Spatial working memory deficits are shown in the rat with abnormal hippocampal neurogenesis, but not in the rat with abnormal cerebellar neurogenesis

2009 ◽  
Vol 65 ◽  
pp. S235
Author(s):  
Kozo Sugioka ◽  
Tomiyoshi Setsu ◽  
Toshio Terashima
2002 ◽  
Vol 22 (13) ◽  
pp. 5619-5629 ◽  
Author(s):  
Sara B. Glickstein ◽  
Patrick R. Hof ◽  
Claudia Schmauss

1996 ◽  
Vol 40 (9) ◽  
pp. 930-932 ◽  
Author(s):  
Cameron Carter ◽  
Lynn Robertson ◽  
Thomas Nordahl ◽  
Marc Chaderjian ◽  
Louis Kraft ◽  
...  

2000 ◽  
Vol 41 (1) ◽  
pp. 277-278
Author(s):  
T. Sigmundsson ◽  
J. Suckling ◽  
K. Greenwood ◽  
E.T. Bullmore ◽  
M. Maier ◽  
...  

1999 ◽  
Vol 46 (3) ◽  
pp. 392-400 ◽  
Author(s):  
Sohee Park ◽  
Jörg Püschel ◽  
Barbara H Sauter ◽  
Markus Rentsch ◽  
Daniel Hell

1995 ◽  
Vol 15 (1-2) ◽  
pp. 111
Author(s):  
C.S. Carter ◽  
L.C. Robertson ◽  
T.E. Nordahl ◽  
M. Chaderjian ◽  
L. Kraft ◽  
...  

2020 ◽  
Vol 21 (9) ◽  
pp. 3365 ◽  
Author(s):  
Hang Thi Nguyet Pham ◽  
Hong Nguyen Tran ◽  
Phuong Thi Nguyen ◽  
Xoan Thi Le ◽  
Khoi Minh Nguyen ◽  
...  

Bacopa monnieri L. Wettst. (BM) is a botanical component of Ayurvedic medicines and of dietary supplements used worldwide for cognitive health and function. We previously reported that administration of BM alcoholic extract (BME) prevents trimethyltin (TMT)-induced cognitive deficits and hippocampal cell damage and promotes TMT-induced hippocampal neurogenesis. In this study, we demonstrate that administration of BME improves spatial working memory in adolescent (5-week- old) healthy mice but not adult (8-week-old) mice. Moreover, improved spatial working memory was retained even at 4 weeks after terminating 1-week treatment of adolescent mice. One-week BME treatment of adolescent mice significantly enhanced hippocampal BrdU incorporation and expression of genes involved in neurogenesis determined by RNAseq analysis. Cell death, as detected by histochemistry, appeared not to be significant. A significant increase in neurogenesis was observed in the dentate gyrus region 4 weeks after terminating 1-week treatment of adolescent mice with BME. Bacopaside I, an active component of BME, promoted the proliferation of neural progenitor cells in vitro in a concentration-dependent manner via the facilitation of the Akt and ERK1/2 signaling. These results suggest that BME enhances spatial working memory in healthy adolescent mice by promoting hippocampal neurogenesis and that the effects of BME are due, in significant amounts, to bacopaside I.


Sign in / Sign up

Export Citation Format

Share Document