4.7 Article

Endogenous neurosteroids pregnanolone and pregnanolone sulfate potentiate presynaptic glutamate release through distinct mechanisms

Journal

BRITISH JOURNAL OF PHARMACOLOGY
Volume 178, Issue 19, Pages 3888-3904

Publisher

WILEY
DOI: 10.1111/bph.15529

Keywords

glutamate; Munc13-1; neurosteroid; phorbol ester; pregnanolone; presynaptic

Funding

  1. BIOCEV-Biotechnology and Biomedicine Centre of the Academy of Sciences and Charles Univeristy in Vestec
  2. European Regional Development Fund [PharmaBrain CZ.02.1.01/0.0/0.0/16_025/0007444]
  3. Czech Science Foundation (Grantova agentura Ceske republiky) [16-03913Y]
  4. Research Project of the Czech Academy of Sciences (Akademieved Ceske republiky) [RVO: 61388963, RVO: 67985823]
  5. Technology Agency of the Czech Republic (Technologicka agentura Ceske republiky) [TN01000013]

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This study demonstrates a novel presynaptic effect of neurosteroids pregnanolone and pregnanolone sulfate in potentiating glutamate release, with the mechanism of pregnanolone partially overlapping with that of PDBu.
Background and Purpose Neurosteroids influence neuronal function and have multiple promising clinical applications. Direct modulation of postsynaptic neurotransmitter receptors by neurosteroids is well characterized, but presynaptic effects remain poorly understood. Here, we report presynaptic glutamate release potentiation by neurosteroids pregnanolone and pregnanolone sulfate and compare their mechanisms of action to phorbol 12,13-dibutyrate (PDBu), a mimic of the second messenger DAG. Experimental Approach We use whole-cell patch-clamp electrophysiology and pharmacology in rat hippocampal microisland cultures and total internal reflection fluorescence (TIRF) microscopy in HEK293 cells expressing GFP-tagged vesicle priming protein Munc13-1, to explore the mechanisms of neurosteroid presynaptic modulation. Key Results Pregnanolone sulfate and pregnanolone potentiate glutamate release downstream of presynaptic Ca2+ influx, resembling the action of a phorbol ester PDBu. PDBu partially occludes the effect of pregnanolone, but not of pregnanolone sulfate. Calphostin C, an inhibitor that disrupts DAG binding to its targets, reduces the effect PDBu and pregnanolone, but not of pregnanolone sulfate, suggesting that pregnanolone might interact with a well-known DAG/phorbol ester target Munc13-1. However, TIRF microscopy experiments found no evidence of pregnanolone-induced membrane translocation of GFP-tagged Munc13-1, suggesting that pregnanolone may regulate Munc13-1 indirectly or interact with other DAG targets. Conclusion and Implications We describe a novel presynaptic effect of neurosteroids pregnanolone and pregnanolone sulfate to potentiate glutamate release downstream of presynaptic Ca2+ influx. The mechanism of action of pregnanolone, but not of pregnanolone sulfate, partly overlaps with that of PDBu. Presynaptic effects of neurosteroids may contribute to their therapeutic potential in the treatment of disorders of the glutamate system.

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