GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
Document type
Keywords
Language
  • 1
    Keywords: Hochschulschrift
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (34 Blatt = 1,6 MB) , Illustrationen, Diagramme
    Language: English
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Keywords: Hochschulschrift
    Type of Medium: Online Resource
    Pages: 1 Online-Ressource (85 Seiten = 8 MB) , Illustrationen, Graphen, Karte
    Edition: Online-Ausgabe 2021
    Language: English
    Note: Zusammenfassung in deutscher und englischer Sprache
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    Kiel : Ozean der Zukunft, Die Kieler Meereswissenschaften
    Keywords: Hochschulschrift
    Type of Medium: Online Resource
    Pages: Online-Ressource ( PDF-Datei : 8 S., 1,2 MB). , Ill.
    Series Statement: Kinder- und Schüleruni Kiel : für Schülerinnen und Schüler von 12 bis 16 Jahren 2008.11,12
    Language: German
    Note: Auch als gedr. Dokument vorh
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Book
    Book
    Kiel : Ozean der Zukunft, Die Kieler Meereswissenschaften
    Keywords: Hochschulschrift
    Type of Medium: Book
    Pages: [8] S. , Ill.
    Series Statement: Kinder- und Schüleruni Kiel : für Schülerinnen und Schüler von 12 bis 16 Jahren 2008.11,12
    Language: German
    Note: Auch als elektronisches Dokument vorh
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Mutations in all four known KCNQ potassium channel α-subunit genes lead to human diseases. KCNQ1 (KvLQT1) interacts with the β-subunit KCNE1 (IsK, minK) to form the slow, depolarization-activated potassium current IKs that is affected in some forms of cardiac ...
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 1432-2013
    Keywords: Key words Chloride secretion ; Electrophysiology ; IsK(minK) ; Rapid amplification of cDNA ends/polymerase chain reaction (RACE/PCR) ; Xenopus oocytes ; 293B
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Functional and pharmacological data point to the involvement of KCNQ1/IsK potassium channels in the basolateral potassium conductance of secretory epithelia. In this study, we report the cloning and electrophysiological characterization of the KCNQ1 protein from the salt secretory rectal gland of the spiny dogfish (Squalus acanthias). The S. acanthias KCNQ1 (s-KCNQ1) cDNA was cloned by polymerase chain reaction (PCR) intensive techniques and showed overall sequence similarities with the KCNQ1 potassium channel subunits of Man, mouse and Xenopus laevis of 64, 70 and 77%, respectively, at the translated amino acid level. Analysis of s-KCNQ1 expression on a Northern blot containing RNA from heart, rectal gland, kidney, brain, intestine, testis, liver and gills revealed distinct expression of 7.4-kb s-KCNQ1 transcripts only in rectal gland and heart. Voltage-clamp analysis of s-KCNQ1 expressed in Xenopus oocytes showed pronounced electrophysiological similarities to human and murine KCNQ1 isoforms, with a comparable sensitivity to inhibition by the chromanol 293B. Coexpression of s-KCNQ1 with human-IsK (h-IsK) induced currents with faster activation kinetics and stronger rectification than observed after coexpression of human KCNQ1 with h-IsK, with the voltage threshold of activation shifted to more negative potentials. The low activation threshold at approximately –60 mV in combination with the high expression in rectal gland cells make s-KCNQ1 a potential candidate responsible for the basolateral potassium conductance.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    ISSN: 1432-2013
    Keywords: Key words cGMP ; Cl ; secretion ; C-type natriuretic peptide ; NaCl secretion ; Squalus acanthia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  We have examined the mechanism whereby C-type natriuretic peptide (CNP), an agonist acting through the second messenger cGMP, enhances NaCl secretion in the rectal gland of Squalus acanthias. Single rectal gland tubules (RGT) were dissected manually, perfused in vitro and equivalent short-circuit current [I sc=transepithelial voltage/transepithelial resistance (R te)] as well as basolateral membrane voltage (V bl) were measured. CNP was added to luminal and basolateral perfusates at concentrations between 1 and 1000 nmol/l and its effects on the above parameters were compared to those of a ”stimulation cocktail” (Stim, containing dibutyryl cAMP, adenosine and forskolin) that maximally enhances cytosolic cAMP, and other agonists and hormones such as guanylin, vasoactive intestinal peptide (VIP), and adenosine. CNP had no effect from the luminal side (n=6). Its effects from the basolateral side consisted of a substantial increase in I sc (–31.6±7.7 to –316±82.2 µA/cm2, n=15). CNP significantly depolarized the luminal membrane from –87.4±1.0 to –82.3±2.6 mV (n=12). V bl was not changed (n=12) but the fractional conductance for K+ was increased (n=3). These effects were qualitatively and even quantitatively comparable to those of other agonists acting via cytosolic cAMP, but were less marked than those caused by Stim (n=64). The effects of VIP and CNP on I sc were not additive (n=5). The cytosolic Ca2+ concentration ([Ca2+]i) was monitored using the fura-2 fluorescence ratio (FFR 340/380 nm) and it was found that CNP, like agonists acting via cAMP, enhances FFR significantly from 1.02±0.05 to 1.32±0.05 (n=8) with a time constant in the 1–2 min in range. Our data suggest that CNP, acting via the second messenger cGMP, induces a marked increase in I sc in the rectal gland. The concomitant fall in R te corresponds to increases in the luminal membrane Cl– conductance and in the basolateral membrane K+ conductance. The latter effect is probably due to an increase in [Ca2+]i.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 1432-2013
    Keywords: BCECF fluorescence Luminal permeability Na+-dependent HCO3–/Cl– exchanger Na+/H+ exchange Short-chain fatty acids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. We investigated disorders and regulation of cytosolic pH (pHi) in isolated perfused crypts from rat distal colon using the pH-sensitive dye BCECF. This preparation allows distinct examination of either luminal or basolateral transport. The effects of luminal weak organic acids and bases on pHi were examined. The physiological concentrations of both luminal CO2/HCO3 – and acetic acid/acetate acidified pHi significantly, but less than when applied from the basolateral side. Corresponding changes (luminal versus basolateral) in pHi were –0.17±0.04 versus –0.39±0.04, (n=8) and –0.15±0.02 versus –0.41±0.04, (n=8), respectively. Basolateral versus luminal application of NH3/NH4 + led to a more marked change in pHi, namely 0.35±0.03 versus 0.008±0.007 pH units, (n=19). The luminal perfusion of NH3/NH4 + was controlled by applying fura-2 acid to the luminal side and at the same time recording fura-2-specific fluorescence. Hence, the influence of luminal acid/base on colonic pHi homeostasis was limited. To examine pHi regulation, we investigated the recovery from an intracellular acid load using the NH3/NH4 + pulse method. Recovery was completely dependent on basolateral Na+, indicating that luminal acid/base transport does not play a major role in pHi homeostasis. The basolateral transporters involved in pHi recovery are probably the EIPA- and HOE694-inhibitable (IC50=0.2 and 2 µmol/l, respectively) Na+/H+ exchanger NHE1 and the DIDS-inhibitable Na+-dependent HCO3 – importer.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 1432-2013
    Keywords: Electrolyte secretion Inwardly rectifying K+ channels (Kir) K+ recycling Rat pancreatic acini
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Previous studies of the whole-cell K+ conductance suggest the presence of inwardly rectifying K+ channels (Kir) in rat pancreatic acini (RPAs). Here we investigate the properties of Kir of RPAs using patch-clamp techniques. The whole-cell current-to-voltage relationship of freshly isolated RPAs was steeper for inward currents than for outward currents when the extracellular K+ concentration ([K+]o) was raised. With a high [K+]o (145 mM), external application of Ba2+ and Cs+ blocked the inward K+ current in a voltage-dependent manner. The apparent IC50 of Ba2+ was 8.5±1.9 µM and 1.1±0.2 µM at –70 mV and –130 mV, respectively (n=5). The IC50 of Cs+ was 3.5±1.1 mM and 0.2±0.1 mM at –60 mV and –120 mV, respectively (n=4). Application of Ba2+ (0.1 mM) to the extracellular solution reversibly depolarized RPAs from –43±1.1 mV to –37±1.2 mV (n=20). In the cell-attached configuration with 145 mM KCl in the pipette solution, we observed inwardly rectifying channels with a high open probability (P o) of 0.85±0.02 (n=6) and a slope conductance (G s) of 30±2.8 pS (n=13). The same type of channel was observed in the outside-out patch. We could also observe a very small conductance K+ channel which was resistant to 0.1 mM Ba2+ and did not show inward rectification (n=11). RT-PCR analysis of RPA confirmed the presence of transcripts for Kir2.1, Kir2.3 and Kir7.1 subfamilies as molecular candidates for the observed channels. The above results demonstrate the presence of Kir channels in the basolateral membrane of the RPA, which may be important for the K+ recycling process during electrolyte secretion as well as for maintaining a hyperpolarized membrane.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 10
    ISSN: 1432-2013
    Keywords: KvLQT1 minK Temperature Clotrimazole Tetrapentylammonium Mefenamic acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract. Previous studies have shown that heteromultimeric KCNQ1/KCNE1 (KvLQT1/minK) channels and homomultimeric KCNQ1 (KvLQT1) channels exhibit different current properties, e.g. distinct kinetics and different sensitivities to drugs. In this study we report on the divergent responses to internal pH changes and further characterize some of the current properties of the human isoforms of KCNQ1 and KCNE1 expressed in Chinese hamster ovary (CHO) cells or Xenopus laevis oocytes. Decreasing the bath temperature from 37 °C to 20 °C increased the half-activation time by a factor of 5 for KCNQ1/KCNE1 currents (I Ks) but by only twofold (not significant) for KCNQ1 currents (I K) in CHO cells. Acidification of cytosolic pH (pHi) increased I Ks but decreased I K whereas intracellular alkalinization decreased I Ks but increased I K. pHi-induced changes in intracellular Ca2+ activity ([Ca2+]i) did not correlate with the current responses. At 20 °C mefenamic acid (0.1 mM) significantly augmented I Ks but slightly decreased I K. It changed the slow activation kinetics of I Ks to an instantaneous onset. The form of the current/voltage (I/V) curve changed from sigmoidal to almost linear. In contrast, at 37 °C, mefenamic acid also increased I Ks but slowed the activation kinetics and shifted the voltage activation to more hyperpolarized values without markedly affecting the sigmoidal shape of the I/V curve. The potassium channel blockers clotrimazole and tetrapentylammonium (TPeA) inhibited I Ks with a lower potency than I K. These results show that coexpression of KCNE1 reversed pH regulation of KCNQ1 from inhibition to activation by acidic pHi. In addition, KCNE1 altered the pharmacological properties and sensitivity to temperature of KCNQ1. The pH-dependence of I Ks might be of clinical and pathophysiological relevance in the pathogenesis of ischaemic cardiac arrhythmias.
    Type of Medium: Electronic Resource
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...