Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.

In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field

Bone tissue, blood lipids and inflammatory profiles in adolescent male athletes from sports contrasting in mechanical load

Exploring the effect of non-impact and impact sports is particular relevant to understand the interaction between skeletal muscle and bone health during growth. The current study aimed to compare total and regional bone and soft-tissue composition, in parallel to measurements of blood lipid and inflammatory profiles between adolescent athletes and non-athletes. Anthropometry, biological maturity, dual energy X-ray absorptiometry (DXA) scans, training load and lipid and inflammatory profiles were assessed in a cross-sectional sample of 53 male adolescents (20 non-athletes, 15 swimmers and 18 basketball players) aged 12-19 years. Multiple comparisons between groups were performed using analysis of variance, covariance and magnitude effects (ES-r and Cohen's d). The comparisons of controls with other groups were very large for high-sensitivity C-reactive protein (d range: 2.17-2.92). The differences between sports disciplines, regarding tissue outputs obtained from DXA scan were moderate for all variables except fat tissue (d = 0.4). It was possible to determine small differences (ES-r = 0.17) between controls and swimmers for bone area at the lower limbs (13.0%). In parallel, between swimmers and basketball players, the gradient of the differences was small (ES-r range: 0.15-0.23) for bone mineral content (24.6%), bone area (11.3%) and bone mineral density (11.1%) at the lower limbs, favoring the basketball players. These observations highlight that youth male athletes presented better blood and soft tissues profiles with respect to controls. Furthermore, sport-specific differences emerged for the lower limbs, with basketball players presenting higher bone mineral content, area and density than swimmers

Produção e qualidade de frutos de tomateiro cultivado em substrato com zeólita Yield and fruit quality of tomato grown in substrate with zeolite

Avaliou-se a produção e a qualidade dos frutos de tomateiro cv. Finestra, cultivado em substrato com zeólita enriquecida com N, P e K. Os tratamentos utilizados foram quatro doses (20; 40; 80 e 160 g por vaso) de zeólitas enriquecidas com H3PO4/apatita, KNO3 e KH2PO4, além de uma testemunha cultivada em solução nutritiva. Foram avaliados a produção de frutos por vaso, firmeza, sólidos totais, pH, acidez titulável e ácido ascórbico dos frutos, dos 80 aos 90 dias de cultivo. O fornecimento de nutrientes através do mineral zeólita enriquecido com N, P e K comprovou ser uma alternativa para o aumento da produção. As maiores produções foram obtidas nos tratamentos com adição de P e K e nas maiores doses de zeólita (160 e 80 g por vaso). A produção de frutos foi 11 a 17% maior em relação à testemunha cultivada com solução nutritiva. Houve efeitos positivos das zeólitas enriquecidas com fontes de fósforo sobre a firmeza e efeito negativo sobre o pH. A firmeza dos frutos variou 104% entre tratamentos, de 7,06 N (ZNK 160) a 14,38 (ZPK 40). O aumento da disponibilidade de potássio contribuiu para o aumento do teor de ácido ascórbico dos frutos.<br>We evaluated yield and quality of tomato fruits, cv. Finestra, grown in a zeolite substrate enriched with N, P and K. Treatments comprised four levels (20; 40; 80 and 160 g per pot) of zeolite enriched with H3PO4/apatite, KNO3 and KH2PO4, and a control grown in a nutrient solution. Fruit production, firmness, total soluble solids, pH, titratable acidity and ascorbic acid were evaluated from 80 to 90 days of plant cultivation. Nutrients supplied through the mineral zeolite enriched with N, P and K was an adequate alternative to increase the production. Higher fruit production was obtained with addition of P and K and higher zeolite dosis (160 and 80 g per pot). Fruit production was 11% and 17% higher when compared to the plants grown in nutritive solution (check treatment). Positive effects were observed in P-enriched zeolites in relation to fruit firmness, and negative effects over fruit pH. Fruit firmness varied 104% among treatments, from 7.06N (ZNK 160) to 14.38N (ZPK 40). The increase of potassium availablity increased the ascorbic acid levels of the fruits