Reduced hippocampal CA1 Ca2+-induced long-term potentiation is associated with age-dependent impairment of spatial learning

1995 ◽  
Vol 686 (1) ◽  
pp. 107-110 ◽  
Author(s):  
Giovanni Diana ◽  
Maria Rosaria Domenici ◽  
Arsenia Scotti de Carolis ◽  
Alberto Loizzo ◽  
Stefano Sagratella
Author(s):  
Alexander Popov ◽  
Alexey Brazhe ◽  
Pavel Denisov ◽  
Oksana Sutyagina ◽  
Natalia Lazareva ◽  
...  

Little is known about age-dependent changes in structure and function of astrocytes and of the impact of these into the cognitive decline in the senescent brain. The prevalent view on age-dependent increase in reactive astrogliosis and astrocytic hypertrophy requires scrutiny and detailed analysis. Using two-photon microscopy in conjunction with 3D reconstruction, Sholl and volume fraction analysis we demonstrate a significant reduction in the number and the length of astrocytic processes, in astrocytic territorial domains and in astrocyte-to-astrocyte coupling in the aged brain. Probing physiology of astrocytes with patch-clamp and Ca2+ imaging revealed deficits in K+ and glutamate clearance, and spatiotemporal reorganization of Ca2+ events in old astrocytes. These changes paralleled impaired synaptic long-term potentiation (LTP) in hippocampal CA1 in old mice. Our findings may explain astroglial mechanisms of age-dependent decline in learning and memory.


2003 ◽  
Vol 17 (2) ◽  
pp. 341-349 ◽  
Author(s):  
Takashi Okada ◽  
Nobuaki Yamada ◽  
Keisuke Tsuzuki ◽  
Hiroshi P. M. Horikawa ◽  
Kohichi Tanaka ◽  
...  

2010 ◽  
Vol 56 (1) ◽  
pp. 77-83 ◽  
Author(s):  
Daisuke Ibi ◽  
Atsumi Nitta ◽  
Kumiko Ishige ◽  
Xiaobo Cen ◽  
Tomohiro Ohtakara ◽  
...  

2002 ◽  
Vol 13 (10) ◽  
pp. 3696-3705 ◽  
Author(s):  
Chin-Hung Cheng ◽  
David Tai-Wai Yew ◽  
Hiu-Yee Kwan ◽  
Qing Zhou ◽  
Yu Huang ◽  
...  

CNG channels are cyclic nucleotide-gated Ca2+-permeable channels that are suggested to be involved in the activity-dependent alterations of synaptic strength that are thought to underlie information storage in the CNS. In this study, we isolated an endogenous RNA transcript antisense to CNGα1 mRNA. This transcript was capable of down-regulating the expression of sense CNGα1 in theXenopus oocyte expression system. RT-PCR, Northern blot, and in situ hybridization analyses showed that the transcript was coexpressed with CNGα1 mRNA in many regions of human brain, notably in those regions that were involved in long-term potentiation and long-term depression, such as hippocampal CA1 and CA3, dentate gyrus, and cerebellar Purkinje layer. Comparison of expression patterns between adult and fetal cerebral cortex revealed that there were concurrent developmental changes in the expression levels of anti-CNG1 and CNGα1. Treatment of human glioma cell T98 with thyroid hormone T3 caused a significant increase in anti-CNG1 expression and a parallel decrease in sense CNGα1 expression. These data suggest that the suppression of CNGα1 expression by anti-CNG1 may play an important role in neuronal functions, especially in synaptic plasticity and cortical development. Endogenous antisense RNA-mediated regulation may represent a new mechanism through which the activity of ion channels can be regulated in the human CNS.


Neuroscience ◽  
1996 ◽  
Vol 74 (2) ◽  
pp. 331-339 ◽  
Author(s):  
F.H Brucato ◽  
E.D Levin ◽  
D.D Mott ◽  
D.V Lewis ◽  
W.A Wilson ◽  
...  

1998 ◽  
Vol 812 (1-2) ◽  
pp. 209-215 ◽  
Author(s):  
Keith B Hoffman ◽  
Jason K Pinkstaff ◽  
Christine M Gall ◽  
Gary Lynch

1998 ◽  
Vol 251 (1) ◽  
pp. 41-44 ◽  
Author(s):  
G Richter-Levin ◽  
K.L Thomas ◽  
S.P Hunt ◽  
T.V.P Bliss

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