Library

feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 368 (1977), S. 83-88 
    ISSN: 1432-2013
    Keywords: Harmaline ; Active Na+ transport ; Na+−K+-ATPase ; HCO 3 − -ATPase ; Renal glucose transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effect of the hallucinogenic drug harmaline was tested on rat kidney proximal tubular solute and water transport, using in vivo micropuncture and electrophysiological techniques as well as in vitro biochemical techniques. During peritubular application harmaline (5 mmol/l) was found to block net tubular volume absorption reversibly (by 85%) through inhibition of active Na+ transport and possibly active HCO 3 − transport. The inhibition was accompanied by a rapid strong depolarization of the tubular cell membranes. As a biochemical equivalent harmaline inhibited the Na+−K+-ATPase and the Mg2+-ATPase of peritubular cell membrane fractions as well as the HCO 3 − -stimulated ATPase of a brush border membrane fraction with similar kinetics. By studying glucose tracer efflux and by measuring cell membrane potential and conductance changes in response to glucose perfusions, no evidence for a direct effect of harmaline on Na+-glucose (or amino acid) cotransport mechanisms in the brush border could be obtained. The data suggest that harmaline does not specifically compete with Na+ for transport sites. Neither are the cotransport systems in the brush border membrane specifically inhibited, nor could the inhibition of the Na+ pump in the peritubular cell membrane simply result from a competition between harmaline and Na+.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 378 (1978), S. 37-45 
    ISSN: 1432-2013
    Keywords: Ion-selective microelectrode ; Renal tubular cell ; Cytoplasmic K+ activity ; Active K+ transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The intracellular K+ activity of rat kidney proximal tubular cells was determined in vivo, using intracellular microelectrodes. In order to minimize damage from the impaling electrodes, separate measurements on separate cells, were performed with single-barrelled KCl-filled non-selective electrodes and single-barrelled, K+-sensitive microelectrodes, which were filled with a liquid K+-exchanger resin that has also a small sensitivity to Na+. Both electrodes had tip diameters of 0.2 μm or below. The proper intracellular localization of the electrodes was ascertained by recording the cell potential response to intermittent luminal perfusions with glucose. The membrane potential measured with the non-selective microelectrodes was −76.3±8.1 mV (n=81) and the potential difference measured with the K+-sensitive microelectrode was −7.2±5.8 mV (n=32). Based on the activity of K+ in the extracellular fluid of ∼3 mmol/l the intracellular K+ activity was estimated to be ∼82 mmol/l. Assuming equal K+-activity coefficients to prevail inside and outside the cell, this figure suggests that the intracellular K+ concentration is ∼113 mmol/l which must be considered as a lower estimate, however. The data indicate that the K+-ion distribution between cytoplasm and extracellular fluid is not in equilibrium with the membrane potential, but that K+ is actively accumulated inside the cell. This result provides direct evidence for the presence of an active K+ pump in the tubular cell membranes, which in view of other observations, must be envisaged as a (not necessarily electroneutral) Na+/K+-exchange pump which operates in the peritubular cell membrane and is eventually responsible for the major part of the tubular solute and water absorption.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...