Effects of blockade of voltage-sensitive Ca(2+)/Na(+) channels by a novel phenylpyrimidine derivative, NS-7, on CREB phosphorylation in focal cerebral ischemia in the rat.

Abstract

NS-7 is a novel blocker of voltage-sensitive Ca(2+) and Na(+) channels, and it significantly reduces infarct size after occlusion of the middle cerebral artery. Persistent activation of cyclic AMP response element binding protein (CREB), which can be induced by increase in intracellular Ca(2+) concentrations or other second messengers, has recently been found to be closely associated with neuronal survival in cerebral ischemia. The present study was therefore undertaken to evaluate the neuroprotective effects of NS-7 by analyzing changes in CREB phosphorylation in a focal cerebral ischemia model. CREB phosphorylation in the brain of rats was investigated immunohistochemically at 3.5-48-h recirculation after 1. 5-h occlusion of the middle cerebral artery. NS-7 (1 mg/kg; NS-7 group) or saline (saline group) was intravenously injected 5 min after the start of recirculation. The NS-7 group showed significantly milder activation of CREB phosphorylation in various cortical regions after 3.5 h of recirculation than the saline group. The inner border zone of ischemia in the NS-7 group subsequently exhibited a moderate, but persistent, increase in number of phosphorylated CREB-positive neurons with no apparent histological damage. By contrast, the saline group displayed a marked, but only transient, increase in number of immunopositive neurons in this border zone after 3.5 h of recirculation, and this was followed by clear suppression of CREB phosphorylation and subsequent loss of normal neurons. These findings suggest that: (1) the marked enhancement of CREB phosphorylation in the acute post-ischemic phase may be triggered largely by an influx of calcium ions as a result of activation of the voltage-sensitive Ca(2+) and Na(+) channels; and that (2) the neuroprotective effects of NS-7 may be accompanied by persistent activation of CREB phosphorylation in the inner border zone of ischemia.

• Authors: K Tanaka, S Nogawa, E Nagata, S Suzuki, T Dembo, A Kosakai, Y Fukuuchi
• Journal: Brain research (Brain Res) Vol. 873 Issue 1 Pg. 83-93 (Aug 04 2000) ISSN: 0006-8993 [Print] Netherlands
• PMID: 10915813 (Publication Type: Journal Article)

Chemical References

• 4-(4-fluorophenyl)-2-methyl-6-(5-piperidinopentyloxy)pyrimidine hydrochloride
• Calcium Channel Blockers
• Calcium Channels
• Cyclic AMP Response Element-Binding Protein
• Neuroprotective Agents
• Pyrimidines
• Sodium Channel Blockers
• Sodium Channels

Topics

• Animals
• Brain (metabolism)
• Brain Ischemia (metabolism)
• Calcium Channel Blockers (pharmacology)
• Calcium Channels (physiology)
• Cyclic AMP Response Element-Binding Protein (metabolism)
• Immunohistochemistry
• Male
• Neuroprotective Agents (pharmacology)
• Phosphorylation (drug effects)
• Pyrimidines (pharmacology)
• Rats
• Rats, Sprague-Dawley
• Sodium Channel Blockers
• Sodium Channels (physiology)