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- W1977821665 abstract "In the light of hypotheses related to the evolution of pain-carrying systems in mammals, terminal projection fields in brainstem and diencephalon of efferents of nucleus caudalis (NC) of the spinal trigeminal complex and spinal cord were determined in hedgehog by using Nauta-Gygax and Fink-Heimer silver techniques for degeneration. Unilateral NC lesions resulted in medullary degeneration in the ventral portion of NC contralaterally and bilaterally in cuneate nucleus (CU) and reticular formation. Pontine degeneration was noted ipsilaterally in medial (PBM) and lateral (PBL) parabrachial, facial motor (VII), and interpolar, oral, and main sensory trigeminal nuclei; degeneration in reticular formation was bilateral. Midbrain degeneration was seen bilaterally in caudal superior colliculus (SC), inferior colliculus (IC), periaqueductal gray, and tegmentum. In thalamus, projections to ventroposterior nucleus (VP) were contralateral and concentrated in a crescent extending along the lateral one-third-to-one-half and ventral border of the nucleus. Bilateral degeneration fields were noted in a dorsomedial sector of the ventral nuclear field, posterior complex (PO), and mediodorsal nucleus (MD), the degeneration always heavier contralaterally in these nuclei. Sparse degeneration was noted in the medial most portions of the medial geniculate nuclei bordering PO and VP. In rostral diencephalon, bilateral degeneration was traced from the inferior thalamic peduncle to the lateral hypothalamic area (LH). Unilateral spinal cord lesions made between C7 and T1 vertebrae resulted in medullary degeneration in NC contralaterally, ipsilaterally in CU and lateral cuneate nucleus, and bilaterally in gracile nucleus, inferior olivary complex, and reticular formation. Pontine degeneration was limited to ipsilateral PBL and bilaterally to VII. Midbrain degeneration was found bilaterally in IC, SC, nucleus sagulum, and tegmentum; a minor projection was noted in interpeduncular nucleus. In thalamus, projections were confined to ipsilateral PO and zona incerta. In rostral diencephalon bilateral fields were noted in LH. NC terminations in PO and VP parallel results of research in hedgehogs on thalamic projections of the dorsal column nuclei (Jane and Schroeder, '71), and particularly the location in VP of most cells responsive to stimulation of the face (Erickson et al., '67). This suggests that somatic input from NC, some of which may be pain-specific, reaches thalamic areas, a portion of whose neurons are characterized as polymodal and at least partially convergent for somatotopy. These results are consistent with the thesis that specific sensory thalamic nuclei evolved from a diffuse sensory region. Response properties of neurons in the dorsomedial portion of the ventral nuclear field, an area which are also received NC efferents, are not known. Last, NC projections to MD and LH implicate the role of limbic aspects of nociception." @default.
- W1977821665 created "2016-06-24" @default.
- W1977821665 creator A5049892960 @default.
- W1977821665 creator A5069031883 @default.
- W1977821665 date "1983-05-10" @default.
- W1977821665 modified "2023-10-16" @default.
- W1977821665 title "Projections of nucleus caudalis and spinal cord to rrainstem and diencephalon in the hedgehog (Erinaceus europaeus andParaechinus aethiopicus): A degeneration study" @default.
- W1977821665 cites W116098567 @default.
- W1977821665 cites W170990903 @default.
- W1977821665 cites W1794801390 @default.
- W1977821665 cites W1872169714 @default.
- W1977821665 cites W1891398114 @default.
- W1977821665 cites W1944937124 @default.
- W1977821665 cites W1963908731 @default.
- W1977821665 cites W1972852833 @default.
- W1977821665 cites W1973967201 @default.
- W1977821665 cites W1976876069 @default.
- W1977821665 cites W1978217305 @default.
- W1977821665 cites W1987736882 @default.
- W1977821665 cites W1987934840 @default.
- W1977821665 cites W1990840741 @default.
- W1977821665 cites W2000437871 @default.
- W1977821665 cites W2001604678 @default.
- W1977821665 cites W2002099931 @default.
- W1977821665 cites W2003164779 @default.
- W1977821665 cites W2003577865 @default.
- W1977821665 cites W2006217500 @default.
- W1977821665 cites W2008102822 @default.
- W1977821665 cites W2017001210 @default.
- W1977821665 cites W2018368339 @default.
- W1977821665 cites W2018588547 @default.
- W1977821665 cites W2019695325 @default.
- W1977821665 cites W2021218675 @default.
- W1977821665 cites W2024689361 @default.
- W1977821665 cites W2028728373 @default.
- W1977821665 cites W2028945301 @default.
- W1977821665 cites W2036396670 @default.
- W1977821665 cites W2036549841 @default.
- W1977821665 cites W2036812284 @default.
- W1977821665 cites W2037131117 @default.
- W1977821665 cites W2038437873 @default.
- W1977821665 cites W2039367971 @default.
- W1977821665 cites W2040578258 @default.
- W1977821665 cites W2042577042 @default.
- W1977821665 cites W2044249049 @default.
- W1977821665 cites W2044299701 @default.
- W1977821665 cites W2046020290 @default.
- W1977821665 cites W2050798099 @default.
- W1977821665 cites W2052754336 @default.
- W1977821665 cites W2052956440 @default.
- W1977821665 cites W2054453410 @default.
- W1977821665 cites W2060085638 @default.
- W1977821665 cites W2062372446 @default.
- W1977821665 cites W2064810982 @default.
- W1977821665 cites W2079620852 @default.
- W1977821665 cites W2082856740 @default.
- W1977821665 cites W2086095601 @default.
- W1977821665 cites W2092085055 @default.
- W1977821665 cites W2093492951 @default.
- W1977821665 cites W2094667628 @default.
- W1977821665 cites W2100528415 @default.
- W1977821665 cites W2101682699 @default.
- W1977821665 cites W2108031671 @default.
- W1977821665 cites W2117459625 @default.
- W1977821665 cites W2134904201 @default.
- W1977821665 cites W2136099176 @default.
- W1977821665 cites W2150296457 @default.
- W1977821665 cites W2150957815 @default.
- W1977821665 cites W2153961094 @default.
- W1977821665 cites W2167153260 @default.
- W1977821665 cites W2169760350 @default.
- W1977821665 cites W2222239144 @default.
- W1977821665 cites W2253176756 @default.
- W1977821665 cites W2276864346 @default.
- W1977821665 cites W2277539688 @default.
- W1977821665 cites W2400935632 @default.
- W1977821665 cites W2405019314 @default.
- W1977821665 cites W2416261878 @default.
- W1977821665 cites W2416304624 @default.
- W1977821665 cites W2423501477 @default.
- W1977821665 cites W2612202155 @default.
- W1977821665 cites W2737366357 @default.
- W1977821665 cites W4236449552 @default.
- W1977821665 cites W4251222195 @default.
- W1977821665 cites W4298355257 @default.
- W1977821665 cites W4321429378 @default.
- W1977821665 cites W4361805901 @default.
- W1977821665 cites W2077382424 @default.
- W1977821665 doi "https://doi.org/10.1002/cne.902160203" @default.
- W1977821665 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/6863599" @default.
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