Histochemistry of implantation in the rabbit

Summary The distribution of glycogen, acid and neutral mucopolysaccharides, hydrolases alkaline phosphatases, and carbohydrate dehydrogenases is described in the rabbit blastocyst and its surroundings over the implantation period from 5 to 9 days.Glycogen is found mainly in the embryonic tissues, where peaks of concentration coincide with differentiation, some is also seen in the uterine epithelium and secretion, and large quantities accumulate in the developing decidua.Neutral mucopolysaccharide is found in the yolk-sac and embryonic endoderm, and as secretion droplets in the uterine epithelium and secretion.Acid mucopolysaccharide occurs in the embryonic coverings and uterine secretion.RNA is associated in the embryo with developing tissues, and accumulates in the developing decidual cells.Hydrolases (acid phosphatase, and B esterase) increase their activity in the trophoblast knobs, in developing syncytiotrophoblast, and in the embryonic endoderm. Degeneration of the uterine epithelium is associated with maximal hydrolase activity.Trophoblastic alkaline phosphatase activity (non-specific and specific) decreases from 5 to 7 days of gestation, then increases markedly in the developing syncytiotrophoblast. AMPase appears in the embryonic mesoderm. In the uterine epithelium intense brush border staining is seen, and TPPase and UDPase become visible for a short period in the Golgi region. Phosphatases increase their activity in the decidua to 8 days and then decrease.Carbohydrate dehydrogenases (except -glycero-phosphate and -hydroxy-butyrate dehydrogenases) increase their activity in embryonic tissues, particularly in the developing syncytiotrophoblast and endoderm. Symplasma formation in the uterine epithelium is also associated with increase in enzyme activity, and a similar increase, up to 8 days of gestation, is seen in the decidua with isocitrate, malate, glucose-6-phosphate, lactate, succinate, and furfuryl alcohol dehydrogenases.Some correlation is found between the histochemical findings and the phenomena of epithelial removal, uterine secretion, decidual formation and function, giant cell function, morphogenesis, and histiotrophic nutrition, and the results are compared with previous findings for the rat in which implantation is morphologically, and probably physiologically a very different process.     

Comparative histochemical distribution of “leucine amino-peptidase” in the placenta and foetal membranes

Summary The distribution of an enzyme, or enzymes hydrolysing l-leucyl--naphthylamide is studied in the placentae, foetal membranes, and uterine structures of the horse, sheep, cat, dog, ferret, rat, rabbit, guinea-pig, and human. Activity is seen mainly in the trophoblast (except that of the cat, dog, and guinea-pig), in the rodent yolk-sac endoderm (except that of the rat), or in the uterine epithelium — surface (sheep and guinea-pig) or glandular (dog). The presence of the enzyme or enzymes is correlated with possible functions in absorption and transport of materials, or in elaboration and release of complex molecules.     

Pulsed-field gel analysis of human immunoglobulin heavy-chain constant region gene deletions reveals the extent of unmapped regions within the locus

The human immunoglobulin heavy-chain constant region gene locus is organized in three main gene groups, the physical distances of which are unknown. Different types of gene deletions, originated by unequal crossingover, have been found to encompass one or more genes in the locus. We have analyzed some of these deletions by means of pulsed-field gel electrophoresis, which allows resolution of large DNA fragments. By identifying a fragment containing two of the main gene groups and by observing the size reduction of this fragment in subjects with deletions, we were able to estimate the distance between the two groups and better locate the pseudogene in-between.     

Internal desynchronization of circadian rhythms and tolerance of shift work

Fifteen male subjects including 12 shift workers (oil refinery operators) volunteered to document circadian rhythms in sleep-wake, grip strength of both hands, peak expiratory flow, heart rate, self-rated drowsiness, fatigue and attention. Each of these variables was measured 4 to 6 times/day for 2 to 3 weeks. In addition, both axillary temperature (with a shielded probe) and wrist activity were almost continuously recorded at 15 min intervals during the same time span. Individual time series were analyzed according to several statistical methods (power spectrum, cosinor, chi 2, etc.), in order to estimate the prominent circadian period tau and to evaluate both individual and subgroup differences with regard to tolerance of shift work, age, duration of shift work. The present study confirms for continuously recorded temperature and wrist activity, grip strength of both hands, heart rate and peak expiratory flow that intolerance of shift work is frequently associated with an internal desynchronization. However, this conclusion cannot be extended to circadian rhythms in self-rated drowsiness, fatigue and attention. The internal desynchronization among several circadian rhythms supports the hypothesis that these latter are driven by several oscillators, with presumable differences between right and left hemispheres as suggested by unequal values of tau in rhythms of both hand grip strength. Since an internal desynchronization can be observed in tolerant shift workers having no complaint, it is likely that symptoms of intolerance are related to the subject's sensitivity to internal desynchronization rather than to the desynchronization itself.