c-Jun N-terminal Kinase 1 ablation protects against metabolic-induced hippocampal cognitive impairments

J Mol Med (Berl). 2019 Dec;97(12):1723-1733. doi: 10.1007/s00109-019-01856-z. Epub 2019 Dec 3.

Abstract

The development of metabolic alterations like insulin resistance has been associated with dysfunctions in mitochondrial oxidative capacity, induction of neuroinflammatory responses, and the appearance of cognitive impairments in the brain. The c-Jun N-terminal Kinase 1 (JNK1) is a potential key modulator of these mechanisms. The current study identifies a protective effect of whole-body JNK1 knockout in the presence of a high-fat diet (HFD). Specifically, the data suggest that mice missing JNK1 show increased insulin sensitivity and mitochondrial activity, as well as reduced body weight, and astrocyte and microglial reactivity. Finally, these animals are also protected against HFD-induced cognitive impairments as assessed through novel object recognition test, the observation of dendritic spines, and the levels of BDNF or other proteins like spinophilin and ARC. Thus, modulation of JNK1 activity seems like a promising approach for the design of therapies aimed at treating metabolic-induced cognitive impairments. KEY MESSAGES: JNK1 is a link between obesity/type 2 diabetes and cognitive loss Inhibition of JNK1 is neuroprotective JNK1 constitutes a therapeutic strategy for cognitive loss.

Keywords: Cognitive impairments; High-fat diet; c-Jun N-terminal Kinase 1.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Astrocytes / metabolism
  • Body Weight / genetics
  • Brain-Derived Neurotrophic Factor / metabolism
  • Cognitive Dysfunction / etiology*
  • Cognitive Dysfunction / genetics
  • Cognitive Dysfunction / metabolism
  • Dendritic Spines / genetics
  • Dendritic Spines / physiology
  • Diabetes Mellitus, Type 2 / complications*
  • Diabetes Mellitus, Type 2 / metabolism
  • Diet, High-Fat / adverse effects
  • Hippocampus / metabolism*
  • Insulin Resistance / genetics
  • Male
  • Memory and Learning Tests
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Microfilament Proteins / metabolism
  • Microglia / metabolism
  • Mitochondria / enzymology
  • Mitochondria / genetics
  • Mitochondria / metabolism*
  • Mitogen-Activated Protein Kinase 8 / genetics
  • Mitogen-Activated Protein Kinase 8 / metabolism*
  • Nerve Tissue Proteins / metabolism

Substances

  • Brain-Derived Neurotrophic Factor
  • Microfilament Proteins
  • Nerve Tissue Proteins
  • neurabin
  • Mitogen-Activated Protein Kinase 8