Global loss of acetylcholinesterase activity with mitochondrial complexes inhibition and inflammation in brain of hypercholesterolemic mice

Sci Rep. 2017 Dec 20;7(1):17922. doi: 10.1038/s41598-017-17911-z.

Abstract

There exists an intricate relationship between hypercholesterolemia (elevated plasma cholesterol) and brain functions. The present study aims to understand the impact of hypercholesterolemia on pathological consequences in mouse brain. A chronic mouse model of hypercholesterolemia was induced by giving high-cholesterol diet for 12 weeks. The hypercholesterolemic mice developed cognitive impairment as evident from object recognition memory test. Cholesterol accumulation was observed in four discrete brain regions, such as cortex, striatum, hippocampus and substantia nigra along with significantly damaged blood-brain barrier by hypercholesterolemia. The crucial finding is the loss of acetylcholinesterase activity with mitochondrial dysfunction globally in the brain of hypercholesterolemic mice, which is related to the levels of cholesterol. Moreover, the levels of hydroxyl radical were elevated in the regions of brain where the activity of mitochondrial complexes was found to be reduced. Intriguingly, elevations of inflammatory stress markers in the cholesterol-rich brain regions were observed. As cognitive impairment, diminished brain acetylcholinesterase activity, mitochondrial dysfunctions, and inflammation are the prima facie pathologies of neurodegenerative diseases, the findings impose hypercholesterolemia as potential risk factor towards brain dysfunction.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylcholinesterase / deficiency*
  • Animals
  • Blood-Brain Barrier / metabolism
  • Blood-Brain Barrier / pathology*
  • Brain / metabolism
  • Brain / pathology*
  • Cholesterol / metabolism
  • Disease Models, Animal
  • Electron Transport Chain Complex Proteins / antagonists & inhibitors*
  • Hypercholesterolemia / complications*
  • Hypercholesterolemia / physiopathology
  • Inflammation / etiology
  • Inflammation / metabolism
  • Inflammation / pathology*
  • Male
  • Mice
  • Mitochondria / metabolism
  • Mitochondria / pathology
  • Mitochondrial Proteins / antagonists & inhibitors*

Substances

  • Electron Transport Chain Complex Proteins
  • Mitochondrial Proteins
  • Cholesterol
  • Acetylcholinesterase