Development of a peripheral nerve stimulator-guided technique for equine pudendal nerve blockade.

The aim of this study was to develop and evaluate a procedure for equine pudendal nerve block using a peripheral nerve locator. In the first experiment, six ponies were used to determine the relationship between elicited muscle contractions (anal, perineal or both) and nerves serving the perineal region (pudendal, caudorectal and perineal nerves) when methylene blue dye was injected using the electrolocation technique. This experiment showed that the pudendal nerve was approached effectively when both anal and perineal twitch were elicited during electrolocation. In a second experiment, seven Thoroughbred horses were used to evaluate the appropriate volume of anaesthetic solution for the nerve block. Immediately after euthanasia, lidocaine/methylene blue solution was injected after positive electrolocation. A stained segment of 2 cm or more of the nerve was considered effective and this was evaluated after dissection. Both 10 and 20 mL per injection site resulted in effective nerve staining. Finally, pudendal nerve block was performed and evaluated in 27 horses admitted for selected reproductive surgical procedures including perineoplasty, urethroplasty, clitorectomy in mares and penile examination, phallectomy and urethrostomy in geldings. Surgical time varied from several minutes to 3 h. The choice between lidocaine, mepivacaine or bupivacaine was based on the duration of analgesia required. In mares and males, a volume of 20 mL and 10 mL, respectively, was injected per site. The use of a peripheral nerve stimulator-guided pudendal nerve block is a feasible, safe and reliable alternative for both epidural and general anaesthesia, to provide peri-operative analgesia in clinical equine patients undergoing specific reproductive surgeries.

A lectin histochemical study of the thoracic respiratory air sacs of the fowl.

The lectin-binding characteristics of the epithelial lining of the thoracic air sacs of the chicken were determined. Con A, LCA and PSA bound to the apical membrane as well as to the cytoplasm distal to the nucleus of the surface epithelium, indicated the presence of a-linked mannose as well as N-acetylchitobiose-linked alpha-fucose residues in the glycoproteins. GSL I bound to the apical membrane and cytoplasm distal to the nucleus, but not to the cilia of the epithelium, where-as MPL, DBA and RCA120 bound to the apical membrane, cilia and cytoplasm, indicated the presence of a-linked N-acetylgalactosamine residues. However, neither SJA or SBA showed any binding, indicating the absence of beta anomers of galactosyl (beta1.3)N-acetylgalactosamine and beta-linked N-acetylgalactosamine residues. UEA I bound to the apical membrane and cilia, as well as to the cytoplasm of a few cells, indicated the presence of alpha-linked fucose residues. PNA bound to the apical membrane of some, but not all, surface epithelium cells, indicated the presence of galactosyl (beta1.3)N-acetylgalactosamine residues. WGA bound to the apical membrane and cilia, as well as to the cytoplasm of a few cells, indicated the presence of neuraminic acid residues.

Ascites and the anatomy of the peritoneal sacs of broilers.

Although the ascites syndrome of broilers is well documented, all the authors fail to describe exactly in which of the various coelomic cavities ascitic fluid is found. Determination of the precise location of this fluid is essential if the pathogenesis of the syndrome is to be understood and explained. Post-mortem examinations were done on 100 broilers that had ascites or had died of the ascites syndrome. In all of them large quantities of fluid were found in the ventral hepatic peritoneal cavities, moderate amounts in the right dorsal hepatic peritoneal cavities and small amounts in the intestinal peritoneal and pericardial cavities. No ascitic fluid was found in the left dorsal hepatic peritoneal cavity. The amount of ascitic fluid effusing from the liver was directly proportional to the surface area of the liver in a given peritoneal cavity.

The topography of the thoraco-abdominal viscera in the ostrich (Struthio camelus).

The topography of the thoraco-abdominal viscera in the ostrich was studied in 20 birds varying in age from 2 weeks to 12 months. The lungs occupied the dorsal third of the thorax, and the heart lay in the cranioventral thorax perpendicular to the long axis of the body. There was no pleural cavity. The liver was situated in the caudoventral part of the thorax, and the proventriculus occupied the left cranial part of the abdomen between the 7th vertebral rib and the acetabulum. The gizzard lay in the cranioventral part of the abdomen, resting on the sternum and abdominal floor. The duodenum formed a loop from right to left, with the pancreas lying between the 2 limbs of the loop. The coiled jejunum and ileum occupied the ventral part of the abdomen between the gizzard and pelvis. The two caeca lay on either side of the terminal ileum with their apices in the pelvis. The rectum was the longest part of the intestine and could be divided into a thick proximal segment situated in the right dorsal part of the abdomen, and a thin distal part that occupied the left caudodorsal part of the abdomen. The trilobed kidneys lay along the ventral surface of the synsacrum, with the adrenal glands at their cranioventral poles. The testes lay ventrally to the cranial divisions of the kidneys, whereas the left ovary was situated ventrally to the cranial division of the left kidney. The spleen lay wedged in between the right kidney, caudal vena cava and proventriculus. The thyroid glands were situated at the cranial borders of the subclavian arteries, and the thymus lay at the base of the neck.

The major blood vessels of the wing of the ostrich (Struthio camelus).

The major blood vessels of the ostrich wing were studied by dissection of the wings of 8 ostriches. The axillary artery entered the caudo-ventral aspect of the wing and divided into the brachial and deep brachial arteries. The deep brachial artery gave rise to the radial and ulnar collateral arteries which supplied the caudodorsal aspect of the brachium. The brachial artery divided in the cubital fossa into the smaller ulnar and large radial arteries. The ulnar artery supplied the cranio-ventral aspect of the antebrachium and manus, and the radial artery the caudo-ventral and dorsal aspects of the antebrachium and manus, including the feathers. With few exceptions the veins corresponded with the arteries that supplied the region they drained. The basilic vein passed along the cranial margin of the wing, unaccompanied by arteries or nerves, to drain the major part of the wing. The brachial artery and the basilic veins were the vessels most accessible for arterio- and venipuncture, respectively.

Osteology of the thoracic limb of the African elephant (Loxodonta africana).

The forelimb bones of 8 elephants (7 adults, 1 juvenile) were studied. In addition, the bones of the digits were dissected and studied in situ in a mature specimen. The scapula, humerus and bones of the antebrachium (particularly the ulna) are massive in comparison to the short, relatively small bones of the manus. There are 8 carpal bones, 5 metacarpal bones and 5 digits. Digits 2-4 consist of 3 phalanges each. The 5th digit consists of 2 phalanges, while the 1st is represented by a single phalanx which is tusk-like and pointed. The distal phalanges of digits 2-4 are very small and do not articulate with the middle phalanges. The proximal sesamoids are well developed and are present on the palmar aspect of all 5 metacarpophalangeal joints. All the bones are illustrated from at least 2 aspects.

The osteology of the African elephant (Loxodonta africana): vertebral column, ribs and sternum.

The vertebral column, sternum and ribs of the African elephant were studied and illustrated. In the cervical series, the vertebrae are characterized by very short (compressed) vertebral bodies and short spinous processes. There are 20-21 thoracic vertebrae that carry ribs, and three lumbar vertebrae. The neural arches of the five sacral vertebrae fuse with each other as well as with the wings of the ilium, while the intervertebral discs do not ossify and the vertebral bodies remain separate. There are 19-21 caudal vertebrae. In the latter, the neural arches of only the first five to six vertebrae fuse dorsally, the vertebral foramens of the other vertebrae as well as the vertebral canal remain open dorsally. The body of the first rib is greatly expanded while that of the last three to four ribs are reduced. The cartilages of the first six ribs articulate with the sternum, the last five to six ribs do not bear costal cartilages and are not attached to the costal arch. The sternum consists of five sternabrae that form three approximately equal, but separate, segments. The first segment is formed by the first sternabra, the second segment is formed by the second to fourth sternabrae and the last segment is formed by the fifth sternabra. The first and second sternabrae articulate with each other by means of a synovial joint, the second to fourth sternabrae are fused to each other and the fourth and fifth sternabrae are loosely attached to each other by connective tissue.

Osteology of the pelvic limb of the African elephant (Loxodonta africana).

The pelvic girdle was characterized by large, transversely-placed ilial wings. The femur was the longest bone of the skeleton and its fovea capitis was situated caudomedially between the epiphyseal line and the articular surface of the femoral head. A wedge-shaped patella articulated with the femoral trochlea. The bones of the crus were approximately half as long as the femur and consisted of the sturdy tibia and slender fibula. The condyles of the tibia were concave and the femoro-tibial joint was congruent with rudimentary menisci. The tarsus consisted of seven bones which were arranged in three rows. There were five metatarsal bones. Only four digits were present, the third and fourth consisted of three phalanges each while the second and fourth digits were smaller and consisted of two phalanges each. The first digit was represented by one proximal sesamoid bone only. A large, cartilagenous rod or prehallux was attached to the first tarsal and metatarsal bones. Proximal sesamoid bones were present on the plantar aspect of the trochleae of metatarsal bones 1-V. The pes was found to be digitigrade and the digits rested on a thick pad of elastic connective tissue and fat.

A light microscopic and immunocytochemical study of the gastrointestinal tract of the ostrich (Struthio camelus L.).

Although the histological features and endocrine cells of the gastro-intestinal tract of the chicken have been well studied, little is known about these features of the gut of the ostrich. The present study was undertaken to elucidate the histology and peptide-storing endocrine cells of the ostrich. As a rule the histological features of the gastro-intestinal tract of the ostrich corresponded to that of the fowl. However, certain differences were observed. The superficial proventricular glands were simple, branched tubular glands, while the deep proventricular glands were restricted to a slipper-shaped area and extended into the muscularis mucosae. The gizzard had a variably developed muscularis mucosae, a feature that seems to be unique to the ostrich. The villi of the small intestine were long and branched profusely, forming a labyrinthine surface. No Paneth cells were observed. The mucosa of the ceca and the first part of the rectum was thrown in large circular folds, forming a compressed spiral. Numerous melanocytes were seen in the submucosa and the connective tissue around the bloodvessels of the muscle layers at the tips of the ceca. A well developed subserosa was present throughout the gastro-intestinal tract. Endocrine cells immunoreactive to somatostatin, glucagon, gastrin, bombesin, neurotensin, substance P and pancreatic polypeptide were detected in the gastro-intestinal tract of the ostrich. The topographical distribution of those endocrine cells immunoreactive to glucagon, bombesin, neurotensin and substance P differed from that of the chicken. The results of this investigation inferred that at least one of the gut peptides of the ostrich (secretin) to be structurally different from its counterparts in mammal and chicken. Molecular heterogeneity of somatostatin was observed in endocrine cells situated in the deep ventricular glands of the ostrich.

Serum- and bone-mineral status of ostriches with tibiotarsal rotation.

Tibiotarsal rotation in ostrich chicks is a serious problem that accounts for considerable financial loss to ostrich farmers. Serum- and bone-mineral analyses of 20 ostrich chicks with tibiotarsal rotation were compared with serum- and bone-mineral analyses of eight normal ostrich chicks of comparable age, sex and body mass, and raised under identical conditions. The serum-zinc values were significantly higher and the bone-calcium and phosphorus values significantly lower in the affected group than in the group of normal ostrich chicks. The results indicated poor mineralization of bone with subsequent reactive osteoid formation.

The skull and mandible of the African elephant (Loxodonta africana).

In the present study the bones of the skull, excluding the hyoid apparatus, are described. All the bones are aerated by sinuses. In the occipital bone the squamous part is aerated from the sinus of the parietal bone, the lateral part is aerated from the tympanic bulla and the basal part from the sinus of the basisphenoid bone. Condylar foramens and hypoglossal canals are absent. A small interparietal bone is present at birth. At an early age it fuses with the surrounding cranial bones. The squamous part of the temporal bone lies sagittally in young animals, but moves progressively to a transverse plane as the animals age. A foramen lacerum is represented by jugular and oval foramens and the carotid canal. The body of the basisphenoid bone is excavated by the massive maxillary tuberosity. The latter extends to the oval foramen and contains the developing molar teeth. The ethmoturbinate, nasal and lacrimal bones are exceptionally small. In old bulls the palatine process of the incisive bones and their sinuses are gradually displaced by the palatine process of the maxillae.

Macroscopic blood supply to the hypophysis and hypothalamus of the ostrich (Struthio camelus).

The branching pattern of the Aa. carotes internae and the macroscopic blood supply to the hypophysis and hypothalamus of the ostrich were studied on ten dissected acrylic vascular-injected heads and ten corrosion preparations of acrylic vascular casts of the head. The A. carotis cerebralis was found to be the only source of blood supply to the hypophysis and hypothalamus. The neurohypophysis was supplied by the caudal hypophyseal and infundibular arteries. The pars distalis was supplied by portal vessels from the ventral hypothalamic region, and it also received arterial blood directly from the infundibular arteries. The hypothalamus received blood from the Aa. infundibulares. A. ventralis tecti mesencephali and A. preopticae.

An anatomical study of the respiratory air sacs in ostriches.

An accurate description of the number, location and relative position of the air sacs and their diverticula in the ostrich is essential for a better understanding of the pathogenesis of air sacculitis in this bird. The air sacs were studied in ten ostriches of varying ages by latex or silicone casting of the respiratory tract and dissection. Results revealed that the air sacs of the ostrich conform to the general pattern in birds. Cervical, lateral and medial clavicular, cranial and caudal thoracic, and abdominal air sacs are present. The left and right medial clavicular air sacs fuse with each other ventrally to the trachea to form a single, median compartment. A unique, large gastric diverticulum which covers the caudal aspects of the proventriculus and gizzard originates from the median compartment of the clavicular air sac. The lateral clavicular air sacs and their diverticula are similar to those of other bird species, with the exception that humeral diverticula are absent. Both abdominal air sacs are relatively small, with the left sac being the larger. Perirenal and femoral diverticula, similar to those found in other bird species, are present. However, the entire femur is aerated by the femoral diverticulum which also forms a large, subcutaneous division caudally and caudo-laterally to the femur. The presence of this subcutaneous part has practical implications for injury and intramuscular injections. The number and location of ostia connecting the air sacs to the bronchial tree are generally similar to those reported in other bird species.

Evidence for cryptosporidial infection as a cause of prolapse of the phallus and cloaca in ostrich chicks (Struthio camelus).

Cloacas of male ostrich chicks that had suffered prolapse of the phallus and cloaca were compared with cloacas of normal ostrich chicks of both sexes from the same area. Heavy infection of the cloacal and bursal tissue with Cryptosporidium sp. was present in all the cases of prolapse, while no cryptosporidia were observed in the normal chicks. Histopathological lesions as described in cryptosporidial infection in other species were present in the infected cloacas. These included loss of the microvillous border and epithelial hyperplasia and degeneration, which was indicated ultrastructurally by vacuolation of the apical cytoplasm, swelling of organelles, and nuclear changes. It is suggested that these lesions, in combination with the anatomy of the male ostrich cloaca, may be responsible for prolapse of the phallus and cloaca.

Sperm-storage tubules in the vagina of the ostrich (Struthio camelus).

Sperm-storage tubules have been described in a number of species of birds. The presence of these tubules in the Rhea has been mentioned, but no description of these structures in ratites is available. The purpose of this study was to determine the presence and morphology of sperm-storage tubules in the vagina of the ostrich. The study was performed with the use of conventional light- and electron-microscopic techniques. Sperm-storage tubules were located in a 200-mm-wide band of the vagina adjacent to the utero-vaginal junction. The tubules were mostly branched and slightly coiled and lined by columnar epithelial cells. The cells contained a basal nucleus and displayed extensive apical junctional complexes. TEM revealed sperm in all the tubules examined.

Unusual anomalies of the arteries at the base of the heart in a dog.

Anomalous blood vessels at the base of the heart in a 6-month-old German Shepherd Dog are described. On the right side, the thoracic vertebral artery was absent and the dorsal intercostal arteries to the first 2 ribs arose directly from the deep cervical artery. The right bronchoesophageal artery was exceptionally large and arose from the right costocervical trunk. An anastomosis was present between the fifth dorsal intercostal artery and the left bronchoesophageal artery. On the left side the left bronchoesophageal artery arose from the left pulmonary artery close to the bifurcation of the pulmonary trunk. Anastomoses were present between the third dorsal intercostal artery and the paraconal interventricular branch of the left coronary artery and between the third dorsal intercostal artery and the left bronchoesophageal artery. Radiographically the anastomoses between the dorsal intercostal artery and the left pulmonary artery via the left bronchoesophageal artery could be confused with a patent ductus arteriosus.

Anomalous origins of the right subclavian and common carotid arteries in the dog.

Anomalous origins of the right subclavian and common carotid arteries in a 6-month old Alsatian bitch are described. The first vessel to branch from the aortic arch was a short bicarotid trunk which divided into left and right common carotid arteries. The right common carotid artery was partially occluded at its origin and its function and area of supply was taken over by the right vertebral artery. The right subclavian artery branched directly from the aortic arch and passed dorsally to the oesophagus, forming an incomplete vascular ring around the oesophagus. Although the oesophagus was constricted between the vessel dorsally and the trachea ventrally, it did not cause obstruction or dysphagia. The right vertebral artery was exceptionally large.

The urethral diverticulum of the bull.

The exact location of the urethral diverticulum of the bull was determined. It was found to lie 80-100 mm caudal to the colliculus seminalis, at the transition from the pelvic to the penile urethra. The presence of the diverticulum makes catheterization of the urinary bladder via the penile urethra very difficult.

Prolapse of the phallus and cloaca in the ostrich (Struthio camelus).

The incidence of cloacal prolapse in ostrich chicks hatched and raised on the Oudtshoorn Experimental Farm during the 1992-1993 breeding season was investigated. The condition which occurred primarily in male chicks, affected 14.65% of the total number of chicks hatched. The mortality rate amongst chicks with cloacal prolapse was very high. Although the pathogenesis and aetiology of the condition is unknown, a species of Cryptosporidium was present in large numbers in affected cloacas. Treatment with systemic antibiotics was found to be effective in some cases.

Evaluation of maxillary arterial blood flow in anesthetized cats with the mouth closed and open.

The mouth-gag is a common tool used in veterinary medicine during oral and transoral procedures in cats but its use has recently been associated with the development of blindness. The goal of this study was to investigate whether maximal opening of the mouth affects maxillary artery blood flow in six anesthetized cats. To assess blood flow, the electroretinogram (ERG), brainstem auditory evoked response (BAER) and magnetic resonance angiography (MRA) were evaluated qualitatively with the mouth closed and open. During dynamic computer tomography (CT) examinations, detection of contrast medium in the maxillary artery was quantified by measuring the Hounsfield units (HUs). The peak HU, time to peak and mean HU were determined. Changes ⩾10% of these parameters were considered indicative of altered blood flow. ERG and BAER were normal with the mouth closed in all cats, but was abnormal with the mouth opened maximally in two cats and one cat, respectively. During MRA, blood flow was undetected in either maxillary artery in one cat and reduced in the right maxillary artery in two cats, when the mouth was open. During CT, the peak HU decreased ⩾10% in three cats, the time to peak was ⩾10% longer in two cats, and the mean HU was ⩾10% lower in one cat when the mouth was open. No cat developed apparent blindness or deafness. Maximal opening of the mouth caused alterations in several indicators of blood flow in some individual cats.