Renal morphology of the hook-lipped African rhinoceros, Diceros bicornis, Linnaeus

The kidney of Diceros bicornis has about 60 lobes, all appearing peripherally. These are separated by interlobar septa, except for small septal defects through which tubules pass. Renal capsule and interlobar septa are fibromuscular and contain small blood vessels. The kidney is about 65% cortex. It contains about 12.5 x 10(6) glomeruli, which form about 7% of the cortical mass and 4.6% of the renal mass. Diameter of a glomerular capsule is about 244 microns, there being no difference in size across the cortex in these adults. The ureter bifurcates into a cephalic and a caudal, fibromuscular, urothelial-lined conduit, into which open about 23 urothelial-lined infundibula. The common large collecting duct, or tubus maximus, of every lobe opens at the apex of its infundibulum. Two tubi may join into one infundibulum. The tubi and their terminal collecting ducts (of Bellini) are part of the inner medulla. Musculature of conduits and infundibula is largely longitudinal. The calyx may be represented by a circular muscle bundle near the apex of every infundibulum. The large intralobar veins are partly adherent to their infundibulum and calyx and receive arcuate veins via valved orifices. Most branches of the renal artery enter via the interlobar septa. Within a septum they branch again and also supply numerous perforators, which thence enter the cortex. Remaining branches of the renal artery enter cortex directly from without. A fibromuscular scaffolding lies deep to arcuate veins where they contact medulla. Where these veins contact cortical tubules; however, their walls become merely endothelium, like the walls of the interlobular veins.     

Circulatory pathways in the sinusal spleen of the dog, studied by scanning electron microscopy of microcorrosion casts

Scanning electron microscopy of microcorrosion casts was used to visualize circulatory pathways in the sinusal spleen of dog. The examination of contracted versus dilated organs and variations of the volume of material injected gave an indication of flow dynamics. Minimal injections of material into contracted spleens produced filling of mainly the fastest routes for flow, whereas injections into dilated spleens primarily filled slower routes. This procedure yielded a more complete, three-dimensional picture of the arterial, intermediate, and venous pathways as a whole, and of the relative amounts of flow through different arterial routes. Evidence of flow from capillary lumina out into ellipsoid sheaths was plentiful in casts from dilated spleens, but rare in casts from contracted organs. The pattern of flow within and out of the marginal sinus has been elucidated: A circumferential filling occurs first, followed by a flow that radiates outward into the marginal zone and red pulp. Venous sinuses filled via two routes in addition to the generally accepted path from the reticular meshwork via fenestrations in sinus walls. First, many venous sinuses extending out from the marginal sinus and surrounding marginal zone originated as open-ended tubes continuous with the reticular spaces of the marginal sinus or marginal zone. Second, direct connections of arterial capillaries with venous sinuses in the red pulp were found. Evidence indicating that some mechanism is controlling the flow via these routes is discussed. The strikingly different arrangement of venous sinuses in the subcapsular region is demonstrated.     

Cortical microvasculature of the feline kidney

Scanning electron microscopy of corrosion casts was used to study the ultrastructural morphology of the microcirculation in the feline kidney. The technique used enabled us to examine the renal microvasculature by obtaining stable and consistent replicas of the vasculature. Corrosion casts were evaluated at three different levels, namely subcapsular, midcortical and the corticomedullary junction. The interlobular arteries, given off by the arcuate arteries, coursed through the cortex in a radial fashion and afferent arterioles were given off at varying intervals. Large afferent arterioles formed the glomerular capillary lobules which consisted of very tortuous capillaries. Smaller-diameter efferent arterioles were formed at the vascular pole and ran in the opposite direction to the afferent arteriole. The peritubular plexuses were seen as interconnecting capillaries at both the subcapsular, midcortical and corticomedullary junction. Numerous efferent arterioles, derived from the corticomedullary glomeruli, were seen as large, radiating vessels running towards the renal papilla.     

An investigation of potential vascular connections between the kidney and the adrenal gland

This study was conducted on two species of monkeys, Macaca fascicularis and Macaca mulatta, to determine if there were vascular connections between the kidney and other abdominal structures such as the adrenal glands. Microfil vascular perfusions, followed by microscopic observations and dissections, were utilized to investigate the existence of these potential connections. Highly anastomotic renal capsular vessels were always observed on the outer surface of the renal capsule. However, these capsular vessels did not make connections with the subcapsular capillary plexus in the majority of monkeys studied. Vascular connections between the adrenal gland and kidney were not observed. It was concluded that, although the region between the adrenal gland and kidney was rich in vasculature, it did not appear to play an anatomical role in anastomosing the extrarenal and intrarenal circulations.     

Microvasculature of the thyroid gland in the common tree shrew (Tupaia glis): microvascular corrosion cast/scanning electron microscopy study.

A thyroid vascular cast of the common tree shrew (Tupaia glis) was obtained by injection of Batson's No. 17 plastic mixture into the ascending aorta. The cast was studied under the scanning electron microscope. It was found that each half of the gland is supplied by a large superior and a rather small inferior thyroid artery. After plunging into the gland, the arteries divide into smaller branches that are the interlobular, intralobular and follicular arteries (afferent vessels). The basket-like capillaries arising from the follicular arteries and encapsulating thyroid follicles are of large diameter and are arranged in a single layer. The follicular side of the capillary casts was observed to contain numerous small and some large projecting knobs compatible with the presence of fenestrations in the endothelial cells. On the other hand, endothelial nuclear imprints were found mainly on the stromal surface of the follicular capillary casts. Transfollicular capillaries connecting the adjacent follicular capillary networks were also observed. Blood from the follicular capillaries either drains into the follicular veins (efferent vessels) or abruptly drains into the intralobular veins before proceeding to intralobular and interlobular veins, respectively. The interlobular veins are collected into a few small superior, a few larger middle and a few even larger inferior thyroid veins. These veins drain directly into the laryngeal vein lying adjacent to the deep surface of the thyroid gland before joining the jugular vein. Venous valves were identified outside the thyroid gland. In addition, the glomerular capillary island of the parathyroid gland was often seen at the cranioanterolateral and sometimes at the cranioposterolateral aspect of the thyroid gland.     

The dynamics of venous return and response to hypervolemia in the toad, Bufo marinus (L.)

Background

Venous return from the posterior region of amphibians travels by either two renal portal veins to the kidney or a central abdominal vein that drains into the hepatic portal system. The relative proportions of blood flow in these vessels has never been measured nor has a modification of flow been determined when venous return increases by changes in blood volume during hypervolemia or during increased volume input from the posterior lymph hearts.

Results

Venous return from the posterior region of Bufo marinus was measured under resting conditions and in response to a systemic hypervolemia. Doppler flow probes were positioned on the renal portal and ventral abdominal veins, and flow was recorded as injections of artificial plasma equaling 100% of the animal's plasma volume were administered through the sciatic artery. Resting flow was found to be 5.54 ± 2.03 ml min^-1 kg^-1 in the paired renal portal veins, and 7.31 ± 0.89 ml min^-1 kg^-1 in the ventral abdominal vein. While renal portal flow was found to increase by a factor of 2.4 times during the first 10 min of hypervolemia, ventral abdominal flow only increased by a factor of 1.3.

Conclusions

Our results quantify the contribution to circulation from posterior venous return in the toad Bufo marinus. A preferential movement of excess fluid through the renal portal pathway was also demonstrated, supporting the possibility of water elimination via the renal portal circulation, especially during periods of high water influx into the animals.     

The fibromuscular basket (Sporta perimedullaris musculosa) in renculi of kidneys from the ringed seal, Phoca hispida (Pinnipedia)

The medulla of renculi from kidneys of Ringed seals (Phoca hispida) is completely enclosed by cortex except at the hilum. Within the renculus, the fibromuscular coat of the calyx separates from the transitional epithelium at the level of the corticomedullary junction, where the intrarencular arteries also diverge into the parenchyma. Flat ribbons of this stromal tissue form an arborized framework near the medullary side of the intrarencular arteries and the larger of the arcuate arteries derived from them. The ribbons, which are clearly distinct from periarterial connective tissue, are composed of coarse collagenous fibers, elastic fibers, and smooth muscle cells, all oriented in the direction of the long axes of the ribbons, and myofibroblasts. The proportion of smooth muscle cells decreases and that of myofibroblasts increases with increasing distance from the calyx. At the base of the medullary pyramid, the elements of the framework diminish in width and ultimately blend with the surrounding interstitial tissue. The stromal framework, or basket, is homologous with the Sporta perimedullaris musculosa of cetacean kidneys.     

The vagal contribution to the rat liver innervation: a demonstration with the cobalt impregnation method

The contribution of the vagus nerves to the innervation of the liver has been studied with the cobaltous chloride impregnation method. With this method we have demonstrated that the fiber plexus in the rat hepatic parenchyma, that we had previously described and stained for acetylcholinesterase, is of a nervous nature and of vagal origin. Our results show that branches from the vagus spread abundantly with the connective tissue at the capsule. From this peripheral location, the fibres expand deeply through the parenchyma in close contact with the hepatocytes towards the central veins. Other branches run with the interlobular connective tissue, distributing to the portal veins, hepatic arteries and biliary ducts. They also have lateral branches which penetrate into the parenchyma.     

Microcirculatory pathways in normal human spleen, demonstrated by scanning electron microscopy of corrosion casts

Confusion regarding microcirculatory pathways in normal human spleen has arisen due to extrapolation from pathological material and from other mammalian spleens, not to mention difficulties in tracing intricate three-dimensional routes from the study of thin sections or cut surfaces of tissue. We examined microcirculatory pathways in normal human spleens freshly obtained from organ transplant donors. A modified corrosion casting procedure was used to obtain an open view of vessels and their connections. Our results demonstrate: 1) "arteriolar-capillary bundles" within lymphatic nodules and extensive branching of arterioles in the marginal zone (MZ); 2) the marginal sinus around lymphatic nodules; 3) the peri-marginal cavernous sinus (PMCS) outside the MZ or immediately adjacent to the nodule itself; the PMCS receives flow via ellipsoid sheaths and MZ, or directly from arterial capillaries, and drains into venous sinuses; 4) fast pathways for flow into venous sinuses via ellipsoid sheaths; 5) arterial capillary terminations in the reticular meshwork of the red pulp or MZ ("open" circulation); direct connections to venous sinuses also occur ("closed" circulation), although rarely; and 6) numerous open-ended venous sinuses in the MZ, allowing a large proportion of the splenic inflow to bypass the red cell filtration sites in the reticular meshwork and at venous sinus walls.     

Sinuses of the dura mater in dogs]

Sinuses of the dura mater were studied in 50 preparations of the venous system in mongrel dogs--10 moist, 40 corrosive prepared from plastics AKP-7 and AKP-15. Sinuses of the fornix--superior, sagittal, straight, transversal, occipital sinusal gutter, and sinuses of the basis--cavernous, intracavernous, petrous-basal, occipital and marginal were detected and their connections were described. Emissary and diploid veins and extracranial venous plexus are demonstrated to mediate a close connection between the sinuses of the dura mater. Common features in the sinusal structure of the human dura mater and those of the animals studied are noted; comparative-anatomical differences which should be taken into account when planning the experiment are presented.     

Comparative histochemical and electron microscopic studies of the sinus and venous walls of the human spleen with special reference to the sinus-venous connections

Sinus and venous walls of normal human spleens were studied with enzyme histochemical and electron microscopic methods. Particular attention was paid to the connections between sinuses and veins. Histochemically the sinus lining cells revealed a distinct naphthol-AS-acetate-esterase activity but no reaction for alkaline phosphatase. Venous endothelial cells were positive for the latter but negative for the former enzyme. In the sinus-venous junctional area there were no endothelial cells with reactivity for both enzymes. Electron microscopically both the sinus lining cells and the venous endothelial cells could be clearly characterized and therefore easily distinguished from one another on morphological grounds. There were no clear ultrastrural indications of transitional forms between sinus lining cells and venous endothelial cells in the sinus-venous area. According to these findings, sinus lining cells represent a specialized endothelium, but one with practically no morphological similarities to the venous endothelium.     

A morphological study of the vertebral venous plexus and its connections in the Cape dune mole‐rat,Bathyergus suillus (Bathyergidae)

Bathyergus suillus are subterranean rodents found in the Western Cape of South Africa, where they inhabit sandy, humid burrows. Vertebral venous plexuses around the vertebral column have been implicated in aiding the maintenance of a constant central nervous system temperature via its connections with muscles and interscapular brown adipose tissue. The morphology of the vertebral venous plexuses and its connections in B.suillus were investigated. Frozen (n = 10) animals were defrosted; the venous system injected with latex and the vertebral venous plexuses, azygos‐ and intercostal veins dissected along the dorsal and ventral aspects of the vertebral column. Specimens (n = 4) were used for histological serial cross sections of the thoracic vertebrae. Veins drained from the interscapular brown adipose tissue to the external vertebral venous plexus, via a dorsal vein at the spinous process of T2 which might represent the “vein of Sulzer” described in rats. The intercostal veins cranial to the level of T8 drained directly into the ventral external vertebral venous plexus instead of into the azygos vein as seen in rats. The azygos vein was situated ventrally on the thoracic vertebral bodies in the median plane as opposed to most rodents that have a left sided azygos vein. The internal vertebral venous plexus consisted of two ventrolateraly placed longitudinal veins in the spinal epidural space. Veins from the forelimbs entered the internal vertebral venous plexus directly at the levels of C7 and T1 and have not been described in other rodents. Serial histological sections, revealed no regulatory valves in vessels leading toward the internal vertebral venous plexus, allowing blood to presumably move in both directions within the vertebral venous plexus. The vertebral venous plexus of B. suillus shows similarities to that of the rat but the vessels from the forelimbs draining directly into to the internal vertebral venous plexus and the position of the azygos vein and the intercostal veins draining into the external vertebral venous plexus are notable exceptions. J. Morphol., 2011. © 2010 Wiley‐Liss, Inc.     

Identification of noradrenergic nerve terminals immunoreactive for neuropeptide Y and vasoactive intestinal peptide in the rat kidney

Cryostat- and vibratome-cut sections of rat kidneys were singly or doubly labeled to visualize immunoreactive tyrosine hydroxylase (THI), dopamine beta-hydroxylase (DBHI), vasoactive intestinal peptide (VIPI), and neuropeptide Y (NPYI). Rats were perfusion fixed with 2-4% paraformaldehyde with or without 0.15% picric acid and rinsed in buffer for 18-48 hr. Single antigens were labeled with horseradish peroxidase in vibratome sections, whereas cryostat sections were used to label one antigen with peroxidase and another with a fluorophore in the same tissue section. A dense plexus of DBHI noradrenergic nerves innervates the renal arterial tree, and such nerves innervate the interlobar veins and renal calyx as well. Immunoreactive NPY is colocalized in most of these nerves, but some intrarenal noradrenergic nerves do not contain NPY but do contain VIP immunoreactivity. The distribution of NPYI nerves resembles that of DBHI nerves, whereas most perivascular noradrenergic nerves immunoreactive for VIP innervate selected arcuate and interlobular arteries. A small population of nonadrenergic, VIPI nerves innervates the renal calyx.     

Arguments justifying the acception of the notion "sublobular artery" in the nomenclature of renal vessels: the "conical" architectonics of the renal cortex

The corrosion technique was used to demonstrate the presence of the "sublobular artery", a constant vessel with a special profile of the dog kidney, generating after two divisions the so-called interlobular arteries as a third generation of branches. More rarely arteriae interlobulares emerge also directly from the arcuate artery. The sublobular arteries (= parent vessels of the interlobular arteries) are characterized by their particular origin, branching type, and by having no or sporadically disposed glomeruli. For this reason, the authors suggest the acception of the term "arteria sublobularis" in the international nomenclature of renal vessels. According to authors' opinion the dog kidney is composed of a number of conical vascular-parenchymatous units, each containing in their axis a sublobular artery of the second order ("conical" architectonics of the renal cortex).     

Blood vessels and excretory apparatus of the kidney in some wild animals.

On 110 preparations of the kidney in some wild animals (hare, fox, wolf, bear, boar and chamois), the blood vessels and the excretory apparatus were studied by dissection, injection-corrosion and microscope. Only the bear has a markedly split kidney, whereas the kidneys of the other animals are unsplit. In the fox there is an obvious split of the renal artery into anterior and posterior branches which supply the anterior and posterior portion, respectively, of the renal parenchyma, being separated from each other, so that we may speak of an anterior and posterior kidney. In the fox, wolf, hare and chamois the interlobar arteries pass through the renal calices in a loop composed of adipose tissue, invested by the epithelium of the renal calyx. The renculi of the bear kidney show complete autonomy in relation to the blood vessels as well as in relation to the excretory apparatus. The relation of the surface of the excretory apparatus to the whole kidney was studied. Thus we have found the fox to have relatively the largest excretory apparatus, whose surface amounts to 31% of the whole kidney. In the remainder of the animals investigated this percentage is considerably less, ranging from 21.7% (boar) to 26.7% (bear).     

江豚的小肾结构指数和尿浓缩能力

对江豚的六项小肾结构指数的测定发现,黄海沿岸江豚的小肾结构指数明显高于长江江豚的。提示前者具有较高的尿浓缩能力。对尿的分析所获结论相同,反映出二者对所栖水域的不同渗透浓度的适应。     

Microvascularization of the spleen in larval and adult Xenopus laevis: Histomorphology and scanning electron microscopy of vascular corrosion casts

Microvascular anatomy and histomorphology of larval and adult spleens of the Clawed Toad, Xenopus laevis were studied by light microscopy of paraplast embedded serial tissue sections and scanning electron microscopy (SEM) of vascular corrosion casts (VCCs). Histology showed i) that white and red pulp are present at the onset of metamorphic climax (stage 57) and ii) that splenic vessels penetrated deeply into the splenic parenchyma at the height of metamorphic climax (stage 64). Scanning electron microscopy of VCCs demonstrated gross arterial supply and venous drainage, splenic microvascular patterns as well as the structure of the interstitial (extravasal) spaces representing the “open circulation routes.” These spaces identified themselves as interconnected resin masses of two distinct forms, namely “broccoli‐shaped” forms and highly interconnected small resin structures. Arterial and venous trees were clearly identified, as were transitions from capillaries to interstitial spaces and from interstitial spaces to pulp venules. Venous sinuses were not diagnosed (nonsinusal spleen). The splenic circulation in Xenopus laevis is “open.” It is hypothesized that red blood cells circulate via splenic artery, central arteries, penicillar arteries, and red pulp capillaries primarily via “broccoli‐shaped” interstitial spaces, pulp venules and veins into subcapsular veins to splenic veins while lymphocytes circulate also via the interstitial spaces represented by the highly interconnected small resin structures in vascular corrosion casts. In physiological terms, the former most likely represent the fast route for blood circulation, while the latter represent the slow route. J. Morphol. 277:1559–1569, 2016. © 2016 Wiley Periodicals, Inc.     

Veins of the human cerebellum

(1) The veins of the human cerebellum, which may be classified into internal and external venous channels, correspond, in this respect, to the veins of the cerebral hemispheres. (2) The external cerebellar veins are arranged in three groups which, in turn, correspond to the three cerebellar surfaces and which communicate extensively. Accordingly, the terminal segments of the cerebellar veins overlap, which implies that no one-to-one relationship exists between the mouths of the individual veins and their respective distributions. (3) The terminal segments of the cerebellar veins are the superior petrosal sinus, the tentorial venous sinuses, the great vein of Galen and the internal vertebral plexus. (4) The tentorial venous channels may form a collateral venous arrangement. (5) The internal cerebellar veins consist of the nuclear veins and the medullary veins. (6) The medullary veins form a cortex-perforating group and a group located in the basal medullary region. The latter form a venous arborization of blood vessels not described thus far. This group of veins opens chiefly into the vein of the lateral recess of the fourth ventricle.(7) Attention is called to a 'venous watershed' corresponding to the one that exists in the cerebral hemispheres. (8) The veins of the dentate nucleus are composed of several venous channels draining its external surface and one single vein draining its internal surface. The latter has not been described thus far. The external veins of the dentate nucleus open into the venous star and the cortex-perforating veins. The internal nuclear vein, on the other hand, emerging from the hilum of the dentate nucleus, runs along the superior cerebellar peduncle. Thus, the term 'vena centralis nuclei dentati' appears to be appropriate to designate this vessel. It ultimately opens into the precentral cerebellar vein. (9) In certain places, various-colored substances used for injection form mixed pools.     

Paravascular connective tissue structures of the veins of the pelvic cavity in man

The data on structure of the paravasal connective tissue formations in some parietal pelvic veins, in the utero-vaginal plexus veins, in the fatty tissue space veins of the rectum, of the vesicular and prostatic plexuses are presented, as well as those on connections between the fascial vaginae for the veins in the human subabdominal part of the pelvis and its fascial nodes. Theoretical interpretation of gaping of the pelvic fundal venous vessels is presented. Participation of the paravasal connective tissue formations in organization of the fascial nodes of the human small pelvis is stated.     

Some aspects concerning the peculiarities of the pterygoid venous plexus in man related to age

The pterygoid venous plexus (pt.v.pl.) was studied in 54 human heads (adults, children, fetuses) halved in the middle sagital plan, using microdissections and injections with PVC, coloured gelatin and roentgenopaque masses. In adults, the pt.v.pl. was closely related to the external pterygoid muscle. The superficial variant (more frequent) maintained connections with the facial vein through a venous network named by us "plexus pterygo-temporo-buccalis". The deep variant (less frequent) could be included in the system of venous plexuses placed at the basis cranii. Its tributaries, accompanying the lingual nerve, established connections with the veins of the sublingual compartment (a fact not yet mentioned in the literature). In children and old humans the pt.v.pl. was formed only by some large veins giving a radiate structure ("starfish-shaped" plexus) corresponding to the first and second portion of the maxillary artery. These results revealed that the pt.v.pl. is a unique formation which could be more developed laterally or medially in comparison with the external pterygoid muscle, in relation with the superficial or deep position of the maxillary artery. The practical importance of the pt.v.pl. is emphasized.