Comparative morphology of the pectinate ligaments of domestic mammals, as observed under the dissecting microscope and the scanning electron microscope.

The pectinate ligaments of ten horses, two donkeys, five oxen, five sheep, ten goats, five dogs, five cats, thirty pigs and two rabbits were studied under the stereomicroscope and the scanning electron microscope. In the horse and the donkey, the pectinate ligament was very prominent and was characterized by sturdy interconnected strands and relatively small intertrabecular spaces. The pectinate ligaments of ruminants were composed of shorter strands, separated by relatively larger spaces. Fusion between adjacent strands, resulting in the formation of fenestrated sheets, was regularly observed in these species, in particular in the superior and inferior ocular segments. In the dog and the cat, the pectinate ligament consisted of slender strands that were separated by large intertrabecular spaces. The strands of the pectinate ligaments of the pig and the rabbit were shorter and their diameters were intermediate between those of the herbivores and the carnivores. The clinical relevance of the normal variability in the structure of the pectinate ligament and proposals for a uniform anatomical nomenclature are discussed.

Development of the retina in the porcine fetus. A light microscopic study.

Morphogenesis of the porcine retina was studied using light microscopy from 4 weeks of gestation until birth (18 to 310 mm crown-rump length), and compared with the adult stage (6 months). Tissue samples were examined from the posterior and peripheral parts of the retina. At 18 mm the retina consists of an inner marginal layer and an outer layer of neuroblastic cells. At 18-40 mm the latter layer is divided into an inner and an outer neuroblastic layer by the transient layer of Chievitz. Subsequently, the development of the different retinal layers begins at the inner retinal border and moves progressively outwards; it also spreads from the posterior to the peripheral part of the neural retina. Many cells of the inner neuroblastic layer are prospective ganglionic cells which migrate inwards, thus forming the ganglion cell layer and the inner plexiform layer at 90 mm. At 120 mm, primitive horizontal cells appear within the outer neuroblastic layer. Separation of this layer into the inner nuclear, outer plexiform and outer nuclear layers is first evident at 180 mm. At this stage all retinal layers are present, except the layer of the photoreceptor cells which is not widespread until at 220 mm. The inner and outer segments of the photoreceptor cells lengthen considerably during the last month of gestation. During the late fetal stage the nerve fiber layer, the inner and outer plexiform layers and the layer of rods and cones all continue to increase in thickness. Concurrently, the ganglion cell layer and the inner and outer nuclear layers have reached their maximal thickness and become thinner. After the total thickness of the neural retina amounts to approximately 180 microns at two to three weeks before birth, it then thins to approximately 160 microns in the adult stage.

The morphology of the equine iridocorneal angle: a light and scanning electron microscopic study.

The present investigation of 20 equine eyes shows that the iridocorneal angle of the horse is characterised by a very distinct pectinate ligament and a large ciliary cleft. The pectinate ligament consists of long and broad pigmented trabeculae which form a firm, flat and dense network that encircles the eye. On meridional sections, the ciliary cleft is visible as a wide triangular space comprising the trabecular meshwork which consists of two parts. The inner part is the larger and forms a three-dimensional network of large pigmented trabeculae with very wide intertrabecular spaces. The outer part occupies a much smaller area and fills the posterior angle of the ciliary cleft. It is a compact annular network consisting of small non-pigmented circularly orientated trabeculae. They enclose very narrow spaces which contain glycosaminoglycans. External to the outer network lies the angular aqueous plexus, which is rudimentary. This discontinuous plexus runs circularly and is composed of small slit-like vessels. The intrascleral venous plexus is also very weakly developed, whereas the internal collector channels and the episcleral venous plexus are clearly visible. The large ciliary cleft is supported by the strong trabeculae of both the pectinate ligament and the inner part of the trabecular meshwork, making collapse of the ciliary cleft practically impossible. This morphology of the equine iridocorneal angle helps to explain the rarity of glaucoma in the horse.

Retinal vascular patterns in domestic animals.

In this paper a morphological study of the retinal vascular patterns in various species of domestic animals is reported. A classification of these patterns into four well-defined groups is described. In the domestic ruminants, pigs and carnivores the retina contains a compact plexus of blood vessels located in the major part of the light-sensitive portion of the retina (euangiotic or holangiotic pattern). In other domestic animals blood vessels are present only in a smaller part of the retina. In the rabbit, vessels are confined to a broad horizontal band coincident with the area of dispersion of the myelinated nerve fibres. The larger of these vessels are readily visible macroscopically (merangiotic pattern). In the horse and the guinea pig the retinal blood vessels are minute and restricted to the direct neighbourhood of the optic disc (paurangiotic pattern). The avian retina is completely avascular (anangiotic pattern), but a densely vascularised pecten oculi is attached to the linear optic nerve head and protrudes far into the inferior part of the vitreous body.

The hyaloid vascular system of the pig. A light and scanning electron microscopic study.

The hyaloid vascular system of the pig was studied from 4 weeks of gestation until 2 weeks after birth by means of semithin sections and vascular corrosion casts. The vascular tunic of the lens is supplied by the posterior lens branches of the hyaloid artery (at the posterior lens pole), by the intermediate lens branches of the proper hyaloid arteries (at the lens equator) and by the anterior lens branches of the radial iridial arteries (at the anterior lens pole). Venous drainage takes place via the venous lens branches which leave the lens anteriorly and drain into the radial iridial veins. Regression of the vascular tunic of the lens occurs during the second half of fetal life and is nearly completed in the first postnatal days. The involution first affects the proper hyaloid arteries and their intermediate lens branches. Subsequently, the posterior lens branches regress, whereas the anterior lens branches in the pupillary membrane disappear in the perinatal period only.

Topography and identification of the parathyroid glands in the calf.

There is considerable controversy in the literature concerning the topography of the parathyroid glands in the calf. In the present study, the position of the parathyroids III (external parathyroids) and of the parathyroids IV (internal parathyroids) was examined in 25 young calves, 10 veal calves and 5 adult oxen. Detailed data for the recognition and the collection of these glands are provided. The parathyroids III are well suited for removal in a fresh state, since they can readily be located. They are situated medial to the carotid bifurcation and ventrolateral to the vagus nerve, where the latter gives off the cranial laryngeal nerve. In all young calves and in most veal calves, they lie embedded in the sub-basilar portion of the thymus, from which they can usually be differentiated easily by their color. However, they should not be confused with lymph nodes and hemal nodes, which are located in the neighborhood. Light-microscopical substantiation is therefore advisable. The parathyroids IV are not suited for collection, since they cannot be distinguished macroscopically from the adjacent thyroid gland.

Effect of intratesticular inoculation with Aujeszky's disease virus on genital organs of boars.

Ten 8-10-month-old Belgian Landrace boars were intratesticularly inoculated with 500 TCID50 of a virulent Belgian Aujeszky's disease virus (ADV) isolate (75V19) in 0.1 ml volume. One control boar was similarly inoculated with phosphate-buffered saline solution. The genital organs of six inoculated boars were examined by virus isolation and immunofluorescence. In spite of high virus titers, the fluorescence in the testicles remained limited to a few small foci in the interstitial connective tissue and tunica albuginea at or close to the inoculation site. Neither virus replication, necrosis nor inflammatory lesions could be demonstrated in the epithelium of the seminiferous tubules. However, virus replication was regularly demonstrated in the serosa covering testicles, plexus pampiniformis, ductus deferens and tunica vaginalis. Virus was also isolated from the scrotal fluid. It is suggested that the serosa is the primary target tissue for ADV. The other four boars were inoculated to study the effect of ADV on semen. Severe morphologic alteration and lowered sperm cell concentrations were observed during several weeks after inoculation or until slaughter at 47, 53 and 58 days post inoculation. Virus was isolated from semen of only two out of four boars examined at 9 and 10 days post inoculation.