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Benzodiazepine receptors in the human spinal cord: a detailed anatomical and pharmacological study
Authors:R L Faull  J W Villiger
Affiliation:1. Singapore Institute for Neurotechnology (SINAPSE), National University of Singapore, 28 Medical Drive, #05-COR 117456, Singapore;2. Department of Electrical & Computer Engineering, National University of Singapore, 4 Engineering Drive 3 117583, Singapore;3. Department of Physical Medicine and Rehabilitation, Chang Gung Memorial Hospital and Chang Gung University, Taoyuan 333, Taiwan, ROC;4. Department of Biomedical Engineering, National University of Singapore, 9 Engineering Drive 1 117575, Singapore;5. Department of Neurology, University of North Carolina, Chapel Hill, NC, USA;6. Department of Biomedical Engineering, National Yang Ming University, No. 155, Sec. 2, Linong St., Taipei 112, Taiwan, ROC;7. Department of Biomedical Engineering, Johns Hopkins University, Traylor 701/720 Rutland Ave, Baltimore, MD 21205, USA;1. The John W. Duckett Center for Pediatric Urology, Children''s Hospital of Philadelphia, The Perelman School of Medicine, University of Pennsylvania, United States;2. The Department of Anethesiology and Critical Care Medicine, Children''s Hospital of Philadelphia, The Perelman School of Medicine, University of Pennsylvania, United States;3. The Proteomics Core Laboratory, Children''s Hospital of Philadelphia, The Perelman School of Medicine, University of Pennsylvania, United States;2. School of Medicine, Southern Illinois University Springfield, Springfield, IL, USA
Abstract:The anatomical distribution and pharmacological characteristics of benzodiazepine receptors in the human spinal cord were examined in four cases aged 20-41 years using in vitro autoradiography and biochemical assays of [3H]flunitrazepam binding. In all cases, the autoradiograms demonstrated that benzodiazepine receptors were distributed in a consistently similar fashion in the gray matter of the cervical, thoracic, lumbar and sacral regions of the human spinal cord. At all levels, the highest densities of benzodiazepine receptors were found to be localized within lamina II of the dorsal horn as defined on cytoarchitectonic, myeloarchitectonic and substance P immunocytochemical criteria. Within this lamina the receptors were concentrated mainly in its deeper, inner portion which lies immediately adjacent to lamina III, with some overlap dorsally into the outer segment of lamina II and ventrally into the adjacent region of lamina III. The lowest density of receptors was found in regions of laminae I, IV, VII and X; in particular, in lamina VII the lowest concentration of receptors was found in the dorsal nucleus of Clarke and the sacral parasympathetic nucleus. The remaining laminae of the spinal gray (laminae, V, VI, VIII and IX) showed a moderate density of receptors. Biochemical assays of membranes prepared from the lumbosacral cord indicated that these [3H]flunitrazepam binding sites have high affinity and have the pharmacological characteristics of the "central" Type II benzodiazepine receptor. These results show a high concentration of Type II benzodiazepine receptors in the substantia gelatinosa of the human spinal cord and suggest a possible role for these receptors in spinal sensory functions.
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