Estrous cycle and stress: influence of progesterone on the female brain

The female brain operates in a constantly changing chemical milieu caused by cyclical changes in gonadal hormones during the estrous cycle (menstrual cycle in women). Such hormones are highly lipophilic and pass readily from the plasma to the brain where they can influence neuronal function. It is b...

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Main Author: T.A. Lovick
Format: Article
Language:English
Published: Associação Brasileira de Divulgação Científica 2012-04-01
Series:Brazilian Journal of Medical and Biological Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012000400005&lng=en&tlng=en
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spelling doaj-d581caa1c938445db393765c62ae91d72020-11-25T00:05:43ZengAssociação Brasileira de Divulgação CientíficaBrazilian Journal of Medical and Biological Research1414-431X2012-04-01454314320S0100-879X2012000400005Estrous cycle and stress: influence of progesterone on the female brainT.A. Lovick0University of BirminghamThe female brain operates in a constantly changing chemical milieu caused by cyclical changes in gonadal hormones during the estrous cycle (menstrual cycle in women). Such hormones are highly lipophilic and pass readily from the plasma to the brain where they can influence neuronal function. It is becoming clear that the rapid reduction in peripheral circulating progesterone, which occurs during the late diestrous phase of the cycle, can trigger a withdrawal-like response, in which changes in GABA A receptor expression render hyper-responsive certain brain areas involved in processing responses to stressful stimuli. The periaqueductal gray matter (PAG) is recognised as an important region for integrating anxiety/defence responses. Withdrawal from progesterone, via actions of its neuroactive metabolite allopregnanolone, triggers up-regulation of extrasynaptic GABA A receptors on GABAergic neurons in the PAG. As a consequence, ongoing GABAergic tone on the output cells decreases, leading to an increase in functional excitability of the circuitry and enhanced responsiveness to stressful stimuli during the late diestrous phase. These changes during late diestrus could be prevented by short-term neurosteroid administration, timed to produce a more gradual fall in the peripheral concentration of allopregnanolone than the rapid decrease that occurs naturally, thus removing the trigger for the central withdrawal response.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012000400005&lng=en&tlng=enFemaleEstrous cycleStressAnxietyProgesteroneNeurosteroid replacement
collection DOAJ
language English
format Article
sources DOAJ
author T.A. Lovick
spellingShingle T.A. Lovick
Estrous cycle and stress: influence of progesterone on the female brain
Brazilian Journal of Medical and Biological Research
Female
Estrous cycle
Stress
Anxiety
Progesterone
Neurosteroid replacement
author_facet T.A. Lovick
author_sort T.A. Lovick
title Estrous cycle and stress: influence of progesterone on the female brain
title_short Estrous cycle and stress: influence of progesterone on the female brain
title_full Estrous cycle and stress: influence of progesterone on the female brain
title_fullStr Estrous cycle and stress: influence of progesterone on the female brain
title_full_unstemmed Estrous cycle and stress: influence of progesterone on the female brain
title_sort estrous cycle and stress: influence of progesterone on the female brain
publisher Associação Brasileira de Divulgação Científica
series Brazilian Journal of Medical and Biological Research
issn 1414-431X
publishDate 2012-04-01
description The female brain operates in a constantly changing chemical milieu caused by cyclical changes in gonadal hormones during the estrous cycle (menstrual cycle in women). Such hormones are highly lipophilic and pass readily from the plasma to the brain where they can influence neuronal function. It is becoming clear that the rapid reduction in peripheral circulating progesterone, which occurs during the late diestrous phase of the cycle, can trigger a withdrawal-like response, in which changes in GABA A receptor expression render hyper-responsive certain brain areas involved in processing responses to stressful stimuli. The periaqueductal gray matter (PAG) is recognised as an important region for integrating anxiety/defence responses. Withdrawal from progesterone, via actions of its neuroactive metabolite allopregnanolone, triggers up-regulation of extrasynaptic GABA A receptors on GABAergic neurons in the PAG. As a consequence, ongoing GABAergic tone on the output cells decreases, leading to an increase in functional excitability of the circuitry and enhanced responsiveness to stressful stimuli during the late diestrous phase. These changes during late diestrus could be prevented by short-term neurosteroid administration, timed to produce a more gradual fall in the peripheral concentration of allopregnanolone than the rapid decrease that occurs naturally, thus removing the trigger for the central withdrawal response.
topic Female
Estrous cycle
Stress
Anxiety
Progesterone
Neurosteroid replacement
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0100-879X2012000400005&lng=en&tlng=en
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