Effects of cervical spinal hemisection on dihydromorphine binding in brainstem and spinal cord in cat
Cats were sacrificed 1–3 weeks after cervical (C 1-C 2) hemisection and receptor binding experiments were carried out with 4.0 and 0.6 nM concentrations of [ 3H]dihydromorphine ([ 3H]DHM); these concentrations were shown by Scatchard analysis to represent the approximate K d values of high and low a...
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Veröffentlicht in: | Brain research 1989-03, Vol.483 (1), p.61-67 |
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description | Cats were sacrificed 1–3 weeks after cervical (C
1-C
2) hemisection and receptor binding experiments were carried out with 4.0 and 0.6 nM concentrations of [
3H]dihydromorphine ([
3H]DHM); these concentrations were shown by Scatchard analysis to represent the approximate K
d values of high and low affinity dihydromorphine binding sites in brain homogenates. Unilateral cervical hemisection produced significant (P < 0.05), bilateral, reductions in the levels of [
3H]DHM binding in the periaqueductal gray (PAG; 35–40%) and mesencephalic reticular formation (MRF; 47–51%), medial pons (40–56%) and medial medulla (30–37%). In paramedial pons and medulla, numerical reductions in [
3H]DHM binding were observed (18 and 28%) which did not achieve statistical significance. In spinal cord, significant reductions were observed in the dorsal (45%) and ventral (29%) ipsilateral but not contralateral quadrants. We believe that these results in the brainstem and spinal cord reflect in part the loss of opiate binding on spinobulbar terminals and bulbospinal terminals, respectively, following orthograde degeneration. These observations support the hypothesis that the analgetic effects of opiates in the brainstem may in part be mediated by the direct inhibition of transmission through spinobulbar terminals. |
doi_str_mv | 10.1016/0006-8993(89)90034-6 |
format | Article |
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1-C
2) hemisection and receptor binding experiments were carried out with 4.0 and 0.6 nM concentrations of [
3H]dihydromorphine ([
3H]DHM); these concentrations were shown by Scatchard analysis to represent the approximate K
d values of high and low affinity dihydromorphine binding sites in brain homogenates. Unilateral cervical hemisection produced significant (P < 0.05), bilateral, reductions in the levels of [
3H]DHM binding in the periaqueductal gray (PAG; 35–40%) and mesencephalic reticular formation (MRF; 47–51%), medial pons (40–56%) and medial medulla (30–37%). In paramedial pons and medulla, numerical reductions in [
3H]DHM binding were observed (18 and 28%) which did not achieve statistical significance. In spinal cord, significant reductions were observed in the dorsal (45%) and ventral (29%) ipsilateral but not contralateral quadrants. We believe that these results in the brainstem and spinal cord reflect in part the loss of opiate binding on spinobulbar terminals and bulbospinal terminals, respectively, following orthograde degeneration. These observations support the hypothesis that the analgetic effects of opiates in the brainstem may in part be mediated by the direct inhibition of transmission through spinobulbar terminals.</description><identifier>ISSN: 0006-8993</identifier><identifier>EISSN: 1872-6240</identifier><identifier>DOI: 10.1016/0006-8993(89)90034-6</identifier><identifier>PMID: 2539891</identifier><identifier>CODEN: BRREAP</identifier><language>eng</language><publisher>London: Elsevier B.V</publisher><subject>Analgesia ; Animals ; Biological and medical sciences ; Brain Stem - cytology ; Brain Stem - metabolism ; Cats ; Dihydromorphine ; Dihydromorphine - metabolism ; Fundamental and applied biological sciences. Psychology ; Medulla ; Morphine Derivatives - metabolism ; Neural Pathways - metabolism ; Opiate binding ; Periaqueductal gray ; Receptors, Opioid - metabolism ; Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors ; Spinal Cord - cytology ; Spinal Cord - metabolism ; Vertebrates: nervous system and sense organs</subject><ispartof>Brain research, 1989-03, Vol.483 (1), p.61-67</ispartof><rights>1989 Elsevier Science Publishers B.V. (Biomedical Division)</rights><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c333t-b955b4ebe97f18be7bb61ab3bb078d9235eb02e66934ac13964d9e77e408be123</citedby><cites>FETCH-LOGICAL-c333t-b955b4ebe97f18be7bb61ab3bb078d9235eb02e66934ac13964d9e77e408be123</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0006899389900346$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=19510554$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2539891$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ramberg, Donald A.</creatorcontrib><creatorcontrib>Yaksh, Tony L.</creatorcontrib><title>Effects of cervical spinal hemisection on dihydromorphine binding in brainstem and spinal cord in cat</title><title>Brain research</title><addtitle>Brain Res</addtitle><description>Cats were sacrificed 1–3 weeks after cervical (C
1-C
2) hemisection and receptor binding experiments were carried out with 4.0 and 0.6 nM concentrations of [
3H]dihydromorphine ([
3H]DHM); these concentrations were shown by Scatchard analysis to represent the approximate K
d values of high and low affinity dihydromorphine binding sites in brain homogenates. Unilateral cervical hemisection produced significant (P < 0.05), bilateral, reductions in the levels of [
3H]DHM binding in the periaqueductal gray (PAG; 35–40%) and mesencephalic reticular formation (MRF; 47–51%), medial pons (40–56%) and medial medulla (30–37%). In paramedial pons and medulla, numerical reductions in [
3H]DHM binding were observed (18 and 28%) which did not achieve statistical significance. In spinal cord, significant reductions were observed in the dorsal (45%) and ventral (29%) ipsilateral but not contralateral quadrants. We believe that these results in the brainstem and spinal cord reflect in part the loss of opiate binding on spinobulbar terminals and bulbospinal terminals, respectively, following orthograde degeneration. These observations support the hypothesis that the analgetic effects of opiates in the brainstem may in part be mediated by the direct inhibition of transmission through spinobulbar terminals.</description><subject>Analgesia</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Brain Stem - cytology</subject><subject>Brain Stem - metabolism</subject><subject>Cats</subject><subject>Dihydromorphine</subject><subject>Dihydromorphine - metabolism</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Medulla</subject><subject>Morphine Derivatives - metabolism</subject><subject>Neural Pathways - metabolism</subject><subject>Opiate binding</subject><subject>Periaqueductal gray</subject><subject>Receptors, Opioid - metabolism</subject><subject>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</subject><subject>Spinal Cord - cytology</subject><subject>Spinal Cord - metabolism</subject><subject>Vertebrates: nervous system and sense organs</subject><issn>0006-8993</issn><issn>1872-6240</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFUctKAzEUDaLUWv0DhdkouhjNYyYz2Qgi9QGCG12HPO7YSCepyVTw701t1Z1CyCWcBzfnIHRI8DnBhF9gjHnZCsFOW3EmMGZVybfQmLQNLTmt8DYa_1B20V5Kr_nJmMAjNKI1E60gYwTTrgMzpCJ0hYH47oyaF2nhfB4z6F3KoAu-yMe62YeNoQ9xMXMeCu28df6lcL7QUTmfBugL5e233IRoV6BRwz7a6dQ8wcFmTtDzzfTp-q58eLy9v756KA1jbCi1qGtdgQbRdKTV0GjNidJMa9y0VlBWg8YUOBesUoYwwSsroGmgwplNKJugk7XvIoa3JaRB5h8YmM-Vh7BMsuFUMCLaf4mkppy2eakJqtZEE0NKETq5iK5X8UMSLFc1yFXGcpVxvuRXDZJn2dHGf6l7sD-iTe4ZP97gKuXEu6i8cenXW9QE13WVeZdrHuTU3h1EmYwDb8C6mJuRNri_F_kEiqOkbA</recordid><startdate>19890327</startdate><enddate>19890327</enddate><creator>Ramberg, Donald A.</creator><creator>Yaksh, Tony L.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>19890327</creationdate><title>Effects of cervical spinal hemisection on dihydromorphine binding in brainstem and spinal cord in cat</title><author>Ramberg, Donald A. ; Yaksh, Tony L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c333t-b955b4ebe97f18be7bb61ab3bb078d9235eb02e66934ac13964d9e77e408be123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Analgesia</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Brain Stem - cytology</topic><topic>Brain Stem - metabolism</topic><topic>Cats</topic><topic>Dihydromorphine</topic><topic>Dihydromorphine - metabolism</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Medulla</topic><topic>Morphine Derivatives - metabolism</topic><topic>Neural Pathways - metabolism</topic><topic>Opiate binding</topic><topic>Periaqueductal gray</topic><topic>Receptors, Opioid - metabolism</topic><topic>Somesthesis and somesthetic pathways (proprioception, exteroception, nociception); interoception; electrolocation. Sensory receptors</topic><topic>Spinal Cord - cytology</topic><topic>Spinal Cord - metabolism</topic><topic>Vertebrates: nervous system and sense organs</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ramberg, Donald A.</creatorcontrib><creatorcontrib>Yaksh, Tony L.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Brain research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ramberg, Donald A.</au><au>Yaksh, Tony L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of cervical spinal hemisection on dihydromorphine binding in brainstem and spinal cord in cat</atitle><jtitle>Brain research</jtitle><addtitle>Brain Res</addtitle><date>1989-03-27</date><risdate>1989</risdate><volume>483</volume><issue>1</issue><spage>61</spage><epage>67</epage><pages>61-67</pages><issn>0006-8993</issn><eissn>1872-6240</eissn><coden>BRREAP</coden><abstract>Cats were sacrificed 1–3 weeks after cervical (C
1-C
2) hemisection and receptor binding experiments were carried out with 4.0 and 0.6 nM concentrations of [
3H]dihydromorphine ([
3H]DHM); these concentrations were shown by Scatchard analysis to represent the approximate K
d values of high and low affinity dihydromorphine binding sites in brain homogenates. Unilateral cervical hemisection produced significant (P < 0.05), bilateral, reductions in the levels of [
3H]DHM binding in the periaqueductal gray (PAG; 35–40%) and mesencephalic reticular formation (MRF; 47–51%), medial pons (40–56%) and medial medulla (30–37%). In paramedial pons and medulla, numerical reductions in [
3H]DHM binding were observed (18 and 28%) which did not achieve statistical significance. In spinal cord, significant reductions were observed in the dorsal (45%) and ventral (29%) ipsilateral but not contralateral quadrants. We believe that these results in the brainstem and spinal cord reflect in part the loss of opiate binding on spinobulbar terminals and bulbospinal terminals, respectively, following orthograde degeneration. These observations support the hypothesis that the analgetic effects of opiates in the brainstem may in part be mediated by the direct inhibition of transmission through spinobulbar terminals.</abstract><cop>London</cop><cop>Amsterdam</cop><cop>New York, NY</cop><pub>Elsevier B.V</pub><pmid>2539891</pmid><doi>10.1016/0006-8993(89)90034-6</doi><tpages>7</tpages></addata></record> |
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subjects | Analgesia Animals Biological and medical sciences Brain Stem - cytology Brain Stem - metabolism Cats Dihydromorphine Dihydromorphine - metabolism Fundamental and applied biological sciences. Psychology Medulla Morphine Derivatives - metabolism Neural Pathways - metabolism Opiate binding Periaqueductal gray Receptors, Opioid - metabolism Somesthesis and somesthetic pathways (proprioception, exteroception, nociception) interoception electrolocation. Sensory receptors Spinal Cord - cytology Spinal Cord - metabolism Vertebrates: nervous system and sense organs |
title | Effects of cervical spinal hemisection on dihydromorphine binding in brainstem and spinal cord in cat |
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