Formation of GABAA receptor complexes containing α1 and α5 subunits is paralleling a multiple T-maze learning task in mice

2016 ◽  
Vol 222 (1) ◽  
pp. 549-561 ◽  
Author(s):  
Maryam Ghafari ◽  
Soheil Keihan Falsafi ◽  
Edit Szodorai ◽  
Eun-Jung Kim ◽  
Lin Li ◽  
...  
2013 ◽  
Vol 714 (1-3) ◽  
pp. 249-253 ◽  
Author(s):  
Zhao-Lin Cai ◽  
Chun-Yang Wang ◽  
Zhong-Jiao Jiang ◽  
Hai-Hang Li ◽  
Wen-Xiao Liu ◽  
...  
Keyword(s):  

2003 ◽  
Vol 13 (1) ◽  
pp. 9-16
Author(s):  
Noah A. Russell ◽  
Arata Horii ◽  
Paul F. Smith ◽  
Cynthia L. Darlington ◽  
David K. Bilkey

In order to investigate whether bilateral peripheral vestibular lesions cause long-term impairment of spatial learning, rats were tested in a reference memory radial arm maze learning task at least 5 weeks following a bilateral labyrinthectomy (BL) or sham control lesion. All control rats reached criterion (i.e., 1 error or less, averaged across 7 trials for 3 consecutive days of training) but only 4 of the 8 BL rats had reached criterion by day 21 of the training sessions. The control rats reached criterion more quickly than the lesioned rats (Control, 7.0 ± 0.63 days, Lesioned, 15.8 ± 1.4 days, t 10 = 5.84, p < 0.0001). This difference resulted from the greater number of errors made by the BL animals. However, the latency to respond was comparable as a result of the increased locomotor activity of the BL group (i.e., ’hyperkinesis), and the overall rate of acquisition of the task, as indicated by analysis of the exponential decrease in errors over the entire training period, was not significantly different between the 2 groups. The results of this study demonstrate that BL in rats produces long-term changes in performance in a spatial reference memory task, which are not simply due to the inability to move but may relate to the way that the brain uses vestibular information to create spatial representations and determines behavioural strategies on the basis of these representations.


1995 ◽  
Vol 18 (4) ◽  
pp. 541-558 ◽  
Author(s):  
Alan D. Pickering ◽  
Amelia Díaz ◽  
Jeffrey A. Gray
Keyword(s):  

1987 ◽  
Vol 82 (1) ◽  
pp. 101-106 ◽  
Author(s):  
Jennifer Ong ◽  
David I.B. Kerr ◽  
Graham A.R. Johnston

1998 ◽  
Vol 14 (1-2) ◽  
pp. 209-221 ◽  
Author(s):  
Enrico Alleva ◽  
Judith Rankin ◽  
Daniela Santucci

Aluminum (Al) is one of the most abundant metals in the earth's crust, and humans can be exposed to it from several sources. It is present in food, water, pharmaceutical compounds, and in the environment, e.g., as a result of acid rain leaching it from the soil. Exposure to Al has recently been implicated in a number of human pathologies, but it has not yet been definitely proved that it plays a major causal role in any of them. In this paper we review the effects of developmental exposure of laboratory animals to Al salts as a model for human pathological conditions. The data presented show behavioral and neurochemical changes in the offspring of AL-exposed mouse dams during gestation, which include alterations in the pattern of ultrasonic vocalizations and a marked reduction in central nervous system (CNS) choline acetyltransferase activity. Prenatal Al also affects CNS cholinergic functions under Nerve Growth Factor (NGF) control, as shown by increased central NGF levels and impaired performances in a maze learning task in young-adult mice. The need for more detailed studies to evaluate the risks for humans associated with developmental exposure to Al, as well as the importance of using more than one strain of laboratory animal in the experimental design, is emphasized.


PLoS ONE ◽  
2014 ◽  
Vol 9 (2) ◽  
pp. e88456 ◽  
Author(s):  
Henrik Sindal Jensen ◽  
Kathryn Nichol ◽  
Deborah Lee ◽  
Bjarke Ebert

1989 ◽  
Vol 34 (2) ◽  
pp. 439-442 ◽  
Author(s):  
D.B. Gilbert ◽  
T.A. Patterson ◽  
S.P.R. Rose

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