Strategies of success for social networks: Mermaids and temporal evolution

The main goal of this article is to investigate techniques that can quickly lead to successful social systems by boosting network connectivity. This is especially useful when starting new online communities where the aim is to increase the system utilization as much as possible. This aspect is very important nowadays, given the existence of many online social networks available on the web, and the relatively high level of competition. In other words, attracting users' attention is becoming a major concern, and time is an essential factor when investing money and resources into online social systems. Our study describes an effective technique that deals with this issue by introducing the notion of mermaids, special attractors that alter the normal evolutive behavior of a social system. We analyze how mermaids can boost social networks, and then provide estimations of fundamental parameters that business strategists can take into account in order to obtain successful systems within a constrained budget

Paracetamol metabolism, hepatotoxicity, biomarkers and therapeutic interventions: a perspective

After over 60 years of therapeutic use in the UK, paracetamol (acetaminophen, N-acetyl-p-aminophenol, APAP) remains the subject of considerable research into both its mode of action and toxicity. The pharmacological properties of APAP are the focus of some activity, with the role of the metabolite N-arachidonoylaminophenol (AM404) still a topic of debate. However, that the hepatotoxicity of APAP results from the production of the reactive metabolite N-acetyl-p-benzoquinoneimine (NAPQI/NABQI) that can deplete glutathione, react with cellular macromolecules, and initiate cell death, is now beyond dispute. The disruption of cellular pathways that results from the production of NAPQI provides a source of potential biomarkers of the severity of the damage. Research in this area has provided new diagnostic markers such as the microRNA miR-122 as well as mechanistic biomarkers associated with apoptosis, mitochondrial dysfunction, inflammation and tissue regeneration. Additionally, biomarkers of, and systems biology models for, glutathione depletion have been developed. Furthermore, there have been significant advances in determining the role of both the innate immune system and genetic factors that might predispose individuals to APAP-mediated toxicity. This perspective highlights some of the progress in current APAP-related research

Potencial alelopático de Annona crassiflora: efeitos sobre plantas daninhas.

A alelopatia pode oferecer novas substâncias químicas com propriedades herbicidas menos prejudiciais ao ambiente e ao homem do que os sintéticos em uso na atual agricultura. Nesse contexto, foi avaliado o efeito de extratos de Annona crassiflora sobre a germinação e o desenvolvimento de Brachiaria brizantha, Euphorbia heterophylla e Ipomoea grandifolia, bem como o efeito do extrato mais promissor sobre a soja (Glycine max). Para isso, foram preparados extratos hidroalcoólicos de sementes, folhas e caules de A. crassiflora, a fim de serem avaliados em testes de germinação e desenvolvimento das plantas daninhas. O extrato da parte mais promissora da planta foi fracionado, utilizando-se solventes em ordem crescente de polaridade. Em relação às partes da planta de A. crassiflora avaliadas, o extrato hidroalcoólico preparado a partir das sementes proporcionou maior interferência nas plantas daninhas; a germinação das sementes de Brachiaria brizantha e Euphorbia heterophylla foi totalmente inibida por esse extrato. De modo geral, as espécies receptoras foram mais sensíveis à fração acetato de etila, mas esta não influenciou o desenvolvimento da soja. Portanto, A. crassiflora apresenta potencial para o manejo de B. brizantha, E. heterophylla e I. grandifolia, em pós-emergência na cultura da soja

Multidisciplinary recommendations for essential baseline functional and laboratory tests to facilitate early diagnosis and management of immune-related adverse events among cancer patients.

Immune checkpoint inhibitors (ICIs) have fundamentally changed the treatment landscape of various cancers. While ICI treatments result in improved survival, quality of life and are cost-effective, the majority of patients experience at least one immune-related adverse event (irAE). Many of these side effects cause little discomfort or are asymptomatic; however, irAEs can affect any organ and are potentially life-threatening. Consequently, early diagnosis and appropriate treatment of irAEs are critical for optimizing long-term outcomes and quality of life in affected patients. Some irAEs are diagnosed according to typical symptoms, others by abnormal findings from diagnostic tests. While there are various guidelines addressing the management of irAEs, recommendations for the early recognition of irAEs as well as the optimal extent and frequency of laboratory tests are mostly lacking. In clinical practice, blood sampling is usually performed before each ICI administration (i.e., every 2-3 weeks), often for several months, representing a burden for patients as well as health care systems. In this report, we propose essential laboratory and functional tests to improve the early detection and management of irAEs and in cancer patients treated with ICIs. These multidisciplinary expert recommendations regarding essential laboratory and functional tests can be used to identify possible irAEs at an early time point, initiate appropriate interventions to improve patient outcomes, and reduce the burden of blood sampling during ICI treatment

Defective monocyte oxidative burst predicts infection in alcoholic hepatitis and is associated with reduced expression of NADPH oxidase

Objective In order to explain the increased susceptibility to serious infection in alcoholic hepatitis, we evaluated monocyte phagocytosis, aberrations of associated signalling pathways and their reversibility, and whether phagocytic defects could predict subsequent infection. Design Monocytes were identified from blood samples of 42 patients with severe alcoholic hepatitis using monoclonal antibody to CD14. Phagocytosis and monocyte oxidative burst (MOB) were measured ex vivo using flow cytometry, luminometry and bacterial killing assays. Defects were related to the subsequent development of infection. Intracellular signalling pathways were investigated using western blotting and PCR. Interferon-γ (IFN-γ) was evaluated for its therapeutic potential in reversing phagocytic defects. Paired longitudinal samples were used to evaluate the effect of in vivo prednisolone therapy. Results MOB, production of superoxide and bacterial killing in response to Escherichia coli were markedly impaired in patients with alcoholic hepatitis. Pretreatment MOB predicted development of infection within two weeks with sensitivity and specificity that were superior to available clinical markers. Accordingly, defective MOB was associated with death at 28 and 90 days. Expression of the gp91phox subunit of nicotinamide adenine dinucleotide phosphate (NADPH) oxidase was reduced in patients with alcoholic hepatitis demonstrating defective MOB. Monocytes were refractory to IFN-γ stimulation and showed high levels of a negative regulator of cytokine signalling, suppressor of cytokine signalling-1. MOB was unaffected by 7 days in vivo prednisolone therapy. Conclusions Monocyte oxidative burst and bacterial killing is impaired in alcoholic hepatitis while bacterial uptake by phagocytosis is preserved. Defective MOB is associated with reduced expression of NADPH oxidase in these patients and predicts the development of infection and death

Coletor de esporos: descrição, uso e resultados no manejo da ferrugem-asiática da soja.

bitstream/item/220504/1/Circ-Tec-167.pd

Monitoramento de Phakopsora pachyrhizi na safra 2019/2020 para tomada de decisão do controle químico da ferrugem-asiática da soja.

bitstream/item/216948/1/Circ-Tec-164.pd