Midkine Is a Novel Regulator of Amphetamine-Induced Striatal Gliosis and Cognitive Impairment: Evidence for a Stimulus-Dependent Regulation of Neuroinflammation by Midkine

Mediators Inflamm. 2016:2016:9894504. doi: 10.1155/2016/9894504. Epub 2016 Dec 4.

Abstract

Midkine (MK) is a cytokine that modulates amphetamine-induced striatal astrogliosis, suggesting a possible role of MK in neuroinflammation induced by amphetamine. To test this hypothesis, we studied astrogliosis and microglial response induced by amphetamine (10 mg/kg i.p. four times, every 2 h) in different brain areas of MK-/- mice and wild type (WT) mice. We found that amphetamine-induced microgliosis and astrocytosis are enhanced in the striatum of MK-/- mice in a region-specific manner. Surprisingly, LPS-induced astrogliosis in the striatum was blocked in MK-/- mice. Since striatal neuroinflammation induced by amphetamine-type stimulants correlates with the cognitive deficits induced by these drugs, we also tested the long-term effects of periadolescent amphetamine treatment (3 mg/kg i.p. daily for 10 days) in a memory task in MK-/- and WT mice. Significant deficits in the Y-maze test were only observed in amphetamine-pretreated MK-/- mice. The data demonstrate for the first time that MK is a novel modulator of neuroinflammation depending on the inflammatory stimulus and the brain area considered. The data indicate that MK limits amphetamine-induced striatal neuroinflammation. In addition, our data demonstrate that periadolescent amphetamine treatment in mice results in transient disruption of learning and memory processes in absence of endogenous MK.

MeSH terms

  • Amphetamines / pharmacology
  • Animals
  • Behavior, Animal
  • Central Nervous System Stimulants / pharmacology
  • Cognition Disorders / chemically induced
  • Cognition Disorders / metabolism*
  • Cognitive Dysfunction / chemically induced
  • Corpus Striatum / drug effects
  • Corpus Striatum / metabolism*
  • Gliosis / metabolism
  • Hippocampus / drug effects
  • Hippocampus / metabolism
  • Inflammation
  • Intercellular Signaling Peptides and Proteins / genetics
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Male
  • Maze Learning
  • Mice
  • Mice, Knockout
  • Midkine

Substances

  • Amphetamines
  • Central Nervous System Stimulants
  • Intercellular Signaling Peptides and Proteins
  • Mdk protein, mouse
  • Midkine