Treatment effects of Cardiotrophin-1 (CT-1) on streptozotocin-induced memory deficits in mice

Exp Gerontol. 2017 Jun:92:42-45. doi: 10.1016/j.exger.2017.03.007. Epub 2017 Mar 8.

Abstract

Increasing evidence has shown that diabetes-associated cognitive impairment is correlated with mitochondrial dysfunction and resultant synaptic injury as well as brain insulin resistance. Cardiotrophin-1 (CT-1), a regulator of energy metabolism, has been shown to exhibit impressive neuroprotective effects. In this study, we evaluated the effects of CT-1 on brain pathological features in intracerebroventrical-streptozotocin (ICV-STZ)-treated mouse model, and explored its potential mechanisms. STZ was injected twice (3mg/kg, ICV) on alternate days (day 1 and day 3) in mice. Daily treatment with CT-1 (1μg/day, ICV) starting from the first dose of STZ for 14days showed that CT-1 significantly improved learning and memory deficits, alleviated mitochondrial dysfunction, and increased synaptic density in the CA1 region of the hippocampus in ICV-STZ-treated mice. Moreover, CT-1 significantly enhanced insulin signaling pathway in the hippocampus of ICV-STZ-treated mice when compared with the control. However, all the protective effects including biochemistry, pathological changes and cognitive function could be blocked by an ICV injection of Compound C, a specific AMPK inhibitor. Taken together, these results suggested that CT-1 improves pathological changes and cognitive impairments via AMPK activation in ICV-STZ mice.

Keywords: AMPK; CT-1; Insulin signal; Mitochondrial dysfunction; Streptozotocin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • AMP-Activated Protein Kinases / antagonists & inhibitors
  • Animals
  • Brain / pathology*
  • Cognition / drug effects
  • Cognitive Dysfunction / drug therapy*
  • Cytokines / pharmacology*
  • Diabetes Mellitus, Experimental / complications*
  • Disease Models, Animal
  • Insulin / metabolism
  • Maze Learning / drug effects
  • Memory / drug effects
  • Memory Disorders / drug therapy*
  • Mice
  • Mice, Inbred C57BL
  • Neuroprotective Agents / pharmacology*
  • Signal Transduction
  • Streptozocin

Substances

  • Cytokines
  • Insulin
  • Neuroprotective Agents
  • Streptozocin
  • cardiotrophin 1
  • AMP-Activated Protein Kinases