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A reconstruction was made of the trajectory of primary spindle afferents from the intercostal muscles in the spinal cord of the cat. Intraaxonal recordings were performed from the primary spindle afferents that were identified by their response to lung inflation and stimulus threshold to activate the action potentials. The afferents were stained by using intraaxonal injection of horseradish peroxidase (HRP). Results were obtained mainly from internal intercostal Ia fibers, which entered the spinal cord and bifurcated into ascending and descending branches. The ascending branches could be traced up to 10.7 mm, and the descending branches could be traced up to 7.3 mm. The ascending branches extended to the next segment. Collaterals ranging from one to six were given off from these branches. The distances between adjacent collaterals ranged from 0.9 mm to 4.7 mm. Each collateral had similar morphological characteristics. The collaterals entered the dorsal horn and ran toward lamina IX through the medial half of the gray matter. Fine branches and boutons were given off in laminae V, VII, VIII, and IX. The aggregations of these branches were found in lamina VII, mainly in the region of Clarke's column and in the ventral and ventrolateral regions thereof and in lamina IX, mainly in the nucleus lateromedialis. Most terminals did not contact the somata of target neurons in all laminae in which terminals were found. However, a few terminals were found to contact large neurons in lamina IX. In addition to these aggregates, there were some terminals scattered throughout the ventral horn. Thus, it was concluded that single intercostal Ia afferents project to the region of Clarke's column, to the intercostal motor nucleus, and to the intermediate regions.

The morphology of jaw-muscle spindle afferents in the rat has been studied by intra-axonal injection of horseradish peroxidase. All stained axons were located in the motor root of the trigeminal nerve and could be traced dorsomedially to the vicinity of the trigeminal motor nucleus, where they divided into an ascending branch in the tract of the mesencephalic nucleus and a descending branch in the tract of Probst. Axon collaterals and swellings on fine collateral branches presumed to be synaptic boutons were located in the following regions: the trigeminal motor nucleus, the region dorsal to the trigeminal motor nucleus including the supratrigeminal nucleus, the parvicellular reticular formation immediately caudal to the trigeminal motor nucleus, the reticular formation at the level of the facial nucleus, and the caudal portion of the mesencephalic nucleus. No evidence of a projection to the cerebellum was observed. Boutons were most numerous in the region surrounding the trigeminal motor nucleus, especially dorsally. Here they were not demonstrated in close proximity to counterstained cells, and therefore it was not possible to determine how many of these contacts are located on cells in this region and how many are on the distal dendrites of trigeminal motorneurons. Boutons located within the trigeminal motor nucleus were always confined to a small portion of the nucleus and were significantly larger than those located dorsally. Some boutons were found in close apposition to trigeminal motorneurons and presumably make somatic contacts. These results suggest that jaw-muscle spindle afferents make somatic and proximal dendritic contacts with only a limited number of trigeminal motorneurons and also project to masticatory interneuronal regions dorsal and caudal to the motor nucleus.

Patterns of innervation were examined in tandem muscle spindles teased from silver-stained muscles of the cat neck. Each tandem spindle was composed of two or more encapsulated receptors linked in series by a shared bag2 fiber. In most tandem spindles, two different types of encapsulation were identified according to differences in their intrafusal fiber content. One type, the b1b2c unit, contained typical bag1, bag2, and chain fibers and was structurally similar to single spindles described in other cat muscles. Each b1b2c unit contained a single primary sensory ending and 1-6 secondary endings. Fusimotor innervation was supplied by many axons. Some fusimotor axons ended in trail ramifications on bag2 and chain fibers, others ended in plates on the bag1 or long chain fiber. The other type of tandem encapsulation, the b2c unit, had only bag2 and chain fibers in its intrafusal fiber bundle. The b2c unit was usually supplied by only one sensory axon that ended on the nucleated part of the intrafusal fiber bundle. This single ending had a more variable terminal morphology than the primary ending in b1b2c units. A few b2c units (3/49) were also supplied by a secondary ending. The fusimotor innervation of the b2c unit was relatively simple. A single pole of the b2c unit was usually supplied by only one to three axons, all ending in trail ramifications. No plate endings were found in b2c units. These morphological specializations suggest that b1b2c and b2c units in tandem spindles differ in both their transductive and fusimotor mechanisms. Thus, the tandem spindle is a specialized structure that may provide additional proprioceptive information beyond that available from single muscle spindles.