Abstract | BACKGROUND AND PURPOSE: EXPERIMENTAL APPROACH: KEY RESULTS:
SU4312 unexpectedly prevented MPP(+) -induced neuronal apoptosis in vitro and decreased MPTP-induced loss of dopaminergic neurons, reduced expression of mRNA for tyrosine hydroxylase and impaired swimming behaviour in zebrafish. In contrast, PTK787/ ZK222584, a well-studied VEGFR-2 inhibitor, failed to prevent neurotoxicity, suggesting that the neuroprotective actions of SU4312 were independent of its anti-angiogenic action. Furthermore, SU4312 exhibited non-competitive inhibition of purified neuronal NOS (nNOS) with an IC(50) value of 19.0 μM but showed little or no effects on inducible and endothelial NOS. Molecular docking simulations suggested an interaction between SU4312 and the haem group within the active centre of nNOS. CONCLUSIONS AND IMPLICATION:
SU4312 exhibited neuroprotection against MPP(+) at least partly via selective and direct inhibition of nNOS. Because SU4312 could reach the brain in rats, our study also offered a support for further development of SU4312 to treat neurodegenerative disorders, particularly those associated with NO-mediated neurotoxicity.
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Authors | Wei Cui, Zaijun Zhang, Wenming Li, Shengquan Hu, Shinghung Mak, Huan Zhang, Renwen Han, Shuai Yuan, Sai Li, Fei Sa, Daping Xu, Zhixiu Lin, Zhong Zuo, Jianhui Rong, Edmond Dik-Lung Ma, Tony Chunglit Choi, Simon My Lee, Yifan Han |
Journal | British journal of pharmacology
(Br J Pharmacol)
Vol. 168
Issue 5
Pg. 1201-14
(Mar 2013)
ISSN: 1476-5381 [Electronic] England |
PMID | 23062100
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Copyright | © 2012 The Authors. British Journal of Pharmacology © 2012 The British Pharmacological Society. |
Chemical References |
- 3-(4-dimethylaminobenzylidene)-1,3-dihydroindol-2-one
- Antineoplastic Agents
- Enzyme Inhibitors
- Indoles
- Neuroprotective Agents
- Nitric Oxide
- 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
- Nitric Oxide Synthase Type I
- 1-Methyl-4-phenylpyridinium
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Topics |
- 1-Methyl-4-phenyl-1,2,3,6-tetrahydropyridine
- 1-Methyl-4-phenylpyridinium
(toxicity)
- Animals
- Antineoplastic Agents
(pharmacology, therapeutic use)
- Behavior, Animal
(drug effects)
- Brain
(metabolism)
- Cell Death
(drug effects)
- Cell Line, Tumor
- Embryo, Nonmammalian
(anatomy & histology, drug effects, physiology)
- Enzyme Inhibitors
(pharmacology, therapeutic use)
- Humans
- Indoles
(pharmacology, therapeutic use)
- Molecular Docking Simulation
- Motor Activity
(drug effects)
- Neurons
(drug effects)
- Neuroprotective Agents
(pharmacology, therapeutic use)
- Nitric Oxide
(metabolism)
- Nitric Oxide Synthase Type I
(antagonists & inhibitors)
- PC12 Cells
- Rats
- Rats, Sprague-Dawley
- Zebrafish
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