Motoharu Oishi

Dimensions of forelimb muscles in orangutans and chimpanzees.

Eight forelimbs of three orangutans and four chimpanzees were dissected and the muscle mass, fascicle length and physiological cross‐sectional area (PCSA) of all forelimb muscles were systematically recorded to explore possible interspecies variation in muscle dimensions. Muscle mass and PCSA were divided by the total mass and total PCSA of the entire forelimb muscles for normalization. The results indicate that the mass and PCSA ratios of the monoarticular elbow flexors (M. brachialis and M. brachioradialis) are significantly larger in orangutans. In contrast, the mass ratios of the biarticular muscles in the upper arm (the short head of M. biceps brachii and the long head of M. triceps brachii) are significantly larger in chimpanzees. For the rotator cuff muscles, the force‐generating capacity of M. subscapularis is significantly larger in orangutans, whereas the opposite rotator cuff muscle, M. infraspinatus, is larger in chimpanzees. These differences in forelimb muscle dimensions of the two species may reflect functional specialization for their different positional and locomotor behaviors.

Muscle architecture of the upper limb in the orangutan

We dissected the left upper limb of a female orangutan and systematically recorded muscle mass, fascicle length, and physiological cross-sectional area (PCSA), in order to quantitatively clarify the unique muscle architecture of the upper limb of the orangutan. Comparisons of the musculature of the dissected orangutan with corresponding published chimpanzee data demonstrated that in the orangutan, the elbow flexors, notably M. brachioradialis, tend to exhibit greater PCSAs. Moreover, the digital II–V flexors in the forearm, such as M. flexor digitorum superficialis and M. flexor digitorum profundus, tend to have smaller PCSA as a result of their relatively longer fascicles. Thus, in the orangutan, the elbow flexors demonstrate a higher potential for force production, whereas the forearm muscles allow a greater range of wrist joint mobility. The differences in the force-generating capacity in the upper limb muscles of the two species might reflect functional specialization of muscle architecture in the upper limb of the orangutan for living in arboreal environments.

Morphology of Brachial Plexus and Axillary Artery in Bonobo (Pan paniscus)

With 1 figure and 1 table

The Brachial Plexus Adapted to the Semi-Elongated Neck in the Okapi

Abstract. The brachial plexus of the okapi showed the evolutionarily intermediate status between the underived ruminants and the giraffe with elongated neck. Whereas the C6 was the thinnest among the roots of the brachial plexus, the C7, C8 and T1 were much thicker in the okapi. From the data we concluded that the okapi was equipped with the intermediate characteristics of the disappearing C6. Although the nerve of the C6 should be elongated in accordance with the long neck in the Giraffidae, the extraordinary elongation of the C6 may have no advantages in the function of the innervations. In the okapi, therefore, we suggest that the function of the C6 has been mainly replaced with that of C7.

Histological Structure and Distribution of Carbonic Anhydrase Isozymes (CA‐I, II, III and VI) in Major Salivary Glands in Koalas

While the mandibular glands usually consist of only mucous acinar cells or a combination of mucous and serous cells in other species of mammals, those of koalas were serous glands. Rabbit mono‐specific polyclonal anti‐canine CA‐I, II, III or VI antiserum showed cross‐reactivity against corresponding koala carbonic anhydrase (CA) isozymes. Although immunohistochemical reactions to CA‐I, II and VI in ductal cells were moderate to strong in the tested salivary glands, no reaction or only slight reactions were observed against CA‐III. In the sublingual glands, moderate immunohistochemical reactions to CA‐I, II and VI were also evident in serous acinar cells and serous demilunes. However, no reactions to the tested isozymes were observed in mucous acinar cells in these glands. With the exception of the histological structure of the mandibular glands, histological features and the distributional profile of CA isozymes of the salivary glands in koalas are relatively close to results obtained from horses.

The Semifossorial Function of the Forelimb in the Common Rice Tenrec (Oryzorictes hova) and the Streaked Tenrec (Hemicentetes hemispinosus)

The forelimb muscles of the two semifossorial species of Tenrecidae (Oryzoryctinae: common rice tenrec; and Tenrecinae: streaked tenrec) were compared macroscopically with those of the unspecialized terrestrial–arboreal species, the Talazac long‐tailed tenrec. The structure of the hand was also observed using three‐dimensional reconstructed images from computed tomography data. The two semifossorial species had similar muscle weight ratios in the lateral and long heads of M. triceps brachii and M. teres major. A similar hand skeleton structure (in which the second, third and fourth metacarpals and phalanges act as a digging apparatus) was observed in both species. Our observations confirm that both these species have muscular–skeletal adaptations supporting fossorial locomotion. As each species belongs to a monophyletic subfamily within the Tenrecidae isolated in Madagascar, such semifossorial adaptations are assumed to have evolved convergently.

Muscle architectural properties in the common marmoset (Callithrix jacchus)

The common marmoset, Callithrix jacchus, is a small New World monkey that has recently gained attention as an important experimental animal model in the field of neuroscience as well in rehabilitative and regenerative medicine. This attention reflects the closer phylogenetic relationship between humans and common marmosets compared to that between humans and other experimental animals. When studying the neuronal mechanism behind various types of neurological motor disorders using the common marmoset, possible differences in muscle parameters (e.g., the force-generating capacity of each of the muscles) between the common marmoset and other animals must be taken into account to permit accurate interpretation of observed motor behavior. Differences in the muscle architectural properties are expected to affect biomechanics, and hence to affect neuronal control of body movements. Therefore, we dissected the forelimbs and hind limbs of two common marmosets, including systematic analysis of the muscle mass, fascicle length, and physiological cross-sectional area (PCSA). Comparisons of the mass fractions and PCSA fractions of the forelimb and hind limb musculature among the common marmoset, human, Japanese macaque, and domestic cat demonstrated that the overall muscle architectural properties of the forelimbs and hind limbs in the common marmoset are very similar to those of the Japanese macaque, a typical quadrupedal primate. However, muscle architectural properties of the common marmoset differ from those of the domestic cat, which has relatively larger hamstrings and pedal digital flexor muscles. Compared to humans, the common marmoset exhibits relatively smaller shoulder protractor, retractor, and abductor muscles and larger elbow extensor and rotator-cuff muscles in the forelimb, and smaller plantarflexor muscles in the hind limb. These differences in the muscle architectural properties must be taken into account when interpreting motor behaviors such as locomotion and arm-reaching movements in the common marmoset.

Muscle dimensions of the foot in the orangutan and the chimpanzee

The hindlimbs of two orangutans and four chimpanzees were dissected, and muscle parameters (mass, fascicle length, and physiological cross‐sectional area: PCSA) were determined to explore possible interspecies variation in muscle dimensions. Muscle mass and PCSA were divided by the total mass and total PCSA of the entire foot muscles for normalization. The results indicate that the pedal interosseous and the intrinsic pedal digital extensor muscles in the orangutans probably have higher capacity for force production due to their relatively larger PCSAs than in chimpanzees. Moreover, the medial components of the intrinsic muscles exhibited relatively larger mass and PCSA ratios in orangutans. The mass and PCSA ratios of the hallucal muscles were larger in chimpanzees. These differences in foot muscle dimensions of the two species suggest that the orangutan is more specialized for hook‐like digital gripping without involvement of the rudimentary hallux, while the chimpanzee is adapted to hallux‐assisted power gripping in arboreal locomotion.

Muscle dimensions in the Japanese macaque hand

Macaques have been used as an important paradigm for understanding the neural control mechanisms of human precision grip capabilities. Therefore, we dissected the forearms and hands of two male Japanese macaques to systematically record the muscle mass, fascicle length and physiological cross-sectional area (PCSA). Comparisons of the mass fractions and PCSA fractions of the hand musculature among the Japanese macaque, chimpanzee, and human demonstrated that the sizes of the thenar and hypothenar eminence muscle groups are more balanced in the macaque and chimpanzee, but those of the thenar eminence group are much larger in the human, indicating that the capacity to generate force at the tip of the thumb is more restricted in macaques, despite their high manual dexterity. In the macaque, however, the extrinsic flexor muscles are much larger, possibly to facilitate weight bearing by the forelimbs in pronograde quadrupedal locomotion and forceful grasping of arboreal supports in gap-crossing movements such as leaping. Taking such anatomical differences imposed on the hand musculoskeletal system into consideration seems to be an important method of clarifying the mechanisms of precision grip in macaques.

The seminiferous epithelial cycle and microanatomy of the koala (Phascolarctos cinereus) and southern hairy-nosed wombat (Lasiorhinus latifrons) testis

The koala (Phascolarctos cinereus) and southern hairy‐nosed wombat (Lasiorhinus latifrons) are iconic Australian fauna that share a close phylogenetic relationship but there are currently no comparative studies of the seminiferous epithelial cell or testicular microanatomy of either species. Koala and wombat spermatozoa are unusual for marsupials as they possess a curved stream‐lined head and lateral neck insertion that superficially is similar to murid spermatozoa; the koala also contains Sertoli cells with crystalloid inclusions that closely resemble the Charcot–Bottcher crystalloids described in human Sertoli cells. Eighteen sexually mature koalas and four sexually mature southern hairy‐nosed (SHN) wombats were examined to establish base‐line data on quantitative testicular histology. Dynamics of the seminiferous epithelial cycle in the both species consisted of eight stages of cellular association similar to that described in other marsupials. Both species possessed a high proportion of the pre‐meiotic (stages VIII, I – III; koala – 62.2 ± 1.7% and SHN wombat – 66.6 ± 2.4%) when compared with post‐meiotic stages of the seminiferous cycle. The mean diameters of the seminiferous tubules found in the koalas and the SHN wombats were 227.8 ± 6.1 and 243.5 ± 3.9 μm, respectively. There were differences in testicular histology between the species including the koala possessing (i) a greater proportion of Leydig cells, (ii) larger Sertoli cell nuclei, (iii) crystalloids in the Sertoli cell cytoplasm, (iv) a distinctive acrosomal granule during spermiogenesis and (v) a highly eosinophilic acrosome. An understanding of the seminiferous epithelial cycle and microanatomy of testis is fundamental for documenting normal spermatogenesis and testicular architecture; recent evidence of orchitis and epididymitis associated with natural chlamydial infection in the koala suggest that this species might be useful as an experimental model for understanding Chlamydia induced testicular pathology in humans. Comparative spermatogenic data of closely related species can also potentially reflect evolutionary divergence and differences in reproductive strategies.