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Neurosci Lett ; 543: 183-8, 2013 May 24.
Article in English | MEDLINE | ID: mdl-23567742

ABSTRACT

Disturbances in Ca(2+) homeostasis have been implicated in a variety of neuro-pathological conditions including Parkinson's disease (PD). In the present study, we investigated the potential protective effect of SKF-96365, an originally identified blocker of receptor-mediated calcium entry, on MPP(+) induced neuronal injury in cultured rat mesencephalic cells. We found that pretreatment with SKF-96365 30 min before injury significantly reduced nuclear damage, decreased LDH release and inhibited apoptotic neuronal death. The results of calcium image also showed that SKF-96365 inhibited the increase of intracellular calcium induced by MPP(+), which was not dependent on the expression and function of TRPC1. In addition, SKF-96365 increased the expression of Homer1a, but decreased the expression of Homer1b/c in the presence or absence of MPP(+). Furthermore, overexpression of Homer1a by using recombinant lentivirus and knockdown of Homer1b/c by short interfering RNA (siRNA) further enhanced protective effects of SKF-96365 against MPP(+) injury. Taken together, these data suggest that SKF-96365 protects cultured rat mesencephalic cells against MPP(+) induced cytotoxicity, and this protection may be at least in part dependent on attenuating intracellular calcium overload, opposite regulatory effects on Homer1a and Homer1b/c expressions.


Subject(s)
1-Methyl-4-phenylpyridinium , Calcium Channel Blockers/pharmacology , Carrier Proteins/physiology , Imidazoles/pharmacology , Mesencephalon/cytology , Neurons/drug effects , Neuroprotective Agents/pharmacology , Animals , Calcium/metabolism , Cell Death , Cells, Cultured , Embryo, Mammalian/cytology , Homer Scaffolding Proteins , Neurons/cytology , Neurons/metabolism , Rats , Rats, Sprague-Dawley , TRPC Cation Channels/metabolism
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