PMID- 10341265 OWN - NLM STAT- MEDLINE DCOM- 19990616 LR - 20231014 IS - 1529-2401 (Electronic) IS - 0270-6474 (Print) IS - 0270-6474 (Linking) VI - 19 IP - 11 DP - 1999 Jun 1 TI - Relationships between the prefrontal cortex and the basal ganglia in the rat: physiology of the cortico-nigral circuits. PG - 4674-81 AB - The prelimbic/medial orbital areas (PL/MO) of the rat prefrontal cortex are connected to substantia nigra pars reticulata (SNR) through three main circuits: a direct nucleus accumbens (NAcc)-SNR pathway, an indirect NAcc-SNR pathway involving the ventral pallidum (VP) and the subthalamic nucleus (STN), and a disynaptic cortico-STN-SNR pathway. The present study was undertaken to characterize the effect of PL/MO stimulation on SNR cells and to determine the contribution of these different pathways. The major pattern of responses observed in the SNR was an inhibition preceded by an early excitation and followed or not by a late excitation. The inhibition resulted from the activation of the direct NAcc-SNR pathway because it disappeared after acute blockade of the glutamatergic cortico-striatal transmission by CNQX application into the NAcc. The late excitation resulted from the activation of the indirect NAcc-VP-STN-SNR pathway via a disinhibition of the STN because it disappeared after either CNQX application into the NAcc or blockade of the GABAergic striato-pallidal transmission by bicuculline application into the VP. The early excitation, which was markedly decreased after blockade of the cortico-STN transmission by CNQX application into the STN, resulted from the activation of the disynaptic cortico-STN-SNR pathway. Finally, the blockade of the cortico-STN-VP circuit by CNQX application into STN or VP modified the influence of the trans-striatal circuits on SNR cells. This study suggests that, in the prefrontal cortex-basal ganglia circuits, the trans-subthalamic pathways, by their excitatory effects, participate in the shaping of the inhibitory influence of the direct striato-nigral pathway on SNR neurons. FAU - Maurice, N AU - Maurice N AD - Chaire de Neuropharmacologie, Institut National de la Sante et de la Recherche Medicale U114, College de France, 75231 Paris Cedex 05, France. FAU - Deniau, J M AU - Deniau JM FAU - Glowinski, J AU - Glowinski J FAU - Thierry, A M AU - Thierry AM LA - eng PT - Comparative Study PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - United States TA - J Neurosci JT - The Journal of neuroscience : the official journal of the Society for Neuroscience JID - 8102140 RN - 0 (Excitatory Amino Acid Antagonists) RN - 0 (GABA Antagonists) RN - 6OTE87SCCW (6-Cyano-7-nitroquinoxaline-2,3-dione) RN - Y37615DVKC (Bicuculline) SB - IM MH - 6-Cyano-7-nitroquinoxaline-2,3-dione/pharmacology MH - Animals MH - Basal Ganglia/*physiology MH - Bicuculline/pharmacology MH - Electric Stimulation MH - Excitatory Amino Acid Antagonists/pharmacology MH - GABA Antagonists/pharmacology MH - Male MH - Neural Pathways/physiology MH - Nucleus Accumbens/drug effects/physiology MH - Prefrontal Cortex/*physiology MH - Rats MH - Rats, Sprague-Dawley MH - Substantia Nigra/drug effects/*physiology PMC - PMC6782607 EDAT- 1999/05/26 00:00 MHDA- 1999/05/26 00:01 PMCR- 1999/12/01 CRDT- 1999/05/26 00:00 PHST- 1999/05/26 00:00 [pubmed] PHST- 1999/05/26 00:01 [medline] PHST- 1999/05/26 00:00 [entrez] PHST- 1999/12/01 00:00 [pmc-release] AID - 3088 [pii] AID - 10.1523/JNEUROSCI.19-11-04674.1999 [doi] PST - ppublish SO - J Neurosci. 1999 Jun 1;19(11):4674-81. doi: 10.1523/JNEUROSCI.19-11-04674.1999.