Abstract

The specific [ 3H]QNB binding and high-affinity uptake of [ 14C]choline in 8 brain regions (cerebral cortex, hippocampus, hypothalamus, thalamus, striatum, midbrain, cerebellum and brainstem) after repeated administration of DFP and atropine to guinea-pigs were simultaneously measured. Following repeated DFP administration, AChE was markedly depressed in each brain region. In these animals, there was a significant decrease in specific [ 3H]QNB binding in the cerebral cortex, hippocampus and striatum, whereas the [ 3H]QNB binding in the rest of brain regions was unchanged. Scatchard analysis revealed a 36% decrease in the B max value for the striatal [ 3H]QNB binding without a change in the K d value, suggesting a change in the receptor density. In contrast, repeated atropine administration produced a significant enhancement in the [ 3H]QNB binding only in the hippocampus and striatum. The B max value in the striatum increased by 21% without a change in the K d value. In addition to the receptor alteration, high affinity uptake of [ 14C]choline in the hippocampus and striatum was significantly decreased by DFP treatment, while that in the striatum increased by atropine treatment. Thus the present study has demonstrated that a prolonged activation and blockade of central muscarinic receptors resulted in specific adaptation in both the receptor density and ACh availability at the synapses in the cerebral cortex, hippocampus and striatum.

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