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 adj acent 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.

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.

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.

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.