Experimental validation of gallium production and isotope-dependent positron range correction in PET

Abstract Positron range (PR) is one of the important factors that limit the spatial resolution of positron emission tomography (PET) preclinical images. Its blurring effect can be corrected to a large extent if the appropriate method is used during the image reconstruction. Nevertheless, this correction requires an accurate modelling of the PR for the particular radionuclide and materials in the sample under study. In this work we investigate PET imaging with 68Ga and 66Ga radioisotopes, which have a large PR and are being used in many preclinical and clinical PET studies. We produced a 68Ga and 66Ga phantom on a natural zinc target through (p,n) reactions using the 9-MeV proton beam delivered by the 5-MV CMAM tandetron accelerator. The phantom was imaged in an ARGUS small animal PET/CT scanner and reconstructed with a fully 3D iterative algorithm, with and without PR corrections. The reconstructed images at different time frames show significant improvement in spatial resolution when the appropriate PR is applied for each frame, by taking into account the relative amount of each isotope in the sample. With these results we validate our previously proposed PR correction method for isotopes with large PR. Additionally, we explore the feasibility of PET imaging with 68Ga and 66Ga radioisotopes in proton therapy.We acknowledge support from the Spanish MINECO through projects FPA2010-17142, FPA2013-41267-P, CSD-2007-00042 (CPAN), and the RTC-2015-3772-1 grant. We also acknowledge support from Comunidad de Madrid via the TOPUS S2013/MIT-3024 project

Circadian glucocorticoid oscillations preserve a population of adult hippocampal neural stem cells in the aging brain.

A decrease in adult hippocampal neurogenesis has been linked to age-related cognitive impairment. However, the mechanisms involved in this age-related reduction remain elusive. Glucocorticoid hormones (GC) are important regulators of neural stem/precursor cells (NSPC) proliferation. GC are released from the adrenal glands in ultradian secretory pulses that generate characteristic circadian oscillations. Here, we investigated the hypothesis that GC oscillations prevent NSPC activation and preserve a quiescent NSPC pool in the aging hippocampus. We found that hippocampal NSPC populations lacking expression of the glucocorticoid receptor (GR) decayed exponentially with age, while GR-positive populations decayed linearly and predominated in the hippocampus from middle age onwards. Importantly, GC oscillations controlled NSPC activation and GR knockdown reactivated NSPC proliferation in aged mice. When modeled in primary hippocampal NSPC cultures, GC oscillations control cell cycle progression and induce specific genome-wide DNA methylation profiles. GC oscillations induced lasting changes in the methylation state of a group of gene promoters associated with cell cycle regulation and the canonical Wnt signaling pathway. Finally, in a mouse model of accelerated aging, we show that disruption of GC oscillations induces lasting changes in dendritic complexity, spine numbers and morphology of newborn granule neurons. Together, these results indicate that GC oscillations preserve a population of GR-expressing NSPC during aging, preventing their activation possibly by epigenetic programming through methylation of specific gene promoters. Our observations suggest a novel mechanism mediated by GC that controls NSPC proliferation and preserves a dormant NSPC pool, possibly contributing to a neuroplasticity reserve in the aging brain

Exigências em treonina para frangos de corte de 22 a 42 dias de idade Threonine requirements of 22 to 42-day-old broilers

Um experimento foi realizado com o objetivo de estabelecer critérios de avaliação das exigências de treonina digestível para frangos de corte de 22 a 42 dias de idade utilizando-se diferentes modelos de regressão (quadrático, exponencial e de retas segmentadas ou Linear Response Plateau). Foram utilizados 1.920 frangos de corte machos com 22 dias de idade, distribuídos em delineamento inteiramente ao acaso, com seis tratamentos (seis níveis de treonina digestível: 0,5904; 0,6441; 0,6977; 0,7514; 0,8051 e 0,8588%) e oito repetições de 40 aves. Utilizou-se como padrão o nível de 0,6977% de treonina digestível. Foram avaliados dados de desempenho e características de carcaça. Com base nos dados, o nível de 0,7642% de treonina digestível, correspondente às relação treonina:lisina digestível de 71,19%, promoveu o melhor resultado de conversão alimentar de acordo com o modelo Linear Response Plateau.<br>The objective of this experiment was to establish different criteria for evaluation of the requirements of digestible threonine for broilers from 22 to 42 d of age, using different regression models (quadratic, exponential, and Linear Response Plateau). A total of 1,920 22-day-old male Cobb broilers were distributed in randomized experimental design, with six treatments (six threonine levels: 0.5904, 0.6441, 0.6977, 0.7514, 0.8051, and 0.8588%) and 8 replications containing 40 broilers each one. The level of 0.6977% digestible threonine was used as standard. Data on performance and carcass characteristics were evaluated. Based on the data, the threonine level of 0.7642%, corresponding to the threonine:digestible lysine ratio of 71.19% had the best result for feed conversion, according to the Linear Response Plateau model