Constipation in Tg2576 mice model for Alzheimer's disease associated with dysregulation of mechanism involving the mAChR signaling pathway and ER stress response

PLoS One. 2019 Apr 12;14(4):e0215205. doi: 10.1371/journal.pone.0215205. eCollection 2019.

Abstract

Background: Although constipation has been researched in various neurological disorders, including Parkinson's disease (PD) and spinal cord injury (SCI), the pathological mechanism of this symptom has not been investigated in Alzheimer's disease (AD) associated with loss of nerve cells in the brain. This study was undertaken to gain scientific evidences for a molecular correlation between constipation and AD.

Methods: To understand the etiology, we measured alterations in various constipation parameters, muscarinic acetylcholine receptors (mAChRs) and endoplasmic reticulum (ER) stress response, in 11-month-old Tg2576 transgenic (Tg) mice showing AD-like phenotypes.

Results: A high accumulation of amyloid beta (Aβ) peptides, a key marker of AD pathology, were detected in the cortex and hippocampus of Tg mice. Furthermore, significant alterations were observed in various constipation parameters including stool weight, histological structure, cytological structure and mucin secretion in Tg2576 mice. Moreover, M2 and M3 expression and the downstream signaling pathways of mAChRs were decreased in the Tg group, as compared with non-Tg (NT) group. Furthermore, activation of ER stress proteins and alteration of ER structure were also detected in the same group.

Conclusions: The results of the present study provide strong novel evidence that the neuropathological constipation detected in Tg2576 mice is linked to dysregulation of the mAChR signaling pathways and ER stress response.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / complications*
  • Alzheimer Disease / genetics
  • Alzheimer Disease / metabolism*
  • Amyloid beta-Peptides / metabolism
  • Amyloid beta-Protein Precursor / genetics
  • Amyloid beta-Protein Precursor / metabolism
  • Animals
  • Brain / metabolism
  • Brain / pathology
  • Colon / pathology
  • Constipation / complications*
  • Constipation / genetics
  • Constipation / metabolism*
  • Disease Models, Animal
  • Endoplasmic Reticulum Stress*
  • Female
  • Humans
  • Male
  • Mice
  • Mice, Transgenic
  • Mucins / metabolism
  • Peptide Fragments / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Muscarinic / genetics
  • Receptors, Muscarinic / metabolism*
  • Signal Transduction

Substances

  • Amyloid beta-Peptides
  • Amyloid beta-Protein Precursor
  • Mucins
  • Peptide Fragments
  • RNA, Messenger
  • Receptors, Muscarinic
  • amyloid beta-protein (1-42)

Grants and funding

This research was supported by the Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education (2017R1D1A3B03032631), (2018R1A6A3A01011498). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.