Defined Electrical Stimulation Emphasizing Excitability for the Development and Testing of Engineered Skeletal Muscle

被引:3
作者
Khodabukus, Alastair [1 ]
Baar, Keith [1 ]
机构
[1] Univ Calif Davis, Div Neurobiol Physiol & Behav, Davis, CA 95616 USA
关键词
NA+-K+ PUMP; RAT SOLEUS MUSCLE; IN-VITRO; RESISTANCE EXERCISE; FIELD STIMULATION; PHOSPHORYLATION; MEMBRANE; CELLS; CALCIUM; DEPOLARIZATION;
D O I
10.1089/ten.tec.2011.0364
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Electrical stimulation is required for the maturation of skeletal muscle and as a way to nondestructively monitor muscle development. However, the wrong stimulation parameters can result in electrochemical damage that impairs muscle development/regeneration. The goal of the current study was to determine what aspect of an electrical impulse, specifically the pulse amplitude or pulse width, was detrimental to engineered muscle function and subsequently how engineered muscle responded to continuous electrical stimulation for 24 h. Acute stimulation at a pulse amplitude greater than six-times rheobase resulted in a 2.4-fold increase in the half-relaxation time (32.3 +/- 0.49 ms vs. 77.4 +/- 4.35 ms; p < 0.05) and a 1.59-fold increase in fatigability (38.2% +/- 3.61% vs. 60.6% +/- 4.52%; p < 0.05). No negative effects were observed when the pulse energy was increased by lengthening the pulse width, indicating electrochemical damage was due to electric fields at or above six-times rheobase. Continuous stimulation for 24 h at electric fields greater than 0.5 V/mm consistently resulted in similar to 2.5-fold increase in force (0.30 +/- 0.04 kN/m(2) vs. 0.67 +/- 0.06 kN/m(2); p < 0.05). Forty per cent of this increase in force was dependent on the mammalian target of rapamycin (RAP) complex 1 (mTORC1), as RAP prevented this portion of the increase in force (CON = 0.30 +/- 0.04 kN/m(2) to 0.67 +/- 0.06 kN/m(2) compared with RAP = 0.21 +/- 0.01 kN/m(2) to 0.37 +/- 0.04 kN/m(2); p < 0.05). Since there was no increase in myosin heavy chain, the remaining increase in force over the 24 h of stimulation is likely due to cytoskeletal rearrangement. These data indicate that electrochemical damage occurs in muscle at a voltage field greater than six-times rheobase and therefore optimal muscle stimulation should be performed using lower electric fields (two-to four-times rheobase).
引用
收藏
页码:349 / 357
页数:9
相关论文
共 51 条
  • [1] Fibrin: A versatile scaffold for tissue engineering applications
    Ahmed, Tamer A. E.
    Dare, Emma V.
    Hincke, Max
    [J]. TISSUE ENGINEERING PART B-REVIEWS, 2008, 14 (02) : 199 - 215
  • [2] CALCITONIN GENE-RELATED PEPTIDE STIMULATES ACTIVE NA+-K+ TRANSPORT IN RAT SOLEUS MUSCLE
    ANDERSEN, SLV
    CLAUSEN, T
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (02): : C419 - C429
  • [3] Dihydropyridine receptors as voltage sensors for a depolarization-evoked, IP3R-mediated, slow calcium signal in skeletal muscle cells
    Araya, R
    Liberona, JL
    Cárdenas, JC
    Riveros, N
    Estrada, M
    Powell, JA
    Carrasco, MA
    Jaimovich, E
    [J]. JOURNAL OF GENERAL PHYSIOLOGY, 2003, 121 (01) : 3 - 16
  • [4] Determination of the chronaxie and rheobase of denervated limb muscles in conscious rabbits
    Ashley, Z
    Sutherland, H
    Lanmuller, H
    Unger, E
    Li, F
    Mayr, W
    Kern, H
    Jarvis, JC
    Salmons, S
    [J]. ARTIFICIAL ORGANS, 2005, 29 (03) : 212 - 215
  • [5] Selective activation of AMPK-PGC-1α or PKB-TSC2-mTOR signaling can explain specific adaptive responses to endurance or resistance training-like electrical muscle stimulation
    Atherton, PJ
    Babraj, JA
    Smith, K
    Singh, J
    Rennie, MJ
    Wackerhage, H
    [J]. FASEB JOURNAL, 2005, 19 (02) : 786 - +
  • [6] Phosphorylation of p70S6k correlates with increased skeletal muscle mass following resistance exercise
    Baar, K
    Esser, K
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 1999, 276 (01): : C120 - C127
  • [7] Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo
    Bodine, SC
    Stitt, TN
    Gonzalez, M
    Kline, WO
    Stover, GL
    Bauerlein, R
    Zlotchenko, E
    Scrimgeour, A
    Lawrence, JC
    Glass, DJ
    Yancopoulos, GD
    [J]. NATURE CELL BIOLOGY, 2001, 3 (11) : 1014 - 1019
  • [8] mTOR signaling and the molecular adaptation to resistance exercise
    Bodine, Sue C.
    [J]. MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 2006, 38 (11) : 1950 - 1957
  • [9] Electric Pulse Stimulation of Cultured Murine Muscle Cells Reproduces Gene Expression Changes of Trained Mouse Muscle
    Burch, Nathalie
    Arnold, Anne-Sophie
    Item, Flurin
    Summermatter, Serge
    Santos, Gesa Brochmann Santana
    Christe, Martine
    Boutellier, Urs
    Toigo, Marco
    Handschin, Christoph
    [J]. PLOS ONE, 2010, 5 (06):
  • [10] Lengthening contractions differentially affect p70s6k phosphorylation compared to isometric contractions in rat skeletal muscle
    Burry, Martin
    Hawkins, David
    Spangenburg, Espen E.
    [J]. EUROPEAN JOURNAL OF APPLIED PHYSIOLOGY, 2007, 100 (04) : 409 - 415