Title of article :
Human Neural Stem Cells Overexpressing Choline Acetyltransferase Restore Unconditioned Fear in Rats with Amygdala Injury
Author/Authors :
Shin, Kyungha College of Veterinary Medicine - Chungbuk National University, Republic of Korea , Cha, Yeseul College of Veterinary Medicine - Chungbuk National University, Republic of Korea , Sei Kim, Kwang College of Veterinary Medicine - Chungbuk National University, Republic of Korea , Choi, Ehn-Kyoung College of Veterinary Medicine - Chungbuk National University, Republic of Korea , Choi, Youngjin College of Veterinary Medicine - Chungbuk National University, Republic of Korea , Guo, Haiyu College of Veterinary Medicine - Chungbuk National University, Republic of Korea , Ban, Young-Hwan College of Veterinary Medicine - Chungbuk National University, Republic of Korea , Kim, Jong-Choon College of Veterinary Medicine - Chonnam National University, Republic of Korea , Park, Dongsun College of Veterinary Medicine - Chungbuk National University, Republic of Korea , Kim, Yun-Bae College of Veterinary Medicine - Chungbuk National University, Republic of Korea
Pages :
9
From page :
1
To page :
9
Abstract :
Amygdala is involved in the fear memory that recognizes certain environmental cues predicting threatening events. Manipulation of neurotransmission within the amygdala affects the expression of conditioned and unconditioned emotional memories such as fear freezing behaviour. We previously demonstrated that F3.ChAT human neural stem cells (NSCs) overexpressing choline acetyltransferase (ChAT) improve cognitive function of Alzheimer's disease model rats with hippocampal or cholinergic nerve injuries by increasing acetylcholine (ACh) level. In the present study, we examined the effect of F3.ChAT cells on the deficit of unconditioned fear freezing. Rats given N-methyl-d-aspartate (NMDA) in their amygdala 2 weeks prior to cat odor exposure displayed very short resting (freezing) time compared to normal animals. NMDA induced neuronal degeneration in the amygdala, leading to a decreased ACh concentration in cerebrospinal fluid. However, intracerebroventricular transplantation of F3.ChAT cells attenuated amygdala lesions 4 weeks after transplantation. The transplanted cells were found in the NMDA-injury sites and produced ChAT protein. In addition, F3.ChAT-receiving rats recuperated freezing time staying remote from the cat odor source, according to the recovery of brain ACh concentration. The results indicate that human NSCs overexpressing ChAT may facilitate retrieval of unconditioned fear memory by increasing ACh level.
Keywords :
Human Neural Stem , Cells Overexpressing , Choline Acetyltransferase , Restore Unconditioned Fear , Rats , Amygdala Injury
Journal title :
Behavioural Neurology
Serial Year :
2016
Full Text URL :
Record number :
2604289
Link To Document :
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