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Optical Recording of Action Potential Initiation and Propagation in Mouse Skeletal Muscle Fibers

机译:小鼠骨骼肌纤维中动作电位的起始和传播的光学记录

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摘要

Skeletal muscle fibers have been used to examine a variety of cellular functions and pathologies. Among other parameters, skeletal muscle action potential (AP) propagation has been measured to assess the integrity and function of skeletal muscle. In this work, we utilize 1-(3-sulfonatopropyl)-4[ [2-(Di- -octylamino)-6-naphtyl]vinyl]pyridinium betaine, a potentiometric dye, and mag-fluo-4, a low-affinity intracellular Ca indicator, to noninvasively and reliably measure AP conduction velocity in skeletal muscle. We used remote extracellular bipolar electrodes to generate an alternating polarity electric field that initiates an AP at either end of the fiber. Using enzymatically dissociated flexor digitorum brevis (FDB) fibers and high-speed line scans, we determine the conduction velocity to be ∼0.4 m/s. We applied these methodologies to FDB fibers under elevated extracellular potassium conditions and confirmed that the conduction velocity is significantly reduced in elevated [K ] . Because our recorded velocities for FDB fibers were much slower than previously reported for other muscle groups, we compared the conduction velocity in FDB fibers to that of extensor digitorum longus (EDL) fibers and measured a significantly faster velocity in EDL fibers than FDB fibers. As a basis for this difference in conduction velocity, we found a similarly higher level of expression of Na channels in EDL than in FDB fibers. In addition to measuring the conduction velocity, we can also measure the passive electrotonic potentials elicited by pulses by applying tetrodotoxin and have constructed a circuit model of a skeletal muscle fiber to predict passive polarization of the fiber by the field stimuli. Our predictions from the model fiber closely resemble the recordings acquired from in vitro assays. With these techniques, we can examine how various pathologies and mutations affect skeletal muscle AP propagation. Our work demonstrates the utility of using 1-(3-sulfonatopropyl)-4[ [2-(Di- -octylamino)-6-naphtyl]vinyl]pyridinium betaine or mag-fluo-4 to noninvasively measure AP initiation and conduction.
机译:骨骼肌纤维已用于检查各种细胞功能和病理。在其他参数中,已测量了骨骼肌动作电位(AP)的传播,以评估骨骼肌的完整性和功能。在这项工作中,我们利用了电位计染料1-(3-磺基磺丙基)-4 [[2-(二-辛基氨基)-6-萘基]乙烯基]吡啶甜菜碱和低亲和力的mag-fluo-4。细胞内Ca指标,以无创且可靠地测量骨骼肌中AP传导速度。我们使用远程细胞外双极电极产生交替极性的电场,该电场在光纤的任一端引发AP。使用酶解的短指屈屈短纤维(FDB)纤维和高速线扫描,我们确定传导速度为〜0.4 m / s。我们将这些方法应用于细胞外钾离子浓度升高的FDB纤维,并确认在[K]升高时传导速度显着降低。因为我们记录的FDB纤维的速度比以前报道的其他肌肉群的速度要慢得多,所以我们将FDB纤维与指长伸肌(EDL)纤维的传导速度进行了比较,并且测得EDL纤维的传导速度明显快于FDB纤维。作为这种传导速度差异的基础,我们发现与FDB纤维相比,EDL中Na通道的表达水平更高。除了测量传导速度外,我们还可以通过应用河豚毒素来测量脉冲引起的被动电渗电位,并构建了骨骼肌纤维的电路模型,以通过场刺激来预测纤维的被动极化。我们对模型纤维的预测与体外测定中获得的记录非常相似。使用这些技术,我们可以检查各种病理和突变如何影响骨骼肌AP的繁殖。我们的工作证明了使用1-(3-磺酰基丙基)-4 [[2-(二-辛基氨基)-6-萘基]乙烯基]吡啶甜菜碱或mag-fluo-4来无创地测量AP起始和传导的实用性。

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