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Neurosteroids

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(New page: <StructureSection load='1ihi' size='340' side='right' caption='Caption for this structure' scene=''> This is a default text for your page '''Neurosteroids'''. Click above on '''edit this p...)
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<StructureSection load='1ihi' size='340' side='right' caption='Caption for this structure' scene=''>
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<StructureSection load='5o8f' size='340' side='right' caption='Structure of a chimaeric beta3-alpha5 GABAA receptor in complex with pregnanolone (based on [[5o8f]]) scene='89/896619/Cv/3'>
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This is a default text for your page '''Neurosteroids'''. Click above on '''edit this page''' to modify. Be careful with the &lt; and &gt; signs.
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Neurosteroids, also known as neuroactive steroids, are endogenous or exogenous steroids that rapidly alter neuronal excitability through interaction with ligand-gated ion channels and other cell surface receptors.
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You may include any references to papers as in: the use of JSmol in Proteopedia <ref>DOI 10.1002/ijch.201300024</ref> or to the article describing Jmol <ref>PMID:21638687</ref> to the rescue.
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== Function ==
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'''[[Inhibitory neurosteroids]]'''
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== Disease ==
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These neurosteroids exert inhibitory actions on neurotransmission. They act as positive allosteric modulators of the [[GABAA receptor]] (especially δ subunit-containing isoforms), and possess, in no particular order, antidepressant, anxiolytic, stress-reducing, rewarding, prosocial, antiaggressive, prosexual, sedative, pro-sleep, cognitive and memory-impairing, analgesic, anesthetic, anticonvulsant, neuroprotective, and neurogenic effects.
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== Relevance ==
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Major examples include <scene name='89/896619/Cv/7'>tetrahydrodeoxycorticosterone</scene> (THDOC; from [[5osb]]), the androstane 3α-androstanediol, the cholestane cholesterol and the pregnanes pregnanolone (eltanolone), allopregnanolone (3α,5α-THP).
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== Structural highlights ==
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'''[[Excitatory neurosteroids]]'''
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This is a sample scene created with SAT to <scene name="/12/3456/Sample/1">color</scene> by Group, and another to make <scene name="/12/3456/Sample/2">a transparent representation</scene> of the protein. You can make your own scenes on SAT starting from scratch or loading and editing one of these sample scenes.
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These neurosteroids have excitatory effects on neurotransmission. They act as potent negative allosteric modulators of the [[GABAA receptor]], weak positive allosteric modulators of the NMDA receptor, and/or agonists of the σ1 receptor, and mostly have antidepressant, anxiogenic, cognitive and memory-enhancing, convulsant, neuroprotective, and neurogenic effects. Major examples include the pregnanes pregnenolone sulfate (PS), epipregnanolone, and isopregnanolone (sepranolone), the androstanes dehydroepiandrosterone (DHEA; prasterone), and dehydroepiandrosterone sulfate (DHEA-S; prasterone sulfate), and the cholestane 24(S)-hydroxycholesterol (NMDA receptor-selective; very potent).
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*<scene name='89/896619/Cv/5'>Pregnenolone alone</scene>.
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*<scene name='89/896619/Cv/4'>Pregnanolone binds beta3-alpha5 GABAA receptor</scene> ([[5o8f]]).
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*<scene name='89/896619/Cv/6'>Pregnanolone binding site is situated between 2 monomers</scene>.
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'''Mixed'''
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Cholesterol: cholest-5-en-3β-ol – NMDA receptor positive allosteric modulator, possible GABAA receptor positive allosteric modulator, many other actions.
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Epipregnanolone sulfate: 5β-pregnan-3β-ol-20-one 3β-sulfate – GABAA and NMDA receptor negative allosteric modulator, Transient receptor potential cation channel subfamily M member 3 (TRPM3) agonist.
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'''[[Pheromones]]'''
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Pheromones are neurosteroids that influence brain activity, notably hypothalamic function, via activation of vomeronasal receptor cells.
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They include the androstanes androstadienol, androstadienone, androstenol ([[1xnx]]), and androstenone and the estrane estratetraenol.
</StructureSection>
</StructureSection>
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SEE ALSO:
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*[[Steroids]]
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*[[Lipid signaling]]
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== References ==
== References ==
<references/>
<references/>

Current revision

PDB ID 5o8f

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SEE ALSO:

References

Proteopedia Page Contributors and Editors (what is this?)

Alexander Berchansky

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