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  • Electronic Resource  (9)
  • Admittance plethysmography  (3)
  • Acetylcholine  (2)
  • Acute myeloblastic leukemia  (2)
  • Arterial compliance  (2)
  • Autolysis  (2)
Material
  • Electronic Resource  (9)
Years
Keywords
  • 1
    ISSN: 0014-5793
    Keywords: Autolysis ; Calcium ; Proteolysis ; m-Calpain
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0014-5793
    Keywords: Autolysis ; Calcium ; Proteolysis ; m-Calpain
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 351 (1995), S. 610-617 
    ISSN: 1432-1912
    Keywords: Key words Ferret ; Ventricular myocytes ; Acetylcholine ; Adenosine ; Muscarinic K+ channel ; G protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract  The properties of the K+ channel activated by acetylcholine (ACh) and adenosine (Ado) were examined in single ferret ventricular myocytes using patch-clamp techniques. In the whole-cell configuration, ACh and Ado induced an inwardly rectifying K+ current and shortened the action potential duration. The effect of ACh was blocked by atropine, while the Ado effect was interrupted by 8-cyclopentyl,1,2-dipropyl xanthine, a specific Ado A1 receptor antagonist. In cell-attached recordings, ACh and Ado added to the pipette solution activated a single population of inwardly rectifying K+ channels, distinct from the i K1 channel. The channel had a slope conductance of ∼40 pS in symmetrical 150 mM K+ solutions and a mean open time of 0.8 ms. Excision of the patch into the inside-out patch configuration in guanosine triphosphate (GTP)-free solution abolished the channel activity. The channel was reversibly reactivated by adding GTP to the intracellular side of the patch. GTPγS activated the channel irreversibly. When the inside-out patch was treated with the A protomer of pertussis toxin (PTX), intracellular GTP no longer activated the K+ channel. The results show that ferret ventricular myocytes possess a K+ channel activated by both muscarinic and Ado A1 receptors. Its electrophysiological properties and the gating by a PTX-sensitive G protein in a membrane-delimited fashion are identical with those of the muscarinic K+ channels in nodal and atrial tissues of other species. In conclusion, the G protein-gated muscarinic K+ channel is expressed in ferret ventricular myocardium and may underlie the direct negative inotropism of ACh and Ado in this tissue.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-1920
    Keywords: Key words Magnetic resonance imaging ; Leukoencephalopathy ; Methotrexate ; Acute myeloblastic leukemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A patient with acute myeloblastic leukaemia showed atypical findings on MRI following combination therapy including intrathecal methotrexate and radiation. MRI findings not previously been reported are ring as well as patchy enhancement, marked mass effect and lesions extending to the putamen and corpus callosum.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1920
    Keywords: Magnetic resonance imaging ; Leukoencephalopathy ; Methotrexate ; Acute myeloblastic leukemia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract A patient with acute myeloblastic leukaemia showed atypical findings on MRI following combination therapy including intrathecal methotrexate and radiation. MRI findings not previously been reported are ring as well as patchy enhancement, marked mass effect and lesions extending to the putamen and corpus callosum.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 351 (1995), S. 610-617 
    ISSN: 1432-1912
    Keywords: Ferret ; Ventricular myocytes ; Acetylcholine ; Adenosine ; Muscarinic K+ ; channel ; G protein
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The properties of the K+ channel activated by acetylcholine (ACh) and adenosine (Ado) were examined in single ferret ventricular myocytes using patch-clamp techniques. In the whole-cell configuration, ACh and Ado induced an inwardly rectifying K+ current and shortened the action potential duration. The effect of ACh was blocked by atropine, while the Ado effect was interrupted by 8-cyclopenty1,1,2-dipropyl xanthine, a specific Ado A1 receptor antagonist. In cell-attached recordings, ACh and Ado added to the pipette solution activated a single population of inwardly rectifying K+ channels, distinct from the i K1 channel. The channel had a slope conductance of ∼ 40 pS in symmetrical 150 mM K+ solutions and a mean open time of 0.8 ms. Excision of the patch into the inside-out patch configuration in guanosine triphosphate (GTP)-free solution abolished the channel activity. The channel was reversibly reactivated by adding GTP to the intracellular side of the patch. GTPγS activated the channel irreversibly. When the inside-out patch was treated with the A protomer of pertussis toxin (PTX), intracellular GTP no longer activated the K+ channel. The results show that ferret ventricular myocytes possess a K+ channel activated by both muscarinic and Ado A1 receptors. Its electrophysiological properties and the gating by a PTX-sensitive G protein in a membrane-delimited fashion are identical with those of the muscarinic K+ channels in nodal and atrial tissues of other species. In conclusion, the G protein-gated muscarinic K+ channel is expressed in ferret ventricular myocardium and may underlie the direct negative inotropism of ACh and Ado in this tissue.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1741-0444
    Keywords: Admittance plethysmography ; Respiration rate ; Stroke volume ; Three-channel telemetry ; Total transthoracic admittance
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract A three-channel frequency-modulation telemetry system for the noninvasive measurement of cardiac output, rate of respiration, e.c.g. and basal transthoracic admittance of the unconstrained human subject is described. Tetrapolar admittance plethysmography has been employed to obtain the transthoracic admittance and its variations corresponding to the cardiac cycle and respiratory changes. Pulse duration modulation has been used in the transmitter system. The nonlinearity of the system is less than ±2·0%. The telemetry transmitter has a range of about 100 m, it weights approximately 200 g and is contained in a box measuring 150×100×50 mm. The batteries used provide a continuous life of 20 h. The system has been used to obtain data from normal subjects in different postures with breath hold and during normal respiration.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 26 (1988), S. 641-646 
    ISSN: 1741-0444
    Keywords: Admittance plethysmography ; Arterial compliance ; Human limb ; Noninvasive measurement ; Volume elastic modulus ; Volume oscillometric method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Arterial elasticity expressed by such indices as volume elastic modulus Ev and compliance Ca were noninvasively measured in various human limb segments; the upper arms, forearms, fingers, thighs, calves and toes. These indices are defined, respectively, as $$E_v = \Delta P/(\Delta V/\bar V_a )$$ and Ca=ΔV/ΔP, where ΔP is pulse pressure, $$\bar V_a $$ mean arterial volume and ΔV its pulsatile variation. ΔP was calculated from systolic Pas and mean Pam arterial pressures determined by volume oscillometric sphygmomanometry using the following equation: $$\Delta P = 3(P_{as} - P_{am} )/2\bar V_a $$ and the ΔV were detected by electrical admittance plethysmography at various transmural pressure Pt levels controlled by a compression cuff. The values obtained in these limb segments were compared with each other at Pt levels 0,30 and 60 mm Hg and the differences between them were discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Medical & biological engineering & computing 23 (1985), S. 43-47 
    ISSN: 1741-0444
    Keywords: Admittance plethysmography ; Arterial compliance ; Arterial volume ; Vascular unloading technique ; Volume elastic modulus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Abstract Static and dynamic (beat-to-beat) arterial viscoelastic properties were measured noninvasively in human fingers and forearms. The volume change and pressure change were detected simultaneously by admittance plethysmography and by sphygmomanometry using the vascular unloading technique in the index and middle finger, or vice versa. These simultaneous measurements were also made on the forearms of one side and the fingers of the other side. The arterial viscoelastic properties in these segments could be successfully determined at different transmural pressure levels from 0 mm Hg to around the mean arterial pressure.
    Type of Medium: Electronic Resource
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