Neurosteroids: Difference between revisions

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<StructureSection load='1ihi' size='340' side='right' caption='Caption for this structure' scene=''>
<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'>
Neurosteroids such as DHEA and allopregnanolone.
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.
 
'''[[Inhibitory neurosteroids]]'''
 
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.
 
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).
 
'''[[Excitatory neurosteroids]]'''
 
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).
*<scene name='89/896619/Cv/5'>Pregnenolone alone</scene>.
*<scene name='89/896619/Cv/4'>Pregnanolone binds beta3-alpha5 GABAA receptor</scene> ([[5o8f]]).
*<scene name='89/896619/Cv/6'>Pregnanolone binding site is situated between 2 monomers</scene>.
 
'''Mixed'''
 
Cholesterol: cholest-5-en-3β-ol – NMDA receptor positive allosteric modulator, possible GABAA receptor positive allosteric modulator, many other actions.
 
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.
 
'''[[Pheromones]]'''
 
Pheromones are neurosteroids that influence brain activity, notably hypothalamic function, via activation of vomeronasal receptor cells.
 
They include the androstanes androstadienol, androstadienone, androstenol ([[1xnx]]), and androstenone and the estrane estratetraenol.


</StructureSection>
</StructureSection>
SEE ALSO:
*[[Steroids]]
*[[Lipid signaling]]
== References ==
== References ==
<references/>
<references/>

Latest revision as of 11:39, 2 January 2022

Structure of a chimaeric beta3-alpha5 GABAA receptor in complex with pregnanolone (based on 5o8f) scene=

Drag the structure with the mouse to rotate

SEE ALSO:

References

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Alexander Berchansky