Abstract
Previous studies from this laboratory have localized and morphologically characterized phrenic motor neurons in the rat spinal cord at light and electron microscopic levels. The present investigation used a modification of the TMB method for the retrograde transport of horseradish peroxidase (HRP) to describe at light microscope levels the origin and distribution of phrenic primary afferent axons in the adult rat spinal cord. Dry HRP crystals were applied to the central stump of the transected phrenic nerve in the neck to label spinal ganglion cell bodies and thus determine the levels of origin of afferent axons in the phrenic nerve. Camera lucida drawings were then made from serial sections through the appropriate spinal cord levels to determine the specific distribution of transganglionically labeled phrenic central axonal processes within the spinal cord. HRP-labeled phrenic primary neurons were observed in the C3 to C7 spinal ganglia. The camera lucida studies indicated that the transganglionically labeled central processes of phrenic primary afferent axons distributed into the dorsal horn at the C4 and C5 levels of the spinal cord. Furthermore, central processes distributing to C5 were more numerous than those that distributed to C4. Afferent axons were never seen in the dorsal horn at C3, C6, or C7. As spinal ganglion cells were labeled at C3 above and C6 and C7 below, it follows that central processes of phrenic afferent fibers descend and ascend in the dorsal columns of the spinal cord before distributing into the dorsal horn. Specifically, the labeled primary afferent axons and their collateral branches were found in the fasciculus cuneatus, and in laminae I, II, III, and IV of the dorsomedial aspect of the dorsal horn. The function of these central axonal processes is unknown, but based on a comparison of our morphologic data with previous physiological and anatomical studies, we suggest that phrenic afferent fibers may arise from (i) proprioceptors (muscle spindles and Golgi tendon organs), (ii) nociceptors, or (iii) rapidly adapting mechanoreceptors (Pacinian corpuscles) within the diaphragm.
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