2008
DOI: 10.1016/j.brainres.2007.11.024
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Adrenalectomy counteracts the local modulation of astroglial fibroblast growth factor system without interfering with the pattern of 6-OHDA-induced dopamine degeneration in regions of the ventral midbrain

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Cited by 19 publications
(25 citation statements)
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“…Primary hippocampal neurons were seeded into 96-well plates and treated with 6-OHDA (50, 100, 150, 200 and 400 μM) for 24 h with or without bFGF (10,20,40 and 80 ng/mL). After 24 h incubation, cell viability was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay.…”
Section: Viability Assaymentioning
confidence: 99%
See 1 more Smart Citation
“…Primary hippocampal neurons were seeded into 96-well plates and treated with 6-OHDA (50, 100, 150, 200 and 400 μM) for 24 h with or without bFGF (10,20,40 and 80 ng/mL). After 24 h incubation, cell viability was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay.…”
Section: Viability Assaymentioning
confidence: 99%
“…Several studies have focused on the relevance of bFGF in the dopaminergic nigrostriatal system. Chadi et al reported that bFGF promotes dopaminergic cell survival in human fetal tissue strands transplanted into immunosuppressed 6-OHDA-lesioned rats [10]. Another group showed that bFGF protects against rotenone-induced dopaminergic cell death [11].…”
mentioning
confidence: 99%
“…Schwann cell FGF-2 and S100ß proteins were assessed by Western blot analysis 14 . The Schwann cells cultures were homogenized in PBS, pH 7.4, containing 1% NP40, 0.5% sodium deoxycholate, 1% sodium dodecyl sulfate, 1 mM ethylenediaminetetraacetic acid, 1 mM ethylene glycol tetraacetic acid, and 1% protease inhibitor cocktail (Sigma).…”
Section: Western Blot Analysis Of Cultured Schwann Cellsmentioning
confidence: 99%
“…To do so, the membranes were incubated with primary antibody against beta-actin diluted at 1:30.000 (Sigma, USA) in TBS-T with 1% Bovine Serum Albumin (BSA) for 1 hour at room temperature, then washed twice for 10 minutes with TBS-T and incubated for 45 minutes at room temperature with the secondary antibody (anti-rabbit, HRP-conjugated, Amersham) diluted at 1:10.000 in TBS-T with 1% BSA. After these incubations, the membranes were washed as previously described, which was followed by reaction and film developing 11 . The films were quantified by optical densitometry using an image analyzing system, as described by Chadi et al Samples were diluted in lysis buffer to obtain 60 µg in 25 µL of buffer.…”
Section: Carboxytherapy Is a Technique Originated In 1930 Inmentioning
confidence: 99%