The ascending fiber projections from the principal sensory trigeminal nucleus in the rat.

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AbstractPersisting reports of uncrossed secondary trigeminothalamic pathways originating from the principal sensory trigeminal nucleus (PrV) are based mainly on data obtained from surgically induced lesions analyzed by methods other than reduced silver impregnation techniques. After complete stereotaxic or direct surgical lesions of PrV, degenerating fibers proceed ventrally and rostrally from the nucleus and cross the midline in the rostral pons, completing their decussation caudal to nucleus interpeduncularis. These fibers form a large trigeminal lemniscus that ascends through the midbrain dorsomedial to the smaller medial lemniscus. PrV fibers terminate in the posterior thalamic nucleus and throughout the medial two‐thirds of the ventrobasal thalamic complex (VBm) contralateral to the side of the lesion. Connections with the ventral part of zona incerta were also found similar to those reported for the medial lemniscus.Another fiber system proceeds dorsad from the parvicellular reticular formation in the PrV region and terminates on cells of the ipsi‐and contralateral motor trigeminal nuclei and the adjacent contralateral parvicellular reticular formation. Differential lesions indicate that these “intertrigeminal” commissural connections arise chiefly from the parvicellular reticular formation that lies between PrV and the motor trigeminal nucleus.These experiments, which also included selective lesions of dorsal and rostral portions of PrV, failed to produce any evidence supporting the existence of an uncrossed principal sensory trigeminothalamic pathway in the rat. While selective, ventral zona incerta PrV connections can be demonstrated, no PrV intralaminar projections appear to exist. Initial findings show that comparable fully decussated PrV–VBm connections also exist in the guinea pig but that some ipsilaterally ascending fibers occur in monkeys (Smith, '72). These and other recent data demonstrate that phyletic neural variations exist in the PrV‐thalamic projections in various mammalian species.