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
    Oxford, UK : Blackwell Publishing Ltd
    Cardiovascular drug reviews 16 (1998), S. 0 
    ISSN: 1527-3466
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1546-170X
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Medicine
    Notes: [Auszug] We recently reported that mice deficient in the programmed cell death-1 (PD-1) immunoinhibitory coreceptor develop autoimmune dilated cardiomyopathy (DCM), with production of high-titer autoantibodies against a heart-specific, 30-kDa protein. In this study, we purified the 30-kDa protein from heart ...
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 433 (1997), S. 390-396 
    ISSN: 1432-2013
    Keywords: Key words Cardiac pacemaker cell ; Sinoatrial node cell ; Spontaneous action potential ; Sustained inward current ; Guinea-pig
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  Single myocytes were dissociated from the sino-atrial (SA) node of guinea-pig hearts. Only a quite small fraction of the cell population showed spontaneous action potentials and these cells were characterized by the presence of the hyperpolarization-activated cation current I f , the delayed rectifier K+ current I K and the L-type Ca2+ current I Ca,L as well as by the absence of both the transient outward current I to and the inward rectifier K+ current I K,1. After blocking I f and I K, depolarizing pulses from –80 mV revealed a large nicardipine-sensitive late current (NSLC). The NSLC was scarcely affected by decreasing extracellular [Ca2+] ([Ca2+]o) from 1.8 to 0.1 mM, while it was decreased significantly by depleting [Na+]o, differently from I Ca,L. NSLC was blocked by nicardipine and was increased by Bay K 8644. NSLC was increased by isoprenaline and the additional application of acetylcholine reversed the increase of this current. We conclude that NSLC is largely composed of I st described in the rabbit SA node pacemaker cells, and that I st is unique for the pacemaker cells in mammalian SA node cells. Most of the quiescent cells showed neither I f nor I st.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    ISSN: 1432-2013
    Keywords: Cardiac Na+ channel ; Patch clamp ; Fluctuation analysis ; Open probability ; Inactivation delay
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Single Na+ channel currents were recorded from guinea-pig ventricular cells in cell-attached patches. The ensemble average current (I) of multi-channel recordings was used to calculate the variance (σ 2) of current fluctuations around the mean in individual current recordings. The relationship between σ 2/I and I was linear and allowed estimation of the number of functional channels in the patch of membrane. The unitary amplitude of channel current obtained from the relation σ 2/I-I was in agreement with that obtained directly by measuring the original records. The number of channels determined at different depolarizing pulses was almost constant in a given patch. The value was nearly equal to that of the maximum current, measured at high depolarizing potentials when most channels are open, divided by the unitary current. The open probability of the channels at the peak time of mean current was calculated based on the estimated number of channels. It increased with increasing depolarization and saturated at about 0.6 at test potentials above −20 mV. The inactivation time-course of the mean current was fitted by a sum of two exponentials. The current amplitude extrapolated to time zero was much larger than the current which could be generated by all channels. This indicates that the inactivation of the Na+ channel develops with delay after the onset of depolarization. The finding is in agreement with a model in which the inactivation rate is accelerated with activation of the Na+ channel.
    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...