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Query: UMLS:C0403608 (ureter)
 9,655 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The sensory innervations of the ureter in the dog were studied using the anterograde and retrograde axonal transport of wheat germ agglutinin-horseradish peroxidase conjugates (WGA-HRP). Following upper ureteral injections, labeled cells were observed in the ipsilateral T7-L3 spinal ganglia to the injection site, with the greatest concentration at the T12-L2 levels. And labeled cells were seen in the contralateral T7--L3 spinal ganglia to the injection site with the greatest concentration at the T10 and L3 ganglia. Lower ureter injections resulted in the labeling of ipsilateral T11-Co1 and contralateral T9-Co1 spinal ganglia, with highest concentration at the ipsilateral L3 and S2 levels. Following thoracic and lumbar spinal ganglia T12, L1-L3 injections labeled fibers bundles were observed in the adventitia of the upper and lower ureter. Some labeled fibers were bifurcated from these bundles and passed through the two layers of the smooth muscles. In tunica submucosa and tunica propria mucosae, many labeled fibers were observed. A few labeled fibers were seen in the epithelium. After injections into the sacral and coccygeal spinal ganglia S1-Co1, labeled fibers were not observed in the upper ureter. Course and distribution of labeled fibers in the lower ureter were similar to those of the case in which injection was done into the thoracic and lumbar spinal ganglia.
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PMID:[An experimental study of sensory innervation of the ureter in the dog using wheat germ agglutinin-horseradish peroxidase conjugates]. 168

The innervation of rat and guinea pig urinary tract was examined using immunohistochemistry, radioimmunoassay and True Blue retrograde tracing techniques and was further assessed following both surgical and chemical denervation experiments. Substantial amounts of calcitonin gene-related peptide-like immunoreactivity (range 20-150 pmol/g) were detected in tissue extracts and localised to nerve fibres distributed throughout the urinary tract of both species, these being concentrated in the ureter and base of the bladder. In the guinea pig, the number and distribution pattern of calcitonin gene-related peptide-like immunoreactive nerves appeared to be identical to that of substance P-containing nerves, whereas in the rat the former predominated. Seven days after injection of the fluorescent dye True Blue into tissues of the urinary tract, retrogradely labelled cells were found in the dorsal root ganglia. These cells had a segmental distribution pattern which was specific for each of the injection sites. Thus, after injection of True Blue into the left kidney hilum a single group of labelled cells were found in the ipsilateral T10-L2 dorsal root ganglia. In contrast, injection into the left ureter produced labelled cells in two separate groups of ipsilateral ganglia (T11-L3 and L6-S1). Injection into the wall of the bladder and upper urethra resulted in bilateral labelling, with most labelled cells occurring in L6 and S1 ganglia. Approximately 90% of labelled cells in T10-L3 dorsal root ganglia displayed calcitonin gene-related peptide-like immunoreactivity, but only 60% of retrogradely labelled bladder neurons in L6-S1 ganglia were immunoreactive for this peptide. Adult guinea pigs and neonatal rats injected systemically with capsaicin subsequently exhibited a marked reduction both in the amount of calcitonin gene-related peptide immunostaining and the concentration of immunoreactive material in the urinary tract, dorsal root ganglia and spinal cord. In rats treated neonatally with capsaicin, there was a significant reduction in the number of retrogradely labelled cells and a hypertrophy of the bladder. Sectioning of the pelvic and hypogastric nerves in the rat also resulted in a depletion of calcitonin gene-related peptide-like immunoreactive nerves in the bladder, whereas chemical sympathectomy appeared to have no effect. The results indicate that calcitonin gene-related peptide immunoreactivity occurs in a major proportion of afferent neurons supplying the urinary tract of the rat and guinea pig.(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Calcitonin gene-related peptide immunoreactivity in afferent neurons supplying the urinary tract: combined retrograde tracing and immunohistochemistry. 242 72

Experiments were done to examine the effect of occlusion of the uppermost portion of the ureter on activity of spinothalamic tract (STT) neurons. Fifteen monkeys (Macaca fascicularis) were anesthetized with alpha-chloralose. Extracellular unit recordings were obtained from 38 STT neurons in the T11-L1 segments. All cells were excited by renal A delta-afferent fibers or by both A delta- and C-fibers. In addition each cell had a somatic receptive field, most commonly located on the left flank and abdomen. Ureteral occlusion increased activity of 16 cells from 4 +/- 1 to a peak of 32 +/- 9 spikes/s. Peak responses occurred, on average, 3 s following the onset of occlusion. Thereafter activity adapted to a lower level. Cells that responded to ureteral occlusion were most often wide dynamic range cells and were significantly more likely to receive both A delta- and C-fiber renal input than the cells that failed to respond. In addition responses of cells with A delta- and C-fiber inputs were significantly greater than cells with only A delta-input. Responsive cells were located primarily in laminae V and VII. Results of these experiments show that occlusion of the uppermost portion of the ureter excites thoracolumbar STT cells. These cells probably play a role in pain of renal origin, including its referral to the flank and abdomen.
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PMID:Primate spinothalamic cell responses to ureteral occlusion. 280 25

Monoclonal antibodies were used to examine the pattern of distribution of lymphocyte subpopulations and macrophages in normal human urothelium. T lymphocytes (T11-positive cells) were demonstrated within the epithelium and within the lamina propria of both the ureter and the urinary bladder. Suppressor/cytotoxic T cells (T8-positive cells) predominated, with the average ratio of suppressor/cytotoxic T cells to the helper/inducer T cells being approximately 8.9 in the epithelium and 1.5 in the lamina propria. Leu M3+ cells (monocytes/macrophages) were detected in both epithelium and lamina propria. The character and distribution of these immunocompetent cells within the urothelium suggest a protective function, especially against infection and in tumour surveillance.
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PMID:Immunohistochemical identification of lymphocyte subsets and macrophages in normal human urothelium using monoclonal antibodies. 353 Mar 63

In rats with hyperalgesia of the obliquus externus muscle (OE) from artificial calculosis of the ipsilateral upper ureter, changes in cell activity were studied in the ipsilateral spinal cord (T11-T12) versus control animals. In cases of hyperalgesia of high degree, in the dorsal horn (0-900 microns) the following were found: significantly higher percentages of cells driven by OE stimulation (P < 0.03) and of spontaneously active cells with OE input (P < 0.02); significantly higher frequency of background discharge of cells with OE input (P < 0.002); among cells driven by OE stimulation, significantly higher percentages of neurons with exclusively deep input (P < 0.0006) and of neurons with low mechanical threshold of activation (P < 0.03). In the intermediate region of the cord (900-1600 microns), a significantly higher percentage was found of spontaneously active cells with OE input (P < 0.009) while in the ventral horn (1600-2300 microns) no changes were detected. The results indicate that referred muscle hyperalgesia of high degree is accompanied by a state of central sensitization probably triggered by the abnormal afferent input from the visceral focus.
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PMID:Changes in activity of spinal cells with muscular input in rats with referred muscular hyperalgesia from ureteral calculosis. 883

Rats with an artificial stone in the left ureter display spontaneous pain behavior (ureteral 'crises') and referred hyperalgesia/contraction in the ipsilateral oblique musculature. To evaluate neuronal activation in both sensitive and motor pathways in this model, c-Fos expression was studied in the spinal cord of calculosis rats vs. sham controls. Fos-labeled cells were never observed in sham controls. In stone rats, they were found in the T10-L2 segments, throughout the dorsal horn, significantly more on the left than the right side (P < 0.002). Fos-labeled cells were also found in lamina IX, containing motoneurons; at the T11-T12 level, these were significantly more on the left than the right side (P < 0.03). Nociceptive input from the ureter thus activates not only sensory but also efferent neurons in the spinal cord, suggesting the triggering of reflex arcs by the visceral focus.
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PMID:c-Fos expression in the spinal cord of female rats with artificial ureteric calculosis. 1513 31