<scp>D1</scp> / <scp>D5</scp> receptor activation promotes long‐term potentiation and synaptic tagging/capture in hippocampal area <scp>CA2</scp>

Hippocampal area CA2 plays an important role in social memory formation. However, CA2 is characterised by plasticity-resistant Schaffer Collateral-CA2 (SC-CA2) synapses and highly plastic entorhinal cortex-CA2 (EC-CA2) synapses. Despite abundant dopaminergic input, the relationship between dopamine signalling and area CA2 synaptic plasticity remains unexplored. Here, we show that SKF-38393-mediated dopamine D1-like receptor (dopamine D<sub>1</sub> and D<sub>5</sub> receptors (D1R and D5R)) activation differentially primes CA2 inputs in an N-methyl-D-aspartate receptor (NMDAR)- and protein synthesis-dependent manner. We defined an inverted U-shape relationship between SKF-38393 concentration and EC-CA2 potentiation. Additionally, we observed a priming effect on SC-CA2 plasticity with 50 μm SKF-38393, relieving plasticity resistance. We also demonstrated that this effect follows canonical protein kinase A (PKA) signalling. Collectively, our results show that D1R activation primes the CA2 for synaptic plasticity. Thus, we propose a link between neuropsychiatric diseases related to impaired dopamine transmission and deficits in hippocampus-dependent social memory.

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Publication Details

Journal
FEBS Journal
Published
2025-09-22
DOI
https://doi.org/10.1111/febs.70266
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
Field-Weighted Citation Impact
0.00

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article

D1 / D5 receptor activation promotes long‐term potentiation and synaptic tagging/capture in hippocampal area CA2

Kevin Chua, Sreedharan Sajikumar, Yee Song Chong
FEBS Journal
Neuroscience and Neuropharmacology Research
article

D1 / D5 receptor activation promotes long‐term potentiation and synaptic tagging/capture in hippocampal area CA2

Kevin Chua, Sreedharan Sajikumar, Yee Song Chong
article en

Abstract

Hippocampal area CA2 plays an important role in social memory formation. However, CA2 is characterised by plasticity-resistant Schaffer Collateral-CA2 (SC-CA2) synapses and highly plastic entorhinal cortex-CA2 (EC-CA2) synapses. Despite abundant dopaminergic input, the relationship between dopamine signalling and area CA2 synaptic plasticity remains unexplored. Here, we show that SKF-38393-mediated dopamine D1-like receptor (dopamine D<sub>1</sub> and D<sub>5</sub> receptors (D1R and D5R)) activation differentially primes CA2 inputs in an N-methyl-D-aspartate receptor (NMDAR)- and protein synthesis-dependent manner. We defined an inverted U-shape relationship between SKF-38393 concentration and EC-CA2 potentiation. Additionally, we observed a priming effect on SC-CA2 plasticity with 50 μm SKF-38393, relieving plasticity resistance. We also demonstrated that this effect follows canonical protein kinase A (PKA) signalling. Collectively, our results show that D1R activation primes the CA2 for synaptic plasticity. Thus, we propose a link between neuropsychiatric diseases related to impaired dopamine transmission and deficits in hippocampus-dependent social memory.

FEBS JournalVol. 293(3)
National University of Singapore (SG), National Neuroscience Institute (SG), National University Health System (SG)
National University Health System
Openalex Percentile: Top 72%
Neuroscience and Neuropharmacology Research
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