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.     

The venous supply of the cecum, ileum, and the proximal loop of the ascending colon in the ox

The present study describes in detail the venous supply to the bovine cecum, ileum, and the proximal loop of the ascending colon. The cecum was supplied by branches from the cecal and accessory cecal veins. The accessory cecal vein was observed in the majority of the specimens examined. The cecal and accessory cecal veins were joined by 7–10 short oblique anastomoses. The ileum was supplied by the ileal branches of the cecal vein, and from the mesenteric ileal and first ileal (cranial mesenteric) veins. The ileal branches of the cecal vein formed a row of antimesenteric ileal arches in the ileal part of the ileocecal fold. The mesenteric ileal vein, in some cases, detached a collateral branch. The first ileal and the mesenteric ileal veins anastomosed on the ventral surface of the ileum. The initial loop of colon was supplied by branches from the ileocolic vein. In the majority of specimens, the common colic, a branch of the cranial mesenteric vein, supplied the first colic branch to the third part of the initial colon. In such cases, the ileocolic vein gave off only the second and third colic branches. However, in one case, the proximal loop of the ascending colon was supplied by three colic branches of the ileocolic vein and by the first colic branch of the common colic vein. In specimens in which the common colic vein was absent, the colic branches to the initial colon were all given off by the ileocolic vein. The third (or fourth) colic branch of the ileocolic vein and the first cecal branch of the cecal vein united on the lateral surface of the ileocecocolic junction to form an ileocecocolic arch. The veins on the medial surface of the ileocecocolic junction did not form an arch. The colic and ileal lymph nodes were supplied by twigs from the colic branches of the ileocolic vein and first ileal vein of the cranial mesenteric, respectively. The small cecal lymph nodes seen only in the specimen from the calf were supplied by fine branches from the cecal vein.     

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.     

Vascular Anatomy of the Descending Colon of the Horse

The blood supply to the descending colon of the horse was studied by gross dissection and methyl methacrylate corrosion casts. The arterial supply is derived from the left colic artery and cranial rectal artery with the left colic artery supplying approximately the proximal three fourths. Each artery gives off four to eight arcuate arteries that form a series of anastomosing arcades. The arcade pattern continues to form a marginal artery that parallels the long axis of the colon. Small branches from the marginal artery anastomose with adjacent branches to form a secondary arcade. The secondary arcade lies approximately 1 cm proximal to the mesenteric teniae and sends off long arteries at regular intervals that course circumferentially around the bowel. The long arteries begin under the serosal mesothelium and perforate the muscular layers to course in the submucosal layer. The long arteries branch off supplying the wall of the colon and arborize over the antimesenteric surface, anastomosing with the vessels from the opposite side. The result is the formation of a series of vascular rings surrounding the colon. Venous return, in general, parallels the arterial supply.     

Arterial Vascularization of the Gastrointestinal Tract of the Pampas Deer (Ozotoceros bezoarticus,Linnaeus, 1758)

Based on gross dissection of fifteen adult animals (11 females, 4 males), we described the arterial supply of the stomach and intestines of the pampas deer (Ozotoceros bezoarticus), a South American endangered species. The coeliac artery emitted the splenic, left gastric and hepatic arteries. The splenic artery directed towards the spleen, and the right ruminal artery, which is its only collateral directed towards the stomach, being the main artery of the rumen. The left gastric artery gave origin to the left ruminal, the reticular and the left gastroepiploic arteries. The left gastroepiploic artery originated the reticular accessory artery. Both arteries, gastric and left gastroepiploic, anastomosed their right counterparts derived from the hepatic artery on the curvatures of the abomasum. The cranial mesenteric artery irrigated the second half of the duodenum until the beginning of the descending colon. The thickest branch emitted by the cranial mesenteric artery was the ileocolic artery, which was destined to the ascending colon, caecum and ileum. The colic branches and the right colic arteries were irradiated on the right surface of the spiral loop of the ascending colon and distributed to both centripetal and centrifugal coils of the ascending colon; the colic branches were also anastomosed with the last jejunals and ileals and with the right colic arteries. There were no variations in the origin of any of the main branches derived from the coeliac and cranial mesenteric arteries. This species had a basic pattern of arterial distribution similar to small domestic ruminants.     

Macroanatomic investigations of the blood supply of thoracic limb of Kangal dogs

In this study, the arterial supply of the thoracic limb was investigated in Kangal dogs. Twelve adult healthy Kangal dogs of either sex were used. Latex was injected into the common carotid artery, and then the axillary artery was dissected. The axillary artery is a continuation of the subclavian artery and supplies the thoracic limb in Kangal dogs. The axillary artery gave off a deltoid branch and external thoracic, lateral thoracic, and subscapular thoracic arteries in its course along the thoracic wall. The axillary artery continues distally as the brachial artery in the arm. The brachial artery gives rise to the cranial humeral circumflex, deep brachial, bicipital, ulnar collateral, superficial brachial, transverse cubital, and common interosseus arteries. It continues as the median artery after giving off the common interosseus artery. It was observed that the deep antebrachial artery arose from the median artery at the proximal third of the forearm. In the distal third of the forearm, the median artery divided into the palmar carpal and dorsal carpal branches. The deep palmar branch of the radial artery and deep branch of the palmar branch of the caudal interosseus artery form the deep palmar arch. The median artery joined the superficial branch of the palmar branch of the caudal interosseus artery to constitute the superficial palmar arch. The radial artery and cranial interosseus artery contributed to the dorsal carpal rete. The ulnar artery contributed to the formation of the deep and superficial palmar arches.     

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.     

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.     

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.     

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.     

The arterial supply of Meckel's diverticulum in geese (Anser anser domesticus).

This study was carried out to describe the arterial supply of Meckel's diverticulum (MD) in geese, using 36 adult healthy geese of both sexes, 50 to 52 weeks of age. The arterial supply of MD was classified into three types, In the first type, MD was supplied by a very distinct branch from the cranial mesenteric artery in 21 geese. In the second type, it was supplied by one terminal branch from the cranial mesenteric artery in 9 geese. In the third type, it was supplied both by one branch from the jejunal artery and by terminal branch from the cranial mesenteric artery in 6 geese. Based on the these types, we found significant differences (p < or = 0.01) in the length of MD between type I and II. The blood supply of the third type was observed more frequently in the male than in the female. Results from this study may contribute to the anatomical knowledge of arterial supply of MD in the geese.     

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.     

初生仔猪腹腔脏器的动脉分枝类型

用乳胶加颜料血管注射的方法,对32例初生仔猪的腹腔脏器的动脉分枝进行观察,其主要结果如下: 腹腔动脉有五个分枝类型,即两枝型(脾动脉、肝动脉)有25例(78.13％);三枝型(脾动脉、胃左动脉、肝动脉)有3例(9.36％);四枝型A(脾动脉、憩室动脉、胃左动脉、肝动脉)有1例(3.13％);四枝型B(两主枝是脾动脉和肝动脉,两侧枝是胃左动脉和憩室动脉)有1例(3.13％);一枝型(只有脾动脉,而肝动脉则来自肠系膜前动脉)有2例(6.25％)。 空肠动脉的分枝,依次形成初级弓、二级弓和网状丛,再由网状丛发出大量的、放射状的小枝分布到肠管上。这些小枝呈两两成对地并列(与同级静脉伴行),到肠管附近,两枝彼此分开,每枝分布到肠管的一个侧面。     

The Arterial Supply of the Carpal Joint in the Bactrian Camel (Camelus Bactrianus)

The arterial supply of the six carpal joints was studied in Bactrian camels. The arterial branches supplying the carpal joints were the proximal medial dorsal, middle medial dorsal, distal medial dorsal, proximal lateral dorsal, distal lateral dorsal, proximal medial palmar, distal medial palmar, lateral palmar, proximal palmar and dorsal palmar carpi and the dorsal interosseous antebrachium branches. Some small unnamed branches supplied the diverticulum and the antebrachiocarpal joint capsule. All these arteries arose from the lateral and medial branches of the radial artery.     

Arteriography in ponies with Strongylus vulgaris arteritis.

Radiographs of the aorta and abdominal arteries were obtained from a normal anesthetized pony following catheterization of a femoral artery for nonselective, semiselective or selective arteriography. The arteries had smooth borders and regular diameters and the branches of the cranial mesenteric artery could be followed distally on the angiogram through to the smaller branches proximal to the bowel wall. Following arteriography, the pony walked normally and there were minimal alterations of the levels of serum muscle enzymes and blood lactate. The procedures for arteriography were repeated in three days. At that time the femoral artery was patent and satisfactory angiograms were obtained. Similiarly, radiographs were obtained from two ponies artificially infected with Strongylus vulgaris. The cranial msenteric artery and some of its branches, the right renal artery and segments of the aorta had irregular borders and were enlarged. Branches of the cranial mesenteric artery could not be followed distally because the flow of the contrast material was blocked. Following the above procedures, euthanasia of all ponies was expedited and the findings of arteritis, thrombosis and dilatation of arteries at necropsy compared favorably with interpretations from the radiographs. At least in the pony, arteriography can be a valuable research and diagnostic tool for the demonstration of lesions associated with verminous arteritis.     

Gross Anatomy of the Canine Portal Vein

The gross anatomy of the portal vein of 21 dogs was studied by venous portography, corrosion casting, and gross dissection. The portal vein in all specimens originated by confluence of the cranial and caudal mesenteric veins. Its large tributaries were the splenic and gastroduodenal veins, which entered the portal vein between its origin and the hepatic porta. At the hepatic porta, the portal vein divided into a short right branch and a larger left branch. The right branch ramified in the caudate process of the caudate lobe and in the right lateral lobe of the liver. The left branch was essentially the continuation of the portal vein from which successive branches passed to each of the remaining lobes of the liver and the papillary process of the caudate lobe.     

Technique for transrectal ultrasonography of the cranial mesenteric artery of the horse

Transrectal ultrasonography was successfully used to image the cranial mesenteric artery and its branches in 23 adult horses. The artery could be imaged from its origin at the aorta distally to identify several bifurcations. The method for transrectal imaging of the cranial mesenteric artery and its major branches required 3 distinct transducer positions. One position was used to locate the cranial mesenteric artery by imaging the caudal portion of the aorta from the aortic bifurcation cranially to the level of the cranial mesenteric artery. The second position was used to image the origin of the cranial mesenteric artery. The third position was used to image the major branches of the cranial mesenteric artery.     

The arterial supply of the eye of the yak (Bos Grunniens)

The heads and necks of 10 yaks were dissected to study the arterial supply to the eye of the yak in the Qinghai-Tibetan Plateau. The supply came from the internal ophthalmic, external eight ophthalmic, superficial temporal and malar arteries. The internal ophthalmic was one of sources of the posterior long ciliary artery. The external ophthalmic artery gave rise to branches to supply the dorsal oblique muscle and otherwise, and to take part in the formation of the ophthalmic rete mirabile. The ophthalmic rete mirabile gave off many branches to supply the rectus muscles of the eye and otherwise. The malar artery was one of the branches derived from the infraorbital artery, and its branches supplied the inferior, superior and third eyelids and otherwise. The superficial temporal artery detached off some branches to supply the lateral angle of the eye and otherwise, and anastomosed with the lacrimal artery of the ophthalmic rete mirabile.     

Macroscopic description of the coronary arteries in Swiss albino mice (Mus musculus)

A total of 25 (13 male, 12 female) adult, healthy Swiss albino mice were used to investigate the origin, course and anastomoses of coronary arteries. Coloured latex was injected into the aortic arch to enable these arteries to be clearly discerned. A. coronaria sinistra was larger than A. coronaria dextra. It was divided into a Ramus interventricularis paraconalis and a Ramus circumflexus sinister. However, in 2 specimens, the septal ramus, was observed to stem directly from the left coronary artery, and only 1 ventricular branch arose from the left circumflex. The collateral branches of the paraconal interventricular ramus had a larger diameter and more extensive distribution was observed in these specimens. The A. coronaria dextra was divided into a Ramus septalis and Ramus circumflexus dexter. The Ramus interventricularis subsinuosis was not detected in this study. The ventricular branches of the left coronary artery run intramyocardially whereas the branches of the right coronary artery course subendocardially.