Functional anatomy of shoulder muscles in the Pacific white-sided dolphin (Lagenorhynchus obliquidens).

Most intrinsic muscles of the forelimb in dolphins are either degenerated or lost; however, the muscles around the shoulder joint are well preserved. We dissected the forelimbs of Pacific white-sided dolphins and constructed a full-scale model of the flipper to compare and examine their movements following dissection. The humerus was oriented at approximately 45° ventrally from the horizontal plane of the dolphin and 45° caudally from the frontal plane. This maintains the neutral position of the flipper. The deltoideus and pectoralis major muscles were inserted into the body of the humerus, and the flipper was moved in the dorsal and ventral directions, respectively. A large tubercle, known as the common tubercle, was observed at the medial end of the humerus. Four muscles were inserted into the common tubercle: the brachiocephalicus, supraspinatus, and cranial part of the subscapularis, which laterally rotated the common tubercle. Subsequently, the flipper swung forward, and its radial edge was lifted. Conversely, the medial rotation of the common tubercle caused by the coracobrachialis and the caudal part of the subscapularis was accompanied by backward swinging of the flipper and lowering of the radial edge. These findings suggest the function of the flipper as a stabilizer or rudder is caused by the rotation of the humerus's common tubercle.

Comparison of the soleus and plantaris muscles in humans and other primates: Macroscopic neuromuscular anatomy and evolutionary significance.

In humans, the soleus is more developed compared to other primates and has a unique architecture composed of anterior bipennate and posterior unipennate parts, which are innervated by different nerve branches. The anterior part of the human soleus was proposed to be important for bipedalism, however, the phylogenetic process resulting in its acquisition remains unclear. Providing insights into this process, the anterior part of the soleus was suggested to be closely related to the plantaris based on the branching pattern of their nerve fascicles. To reveal the phylogeny of the soleus and plantaris in primates, the innervation patterns of the posterior crural muscles were compared among a wide range of species. From their branching pattern, posterior crural muscles could be classified into superficial and deep muscle groups. The anterior part of the soleus and plantaris both belonged to the deep muscle group. In all the examined specimens of ring-tailed lemurs and chimpanzees, as well as in one out of two specimens of siamang, the nerve branches corresponding to those innervating the anterior part of the human soleus were found. The muscular branches innervating the anterior part of the soleus and plantaris formed a common trunk or were connected in all the specimens. These results indicate that the anterior part of the soleus is closely related to the plantaris across different species of primates. In turn, this suggests that the anterior part of the soleus is maintained among primates, and especially in humans, where it develops as the characteristic bipennate structure.

Congenital diaphragmatic eventration with absent left phrenic nerve in the fetal pig.

We encountered a fetal pig with eventration of the diaphragm and pulmonary hypoplasia accompanied by phrenic nerve agenesis. The fetal pig was female measuring 34 cm in crown-rump length and about 1500 g in body weight. The diaphragm was a complete continuous sheet, but comprised a translucent membrane with residual muscular tissue only at the dorsolateral area of the right leaf of the diaphragm. The left leaf protruded extraordinarily toward the thoracic cavity. The left phrenic nerve was completely absent, while there was a slight remnant of the right phrenic nerve that supplied the dorsolateral muscular area of the right leaf. Both lungs were small, and the number of smaller bronchioles arising from the bronchioles was decreased to about half of that of the normal lung. Additionally, the right and left subclavius muscles and nerves could not be identified. These findings imply that the diaphragm, the subclavius muscle and nerves innervating them comprise a developmental module, which would secondarily affect lung development. It is considered that the present case is analogous to the animal model of congenital eventration of the diaphragm in humans.

Pseudoganglion on the connecting branch between the deep branch of the lateral plantar nerve and medial plantar nerve.

The connecting branch between the deep branch of the lateral plantar nerve and medial plantar nerve often has an enlarged site. We investigated these enlarged sites of the connecting branches. We observed the 22 human feet of 20 Japanese cadavers. We investigated the connecting branch macroscopically and histologically. We found the connecting branches between the deep branch of the lateral plantar nerve and medial plantar nerve in 19 feet out of 22 feet. This connecting nerve branch was interposed between the tendon of the flexor hallucis longus and the flexor hallucis brevis, and there enlarged in the anteroposterior direction. After penetration, numbers of fascicles of this connecting branch were increased at the enlarged site. In this region, the connective tissues surrounding the nerve fascicles and vessels were more developed compared with the adjoining sides of this branch. A few fascicles at this enlarged site innervated the first metatarsophalangeal joint capsule. Other nerve fascicles arose from the connecting branch and branched off muscular branches to the flexor hallucis brevis. This branch possibly receives the physical exertion or friction during gait due to its position. Deformity and overload of the foot can cause sensory disorders of the foot, but the anatomical basis for the relationship between the deformity/overload and sensory disorders of the foot is unclear. We discussed that this connecting branch can be a potential cause of pressure neuropathies in the human foot.

[Reexamination of the communicating branch between the sural and tibial nerves].

Reexamination of communicating branches between the sural and tibial nerves ventral to the calcanean tendon was carried out on 52 legs of 26 Japanese cadavers which were used for ordinary dissection practices at the Niigata University School of Medicine. Communicating branches were found in 7 out of 52 dissections (13.5% of cases). In three of the 7 specimens, the communicating branch, the sural nerve and the tibial nerve with the deep crural fascia were removed from the legs and demonstrated by a modified Sihler's staining technique. Three types of communicating branches, Y, U and N, were distinguished on the basis of their shapes. In type Y, a medial branch from the sural nerve and a branch from the tibial nerve joined in Y-shape and become one terminal branch. In type U, the both branches formed a loop between the sural and tibial nerves. The type N communicating branch ran obliquely and medially to reach the tibial nerve distally. Only the Y type appeared in 5 specimens. Both the Y and U type and the Y and N types occurred in one specimen each. We assume that the communicating branch of the N type contains motor fibers which are derived from the sural nerve and innervate some plantar muscles, because this type is correspond to the communication type of some animals in which motor fibers have been demonstrated. Therefore, if the sural nerve biopsy is performed to examine a pure sensory nerve, removal of the more distal part of the sural nerve than a diverging point of a communicating branch is recommended. This study also indicated that the modified Sihler's staining technique is useful to examine distributions of cadaveric peripheral nerves after medical students' dissection course.

Intramuscular nerve distribution pattern of the oblique and transverse heads of the adductor hallucis muscles in the human foot.

To understand which layer of the intrinsic muscles of the foot the adductor hallucis muscle belongs to, it is essential to investigate the innervation patterns of this muscle. In the present study, we examined the innervation patterns of the adductor hallucis muscles in 17 feet of 15 Japanese cadavers. We investigated the intramuscular nerve supplies of the adductor hallucis muscles in six feet and performed nerve fiber analysis in three feet. The results indicate that: (i) the oblique head of the adductor hallucis muscle is divided into three compartments (i.e. lateral, dorsal and medial parts) or two compartments (i.e. dorsal and medial parts) based on its intramuscular nerve supplies, but we could not classify the transverse head into any parts; (ii) the communicating twig between the lateral and medial plantar nerves penetrated the oblique head of the adductor hallucis muscle in 13 of 17 feet (76.5%); (iii) the penetrating twig entered between the lateral and dorsal parts of the oblique head, passed between the lateral and medial parts of this muscle and then connected with the medial plantar nerve; and (iv) the majority of the nerve fibers of the penetrating twig derived from the lateral plantar nerve. The present study demonstrated that only the lateral part of the oblique head of the adductor hallucis muscle had a unique innervating pattern different from other parts of this muscle, suggesting that the lateral part of the oblique head has a different origin from other parts of this muscle.

Formation and distribution of the sural nerve based on nerve fascicle and nerve fiber analyses.

The formation and distribution of the sural nerve are presented on the basis of an investigation of 31 legs of Japanese cadavers using nerve fascicle and fiber analyses. Nerve fibers constituting the medial sural cutaneous nerve were designated as 'T', whereas those constituting the peroneal communicating branch were designated as 'F'. In 74.2% of cases (23/31), the T and F fibers joined each other in the leg, whereas in 9.7% of cases (3/31) they descended separately. In 16.1% of cases (5/31), the sural nerve was formed of only the T fibers. The sural nerve gave off lateral calcaneal branches and medial and lateral branches at the ankle. The lateral calcaneal branches always contained T fibers. The medial branches consisted of only T fibers, whereas most of the lateral branches consisted of only F fibers (71.0%; 22/31). In addition to the T and F fibers, P fibers, which derived from the superficial and deep peroneal nerves, formed the dorsal digital nerves. The P fibers were entirely supplied to the medial four and one-half toes. However, they were gradually replaced by the T and F fibers in the lateral direction. The 10th proper dorsal digital nerve consisted of T fibers only (38.7%; 12/31), of F fibers only (19.4%; 6/31) or of both T and F fibers (38.7%; 12/31). These findings suggest that the T fibers are essential nerve components for the skin and deep structures of the ankle and heel rather than the skin of the lateral side of the fifth toe. The designation of the medial sural cutaneous nerve should be avoided and only the T fibers are appropriate components for naming as the sural nerve.

[Application of the modified Sihler's stain technique to cadaveric peripheral nerves after medical students' dissection course].

The exact ramification and distribution pattern of the peripheral nerves is one of the most important information for anatomists and clinicians. However, it is very difficult to pursue perfectly all of the fine twigs of nerve branches even if we use a stereoscopic microscope. Recently, Liu et al. (Anat. Rec., 247: 137, 1997) applied a modified Sihler's stain technique to study the distribution of intramuscular nerve branches in mammalian skeletal muscles. Then, we attempted to apply this technique to plantar nerves of human foot removed from cadavers which were used for ordinary dissection practices at the School of Medicine. Intrinsic muscles of the foot with motor and sensory nerve branches were removed en bloc from bones of the foot. They were macerated and depigmented in 3% aqueous potassium hydroxide, decalcified in Sihler's solution 1. Then, after staining in Sihler's solution II, they were destained in Sihler's solution I, neutralized in 0.05% lithium carbonate, and cleared in increasing concentrations of glycerin. As a result, each nerve fascicle, which are bundles of nerve fibers invested by the perineurium, was very clearly visualized, since only nerve fibers were stained deep blue-purple, while muscles, the epineurium and the perineurium were made transparent in glycerin. We found an anastomosis between a deep branch of the lateral plantar nerve and the medial plantar nerve, composed of several nerve fascicles. Therefore, the modified Sihler's stain technique can be applied to cadaveric peripheral nerves after medical students' dissection course.

Ramification pattern of the deep branch of the lateral plantar nerve in the human foot.

To understand how the oblique and transverse heads of the adductor hallucis muscle of the human foot are phylogenitically and ontogenetically developed, it is essential to know nerve supplies of these two heads of the muscle. In the present study, we dissected seven feet of five Japanese cadavers in detail to clarify the ramification patterns of the deep branch of the lateral plantar nerve by peeling off its epineurium (the nerve fascicle analysis method). We found that the muscular branch to the oblique head of the adductor hallucis muscle directly separated from nerve fascicles constituting the deep branch of the lateral plantar nerve, whereas the muscular branch to the transverse head arose in common with branches which innervated other intrinsic muscles of the foot, i.e., the 2nd and 3rd lumbrical muscles and the 1st and 2nd dorsal interossei muscles. The present study revealed that two heads of the adductor hallucis muscle, the oblique and transverse, had different innervating patterns, suggesting that two heads of the human adductor hallucis muscle develop from different primordia, and not from common ancestors.

Sural-tibial nerve communications in humans.

We investigated the occurrence of a communication between the sural and tibial nerves in 49 legs of 28 Japanese cadavers. In front of the calcanean tendon, we found the communication in 7 legs (14.3%) or in 5 cadavers (18.9%). The sural nerve gave rise to a number of medial and lateral branches, including the lateral calcanean branch at the lateral side of the ankle. The communicating branch with the tibial nerve arose from the first medial branch and pierced the deep fascia of the leg. In 4 cases, the U-shaped communication was formed between the sural and tibial nerves, and in 3 cases, the Y-shaped communication. Electrophysiological evidence of an anomalous motor function of the sural nerve has been reported recently. We consider that the U-shaped communication between the sural and tibial nerves gives a morphological basis to the motor function of the sural nerve.