Cerebral microvascular architecture in the common tree shrew (Tupaia glis) revealed by plastic corrosion casts.

The vascularization of the cerebrum (cerebral cortex and basal ganglia) in the common tree shrew (Tupaia glis) has been studied in detail using vinyl injection and vascular corrosion cast/SEM techniques. It is found that the arterial supply of the cerebral cortex are from cortical branches of the middle cerebral artery (MCA) and of the anterior cerebral artery (ACA). These arteries are in turn branches of the internal carotid artery (ICA). In addition, the cerebral cortex receives the blood from the cortical branches of the posterior cerebral artery (PCA) that originates from the basilar artery (BA). These cortical arteries gives rise to rectilinear orientated intracortical arteries that are divided into dense capillary networks to supply the cerebral cortex. The capillary networks drain the blood into intracortical veins and then into the tributaries of major superficial cerebral veins. The basal ganglia (caudate and lentiform nuclei) are supplied by central or perforating branches of the ACA and MCA. These central or medullary arteries give rise to arterioles that ramify into dense capillary plexuses. The venous blood from both nuclei drains into venules and finally into the tributaries of internal cerebral veins. It is obvious that on the ventral aspect, the diameter of the lateral striate artery (LSA) and of the penetrating arterioles from the MCA are much smaller than that of the MCA. These arterioles have few side branches while the peripheral branches of the superficial cerebral arteries exhibit several series of branches that are gradually reduced in diameter before branching into intracortical arteries. This could be one of the reasons why the rupture of cerebral arteries in man mostly occurs in the those originating from the ventral surface rather than from the dorsolateral surface.

Adrenal microvascularization in the common tree shrew (Tupaia glis) as revealed by scanning electron microscopy of vascular corrosion casts.

The blood supply of the adrenal gland in the common tree shrew (Tupaia glis) was studied by use of transmission electron microscopy and vascular corrosion cast/scanning electron microscopy techniques. It was found that the gland receives its blood supply from branches of the inferior phrenic, aorta and renal arteries. Upon reaching the gland, these arteries divide into cortical and medullary arteries. The cortical arteries give rise to the subcapsular capillary plexuses which partially enclose the clusters of cells in the zona glomerulosa (ZG) and appear as lobular-like microvascular networks before running among the cellular cords in the zona fasciculata (ZF) and zona reticularis (ZR). It was noted that the capillaries in ZG and ZR are with more anastomoses than those in the ZF. Capillaries from the ZR become the sinusoidal capillaries in the adrenal medulla before proceeding to the peripheral radicles of the central vein. The medullary arteries penetrate the adrenal cortex and occasionally give off small branches to supply the inner cortex, especially the ZR. Their main branches break up into small or conventional capillaries in the adrenal medulla. These capillaries drain the blood into the peripheral radicles of the central vein and medullary collecting veins which proceed further into a very large central vein. The present findings illustrate that the adrenal medulla receives two blood supplies that yield somewhat different influences upon the adrenal medulla. The portal blood vessel could not be illustrated in the tree shrew adrenal gland.

Testicular microvascularization in the common tree shrew (Tupaia glis) as revealed by vascular corrosion cast/SEM and by TEM.

Testicular angioarchitecture in lower primates has not been established and the route of androgens from Leydig cells entering the systemic circulation is still a matter of controversy. In the present study, the common tree shrew (Tupaia glis) was used as the model for vascular corrosion cast/SEM and conventional TEM studies. With vascular corrosion cast/SEM, it was revealed that while coursing in the spermatic cord, the testicular artery convoluted and gave off branches to supply the epididymis, the coverings of the spermatic cord and the pampiniform plexus. Upon approaching the testis, it encircled the organ, then penetrated into the testicular parenchyma near the rostro-medial pole before further dividing into arterioles that gave rise to capillary plexuses looping around the seminiferous tubules. These capillaries converged into the intratesticular venules, then into larger venules on ventral and dorsal surfaces of the testis and finally into the collecting veins on medial and lateral borders of the testis. In addition, the capillaries in the central or medullary portion of the gland collected the blood into the medullary venules and central (medullary) vein, respectively. The collecting veins as well as central vein joined together before dividing into pampiniform plexus. With transmission electron microscopy, the capillaries in the testis were shown to be of the thick basement membrane and continuous type. The Leydig cells were found adjacent to lymphatic vessels among the seminiferous tubules. This structure is compatible with the idea that most of the androgens drain into the lymphatic vessels rather than into the capillaries.

Angioarchitecture of the coeliac sympathetic ganglion complex in the common tree shrew (Tupaia glis).

The angioarchitecture of the coeliac sympathetic ganglion complex (CGC) of the common tree shrew (Tupaia glis) was studied by the vascular corrosion cast technique in conjunction with scanning electron microscopy. The CGC of the tree shrew was found to be a highly vascularised organ. It normally received arterial blood supply from branches of the inferior phrenic, superior suprarenal and inferior suprarenal arteries and of the abdominal aorta. In some animals, its blood supply was also derived from branches of the middle suprarenal arteries, coeliac artery, superior mesenteric artery and lumbar arteries. These arteries penetrated the ganglion at variable points and in slightly different patterns. They gave off peripheral branches to form a subcapsular capillary plexus while their main trunks traversed deeply into the inner part before branching into the densely packed intraganglionic capillary networks. The capillaries merged to form venules before draining into collecting veins at the peripheral region of the ganglion complex. Finally, the veins coursed to the dorsal aspect of the ganglion to drain into the renal and inferior phrenic veins and the inferior vena cava. The capillaries on the coeliac ganglion complex do not possess fenestrations.

Microvascularization in trigeminal ganglion of the common tree shrew (Tupaia glis).

Since there is only a limited number of studies of the blood supply to the trigeminal ganglion (TG) in mammalian species, the TG from 16 common tree shrews (Tupaia glis) were investigated by light microscope, transmission electron microscope (TEM) and the corrosion cast technique in conjunction with scanning electron microscope (SEM). It was found that the TG contained clusters of neurons in the peripheral region whereas the bundles of nerve fibers were located more centrally. Each ganglionic neuron had a concentric nucleus and was ensheathed by satellite cells. It was noted that blood vessels of a continuous type were predominantly found in the area where the neurons were densely located and were much less frequently observed in the area occupied by nerve fibers. With TEM, the TG was shown to be mainly associated with large neurons containing big nuclei and prominent nucleoli. The blood supply of the TG is derived from the most rostral branch of the pontine artery, from the stapedial artery or sometimes from the supraorbital artery, and from the accessory meningeal artery which is a branch of the maxillary artery passing through the foramen ovale. These arteries give off branches and become capillary networks in the ganglion before draining blood to the peripheral region. The veins at the medial border drained into the cavernous sinus directly or through the inferior hypophyseal vein, while those at the lateral side of the ganglion carried the blood into the pterygoid plexus via an accessory meningeal vein. The veins along the trigeminal nerve root joined the posterior part of the cavernous sinus. These studies establish a unique anatomical distribution of the TG blood supply in the tree shrew and the utility of the cast/SEM technique in discerning detailed features of the blood supply in the nervous system.

Cytoarchitecture of the common tree shrew (Tupaia glis) superior cervical ganglion. A scanning electron microscope study on vascular cast/enzyme-digested superior cervical ganglia.

The cytoarchitecture of the superior cervical ganglion of the common tree shrew was investigated by scanning electron microscopy using the vascular cast technique in conjunction with digestion by collagenase-hyaluronidase/HCl. The main cellular constituents were found to be multipolar neurons that were densely distributed throughout the ganglion. These neurons were covered with a smooth cytoplasmic sheath of satellite cells. After the removal of this sheath by digestion of increased duration, the blebs or knobs on the neuronal surfaces became evident. A meshwork of nerve fibers over the surface of neurons was also observed. Preganglionic sympathetic nerve fibers, giving rise to fine branches that ran toward the postganglionic sympathetic neurons before forming synapses, were demonstrated. Groups of neurons surrounded by capillary loops were also frequently observed.

Microvascularization of the common tree shrew (Tupaia glis) superior cervical ganglion studied by vascular corrosion cast with scanning electron microscopy.

Microvascularization of the superior cervical ganglion (SCG) of the common tree shrew (Tupaia glis) was investigated by the vascular-corrosion-cast technique in conjunction with scanning electron microscopy. It was found that the SCG of the tree shrew is a highly vascularized organ. It receives arterial blood from branches of the external and common carotid arteries which enter the rostral and caudal portions of the ganglion. These arteries give rise to a subcapsular capillary plexus before branching off to form a group of densely packed intraganglionic capillaries. Moreover, the intraganglionic capillaries tend to follow a tortuous course that is essentially parallel to the longitudinal axis of the ganglion, and they form anastomoses with each other. In addition, the intraganglionic capillaries are also connected to a subcapsular capillary plexus. The capillaries of the SCG converge into venules and collecting veins which subsequently drain rostrally and caudally into the systemic veins. However, neither a pattern of blood vessels resembling glomeruli nor a portal-like intraganglionic microcirculation was observed.

Microvascularization of the rat superior cervical ganglion. A three-dimensional observation.

The three-dimensional image of the microvascularization of the rat superior cervical ganglion (SCG) was examined using the vascular corrosion cast technique in conjunction with scanning electron microscopy. It was found that the rat SCG was a highly vascularized organ. Arteries supplying the ganglion gave rise to a subcapsular capillary plexus before branching off to become intraganglionic capillaries. Two types of intraganglionic capillaries, large and small, were observed throughout the organ. Numerous anastomoses among these capillaries were found before they converged into venules and collecting veins. However, a pattern of blood vessels resembling portal-like intraganglionic microcirculation could not be demonstrated.

Pancreatic microcirculation in the common tree shrew (Tupaia glis) as revealed by scanning electron microscopy of vascular corrosion casts.

Pancreatic vascular casts of the common tree shrew (Tupaia glis) were prepared by infusion of Batson's No. 17 plastic mixture into the blood vessels and examined by scanning electron microscopy (SEM). Routine histological study of the pancreas was also performed. It was found that the A and D cells appeared to occupy the core whereas the B cells were found at the periphery of the islets of Langerhans. With SEM, the insular arteriole, a branch of the interlobular artery, was shown to penetrate deeply into the core of the islets before branching off into the glomerular capillary network supplying the islets. These capillaries reunited at the periphery of the islets to become vasa efferentia and then gave off capillaries to anastomose with those in the exocrine part of the pancreas, the insuloacinar portal system. Such an insuloacinar portal system found in the pancreas of the tree shrew was similar to that found in the horse and monkey. However, there were some intralobular arterioles which did not end in the islets but directly branched into the interacinar capillary network and periductular plexus. The capillaries in the exocrine part not only gathered into intralobular venules which confluently formed the interlobular vein but also supplied the duct system. The periductular plexus also collected blood into the intralobular venule and interlobular vein, respectively.

SEM study on the dorsal lingual surface of the common tree shrew, Tupaia glis.

The dorsal lingual surface of the common tree shrew was examined by SEM after treating it with HCl to remove the mucous substance. Filiform (FI), fungiform (FU) and circumvallate papillae (CI) were observed. The FI exhibited a small circular bulge surrounded by anterior and posterior filamentous processes. FU were scattered among the FI. There were 3 CI separating the anterior 4/5 from the posterior 1/5 of the tongue. In addition, a group of conical projections with caudal orientation was found anterior to the palatoglossal fold on each side of the tongue. Microridges were widely observed on the entire dorsal lingual surface, except on the free surface of FI processes.

Hypophyseal angioarchitecture of common tree shrew (Tupaia glis) revealed by scanning electron microscopy study of vascular corrosion casts.

The vascular corrosion cast technique in conjunction with scanning electron microscopy (SEM) was used for the study of pituitary microvascularization in the common tree shrew (Tupaia glis). The pituitary vascular casts were obtained by infusion of low viscosity methyl methacrylate plastic (Batson's no.17) mixture. It was found that the blood supplies to the pituitary complex were from branches of the circle of Willis and could be divided into two groups. The first group consisted of two to four superior hypophyseal arteries (SHAs) branching off from the internal carotid artery supplying each half of the median eminence (ME), infundibular stalk (IS), and pars distalis (PD). The SHAs supplying the ME branched into internal and external capillary plexi. The internal plexus had a larger capillary size (approximately 15 microns in diameter), was deeper in position, and had denser and more complex capillary loops than those in the external plexus. The capillaries of the external plexus were approximately 10 microns in diameter. The two plexi drained into 15-20 hypophyseal portal veins (HPVs) which were located mainly along the ventral and ventrolateral surfaces of the IS before breaking up into large capillaries (approximately 18 microns in diameter) with an anteroposterior arrangement within the PD. The second group consisted of one inferior hypophyseal artery (IHA) on each side branching off from the internal carotid artery. These arteries gave off branches to pierce the dorsolateral and ventrolateral aspects of infundibular process (IP) before branching off to form a capillary network. They also gave rise to radiating capillaries to supply the pars intermedia (PI) surrounding the cortical area of the IP. The hypophyseal cleft separating the PI from the PD was clearly seen with very few blood vessels. The capillaries in both PD and IP joined to form confluent hypophyseal veins draining the blood into the cavernous sinus.

Scanning electron microscopic study on pineal vascularization of the common tree shrew (Tupaia glis).

The detailed blood supply including microvascularization of pineal gland in the common tree shrew (Tupaia glis) was investigated using a vascular corrosion cast technique in conjunction with scanning electron microscopy. Adult common tree shrews of both sexes, divided into 3 groups, were injected with red latex, blue vinyl resin, and Batson's No. 17 plastic mixture for the studies of arterial supply, venous drainage, and microvasculature of the pineal gland, respectively. It was found that the pineal gland is a highly vascularized organ. It receives two to four branches from the medial posterior choroidal arteries. Two types of capillary arrangements, fan-like and network, are observed. As in the human, usually one and occasionally two pineal veins, draining directly into the great cerebral vein of Galen, are observed. A pineal portal system is not demonstrated.

Scanning electron microscopic study of the splenic vascular casts in common tree shrew (Tupaia glis).

Splenic vascular casts of the common tree shrew, Tupaia glis, were constructed with Batson's No. 17 plastic mixture and studied with the scanning electron microscope (SEM). Fifteen adult animals of both sexes, weighing between 120 and 180 g were used. Under ether anaesthesia, each animal was injected with 0.05 ml heparin intracardially; the right atrium was cut open and then 250 ml of 0.9% NaCl, followed by 50 ml of 10% neutral formalin, (in four animals) was injected through the left ventricle. Plastic mixture was injected through the same opening. After complete polymerization of the plastic, the spleen and surrounding tissues were removed and macerated in 40% KOH. The air-dried casts were then coated with carbon and gold before viewing and photographing under SEM at 15 kV. It was found that the splenic arteries penetrated deep into the organ before they divided into trabecular arteries and divided again into central arterioles. Each central arteriole sent out 15 to 30 radiating arterioles, called penicillar arterioles, and further divided into smaller vessels entering the marginal zone and red pulp. In this area each arteriole continued directly into either marginal or red pulp sinusoids. The sinusoids emptied into pulp venules which joined to form trabecular veins. Most of the trabecular veins travelled to the cortical area underneath the splenic capsule before approaching the hilum, where they finally drained into splenic and short gastric veins. It is likely that the spleen of the common tree shrew has a closed circulation.

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.

A re-examination of the cerebellar projections from the gracile, main and external cuneate nuclei in the cat.

Cerebellar projections from the dorsal column and external cuneate nuclei in the cat have been studied by means of retrograde axonal transport of horseradish peroxidase. Localized injections covering the entire cerebellar cortex and nuclei show that the gracile nucleus has a weak projection only to the cortex of the anterior lobe, but that there is a conspicuous projection from the main cuneate nucleus to the cerebellum. Most of these fibres reach lobule V and the adjacent parts of lobules IV and VI, and there is also a heavy projection to the paramedian lobule. Some fibres reach lobule IX and possibly also lobules II, III and VIIIB, and nuclear afferents also reach the fastigial and interposite nuclei. Three cerebellar cortical regions are the main targets for the fibres from the external cuneate nucleus, viz. lobule V with the adjacent regions of lobules IV and VI, lobules I and II and lobule IX (the anterior part). Other important afferent regions are the paramedian lobule and the cerebellar nuclei, especially the anterior interposite, and some fibres reach the flocculus. The projections are predominantly ipsilateral. The investigation is the first detailed study of the cerebellar projections from the three nuclei and the findings are discussed in relation to previous experimental observations.

Cerebellar afferents from the trigeminal sensory nuclei in the cat.

The cerebellar afferent projection from the trigeminal sensory nuclei (TSN) was studied by means of retrograde axonal transport of horseradish peroxidase (HRP). The projection is almost exclusively ipsilateral. Three cortical regions, viz., the intermediate-lateral part of lobulus simplex with the adjacent area of lobule V, the rostralmost folia of the paramedian lobule with the surrounding parts of crus I and II, and lobule IX, especially its rostral two folia, are the main targets for the cerebellar afferent fibres. A few fibres reach also the other cerebellar regions, as shown in Fig. 3. Most of the cerebellar afferent fibres originate in the nucleus interpolaris with nucleus oralis as the second most important region. The projection from the principal nucleus is moderate and reaches primarily the area of the crura bordering on the paramedian lobule and lobule IX. The projections from the nucleus caudalis and nucleus mesencephalicus are scanty. The fibres from the latter reach only the vermal region. The findings are discussed in relation to previous anatomical and physiological observations.

The cerebellar projection from the paratrigeminal nucleus in the cat.

The cerebellar afferent projection from the paratrigeminal nucleus (PTN) was studied in the cat by means of retrograde axonal transport of horseradish perioxidase (HRP). Most of the afferent fibres reach the cerebellar lobules I, II, V (hemispheral part), VIIIB and IX, the paramedian lobule and the fastigial nucleus. The total distribution of the cerebellar afferents is shown in Fig. 2. The findings extend Chan-Palay's [2,3] recent studies on the cytology, synaptic organization and neurotransmitter content of the paratrigeminal nucleus in monkey and rat.

Cerebellar afferents from the nucleus of the solitary tract.

The cerebellar afferents from the nucleus of the solitary tract were studied in cat by means of retrograde axonal transport of horseradish peroxidase. Labelled cells occurred bilaterally in the nucleus of the solitary tract following injections in various folia of the cerebellar vermis and in the flocculus (the positive cases are shown in Fig. 1A). Injections in the anterior lobe vermis labelled cells in the caudal part of the nucleus, injections in the posterior vermis labelled cells in the rostral part (Fig. 2). The findings are discussed in relation to other efferent and afferent connections of the nucleus of the solitary tract.