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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 55 (1977), S. 823-824 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 43 (1965), S. 410-413 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Summary In micropuncture experiments of the rat kidney solutions of various electrolyte compositions were injected into the tubule near the site of the macula densa cells. In kidneys with high renin an increase in Na+-concentration at this site by injection of 150 mMol/l NaCl or NaBr produced a transient collapse of the proximal convolution only of the same nephron. The collapse occurred within 10 sec after injection and the tubule was completely reopened within 60 sec after injection was stopped. The reaction was often repeated in the tubule 20 times. 150 mMol/l cholinchloride and 300 mMol/l Mannitol injections were not followed by collapse. This indicates that the osmolar concentrationper se is not the primary cause of the reaction. The Na+-specific reaction was absent or almost abolished in renin depleted kidneys. The macula densa cells are part of the juxtaglomerular apparatus and in direct contact with the renin producing cells of the afferent arteriole of the same nephron. We would like to suggest that the proximal collapse is the result of constriction of the afferent arteriole due to stimulation of renin secretion by increased Na+-concentration at the macula densa site. This inverse relation between [Na+] at the macula densa site and glomerular filtration would in effect be a feedback mechanism for the regulation of tubular sodium load, GFR, and RBF.
    Notes: Zusammenfassung In Mikropunktionsversuchen an der Ratte wurde die Elektrolytzusammensetzung am Macula densa-Segment eines einzelnen Nephrons experimentell verändert. In Nieren mit hohem Reningehalt ließ sich durch Erhöhung der NaCl-Konzentration eine vorübergehende Unterbrechung des Glomerulumfiltrates dieses einzelnen Nephrons hervorrufen. Eine gleiche Wirkung hat NaBr, dagegen sind Cholinchlorid und elektrolytfreie Mannitollösung ohne Effekt. Diese Na+-spezifische Reaktion ist an stark reninverarmten Nieren nicht oder nur in geringem Ausmaß nachweisbar. Die Verminderung des Einzelnephronfiltrates setzt innerhalb von 10 sec nach Erhöhung der Na+-Konzentration im Macula densa-Segment ein. Das Macula densa-Segment steht als Bestandteil des juxtaglomerulären Apparates in direktem Kontakt mit den reninbildenden Epitheloidzellen der afferenten Arteriole der gleichen Nephroneinheit. Es ist naheliegend anzunehmen, daß die Filtratunterbrechung durch eine präglomeruläre Vasoconstriction, ausgelöst durch eine lokale Aktivierung des Renin-Angiotensin-systems, zustande kommt. Auf Grund unserer Befunde wird zwischen dem Macula densa-Segment und der afferenten Arteriole ein intrarenaler Rückkoppelungs-mechanismus zur Regulation des tubulären Na+-Loads postuliert, an dem das Renin-Angiotensinsystem beteiligt ist.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 50 (1972), S. 221-225 
    ISSN: 1432-1440
    Keywords: Tubular function ; single nephron filtration rate ; juxtaglomerular apparatus ; renin-angiotensin system ; urea reabsorption ; Tubuläre Funktion ; Einzelnephronfiltrat ; juxtaglomerulärer Apparat ; Renin-Angiotensin-System ; Harnstoffresorption
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung In der Nierenphysiologie stehen Fragen über die Mechanismen der tubulären NaCl-Resorption, der intrarenalen Regulation der NaCl-Ausscheidung sowie der tubulären Behandlung von Nicht-Elektrolyten im Mittelpunkt zahlreicher experimenteller Bemühungen. 1. Für den tubulären Na-Transport ergeben sich Anhalte, daß die enge Koppelung zwischen H+-Sekretion und Na-Resorption eine Abhängigkeit des aktiven Transportschrittes vom intracellulären pH reflektiert. 2. Zur Frage der intrarenalen Mechanismen, die die Na-Ausscheidung entsprechend der Na-Aufnahme einstellen, gewinnen Vorstellungen zunehmende Bedeutung, wonach Filtrate einzelner Glomerula in unterschiedlichen Schichten der Nierenrinde ungleichen Veränderungen unterliegen. Für die Einstellung dieser Einzelnephronfiltrate erlangt die Funktion des einzelnen juxtaglomerulären Apparates mit seinem Renin-Angiotensinsystem eine zunehmende Bedeutung. 3. Die Vorstellungen über einen aktiven Harnstoff-Transport in der Niere basieren zum Großteil auf Clearance-Befunden an Fischen aus der Klasse der Elasmobranchier, deren Blutosmolarität durch Harnstoffretention der Osmolarität des Meerwassers angepaßt ist. Das Konzept einer aktiven Harnstoffresorption bedarf möglicherweise einer Revision, da die Nephrone eine typische Gegenstromanordnung aufweisen, mit deren Hilfe eine Nettoresorption von Harnstoff ohne aktiven Transportschritt möglich ist (anatomical support).
    Notes: Summary Renal physiology has been concerned with questions about mechanisms of tubular Na reabsorption, the intrarenal regulation of Na excretion and the tubular handling of non-electrolytes. 1. The close coupling between Na reabsorption and H+ secretion reflects a dependency of the active transport step on intracellular pH. 2. Concerning the intrarenal mechanisms for the adjustment of Na excretion it appears that single nephron filtration rate in the different cortical layers is independently regulated. There is growing evidence that the function of the juxtaglomerular apparatus, in particular its renin-angiotensin system, is involved. 3. The postulate of active urea transport in the kidney rests largely on clearance data obtained from experiments performed on cartilagenous fish. These elasmobranchs retain urea in order to increase their plasma osmolarity to that of sea level. The concept of active urea reabsorption in these fish may need revision since a countercurrent system has been found which provides a mechanism by which urea may be passively retained (anatomical support to fascilitate net movement of substances lacking active transport).
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 52 (1974), S. 654-656 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 52 (1974), S. 703-704 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 55 (1977), S. 1177-1178 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 57 (1979), S. 993-999 
    ISSN: 1432-1440
    Keywords: Electron microprobe analysis ; Intracellular electrolytes ; Kidney ; Ischaemia ; Elektronenstrahl-Mikroanalyse ; Intrazelluläre Elektrolyte ; Niere ; Ischämie
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In order to be able to examine the processes involved in transepithelial transport in tissues, which are not composed of a single cell type, methods are required, which permit analysis at a cellular level. The technique of electron microprobe analysis permits the intracellular concentrations of many elements to be determined simultaneously in various portions of the cell. The application of this method to renal cortical tissue has shown that the best estimates of the cytoplasmic concentrations are to be obtained in regions close to the nucleus, farthest from the basolateral infoldings and microvilli, which separate the intracellular environment from the extracellular space. The nuclear concentrations of Na and K do not differ from those in the surrounding cytoplasm, although those of P and C1 are somewhat higher in cytoplasm. The intracellular element concentrations in the different cell types vary somewhat, proximal tubular cells contain higher concentrations of Na and C1 and lower ones of P than distal tubular cells. Following ischaemia, a manoeuvre know to result in a disturbance of intracellular electrolytes, Na was observed to rise and K to fall only in the non-surface cells of kidneys exposed to the air, but in all cells, if the kidneys were kept air-free in an atmosphere of N2. The proximal and distal tubular cells showed a variable resistance to ischaemia, the distal tubular cells being much more resistant. Despite the severity of the electrolyte disturbance following ischaemia, the intracellular composition was completely restored one hour after re-introducing renal blood flow.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 26 (1948), S. 663-663 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary The electrolyte composition of toad urinary bladder epithelial cells has been measured using the technique of electron microprobe analysis. Portions of hemi-bladders, which had been mounted in chambers and bathed with a variety of media, were layered with albumin solution on their mucosal surfaces and immediately shock-frozen in liquid propane at −180°C. From the frozen material 1–2μm thick cryosections were cut and promptly freeze-dried for 12 hr at −80°C and 10−6 Torr. Electron microprobe analysis using a scanning electron microscope, an energy dispersive X-ray detector, and a computer programme, to distinguish between characteristic and uncharacteristic radiations, allowed quantification of cellular ionic concentrations per kg tissue wet wt by comparison of the intensities of the emitted radiations from the cells and from the albumin layer. Granular, mitochondrial-rich, and basal cells, and the basal portions of goblet cells, showed a similar composition, being high in K (about 110mm/kg wet wt) and low in Na (about 13mm/kg wet wt). The apical portions of goblet cells were higher in Ca and S and lower in P and K, presumably reflecting the composition of the mucus within them. With Na-Ringer's as the mucosal medium, cells gained Na and lost K, when their serosal surfaces were exposed to ouabain, 10−2 m. Replacement of mucosal Na by choline virtually prevented these ouabain-induced changes. Cellular ion contents were unchanged when Na in the serosal medium was replaced by choline. No differences in Na and K concentrations were detected between nuclei and cytoplasm. These results provide independent support for the hypothesis that the cellular Na transport pool in toad bladder epithelial cells derives exclusively from the mucosal medium and that no important recycling of Na occurs from the serosal medium to the cells.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 1432-1424
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary For elucidation of the functional organization of frog skin epithelium with regard to transepithelial Na transport, electrolyte concentrations in individual epithelial cells were determined by electron microprobe analysis. The measurements were performed on 1-μm thick freeze-dried cryosections by an energy-dispersive X-ray detecting system. Quantification of the electrolyte concentrations was achieved by comparing the X-ray intensities obtained in the cells with those of an internal albumin standard. The granular, spiny, and germinal cells, which constitute the various layers of the epithelium, showed an identical behavior of their Na and K concentrations under all experimental conditions. In the control, both sides of the skin bathed in frog Ringer's solution, the mean cellular concentrations (in mmole/kg wet wt) were 9 for Na and 118 for K. Almost no change in the cellular Na occurred when the inside bathing solution was replaced by a Na-free isotonic Ringer's solution, whereas replacing the outside solution by distilled water resulted in a decrease of Na to almost zero in all layers. Inhibition of the transepithelial Na transport by ouabain (10−4 m) produced an increase in Na to 109 and a decrease in K to 16. The effect of ouabain on the cellular Na and K concentrations was completely cancelled when the Na influx from the outside was prevented, either by removing Na or adding amiloride (10−4 m). When, after the action of ouabain, Na was removed from the outside bathing solution, the Na and K concentration in all layers returned to control values. The latter effect could be abolished by amiloride. The other cell types of the epithelium showed under some experimental conditions a different behavior. In the cornified cells and the light cells, which occurred occasionally in the stratum granulosum, the electrolyte concentrations approximated those of the outer bathing meium under all experimental conditions. In the mitochondria-rich cells, the Na influx after ouabain could not be, prevented by adding amiloride. In the gland cells, only a small change in the Na and K concentrations could be detected after ouabain. The results of the present study are consistent with a two-barrier concept of transepithelial Na transport. The Na transport compartment comprises all living epithelial layers. Therefore, with the exception of some epithelial cell types, the frog skin epithelium can be regarded as a functional syncytium for Na.
    Type of Medium: Electronic Resource
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