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本文引用的文献

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An analysis of the mechanical components in frog's striated muscle.青蛙横纹肌中机械成分的分析。
J Physiol. 1958 Oct 31;143(3):515-40. doi: 10.1113/jphysiol.1958.sp006075.
2
The relationship between tension and slowly varying intracellular calcium concentration in intact frog skeletal muscle.完整青蛙骨骼肌中张力与缓慢变化的细胞内钙浓度之间的关系。
J Physiol. 1997 Apr 1;500 ( Pt 1)(Pt 1):177-92. doi: 10.1113/jphysiol.1997.sp022008.
3
Calmidazolium alters Ca2+ regulation of tension redevelopment rate in skinned skeletal muscle.氯氮䓬改变了去表皮骨骼肌中钙离子对张力重建速率的调节。
Biophys J. 1996 Nov;71(5):2786-94. doi: 10.1016/S0006-3495(96)79471-7.
4
Calcium alone does not fully activate the thin filament for S1 binding to rigor myofibrils.单独的钙并不能完全激活细肌丝,以使肌球蛋白头部(S1)与僵直肌原纤维结合。
Biophys J. 1996 Oct;71(4):1891-904. doi: 10.1016/S0006-3495(96)79388-8.
5
Fatigue vs. shortening-induced deactivation in striated muscle.横纹肌中疲劳与缩短诱导的失活
Acta Physiol Scand. 1996 Mar;156(3):183-92. doi: 10.1046/j.1365-201X.1996.t01-1-198000.x.
6
Osmotic compression of skinned cardiac and skeletal muscle bundles: effects on force generation, Ca2+ sensitivity and Ca2+ binding.渗透压缩去膜心肌和骨骼肌束:对力产生、Ca2+敏感性和Ca2+结合的影响。
J Mol Cell Cardiol. 1995 Jun;27(6):1235-44. doi: 10.1016/s0022-2828(05)82385-5.
7
Fluorescence signals from the Mg2+/Ca2+ indicator furaptra in frog skeletal muscle fibers.青蛙骨骼肌纤维中Mg2+/Ca2+指示剂呋喃普拉的荧光信号。
Biophys J. 1993 Jan;64(1):223-39. doi: 10.1016/S0006-3495(93)81359-6.
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Variation in myoplasmic Ca2+ concentration during contraction and relaxation studied by the indicator fluo-3 in frog muscle fibres.利用荧光指示剂fluo-3研究蛙肌纤维收缩和舒张过程中肌浆Ca2+浓度的变化。
J Physiol. 1994 Jul 1;478 ( Pt 1)(Pt 1):137-48. doi: 10.1113/jphysiol.1994.sp020237.
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The effects of muscle length on intracellular calcium transients in mammalian cardiac muscle.肌肉长度对哺乳动物心肌细胞内钙瞬变的影响。
J Physiol. 1982 Jun;327:79-94. doi: 10.1113/jphysiol.1982.sp014221.
10
Depression of mechanical performance by active shortening during twitch and tetanus of vertebrate muscle fibres.脊椎动物肌纤维单收缩和强直收缩期间主动缩短导致的力学性能降低。
Acta Physiol Scand. 1980 May;109(1):15-26. doi: 10.1111/j.1748-1716.1980.tb06559.x.

快速缩短对完整青蛙骨骼肌纤维中力量再生速率和肌浆[Ca2+]的影响。

Effects of rapid shortening on rate of force regeneration and myoplasmic [Ca2+] in intact frog skeletal muscle fibres.

作者信息

Vandenboom R, Claflin D R, Julian F J

机构信息

Department of Anesthesia Research Laboratories, Brigham and Women's Hospital, Harvard Medical School, 75 Francis Street, Boston, MA 02115, USA.

出版信息

J Physiol. 1998 Aug 15;511 ( Pt 1)(Pt 1):171-80. doi: 10.1111/j.1469-7793.1998.171bi.x.

DOI:10.1111/j.1469-7793.1998.171bi.x
PMID:9679172
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2231114/
Abstract
  1. The effect of rapid shortening on rate of force regeneration (dF/dtR) was examined in single, intact frog (Rana temporaria) skeletal muscle fibres (3.0 C). Step releases leading to unloaded shortening were applied after 500 ms of stimulation, during the plateau of an isometric tetanus. Initial mean sarcomere length ranged from 2.05 to 2.35 micrometer; force regeneration after shortening was at 2.00 micrometer. 2. Values for dF/dtR following a 25 nm half-sarcomere-1 release were 3.17 +/- 0.17 (mean +/- s.e.m., n = 8) times greater than the initial rate of rise of force before release (dF/dtI). As release size was increased from 25 to 175 nm half-sarcomere-1, the relationship between release size and dF/dtR decreased sharply before attaining a plateau value that was 1.34 +/- 0.09 times greater than dF/dtI. Despite wide variations in dF/dtR, the velocity of unloaded shortening remained constant (2.92 +/- 0.08 micrometer half-sarcomere-1 s-1; n = 8) for the different release amplitudes used in this study. 3. To investigate its role in the attenuation of dF/dtR with increased shortening, the effects of rapid ramp (constant velocity) shortening on intracellular free Ca2+ concentration ([Ca2+]i) were monitored using the Ca2+-sensitive fluorescent dye furaptra. Compared with an isometric contraction, rapid fibre shortening was associated with a transient increase in [Ca2+]i while force regeneration after shortening was associated with a transient reduction in [Ca2+]i. The greatest reductions in [Ca2+]i were associated with the largest amplitude ramps. 4. Cross-bridge-mediated modifications of the Ca2+ affinity of troponin C (TnC) may explain the fluctuations in [Ca2+]i observed during and after ramps. Associated fluctuations in TnC Ca2+ occupancy could play a role in the reduction of dF/dtR with increasing release size.
摘要
  1. 在单个完整的青蛙(林蛙)骨骼肌纤维(3.0℃)中,研究了快速缩短对力再生速率(dF/dtR)的影响。在等长强直收缩的平台期,刺激500毫秒后施加导致无负荷缩短的阶跃释放。初始平均肌节长度范围为2.05至2.35微米;缩短后力再生时的肌节长度为2.00微米。2. 半肌节-1释放25纳米后的dF/dtR值比释放前力的初始上升速率(dF/dtI)大3.17±0.17(平均值±标准误,n = 8)倍。当释放大小从25纳米半肌节-1增加到175纳米半肌节-1时,释放大小与dF/dtR之间的关系在达到比dF/dtI大1.34±0.09倍的平台值之前急剧下降。尽管dF/dtR存在很大差异,但本研究中使用的不同释放幅度下,无负荷缩短的速度保持恒定(2.92±0.08微米半肌节-1秒-1;n = 8)。3. 为了研究其在随着缩短增加而导致dF/dtR衰减中的作用,使用钙敏感荧光染料呋喃甲酰三氟丙酮监测快速斜坡(恒定速度)缩短对细胞内游离Ca2+浓度([Ca2+]i)的影响。与等长收缩相比,快速纤维缩短与[Ca2+]i的短暂增加相关,而缩短后力再生与[Ca2+]i的短暂降低相关。[Ca2+]i的最大降低与最大幅度的斜坡相关。4. 肌钙蛋白C(TnC)的Ca2+亲和力的横桥介导修饰可能解释了斜坡期间和之后观察到的[Ca2+]i波动。TnC Ca2+占有率的相关波动可能在随着释放大小增加而导致的dF/dtR降低中起作用。