Literature DB >> 2438589

Opiate receptors in the human spinal cord: a detailed anatomical study comparing the autoradiographic localization of [3H]diprenorphine binding sites with the laminar pattern of substance P, myelin and nissl staining.

R L Faull, J W Villiger.   

Abstract

The anatomical localization of opiate receptors in the human spinal cord has been examined in six cases aged 7-41 years using quantitative autoradiographic methods following the incubation of fresh, unfixed cryostat sections with [3H]diprenorphine. In order to precisely localize the distribution of receptors in the spinal cord, the laminar anatomy of the spinal grey was demonstrated at each spinal level examined using 50-microns sections stained for myelin, Nissl substance and substance P. In all cases, autoradiograms demonstrated that opiate receptors were distributed in a similar fashion in the grey matter of the cervical, thoracic, lumbar, sacral and coccygeal regions of the human spinal cord. At all 25 spinal levels examined, opiate receptors were mainly localized within the upper laminae of the dorsal horn (laminae I-III) and within the tract of Lissauer. The highest density of opiate receptors was localized within the inner segment of lamina II where the receptors formed a very dense band lying immediately dorsal to lamina III. The density of receptors in this inner region of lamina II (33 +/- 2 fmol/mg) was more than two-and-one-half times greater than that in the remaining upper laminae which showed moderate receptor densities: lamina I (12 +/- 4 fmol/mg) and outer lamina II (13 +/- 3 fmol/mg) both showed similar receptor densities which were higher than those in lamina III (10 +/- 3 fmol/mg) The tract of Lissauer (11 +/- 2 fmol/mg) also showed a moderate density of opiate receptors which was intermediate between the densities in laminae I/IIo and the density of lamina III. The density of receptors in the remaining laminae of the spinal cord varied from moderately low to virtually zero. Moderately low densities of receptors were found in laminae V, VI, VIII, IX and X with very low levels within laminae IV and VII. In particular, in lamina VII opiate receptors were unable to be detected above normal background levels in the dorsal nucleus of Clarke. These results show that, as in other mammalian species, opiate receptors in the human spinal cord are mainly concentrated in the upper laminae of the dorsal horn and in the tract of Lissauer. The possible role of these receptors in modulating spinal nociceptive information is discussed with respect to previous findings on the relationship of opiate receptors to primary afferent fibres in the spinal cord.

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Year:  1987        PMID: 2438589     DOI: 10.1016/0306-4522(87)90100-x

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  9 in total

1.  Mu opioid receptors in developing human spinal cord.

Authors:  S B Ray; S Wadhwa
Journal:  J Anat       Date:  1999-07       Impact factor: 2.610

2.  Actions of opioids on excitatory and inhibitory transmission in substantia gelatinosa of adult rat spinal cord.

Authors:  T Kohno; E Kumamoto; H Higashi; K Shimoji; M Yoshimura
Journal:  J Physiol       Date:  1999-08-01       Impact factor: 5.182

Review 3.  Intrathecal drug administration. Present use and future trends.

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Authors:  Akiko Koga; Tsugumi Fujita; Tadahide Totoki; Eiichi Kumamoto
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5.  Opioid analgesia alters corticospinal coupling along the descending pain system in healthy participants.

Authors:  Christian Sprenger; Christian Büchel; Alexandra Tinnermann
Journal:  Elife       Date:  2022-04-26       Impact factor: 8.713

6.  Suppression of noxious stimulus-evoked activity in the ventral posterolateral nucleus of the thalamus by a cannabinoid agonist: correlation between electrophysiological and antinociceptive effects.

Authors:  W J Martin; A G Hohmann; J M Walker
Journal:  J Neurosci       Date:  1996-10-15       Impact factor: 6.167

7.  kappa-Opioid receptor in humans: cDNA and genomic cloning, chromosomal assignment, functional expression, pharmacology, and expression pattern in the central nervous system.

Authors:  F Simonin; C Gavériaux-Ruff; K Befort; H Matthes; B Lannes; G Micheletti; M G Mattéi; G Charron; B Bloch; B Kieffer
Journal:  Proc Natl Acad Sci U S A       Date:  1995-07-18       Impact factor: 11.205

8.  Chronic opioid therapy and opioid tolerance: a new hypothesis.

Authors:  Joel S Goldberg
Journal:  Pain Res Treat       Date:  2013-01-14

9.  DAMGO modulates two-pore domain K(+) channels in the substantia gelatinosa neurons of rat spinal cord.

Authors:  Pyung Sun Cho; Han Kyu Lee; Sang Hoon Lee; Jay Zoon Im; Sung Jun Jung
Journal:  Korean J Physiol Pharmacol       Date:  2016-08-26       Impact factor: 2.016

  9 in total

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