Neonatal ethanol causes profound reduction of cholinergic cell number in the basal forebrain of adult animals

Alcohol ◽  
2021 ◽  
Vol 97 ◽  
pp. 1-11
Author(s):  
John F. Smiley ◽  
Cynthia Bleiwas ◽  
Stefanie Canals-Baker ◽  
Sharifa Z. Williams ◽  
Robert Sears ◽  
...  
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Kana Okada ◽  
Kayo Nishizawa ◽  
Tomoko Kobayashi ◽  
Shogo Sakata ◽  
Kouichi Hashimoto ◽  
...  

AbstractSocial behaviour is a complex construct that is reported to include several components of social approach, interaction and recognition memory. Alzheimer’s disease (AD) is mainly characterized by progressive dementia and is accompanied by cognitive impairments, including a decline in social ability. The cholinergic system is a potential constituent for the neural mechanisms underlying social behaviour, and impaired social ability in AD may have a cholinergic basis. However, the involvement of cholinergic function in social behaviour has not yet been fully understood. Here, we performed a selective elimination of cholinergic cell groups in the basal forebrain in mice to examine the role of cholinergic function in social interaction and social recognition memory by using the three-chamber test. Elimination of cholinergic neurons in the medial septum (MS) and vertical diagonal band of Broca (vDB) caused impairment in social interaction, whereas ablating cholinergic neurons in the nucleus basalis magnocellularis (NBM) impaired social recognition memory. These impairments were restored by treatment with cholinesterase inhibitors, leading to cholinergic system activation. Our findings indicate distinct roles of MS/vDB and NBM cholinergic neurons in social interaction and social recognition memory, suggesting that cholinergic dysfunction may explain social ability deficits associated with AD symptoms.


Neuroscience ◽  
2002 ◽  
Vol 115 (3) ◽  
pp. 815-827 ◽  
Author(s):  
E.S Tsai ◽  
S.J Haraldson ◽  
J Baratta ◽  
A.D Lander ◽  
J Yu ◽  
...  

Neuroscience ◽  
2001 ◽  
Vol 103 (4) ◽  
pp. 1025-1031 ◽  
Author(s):  
J.R Martı́nez-Morales ◽  
I López-Coviella ◽  
J.G Hernández-Jiménez ◽  
R Reyes ◽  
A.R Bello ◽  
...  

1986 ◽  
Vol 64 (3) ◽  
pp. 318-324 ◽  
Author(s):  
Pierre Etienne ◽  
Yves Robitaille ◽  
Serge Gauthier ◽  
N. P. V. Nair

All our advanced severe cases of Alzheimer's disease had dramatic cholinergic cell loss in the basal forebrain, even after correction for cell or nucleolus shrinkage. We examined the relation between cell loss in the various subdivisions of the nucleus basalis of Meynert and plaque counts in corresponding and noncorresponding projection areas. This relation was not interpretable because of the ambiguity in the data.


2020 ◽  
Author(s):  
Kana Okada ◽  
Kayo Nishizawa ◽  
Tomoko Kobayashi ◽  
Shogo Sakata ◽  
Kouichi Hashimoto ◽  
...  

Abstract Social behaviour is a complex construct that is reported to include several components of social approach, interaction and recognition memory. Alzheimer’s disease (AD) is mainly characterized by progressive dementia and is accompanied by cognitive impairments, including a decline in social ability. The cholinergic system is a potential constituent for the neural mechanisms underlying social behaviour, and impaired social ability in AD may have a cholinergic basis. However, the involvement of cholinergic function in social behaviour has not yet been fully understood. Here, we performed a selective elimination of cholinergic cell groups in the basal forebrain in mice to examine the role of cholinergic function in social interaction and social recognition memory by using the three-chamber test. Elimination of cholinergic neurons in the medial septum (MS) and vertical diagonal band of Broca (vDB) caused impairment in social interaction, whereas ablating cholinergic neurons in the nucleus basalis magnocellularis (NBM) impaired social recognition memory. These impairments were restored by treatment with cholinesterase inhibitors, leading to cholinergic system activation. Our findings indicate distinct roles of MS/vDB and NBM cholinergic neurons in social interaction and social recognition memory, suggesting that cholinergic dysfunction may explain social ability deficits associated with AD symptoms.


2000 ◽  
Vol 875 (1-2) ◽  
pp. 144-151 ◽  
Author(s):  
Ronald L Klein ◽  
Aaron C Hirko ◽  
Craig A Meyers ◽  
Jeremy R Grimes ◽  
Nicholas Muzyczka ◽  
...  

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