This review surveys the potential of plastination, a technique of tissue preservation introduced eight years ago. In this process, water and lipids in biological tissues are replaced by curable polymer which are subsequently hardened, resulting in dry, odorless and durable specimens. The procedure consists of the following steps - fixation, dehydration, forced impregnation in a vacuum, and hardening. The properties of the finished specimen are determined by the class of polymer used. Silicone yields flexible, resilient specimens, allows the broadest range of application, and provides satisfactory results with minimum equipment. Specimens plastinated with an epoxy-silicone copolymer are rigid enough to be polished, but are not unbreakable. This resin is used for thick, opaque body slices and showcase specimens. Epoxy resins are used for thin (2.5 mm), transparent body or organ slices. They are cast between polyester foils or glass plates and can be used for histological investigations. Polyester resin is used for the production of opaque brain slices, which gives excellent differentiation between grey and white matter. The application of plastination in research and the production of teaching specimens is discussed with special regard to the equipment required, cost, and feasibility of the processing.

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The occurrence and distribution of renin was investigated in meso- and metanephric kidneys of pig embryos in various gestational stages. The immunohistochemical peroxidase-antiperoxidase-method (PAP) was used on paraffin sections after application of an antiserum against mouse renin which cross reacts with pig renin. Renin immunoreactivity was already found in the mesonephros of 21 day pig embryos (crown-rump(CR)-length 12 mm) with the strongest reaction in the media of the juxtaglomerular afferent arteriole. Efferent vessels, mesonephric arteries, and the aortic wall also contained scattered renin-positive cells. In the definitive kidney, renin was not detected prior to the 25 mm CR-length-stage. In 45 mm embryos, immunocytochemical staining was observed not only in the media of kidney arteries and arterioles, but also in proximal tubules after pinocytic absorption of filtered renin. TEM-studies revealed that the media of both the mesonephric and the developing metanephric arteries and arterioles contains epithelioid cells whose ultrastructure is very similar to that of renin-producing cells in the adult organ. The observed distribution of renin-producing cells along the entire renal arterial tree points to the possibility that the major function of the renin-angiotensin system in the fetal animal is to participate in the stabilization of renal perfusion pressure.

Plastinated hearts are natural specimens, preserved in a firm or flexible state, which thus can be grasped in the hand. They are fixed in a dilated state. Their tissue water and lipids are replaced by polymerized synthetic resins or elastomers. The final specimens show doubly injected coronary vessels, opened atria and ventricles, thus exhibiting all finer external and internal details. The procedure described consists of the removal of the heart; intermediate storage facilities; dilatation with water under hydrostatic pressure; color injection of the coronary vessels; fixation; dehydration in acetone under hydrostatic pressure; forced impregnation in a vacuum chamber; and hardening with aftercare. Technical variations and pitfalls are discussed, as well as the required equipment.