Increased c-fos expression in spinal neurons induced by electrical stimulation of the ureter in the rat |
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Authors: | Genichi Matsumoto Margaret A. Vizzard Tadashi Hisamitsu William C. de Groat |
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Affiliation: | aDepartment of Pharmacology, University of Pittsburgh, School of Medicine, W1352 Biomedical Science Tower, Pittsburgh, PA 15261, USA;bDepartment of Physiology, Showa University, Tokyo, Japan |
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Abstract: | The spinal processing of afferent input from the ureter was examined using an immunocytochemical technique to detect the expression of c-fos, an immediate early gene. Proximal and distal sites in one ureter were electrically stimulated separately or together at intensities that elicited a pseudo-affective response (an increase in arterial pressure). Very few Fos + cells (range: 0.6–6.6 cells/half section were present in the L1-L2, L5-S2 spinal segments in sham operated control animals; however, following stimulation of the ureter, a significant increase in the numbers of Fos + cells was detected at spinal levels L1-L2 (mean 24.5–33.1 cells/half section) and L6-S1 (mean 17.4–33.0 cells/half section). In L6-S1,the numbers of Fos + cells were significantly greater ipsilateral (mean 25.2 cells/half section) vs. contralateral (12.3 cells/half section) to stimulation; whereas in L1-L2, the numbers were similar on both sides of the spinal cord. In L1-L2, a greater percentage of Fos + cells was present in superficial medial (MDH, 49.7%) and lateral dorsal hom (LDH, 40.8%); whereas in L6-S1, the cells were more numerous in sacral parasympathetic nucleus (SPN, 38.7%) and LDH (25.6%) regions. This distribution of Fos + cells varies in a number of respects from that noted in previous experiments after chemical irritation of the urinary bladder and urethra which activated neurons only in L6-S1 and primarily in the DCM and MDH. The results indicate that nociceptive afferent inputs from different areas of the urinary tract are processed in different regions of the spinal cord. |
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Keywords: | c-fos Ureter Electrical stimulation Rat Spinal cord Afferent input |
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