Edman K A P, Radzyukevich T, Kronborg B
Department of Physiological Sciences, Biomedical Centre, F11, University of Lund, Sweden.
J Physiol. 2002 Jun 15;541(Pt 3):905-16. doi: 10.1113/jphysiol.2001.016220.
Force and isotonic shortening velocities were studied (0.6-4.0 degrees C) in isolated single muscle spindles from the anterior tibialis muscle of Rana temporaria using techniques that enabled measurements both from the spindle as a whole and from marked segments of the preparation. The force-velocity relationship during tetanic stimulation exhibited the same biphasic shape as previously described for extrafusal muscle fibres. However, the maximum speed of shortening of the spindle fibres was merely 0.95 +/- 0.006 lengths s(-1) (mean +/- S.E.M., n = 11), which is approximately half the value recorded in extrafusal fibres of the same muscle. The maximum tetanic force, 91 +/- 10 kN m(-2), n = 14, was likewise only approximately half that produced by extrafusal fibres. The force generated by the capsule segment was lower than that produced by the whole spindle resulting in elongation of the capsule region during a fixed-end tetanus. The intracellular calcium ion concentration reached during the plateau of the tetanus, 1.7 +/- 0.1 microM (n = 8), was substantially lower than the value attained in extrafusal fibres under equivalent conditions. In accordance, the spindle fibres did not become fully activated during supramaximal electrical stimulation as indicated by the finding that the tetanic force could be further increased by 16.6 +/- 0.04 % (n = 5) on addition of 0.5 mM caffeine. Inadequate activation may thus, to a certain extent, account for the relatively low force per cross-sectional area of the spindle fibres. The contractile properties of the intrafusal fibres should make the spindle organ suited to provide feedback control during eccentric (forced lengthening) and static (isometric) contractions and, with reduced effectiveness, during slow muscle shortening.
利用能够对整个肌梭以及制备标本的标记节段进行测量的技术,研究了(0.6 - 4.0摄氏度)来自林蛙胫前肌的分离单根肌梭的力和等张缩短速度。强直刺激期间的力 - 速度关系呈现出与先前描述的梭外肌纤维相同的双相形状。然而,肌梭纤维的最大缩短速度仅为0.95±0.006长度·秒⁻¹(平均值±标准误,n = 11),约为同一肌肉梭外纤维记录值的一半。最大强直力为91±10 kN·m⁻²,n = 14,同样仅约为梭外纤维产生力的一半。在固定端强直期间,被膜节段产生的力低于整个肌梭产生的力,导致被膜区域伸长。强直平台期达到的细胞内钙离子浓度为1.7±0.1微摩尔(n = 8),大大低于同等条件下梭外纤维达到的值。相应地,在超强电刺激期间肌梭纤维未完全激活,这一发现表明,添加0.5 mM咖啡因后强直力可进一步增加16.6±0.04%(n = 5)。因此,激活不足可能在一定程度上解释了肌梭纤维每横截面积相对较低的力。肌梭内纤维的收缩特性应使肌梭器官适合在离心(强制延长)和静态(等长)收缩期间提供反馈控制,而在缓慢肌肉缩短期间效果会降低。