TY - JOUR
T1 - Gradual Cerebral Hypoperfusion Impairs Fear Conditioning and Object Recognition Learning and Memory in Mice
T2 - Potential Roles of Neurodegeneration and Cholinergic Dysfunction
AU - Mehla, Jogender
AU - Lacoursiere, Sean
AU - Stuart, Emily
AU - McDonald, Robert J.
AU - Mohajerani, Majid H.
N1 - Funding Information:
This work was supported by Natural Sciences and Engineering Research Council of Canada (NSERC)
Funding Information:
Discovery Grant #40352 and #06347 to MHM and RJM respectively, Campus Alberta for Innovation Program Chair (MHM), Alberta Alzheimer Research Program (MHM & RJM), Alzheimer Society of Canada (MHM & RJM), NSERC CREATE graduate scholarship (SL) and NSERC undergraduate student research award (ES). We thank Di Shao and Behroo Mirza Agha for animal breeding.
PY - 2018
Y1 - 2018
N2 - In the present study, male C57BL/6J mice were subjected to gradual cerebral hypoperfusion by implanting an ameroid constrictor (AC) on the left common carotid artery (CCA) and a stenosis on the right CCA. In the sham group, all surgical procedures were kept the same except no AC was implanted and stenosis was not performed. One month following the surgical procedures, fear conditioning and object recognition tests were conducted to evaluate learning and memory functions and motor functions were assessed using a balance beam test. At the experimental endpoint, mice were perfused and brains were collected for immunostaining and histology. Learning and memory as well as motor functions were significantly impaired in the hypoperfusion group. The immunoreactivity to choline acetyltransferase was decreased in dorsal striatum and basal forebrain of the hypoperfusion group indicating that cholinergic tone in these brain regions was compromised. In addition, an increased number of Fluoro-Jade positive neurons was also found in cerebral cortex, dorsal striatum and hippocampus indicating neurodegeneration in these brain regions. Based on this pattern of data, we argued that this mouse model would be a useful tool to investigate the therapeutic interventions for the treatment of vascular dementia. Additionally, this model could be employed to exploit the effect of microvascular occlusions on cognitive impairment in the absence and presence of Alzheimer's disease pathology.
AB - In the present study, male C57BL/6J mice were subjected to gradual cerebral hypoperfusion by implanting an ameroid constrictor (AC) on the left common carotid artery (CCA) and a stenosis on the right CCA. In the sham group, all surgical procedures were kept the same except no AC was implanted and stenosis was not performed. One month following the surgical procedures, fear conditioning and object recognition tests were conducted to evaluate learning and memory functions and motor functions were assessed using a balance beam test. At the experimental endpoint, mice were perfused and brains were collected for immunostaining and histology. Learning and memory as well as motor functions were significantly impaired in the hypoperfusion group. The immunoreactivity to choline acetyltransferase was decreased in dorsal striatum and basal forebrain of the hypoperfusion group indicating that cholinergic tone in these brain regions was compromised. In addition, an increased number of Fluoro-Jade positive neurons was also found in cerebral cortex, dorsal striatum and hippocampus indicating neurodegeneration in these brain regions. Based on this pattern of data, we argued that this mouse model would be a useful tool to investigate the therapeutic interventions for the treatment of vascular dementia. Additionally, this model could be employed to exploit the effect of microvascular occlusions on cognitive impairment in the absence and presence of Alzheimer's disease pathology.
KW - Ameroid constrictor
KW - balance beam test
KW - choline acetyltransferase
KW - fear conditioning test
KW - gradual hypoperfusion
KW - neurodegeneration
KW - novel object recognition test
KW - vascular dementia
UR - https://www.scopus.com/pages/publications/85036528435
U2 - 10.3233/JAD-170635
DO - 10.3233/JAD-170635
M3 - Article
C2 - 29154281
AN - SCOPUS:85036528435
SN - 1387-2877
VL - 61
SP - 283
EP - 293
JO - Journal of Alzheimer's Disease
JF - Journal of Alzheimer's Disease
IS - 1
ER -