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Join Date: Aug 2006
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15 yr Member
reverett123 reverett123 is offline
In Remembrance
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Join Date: Aug 2006
Posts: 3,772
15 yr Member
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1. Brain Res Mol Brain Res. 1994 Jul;24(1-4):70-6.

1,25-dihydroxyvitamin D3 regulates the synthesis of nerve growth factor in
primary cultures of glial cells.

Neveu I, Naveilhan P, Jehan F, Baudet C, Wion D, De Luca HF, Brachet P.

Institut National de la Santé et de la Recherche Médicale, Unité U.298, Centre
Hospitalier Régional et Universitaire, Angers, France.

The effect of 1,25-dihydroxyvitamin D3 (1,25-(OH)2 D3) on nerve growth factor
(NGF) synthesis was investigated in primary cultures of astrocytes prepared from
brain of neonatal rats. 1,25-(OH)2 D3 elicited a dose-dependent increase of NGF
mRNA with a maximal effect at 10(-7) M, which persisted for at least 48 h.
Northern blot analysis revealed an expression of the vitamin D3 receptor (VDR)
gene in primary glial cells. Treatment of cells with 1,25-(OH)2 D3 led to an
increase in the VDR mRNA levels. Similar results were obtained in C6 glioma
cells. Exposure of primary glial cells to 10(-8) M 1,25-(OH)2 D3 caused only a
2-fold increase of the levels of cell-secreted NGF after 3 days of treatment.
However, a 5-fold increase was observed three days after a second addition of
vitamin D3. Likewise, a pretreatment with lower doses of hormone such as 10(-10)
M or 10(-9) M enhanced the responsiveness of the cells to a 24 h treatment with
10(-8) M hormone. It appears, therefore, that the duration of the treatment
influences the level of synthesis of NGF, possibly as a consequence of the
increase of the VDR gene expression. The specificity of 1,25-(OH)2 D3 is
supported by the fact that a concentration of 10(-7) M of an another vitamin D3
metabolite, 24,25-(OH)2 D3, had no effect on NGF synthesis. Several lines of
evidence indicate that astrocytes constitute the major cell type responsive to
1,25-(OH)2 D3 in primary cultures of glial cells.(ABSTRACT TRUNCATED AT 250
WORDS)


PMID: 7968379 [PubMed - indexed for MEDLINE]

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1. Neuroreport. 1996 Sep 2;7(13):2171-5.

1,25-Dihydroxyvitamin D3, an inducer of glial cell line-derived neurotrophic
factor.

Naveilhan P, Neveu I, Wion D, Brachet P.

Institut National de la Santé et la Recherche Médicale, Centre Hospitalier
Universitaire, Angers, France.

Glial cell line-derived neurotrophic factor (GDNF) has significant therapeutic
potentials, in particular for neurodegenerative disorders. To determine factors
that would enhance GDNF expression, we analysed the effect of 1,25-(OH)2 D3 in C6
glioma cells. Treatment of C6 cells with 10(-7) M, 1,25-(OH)2 D3 for 48 h
elicited an 18.5-fold increase in the level of GDNF mRNA. In addition, our
results indicate that 1,25-(OH)2 D3 is effective at concentrations as low as
10(-10) M and that retinoic acid has additive effects. These data indicate that
1,25-(OH)2 D3 is a potent inducer of GDNF expression and suggest that 1,25-(OH)2
D3 may contribute to the regulation of GDNF in vivo.


PMID: 8930983 [PubMed - indexed for MEDLINE]

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1. Brain Res Mol Brain Res. 2002 Dec;108(1-2):143-6.

1,25-Dihydroxyvitamin D(3) increases striatal GDNF mRNA and protein expression in
adult rats.

Sanchez B, Lopez-Martin E, Segura C, Labandeira-Garcia JL, Perez-Fernandez R.

Department of Physiology, School of Medicine, University of Santiago de
Compostela, Spain.

Glial cell line-derived neurotrophic factor (GDNF) has been postulated as a
possible candidate for therapeutic treatment in Parkinson's disease (PD). Recent
in vitro data suggest that 1,25-dihydroxyvitamin D3 [1,25(OH)(2)D(3)] treatment
may enhance GDNF mRNA expression. In the present study, using semiquantitative
RT-PCR and Western blot, we have shown that 1,25(OH)(2)D(3) administration
intraperitoneally, significantly increases GDNF mRNA and protein levels in the
striatum of adult rats.


PMID: 12480187 [PubMed - indexed for MEDLINE]

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1. J Neurosci Res. 2009 Feb 15;87(3):723-32.

1,25-Dihydroxyvitamin D3 administration to 6-hydroxydopamine-lesioned rats
increases glial cell line-derived neurotrophic factor and partially restores
tyrosine hydroxylase expression in substantia nigra and striatum.

Sanchez B, Relova JL, Gallego R, Ben-Batalla I, Perez-Fernandez R.

Department of Physiology, School of Medicine, University of Santiago de
Compostela, Santiago de Compostela, Spain.

It has previously been demonstrated that 1,25-dihydroxyvitamin D(3)
[1,25(OH)(2)D(3)] administration, whether in cell cultures or in vivo to rats,
increases glial cell line-derived neurotrophic factor (GDNF) expression levels,
suggesting that this hormone may have beneficial effects in neurodegenerative
disorders. This study was carried out to explore the effects of 1,25(OH)(2)D(3)
administration in a 6-OHDA-lesioned rat model of Parkinson's disease on GDNF and
tyrosine hydroxylase (TH) expression in substantia nigra (SN) and striatum. Two
groups of animals received 1,25(OH)(2)D(3) intraperitoneally, the first group 7
days before the unilateral injection of 6-OHDA into the medial forebrain bundle
(MFB) and the second group 21 days (days 21-28) after the unilateral injection of
6-OHDA. Animals of both groups were sacrificed on day 28. In addition, two other
groups received a unilateral injection of either saline or 6-OHDA into the MFB.
Rats were killed, and the SN and striatum were then removed for GDNF and TH
determination. Striatal GDNF protein expression was increased on the ipsilateral
with respect to the contralateral side after 6-OHDA injection alone as well as in
1,25(OH)(2)D(3)-treated rats before or after 6-OHDA administration. As expected,
6-OHDA injection induced an ipsilateral decrease in TH-immunopositive neuronal
cell bodies and axonal terminals in the SN and striatum. However, treatment with
1,25(OH)(2)D(3) before and after 6-OHDA injection partially restored TH
expression in SN. These data suggest that 1,25(OH)(2)D(3) may help to prevent
dopaminergic neuron damage.


PMID: 18816795 [PubMed - indexed for MEDLINE]
__________________
Born in 1953, 1st symptoms and misdiagnosed as essential tremor in 1992. Dx with PD in 2000.
Currently (2011) taking 200/50 Sinemet CR 8 times a day + 10/100 Sinemet 3 times a day. Functional 90% of waking day but fragile. Failure at exercise but still trying. Constantly experimenting. Beta blocker and ACE inhibitor at present. Currently (01/2013) taking ldopa/carbadopa 200/50 CR six times a day + 10/100 form 3 times daily. Functional 90% of day. Update 04/2013: L/C 200/50 8x; Beta Blocker; ACE Inhib; Ginger; Turmeric; Creatine; Magnesium; Potassium. Doing well.
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