scholarly journals Protection of dopamine neurons by CDNF and neurturin variant N4 against MPP+ in dissociated cultures from rat mesencephalon

PLoS ONE ◽  
2021 ◽  
Vol 16 (2) ◽  
pp. e0245663
Author(s):  
Juliann D. Jaumotte ◽  
Mart Saarma ◽  
Michael J. Zigmond

Parkinson’s disease is associated with the loss of dopamine (DA) neurons in ventral mesencephalon. We have previously reported that no single neurotrophic factor we tested protected DA neurons from the dopaminergic toxin 1-methyl-4-phenylpyridinium (MPP+) in dissociated cultures isolated from the P0 rat substantia nigra, but that a combination of five neurotrophic factors was protective. We now report that cerebral DA neurotrophic factor (CDNF) and a variant of neurturin (NRTN), N4, were also not protective when provided alone but were protective when added together. In cultures isolated from the substantia nigra, MPP+ (10 μM) decreased tyrosine hydroxylase-positive cells to 41.7 ± 5.4% of vehicle control. Although treatment of cultures with 100 ng/ml of either CDNF or N4 individually before and after toxin exposure did not significantly increase survival in MPP+-treated cultures, when the two trophic factors were added together at 100 ng/ml each, survival of cells was increased 28.2 ± 6.1% above the effect of MPP+ alone. In cultures isolated from the ventral tegmental area, another DA rich area, a higher dose of MPP+ (1 mM) was required to produce an EC50 in TH-positive cells but, as in the substantia nigra, only the combination of CDNF and N4 (100 ng/ml each) was successful at increasing the survival of these cells compared to MPP+ alone (by 22.5 ± 3.5%). These data support previous findings that CDNF and N4 may be of therapeutic value for treatment of PD, but suggest that they may need to be administered together.

1999 ◽  
Vol 82 (4) ◽  
pp. 1974-1981 ◽  
Author(s):  
Ezia Guatteo ◽  
Nicola B. Mercuri ◽  
Giorgio Bernardi ◽  
Thomas Knöpfel

Metabotropic glutamate receptors modulate neuronal excitability via a multitude of mechanisms, and they have been implicated in the pathogenesis of neurodegenerative processes. Here we investigated the responses mediated by group I metabotropic glutamate receptors (mGluRs) in dopamine neurons of the rat substantia nigra pars compacta, using whole cell patch-clamp recordings in combination with microfluorometric measurements of [Ca2+]i and [Na+]i. The selective group I mGluR agonist (S)-3,5-dihydroxyphenylglycine (3,5-DHPG) was bath-applied (20 μM, 30 s to 2 min) or applied locally by means of short-lasting (2–4 s) pressure pulses, delivered through an agonist-containing pipette positioned close to the cell body of the neuron. 3,5-DHPG evoked an inward current characterized by a transient and a sustained component, the latter of which was uncovered only with long-lasting agonist applications. The fast component coincided with a transient elevation of [Ca2+]i, whereas the total current was associated with a rise in [Na+]i. These responses were not affected either by the superfusion of ionotropic excitatory amino acid antagonists 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX) and d-2-amino-5-phosphono-pentanoic acid (d-APV), nor by the sodium channel blocker tetrodotoxin (TTX). (S)-α-methyl-4-carboxyphenylglycine (S-MCPG) and the more selective mGluR1 antagonist 7(hydroxyimino)cyclopropa[b]chromen-1a-carboxylate (CPCCOEt) depressed both 3,5-DHPG–induced inward current components and, although less effectively, the associated [Ca2+]i elevations. On repeated agonist applications the inward current and the calcium transients both desensitized. The time constant of recovery from desensitization differed significantly between these two responses, being 67.4 ± 4.4 s for the inward current and 28.6 ± 2.7 s for the calcium response. Bathing the tissue in a calcium-free/EGTA medium or adding thapsigargin (1 μM) to the extracellular medium prevented the generation of the [Ca2+]i transient, but did not prevent the activation of the inward current. These electrophysiological and fluorometric results show that the 3,5-DHPG–induced inward current and the [Ca2+]i elevations are mediated by independent pathways downstream the activation of mGluR1.


2003 ◽  
Vol 18 (10) ◽  
pp. 2743-2750 ◽  
Author(s):  
E. Paolucci ◽  
N. Berretta ◽  
A. Tozzi ◽  
G. Bernardi ◽  
N. B. Mercuri

1987 ◽  
Vol 26 (12) ◽  
pp. 1795-1797 ◽  
Author(s):  
P. Cumming ◽  
H. Kamo ◽  
E.G. McGeer ◽  
P.L. McGeer

2012 ◽  
Vol 33 (3) ◽  
pp. 429-435 ◽  
Author(s):  
Adam C. Munhall ◽  
Yan-Na Wu ◽  
John K. Belknap ◽  
Charles K. Meshul ◽  
Steven W. Johnson

2009 ◽  
Vol 41 (4) ◽  
pp. 440-447 ◽  
Author(s):  
Tinmarla F. Oo ◽  
Deanna M. Marchionini ◽  
Olga Yarygina ◽  
Paul D. O'Leary ◽  
Richard A. Hughes ◽  
...  

Synapse ◽  
1993 ◽  
Vol 15 (3) ◽  
pp. 229-238 ◽  
Author(s):  
G�ran Engberg ◽  
Torben Kling-Petersen ◽  
Hans Nissbrandt

Synapse ◽  
2002 ◽  
Vol 47 (3) ◽  
pp. 236-239 ◽  
Author(s):  
Luigi Caputi ◽  
C. Peter Bengtson ◽  
Ezia Guatteo ◽  
Giorgio Bernardi ◽  
Nicola B. Mercuri

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