Substance P induces plasticity and synaptic tagging/capture in rat hippocampal area CA2

Proc Natl Acad Sci U S A. 2017 Oct 10;114(41):E8741-E8749. doi: 10.1073/pnas.1711267114. Epub 2017 Sep 25.

Abstract

The hippocampal area Cornu Ammonis (CA) CA2 is important for social interaction and is innervated by Substance P (SP)-expressing supramammillary (SuM) nucleus neurons. SP exerts neuromodulatory effects on pain processing and central synaptic transmission. Here we provide evidence that SP can induce a slowly developing NMDA receptor- and protein synthesis-dependent potentiation of synaptic transmission that can be induced not only at entorhinal cortical (EC)-CA2 synapses but also at long-term potentiation (LTP)-resistant Schaffer collateral (SC)-CA2 synapses. In addition, SP-induced potentiation of SC-CA2 synapses transforms a short-term potentiation of EC-CA2 synaptic transmission into LTP, consistent with the synaptic tagging and capture hypothesis. Interestingly, this SP-induced potentiation and associative interaction between the EC and SC inputs of CA2 neurons is independent of the GABAergic system. In addition, CaMKIV and PKMζ play a critical role in the SP-induced effects on SC-CA2 and EC-CA2 synapses. Thus, afferents from SuM neurons are ideally situated to prime CA2 synapses for the formation of long-lasting plasticity and associativity.

Keywords: CA2 region; Substance P; long-term potentiation; social memory; synaptic tagging.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CA2 Region, Hippocampal / drug effects
  • CA2 Region, Hippocampal / physiology*
  • Cells, Cultured
  • Electric Stimulation
  • Long-Term Potentiation
  • Neuronal Plasticity / drug effects
  • Neuronal Plasticity / physiology*
  • Neurons / cytology
  • Neurons / drug effects
  • Neurons / metabolism*
  • Rats
  • Substance P / pharmacology*
  • Synapses / drug effects
  • Synapses / physiology*
  • Synaptic Transmission / drug effects
  • Synaptic Transmission / physiology*

Substances

  • Substance P