Rowlerson A, Mascarello F, Veggetti A, Carpene E
J Muscle Res Cell Motil. 1983 Aug;4(4):443-72. doi: 10.1007/BF00711949.
A combination of standard histochemical techniques and immunohistochemical staining using myosin type-specific antisera was used to determine the fibre-type composition of the muscles of first branchial arch origin (that is, masseter, temporalis, pterygoideus medialis and lateralis, tensor veli palatini, tensor tympani, anterior digastricus and mylohyoideus) in a wide range of the Carnivora and the Primates. The rare IIM fibre type was found in the first branchial arch muscles of most of the species examined, but never in the limb muscles used as controls for this study. The jaw-closer muscles (masseter, temporalis and pterygoideus medialis) were found to contain IIM fibres in all the Carnivora except the lesser panda and in all the Primates except man. When present, the IIM fibres were usually the predominant fibre type, and the only other fibre types present were types I, II or IIC. The presence of IIM fibres in the jaw-closer muscles of most of the Carnivora and the Primates seems to be associated with an aggressive bite which is required for predation by the former and defence by the latter. In both groups of species there was the member which does not have an aggressive bite, the lesser panda and man, respectively, and these (like all other orders of mammals such as Lagomorpha, Rodentia, etc.) were found to have no IIM fibres in the jaw-closer muscles. The two muscles of the first branchial arch group which are derived from the ventral constrictor muscles of the (phylogenetically) original mandibular arch never contained IIM fibres, and were composed of type I and II fibres similar to those found in the control muscles of the limb. Tensor veli palatini and tensor tympani showed species-dependent variations in fibre-type composition and did not always reflect the composition of the jaw-closer muscles. Thus their common origin with the jaw-closers cannot be responsible for the occurrence of IIM fibres in tensor veli palatini and tensor tympani in some species. Furthermore, in tensor tympani but not in tensor veli palatini, the presence of IIM fibres was always accompanied by immunohistochemically slow-tonic fibres. Finally, the regard to the association of oxidative activity with the fibre type as defined by the myofibrillar ATPase method and by the isoform of myosin present, we suggest that in the first branchial arch muscles this is probably not directly comparable to the situation in the typical limb muscle.
采用标准组织化学技术与使用肌球蛋白类型特异性抗血清的免疫组织化学染色相结合的方法,来确定广泛的食肉目动物和灵长目动物中第一鳃弓起源肌肉(即咬肌、颞肌、内侧翼肌和外侧翼肌、腭帆张肌、鼓膜张肌、二腹肌前腹和下颌舌骨肌)的纤维类型组成。在所检查的大多数物种的第一鳃弓肌肉中发现了罕见的IIM纤维类型,但在本研究用作对照的肢体肌肉中从未发现。除小熊猫外的所有食肉目动物以及除人类外的所有灵长目动物的咬肌(咬肌、颞肌和内侧翼肌)中都发现含有IIM纤维。当存在IIM纤维时,它们通常是主要的纤维类型,且仅存在的其他纤维类型为I型、II型或IIC型。大多数食肉目动物和灵长目动物的咬肌中存在IIM纤维,这似乎与前者捕食和后者防御所需的攻击性咬合力有关。在这两组物种中,分别有不具有攻击性咬合力的成员,即小熊猫和人类,并且发现这些动物(与所有其他哺乳动物目如兔形目、啮齿目等一样)的咬肌中没有IIM纤维。第一鳃弓肌群中源自(系统发育上)原始下颌弓腹侧收缩肌的两块肌肉从未含有IIM纤维,且由与肢体对照肌肉中发现的I型和II型纤维组成。腭帆张肌和鼓膜张肌在纤维类型组成上表现出物种依赖性变化,并不总是反映咬肌的组成。因此,它们与咬肌的共同起源并不能解释某些物种的腭帆张肌和鼓膜张肌中出现IIM纤维的原因。此外,在鼓膜张肌而非腭帆张肌中,IIM纤维的存在总是伴随着免疫组织化学慢张力纤维。最后,关于氧化活性与由肌原纤维ATP酶方法和存在的肌球蛋白同工型所定义的纤维类型之间的关联,我们认为在第一鳃弓肌肉中,这可能与典型肢体肌肉的情况没有直接可比性。