60 research outputs found
Характеристика впливу електромагнітних полів на організм людини
Вивчення механізмів дії ЕМП на біологічні об’єкти і організм людини в даний час знаходиться на стику різних напрямків - фізики, біології, медицини, біофізики, радіоелектроніки, екології і т. д. Зі зростанням інтенсивності високочастотних електромагнітних полів з’явилися смертельні випадки від їх впливу. Встановлено, що найбільш чутливою до дії ЕМП є нервова система, особливо її вищі відділи. Під впливом ЕМП низької інтенсивності у новонароджених організмів страждає пам’ять. Особливу чутливість до ЕМП проявляє імунна система. Є повідомлення, що під впливом мікрохвиль порушуються процеси імунітету, частіше в бік їх пригнічення.Изучение механизмов действия ЭМП на биологические объекты и организм человека в настоящее время находится на стыке разных направлений - физики, биологии, медицины, биофизики, радиоэлектроники, экологии и т. Д. С ростом интенсивности высокочастотных электромагнитных полей появились смертельные случаи от их влияния. Установлено, что наиболее чувствительной к действию ЭМП является нервная система, особенно ее высшие отделы. Под влиянием ЭМП низкой интенсивности у новорожденных организмов страдает память. Особую чувствительность к ЭМП проявляет иммунная система. Есть сообщения, что под влиянием микроволн нарушаются процессы иммунитета, чаще в сторону их угнетения.Studying the mechanisms of action of EMF on biological objects and the human body is currently at the crossroads of different areas - physics, biology, medicine, biophysics, electronics, environment and so on. D. With the growing intensity of high-frequency electromagnetic fields were the deaths of their influence. Found that the most sensitive to EMF is the nervous system, especially its higher parts. Under the influence of low intensity electromagnetic fields in newborn organisms suffer memory. Particular sensitivity to EMF exhibits immune system. There are reports that exposure to microwaves disrupt the immune system, often in the direction of their oppression
Trajetórias, transições e âncoras de carreiras: um estudo comparativo e de recursos humanos
Generation of Glucose-Responsive Functional Islets with a Three-Dimensional Structure from Mouse Fetal Pancreatic Cells and iPS Cells In Vitro
Islets of Langerhans are a pancreatic endocrine compartment consisting of insulin-producing β cells together with several other hormone-producing cells. While some insulin-producing cells or immature pancreatic cells have been generated in vitro from ES and iPS cells, islets with proper functions and a three-dimensional (3D) structure have never been successfully produced. To test whether islets can be formed in vitro, we first examined the potential of mouse fetal pancreatic cells. We found that E16.5 pancreatic cells, just before forming islets, were able to develop cell aggregates consisting of β cells surrounded by glucagon-producing α cells, a structure similar to murine adult islets. Moreover, the transplantation of these cells improved blood glucose levels in hyperglycemic mice. These results indicate that functional islets are formed in vitro from fetal pancreatic cells at a specific developmental stage. By adopting these culture conditions to the differentiation of mouse iPS cells, we developed a two-step system to generate islets, i.e. immature pancreatic cells were first produced from iPS cells, and then transferred to culture conditions that allowed the formation of islets from fetal pancreatic cells. The islets exhibited distinct 3D structural features similar to adult pancreatic islets and secreted insulin in response to glucose concentrations. Transplantation of the islets improved blood glucose levels in hyperglycemic mice. In conclusion, the two-step culture system allows the generation of functional islets with a 3D structure from iPS cells
Islet Formation during the Neonatal Development in Mice
The islet of Langerhans is a unique micro-organ within the exocrine pancreas, which is composed of insulin-secreting beta-cells, glucagon-secreting alpha-cells, somatostatin-secreting delta-cells, pancreatic polypeptide-secreting PP cells and ghrelin-secreting epsilon-cells. Islets also contain non-endocrine cell types such as endothelial cells. However, the mechanism(s) of islet formation is poorly understood due to technical difficulties in capturing this dynamic event in situ. We have developed a method to monitor beta-cell proliferation and islet formation in the intact pancreas using transgenic mice in which the beta-cells are specifically tagged with a fluorescent protein. Endocrine cells proliferate contiguously, forming branched cord-like structures in both embryos and neonates. Our study has revealed long stretches of interconnected islets located along large blood vessels in the neonatal pancreas. Alpha-cells span the elongated islet-like structures, which we hypothesize represent sites of fission and facilitate the eventual formation of discrete islets. We propose that islet formation occurs by a process of fission following contiguous endocrine cell proliferation, rather than by local aggregation or fusion of isolated beta-cells and islets. Mathematical modeling of the fission process in the neonatal islet formation is also presented
Incretin Receptor Null Mice Reveal Key Role of GLP-1 but Not GIP in Pancreatic Beta Cell Adaptation to Pregnancy
Islet adaptations to pregnancy were explored in C57BL6/J mice lacking functional receptors for glucagon-like peptide 1 (GLP-1) and gastric inhibitory polypeptide (GIP). Pregnant wild type mice and GIPRKO mice exhibited marked increases in islet and beta cell area, numbers of medium/large sized islets, with positive effects on Ki67/Tunel ratio favouring beta cell growth and enhanced pancreatic insulin content. Alpha cell area and glucagon content were unchanged but prohormone convertases PC2 and PC1/3 together with significant amounts of GLP-1 and GIP were detected in alpha cells. Knockout of GLP-1R abolished these islet adaptations and paradoxically decreased pancreatic insulin, GLP-1 and GIP. This was associated with abolition of normal pregnancy-induced increases in plasma GIP, L-cell numbers, and intestinal GIP and GLP-1 stores. These data indicate that GLP-1 but not GIP is a key mediator of beta cell mass expansion and related adaptations in pregnancy, triggered in part by generation of intra-islet GLP-1
MAPEAMENTO DE COMPETÊNCIAS DE SUPORTE E DE APOIO PEDAGÓGICO E ADMINISTRATIVO DE PROFISSIONAIS QUE ATUAM NA MODALIDADE A DISTÂNCIA
Narrative approach to understand people's comprehension of acquaintance rape: The role of Sex Role Stereotyping
One of the most unreported crimes is acquaintance rape. This may be the result of people's understanding of what rape is because of their rape script and their stereotypes of victim characteristics. These judgements may be moderated by sex role stereotyping (SRS). We utilised a narrative approach to understand low and high SRS participants' rape scripts. Young-adult participants described what they believed a typical rape was, followed by describing an acquaintance rape and then what they believed the stereotypical victim of each crime would be. A narrative analysis was conducted on the data. We found that the blitz script is still held by 44% of low SRS and 47% of high SRS people despite 90% of rapes being committed by an acquaintance. While acquaintance rape scripts existed, the emotional imagery and content of these depended on participants level of SRS. Stereotypical victim characteristics also depended on SRS: those with high SRS were more likely to endorse rape myth ideals in describing victims than those with low SRS. These results have implications for educating people about what rape is so that victims might feel more confident in reporting rape
Cardiopoietic cell therapy for advanced ischemic heart failure: results at 39 weeks of the prospective, randomized, double blind, sham-controlled CHART-1 clinical trial
Cardiopoietic cells, produced through cardiogenic conditioning of patients' mesenchymal stem cells, have shown preliminary efficacy. The Congestive Heart Failure Cardiopoietic Regenerative Therapy (CHART-1) trial aimed to validate cardiopoiesis-based biotherapy in a larger heart failure cohort
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