Iatrogenic hypothyroidism in a hyperthyroid cat treated with 131 I = Iatrogene hypothyroïdie bij een hyperthyroïde kat behandeld met 131 I

A thirteen-year-old, male, castrated, non-azotemic European Shorthair was presented for treatment of hyperthyroidism. Thyroid scintigraphy using Tc-99m showed bilaterally enlarged thyroid glands with an increased thyroid to salivary (T/S) ratio. The cat was treated with an intravenous injection of 4.84 mCi (179MBa) I-131. One year later, the cat showed clinical deterioration, including lethargy, weight loss and a louder heart murmur; iatrogenic hypothyroidism was diagnosed. Concurrently, renal parameters were elevated compared to the pre-treatment values. Supplementation with levothyroxine was started. Four months later, the cat was euthyroid and improved creatinine values were noted. In this case report, the diagnosis and management of iatrogenic hypothyroidism in cats and the interplay with renal function are described. An algorithm with recommendations regarding diagnosis, monitoring and treatment of these cats is presented

Shape analysis of the nasal complex among South African groups from CBCT scans

Three-dimensional (3D) anatomical extraction techniques could help the forensic anthropologist in a precise and inclusive assessment of biological phenotypes for the development of facial reconstruction methods. In this research, the nose morphology and the underlying hard tissue of two South African populations were studied. To this end, a 3D computer-assisted approach based on an automated landmarking workflow was used to generate relevant 3D anatomical components, and shape discrepancies were investigated using a data set of 200 cone-beam computer tomography (CBCT) scans. The anatomical landmarks were placed on the external nose and the mid-facial skeleton (the nasal bones, the anterior nasal aperture, the zygoma, and the maxilla). Shape differences related to population affinity, sex, age, and size were statistically evaluated and visualised using geometric morphometric methods. Population affinity, sexual dimorphism, age, and size affect the nasal complex morphology. Shape variation in the mid-facial region was significantly influenced by population affinity, emphasising that shape variability was specific to the two population groups, along with the expression of sexual dimorphism and the effect of ageing. In addition, nasal complex shape and correlations vary greatly between white and black South Africans, highlighting a need for reliable population-specific 3D statistical nose prediction algorithms. Significance: • 3D anatomical structures were acquired and extracted from 200 CBCT scans of modern South Africans. • Geometric morphometric methods were applied. • Soft- and hard-tissue nasal complex morphology vary across South African groups

Amyloid-β Oligomers Regulate ADAM10 Synaptic Localization Through Aberrant Plasticity Phenomena

A disintegrin and metalloproteinase 10 (ADAM10) is a synaptic enzyme that has been previously shown to limit amyloid-\u3b21-42 (A\u3b21-42) peptide formation in Alzheimer's disease (AD). Furthermore, ADAM10 participates to spine shaping through the cleavage of adhesion molecules and its activity is under the control of synaptic plasticity events. In particular, long-term depression (LTD) promotes ADAM10 synaptic localization triggering its forward trafficking to the synapse, while long-term potentiation elicits ADAM10 internalization. Here, we show that a short-term in vitro exposure to A\u3b21-42 oligomers, at a concentration capable of inducing synaptic depression and spine loss, triggers an increase in ADAM10 synaptic localization in hippocampal neuronal cultures. However, the A\u3b21-42 oligomers-induced synaptic depression does not foster ADAM10 delivery to the synapse, as the physiological LTD, but impairs ADAM10 endocytosis. Moreover, A\u3b21-42 oligomers-induced inhibition of ADAM10 internalization requires neuronal activity and the activation of the NMDA receptors. These data suggest that, at the synaptic level, A\u3b21-42 oligomers trigger an aberrant plasticity mechanism according to which A\u3b21-42 oligomers can downregulate A\u3b2 generation through the modulation of ADAM10 synaptic availability. Moreover, the increased activity of ADAM10 towards its synaptic substrates could also affect the structural plasticity phenomena. Overall, these data shed new lights on the strict and complex relationship existing between synaptic activity and the primary mechanisms of AD pathogenesis

New data on OZI rule violation in bar{p}p annihilation at rest

The results of a measurement of the ratio R = Y(phi pi+ pi-) / Y(omega pi+ pi-) for antiproton annihilation at rest in a gaseous and in a liquid hydrogen target are presented. It was found that the value of this ratio increases with the decreasing of the dipion mass, which demonstrates the difference in the phi and omega production mechanisms. An indication on the momentum transfer dependence of the apparent OZI rule violation for phi production from the 3S1 initial state was found.Comment: 11 pages, 3 PostScript figures, submitted to Physics Letter

Towards a Learning System for University Campuses as Living Labs for Sustainability

Universities, due to their sizeable estates and populations of staff and students, as well as their connections with, and impact within, their local and wider communities, have significant environmental, social and economic impacts. There is a strong movement for universities to become leaders in driving society towards a more sustainable future, through improving the sustainability of the built environment and the universities’ practices and operations, and through their educational, research and wider community engagement missions. Around the globe the concept of ‘Living Labs’ has emerged as an instrument to integrate these different aspects to deliver sustainability improvements, through engaging multiple stakeholders in all of these areas, and through the co-creation of projects to improve the sustainability of the campus environment and operations, and to link these to the education, research, and wider community missions of the institution. This chapter describes a living, shared framework and methodology, the ‘Campus as Living Lab’ learning system, created through global participatory workshops and Living Lab literature, aimed at supporting universities and their Sustainability (Coordinating) Offices in the development and monitoring of Living Lab projects. The framework includes seven categories of supportive data collection and three levels of details to meet different requirements of potential users. The Living Lab framework presented in this chapter, aims to create value and help universities maximise the benefit of Living Lab projects within an institution, support monitoring, reflection and learning from projects, and facilitate communication with stakeholders, and the sharing of practices and learning between peers across the globe. As a living shared, framework and learning system, the framework will adapt and develop over time and within different contexts. To provide feedback and fast (practical) learning from users, the system will be further developed to facilitate transparent peer reviewing