Regulation of dihydropyridine calcium antagonist binding sites in the rat hippocampus following neurochemical lesions

J Neurosci Res. 1987;17(3):285-90. doi: 10.1002/jnr.490170313.

Abstract

The effects of catecholaminergic, cholinergic, serotonergic, and glutaminergic terminal destruction and neurotransmitter depletion on [3H]nitrendipine binding to rat brain membranes were determined using the neurotoxins 6-hydroxydopamine, 5,7-dihydroxytryptamine, and kainic acid and the neurotransmitter-depleting agent reserpine. Following intracisternal injection of 6-hydroxydopamine there were time-dependent increases (14-23%) in the density but not change in the affinity of hippocampal [3H]nitrendipine binding sites. 6-Hydroxydopamine significantly increased [3H]nitrendipine binding in the hippocampus 4 and 10 days following injection. However, no significant change in binding was observed at 16 and 26 days. [3H]Nitrendipine binding in the cerebral cortex, striatum, cerebellum, and brain stem was unaffected by 6-hydroxydopamine. Neither 5,7-dihydroxytryptamine nor kainic acid affected [3H]nitrendipine binding in the hippocampus and cerebral cortex. Acute and chronic reserpinization also did not affect [3H]nitrendipine binding in the hippocampus and cerebral cortex. These results indicate that dihydropyridine calcium antagonist bindings sites in rat brain are subject to brain region-specific regulation following neurochemical lesions and may be present in their largest densities on postsynaptic membranes.

Publication types

  • Comparative Study

MeSH terms

  • Adrenergic Fibers / physiology
  • Animals
  • Calcium Channels
  • Catecholamines / physiology
  • Cholinergic Fibers / physiology
  • Glutamine / physiology
  • Hippocampus / analysis*
  • Hippocampus / drug effects
  • Male
  • Rats
  • Rats, Inbred Strains
  • Receptors, Nicotinic / analysis*
  • Serotonin / physiology
  • Synaptic Transmission

Substances

  • Calcium Channels
  • Catecholamines
  • Receptors, Nicotinic
  • Glutamine
  • Serotonin