Loss of response to levodopa in Parkinson’s disease and co-occurrence with dementia: role of D 3 and not D 2 receptors

Abstract

Previous data suggest a relationship between the loss of response to levodopa in Parkinson’s disease (PD) patients with the co-occurrence of dementia, but the role of alterations in the dopamine system has not been explored. We measured the extent of striatal DA loss and changes in striatal DA D 2 and D 3 receptors in postmortem striatum of PD patients who historically had or had not lost their clinical response to dopaminergic drugs and/or had an additional diagnosis of dementia. Clinical evaluation and retrospective chart reviews for PD and dementia, and neuropathological diagnoses were obtained. All PD cases (±dementia), regardless of response to dopaminergic drugs, exhibited a significant and similar degree and pattern of loss of tyrosine hydroxylase immunocytochemistry and DA transporter binding in striatum, and loss of tyrosine hydroxylase-immunoreactive neurons and brain-derived neurotrophic-immunoreactive neurons from the ventral midbrain. D 2 receptor concentrations were modestly elevated in the rostral striatum of all the PD cases (±dementia), whether or not they continued to respond to dopaminergic drugs. In contrast, loss of D 3 receptor concentration correlated with loss of response to dopaminergic drugs, independent of the presence or absence of dementia. A maintained response to dopaminergic drugs correlated with an elevation of D 3 receptors. Dementia with PD was highly correlated with a loss of response to dopaminergic drugs, and was also correlated with reduced D 3 receptors. The alterations in D 3 receptor concentrations were greatest in the nucleus accumbens, caudal striatum, and globus pallidus. Thus, loss of dopamine D 3 receptors may be a more important contributing factor to a loss of response to dopaminergic drugs than changes in the D 2 receptor.