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AI InsightWe propose that the main effect of the straight spinal input into the limbic system is to facilitate nociceptive sensitivity, but not to suppress nociceptive trans-mission on the level of the spinal cord.
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Özet
In the present study, we made an attempt to detect more exactly the laminar distribution of spinomesencephalic, spinothalamic and spinotelencephalic tract neurons and to estimate the character of axonal collateralization in these spinosupraspinal pathways in the rat by means of retrograde double-labelling of cells with Fluoro-Gold (FG) and Primuline O (Pr). We found that sources of spino-supraspinal pathways to the upper centers of the brain stem, nucleus accumbens and septal nuclei were mixed together in the marginal zone, deep dorsal horn, reticulated area, lamina X and the lateral spinal nucleus, but have as a rule their own discrete projection fields. Thus, spinosupraspinal projections could be characterized as extensive but not diffuse according to the current concept of structural and functional organization of the ascending spinal systems related with pain or motivational-affective reactions connected with pain. It was shown recently that suppression of tonic activity in an ascending spino-supraspinal pathway activates a descending supraspinal anti-nociceptive circuit with an opioid link in nu-cleus accumbens. We propose that the main effect of the straight spinal input into the limbic system is to facilitate nociceptive sensitivity, but not to suppress nociceptive trans-mission on the level of the spinal cord.
Abstract
In the present study, we made an attempt to detect more exactly the laminar distribution of spinomesencephalic, spinothalamic and spinotelencephalic tract neurons and to estimate the character of axonal collateralization in these spinosupraspinal pathways in the rat by means of retrograde double-labelling of cells with Fluoro-Gold (FG) and Primuline O (Pr). We found that sources of spino-supraspinal pathways to the upper centers of the brain stem, nucleus accumbens and septal nuclei were mixed together in the marginal zone, deep dorsal horn, reticulated area, lamina X and the lateral spinal nucleus, but have as a rule their own discrete projection fields. Thus, spinosupraspinal projections could be characterized as extensive but not diffuse according to the current concept of structural and functional organization of the ascending spinal systems related with pain or motivational-affective reactions connected with pain. It was shown recently that suppression of tonic activity in an ascending spino-supraspinal pathway activates a descending supraspinal anti-nociceptive circuit with an opioid link in nu-cleus accumbens. We propose that the main effect of the straight spinal input into the limbic system is to facilitate nociceptive sensitivity, but not to suppress nociceptive trans-mission on the level of the spinal cord.