NEURONAL POPULATIONS OF RAT CEREBRAL CORTEX AND HIPPOCAMPUS EXPRESSED A HIGHER DENSITY OF L-TYPE Ca²⁺ CHANNEL THAN CORRESPONDING CEREBRAL VESSELS

Abstract

Dihydropyridine (DHP)-type Ca²⁺ antagonists block primarily L-type Ca²⁺ channels and are used in the therapy of hypertension. They were also proposed for the treatment of several central nervous system disorders. In brain, these compounds bind both neuronal and vascular Ca²⁺ channels, but no studies have evaluated comparatively their density at neuronal and vascular level. This study has analyzed the pharmacological profile and the anatomical localization of L-type Ca²⁺ channels in rat frontal cortex, hippocampus and in forebrain pial and intracerebral arteries by radioligand binding assay and high resolution light microscope autoradiography. The DHP derivative [³H]nicardipine was used as a radioligand. Binding of [³H]nicardipine was consistent with the labeling of L-type Ca²⁺ channels. In frontal cortex, the highest density of binding sites was found in nerve cell body region, followed by the neuropil and the wall of intracerebral arteries.

In hippocampus, the density of binding sites was higher in the nerve cell body region than in the neuropil of CA1, CA3, and CA4 subfields. In the dentate gyrus, a higher density of silver grains was developed in neuropil than in nerve cell body of granule neurons. With the exception of dentate gyrus, neuronal binding sites were more expressed than vascular binding sites in the hippocampus. In pial arteries [³H]nicardipine binding density decreased concomitant with the reduction of vessel diameter, whereas in intracerebral arteries [³H]nicardipine binding density displayed an opposite pattern. The above findings indicate that in brain the density of neuronal L-type Ca²⁺channels was significantly higher than that of vascular ones. This may account for more pronounced neuronal than vascular effects after pharmacological manipulation of cerebral Ca²⁺ channels.

• Calcium channels
• [³H]nicardipine
• Autoradiography
• Brain
• Nerve cells
• Cerebral vasculature