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spelling paper:paper_13895575_v12_n11_p1081_deNicola2023-06-08T16:13:09Z Neuroprotection and sex steroid hormones: Evidence of estradiol- mediated protection in hypertensive encephalopathy Estradiol Hippocampus Hypertension Hypothalamus Neuroprotection arginine aromatase brain derived neurotrophic factor broxuridine doublecortin estradiol estradiol receptor messenger RNA vasopressin vasopressin V1b receptor aging article astrocyte astrocytosis blood pressure brain cell dentate gyrus diabetes mellitus essential hypertension hippocampus human hypertension encephalopathy hypothalamus nerve cell nervous system development neuroprotection nonhuman protein expression spontaneously hypertensive rat Animals Blood Pressure Brain Estradiol Humans Hypertensive Encephalopathy Neuroprotective Agents Besides their effects on reproduction, estrogens exert neuroprotective effects for brain diseases. Thus, estrogens ameliorate the negative aspects of aging and age-associated diseases in the nervous system, including hypertension. Within the brain, the hippocampus is sensitive to the effects of hypertension, as exemplified in a genetic model, the spontaneously hypertensive rat (SHR). In the dentate gyrus of the hippocampus, SHR present decreased neurogenesis, astrogliosis, low expression of brain derived neurotrophic factor (BDNF), decreased number of neurons in the hilus and increased basal levels of the estrogen-synthesizing enzyme aromatase, with respect to the Wistar Kyoto (WKY) normotensive strain. In the hypothalamus, SHR show increased expression of the hypertensinogenic peptide arginine vasopressin (AVP) and its V1b receptor. From the therapeutic point of view, it was highly rewarding that estradiol treatment decreased blood pressure and attenuated brain abnormalities of SHR, rendering hypertension a suitable model to test estrogen neuroprotection. When estradiol treatment was given for 2 weeks, SHR normalized their faulty brain parameters. This was shown by the enhancement of neurogenesis in the dentate gyrus, according to increased bromodeoxyuridine incorporation and doublecortin labeling, decreased reactive astrogliosis, increased BDNF mRNA and protein expression in the dentate gyrus, increased neuronal number in the hilus of the dentate gyrus and a further hyperexpression of aromatase. The presence of estradiol receptors in hippocampus and hypothalamus suggests the possibility of direct effects of estradiol on brain cells. Successful neuroprotection produced by estradiol in hypertensive rats should encourage the treatment with non-feminizing estrogens and estrogen receptor modulators for age-associated diseases. © 2012 Bentham Science Publishers. 2012 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13895575_v12_n11_p1081_deNicola http://hdl.handle.net/20.500.12110/paper_13895575_v12_n11_p1081_deNicola
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Estradiol
Hippocampus
Hypertension
Hypothalamus
Neuroprotection
arginine
aromatase
brain derived neurotrophic factor
broxuridine
doublecortin
estradiol
estradiol receptor
messenger RNA
vasopressin
vasopressin V1b receptor
aging
article
astrocyte
astrocytosis
blood pressure
brain cell
dentate gyrus
diabetes mellitus
essential hypertension
hippocampus
human
hypertension encephalopathy
hypothalamus
nerve cell
nervous system development
neuroprotection
nonhuman
protein expression
spontaneously hypertensive rat
Animals
Blood Pressure
Brain
Estradiol
Humans
Hypertensive Encephalopathy
Neuroprotective Agents
spellingShingle Estradiol
Hippocampus
Hypertension
Hypothalamus
Neuroprotection
arginine
aromatase
brain derived neurotrophic factor
broxuridine
doublecortin
estradiol
estradiol receptor
messenger RNA
vasopressin
vasopressin V1b receptor
aging
article
astrocyte
astrocytosis
blood pressure
brain cell
dentate gyrus
diabetes mellitus
essential hypertension
hippocampus
human
hypertension encephalopathy
hypothalamus
nerve cell
nervous system development
neuroprotection
nonhuman
protein expression
spontaneously hypertensive rat
Animals
Blood Pressure
Brain
Estradiol
Humans
Hypertensive Encephalopathy
Neuroprotective Agents
Neuroprotection and sex steroid hormones: Evidence of estradiol- mediated protection in hypertensive encephalopathy
topic_facet Estradiol
Hippocampus
Hypertension
Hypothalamus
Neuroprotection
arginine
aromatase
brain derived neurotrophic factor
broxuridine
doublecortin
estradiol
estradiol receptor
messenger RNA
vasopressin
vasopressin V1b receptor
aging
article
astrocyte
astrocytosis
blood pressure
brain cell
dentate gyrus
diabetes mellitus
essential hypertension
hippocampus
human
hypertension encephalopathy
hypothalamus
nerve cell
nervous system development
neuroprotection
nonhuman
protein expression
spontaneously hypertensive rat
Animals
Blood Pressure
Brain
Estradiol
Humans
Hypertensive Encephalopathy
Neuroprotective Agents
description Besides their effects on reproduction, estrogens exert neuroprotective effects for brain diseases. Thus, estrogens ameliorate the negative aspects of aging and age-associated diseases in the nervous system, including hypertension. Within the brain, the hippocampus is sensitive to the effects of hypertension, as exemplified in a genetic model, the spontaneously hypertensive rat (SHR). In the dentate gyrus of the hippocampus, SHR present decreased neurogenesis, astrogliosis, low expression of brain derived neurotrophic factor (BDNF), decreased number of neurons in the hilus and increased basal levels of the estrogen-synthesizing enzyme aromatase, with respect to the Wistar Kyoto (WKY) normotensive strain. In the hypothalamus, SHR show increased expression of the hypertensinogenic peptide arginine vasopressin (AVP) and its V1b receptor. From the therapeutic point of view, it was highly rewarding that estradiol treatment decreased blood pressure and attenuated brain abnormalities of SHR, rendering hypertension a suitable model to test estrogen neuroprotection. When estradiol treatment was given for 2 weeks, SHR normalized their faulty brain parameters. This was shown by the enhancement of neurogenesis in the dentate gyrus, according to increased bromodeoxyuridine incorporation and doublecortin labeling, decreased reactive astrogliosis, increased BDNF mRNA and protein expression in the dentate gyrus, increased neuronal number in the hilus of the dentate gyrus and a further hyperexpression of aromatase. The presence of estradiol receptors in hippocampus and hypothalamus suggests the possibility of direct effects of estradiol on brain cells. Successful neuroprotection produced by estradiol in hypertensive rats should encourage the treatment with non-feminizing estrogens and estrogen receptor modulators for age-associated diseases. © 2012 Bentham Science Publishers.
title Neuroprotection and sex steroid hormones: Evidence of estradiol- mediated protection in hypertensive encephalopathy
title_short Neuroprotection and sex steroid hormones: Evidence of estradiol- mediated protection in hypertensive encephalopathy
title_full Neuroprotection and sex steroid hormones: Evidence of estradiol- mediated protection in hypertensive encephalopathy
title_fullStr Neuroprotection and sex steroid hormones: Evidence of estradiol- mediated protection in hypertensive encephalopathy
title_full_unstemmed Neuroprotection and sex steroid hormones: Evidence of estradiol- mediated protection in hypertensive encephalopathy
title_sort neuroprotection and sex steroid hormones: evidence of estradiol- mediated protection in hypertensive encephalopathy
publishDate 2012
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_13895575_v12_n11_p1081_deNicola
http://hdl.handle.net/20.500.12110/paper_13895575_v12_n11_p1081_deNicola
_version_ 1768542902577790976