1 globus pallidus; the lateral septum; and the islands of Calleja).

2 ns, including hippocampal region CA1 and the islands of Calleja.

3 he brain, including suprachiasmatic nucleus, islands of Calleja and medial preoptic area, olfactory b

4 c [3H]7-OH-DPAT binding were detected in the islands of Calleja and nucleus accumbens but in addition

5 high expression in the ventral pallidum, the islands of Calleja and pars compacta of the substantia n

6  divisions of the spinal trigeminal nucleus, islands of Calleja and presubiculum.

7 ity was also observed in olfactory tubercle, islands of Calleja, cerebral cortex, striatum, thalamic

8 (type 2) nuclear positive neurons within the islands of Calleja, endopiriform nucleus, lateral septum

9 buted with highest densities observed in the islands of Calleja, followed by the nucleus accumbens.

10                Prior to agonist application, island of Calleja granule cells displayed spontaneous st

11 e nucleus accumbens (NACC) (52--83%) and the islands of calleja (IC) (67%), all of which returned to

12 -like receptors) binding in Acc (by 84%) and islands of Calleja (IC; 44%), without affecting [3H](+)-

13 le where DCL is found in the neuropil of the islands of Calleja (ICj).

14 ted compounds on granule neurones within the islands of Calleja in vitro, in slices if approximately

15 he reported presence of gap junctions in the islands of Calleja offers the explanation that these eff

16 rved in the superior and inferior colliculi, islands of Calleja, subiculum, lateral septum, lateral a

17 ry bulb, the anterior olfactory nucleus, the islands of Calleja, the CA1-CA3 fields of the hippocampu

18 l preoptic area, anterior olfactory nucleus, islands of Calleja, the dorsal endopiriform n, piriform

19  populated neuron rich regions including the Islands of Calleja, the olfactory bulb, and the internal

20 ven the reported lack of D2 receptors in the islands of Calleja, these findings indicate a direct act