A systematic review of genetic polymorphisms associated with binge eating disorder

The genetic polymorphisms involved in the physiopathology of binge eating disorder (BED) are currently unclear. This systematic review aims to highlight and summarize the research on polymorphisms that is conducted in the BED. We looked for observational studies where there was a genetic comparison between adults with BED, in some cases also with obesity or overweight, and healthy controls or obesity/overweight without BED. Our protocol was written using PRISMA. It is registered at PROSPERO (identification: CRD42020198645). To identify potentially relevant documents, the following bibliographic databases were searched without a time limit, but until September 2020: PubMed, PsycINFO, Scopus, and Web of Science. In total, 21 articles were included in the qualitative analysis of the systematic review, as they met the eligibility criteria. Within the selected studies, 41 polymorphisms of 17 genes were assessed. Overall, this systematic review provides a list of potentially useful genetic polymorphisms involved in BED: 5-HTTLPR (5-HTT), Taq1A (ANKK1/DRD2), A118G (OPRM1), C957T (DRD2), rs2283265 (DRD2), Val158Met (COMT), rs6198 (GR), Val103Ile (MC4R), Ile251Leu (MC4R), rs6265 (BNDF), and Leu72Met (GHRL). It is important to emphasize that Taq1A is the polymorphism that showed, in two different research groups, the most significant association with BED. The remaining polymorphisms need further evidence to be confirmed

Multi-compartment 3D-cultured organ-on-a-chip: Towards a biomimetic lymph node for drug development

The interaction of immune cells with drugs and/or with other cell types should be mechanistically investigated in order to reduce attrition of new drug development. However, they are currently only limited technologies that address this need. In our work, we developed initial but significant building blocks that enable such immune-drug studies. We developed a novel microfluidic platform replicating the Lymph Node (LN) microenvironment called LN-on-a-chip, starting from design all the way to microfabrication, characterization and validation in terms of architectural features, fluidics, cytocompatibility, and usability. To prove the biomimetics of this microenvironment, we inserted different immune cell types in a microfluidic device, which showed an in-vivo-like spatial distribution. We demonstrated that the developed LN-on-a-chip incorporates key features of the native human LN, namely, (i) similarity in extracellular matrix composition, morphology, porosity, stiffness, and permeability, (ii) compartmentalization of immune cells within distinct structural domains, (iii) replication of the lymphatic fluid flow pattern, (iv) viability of encapsulated cells in collagen over the typical timeframe of immunotoxicity experiments, and (v) interaction among different cell types across chamber boundaries. Further studies with this platform may assess the immune cell function as a step forward to disclose the effects of pharmaceutics to downstream immunology in more physiologically relevant microenvironments

A microfabricated physical sensor for atmospheric mercury monitoring,”

Abstract A new microfabricated physical sensor for elemental gaseous mercury (Hg 0 ) determinations has been developed and experimentally tested by the authors. Hg 0 represents 90-99% of atmospheric mercury forms. The sensor is based on the technique of resistivity variation of thin gold film, characterised by high selectivity and absence of optical parts. The sensor consists of four identical thin gold film resistors mounted in Wheatstone bridge configuration. Two resistors work as sensitive elements and the others as reference, in order to minimise the influence of temperature variation. The absorption of Hg 0 on the gold film produces a change in the resistivity of the amalgam. Far from the saturation, this change is proportional to the amount of the absorbed Hg 0 . The adsorption behaviour of the sensor deposited by sputtering on two different substrates (glass and Printed Circuit Board (PCB)) have been investigated. The sensors showed to work in a large range of linearity and need a low power during the regeneration process. Sensors on glass and PCB substrates underwent numerous regeneration cycles without inflicting any mechanical or electrical damages to the resistors. The presented experimental results describe the features of both sensors pointing out advantages and drawbacks of the used substrates. The PCB substrate seems to have more suitable characteristics for developing a new mercury 'smart' sensor

ODEs model of foreign body reaction around peripheral nerve implanted electrode

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