.Quadrupole time of flight mass spectrometric identification of differentially expressed uterine proteins with respect to pregnancy

We consider a differentiated duopoly where firms invest in research and development (R&D) to reduce their production cost. The objective of this study is to derive and compare Bertrand and Cournot equilibria, and then examine the robustness of the literature's results, especially those of Qiu (1997). We find that The main results of this study are as follows: (a) Bertrand competition is more efficient if R&D productivity is low, industry spillovers are weak, or products are very different. (b) Cournot competition is more efficient if R&D productivity is high and R&D spillovers and products' degree of substitutability are not very small. (c) Cournot competition may lead to higher Outputs, higher consumer surpluses and lower prices, provided that R&D productivity is very high and spillovers and degree of substitutability of firms' products are moderate to high, (d) Cournot competition results in higher R&D Investments compared to Bertrand's. These results show that the relative efficiencies of Bertrand and Cournot equilibria are sensitive to the suggested specifications, and hence far from being robust.

.Protein expression in human granulosa cell subtypes

We consider a differentiated duopoly where firms invest in research and development (R&D) to reduce their production cost. We show that if the firms play a one stage game, i.e., they choose R&D and price (in Bertrand game) or quantity (in Cournot game)at the same time, then the usual result stating that Bertrand competition is more efficient than Cournot competition still holds.

Using an infinite-horizon two-player differential game, we derive and compare Bertrand and Cournot equilibria for a differentiated duopoly engaging in the process of R&D competition. The main findings of this study are as follows. First, Bertrand competition is more efficient if either R&D productivity is low or products are very different. Second, Cournot competition is more efficient provided that R&D productivity is high, products are close substitutes, and spillovers are not close to zero. This last result is different from what has been obtained in the literature. Hence, this shows that considering a dynamic model and more general investment costs does have an impact on the efficiency results.

Objective: The present study investigates the effects of alprazolam (ALP) and nifedipine alone or in combination on behavior and on g-aminobutyric acid (GABA) levels, in discrete brain regions of albino rats.

Methods: The anxiolytic effect was studied using a plus maze model and brain levels of GABA were measured using high performance liquid chromatography. Four acute treatment groups of rats were used. In the first they were treated with 1% Tween 80 (1ml/kg), in the second with nifedipine (10mg/kg), in the third with ALP (2mg/kg) and in the fourth with ALP in addition to nifedipine in the respective doses. The work was carried out at the Faculty of Pharmacy of Al-Fateh University, Tripoli, Libya in the first half of 2002.

Results: The results indicate that the anxiolytic effect of ALP was not modified by nifedipine. Nifedipine by itself significantly decreased the motor activity (decrease in total lines crossed), this effect was apparently antagonized by ALP. Alprazolam administration produced an increase of GABA levels in cerebellum and striatum and a decrease in the brain stem. Nifedipine per-se had no effect on GABA levels in the brain stem but it partially antagonized ALP-induced inhibitory effect on GABA in this region. Alprazolam significantly increased GABA levels in the striatum, while nifedipine alone had no effect on neurotransmitter levels and did not modify the ALP effect in this brain region. Alprazolam or nifedipine had no significant effect on GABA levels in midbrain, cerebral cortex and whole brain. There were no significant changes in GABA levels in midbrain and whole brain with drug combination. However, the combination decreased GABA levels significantly in the cerebral cortex.

Conclusion: It may be concluded that, the anxiolytic effect of ALP possibly occurs through changes in brain GABA levels (an increase in cerebellum and striatum with a decrease in brain stem). The effect was not modified by nifedipine which per se had no affect on GABA levels in any brain area. The significant decrease in GABA levels in cerebral cortex by ALP-nifedipine combination may be due to the mutual closure of calcium channel (mentioned in literature) resulting in inhibition of the EAA-ergic input to GABA-ergic neuron.

Liver cells of the twenty-one day old rat embryo are isolated by a modified method and autophagy is studied in them by electron microscopic morphology and morphometry. Immediately after isolation or 2.5 h incubation in nutrient-free medium, embryonic hepatocytes contain high amount of glycogen and only very few autophagic vacuoles. In contrast, all glycogen is lost and 15% of the cytoplasmic volume is occupied by late autophagic vacuoles in hepatocytes after 18 h in the same medium. Presence of 3- methyladenine in the latter case inhibits both the loss of glycogen and the appearance of autophagic vac- uoles while enlarging the multivesicular body compartment. Our findings reveal major differences between isolated embryonic and adult hepatocytes concerning autophagy. Several types of autophagic vacuoles are described in the cell types of the erythropoietic cell lineage. This means that autophagy is an …