The ketamine metabolite (2R,6R)-hydroxynorketamine rescues hippocampal mRNA translation, synaptic plasticity and memory in mouse models of Alzheimer's disease

Alzheimers Dement. 2024 Aug;20(8):5398-5410. doi: 10.1002/alz.14034. Epub 2024 Jun 27.

Abstract

Introduction: Impaired brain protein synthesis, synaptic plasticity, and memory are major hallmarks of Alzheimer's disease (AD). The ketamine metabolite (2R,6R)-hydroxynorketamine (HNK) has been shown to modulate protein synthesis, but its effects on memory in AD models remain elusive.

Methods: We investigated the effects of HNK on hippocampal protein synthesis, long-term potentiation (LTP), and memory in AD mouse models.

Results: HNK activated extracellular signal-regulated kinase 1/2 (ERK1/2), mechanistic target of rapamycin (mTOR), and p70S6 kinase 1 (S6K1)/ribosomal protein S6 signaling pathways. Treatment with HNK rescued hippocampal LTP and memory deficits in amyloid-β oligomers (AβO)-infused mice in an ERK1/2-dependent manner. Treatment with HNK further corrected aberrant transcription, LTP and memory in aged APP/PS1 mice.

Discussion: Our findings demonstrate that HNK induces signaling and transcriptional responses that correct synaptic and memory deficits in AD mice. These results raise the prospect that HNK could serve as a therapeutic approach in AD.

Highlights: The ketamine metabolite HNK activates hippocampal ERK/mTOR/S6 signaling pathways. HNK corrects hippocampal synaptic and memory defects in two mouse models of AD. Rescue of synaptic and memory impairments by HNK depends on ERK signaling. HNK corrects aberrant transcriptional signatures in APP/PS1 mice.

Keywords: Alzheimer's disease; hydroxynorketamine; mRNA translation; memory; synaptic plasticity.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, N.I.H., Extramural

MeSH terms

  • Alzheimer Disease* / drug therapy
  • Alzheimer Disease* / metabolism
  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Protein Precursor / genetics
  • Amyloid beta-Protein Precursor / metabolism
  • Animals
  • Disease Models, Animal*
  • Hippocampus* / drug effects
  • Hippocampus* / metabolism
  • Humans
  • Ketamine* / analogs & derivatives
  • Ketamine* / pharmacology
  • Long-Term Potentiation / drug effects
  • Male
  • Memory / drug effects
  • Memory Disorders / drug therapy
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic*
  • Neuronal Plasticity* / drug effects
  • Presenilin-1 / genetics
  • Protein Biosynthesis / drug effects
  • RNA, Messenger / metabolism
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Ketamine
  • Amyloid beta-Peptides
  • 6-hydroxynorketamine
  • TOR Serine-Threonine Kinases
  • RNA, Messenger
  • Amyloid beta-Protein Precursor
  • Presenilin-1