Microvasculature of the hamster eye: scanning electron microscopy of vascular corrosion casts

The architecture of the retina, choroid and anterior eye segment was investigated in 12 Syrian hamsters using scanning electron micrographs of methylmethacrylate corrosion casts. The hamster eye receives its primary blood supply from the long posterior ciliary artery, which directly enters the optic nerve head, and divides into three branches: the central retinal artery and medial and lateral long posterior ciliary arteries. In the retina the central retinal artery divides into six radiating branches. Retinal arterioles form a slender and long course to capillaries. Retinal capillaries are extremely thin in diameter and form a sparse capillary network. The choroid is supplied by the long posterior ciliary arteries. Choroidal arterioles exhibit a thick and short course to the choriocapillaris. The choriocapillaris is thick and sinusoid-like, forming a dense network in the choroid. The ciliary body, iris and bulbar conjunctiva are supplied by the anterior ciliary arteries, which are branches of the long posterior ciliary arteries. Capillaries supplying the anterior margin of the ciliary process are large in diameter with an irregular bore, forming a thoroughfare channel draining blood in the ciliary arterioles into the pars plana vessels. Blood from the retina is drained by the central retinal veins. Venules from the anterior eye segment empty into the vortex veins via the pars plana vessels. Venous blood from the choroid is drained only by vortex veins via the choroidal veins. The functional significance of the vascular architecture and species differences are discussed.     

Angioarchitecture of the Branchial Arterial System of Carp (Cyprinus carpio L.)

The arterial system of the gills of carp and its histological structure were studied light and electron microscopically by making Mercox or Neoplane Latex corrosion cast preparations. Four pairs of afferent and efferent branchial arteries, and a pair of afferent and efferent pseudobranchial arteries were identified in the branchial arterial system. The 1st and 2nd afferent branchial arteries are given off directly from the ventral aorta, and the 3rd and 4th afferent arteries originate from their common trunk, which is branched off from the ventral aorta caudal to the origin of the former branchial arteries. Numerous afferent filamental arteries are connected to the lamellar blood capillary networks in the gill lamellae via afferent lamellar arterioles, and efferent filamental arteries followed the efferent lamellar arterioles are converged into four efferent branchial arteries that are connected to the dorsal aorta. To the pseudobranchia, afferent pseudobranchial arteries are connected with the ventral branches of the 1st efferent branchial arteries to provide arterial blood to the organ through the afferent mandibular arteries. Afferent pseudobranchial lamellar arterioles originating from the afferent pseudobranchial filamental arteries are connected with the blood capillary networks in the pseudobranchial lamellae, and blood in the capillary networks is drained into the efferent pseudobranchial filamental arteries via 2-4 pseudobranchial lamellar arterioles. Branches of the efferent pseudobranchial filamental arteries are connected with the arteries to the eyeballs and provide blood to choroid of the vascular tunic of them. Pseudobranchial cells surrounding lamellar capillaries in the pseudobranchia are furnished with abundant mitochondria and tubular structures, and the histological findings suggest the cells may share an ability to exchange physiological materials between the cells and the blood in the capillary networks of pseudobranchia.     

Risks of intravenous injection into the tail of cattle

Since several years collecting blood from the tail vessels in bovine practice gained a wider range of propagation. Recently veterinarians tried to inject drugs intravenously into the tail vessels of the bovine tail. Therefore we carried out anatomical studies concerning the position of the blood vessels of the bovine tail. 24 tails of slaughtered cattle, which were of different breeds and age (1-4 years old), were examined in respect to the course of their arteries and veins as well on the ventral side. By means of necropsy, frozen cross sections, corrosion anatomy and radiography the position of the tail vessels to each other were compared. In the area of the 2nd to 7th coccygeal vertebra the position of the arteries and veins were being determined. Following results were obtained: 1. The A. cocc. med. runs always ventral in the midline of the tail. 2. The number of ventral veins proximal on the tail varies from 1 to 3. 3. The course of the Vena(ae) cocc. mediana(ae) in the tail region examined is inconstant. The vein lies either left, right, dorsal or ventral of the A. cocc. med. The vein can also cross the area. 4. In 8 of 19 examined cases the V. cocc. med. was closely left to the artery (area of the 5th coccygeal vertebra). After radiologic examination it can be stated that this region can be used for collecting blood of the V. cocc. med. In case of intravenous application of considerable amounts of drugs into the vein of the tail a certain portion can get easily into the closely attached artery and severe complications, as necrosis of the tail can occur. Therefore our clinic recommends generally the use of the Vena jugularis externa for intravenous injection.     

La vascularisation du feuillet du boeuf)

The blood vascular system of the bovine omasum The blood vessels supplying and draining the omasal wall and laminae are described and are compared with those of other ruminants. A detailed study revealed that the subepithelial vascular networks in the papillae were in part similar to those of intestinal villi. One or more arterioles branch radially and form a capillary network which does not, as in the villus, drain into a central venule but is succeeded by several subepithelial venules. Capillaries and venules differ only in diameter which are 10 μm. and 40 μm. respectively. The walls of both have a complete basal membrane, perforated endothelium and pinocytotic vesicles. This emphasizes their significance in resorption. Inside and between the papillae the capillaries form a dense network which is separated from the basal cells by a thin layer of connective tissue 5 to 6 μm. thick. Hemodynamic problems related to the presence of elastic connective tissue and to the motor activity of the omasum are discussed.     

Microvascular architecture of the rabbit eye: a scanning electron microscopic study of vascular corrosion casts

The microvasculature of the eyes of 5 rabbits was investigated using scanning electron microscopy on corrosion casts. The study revealed that the pars plana vessels draining blood from the iris and ciliary body coursed directly into the anterior vortex venous system constituting the scleral venous plexus (the venous circle of Hovius). The episcleral vasculature was found to possess a specialized morphology, with channels draining the aqueous humor. The capillaries of the third palpebral, bulbar and palpebral conjunctiva formed a single-layered capillary network approximately parallel to the epithelium and formed a well-developed venous plexus in the stroma. The retina was found to be merangiotic, meaning that vessels were present only in a small part of the retina, extending in a horizontal direction to form bands on either side of the optic disc. Channels representing the aqueous veins that drained blood mixed with aqueous humor were found to derive directly from the suprachoroidal space and communicate with the scleral venous plexus via the anterior vortex veins. The functional significance of the microvasculature of the iris, cilia, retina and choroid is discussed in this report as well. The elaborate microvasculature of the conjunctiva may be a prerequisite for the exchange of nutrients and gasses between the cornea and the vessels across the conjunctival epithelium when the eyelids are shut during sleep, and possibly for the dynamics of eye drop delivery. The scleral venous plexus in rabbits may be analogous to the scleral venous sinus (Schlemm's canal) in rats, primates and humans.     

Microvascular circulation of the small intestine in horses.

The microvascular anatomic features of the small intestine was described by correlating results of microangiography, light microscopy, gross studies, and scanning electron microscopy of vascular replicas in 14 horses. After heparinization, the horses were euthanatized, a length of jejunum was transected, and blood was flushed free of the circulation, using isotonic NaCl solution. In six horses, the circulatory system was perfused with a modified radiopaque medium and evaluated radiographically. These sections were then evaluated by standard histologic methods. Sections from 8 horses were perfused with 1 of 2 types of plastics and studied grossly or by scanning electron microscopy. The marginal arterial arcade gives rise to vessels that enter the jejunum at the mesenteric angle. These vessels penetrated either directly, by branching and entering on both sides of the mesenteric angle, or supplying only 1 side of the mesenteric angle. All these vessels continued in the submucosa branching extensively, forming a submucosal plexus. This submucosal plexus supplied the tunica muscularis, tunica serosa, and the mucosa. Vessels within the 2 muscle layers ran parallel to the muscle fibers and, consequently, perpendicular to each other. The arterial supply to the mucosa penetrated the muscularis mucosae and branched to supply 2 mucosal capillary networks. An eccentrically placed arteriole penetrated the base of the villus and spiralled to the tip where it "fountained" into a mesh-like capillary network, which descended peripherally in the villus to drain via 1 to 3, but most commonly 2 venules. Venules from adjacent villi united and drained via the submucosal veins.(ABSTRACT TRUNCATED AT 250 WORDS)     

Microvascular anatomy of the pig eye: scanning electron microscopy of vascular corrosion casts

The microvasculature of the eye of 10 pigs was investigated using scanning electron micrographs of corrosion casts. The ciliary body, iris and bulbar conjunctiva were supplied by the iridociliary ring artery via the long posterior ciliary artery. Capillaries of the ciliary process were of large diameter (23.2-27.5 microm) with an irregular bore, forming a thoroughfare channel draining blood in the ciliary arterioles into the pars plana venous vessels. Arterioles and venules in the iris exhibited a zigzag or spiral features. The third palpebra was supplied by the anterior ciliary artery. The capillary bed of the third palpebra was dense and was formed by many rows of fine hair-pin loops. Capillaries in the bulbar conjunctiva formed a sparse network disposing approximately parallel to the epithelium and formed a well-developed venous plexus, draining into the vortex veins. Retinal arterioles formed a slender and long course to capillaries. Retinal capillaries were extremely thin (3.0-4.0 microm in diameter). The choroid was supplied by the short posterior ciliary arteries. Choroidal arterioles exhibited a thick and short course to the choriocapillaris. The choriocapillaris was flat and sinusoid-like (8.9-13.9 microm in diameter), forming a dense sheet-like network. Blood from the choroid emptied into the episcleral vein via the vortex vein. Blood from the retina was drained by the posterior ciliary veins. The functional significance of this vascular architecture was discussed.     

Vascularization of the Fleshy Comb in the Domestic Chicken

Up to now little is known about the vascularization of the chicken fleshy comb (crista carnosa). In order to evaluate the vascularization of the crista carnosa of the cook (breed White Leghorn), corrosion casts were created by injecting Plastoid into the internal carotid as described by Schummer (1951). Specimens were investigated by stereomicroscopy and scanning electron microscopy (SEM). Generally the dermis is highly vascularized by two capillary networks, which are localized beneath the epithelium and beneath the dermal papillas. The dense subepithelial network is characterized by the presence of sinusoid vessels. In the subcutaneous plexus numerous arteriovenous anastomoses of different types occur. Additionally there are arteriovenous anastomoses between the main vessels reaching the indentations of the comb. Our results show the presence of superficial and dense capillary networks and arteriovenous anastomoses are the anatomical basis for the functions of the chicken comb in mating behaviour and thermoregulation.
Reference  Schummer, A. 1951: Simplified method for plastoid corrosion. Anat. Anaz. 98 , 288–290.     

Das Blutgefäßsystem des Enddarms vom Hund (Canis lupus f. familiaris)

The Vascular System in the Large Intestine of Dog (Canis lupus f. familiaris) The vascular System of the large intestine of 10 dogs was examined by means of vascular corrosion casts, histology and transmission-electron microscopy. The tela submucosa contains an arterial and a venous vascular plexus. In broader areas of the submucosa, a deep and a superficial vascular plexus, which are interconnected, can be found. The plexus are orientated parallel to the layers of the intestinal wall. On the one hand, these vessels naturally provide self-sufficiency and drainage of the submucosa, and, moreover, direct branches to the stratum circulare of the muscular layer. On the other hand, the submucosal vascular plexus is the ‘distributional network’ for the functional plexus of the tunica mucosa. The arteries, which ascend to the tunica mucosa, supply a flat arterial network underneath the intestinal glands. Bundles of only a few arteriolae originate from this in order to supply the pericryptal capillaries. In the vicinity of the cryptai orifices, these turn into a network of subepithelial capillaries, which is post-connected to the periglandular capillary plexus. From this ‘terminal circulatory pathway’, the blood is drained off by veins that enter the submucosal plexus. It is characteristic that the postcapillary venules often begin as part of the capillary network. As in other species, the subepithelial capillaries are predominantly lined with a ‘fenestrated endothelium’, whereas the capillaries of the pericryptal areas show a continuous endothelium. The latter contains multiple vesicles that may fuse in order to form transcytoplasmic channels as a morphological equivalent for transcappillar-epithelial and vice versa occurring transport of substances.     

Three-dimensional reconstruction of the angioarchitecture of the ciliary body of the West Indian manatee (Trichechus manatus)

OBJECTIVE: To examine the angioarchitecture of the ciliary body in the West Indian manatee (Trichechus manatus), through the use of three-dimensional reconstruction. PROCEDURE: Specimens from West Indian manatee were preserved in 10% buffered formalin, embedded in paraffin, serial sectioned and stained by Masson trichrome for light microscopic three-dimensional reconstruction and evaluation. RESULTS: The network of blood vessels in the ciliary processes of the West Indian manatee is fed by the major arterial circle that lies mostly near the base of the iris. The branching arterioles give rise to a capillary-sinusoidal bed that extends internally along each process, emptying into two sets of veins, one being elevated. The elevated and nonelevated veins join posteriorly before emptying into the choroidal venous system. CONCLUSIONS: The angioarchitecture of the ciliary body of the West Indian manatee is clearly unique when compared to those previously examined in land mammals. Three-dimensional reconstruction of paraffin sections is an effective means to evaluate vascular patterns in ocular specimens, especially those unavailable for corrosion casting.     

Light and scanning electron microscopic study on the blood vascular system of the donkey placenta

The donkey placenta is diffuse and epitheliochorial with numerous microplacentomes consisting of a fetal microcotyledonary and a maternal microcaruncular part. The microplacentomal vasculature during the last third of pregnancy has been investigated by light microscopy in comparison to scanning electron microscopy of the materno-fetal contact surface and corrosion casts of blood vessels after plastic instillation from either the microcotyledonary or the microcaruncular side, and, for the first time in a perissodactyle, from both sides. Morphological data were semiquantitatively evaluated. The supplying parts of both, the microcotyledonary and the microcaruncular vascular system are strictly proximo-distally oriented, thus reaching the capillary systems or working parts in the shortest way possible. The straight course of the vasculature, particularly on the fetal side, suggests the occurrence of venulo-arteriolar back diffusion. The fetal capillary system consists of convolutes confronting the maternal septal capillary complexes in a countercurrent way. This materno-fetal blood flow interrelationship is highly efficient in terms of placental exchange, which is further supported (1) by dilations and increasing coiling of the fetal venular capillary limbs in particular and (2) by a decrease in the interhaemal distance from 12.5 to 7.2 microm between the two capillary systems. Besides the countercurrent blood flow interrelationship, some maternal branch arterioles reach the septal capillary system from the maternally oriented pole of the microplacentome or microcaruncle, respectively, resulting in the less efficient crosscurrent blood flow. Hence, in the donkey placenta fetal and maternal blood vessels meet in a mix of countercurrent and crosscurrent flow patterns.     

Morphologic Peculiarities of the Renal Cortical Vasculature Connected with Blood Redistribution in the Kidney of the Domestic Pig

The cortical blood vessels from 2 to 8 month old Camborow hybrid pigs and Belgium landrace pigs were studied using histologic and semithin sections as well as corrosion casts and cleared preparations of intravascular injection. It was established that the cortical blood vessels of the porcine kidney possess peculiarities that may regulate the redistribution of blood in the cortex. These peculiarities were found in the interlobular arteries, in the efferent arterioles of midcortical nephrons, in afferent arterioles of juxtamedullar glomeruli, and in the glomerular capillary networks. It was established that the number of renal corpuscles is different in the various zones of the cortex.     

Microvasculature in the terminal air spaces of the lungs of the Baird's beaked whale (Berardius bairdii)

Lungs were obtained from five adult Baird's beaked whales (Berardius bairdii) and examined by means of light microscopy and scanning electron microscopy of corrosion casts. The alveolar septa of these whales are thick with a connective tissue core and a bi-layer capillary bed. A double capillary network is regularly found in the alveolar duct and alveolar septa. Occasionally, septa adjacent to alveoli and alveoli themselves show only a single capillary layer. The distance between the two capillary layers has a tendency to decrease toward the end of airspaces, suggesting an end result of capillary fusion. Vascular replicas of venous vessels have annular furrows at regular intervals of 50 to 100 microm, which are caused by focal aggregations of collagen fibers circularly oriented and located immediately underneath the endothelium. The first valves appear in the collecting venules gathering alveolar capillaries. These valves are quite characteristic of flap-, funnel-and/or chimney like structures.     

Microvascularization of the Third Eyelid in Dogs

The third eyelid protects the eye, contribute to the aqueous portion of the pre‐ocular film and its distribution over the corneal surface, as well as removal of foreign material from the anterior surface of the eye. It is rather vulnerable during fights and clinicians often have to perform surgery for third eyelid neoplasia. In dogs, this lid has a triangular shape, being widest at its free margin. It is vascularized by branches of the malar artery. Being of such importance as an adnexa of the eye, the authors concentrated their attention on its vascularization, which is not well defined. Methods: Scanning Electronic Microscopy of vascular corrosion casts and intact tissue. Observations: It was quite interesting to notice the presence of two patterns of vascularization inside the third eyelid. One can say that there are two segmental levels of vessels. In one of these there is a predominance of arteries and veins, while in the other a meshwork of third order arteries, capillaries and post‐capillary venules are present. In fact, the branch of the malar artery that reaches the base of the third eyelid divides into smaller branches that cross almost the complete length of the lid giving only a few collateral vessels, in a monopodical way, and only near the free margin of the lid is possible to observe dicothomical ramifications that became rather anastomotic (being anastomoses of type I and II are present) and contribute to the microvascular meshwork. This microvascular net is drained by post‐capillary venules and veins that empty as a brush into bigger veins that occupy the same segmental level as the third eyelid artery. Remarks: This uncommon angioarchitecture is probably an adaptation to the fact that in the medial canthus of the eye this lid has a smaller space and the way of obtaining an efficient vascularization is by going straight to the top of the lid.     

Microvascularization of the canine hepatic ducts

The angioarchitecture of the proximal and distal segments of the hepatic duct in the dog was investigated by means of vascular corrosion casts under a scanning electron microscope. The results of observations indicated a change of the pattern of vascularization of the hepatic duct along with the increasing distance of the hepatic duct from the liver and increasing diameter of the duct. In the proximal hepatic duct, the main blood vessels run along the duct as a pair of supplying arteriole and voluminous collecting venule, while in the distal segments of the hepatic duct on the opposite margin of the duct two vascular triads were observed, composed of two venules and one medial arteriole. On the surface of both segments of the hepatic duct, there are well-anastomosed outer venous plexuses. In the distal segments of the hepatic duct, the outer venous plexus accompanies a fine outer arterial rete. Observations of the intramural network indicate the presence of single terminal arterioles running to mucosa and supplying a subepithelial capillary network. Differences were observed in the blood drainage from the mucosa, as in the proximal segment of the hepatic duct single post-capillary venules are found, while in the distal segment in the mucosa a well-developed mucosal venous plexus is formed. In the well-developed venous system of the hepatic duct no valves were observed.     

Study of the distribution of retinal blood vessels in buffaloes (Bos bubalis)

The distribution of retinal blood vessels in the eye of buffalo was studied macroscopically and microscopically in twenty-two eyes of healthy animals. After macroscopic observation, 12 of 22 eyes were used for histological study. Ten eyes were stained with hematoxylin and eosin and two eyes with PAS stain. The present findings revealed that the eye of the buffalo was characterized by the complex network of retinal blood vessels (holangiotic or euangiotic). The central retinal artery and vein pierced the eye through the optic disc and gave off several branches. There were four pairs of primary vessels that were named dorsal, ventral, nasal and temporal retinal arteries and veins. The veins anastmosed with each other at the optic disc to form a somewhat circle. Three patterns of the distribution of blood vessels were described. The distribution of the arteries and veins was the same.     

Microvascular anatomy of ovary and oviduct in the adult African Clawed Toad (Xenopus laevis DAUDIN, 1802)–Histomorphology and scanning electron microscopy of vascular corrosion casts

Ovaries and oviducts of the adult African Clawed Toad (Xenopus laevis DAUDIN, 1802) were studied by light microscopy (LM) of paraplast embedded tissue sections and scanning electron microscopy (SEM) of vascular corrosion casts (VCCs). Histomorphology revealed that ovarian vessels located in the thecal layers. Ovarian and interlobar arteries displayed a horse-shoe shaped longitudinally running bundle of vascular smooth muscle cells. Follicular blood vessels showed flattened profiles, which were confirmed by scanning electron microscopy in vascular corrosion casts. The flattened profiles obviously led to high intravasal pressures, which locally prevented filling of the follicular capillary bed. Oviduct arteries pierced the fibrous stroma surrounding the oviduct mucosa. In the pars convoluta, the mucosa consisted of a ciliated simple columnar epithelium and tubular oviduct glands that opened between ciliated epithelial cells into the oviduct lumen. Oviduct arteries branched at the basolateral surfaces of tubular glands. After a short tangential course, arterioles branched into capillaries which ran radially between oviduct glands towards the subepithelium. Anastomoses at different heights connected capillaries of neighbouring glands. Subepithelially, capillaries ran longitudinally and undulated. Postcapillary venules radiated centrifugally towards the stroma to finally drain into oviduct veins located in the stroma. Oviduct vascular densities clearly reflected non-ovulatory and ovulatory states.     

The vascularization of the epididymis of the boar with special reference to perfusion fixation

Vasculature of the epididymis was investigated by means of corrosion casts. In the boar, epididymal arteries form a complex network around their stem vessel, the testicular artery. Proper perfusion fixation or complete casting therefore require direct injection into one of these branches. To reach the distal cauda, cannulation of the deferential artery is further needed. Connections between all of these feeding vessels occur at the level of the vascular cone. A prominent anastomosis between an epididymal branch and the testicular artery is regularly observed under the caput epididymis. Epididymal veins drain to a large extent into the pampiniform plexus. Unlike the situation in other species, vascularization of testis and epididymis are closely associated in the boar.