Gemballa Sven, Vogel Felix
Evolution, Bio-Geosphere Dynamics Program (EBID), University of Tübingen, Systematic Zoology, Auf der Morgenstelle 28, D-72076 Tubingen, Germany.
Comp Biochem Physiol A Mol Integr Physiol. 2002 Dec;133(4):1013-37. doi: 10.1016/s1095-6433(02)00186-1.
We describe the arrangement of white muscle fibers and tendinous myoseptal structures and the relation of these structures to each other in order to provide an anatomical framework for discussions and experimental research on fish swimming mechanics. For the three major craniate groups, the petromyzontids, myxinids and gnathostomes, we identify three conditions that differ remarkably. Myxinids are characterized by asymmetrical myosepta with long cones. Within a single myoseptum these are connected by collagenous fibers that are almost oriented longitudinally. Distinct tendons are absent in myxinid myosepta. Petromyzontid myosepta lack cones and distinct myoseptal tendons, whereas gnathostomes bear cones and distinct tendinous structures: the lateral band, epineural (epipleural) tendon and myhabdoid tendon. Myoseptal fibers of petromyzontids and myoseptal tendons of gnathostome myosepta are firmly anchored in the skin. Myxinids lack firm myoseptal-skin-connections. Their muscular arrangement is neither comparable to that of petromyzontids nor to that of gnathostomes. The latter two bear archlike arrangements of muscle fibers spanning several segments that are hypothesized to play a role during bending. In gnathostomes, archlike helical muscle fiber arrangements (HMFAs) are present that span the length of several body segments and are multiply intersected by myosepta. Hence, a series of tendinous lateral bands of myosepta is embedded in HMFAs. The posterodorsally oriented HMFAs are underlain by posteroventrally oriented crossing muscle fibers (CMFs). Bending may be generated by contraction of the muscle fibers belonging to an HMFA and the simultaneous counteraction of CMFs. Moving caudally, this anterior muscle fiber arrangement gradually changes, eventually becoming the posterior muscle fiber arrangement. This pattern suggests that the function of the myomeres will also change. Three additional putative roles of myoseptal tendons can be deduced from their relations to white muscle fibers in gnathostomes (and in part in petromyzontids): (1) Posterior transmission of anteriorly generated muscular forces via lateral bands and/or myorhabdoid tendons. These tendons are more robust posteriorly. Anterior and posterior cones appear to play an important role in force transmission. (2) Pulling on collagen fibers of the skin via lateral bands and myorhabdoid tendons, suggesting a transmission of muscular forces that puts the skin into tension. (3) Resisting radial expansion of contracting muscle fibers by epineural (epipleural) tendons. By the latter two mechanisms modulation of body stiffness is likely to be achieved.
我们描述了白肌纤维和腱性肌隔结构的排列以及这些结构之间的相互关系,以便为鱼类游泳力学的讨论和实验研究提供一个解剖学框架。对于三个主要的有头类动物群体,即七鳃鳗类、盲鳗类和颌口类,我们确定了三种明显不同的情况。盲鳗类的特征是具有长锥形的不对称肌隔。在单个肌隔内,这些长锥形结构由几乎纵向排列的胶原纤维相连。盲鳗类的肌隔中没有明显的肌腱。七鳃鳗类的肌隔没有锥形结构和明显的肌隔肌腱,而颌口类则有锥形结构和明显的腱性结构:外侧带、神经上(胸膜上)肌腱和肌habdoid肌腱。七鳃鳗类的肌隔纤维和颌口类肌隔的肌腱牢固地附着在皮肤上。盲鳗类缺乏牢固的肌隔 - 皮肤连接。它们的肌肉排列既不像七鳃鳗类,也不像颌口类。后两者具有跨越几个节段的拱形肌纤维排列,据推测在弯曲过程中起作用。在颌口类中,存在跨越几个身体节段长度的拱形螺旋肌纤维排列(HMFAs),并且被肌隔多次交叉。因此,一系列肌隔的腱性外侧带嵌入在HMFAs中。向后上方定向的HMFAs下方是向后下方定向的交叉肌纤维(CMFs)。弯曲可能由属于一个HMFA的肌纤维收缩以及CMFs的同时反作用产生。向尾部移动时,这种前部肌纤维排列逐渐变化,最终变成后部肌纤维排列。这种模式表明肌节的功能也会发生变化。从颌口类(部分七鳃鳗类)的肌隔肌腱与白肌纤维的关系中可以推断出肌隔肌腱的另外三个假定作用:(1)通过外侧带和/或肌habdoid肌腱将前部产生的肌肉力量向后传递。这些肌腱在后部更强壮。前后锥形结构似乎在力量传递中起重要作用。(2)通过外侧带和肌habdoid肌腱拉动皮肤的胶原纤维,表明肌肉力量传递使皮肤处于张力状态。(3)通过神经上(胸膜上)肌腱抵抗收缩肌纤维的径向扩张。通过后两种机制,可能实现身体刚度的调节。