Akt and AMPK activators rescue hyperexcitability in neurons from patients with bipolar disorder

EBioMedicine. 2024 Jun:104:105161. doi: 10.1016/j.ebiom.2024.105161. Epub 2024 May 20.

Abstract

Background: Bipolar disorder (BD) is a multifactorial psychiatric illness affecting ∼1% of the global adult population. Lithium (Li), is the most effective mood stabilizer for BD but works only for a subset of patients and its mechanism of action remains largely elusive.

Methods: In the present study, we used iPSC-derived neurons from patients with BD who are responsive (LR) or not (LNR) to lithium. Combined electrophysiology, calcium imaging, biochemistry, transcriptomics, and phosphoproteomics were employed to provide mechanistic insights into neuronal hyperactivity in BD, investigate Li's mode of action, and identify alternative treatment strategies.

Findings: We show a selective rescue of the neuronal hyperactivity phenotype by Li in LR neurons, correlated with changes to Na+ conductance. Whole transcriptome sequencing in BD neurons revealed altered gene expression pathways related to glutamate transmission, alterations in cell signalling and ion transport/channel activity. We found altered Akt signalling as a potential therapeutic effect of Li in LR neurons from patients with BD, and that Akt activation mimics Li effect in LR neurons. Furthermore, the increased neural network activity observed in both LR & LNR neurons from patients with BD were reversed by AMP-activated protein kinase (AMPK) activation.

Interpretation: These results suggest potential for new treatment strategies in BD, such as Akt activators in LR cases, and the use of AMPK activators for LNR patients with BD.

Funding: Supported by funding from ERA PerMed, Bell Brain Canada Mental Research Program and Brain & Behavior Research Foundation.

Keywords: Akt and AMPK pathways; Bipolar disorder; Lithium responsiveness; Phosphoproteomics; iPSC-derived neurons.

MeSH terms

  • AMP-Activated Protein Kinases* / metabolism
  • Bipolar Disorder* / drug therapy
  • Bipolar Disorder* / metabolism
  • Gene Expression Profiling
  • Humans
  • Induced Pluripotent Stem Cells* / cytology
  • Induced Pluripotent Stem Cells* / metabolism
  • Lithium / pharmacology
  • Lithium / therapeutic use
  • Neurons* / metabolism
  • Proto-Oncogene Proteins c-akt* / metabolism
  • Signal Transduction
  • Transcriptome

Substances

  • AMP-Activated Protein Kinases
  • Proto-Oncogene Proteins c-akt
  • Lithium