TRANSRECTAL ULTRASONOGRAPHY OF THE LEFT ADRENAL GLAND IN HEALTHY HORSES

Little information is available on medical imaging of the adrenal glands in horses. We investigated the feasibility of transrectal ultrasonography to characterize the normal equine adrenal gland. Transrectal ultrasonography was performed in 25 healthy horses using a 7.5 MHz linear array probe at a displayed depth of 8 cm. Transrectal ultrasonography of the right adrenal gland was not feasible. For the left adrenal gland, the left kidney, the abdominal aorta, the left renal artery, the left renal vein, and the cranial mesenteric artery were used as landmarks. The size of the left adrenal gland was variable, but it generally appeared as a long, flat structure with a hyperechoic medulla surrounded by a hypoechoic cortex. The most cranial part of the gland could not be delineated appropriately in 11 horses (44%). The mean (±SD) thickness of the gland and medulla was 0.66±0.15 cm (n=25) and 0.28±0.09 cm (n=25) near the caudal pole, 0.87±0.25 cm (n=14) and 0.40±0.18 cm (n=12) near the cranial pole, and 0.89±0.18 cm (n=25) and 0.36±0.13 cm (n=25) in the middle of the gland, respectively. The mean (±SD) length of the entire adrenal gland and of the medulla was 6.22±0.77 cm (n=14) and 5.45±0.71 cm (n=6), respectively. Transrectal ultrasonography allowed adequate visualization of the left adrenal gland in horses.     

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.     

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.     

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.     

Branching patterns of the adrenal arteries in the degu (Octodon degus)

The degu has drawn increasing attention for use as an experimental animal in stress response studies due to its physiological features, such as diurnality and seasonal breeding, which differ from conventional laboratory rodents. Stress response is elicited by steroid hormones secreted by the adrenal gland, whose functions are controlled by pituitary hormones reaching through the adrenal arteries. However, knowledge of the arterial anatomy of the degu adrenal gland remains insufficient. To address this issue, we observed adrenal arteries in 20 male degus injected with red-colored latex. Adrenal arterial branching patterns were classified into Types 1–4, which respectively have 1 to 4 parent arteries that give rise to the adrenal arteries. Based on the combination of the parent arteries, Types 2 and 3 were categorized into subtypes a to c, while Type 4 was categorized into subtypes a and b. On the left side, Type 2 (45%) and Type 3 (45%) were predominant, whereas Type 1 (5%) and Type 4 (5%) were infrequent. On the right side, Type 2 (50%) and Type 3 (45%) were predominant, whereas Type 4 (5%) was infrequent. Type 1 was not present. There were 0 to 4 cranial, 1 to 4 middle and 1 to 4 caudal adrenal arteries, with the total number varying from 2 to 9. The present observation provides knowledge of comparative anatomical features of the degu adrenal arteries, which can serve as an anatomical basis for comparative endocrinological studies.     

Coronary arteries of the roe deer (Capreolus capreolus; Linnaeus 1758) heart

A study of the coronary arteries of the roe deer heart was performed on 21 hearts of animals of both sexes and various ages. The roe deer heart is supplied by two arteries: the left coronary artery and the right coronary artery. The left coronary artery arises from the left aortic sinus and forms a short common trunk. The left coronary artery reaches the coronary groove, then divides into the paraconal interventricular branch and the circumflex branch. The circumflex branch gives off several branches to the left ventricle wall and terminates in the subsinuosal interventricular groove as the subsinuosal interventricular branch. The right coronary artery is less pronounced than the left coronary artery. It arises from the right aortic sinus and enters the coronary groove as the right circumflex branch. We found the left arterial cone branch in 75% and the right arterial cone branch in 80% of the cases investigated. The coronary arteries of the heart run subepicardially. In 9 cases we found muscular bridges over the coronary arteries, mostly on the paraconal interventricular branch. In conclusion we affirm the left type of the arterial vascularisation in the roe deer heart.     

Effect of histamine on blood flow to the adrenal glands of pigs

Blood flow to the adrenal glands was measured with radioactive microspheres labeled with⁸⁵Sr in 25–37 kg pigs following the intravenous infusion of physiological saline solution or histamine solution (2 ug/kg/min) for 60 minutes. Total blood flow averaged 2.28 ml/min/gland for control pigs and 4.38 ml/min/gland for histamine-treated pigs (P<.0005). Mean blood flow to the adrenal glands of histamine-treated pigs (3.15 ml/min/g) was 82% higher than that of control pigs (1.73 ml/min/g); the difference was highly significant (P<.0005). The result of this study showed that histamine caused an increased blood flow to the porcine adrenal glands.     

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.     

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.     

CONTRAST‐ENHANCED ULTRASONOGRAPHY OF THE NORMAL CANINE ADRENAL GLAND

Contrast‐enhanced ultrasonography is useful in differentiating adrenal gland adenomas from nonadenomatous lesions in human patients. The purposes of this study were to evaluate the feasibility and to describe contrast‐enhanced ultrasonography of the normal canine adrenal gland. Six healthy female Beagles were injected with an intravenous bolus of a lipid‐shelled contrast agent (SonoVue^®). The aorta enhanced immediately followed by the renal artery and then the adrenal gland. Adrenal gland enhancement was uniform, centrifugal, and rapid from the medulla to the cortex. When maximum enhancement was reached, a gradual homogeneous decrease in echogenicity of the adrenal gland began and simultaneously enhancement of the phrenicoabdominal vessels was observed. While enhancement kept decreasing in the adrenal parenchyma, the renal vein, caudal vena cava, and phrenicoabdominal vein were characterized by persistent enhancement until the end of the study. A second contrast enhancement was observed, corresponding to the refilling time. Objective measurements were performed storing the images for off‐line image analysis using Image J (ImageJ^©). The shape of the time–intensity curve reflecting adrenal perfusion was similar in all dogs. Ratios of the values of the cortex and the medulla to the values of the renal artery were characterized by significant differences from initial upslope to the peak allowing differentiation between the cortex and the medulla for both adrenal glands only in this time period. Contrast‐enhanced ultrasonography of the adrenal glands is feasible in dogs and the optimal time for adrenal imaging is between 5 and 90 s after injection.     

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.     

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.     

The Macroscopic Vascular Anatomy of the Equine Ethmoidal Area

The vascular anatomy of the ethmoidal area in six normal horses and two normal ponies was studied using vascularcorrosion casts. The major arterial supply to the ethmoidal area sterns from an intracranial source. The internal and external ethmoidal arteries anastomose on the rostral intracranial surface of the cribriform plate to form the arterial ethmoidal rete which arborizes and passes through the perforations of the cribriform plate to supply the ethmoid labyrinth. A minor arterial supply to the ventral portion of the ethmoid labyrinth sterns from a small caudal nasal branch of the sphenopalatine artery. Multiple parallel venules drain the ethmoid labyrinth rostrally to its apex then join the venous drainage from the surrounding sinuses.     

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.     

Pharmacokinetic study of meropenem in healthy beagle dogs receiving intermittent hemodialysis

Meropenem, a second carbapenem antimicrobial agent with a broad spectrum of activity, is used to treat sepsis and resistant‐bacterial infections in veterinary medicine. The objective of this study was to identify the pharmacokinetics of meropenem in dogs receiving intermittent hemodialysis (IHD) and to determine the proper dosing in renal failure patients receiving IHD. Five healthy beagle dogs were given a single i.v. dose of 24 mg/kg of meropenem and received IHD. The blood flow rate, dialysate flow, and ultrafiltration rate were maintained at 40 mL/min, 300 mL/min, and 40 mL/h, respectively. Blood samples were collected for 24 h from the jugular vein and from the extracorporeal arterial and venous line. Urine samples and dialysate were also collected. The concentrations of meropenem were assayed using HPLC/MS/MS determination. The peak plasma concentration was 116 ± 37 μg/mL at 15 min. The systemic clearance was 347 ± 117 mL/h/kg, and the steady‐state volume of distribution was 223 ± 67 mL/kg. Dialysis clearance was 71.1 ± 34.3 mL/h/kg, and the extraction ratio by hemodialysis was 0.455 ± 0.150. The half‐life (T_1/2) in dogs with IHD decreased compared with those without IHD, and the reduction in T_1/2 was greater in renal failure patients than in normal patients. Sixty‐nine percent and 21% of the administered drug were recovered by urine and dialysate in the unchanged form, respectively. In conclusion, additional dosing of 24 mg/kg of meropenem after dialysis could be necessary according to the residual renal function of the patient based on the simulated data.     

Renal Anatomy of the Pigmy Hippopotamus (Choeropsis liberiensis): An Overview

The adult kidney of Choeropsis liberiensis is 74.8 % cortex and 22.9 % medulla. The neonatal cortex is relatively less. A single kidney has about 3 × 10⁶ glomeruli. These form 5 % of renal mass in the adult but more so in neonates.
The primary tubus maximus, TM₁, follows the lateral curvature of the kidney. It gives off, toward the hilum, dorso-ventrally paired secondary tubi maximi, TM₂. The tubi are a single layer of high cuboidal epithelium from which terminal collecting ducts arise throughout the surrounding inner medulla. The cranial and caudal limbs of TM₁, open at a diminutive pelvis which receives a small papilla in continuity with TM₁.
The medulla is continuous although variably distorted by folds of cortex at the lateral curvature of the kidney. The renal lobes project toward the medial border and consist of cortex, medulla and TM₂. The lobar cortex is continuous with the common cortex of the lateral curvature. The kidney, although strongly lobed, has no infundibula or rencules.
A main peripheral vein courses medial and parallel to TM. It is apparently a modified large arcuate vein and receives arcuate and interlobar tributaries. At the level of the papilla it joins the main renal vein.
The arterial supply is mainly by interlobar arteries but there are also sizeable external perforator arteries which branch from the main renal artery and perforate the cortex of lobes about the hilum. The sourse of the arteries is illustrated.     

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.     

Das Blutgefäßsystem der Magenwand der Katze*

The blood vascular system of the stomach wall in the cat The results of 19 vascular-injections of the stomach wall in the cat are given. The arterial supply to the parietal surface is derived principally from the left gastric artery, that of the visceral surface from the short gastric branches of the splenic artery. Thus the arterial distribution is similar to the venous drainage. The blood supply of the tunica serosa and the tunica muscularis in the fornix and body regions arises from a common subserosal and muscular plexus. In the pyloric canal the blood supply arises from separate subserosal and intermuscular plexus. The submucosal plexus consists of both arteries and veins: from this, mucosal arteries ascend to a subglandular plexus and thence arterioles supply the capillary plexus of the lamina propria. Venules return the blood through collecting veins to a basal venous plexus, thence through mucosal veins to the submucosal plexus.     

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。     

双峰驼肾动脉分布

应用大体解剖学和血管铸型方法,研究了12峰双峰驼肾动脉的分支分布。结果显示,肾脏的肾动脉在进入肾门之前均分成一背干和一腹干,在肾窦内,背干分为一前支,再由前、后支分别发出背部贤脏的各肾段动脉。腹干不分前、后支,而由主干直接发出腹部肾脏的各肾段动脉。不仅各肾段动脉之间未见吻合,背干及其分支与腹干及其分支之间也无吻合。左肾肾段动脉共13条,右肾肾段动脉12条。表明,双峰驼不仅左、右肾的肾动脉与肾段动脉不尽相同,各肾的背部和腹部的动脉供应也存在差异。肾动脉的背干和腹干是相对独立的。