[Effect of aeration on composting of date palm residues contaminated with Fusarium oxysporum f.sp. albedinis]. / Incidence de l'aération sur le traitement par compostage des sous-produits du palmier dattier contaminés par Fusarium oxysporum f.sp. albedinis.

Composting of date palm (Phoenix dactylifera L.) residues contaminated with Fusarium f.sp oxysporum albedinis, causal agent of the vascular wilt (Bayoud) of the date palm, has been achieved. The effect of the aeration of the piles by manual turning has been studied. The maintenance of an adequate humidity of 60%-70%, necessary to the good progress of the composting process, required the contribution of 11.4 L of water/kg of the dried residues. The evolution of the temperatures in the three piles presents the same phases. A latency phase, followed after 2-3 d of composting by a thermophilic phase, which lasts about 24 d, where the temperature remains elevated between 50 and 70 degrees C. Then a cooling phase that takes about 15 d, during which the temperatures fall to values between 25 and 35 degrees C, near room temperature. Fusarium f.sp oxysporum albedinis is eliminated completely during the thermophilic phase of composting, and increasing frequencies of turning accelerate its disappearance to a certain extent. On the other hand, pH remained steady and relatively basic oscillating between 8.2 and 8.7. Ninety percent (90%) of the the date palm residues are composed exclusively of organic matters. The total nitrogen represents only 0.4%. The contribution of manure decreases the ratio of carbon to nitrogen (C/N) from 115 to 48 in the initial mixture. After 80 d of composting and according to the frequency of return up, there is a reduction of the granulometry of the substratum, the C/N ratio (from 29% to 44%), the organic matter (from 15% to 23%), the total volume (from 25% to 35%), and of the dry weight of the swaths (from 16% to 24%). On the other hand there is an increase in total nitrogen rate (from 20% to 40%) and in the mineral matter (from 23% to 35%).

Inhibition of proteoglycan synthesis induces an increase in follicle stimulating hormone (FSH)-stimulated estradiol production by immature rat Sertoli cells.

In order to define the possible involvement of proteoglycans (PG) in the regulation of Sertoli cell functions, we have examined the effect of para-nitrophenyl-beta-D-xyloside (PNPX), a specific inhibitor of PG synthesis, on follicle stimulating hormone (FSH)-dependent estradiol production by immature rat Sertoli cells. Addition of PNPX to the culture medium induced a dose-dependent inhibition of 35S-labeled PG synthesis in Sertoli cells both in the medium and the cell layer. Simultaneously there was a drastic increase in 35S-labeled secreted glycosaminoglycans. By 1 mM PNPX, syntheses of chondroitin sulfate proteoglycans released into culture medium and of heparan sulfate proteoglycans associated with the cell layer were 35% of values from untreated cells. Simultaneously, PNPX induced a twofold (mean of seven experiments, range 17-250%) enhancement of FSH (100 ng/ml)-stimulated estradiol production. In each individual experiment, there was an inverse relationship between the amplitude of PNPX-induced increase in FSH responsiveness and the FSH capability to stimulate basal estradiol production in cultured rat Sertoli cells. The effect of PNPX on FSH-stimulated aromatase activity was not mimicked by para-nitrophenyl-beta-D-galactoside, a structural analog of PNPX that has no effect on PG synthesis. The (Bu)2cAMP-stimulated estradiol synthesis was not modified in the presence of PNPX. Moreover, PNPX enhancement of FSH-stimulated estradiol synthesis disappeared when Sertoli cells were cultured in the presence of 1-methyl-3-isobutylxanthine, an inhibitor of phosphodiesterase activity. These findings suggest that inhibition of PG synthesis under PNPX conditions did not affect signal transduction steps distal to cAMP but rather decreased the phosphodiesterase activity in Sertoli cells.(ABSTRACT TRUNCATED AT 250 WORDS)

Proteoglycan biosynthesis by rabbit articular chondrocytes treated with D-penicillamine.

Rabbit articular chondrocytes in confluent monolayer cultures were treated with D-Penicillamine (D-Pen) during 3 or 5 days. The [35S]-sulfate incorporation in neosynthesized proteoglycans was not modified by D-Pen doses ranging from 50 to 800 micrograms/ml. After treatment during 5 days with D-Pen concentrations of 50 or 400 micrograms/ml, the chemical characteristics of proteoglycans from medium and cell-layer were determined. The aggregation capacity of proteoglycans from medium, the monomer molecular size, the glycosaminoglycan chain length and the relative rates of the different glycosaminoglycans (chondroitins, chondroitin 6-sulfate, chondroitin 4-sulfate, hyaluronic acid) remained unchanged. These results suggest that D-Pen does not alter some of the cartilage mechanical properties due to the presence of proteoglycans.

Calcium ionophore and phorbol myristate acetate synergistically inhibited proteoglycan biosynthesis in articular chondrocytes by prostaglandin independent mechanism.

In rabbit articular chondrocytes, phorbol myristate acetate (PMA), 1,2-dioctanoyl-sn-glycerol (DG) and calcium ionophore (A23187), reduced the proteoglycan synthesis, in a dose-dependent manner. The combined treatment by PMA and A23187 resulted in an enhanced inhibition of proteoglycan production, indicating a synergistic effect. In presence of PMA or A23187, the release of prostaglandin E2 (PGE2) was dramatically increased. The addition of indomethacin and BW755c to chondrocytes stimulated by PMA or A23187, suppressed the liberation of PGE2, but did not stop the decrease of proteoglycan synthesis.