Hypothalamospinal tract
The hypothalamospinal tract is an unmyelinated[1] non-decussated[2] descending nerve tract that arises in the hypothalamus and projects to the brainstem and spinal cord to synapse with pre-ganglionic autonomic (both sympathetic and parasympathetic) neurons. The direct autonomic projections of the hypothalamospinal tract represent a minority of the autonomic output of the hypothalamus; most is thought to project to various relay structures.[3] AnatomyOriginThe tract originates mainly from the paraventricular nucleus of hypothalamus,[4][2] with minor contributions from the dorsomedial, ventromedial, and posterior nuclei of hypothalamus,[4] and lateral hypothalamus.[5][verification needed] The neurons of the hypothalamospinal tract receive direct afferents from the ascending nociceptive sensory spinohypothalamic tract to mediate the autonomic response to painful stimuli.[3] The tract terminates upon pre-ganglionic autonomic neurons in the brainstem,[3] and spinal segments T1-L3 (sympathetic outflow), and S2-S4 (parasympathetic outflow).[1][3] Course/relationsThe tract descends through the periaqueductal gray,[5] through the dorsal longitudinal fasciculus,[1] and adjacent to the reticular formation.[5] In the brainstem, it descends in the lateral tegmentum of the midbrain, pons, and medulla oblongata. In the spinal cord, it descends in the dorsolateral quadrant of the lateral funiculus.[6] FunctionFibers of the tract terminating at the spinal segment T1 synapse with second-order neurons which in turn synapse in the superior cervical ganglion with third-order neurons which provide sympathetic innervation to the eyelids, pupil, and skin of the face.[7] The hypothalamospinal tract includes fibres by which the hypothalamus projects to the ciliospinal center in the spinal cord, a part of a brain circuit regulating pupillary dilatation as part of the pupillary reflex.[3] Some axons of the tract contain oxytocin.[1] Clinical significanceLesions of the hypothalamospinal tract above spinal cord level T1 cause ipsilateral Horner's syndrome, which is characterized by a triad of ptosis, miosis, and anhidrosis due to sympathetic denervation of the face.[6] References
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