J Drouet’s scientific contributions

The phagocytic activity of rat alveolar macrophages was studied in vitro for up to six weeks after whole-body gamma irradiation (7.5 Gy). Ingestion of fluorescent latex microspheres was evaluated using both microscopic examination and flow cytometric quantitation. After a transient decrease on first day post-irradiation, a slight increase in the phagocytic ability was observed from day 14 to day 28, with a maximum on day 21. From day 35 onwards, phagocytic capacities returned approximately to those of the controls. The percentage of phagocytic cells (cells having ingested one microsphere or more) increased by 75 per cent on day 21 after irradiation and the phagocytic index (percentage of phagocytic cells X the average number of ingested microspheres per cell) increased by 250 per cent while at the same time, the number of recovered alveolar cells decreased by 37 per cent. The augmentation of phagocytic capacities after irradiation was particularly characterized by an increase in the percentage of cells ingesting more than five microspheres. Flow cytometric studies showed a significant increase in mean cell size on day 21 post-irradiation. The augmentation of the phagocytic activity was not found when macrophages from control rats were incubated with serum or alveolar lavage fluid from an irradiated donor. Augmentation of phagocytic capacity was also observed after 8.5 Gy but no effect could be observed after 6.5 Gy.

The activity of microsomal glucose-6-phosphatase (EC 3.1.3.9) on male rat liver was measured 1-9 days after whole-body gamma-irradiation. A marked fall of activity, expressed per whole liver, was observed reaching a minimum on the 4th day following irradiation. The enzyme activity is partially and momentarily restored (on day 7), before a new decrease occurred. Furthermore, when the results are expressed per milligram of microsomal proteins, there was no change. Cysteamine, when injected in vivo, kept up the glucose-6-phosphatase of whole liver. On day 4, a histochemical demonstration of the enzyme in liver cells is in accordance with enzyme measures. These observations suggested that the enzyme quantity was altered during the acute radiation syndrome in the rat.

The finding of acute eczematous dermatitis in fishermen of the Baie de Seine led us to look for the property of the marine bryozoa Alcyonidium gelatinosum to produce skin hypersensitivity reactions. A. gelatinosum does in fact produce such reactions in the guinea-pig sensitized by the natural routes, percutaneous or respiratory. A prolonged period of sensitization is not necessary for the installation of a state of hypersensitivity. However, a second exposure of sensitization can change the characteristics of the allergic response. The skin reactions seen would appear to be a mixture of cell-mediated hypersensitivity and humoral hypersensitivity whose nature remains to be defined.

The appearance of acute eczematous dermatitis in fishermen from the estuary of the Seine, about which the responsibility of Alcyonidium gelatinosum (L.) is still under discussion, led us to estimate the ability of this Bryozoa to induce cutaneous responses of delayed hypersensitivity. Intradermal tests carried out in guinea-pigs after subcutaneous, respiratory or percutaneous sensitization, gave evidence of a clear allergenic ability of this alcyonelline. The deposit of the biological product on normal skin during four consecutive days is enough to induce strong responses of delayed hypersensitivity. This experimental study needs further investigations in which the possible existence of anaphylactic reactions should be confirmed.

Osseous cells in culture synthesize and excrete glycosaminoglycans, collagen and alkaline phosphatases, revealed by the classical histochemical reactions. Observation of the living cells iwth the polarizing microscope, after a five day-culture, reveals the presence of micro-crystals of mineral salts only at the level of cells and cellular groupings.

A technique of osseous cells culture has been perfected through discontinuous enzymatic digestion of young Mice prietal bones and using a chemically defined medium buffered by means of hepes. The cultural characteristics observed seem to correspond to those of osteogenic cells.

In the irradiated dog at different doses 250-400 R., a level plasma AMPc rise has been shown since the fourth hour with a maximum at 24 hours, returning to normal values about the thirtieth day. In irradiated at 250-300 R and secondarily enterectomised animals, nucleotide level rises 24 hours later, however this phenomenon is less intensive and later irradiated at 350 and 400 R.

The use of histo-enzymological techniques for visualizing the cholinesterasic spots on the motory plate is turned to account by the authors to point out the inhibition of the cholinesterasic processes, by some fractions of the ciguatoxins at the level of the neuro-mucular synapsis. The results obtained confirm, on one hand, the efficiency of the method to test the anti-cholinesterasic activity of some fractions of the ciguateric extracts, and, on the other hand, enable the establishment of the fact that even clinically non toxic individuals from fishspecies, dwelling in tropical coral biotops, can provoke a slightly marked but real inhibition of the cholinesterases, provided the contact between the fish extract and the neuro-motory plate is long enough in time. This observation reinforces the thesis of the ecological origin of the toxins along the alimentary chain of the reef biocoenosis.