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  • 1
    ISSN: 1432-1424
    Keywords: calcium current ; skeletal muscle ; sulfhydryl ; invertebrate muscle
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Summary Voltage-clamp experiments using the three-microelectrode voltage clamp technique were performed on ventroabdominal flexor muscles of the crustacean Atya lanipes. Potassium and chloride currents were found to underlie the normal, passive response of the muscle. Blocking potassium currents with tetraethylammonium and replacing chloride ions with methanesulfonate did not unmask an inward current. By treating the muscle with the sulfhydryl-alkylating agent 4-cyclopentene-1,3-dione an inward current was detected. The current induced by the agent is carried by Ca2+, since it is abolished in Ca2+-free solutions. The induced Ca+current is detected at about -40 mV and reaches a mean maximum value of -78 μA/cm2 at ca. -10 mV. At this potential the time to peak is close to 15 msec.The induced Ca2+ current inactivated with 1-sec prepulses which did not elicit detectable Ca2+ current; the fitted h xcurve had a midpoint of-38 mV and a steepness of 5.0 mV. Measurements of isometric tension were performed in small bundles of fibers, and the effects of the sulfhydryl-alkylating agents 4-cyclopentene-1,3-dione andN-ethylmaleimide were investigated. Tetanic tension was enhanced in a strictly Ca2+-dependent manner by 4-cyclopentene1,3-dione. The amplitude of K+ contractures increased after treatment with N-ethylmaleimide. It is concluded that Ca2+ channels are made functional by the sulfhydryl-specific reagents and that the increase in tension is probably mediated by an increase in Ca2+ influxthrough the chemically induced Ca2+ channels.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Palo Alto, Calif. : Annual Reviews
    Annual Review of Medicine 44 (1993), S. 335-342 
    ISSN: 0066-4219
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1432-2242
    Keywords: Wheat ; Aegilops ventricosa ; Heterodera avenae ; Cyst nematode ; Resistance gene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Transfer of resistance toHeterodera avenae, the cereal cyst nematode (CCN), by a “stepping-stone” procedure from the wild grassAegilops ventricosa to hexaploid wheat has been demonstrated. The number of nematodes per plant was lower, and reached a plateau much earlier, in the resistant introgression line H93-8 (1–2 nematodes per plant) than in the recipient H10-15 wheat (14–16 nematodes per plant). Necrosis (hypersensitive reaction) near the nematode, little cell fusion, and few, often degraded syncytia were observed in infested H93-8 roots, while abundant, well-formed syncytia were present in the susceptible H10-15 wheat. Line H93-8 was highly resistant to the two Spanish populations tested, as well as the four French races (Fr1-Fr4), and the British pathotype Hall, but was susceptible to the Swedish pathotypes HgI and HgIII. Resistance was inherited as though determined by a single quasi-dominant factor in the F2 generations resulting from crosses of H93-8 with H10-15 and with Loros, a resistant wheat carrying the geneCre1 (syn.Ccn1). The resistance gene in H93-8 (Cre2 orCcn2) is not allelic with respect to that in Loros. RFLPs and other markers, together with the cytogenetical evidence, indicate that theCre2 gene has been integrated into a wheat chromosome without affecting its meiotic pairing ability. Introduction ofCre2 by backcrossing into a commercial wheat backgroud increases grain yield when under challenge by the nematode and is not detrimental in the absence of infestation.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of muscle research and cell motility 13 (1992), S. 354-365 
    ISSN: 1573-2657
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Measurements of isometric tension were performed in single twitch skeletal muscle fibres and the effect of extracellular Na+ removal on contraction was investigated. Na+ withdrawal brought about an increase in the amplitude of K+ contractures and their time course became faster. The potentiation of K+ contractures depended strongly on extracellular Ca2+ and developed slowly following an exponential time course with a time constant of approximately 8 min. Removal of extracellular Na+ greatly increased the amplitude of caffeine contractures and lowered its threshold: caffeine (0.5 mM) had no effect on resting tension in Ringer's but produced contractures in Na+-free solutions. Intramembrane charge movement (charge 1) was monitored in contracting voltage-clamped segments of frog skeletal muscle fibres using the triple-Vaseline-gap technique. Movement of charge 1 did not depend on the presence of extracellular Na+. However, the mechanical threshold decreased by approximately 10 mV at several pulse durations and the charge which produced just detectable contractions decreased by approximately 5 nC μF−1 in the absence of extracellular Na+. Intracellular heparin (40 mg ml−1) increased the mechanical threshold by approximately 20 mV without affecting the movement of charge 1. The effect of Na+-free solutions on the mechanical threshold was additive to that of heparin. It is concluded that the effects of Na+-withdrawal on contraction take place at a location beyond the voltage sensor of excitation-contraction coupling.
    Type of Medium: Electronic Resource
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