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  • 1990-1994  (3)
  • 1991  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 47 (1991), S. 684-686 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Pflügers Archiv 419 (1991), S. 371-379 
    ISSN: 1432-2013
    Keywords: Adrenaline ; α 1-Adrenoceptor ; Ca2+ release ; Ca2+-dependent K+ conductance ; Patch clamp ; Mouse peritoneal macrophage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Responses to adrenaline in mouse peritoneal macrophages were investigated with perforated and cell-attached patch-clamp recording, and with a combination of the perforated-patch recording and fura-2 fluorescence measurements. Extracellularly applied adrenaline induced a transient outward current (4–10s in duration, 100–500 pA in amplitude) at −40 mV associated with a marked increase in conductance. The adrenaline-induced current [I o (Adr)] reversed polarity near −80 mV. The reversal potential depended distinctly on the external K+ concentration but not on external Cl− concentration. Removal of external Ca2+ did not affect I o(Adr) within 2–4 min but subsequent responses to adrenaline were progressively depressed. In contrast, treatment with an intracellular Ca2+ chelator, the acetoxymethyl ester of 1,2-bis-(2-aminophenoxy)ethane-N,N,N′,N′-tetraacetic acid completely abolished I o(Adr). Furthermore, I o(Adr) was blocked by bath-applied quinidine and charybdotoxin, but not by tetraethylammonium or apamin. Extracellular application of an α 1-adrenoceptor agonist phenylephrine and of noradrenaline mimicked I o(Adr). On the other hand, I o(Adr) was antagonized by a non-selective α-adrenoceptor antagonist phentolamine (0.2 μM) and an α 1-adrenoceptor antagonist prazosin (0.2 μM), but was not affected by an α2-adrenoceptor antagonist yohimbine (1 μM) or a β-adrenoceptor antagonist propranolol (1 μM). Cell-attached single-channel recordings with the pipette solution containing 145 mM KCl revealed the activation of single-channel currents with a conductance of 40 pS during application of adrenaline outside the patch. Parallel measurements of membrane current and fura-2 fluorescence in the same cell demonstrated a correlation between the rise in [Ca2+]i and an increase in K+ conductance. Therefore, it is concluded that adrenaline activates a Ca2+-dependent K+ conductance by release of Ca2+ from internal stores through an activation of an α 1-adrenoceptor.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European journal of plastic surgery 14 (1991), S. 149-150 
    ISSN: 1435-0130
    Keywords: Wound opener ; Instrument ; Wound speculum ; Deep wound
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A wound speculum, or an operator-controlled wound retractor, was devised to facilitate surgery in a narrow and deep field. It is specifically designed to make hemostasis and suturing easy as well as accurate. The blades of the speculum are teflon-coated for electrical insulation on electrocoagulation, and made in the shape of a frame with a narrow opening at the side for the convenience of suturing.
    Type of Medium: Electronic Resource
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