glycogen and Schistosomiasis-mansoni

It had been suggested that chronic exposure to Schistosoma mansoni prevents the onset of Th1-mediated diseases such as diabetes mellitus. The present study was carried out on four groups of mice: (1) control group, (2) group infected with S. mansoni, (3) group injected with streptozotocin to induce diabetes, and (4) group infected and then 3 months postinfection injected with streptozotocin. No differences were detected between the infected non-diabetic and infected diabetic groups regarding worm burden, tissue egg count, and oogram. At the same time, results showed a reducing effect of S. mansoni infection on the rate of glucose uptake by the diaphragm with reduction in glycogen content of soleus muscle. This an important issue since skeletal muscle is the primary site for insulin-stimulated glucose disposal. In conclusion, because of the detected depressed peripheral glucose uptake by the diaphragm, the protecting effect of helminths infection in diabetes should be reconsidered, to be able to devise therapeutic strategies for the treatment of autoimmune diseases.

Topics: Animals; Diabetes Mellitus, Experimental; Diaphragm; Female; Glucose; Glycogen; Intestines; Liver; Mice; Muscle, Skeletal; Parasite Egg Count; Schistosoma mansoni; Schistosomiasis mansoni

Hamsters infected with Schistosoma mansoni were operated upon to install a permanent canula into their blood stream. After recovery of the hamster, this canula was used for the injection of radioactively labelled glucose. In this way the glycogen metabolism of S. mansoni could be studied while the parasites remained undisturbed in their natural habitat. The consecutive injection of [U-14C]glucose and [1-3H]glucose permitted an analysis of possible changes in the glycogen synthesis of individual worm pairs with time. The results showed that the synthesis of glycogen by each worm pair was fairly constant with time. Furthermore, all individual worm pairs synthesised glycogen continuously; not even 2 min passed without its formation. Only small differences in glycogen synthesis were observed between parasites isolated from different locations in the veins of the hamster. These results exclude the possibility that the worm pairs had alternating periods of glycogen synthesis and degradation, and they also disprove the idea that synthesis and degradation occur at two different sites in the bloodstream of the hamster. The experiments further showed that glycogen synthesis was proportional to the amount of glycogen already present, which in turn was shown to be proportional to the size of the parasite. From this study it can be concluded that the replenishment of the endogenous glycogen reserves of S. mansoni is not induced by a marked decrease in the glycogen levels, but occurs slowly and continuously.

Topics: Animals; Cricetinae; Glucose; Glycogen; Helminth Proteins; Injections, Intravenous; Kinetics; Schistosoma mansoni; Schistosomiasis mansoni

Topics: Animals; Cricetinae; Glycogen; Schistosoma mansoni; Schistosomiasis mansoni

A detailed study was made of the changes in the carbohydrate metabolism of Schistosoma mansoni occurring during both the penetration of the skin of a hamster and the subsequent development of the schistosome in the lung, liver, and mesenteric veins of the host. During infection, within a few hours a transition occurs from a fully aerobic to a largely anaerobic energy metabolism. By 5 h postinfection, about 6% of carbohydrate breakdown occurs in the aerobic reactions of the Krebs cycle, whereas the rest occurs in the anaerobic formation of lactate. The contribution of aerobic processes to carbohydrate breakdown remains at this level of 6% until 3 weeks postinfection and then gradually declines to the adult level of 2.5%. Measurement of the protein content of developing schistosomes shows that an exponential growth occurs over a 15-day period after the arrival of the schistosomes in the liver (days 11-25 postinfection). During this period the protein content of the parasites increases about 100-fold, but despite this change in size, no major changes occur in the end-product pattern of carbohydrate breakdown. We conclude that during this period the rate of oxygen diffusion into the tissues is not a limiting factor for aerobic metabolism. A limited diffusion of oxygen may play a role in the decreasing contribution of aerobic processes during the later stages of maturation of the schistosomes.

Topics: Aerobiosis; Anaerobiosis; Animals; Carbohydrate Metabolism; Carbon Dioxide; Citric Acid Cycle; Cricetinae; Energy Metabolism; Glycogen; Lactates; Lung; Proteins; Schistosoma mansoni; Schistosomiasis mansoni; Skin

Within 24 hr of treatment of the mouse host with BW484C, 2-[5-nitro-2-(pivaloylimino)-4-thiazoline-3-yl]diacetamide, pairs of Schistosoma mansoni exhibited "hepatic shift" and began to leave the mesenteric veins. The tegument of the males was altered, both morphologically and physiologically, while that of females was unaffected. This morphological damage to males correlated well with therapeutic efficacy against both sexes in a range of analogues of BW484C. However, parasites removed from mice after treatment but before the hepatic shift and then maintained in vitro were far from moribund as treated males could be maintained for 8 days in vitro, although this was 5 days less than males from untreated mice. Females survived as well as control worms. In contrast, male and female S. mansoni remaining in their host after therapy were invaded by host cells in the liver after 2 days. The morphological effects and reduction of the in vitro survival of males treated in the mouse and removed after 24 hr could be simulated by in vitro exposure for 24 hr to 10(-5) M BW484C. Females were not susceptible to this regime. It was concluded that worm pairs were swept to the liver as a result of drug dependent damage to the tegument of the male and that phagocytic invasion of male and female schistosomes by host cells within the liver was an important factor in the efficacy of BW484C. The biochemical events underlying the effects on the tegument of male worms remain unknown.

Topics: Animals; Female; Glucose; Glycogen; Imines; Liver; Male; Mice; Microscopy, Electron; Phagocytosis; Schistosoma mansoni; Schistosomiasis mansoni; Schistosomicides; Thiazoles