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[Abstract Title]. - Society for Neuroscience

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Support: CONACyT 50427Q<br />

<strong>Title</strong>: Dopamine modulates the input from globus pallidus to thalamic reticular nucleus via<br />

presynaptic D4 receptos<br />

Authors: D. GASCA 1 , A. HERNÁNDEZ 1,2 , A. SIERRA 1 , R. VALDIOSERA 1 , B. FLORÁN 1 ,<br />

D. ERLIJ 1 , *J. ACEVES 1 ;<br />

1 Dept Physiol Biophy & Neurosci, Ctr. Investigacion Del IPN, Mexico DF 07000, Mexico; 2 Inst.<br />

de Fisiología Celular, UNAM, Mexico D.F., Mexico<br />

<strong>Abstract</strong>: Thalamic reticular nucleus (TRn) receives dopaminergic afferents from substantia<br />

nigra pars compacta (SNc) and GABAergic afferents from globus pallidus in the rat. In addition,<br />

D1 and D4 dopamine receptors are expressed in the TRn. Our laboratory previously has shown<br />

that D4 dopamine receptors inhibit the depolarization-induced [H 3 ]GABA release in TRn slices<br />

(Florán et al., 2004a), suggesting a presynaptic modulation of the GABAergic transmission. Here<br />

we have studied the source of the inhibitory synaptic currents modulated by D4 dopamine<br />

receptors in TRn slices from neonatal (14-21 days) rats.<br />

The inhibitory postsynaptic currents were evoked by local electrical stimulation (eIPSCs) in the<br />

presence of CNQX and AP-5. The miniature inhibitory posynaptic currents (mIPSCs) were<br />

recorded in the presence of TTX. At the end of the experiments the synaptic currents were<br />

blocked by bicuculline, confirming their GABAergic nature.<br />

The amplitude of the eIPSCs was reduced 40% by PD168,077 (selective D4 agonist) and this<br />

effect was blocked by L-745870 (selective antagonist). This effect was accompanied by a 23%<br />

increase in the paired pulse ratio, indicating a presynaptic effect. It was also observed that<br />

PD168,077 reduced by 40% the frequency of the mIPSCs without affecting their amplitude. This<br />

effect was blocked by L-745870, indicating that it was mediated by a specific activation of D4<br />

dopamine receptors. Dopamine also inhibited both eIPSCs and mIPSCs, and the inhibition was<br />

blocked by L-745,870. These results together indicate a dopamine modulation of GABAergic<br />

synaptic transmission by presynaptic D4 dopamine receptors in the TRn. Previous lesion of the<br />

globus pallidus eliminated completely the effect of the activation of D4 dopamine receptors on<br />

the GABAergic transmission, judged by its effect on evoked or spontaneous IPSCs. These results<br />

indicate that D4 dopamine receptors are located on the GABAergic pallidal terminals in the TRn,<br />

where they modulate the pallidal input.<br />

Disclosures: D. Gasca, None; J. Aceves , None; A. Hernández, None; A. Sierra, None; R.<br />

Valdiosera, None; B. Florán, None; D. Erlij, None.<br />

Poster<br />

274. Basal Ganglia: Transmitters and Neuromodulation II<br />

Time: Sunday, November 16, 2008, 1:00 pm - 5:00 pm

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