Arterial Vascularization and Morphological Characteristics of Adrenal Glands in the Pampas Deer (Ozotoceros bezoarticus,Linnaeus 1758)

This research presents morphological characteristics of adrenal glands and a demonstration of arterial vascularization in the Pampas deer, which is considered to be in extreme danger of extinction. A total of ten deer constituted the material of the study. Vascularization of organs was investigated by using latex injection technique. Left adrenal glands were basically supplied by coeliac, cranial mesenteric, renal and lumbal arteries. The arterial vascularization of the left adrenal glands was very complex in comparison with right adrenal glands. In two examples, branch of the lumbal artery was divided into phrenic caudal artery and cranial adrenal artery. In six examples, it was observed that the caudomedial and ventral regions of the left adrenal glands were also supplied by thinner branches that stemmed from second left lumbal artery. Besides, coeliac and cranial mesenteric arteries also gave off shorter branches supplying the cranial region of the left adrenal glands in five examples. It was determined that two branches originated from abdominal aorta directly for supplying left adrenal glands in only two examples. In four examples, two caudal adrenal arteries stemmed separately from left renal artery in a short distance. Arterial vascularization of right adrenal glands was more constant and supplied by lumbal and renal arteries. The adrenal glands were generally oval or round shaped. In only two examples, left adrenal glands were ‘V‐’ or heart‐shaped. There was no significant difference (P > 0.05) in sizes between right and left adrenal glands.     

Arterial and venous supply to the bovine jejunum and proximal part of the ileum

The blood vasculature of the bovine jejunum and proximal part of the ileum was studied in 20 mature dairy cows at slaughter. The cranial mesenteric artery and vein supplied the jejunum and ileum, and their major branches were present in all specimens and supplied similar regions of the intestinal tract. Proximal branches of the cranial mesenteric artery were pancreatic arteries, caudal pancreaticoduodenal artery, middle colic artery, and ileocolic artery. A large collateral branch arose from the proximal segment of the cranial mesenteric artery, anastomosing with the continuation of the cranial mesenteric artery distally along the jejunum. Jejunal arteries arose from the continuation of the cranial mesenteric artery, forming a series of anastomosing arches. Straight vessels arising from these arches did not branch or anastomose before entering the serosal layer of the intestine. The proximal part of the ileum was supplied by branches from the continuation of the cranial mesenteric artery; these branches anastomosed with the mesenteric ileal (ilei mesenterialis) artery, a branch of the ileocolic artery. The venous supply paralleled the arterial supply in all specimens.     

Reproductive tract vasculature of the female emu (dromaius novaehollandiae)

The arterial supply of the ovary and oviduct is provided by the ovarian artery, cranial oviductal artery, accessory cranial oviductal artery, middle oviductal artery, caudal oviductal artery and the medial and lateral vaginal arteries. These arteries supply various regions of the oviduct and are branches of either the left cranial renal artery, left external iliac artery, left middle renal artery, left lateral caudal artery or the left pudendal artery. The veins that drain the reproductive tract are satellite vessels to each artery that supplied the tract.     

Arterial vascularization of the pineal gland in the fetus of Zavot-bred cattle

This study aimed at revealing arterial vascularization of the pineal gland of the Zavot-bred foetus. Twenty foetuses, regardless of their sex, at the age of 2-7 months were used. Coloured-latex was injected by way of both the right and left common carotid arteries. Then, dissection was performed and vessels nourishing the pineal gland were documented. The pineal gland is vascularized by a number of 2-5 central rami. A small vessel arising from each of the central rami in two foetuses (10%) was shown anastomosing with a branch of the cranial cerebral artery, which advances in cranio-caudal direction in the callosal groove. Hence, anastomoses were observed between several sub-branches of each caudal cerebral and cranial cerebellar arteries.     

Macroscopic features of the arterial supply to the reproductive system of the male ostrich (Struthio camelus)

The macroscopic features of the arterial supply to the reproductive system of the male ostrich was studied in 16 pre-pubertal and eight sexually mature and active birds. The left and right cranial renal arteries arise from the aorta, between the cranial divisions of the kidneys. These vessels supply the cranial divisions of the kidneys, the testes, the epididymides and the cranial segments of the ducti deferentia. Accessory testicular arteries which arise directly from the aorta are present in 45.8% of the specimens. They supply the testes and cranial parts of the ducti deferentia. They are variable in number and origin, and four variants are identified. A cranial ureterodeferential branch originates from the cranial renal artery, supplies the cranial portion of the ductus deferens and ureter, and runs caudally to anastomose with the middle renal artery. The sciatic artery arises laterally from the aorta, just caudal to the acetabulum, and gives rise, ventrally, to a common trunk, the common renal artery, which divides into the middle and caudal renal arteries. The middle renal artery gives rise to the middle ureterodeferential branch which supplies the middle part of the ductus deferens and ureter. A few centimetres caudal to the kidney, the aorta terminates in three branches, namely, the left and right internal iliac arteries and the median caudal artery. The internal iliac artery divides into the lateral caudal artery and the pudendal artery; the latter gives off caudal ureterodeferential branches that supply the caudal segments of the ductus deferens and ureter. In addition, the pudendal artery gives off vessels that supply the cloaca, some of which continue to the base of the phallus, where they form an arterial network. In conclusion, the pattern of the blood supply to the reproductive organs of the male ostrich is, in general, similar to that of the domestic fowl and pigeon, although there are a few highlighted distinctive features.     

北京鸭输卵管血管分布的形态学研究

采用大体解剖学方法，观察了20羽北京鸭输卵管血管分布。结果表明：北京鸭输卵管动脉有输卵管前、中、后动脉和阴道动脉；输卵管静脉通常与同名动脉伴行，但缺输卵管后静脉，这些血管均位于鸭体左侧。输卵管前动脉一般有1条，起始于左髂外动脉的耻动脉，分布于输卵管漏斗部和膨大部；输卵管中动脉起于左肾后动脉，主要分布于输卵管峡部和子宫前部；输卵管后动脉起始于左髂内动脉或左阴部外动脉，主要供应子宫后部的血液；阴道动脉起于左阴部内动脉，分布于阴道部。     

Arterial vascularization of the uropygial glands (gl. uropygialis) in the Japanese quail (Coturnix coturnix japonica) and silver polish (Gallus gallus domesticus)

This study focused on the morphological characteristics of the uropygial glands of the Japanese quail and silver polish, particularly the arterial nourishment. With this respect, coloured-latex injected animals were dissected and their glands and related arteries were observed. The gland in the Japanese quail was relatively longer than that in the silver polish. The first caudal segmental arteries in the Japanese quail were specialized as the uropygial gland artery while the fourth caudal segmental ones were continued as the uropygial gland artery in the silver polish. Branches from the second and third caudal segmental arteries and skin also contributed bilaterally to the vascularization of the gland in the Japanese quail. Observing the more complex arterial structure in the Japanese quail suggests more active uropygial gland in this species, when compared with the silver polish.     

ULTRASONOGRAPHIC EVALUATION OF THE PARATHYROID GLANDS IN HYPERCALCEMIC DOGS

Two hyperplastic parathyroid glands and three solitary parathyroid adenomas were identified using high-resolution ultrasonography in five adult dogs with persistent hypercalcemia. Ultrasonographic features of parathyroid adenomas included visualization of a round or oval, 5 mm or larger, hypoechoic mass in the cranial pole of one thyroid lobe. Each mass had well-defined margins between the thyroid gland and parathyroid adenoma, reduced echogenicity of the adenoma compared to surrounding thyroid parenchyma, and distal enhancement. Ultrasonographic features of the hyperplastic parathyroid glands included hypoechogenicity, compared to surrounding thyroid parenchyma, and a size of approximately 2 mm. Hyperplastic parathyroids were well marginated in one dog and poorly marginated in another dog.     

Vascular anatomy of the equine small colon

The vasculature of 22 small colons from dead adult ponies was perfused with latex or barium sulphate solution. The vascular anatomy was studied by use of dissection and alkali digestion of the latex specimens and microangiography of the barium sulphate-perfused specimens. The small colon is supplied by the caudal mesenteric artery. The left colic artery arises from the caudal mesenteric artery, which then becomes the cranial rectal artery. Branches from the left colic and cranial rectal arteries form anastomosing arcades that become narrower distally along the length of the small colon. From these arcades arise terminal arteries, which enter the small colon wall and give rise to a subserosal, an intermuscular, and a large submucosal plexus, with frequent anastomoses between them. The venous drainage closely parallels the arterial supply, except near to its origin from the portal vein, when the left colic vein and caudal mesenteric vein are separate from the corresponding arteries.     

Arterial supply to the rat colon

Rats are often used as animal models in studies such as on intestinal transplantation and anastomosis healing, which require colectomy. Although detailed information regarding arterial supply is important to establish accurate and reproducible experimental procedures, this has not been studied in the rat colon. Therefore, we analysed the detailed arterial distribution pattern and its individual variations in the colon of 34 rats. The rat colon received colic branches of the ileocolic artery, and the right, middle and left colic arteries. The single left colic artery constantly arose from the caudal mesenteric artery and was distributed to the descending colon, whereas the others showed variations in number and distribution. The ileocolic artery gave rise to one (12%) or two (88%) colic branches supplying the proximal ascending colon, and these branches formed rich, mesh-like anastomoses along the initial portion of the ascending colon. One (74%) or two (26%) right colic arteries originated from the cranial mesenteric artery and supplied the ascending colon and right colic flexure. Moreover, one (38%), two (56%) or three (6%) middle colic arteries emerged from the cranial mesenteric artery and were distributed to the transverse colon, left colic flexure and proximal descending colon. In total, we categorized the individual variations in arterial branching and anastomosis into 11 patterns. Arterial supply to the rat colon showed a specific pattern and frequent individual variations. These findings thus provide essential information for establishing reproducible models of rat colic surgery.     

The Hindlimb Arterial Vessels in Lowland paca (Cuniculus paca,Linnaeus 1766)

This study aims to describe the origin and distribution of the hindlimb arterial vessels. Five adult lowland pacas (Cuniculus paca) were used. Stained and diluted latex was injected, caudally to the aorta. After fixation in 10% paraformaldehyde for 72 h, we dissected to visualize and identify the vessels. It was found out that the vascularization of the hindlimb in lowland paca derives from the terminal branch of the abdominal aorta. The common iliac artery divides into external iliac and internal iliac. The external iliac artery emits the deep iliac circumflex artery, the pudendal epigastric trunk, the deep femoral artery; the femoral artery originates the saphenous artery, it bifurcates into cranial and caudal saphenous arteries. Immediately after the knee joint, the femoral artery is called popliteal artery, which divides into tibial cranial and tibial caudal arteries at the level of the crural inter‐osseous space. The origin and distribution of arteries in the hindlimb of lowland paca resembles that in other wild rodents, as well as in the domestic mammals.     

Descriptive anatomic study of the great vessels of the heart in the capuchin monkey Cebus apella (Linnaeus, 1758)

The aim of this study was to describe the anatomy of the great vessels of the heart in capuchin monkey (Cebus apella) and to compare with those of other primates, including humans. The hearts were prepared through fixation in 10% formalin and subsequently dissected using standard techniques and instruments. The arterial and venous systems were perfused with colored latex solution via the femoral vessels. An ascending cylindrical branch with relatively great caliber was identified in the aorta artery, in addition to an aortic arch, from which three great arteries were originated, the brachiocephalic trunk, the left common carotid artery and the left subclavian artery. After a course of variable extension, the pulmonary trunk divided into right and left pulmonary arteries. The caudal vena cava was morphologically similar to that of humans, except for its association with the cardiac lobe of the right lung, whereas the cranial vena cava was formed by the two braquiocephalic veins and received the azygos vein close to right atrium. The pulmonary veins, in number of six, ended at the posterior face of the left atrium, differently from both humans and other primates. In conclusion, the morphology of the great vessels of the heart in Cebus apella was similar to that of humans and other primates, although some differences are evidenced with regards to topography and number of anatomic structures, particularly the relationship of the caudal vena cava with the cardiac lobe of the right lung and the presence of six pulmonary veins in Cebus apella.     

MAGNETIC RESONANCE IMAGING OF THE PRESUMED NORMAL CANINE ADRENAL GLANDS

Forty-three dogs without evidence of endocrine disease that underwent spinal or abdominal magnetic resonance imaging (MRI) for clinical reasons were studied. Because the procedures were not optimized for inclusion of the adrenal glands, they were not always visible in all planes. Eighty-five of the 86 adrenal glands were seen and only the left gland in a 6-month-old Irish wolfhound could not be found. The right adrenal gland lay cranial to the left in all of the animals in which both glands were seen. The best landmarks for localization of the glands were vascular; both adrenal glands were always cranial to the ipsilateral renal vessels and in the region of the celiac and cranial mesenteric arteries. Various measurements were made on all the available scan planes. In some dogs the whole adrenal gland was difficult to visualize clearly, and this hindered the measuring process, especially when the right adrenal gland was in close contact with the caudal vena cava. The adrenal glands were mainly linear in shape but also had a variable degree of modification of their poles, especially the cranial pole of the right adrenal gland, which tended to be consistently wider and to present different shapes (rounded, arrowhead, inverted P, hook-shaped, triangular, or dome-shaped). Two main patterns of signal intensity were seen on fast spin echo (FSE) sequences (T2-weighted, T1-weighted, and T1-weighted after administration of a paramagnetic contrast medium): homogeneous and hypointense to surroundings or a corticomedullary type pattern with a hyperintense central area surrounded by a hypointense rim of tissue. The outline of the left adrenal gland was always very clear. The clarity of outline of the right adrenal gland was more variable, especially if it was in contact with the liver or the caudal vena cava. It was felt that the amount of retroperitoneal fat was not as important as stated in the human literature for visualization of the adrenal glands and that with an appropriate selection of scan planes and pulse sequences good assessment of the adrenal glands can be performed with MRI in canine patients.     

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.     

Untersuchungen zur Form der Schilddrüse (Glandula thyreoidea) beim Geflügel mit besonderer Berücksichtigung der jahreszeitlichen Schwankungen

The thyroid glands of 31 chickens at the age of 17 to 24 months were investigated. Different methods of anatomical preparation, casts of vessels and scanning electron microscopy were used. The thyroid gland of birds is a paired organ. It is located on the ventral surface of the base of the neck within the thoracic inlet. The left thyroid gland is placed more cranially than the right one. Each thyroid gland is closely connected to the common carotid artery on the medial side, from which it is supplied and to the jugular vein on the lateral side. It is a reddish-brown organ and of lenticular profile. The gland measures on average 10 mm in length, 6 mm in width and 2 mm in thickness, and is covered by a thin connective tissue capsule which holds adipose cells. It seems that each thyroid follicle is surrounded by a net of capillaries. The investigation by scanning electron microscopy proved that the follicles are oval with a pyramidal top on each end. The cuboidal epithelium cells leave impressions in the colloid. Epithelium cells carry microvilli on the follicle side surface. Described seasonal changes of the thyroid gland in size and activity were able to be confirmed by the examination of the organ in July and December. In winter the follicular cells were higher and the follicles had a greater volume.     

The Arterial Supply to the Ileum, Cecum and Proximal Loop of the Ascending Colon in the Ox*

This study describes in detail the arteries supplying the ileum, cecum and proximal loop of the ascending colon in the ox important to the veterinary surgeon treating disorders of these segments of the intestinal tract. The ileum was vascularized by the mesenteric ileal artery (from the ileocolic), the first ileal artery (from the cranial mesenteric) and by the ileal branches of the cecal artery which, by means of their anastomoses, form a row of antimesenteric arches in the ileal part of the ileocecal fold. The termination of the ileum was also supplied by twigs from the ileocecocolic arch. The ileum appears to be the most vascular part of the small intestine. The cecum was supplied mainly by the cecal branches of the cecal artery. The proximal end of the cecum was also vascularized by branches from the ileocecocolic arch. The proximal loop of the colon was vascularized by the three colic branches of the ileocolic. The first colic branch supplied the third part of the loop, the second colic branch supplied the first and the second parts of the loop and the third colic branch supplied the first part and, together with the first cecal branch of the cecal artery, formed the ileocecocolic arch at the dorsolateral surface of the ileocecocolic junction. The terminal branches of the arteries to the ileum, cecum and proximal loop of the colon detached lateral branches in the tunica muscularis which anastomosed with similar branches from neighboring arteries in an arcuate manner in the tunica submucosa. The terminal branches from both sides terminated in the free border, releasing branches which anastomosed with each other in the tunica submucosa. The colic lymph nodes were supplied by the colic branches of the ileocolic artery, die two largest nodes being perforated by some of the branches of the first two colic branches. The ileal lymph nodes were supplied by the ileal arteries of the cranial mesenteric. They were also perforated by these arteries. Cecal lymph nodes were seen only in the specimen from the calf. They were much smaller than the colic and ileal nodes and were supplied by the first two or three cecal branches of the cecal artery and also by twigs arising directly from the cecal artery.     

Gross anatomy of the portal vein and hepatic artery ramifications in dogs: corrosion cast study

The anatomical variations of the portal vein and the hepatic artery ramifications were analysed on liver corrosion casts in 20 dogs as a possible aid in the surgical management of the organ. The portal vein ramified similarly in all dogs. It divided into the smaller right portal branch from which vessels for the caudate process and both right lobes arose and the substantial left portal branch, which supplied the remaining liver portions and in 12 cases also the dorsal part of the right lateral lobe. Right lateral, right medial and left branches are the major arteries originating from the hepatic artery; however, their origin and course varied among individual animals. In 10 livers, the right lateral and the left branches originated from the hepatic artery, while the right medial branch arose from the left branch and usually supplied the right medial lobe solely. In nine livers, the right medial branch arose directly from the hepatic artery and supplied quadrate lobe and gallbladder as well, while in one liver the common artery, which subsequently divided into lobar branches, branched away from the hepatic artery. An additional branch for the caudate process, originating directly from the hepatic artery, was observed in 10 livers. Certain liver portions received the arterial blood from two major branches, which was particularly characteristic for the right medial lobe (six livers) and caudate process (10 livers). The course of the major arterial branches was also variable, although they proceeded in close anatomical relationship with the portal vein branches. The left arterial branch accompanied the left portal branch on its dorsal aspect (15 cases) or crossed it from the caudal aspect (five cases). The right lateral branch crossed the initial parts of the left and right portal branches either from cranial (12 cases) or caudal aspects (eight cases), while the right medial branch always crossed the left portal branch from its caudal aspect.     

Observations on the Equine Hypophysial Portal System

The blood supply to the equine pituitary gland, with special attention to its portal system, was studied by the aid of vascular injections and histological serial sections. The primary capillary plexus of the median eminence was supplied by the rostroventral and rostrodorsal infundibular arteries, which were branches of the internal carotid arteries and the ramus communicans caudalis, respectively. The neural lobe was supplied by the caudal infundibular arteries, which originated from the arteria intercarotica caudalis. Dorsal and ventral groups of the portal vessels were described. Their regional distribution into the sinusoidal capillaries of the pars distalis was discussed. Results of this investigation indicated that the portal vessels were the sole supply to the equine pars distalis. No direct arterial supply to this part of the adenohypophysis was observed.     

Subgross investigation of vessels originating from arcus aortae in guinea-pig (Cavia porcellus)

The vessels that originate from the aortic arch were studied in 16 adult guinea-pigs. Two major vessels, the left subclavian artery and the brachiocephalic trunk, were easily identified as they were branching off from the aortic arch. The brachiocephalic trunk, at first branched off to the left common carotid artery and continued as a common trunk, which was then divided into the right subclavian artery and the right common carotid artery. The left subclavian artery branched off to the following vessels: the costacervical trunk, the internal thoracic artery, a common trunk from which the dorsal scapular artery and the vertebral artery originated, and the superficial cervical artery. The right subclavian artery branched off to the bronchoesophageal artery (in five cadavers), the caudal thyroid artery (in three cadavers) and the tracheal artery (in three cadavers) in addition to the above vessels. There were two vertebral arteries branching off to the right subclavian artery in all dissected cadavers. However, only 10 cadavers had two vertebral arteries originating from the left subclavian artery. The first vertebral artery originated from the common trunk, whereas the second vertebral artery arose from the dorsal scapular artery. The second vertebral artery entered the foramen transversarium of the seventh cervical vertebrae and anastomosed with the first vertebral artery just before entering the foramen transversarium of the sixth cervical vertebrae.     

Arterial supply of the superior cervical ganglion in the guinea-pig (Cavia porcellus)

The vascularization of the cranial cervical ganglion [superior cervical ganglion (SCG)] of 10 adult guinea-pigs (Cavia porcellus) was investigated by latex injection and dissection techniques. Compared with other species, there were differences in the arterial supply of SCG and in the number of branches originating from these vessels. The SCG received arterial blood from branches of the ascending pharyngeal and internal carotid arteries. In addition, it was demonstrated that the superior thyroid and occipital arteries contribute rarely to the vascularization of the SCG.