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Inhibitors of type IV phosphodiesterases reduce the toxicity of MPTP in substantia nigra neurons in vivo.

Abstract:
The neuropathology of Parkinson's disease is characterized by the degeneration of dopaminergic neurons in the substantia nigra. We have recently shown that the activation of protein kinase A improves the survival of dopaminergic neurons in culture and, furthermore, protects them from the dopaminergic neurotoxin, 1-methyl-4-phenylpyridinium ion (MPP+) in vitro. We have now analysed the potential of phosphodiesterase inhibitors to increase cAMP levels in dopaminergic neurons, to improve their survival in culture and to protect them from the toxicity of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) in vivo. Increasing intracellular cAMP with phosphodiesterase type IV-specific inhibitors enhanced the survival of dopaminergic neurons in culture. Inhibitors of other phosphodiesterase types were not active. In vivo, phosphodiesterase type IV inhibitors reduced the MPTP-induced dopamine depletion in the striatum of C57BL/6 mice. Furthermore, the loss of tyrosine hydroxylase-immunopositive neurons in the substantia nigra of these animals was diminished. After Nissl staining, a similar reduction of the MPTP-induced loss of neurons was observed in the substantia nigra. The protective effect of protein kinase A activation did not appear to be due to the blocking of MPP+ uptake into dopaminergic neurons. This was not decreased after treatment with forskolin or 8-(4-chlorophenylthio)-cAMP. Thus, protein kinase A regulates the survival and differentiation of dopaminergic substantia nigra neurons in vivo, implicating a therapeutic potential for substances which regulate cAMP turnover in these neurons.
Publication status:
Published

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Publisher copy:
10.1111/j.1460-9568.1995.tb01041.x

Authors

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Institution:
University of Oxford
Division:
MSD
Department:
NDORMS
Role:
Author


Journal:
European journal of neuroscience More from this journal
Volume:
7
Issue:
12
Pages:
2431-2440
Publication date:
1995-12-01
DOI:
EISSN:
1460-9568
ISSN:
0953-816X


Language:
English
Keywords:
Pubs id:
pubs:107392
UUID:
uuid:f2743b24-b523-44d4-a251-7a4d0e2ad15b
Local pid:
pubs:107392
Source identifiers:
107392
Deposit date:
2012-12-19
ARK identifier:

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