2016 Apr 28. pii: S0896-6273(16)30025-3. doi: 10.1016/j.neuron.2016.03.034.
[Epub ahead of print]
Stempel AV1, Stumpf A2, Zhang HY3, Özdoğan T2, Pannasch U2, Theis AK2, Otte DM4, Wojtalla A4, Rácz I4, Ponomarenko A5, Xi ZX3, Zimmer A4, Schmitz D6.
Abstract
Endocannabinoids (eCBs) exert major control over neuronal activity by activating cannabinoid receptors (CBRs). The functionality of the eCB system is primarily ascribed to the well-documented retrograde activation of presynaptic CB1Rs. We find that action potential-driven eCB release leads to a long-lasting membrane potential hyperpolarization in hippocampal principal cells that is independent of CB1Rs. The hyperpolarization, which is specific to CA3 and CA2 pyramidal cells (PCs), depends on the activation of neuronal CB2Rs, as shown by a combined pharmacogenetic and immunohistochemical approach. Upon activation, they modulate the activity of the sodium-bicarbonate co-transporter, leading to a hyperpolarization of the neuron. CB2R activation occurred in a purely self-regulatory manner, robustly altered the input/output function of CA3 PCs, and modulated gamma oscillations in vivo. To conclude, we describe a cell type-specific plasticity mechanism in the hippocampus that provides evidence for the neuronal expression of CB2Rs and emphasizes their importance in basic neuronal transmission.
Copyright © 2016 Elsevier Inc. All rights reserved.
Copyright © 2016 Elsevier Inc. All rights reserved.
- PMID:
- 27133464
- [PubMed – as supplied by publisher]