Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UMLS:C0403608 (ureter)
9,655 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The innervation of the male genital tract and kidney in three anuran species was studied by the fluorescence histochemical method of Falck-Hillarp for the demonstration of monoamines whose identity was secured by thin-layer chromatography, and by electron microscopy including administration of 5- or 6- hydroxydopamine (5- and 6-ODHA). The genital tract comprises testis, intra- and extratesticular and intrarenal seminal efferent ducts, Bidder's canal, renal dorsal transverse ducts, and ureter. In addition--depending on the species studied--renal corpuscles and the various portions of uriniferous tubules may be involved in sperm transport. 1. Adrenaline is the main transmitter in nerves supplying the male genital tract and kidney. Only in Xenopus is it possible to demonstrate the presence of noradrenaline, which was confirmed in the chromatographic analysis. No obvious changes are observed with regard to the distribution, amount, and fluorescence intensity of adrenergic fibers and their susceptibility towards 5- and 6-OHDA when comparing animals killed in late autumn and winter, or in late spring, respectively. Non-adrenergic nerve fibers have not been observed. 2. The adrenergic innervation in the testis is only scarce and confined to blood vessels. Neuro-endocrine contacts on Leydig cells are not established. The gonadal ducts and the specific (i.e. non-vascular) are intratesticular smooth muscle cells in Xenopus are not innervated. 3. Apart from the uriniferous tubules (see below), only the ureter receives an adrenergic innervation which, however, is scarce even around the time of spermiation. Bundles of non-terminal and terminal axons are seen running contiguous to the superficial bundles of smooth muscle or smooth muscle-like cells. Neuromuscular relationships comprise synapses at distances of 2000-5--- A, but no close contacts. In the seminal vesicle of Rana the same mode of apposition of adrenergic terminals to muscle cells is observed. In addition, a direct innervation of the epithelium is seen in a few instances. 4. In the kidney the renal arteries, afferent arterioles, and the main branches of the kidney the renal arteries, afferent arterioles, and the main branches of the portal veins are supplied by a dense plexus of adrenergic nerves. Small groups of intensely fluorescent cells are found in the walls of the renal portal veins and veins proper. The density of the arteriolar plexus is more pronounced in Rana and Bufo than in Xenopus. In Rana and Bufo the arteriolar innervation comprises terminals at "ordinary" smooth musculature with membrane-to-membrane appositions, as well as contacts at a distance of 800 to 4000 A on juxtaglomerular epitheloid cells...
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PMID:Innervation of the male genital tract and kidney in the amphibia, Xenopus laevis Daudin, Rana temporaria L., and Bufo bufo L. 80 32

Investigations on the isolated pieces from upper part of human ureters and upper and lower parts of dog ureters were performed. Isometric contractions during electrical stimulation in Lock solution (37 degrees C) and their changes after adrenomimetic drug and adrenoblocking drug perfusion were studied. The pieces of human ureters had more average weight and rest tension, but less isometric tension during rhythmic electrical stimulation and more pronounced hypersodium contracture in contrast to dog ureters. Adrenaline and noradrenaline augmented contractions of human and dog ureters. Isadrin increased the contractility of the upper parts of human ureters and the lower parts of dog ureters, but decreased--the upper segments of dog ureters. Adrenoblocking agents modified the action of adrenomimetics. After blockade of alpha-receptors by phentolamine, isadrin decreased the contractions of all studied pieces of ureters, however, adrenaline decreased contractility of human ureters but increased--dog ureters. It may be proposed, that there are alpha 1 and alpha 2 receptors, that stimulated the contractility of human and dog ureters, beta 1 adrenoreceptors, that inhibited the contractions during blockade of alpha-receptors, and beta 2-receptors, that in these conditions increased the contractions of dog ureter but decreased the contractions of human ureters.
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PMID:[Adrenergic regulation of the contractility of the human and canine ureters]. 132 82

1. We have studied the effects of alpha- and beta-adrenoceptor agonists and antagonists on both phasic peristaltic activity and basal tone of the isolated intravesical ureter of the pig by means of isometric techniques in vitro. 2. Spontaneous phasic activity was exhibited by 21% of pig intravesical ureter preparations manifested as rhythmic contractions with average frequency and amplitude of 2.54 +/- 0.18 min-1 and 1.48 +/- 0.16 g (n = 31), respectively. 3. Adrenaline, noradrenaline and phenylephrine induced concentration-dependent increases in both phasic activity and basal tone of ureteral preparations, all three agonists being more potent in modifying ureteral phasic activity than baseline tone. B-HT 920, B-HT 933 and clonidine had no significant effect. 4. Phentolamine (10(-9)-10(-7) M) and prazosin (3 x 10(-11)-3 x 10(-8) M) significantly inhibited increases in both frequency of phasic activity and baseline tone induced by a submaximal dose of noradrenaline. Rauwolscine (10(-9)-10(-7) M) affected only the tone evoked by noradrenaline and higher concentrations of this antagonist were needed to block phasic activity. 5. Pretreatment of ureteral strips with the beta-adrenoceptor antagonist, propranolol (10(-6) M), significantly increased the maximum contraction evoked by noradrenaline. After incubation with phentolamine (10(-6) M), noradrenaline (10(-7)-10(-6) M) decreased phasic activity induced by prostaglandin F2 alpha (10(-5) M). Isoprenaline and salbutamol also abolished PGF2 alpha-induced phasic activity. Pafenolol (10(-6) M) and butoxamine (10(-6) M) blocked the inhibitory effect of noradrenaline, isoprenaline, and salbutamol on PGF2 alpha-induced phasic activity. 6. These results suggest that noradrenaline may modulate both phasic peristaltic activity and basal tone of pig intravesical ureter through both alpha- and beta-adrenoceptors.
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PMID:Noradrenaline modulates smooth muscle activity of the isolated intravesical ureter of the pig through different types of adrenoceptors. 136 2

1. A method of recording the peristaltic frequency and the rate of transport of fluid (perfusion rate) in the rat ureter in vivo is described.2. Acetylcholine and atropine did not alter ureteral activity. Histamine increased the rate of peristalsis by up to 15% and the rate of perfusion by up to 10%. Low doses of 5-hydroxytryptamine increased peristaltic frequency whereas high doses decreased peristaltic frequency; all doses reduced the rate of perfusion.3. Morphine reduced the rate of perfusion by 5-10% at all dose levels, but only the highest dose used reduced the frequency of ureteral peristalsis.4. (-)-Adrenaline, (-)-noradrenaline and (+/-)-isoprenaline reduced the frequency of peristalsis. The order of potency was isoprenaline>noradrenaline>adrenaline. The response was dose-related and blocked by propranolol, which itself did not affect ureteral activity.
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PMID:The pharmacology of the rat ureter in vivo. 504 47

The mechanical activity of isolated strips from different areas of the pyeloureteral system was investigated in 10 pigs: calyx, renal pelvis, pyeloureteral junction and ureter. Additionally, electrical activity was measured in some pyeloureteral preparations using the sucrose-gap technique. Regular spontaneous activity with an average frequency of 9.5/min was recorded in calyceal strips, decreasing to 5.4/min in renal pelvis, 5.7/min in pyeloureteral preparations and to 1.2/min in ureteral preparations. The activity of renal pelvis, pyeloureteral and ureteral preparations was less regular, and bursts of fast activity (near 10/min) could be observed in all these preparations. The membrane potential of pyeloureteral strips showed spontaneous generator oscillations of about 10/min. Variations in the pattern of ureteral peristalsis are due to different coupling ratios of membrane potential oscillations to contractions. Adrenaline (10(-5) mol/l) increased the frequency of the oscillations and enhanced their manifestation in the mechanical recordings, whereas tetraethylammonium (5-20 mmol/l) only increased the coupling ratio. The following concept for the generation of ureteral peristalsis in multicalyceal kidneys is developed: several (primary) oscillators exist in the calyces; in the pyeloureteral junction a (secondary) pacemaker exists which has an intrinsic frequency similar to that of the calyceal pacemakers; both processes cooperate in the generation of ureteral peristalsis.
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PMID:Pacemaker process of ureteral peristalsis in multicalyceal kidneys. 713 75