4.7 Article

Induction of Anti-Hebbian LTP in CA1 Stratum Oriens Interneurons: Interactions between Group I Metabotropic Glutamate Receptors and M1 Muscarinic Receptors

Journal

JOURNAL OF NEUROSCIENCE
Volume 35, Issue 40, Pages 13542-13554

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.0956-15.2015

Keywords

hippocampus; interneuron; LTP; metabotropic glutamate receptors; muscarinic receptors

Categories

Funding

  1. INSERM
  2. UPMC
  3. ICM
  4. IHU
  5. medical Research Council
  6. Welcome Trust
  7. European Research council
  8. Medical Research Council [G0501424, G0802158, G0801316, G116/147, MR/L01095X/1, MR/K000608/1] Funding Source: researchfish
  9. Wellcome Trust [104033/Z/14/Z] Funding Source: researchfish
  10. MRC [G0802158, G0801316, G116/147, G0501424, MR/K000608/1, MR/L01095X/1] Funding Source: UKRI

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An anti-Hebbian form of LTP is observed at excitatory synapses made with some hippocampal interneurons. LTP induction is facilitated when postsynaptic interneurons are hyperpolarized, presumably because Ca2+ entry through Ca2+-permeable glutamate receptors is enhanced. The contribution of modulatory transmitters to anti-Hebbian LTP induction remains to be established. Activation of group I metabotropic receptors (mGluRs) is required for anti-Hebbian LTP induction in interneurons with cell bodies in the CA1 stratum oriens. This region receives a strong cholinergic innervation from the septum, and muscarinic acetylcholine receptors (mAChRs) share some signaling pathways and cooperate with mGluRs in the control of neuronal excitability. We therefore examined possible interactions between group I mGluRs and mAChRs in anti-Hebbian LTP at synapses which excite oriens interneurons in rat brain slices. We found that blockade of either group I mGluRs or M1 mAChRs prevented the induction of anti-Hebbian LTP by pairing presynaptic activity with postsynaptic hyperpolarization. Blocking either receptor also suppressed long-term effects of activation of the other G-protein coupled receptor on interneuron membrane potential. However, no crossed blockade was detected for mGluR or mAchR effects on interneuron after-burst potentials or on the frequency of miniature EPSPs. Paired recordings between pyramidal neurons and oriens interneurons were obtained to determine whether LTP could be induced without concurrent stimulation of cholinergic axons. Exogenous activation of mAChRs led to LTP, with changes in EPSP amplitude distributions consistent with a presynaptic locus of expression. LTP, however, required noninvasive presynaptic and postsynaptic recordings.

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