The close anatomical and physiological relationship between the implanting blastocyst and the associated uterine epithelium was early indicated when Alden (1947) observed that lipid droplets became scarce or wanting in the apical regions of the maternal epithelial cells in the immediate neighbourhood of the rat blastocyst. However, neither Krehbiel (1937) nor Enders & Schlafke (1967) found significant changes in the uterine epithelial lipids, and Potts (1969) stated that at the time of implantation the lipid spread from the basal part of the cell to the supranuclear zone.After biochemical analyses of whole uterine homogenates, Beall & Werthessen (1971) concluded that triglycerides, accumulated in the uterine tissues before implantation, were depleted from implantation sites by Day 7. Triglycerides are the principal components of neutral lipids, and these compounds vary in quantity and intracellular distribution within the rat uterine epithelium during the oestrous cycle (Boshier & Holloway, 1973). The periodic variations in concentrations of neutral lipids result from increased non-specific esterase activity in the uterine epithelium caused by increasing levels of circulating oestrogen (Boshier & Katz, 1975). This communication reports the results of histochemical investigations of the effect of the blastocyst on neutral lipids and nonspecific esterases in the uterine epithelium at the implantation site.Mature virgin female rats of a hooded strain were maintained under normal animal house condi¬ tions as has been described (Boshier & Holloway, 1973). After two complete 4-day oestrous cycles, females were caged, usually at the following metoestrus, with males of proven fertility and the day the copulation plug or spermatozoa in the vaginal smear were found was recorded as Day 1 of pregnancy. On the morning of Day 6 (128 hr post coitum), 0-5 ml (per 100 g body wt) of 1 % Pontamine Sky Blue (Gurr's) in sterile injection saline was infused under ether anaesthesia into the jugular vein to assist in localizing the implantation sites (Psychoyos, 1960). Animals were then killed by cervical dislocation and the uterine horns excised and pinned out to their intra-abdominal length under Baker's formol calcium. The uteri were fixed for 24 hr at 4°C and then soaked for 24-48 hr in 25% aqueous sucrose at 4°C. Preliminary experiments used freshly frozen tissues, but it was found that implantation sites sectioned more easily, stained as intensely, and retained their morphological integrity better after being soaked in the aqueous sucrose.Transverse sections of the implantation sites and inter-implantation areas were cut at 6-8 pm in a microtome cryostat at -25°C and air-dried onto microscope slides. The maternal and embryonic tissues were stained for neutral lipids with Oil Red O (Pearse, 1968) and for esterase activity by the a-naphthyl acetate technique of Chayen, Bitensky, Butcher & Poulter (1969). Ten females, with an average of 8 implantation sites/uterus, were each examined for neutral lipids and esterases.Between the im...