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Epipregnanolone as a Positive Modulator of GABA(A) Receptor in Rat Cerebellar and Hippocampus Neurons

Epipregnanolone (3β-hydroxy-5β-pregnan-20-one, Epi) is an endogenous steroid with important physiological effects and high affinity for GABA(A) receptors. The effect of Epi on GABA-induced chloride current (I(GABA)) in native neurons has hardly been studied. In this work, we studied the influence of...

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Detalles Bibliográficos
Autores principales: Bukanova, Julia, Solntseva, Elena, Kondratenko, Rodion, Kudova, Eva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8225200/
https://www.ncbi.nlm.nih.gov/pubmed/34074021
http://dx.doi.org/10.3390/biom11060791
Descripción
Sumario:Epipregnanolone (3β-hydroxy-5β-pregnan-20-one, Epi) is an endogenous steroid with important physiological effects and high affinity for GABA(A) receptors. The effect of Epi on GABA-induced chloride current (I(GABA)) in native neurons has hardly been studied. In this work, we studied the influence of Epi on the I(GABA) in the Purkinje cells of rat cerebellum and pyramidal neurons of rat hippocampus with the patch clamp technique. We showed that Epi is a positive modulator of the I(GABA) with EC(50) of 5.7 µM in Purkinje cells and 9.3 µM in hippocampal neurons. Epi-induced potentiation of the I(GABA) was more potent at low vs. high GABA concentrations. Isopregnanolone (3β-hydroxy-5α-pregnan-20-one, Iso) counteracted Epi, reducing its potentiating effect by 2–2.3 times. Flumazenil, a nonsteroidal GABA(A) receptor antagonist, does not affect the Epi-induced potentiation. Comparison of the potentiating effects of Epi and allopregnanolone (3α-hydroxy-5α-pregnan-20-one, ALLO) showed that ALLO is, at least, a four times more potent positive modulator than Epi. The combined application of ALLO and Epi showed that the effects of these two steroids are not additive. We conclude that Epi has a dual effect on the I(GABA) increasing the current in the control solution and decreasing the stimulatory effect of ALLO.