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A cross-bridge mechanism can explain the thixotropic short-range elastic component of relaxed frog skeletal muscle

机译:跨桥机制可以解释松弛青蛙骨骼肌的触变性短程弹性成分

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摘要

class="enumerated" style="list-style-type:decimal">The passive tension and sarcomere length of relaxed frog skeletal muscle fibres were measured in response to imposed length stretches. The tension response to a constant-velocity stretch exhibited a clear discontinuity. Tension rose more rapidly during the initial ∼ 0.4%L0 of the stretch than during the latter stages (where L0 is the resting length of the fibre). This initial tension response is attributed to the short-range elastic component (SREC).The use of paired triangular stretches revealed that the maximum tension produced during the SREC response of the second stretch was significantly reduced by the first stretch. This history-dependent behaviour of the SREC reflects thixotropic stiffness changes that have been previously described in relaxed muscle.The biphasic nature of the SREC tension response to movement was most apparent during the first imposed length change after a period at a fixed length, irrespective of the direction of movement.If a relaxed muscle was subjected to an imposed triangular length change so that the muscle was initially stretched and subsequently shortened back to its original fibre length, the resting tension at the end of the stretch was reduced relative to its initial pre-stretch value. Following the end of the stretch, tension slowly increased towards its initial value but the tension recovery was not accompanied by a contemporaneous increase in sarcomere length. This finding suggests that the resting tension of a relaxed muscle fibre is not entirely due to passive elasticity. The results are compatible with the suggestion that a portion of the resting tension - the filamentary resting tension (FRT) - is produced by a low level of active force generation.If a second identical stretch was imposed on the muscle at a time when the resting tension was reduced by the previous stretch, the maximal tension produced during the second stretch was the same as that produced during the first, despite the second stretch commencing from a lower initial resting tension.In experiments using paired triangular length changes, an inter-stretch interval of zero did not produce a substantially greater thixotropic reduction in the second stretch elastic limit force than an inter-stretch interval in the range 0.5-1 s.A theoretical model was developed in which the SREC and FRT arise as manifestations of a small number of slowly cycling cross-bridges linking the actin and myosin filaments of a relaxed skeletal muscle. The predictions of the model are compatible with many of the experimental observations. If the SREC and FRT are indeed due to cross-bridge activity, the model suggests that the cross-bridge attachment rate must increase during interfilamentary movement. A mechanism (based on misregistration between the actin binding sites and the myosin cross-bridges) by which this might arise is presented.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 响应于施加的长度拉伸,测量了松弛的青蛙骨骼肌纤维的被动张力和肌节长度。对恒定速度拉伸的张力响应表现出明显的不连续性。在拉伸的最初〜0.4%L0期间,张力的上升比后面阶段(其中L0是纤维的静止长度)快得多。该初始张力响应归因于短程弹性分量(SREC)。 使用成对的三角拉伸显示,第二拉伸的SREC响应期间产生的最大拉伸力被第一拉伸明显降低。伸展。 SREC的这种与历史有关的行为反映了先前在松弛的肌肉中描述的触变刚度变化。 SREC张力对运动的双相性质在一段时间后首次施加的长度变化中最明显 如果松弛的肌肉受到强加的三角形长度改变,从而使该肌肉最初被拉伸,然后又缩短回到其原始纤维长度,则静止拉伸结束时的张力相对于其初始预拉伸值有所降低。拉伸结束后,张力缓慢增加至其初始值,但张力恢复并未伴随着肌节长度的同时增加。这一发现表明,松弛的肌肉纤维的静息张力并不完全是由于被动弹性。该结果与以下建议相吻合:一部分静息张力-丝状静息张力(FRT)-是由较低水平的主动力产生的。 如果第二次施加相同的张力肌肉在静息张力降低前一次拉伸的同时,第二次拉伸产生的最大张力与第一次拉伸产生的最大张力相同,尽管第二次拉伸是从较低的初始静息张力开始的。 < li>在使用成对的三角形长度变化的实验中,零拉伸间隔时间不会使第二拉伸弹性极限力的触变减小幅度大于0.5-1 s的拉伸间隔时间。 [li]建立了一个理论模型,其中SREC和FRT表现为少量缓慢循环的交叉桥的表现,这些桥将松弛的骨骼肌的肌动蛋白丝和肌球蛋白丝连接在一起。该模型的预测与许多实验观察结果兼容。如果SREC和FRT确实是由于跨桥活动引起的,则该模型表明,跨丝附着率必须在丝间运动期间增加。提出了一种机制(基于肌动蛋白结合位点和肌球蛋白跨桥之间的配准错误)。

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