Spectrum Slicing for Multiple Access Channels with Heterogeneous Services.

Wireless mobile networks from the fifth generation (5G) and beyond serve as platforms for flexible support of heterogeneous traffic types with diverse performance requirements. In particular, the broadband services aim for the traditional rate optimization, while the time-sensitive services aim for the optimization of latency and reliability, and some novel metrics such as Age of Information (AoI). In such settings, the key question is the one of spectrum slicing: how these services share the same chunk of available spectrum while meeting the heterogeneous requirements. In this work we investigated the two canonical frameworks for spectrum sharing, Orthogonal Multiple Access (OMA) and Non-Orthogonal Multiple Access (NOMA), in a simple, but insightful setup with a single time-slotted shared frequency channel, involving one broadband user, aiming to maximize throughput and using packet-level coding to protect its transmissions from noise and interference, and several intermittent users, aiming to either to improve their latency-reliability performance or to minimize their AoI. We analytically assessed the performances of Time Division Multiple Access (TDMA) and ALOHA-based schemes in both OMA and NOMA frameworks by deriving their Pareto regions and the corresponding optimal values of their parameters. Our results show that NOMA can outperform traditional OMA in latency-reliability oriented systems in most conditions, but OMA performs slightly better in age-oriented systems.

Effect of carbamates on mRNA encoding lipid enzymes in hamster flank organs.

Flank organs are an androgen-dependent pilosebaceous complex present in male and female hamsters. These organs have been used for the evaluation of antiandrogenic drugs, which could be used for the treatment of androgen-dependent afflictions. This study demonstrated the role of four different steroidal carbamates 7-10 in the expression of mRNAs coding for different enzymes involved in the lipid metabolism in flank organs. To determine the biological effects of compounds 7-10 on the expression of mRNA coding for lipid enzymes, steroids 7-10, testosterone (T), progesterone (P), and/or 7-10 were applied on the flank organs. Later, the mRNA expression for the enzymes was determined by polymerase chain reaction. The binding of 8 and 9 to the progesterone receptor (PR) as well as their effects on the activity of 5α-reductase were also evaluated. Treatments with T, P, and 7-10 increased the mRNA expression for glycerol 3-phosphate acyl transferase (GPAT), ß-hydroxy-ß-methylglutaryl-CoA synthase (HMG-CoA-S), ß-hydroxy-ß-methylglutaryl-CoA reductase (HMG-CoA-R), phosphatidylinositol synthase (PI-S), and squalene-synthase (SQ-S). However, the combined treatments with P + 7-10 decreased the expression of GPAT, HMG-CoA-S, and HMG-CoA-R. Expression of mRNA for all enzymes was variable under treatment with T + 7-10. Data showed that these carbamates did not bind to the PR, but inhibited the activity of 5α-reductase. Carbamates 7-10 changed the mRNA expression model induced by T and P in flank organs.