Connections of the bullfrog striatum: efferent projections.

Abstract

AbstractAutoradiographic and degeneration techniques were used to describe striatal efferents in the bullfrog (Rana catesbeiana). Horseradish peroxidase (HRP) was then placed in the major terminal fields to reveal the striatal cells responsible for these projections. Except for the small ventral eminence of the lateral pallium immediately adjacent to the dorsal striatum, no pallial region receives a striatal projection. Most striatal efferents descend in the lateral forebrain bundle (LFB), passing through the anterior entopedun‐cular nucleus, where one large fascicle decussates in the anterior commissure and innervates the contralateral anterior entopeduncular nucleus and caudal ventral striatum. A smaller fascicle exits the LFB to terminate in the ipsilateral lateral amygdala. The remaining efferents continue caudal in the LFB through the posterior entopeduncular nucleus, with sparse projections to the ventral thalamus, the adjacent preoptic areas, and the posterior tuberculum leaving the bundle at various points. At pretectal levels, some efferents leave the LFB to run dorsally, through the caudal pole of the central thalamic nucleus and into the posterior division of the lateral nucleus and the lateral portion of the posterior thalamic nucleus. Efferents also continue caudal, through the superficial tegmental cell groups (nucleus profundus mesencephali and superficial isthmal reticular nucleus) before turning dorsomedially into the ventral anterodorsal, lateral anteroventral, and rostral pole of the posterodorsal tegmental fields. A small superficial projection continues to isthmal levels but cannot be traced beyond. Tegmental HRP injections retrogradely fill cells in the dorsal and ventral striatum as well as nucleus accumbens and the anterior entopeduncular nucleus. Pretectal HRP injections fill cells only in the caudal ventral striatum and anterior entopeduncular nucleus. Anterior entopeduncular nucleus HRP injections fill numerous cells in all striatal divisions, but some of this filling may be due to interrupted fibers of passage. Thus the anuran striatum, which receives its major input from thalamic nuclei relaying tectal and toral input, can in turn influence the midbrain roof via several disynaptic pathways: through the anterior entopeduncular nucleus, pretectum, and tegmentum, all of which project directly to the tectum and torus (Wilczynski and Northcutt, ′77; Wilczynski, ′81). Additional trisynaptic routes through the anterior entopeduncular nucleus and its pretectal and tegmental connections parallel the striatal routes.