Chemokine CCL2 impairs spatial memory and cognition in rats via influencing inflammation, glutamate metabolism and apoptosis-associated genes expression- a potential mechanism for HIV-associated neurocognitive disorder

Life Sci. 2020 Aug 15:255:117828. doi: 10.1016/j.lfs.2020.117828. Epub 2020 May 23.

Abstract

Aims: To explore the role of chemokine CC motif ligand 2 (CCL2) in spatial memory and cognition impairment, and the underlying mechanisms focused on inflammatory, glutamate metabolistic and apoptotic- associated mRNA expression.

Materials and methods: Stereotaxic surgery was performed here to establish a rat model by bilateral intra-hippocampal injection of CCL2. Morris water maze (MWM) and Novel object recognition test (NORT) were used to assess the learning, memory and cognitive ability respectively. RT-PCR was used to detect the relative mRNA expression of inflammatory, glutamate metabolistic and apoptotic- associated indexes. Nissl and TUNEL staining were performed to observe the morphological changes of hippocampal CA1 zone and quantified the apoptosis of hippocampal neurons of CA1 zones respectively.

Key findings: We found CCL2 injured cognitive function in rats. Six days after CCL2 injection, we revealed the following obvious mRNA expression changes: (1) increasing of the neuroinflammatory cytokines IL-1β, CXCL-10, IL-6; (2) decreasing of the glutamate transporters GLT-1 and GLAST and increasing of PAG; (3) increasing of the apoptotic genes caspase-8, caspase-3 and Bax, while decreasing the anti-apoptotic gene Bcl-2. Further, Nissl staining and TUNEL confirmed the injury of the structure of hippocampal CA1 zones and the apoptosis of hippocampal neurons.

Significance: Our results indicated that CCL2 impaired spatial memory and cognition, the involving mechanisms may link to the up-regulation of mRNA expression of the three major pathological events: inflammation, excitotoxicity and neuronal apoptosis, which were involved in HIV-associated neurocognitive disorder (HAND). Taken together, these findings suggest a potential therapeutic strategy against CCL2.

Keywords: Apoptosis; CCL2; Cognition; Glutamate metabolism; Inflammation; Spatial memory.

MeSH terms

  • Animals
  • Apoptosis / physiology
  • Chemokine CCL2 / administration & dosage
  • Chemokine CCL2 / metabolism*
  • Cognition / physiology
  • Disease Models, Animal
  • Glutamic Acid / metabolism
  • HIV Infections / complications*
  • Hippocampus / pathology
  • Inflammation / pathology*
  • Male
  • Maze Learning / physiology
  • Memory Disorders / physiopathology*
  • Neurocognitive Disorders / physiopathology*
  • Neurocognitive Disorders / virology
  • Neurons / pathology
  • Rats
  • Rats, Sprague-Dawley
  • Spatial Memory / physiology

Substances

  • Ccl2 protein, rat
  • Chemokine CCL2
  • Glutamic Acid