Vergara Julio L, Difranco Marino
Department of Physiology, David Geffen School of Medicine, University of California at Los Angeles (UCLA), Los Angeles, CA 90095-1751, USA.
Biol Res. 2006;39(3):567-81. doi: 10.4067/s0716-97602006000300017. Epub 2006 Nov 7.
The effects of caffeine on the process of excitation-contraction coupling in amphibian skeletal muscle fibers were investigated using the confocal spot detection technique. This method permits to carefully discriminate between caffeine effects on the primary sources of Ca2+ release at the Z-lines where the triads are located and secondary actions on other potential Ca Release sources. Our results demonstrate that 0.5 mM caffeine potentiates and prolongs localized action-potential evoked Ca2+ transients recorded at the level of the Z-lines, but that 1mM only prolongs them. The effects at both doses are reversible. At the level of the M-line, localized Ca2+ transients displayed more variability in the presence of 1 mM caffeine than in control conditions. At this dose of caffeine, extra-junctional sources of Ca2+ release also were observed occasionally.
利用共焦光斑检测技术研究了咖啡因对两栖类骨骼肌纤维兴奋-收缩偶联过程的影响。该方法能够仔细区分咖啡因对位于三联体的Z线处Ca2+释放主要来源的作用以及对其他潜在Ca释放源的次要作用。我们的结果表明,0.5 mM咖啡因可增强并延长在Z线水平记录到的局部动作电位诱发的Ca2+瞬变,但1 mM咖啡因仅能延长它们。两种剂量的作用都是可逆的。在M线水平,1 mM咖啡因存在时局部Ca2+瞬变比对照条件下表现出更大的变异性。在该咖啡因剂量下,偶尔也会观察到Ca2+释放的结外来源。