation in the diabetic mouse brain. Our results demonstrated a complete reversibility of dentate gyrus cell proliferation in oestrogen-treated diabetic mice. This plasticity change was not exclusive to the hippocampus because oestrogen treatment restored BrdU incorporation into newborn cells of the SVZ region of diabetic animals. Oestrogen treatment did not alter the hyperglycemic status of STZ-diabetic mice. Moreover, oestrogen did not modify BrdU incorporation in control animals. These data show that oestrogen treatment strongly stimulates brain neurogenesis of diabetic mice and open up new venues for understanding the potential neuroprotective role of steroid hormones in diabetic encephalopathy. © 2004 Blackwell Publishing Ltd.
title Oestradiol restores cell proliferation in dentate gyrus and subventricular zone of streptozotocin-diabetic mice
title_short Oestradiol restores cell proliferation in dentate gyrus and subventricular zone of streptozotocin-diabetic mice
title_full Oestradiol restores cell proliferation in dentate gyrus and subventricular zone of streptozotocin-diabetic mice
title_fullStr Oestradiol restores cell proliferation in dentate gyrus and subventricular zone of streptozotocin-diabetic mice
title_full_unstemmed Oestradiol restores cell proliferation in dentate gyrus and subventricular zone of streptozotocin-diabetic mice
title_sort oestradiol restores cell proliferation in dentate gyrus and subventricular zone of streptozotocin-diabetic mice
publishDate 2004
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09538194_v16_n8_p704_Saravia
http://hdl.handle.net/20.500.12110/paper_09538194_v16_n8_p704_Saravia
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