Literature DB >> 19075729

Neuroactive steroids as endogenous modulators of anxiety.

Daniela Eser1, Thomas C Baghai, Cornelius Schüle, Caroline Nothdurfter, Rainer Rupprecht.   

Abstract

In the past decades considerable evidence has emerged that certain so called neuroactive steroids not only act as transcription factors in the regulation of gene expression but may also alter neuronal excitability through interaction with specific neurotransmitter receptors such as gamma-aminobutyric acid type A (GABA(A)), N-methyl-D-aspartate (NMDA) and glutamate receptors. There is growing evidence that neuroactive steroids play an important role as endogenous modulators of neuronal function and behavioural processes and that alterations of endogenous neuroactive steroid concentrations may contribute to the pathophysiology of affective disorders. In view of their positive allosteric potential at GABA(A)-receptors, especially 3alpha-reduced neuroactive steroids have been suggested to play a major role in the pathophysiology of anxiety disorders. In panic disorder patients a dysequilibrium of neuroactive steroid composition has been observed, which may represent counterregulatory mechanisms against the occurrence of spontaneous panic attacks. Therefore, attenuation of neuroactive steroid concentrations either by synthetic derivates of neuroactive steroids or by modulation of endogenous neurosteroid synthesis might constitute a promising novel strategy for the treatment of anxiety disorders. In conclusion, neuroactive steroids are important endogenous modulators of depression and anxiety and may provide a basis for development of novel therapeutic agents in the treatment of affective disorders.

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Year:  2008        PMID: 19075729     DOI: 10.2174/138161208786848838

Source DB:  PubMed          Journal:  Curr Pharm Des        ISSN: 1381-6128            Impact factor:   3.116


  17 in total

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Review 2.  Neurosteroids: endogenous role in the human brain and therapeutic potentials.

Authors:  Doodipala Samba Reddy
Journal:  Prog Brain Res       Date:  2010       Impact factor: 2.453

3.  Inhibition of 5α-reductase attenuates behavioral effects of D1-, but not D2-like receptor agonists in C57BL/6 mice.

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4.  Chronic intermittent ethanol exposure during adolescence: effects on social behavior and ethanol sensitivity in adulthood.

Authors:  Elena I Varlinskaya; Eric Truxell; Linda P Spear
Journal:  Alcohol       Date:  2014-05-15       Impact factor: 2.405

Review 5.  Social consequences of ethanol: Impact of age, stress, and prior history of ethanol exposure.

Authors:  Elena I Varlinskaya; Linda P Spear
Journal:  Physiol Behav       Date:  2014-11-26

6.  Mechanisms responsible for progesterone's protection against lordosis-inhibiting effects of restraint II. Role of progesterone metabolites.

Authors:  Chandra Suma Johnson Miryala; James Hassell; Sarah Adams; Cindy Hiegel; Ndidi Uzor; Lynda Uphouse
Journal:  Horm Behav       Date:  2011-05-20       Impact factor: 3.587

7.  Effects of progesterone and testosterone on cocaine self-administration and cocaine discrimination by female rhesus monkeys.

Authors:  Nancy K Mello; Inge M Knudson; Maureen Kelly; Peter A Fivel; Jack H Mendelson
Journal:  Neuropsychopharmacology       Date:  2011-07-27       Impact factor: 7.853

8.  Allopregnanolone's attenuation of the lordosis-inhibiting effects of restraint is blocked by the antiprogestin, CDB-4124.

Authors:  Lynda Uphouse; Cindy Hiegel
Journal:  Pharmacol Biochem Behav       Date:  2014-03-18       Impact factor: 3.533

9.  An antiprogestin, CDB4124, blocks progesterone's attenuation of the negative effects of a mild stress on sexual behavior.

Authors:  Lynda Uphouse; Cindy Hiegel
Journal:  Behav Brain Res       Date:  2012-11-12       Impact factor: 3.332

10.  RU486 blocks effects of allopregnanolone on the response to restraint stress.

Authors:  Lynda Uphouse; Sarah Adams; Chandra Suma Johnson Miryala; James Hassell; Cindy Hiegel
Journal:  Pharmacol Biochem Behav       Date:  2012-10-06       Impact factor: 3.533

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