2003
DOI: 10.1016/s0022-510x(03)00180-1
|View full text |Cite
|
Sign up to set email alerts
|

The neuroprotective effect of ONO-1714 on NMDA-mediated cytotoxicity in vitro

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

0
7
0

Year Published

2006
2006
2010
2010

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 15 publications
(7 citation statements)
references
References 22 publications
0
7
0
Order By: Relevance
“…Primary cultures of rat cerebral neurons were prepared from cerebral cortex of 1-day-old newborn rats as described previously (Shibuta et al, 2003;Varathan et al, 2001). Neurons were plated at a density of 5 × 10 5 cells/mL on poly-L-lysineprecoated 24-well plates.…”
Section: Methodsmentioning
confidence: 99%
“…Primary cultures of rat cerebral neurons were prepared from cerebral cortex of 1-day-old newborn rats as described previously (Shibuta et al, 2003;Varathan et al, 2001). Neurons were plated at a density of 5 × 10 5 cells/mL on poly-L-lysineprecoated 24-well plates.…”
Section: Methodsmentioning
confidence: 99%
“…This suspension was placed on a poly-L-lysine-coated 35 mm diameter tissue culture dish (1.5 ml per well) with a 2 mm grid (Nunc, Naperville, IL, USA) used to observe the same neurones in a given area over time. 16 After 4 days in culture, cells were treated with 5 mg ml 21 of 5-FU for 3 days to prevent proliferation of non-neuronal cells. The neurones were maintained in DMEM containing 8% FCS and 4% HS in an atmosphere of 5% CO 2 and 95% air, and under 100% humidity at a temperature of 378C.…”
Section: Cell Culturementioning
confidence: 99%
“…Red, neurons; green, glial cells. The proportion of red cells (neurons) was more than 90% [20,21]. Photomicrographs of three or four areas within the dish were taken shortly before the exposure to glutamate.…”
Section: Cell Viabilitymentioning
confidence: 99%