CT sialography in the dog - a cadaver study

To document computed tomographic topography of salivary glands and their ducts in dogs, a retrograde filling with methylcellulose and iodinated contrast medium was performed in three cadavers. Demarcation of the parotid, mandibular and zygomatic glands was achieved. Surrounding structures were imaged without beam hardening artefacts. Landmarks for the parotid, mandibular and zygomatic glands were the external acoustic canal, the mandibular angle and the pterygopalatine fossa, respectively. Sialograms of the parotid, mandibular and zygomatic ducts were achieved, whereas neither the sublingual glands nor their ducts could be contrasted. The images provide a three-dimensional visualization of the salivary glands and their ducts.     

妊娠期牦牛肉阜间区子宫腺的形态计量学分析

运用形态计量学方法对31头牦牛肉阜间区子宫腺的相关组织学数据进行了测定,并进行统计分析。研究发现,除了妊娠151~180 d,牦牛肉阜间区子宫腺上皮高度随着妊娠时间的增长极显著降低(P0.01);妊娠期子宫腺管周长和面积非常明显增大(P0.01);不同妊娠阶段之间体积密度差异极显著(P0.01),先增加后下降,而表面密度无显著差异(P0.05);除了妊娠151~180 d,扭曲腺管和管状腺管的比例随着妊娠时间的增长分别非常显著地增大或减小(P0.01);分泌腺管的比例在妊娠期间有明显变化(P0.05),牦牛肉阜间区还存在嵌套腺管。结果显示,妊娠期牦牛肉阜间区子宫腺形态结构有明显的变化,子宫腺变的更大、更长,形状更加扭曲。     

Glandular structures in the major interlobular and extrapancreatic ducts in the guinea pig

The morphology of the pancreatic duct system did not receive much attention as compared to the microanatomy of the exocrine and endocrine pancreas. The histological peculiarities of the excretory duct system are of major importance especially in laboratory animals like guinea pigs. The paper describes the histological peculiarities of the major interlobular and extrapancreatic ducts in guinea pigs. The pancreatic tissue samples were collected from five guinea pigs. For histological investigation, several pancreatic fragments underwent fixation in 10% buffered formalin and were later processed by the standard paraffin technique. Subsequentially, tissue sections were stained by Goldner's trichrome staining. The mucous substances were assessed by Alcian blue and Periodic acid–Schiff staining methods. The interlobular and main pancreatic ducts in the guinea pig present a simple columnar epithelium surrounded by a thick layer of dense connective tissue. The aforementioned epithelium of the main pancreatic ducts includes principal cells, goblet cells and basal cells. Additionally, the ductal epithelium presents occasional unicellular multiloculated intraepithelial mucous glands and prominent extraepithelial glands. The latter adopts a simple or compound tubular feature. The mucus elaborated by the three glandular types is mostly neutral in goblet cells, predominantly acidic in extraepithelial ductal glands, and a similar amount of acidic and neutral mucin in intraepithelial glands. In conclusion, the epithelium-associated mucous glands in the interlobular and main pancreatic ducts in the guinea pig are restricted not only to goblet cells. A substantial mucous discharge probably with a protecting role against irritative pancreatic juice derives from the main ductal intraepithelial and extraepithelial glands.     

Ultrastructural study of sheep lacrimal glands.

Sheep lacrimal glands are mixed glands, consisting of tubulo-acinar units succeeded by ducts of simple morphology. The secretory portions consist of three cell types: mucous, seromucous and serous, which may be intermingled in the same acinus or may form acini wholly made of only serous or mucous cells. Mucous cells show a rough endoplasmic reticulum that is reduced to a few cisternae located near the cell base and among the interstices of the secretory droplets. Mucous granules appear uniformly electron-lucent. Serous cells display a typical structure; serous granules can be uniformly electron-dense or composed of dense inclusions dispersed in an electron-lucent matrix. The seromucous granules have a bizonal substructure: a dense core is embedded in a highter matrix. Secretory acini are succeeded by intercalated ducts; the epithelium of these ducts gradually increases in height to form a kind of excretory duct, without the intervention of striated ducts.     

Immunocompetent cells in avian paraocular glands

A study was made of the Harderian and lachrymal glands of fowls, pheasants, turkeys and pigeons. Accumulation of heterophils and plasma cells commenced soon after hatching, was well advanced by four weeks of age and was always greater in the Harderian than in the lachrymal glands. Plasmablasts entered via interlobular capillaries, maturing as they migrated to and congregated round the lobular collecting ducts. Their secreted immunoglobulin was readily demonstrated in the duct lumen. Russell body containing cells of diverse morphology were a consistent feature of infiltrated Harderian glands. Though scant in the glands proper, lymphoid tissue was abundant in the walls of their draining ducts.     

Nachweis verschiedener Hydroxysteroid-Dehydrogenasen in Circumanaldrüsen adulter Hunde

Ligh-, electronmicroscopical and histochemical examinations of the circumanal glands of adult dogs suggest that these glands take part in steroid metabolism. The glands have no excretory ducts.     

Pathogenesis of sialodacryoadenitis in gnotobiotic rats.

The pathogenesis of sialodacryoadenitis was studied in gnotobiotic CD rats inoculated intranasally with the causal virus. Virus replication was detected sequentially in the nasopharynx, tracheobronchial tree, cervical lymph nodes, submaxillary and parotid salivary glands, exorbital gland, and Harderian gland. Acute rhinitis appeared within 2 days after inoculation, and salivary glands had lesions in 4 days. Early changes in salivary and exorbital glands were characterized by necrosis of ductal epithelium, which rapidly progressed to widespread acinar necrosis, marked inflammation, edema and total effacement of glandular architecture. Harderian glands also had massive necrosis of tubuloalveolar units. Repair in all glands was characterized by marked squamous metaplasia of tubuloalveolar units. Repair in all glands was characterized by marked squamous metaplasia of ducts. Neutralizing and complement-fixing antibodies were detected in 7 days, and there was a concomitant decrease in tissue-virus titers. There was no detectable evidence for hematogenous spread of virus or for retrograde infection by way of major salivary ducts.     

Microscopy of the echidna sublingual glands

The secretory units and duct system of the echidna sublingual glands exhibit subtle architectural modifications to accommodate the viscous secretion produced by these glands. The glands are compound tubular glands, the secretory units of which are elongate with open lumina and consist only of mucous cells. Closely packed spindle-shaped myoepithelial cells invest the secretory units, but are absent around the ducts. The branched secretory tubules open into an abbreviated duct system characterized by wide lumina. Striated ducts normally associated with the second portion of the intralobular duct system are absent. The duct system shows the most obvious modification of general salivary gland architecture presumably to accommodate the viscous secretion propelled from the secretory units by surrounding myoepithelial cells.     

Sialography of sheep parotid and mandibular salivary glands

The anatomy of ovine salivary glands was studied on cadaver heads. The mandibular duct enters the oral cavity on the ventral surface of sublingual caruncles, which are located medial to the orifice of the ventral sublingual gland duct. The parotid gland duct enters the oral cavity on the cheek opposite the upper 2nd molar. Prior to applying sialography to live animals, the procedure was carried out on cadaver heads then the live animals were sedated, the mandibular and parotid ducts catheterized and contrast medium was injected into each gland. Lateral radiographs were made immediately after the injection. The normal sheep mandibular and parotid salivary glands have a multilobular appearance in cadaver heads, but in live animal only the ducts and their smaller branches could be identified. The mean diameter of mandibular and parotid duct were 1.4+/-0.3 mm and 3. 1+/-1.0 mm respectively. The monostomatic sublingular gland had a slender shape in the sialogram. In conclusion sialography of mandibular, parotid and sublingual salivary glands in sheep is practical and can be helpful in diagnosis of pathological conditions of these glands.     

Cytoarchitectural differences of myoepithelial cells among goat major salivary glands

Previously, the distribution of myoepithelial cells (mecs) in the salivary glands was studied by both immunohistochemistry, and transmission electron microscopy; however, little was elucidated concerning their morphological features, especially in goats. This study was performed to investigate the correlation between the cytoarchitecture of the mecs in goat major salivary glands (parotid, mandibular, and sublingual glands) and the nature of the saliva secretion. The cytoarchitectural features of the mecs were examined by scanning and transmission electron microscopy as well as immunohistochemically. The secretory endpieces in the parotid gland are of the pure serous type, but in both the mandibular and sublingual glands they are of the mixed type. In all studied glands, the intercalated ducts were covered by mecs which, unlike the large stellate cells that surrounded the secretory endpieces, were spindle-shaped with few cytoplasmic processes. Interestingly, the mecs were found to bulge on the basal surfaces of the serous acini and intercalated ducts in all glands and to be in close contact to the seromucous tubules surface in the mandibular and sublingual glands forming a continuous network around it. In conclusion, the differences in the degree of development of the mecs as well as the number of their cytoplasmic processes may be correlated with the nature of the secretion and the number of the secretory granules. Thus these observations may have some relevance in the diagnosis of atrophy and pathogenic conditions of these glands.     

Transrectal ultrasonography for the evaluation of stallion accessory sex glands.

This article reviews the capabilities of transrectal ultrasonography for determining the distribution of fluid and tissue within stallion accessory sex glands. Emphasis is placed on describing the normal ultrasonographic appearance of the accessory sex glands, excurrent ducts, and pelvic urethra of stallions during rest, after teasing, and after ejaculation and using this information to detect glandular abnormalities.     

Renin in Exocrine Glands of Different Mouse Strains

The renin-angiotensin system (RAS) controls the regulation of blood pressure and water-mineral balance. Recently, renin has been reported to be synthesized and secreted outside the kidney. The present study investigated immunohistochemically the distribution of renin in exocrine glands, i.e. salivary glands and coagulating glands, in male mice of 13 strains. In some strains, renin was detected in the sublingual and submandibular salivary glands, but not in the parotid glands. It was restricted to the striated or granular portions of excretory ducts. In coagulating glands, variable staining patterns were found. These results demonstrate the existence of variations in renin content in mouse strains and offered a selection of mouse strains for investigation of exocrine gland renin.     

Structure of the Oesophagus and Morphometric, Histochemical–Immunohistochemical Profiles of the Oesophageal Gland During the Post-hatching Period of Japanese Quails (Coturnix coturnix japonica)

In the oesophagus, mucins, which originate from oesophageal submucosal glands, play an important role in the mucosal protection as a pre-epithelial barrier. In this study, the structure of cervical and thoracic parts of oesophagus of Japanese quail during the post-hatching period was compared, and the contents of carbohydrate and gastric mucin MUC5AC of the oesophageal glands in these parts were analysed at the light microscope levels by applying conventional histochemical and immunohistochemical methods. The oesophageal glands were present at hatching, located in the laminae propria. The numbers of glands were different in the cervical and thoracic parts, but the differences were found to be insignificant. The thoracic part has the oesophageal tonsils which are associated with the glands. Oesophageal tonsil was formed from day 5 after hatching. In quail of all ages, the secretory epithelium of glands contained neutral sialomucins and weakly sulphomucins. The cells in the neck region of secretory units contained sialomucins, while the cells of excretory ducts had strongly sulphomucins. Sialomucin containing cells in the secretory units increased with the advance of age and glandular development. But, in the secretory units, the sulphomucin content of glands was more in the thoracic part. The secretory epithelium of tonsil-associated glands contained mostly sulphomucins and a little sialomucin. From the hatching, MUC5AC mucin was detected in the cells of excretory ducts. Although the lymphoepithelium of the tonsil units exhibited negative reactions to all histochemical methods, it showed positive reaction to MUC5AC mucin antibody. In conclusion, the cervical and thoracic parts may be functionally different and the thoracic part of oesophagus was transformed into an immunological organ following day 5 after hatching.     

Microscopic Anatomy and Enzyme Histochemistry of the Canine Anal Canal

The microscopic anatomy of the anal canal was studied using routine histological methods and the light microscope in male and female dogs ranging from six months to 10 years of age. Precise anatomical boundaries were established for the zona columnaris , the zona intermedia , and the beginning of the zona cutanea. In an effort to clarify conflicting terminology concerning the anal canal, the term "anal sinus" ( sinus anales ) is applied to the shallow troughs located between the longitudinal mucosal ridges or columns (columnae anales) characteristic of the canine and human zona columnaris ; and the term "anal crypt" is used to represent and distinguish the terminal blind pockets of anal sinuses which extend into the lamina propria of the zona intermedia .
Anal glands were identified routinely in the z. columnaris and z. intermedia of the anal canal; dilated excretory ducts of the anal glands were frequently encountered, often filled with inflammatory cells. PAS-positive but Sudan Black-negative secretion was demonstrated in these ducts as well as within the secretory acini. Sebaceous, circumanal and apocrine sweat glands were restricted to the z. cutanea . Moderate to high alkaline phosphatase activity in the basement membrane of circumanal glands may suggest the presence of myoepithelial cells.     

SIALOGRAPHY IN CATTLE: TECHNIQUE AND NORMAL APPEARANCE

Sialography of the bovine mandibular and parotid salivary glands was performed by injecting iodinated, water soluble contrast medium into the respective ducts. The anatomy of the above mentioned salivary glands was studied on cadaver heads. The mandibular duct enters the oral cavity on the ventral surface of the sublingual caruncles, which are located medial to the orifice of the ventral sublingual gland duct. The parotid gland duct enters the oral cavity on the cheek opposite the upper 2nd molar (Sth cheek tooth). Prior to applying sialography to live animals, the technique of catheterization, injection and radiography had to be developed, which was carried out on cadaver heads. Subsequently the technique was applied to 5 live animals. The animals were sedated, the mandibular and parotid ducts catheterized, and contrast medium was injected into each gland. Latero-lateral radiographs were made immediately after the injection. The normal bovine mandibular and parotid glands, as depicted on sialograms, have a multilobutated appearance in cadaver heads, but in the live animal only the ducts and their smaller branches could be identified. The parotid duct leaves the deep surface of the rostral end of the gland and courses along the border of the masseter muscle before it enters the mouth. The mean diameter of the duct was 4.2 ± 0.3 mm. The mandibular duct is composed of a rostral and a caudal branch. The caudal branch describes a semi circular turn prior to joining the rostral branch. The mean diameter of the main duct was 2.8 ± 0.4 mm.     

Histochemistry of Complex Carbohydrate in the Major Salivary Glands of Hoary Bamboo Rats (Rhizomys purinosus)

The major salivary glands (parotid glands, monostomatic sublingual glands and submandibular glands) were obtained from hoary bamboo rats (Rhizomys purinosus) and fixed in Bouin's solution. Paraffin sections were subjected to a battery of staining methods including lectin staining for demonstration of complex carbohydrates. Among the three major salivary glands, unique histochemical features were observed in the submandibular gland. Different from most myomorpha species, submandibular glands of the hoary bamboo rats have two types of secretory cells in the secretory endpieces. One type of cells showed positive reactions with Alcian blue (AB)(pH2.5), periodic acid-Schiff (PAS) and some lectins (peanuts agglutinin, Griffonia simplicifolia I. Machura pomifera agglutinin). The granular ducts, which exist in animals belonging to suborder myomorpha, were not observed in the submandibular glands of this animal.     

Vallate papillae in the domestic rabbit (Oryctolagus cuniculus f. domestica)

On the root of the tongue in the rabbit there are two symmetrically located vallate papillae, covered by nonkeratinized stratified squamous epithelium. The epithelium is characterized by variable thicknesses, forming epithelial streaks of different length and irregular shape. Taste buds are found both in the epithelium covering the papillae and in the epithelium of the outer walls of the papillae from the side of the furrows. The outer wall of the vallate papillae is gradually transformed with no visible boundary into the surface of the root of the tongue devoid of papillae. The surface of the vallate papillae is uneven. The connective tissue core of the papillae is formed by numerous, irregularly shaped connective tissue papillae, between which epithelial streaks are arranged. Around the connective tissue core of the papillae there is a circular connective tissue fold, with a furrow located on its circumference and the core of the outer wall of the vallate papillae. Numerous excretory ducts of the posterior serous lingual glands (Ebner's glands) open on the fundus of the circular furrow of each vallate papilla. Sometimes excretory ducts of these glands open directly onto the surface of a vallate papilla and then in their vicinity taste buds are found. The results of this study show the structure of vallate papillae on the tongue of adult rabbits, at the same time indicating differences in their structure in comparison to the vallate papillae of other animal species.     

Lectin histochemistry of dog major and minor salivary glands

The distribution of different carbohydrates in dog major and minor salivary glands was investigated using a peroxidase-labelled avidin-biotin method to demonstrate binding of six lectins (Canavalia ensiformis agglutinin [Con A], Dolichos biflorus agglutinin [DBA], Arachis hypogaea (peanut) agglutinin [PNA], Glycine max agglutinin [SBA], Tetragonolobus purpurea agglutinin [TGP] and wheat germ agglutinin [WGA]). With PNA, there was only weak staining in serous acini of parotid glands. Other lectins bound, to different degrees, to different components of the salivary glands; differences could be detected between glands and between binding of different lectins to serous and mucous acinar cells and to the epithelial cell cytoplasm, luminal surface and contents of ducts. These results provide a basis for the comparison of possible changes in carbohydrates which may occur in salivary gland diseases.     

Zur pränatalen Entwicklung der Glandula mandibularis und Glandula parotis der Katze

The prenatal development of the cat's mandibular and parotid gland was examined by means of serial section of 36 cat embryos at 14–62 days of development. Both glands were excised from the epithelium of the primitive oral cavity and branched up to day 36 of the branching phase into a specific connective tissue. This tissue contained besides fine collagenous fibres, a high amount of proteoglycans. In the subsequent separation phase, ducts and acini differentiated themselves in primitive lobules which were separated by connective tissue. In the prenatal differentiation phase, from about day 50 up to birth, intercalated ducts and striated ducts were formed. In the acini, mucous and serous cells contained different amounts of complex carbohydrates. This secretory component changed shortly before birth.