75 research outputs found

    Hydrocephalus 2008, 17–20th September, Hannover Germany: a conference report

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    Hydrocephalus 2008 was held 17–20 September in Hannover, Germany, at the invitation of Petra M Klinge (President), co-hosted by Joachim K. Krauss (Vice President), and Madjid Samii (Honorary President). This meeting was a successor to Hydrocephalus 2006 held in GΓΆteborg, Sweden, organised by Past-President, Carsten Wikkelso. The conference began with a general introductory session of six talks including three invited lectures, followed by eighteen parallel sessions. Subjects covered were hydrocephalus signs, symptoms and diagnosis, especially in normal pressure hydrocephalus; cerebrospinal fluid (CSF) physics and dynamics; CSF function and modelling of function; dementia and quality of life, economy, health care and rehabilitation; neuropsychology, cognition and outcome assessment; neuroimaging, functional imaging and non-invasive diagnostics; paediatric and adolescent hydrocephalus; intelligent shunt and valve design (e.g. telemetry, adjustable and antimicrobial shunts); endoscopic third ventriculostomy; technical advances and image-guided surgical approaches in the treatment of hydrocephalus; brain metabolism, biomarkers and biophysics; co-morbidity, classification and aetiology; epidemiology, registries and clinical trials; experimental hydrocephalus; and pharmaceutical modulation of central nervous system function (CNS drug delivery). Each session began with introductory talks from the invited chairpersons followed by six to eight submitted oral presentations. Overall, 136 oral presentations and 18 posters were presented, the abstracts of which were published elsewhere [1]. We present here an account of the introductory session, the invited chairperson's talks and the concluding remarks by Anthony Marmarou

    Therapeutic concentrations of glucagon-like peptide-1 in cerebrospinal fluid following cell-based delivery into the cerebral ventricles of cats

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    <p>Abstract</p> <p>Background</p> <p>Neuropeptides may have considerable potential in the treatment of acute and chronic neurological diseases. Encapsulated genetically engineered cells have been suggested as a means for sustained local delivery of such peptides to the brain. In our experiments, we studied human mesenchymal stem cells which were transfected to produce glucagon-like peptide-1 (GLP-1).</p> <p>Methods</p> <p>Cells were packed in a water-permeable mesh bag containing 400 polymeric microcapsules, each containing 3000 cells. The mesh bags were either transplanted into the subdural space, into the brain parenchyma or into the cerebral ventricles of the cat brain. Mesh bags were explanted after two weeks, and cell viability, as well as GLP-1 concentration in the cerebrospinal fluid (CSF), was measured.</p> <p>Results</p> <p>Viability of cells did not significantly differ between the three implantation sites. However, CSF concentration of GLP-1 was significantly elevated only after ventricular transplantation with a maximum concentration of 73 pM (binding constant = 70 pM).</p> <p>Conclusions</p> <p>This study showed that ventricular cell-based delivery of soluble factors has the capability to achieve concentrations in the CSF which may become pharmacologically active. Despite the controversy about the pharmacokinetic limitations of ventricular drug delivery, there might be a niche in this for encapsulated cell biodelivery of soluble, highly biologically-effective neuropeptides of low molecular weight like GLP-1.</p

    ΠŸΡ€ΠΎΠ΅ΠΊΡ‚ ΠΏΠ»Π°Π½ΠΈΡ€ΠΎΠ²ΠΊΠΈ ΠΈ мСТСвания Ρ‚Π΅Ρ€Ρ€ΠΈΡ‚ΠΎΡ€ΠΈΠΈ ΠΊΠ²Π°Ρ€Ρ‚Π°Π»Π° Π² производствСнно-Π΄Π΅Π»ΠΎΠ²ΠΎΠΉ Π·ΠΎΠ½Π΅ Π³. Вомска

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    ΠŸΠΎΠ΄Π³ΠΎΡ‚ΠΎΠ²ΠΊΠ° ΠΏΡ€ΠΎΠ΅ΠΊΡ‚Π° мСТСвания осущСствляСтся ΠΏΡ€ΠΈΠΌΠ΅Π½ΠΈΡ‚Π΅Π»ΡŒΠ½ΠΎ ΠΊ Ρ‚Π΅Ρ€Ρ€ΠΈΡ‚ΠΎΡ€ΠΈΠΈ, располоТСнной Π² Π³Ρ€Π°Π½ΠΈΡ†Π°Ρ… элСмСнта ΠΏΠ»Π°Π½ΠΈΡ€ΠΎΠ²ΠΎΡ‡Π½ΠΎΠΉ структуры – Π½Π΅ΠΆΠΈΠ»ΠΎΠ³ΠΎ ΠΊΠ²Π°Ρ€Ρ‚Π°Π»Π°, ΠΎΠ³Ρ€Π°Π½ΠΈΡ‡Π΅Π½Π½ΠΎΠ³ΠΎ проспСктом ΠšΠΈΡ€ΠΎΠ²Π°, ΡƒΠ»ΠΈΡ†Π°ΠΌΠΈ КиСвская, Усова, Артёма. Π“Ρ€Π°Π½ΠΈΡ†Ρ‹ ΠΊΠ²Π°Ρ€Ρ‚Π°Π»Π° ΠΎΠΏΡ€Π΅Π΄Π΅Π»Π΅Π½Ρ‹ Π³Π΅Π½Π΅Ρ€Π°Π»ΡŒΠ½Ρ‹ΠΌ ΠΏΠ»Π°Π½ΠΎΠΌ Π³ΠΎΡ€ΠΎΠ΄Π° Вомска, Π° Ρ‚Π°ΠΊΠΆΠ΅ ΠΏΡ€Π°Π²ΠΈΠ»Π°ΠΌΠΈ зСмлСпользования ΠΈ застройки Π³ΠΎΡ€ΠΎΠ΄Π° Вомска. ΠŸΡ€ΠΎΠ΅ΠΊΡ‚ мСТСвания ΠΊΠ²Π°Ρ€Ρ‚Π°Π»Π° подготавливаСтся Π½Π° основС ΠΏΡ€ΠΎΠ΅ΠΊΡ‚Π° ΠΏΠ»Π°Π½ΠΈΡ€ΠΎΠ²ΠΊΠΈ Π΄Π°Π½Π½ΠΎΠΉ Ρ‚Π΅Ρ€Ρ€ΠΈΡ‚ΠΎΡ€ΠΈΠΈ Π² цСлях установлСния Π³Ρ€Π°Π½ΠΈΡ† Π·Π΅ΠΌΠ΅Π»ΡŒΠ½Ρ‹Ρ… участков ΠΈ содСрТит Π³Ρ€Π°Ρ„ΠΈΡ‡Π΅ΡΠΊΡƒΡŽ ΠΈ Ρ‚Π΅ΠΊΡΡ‚ΠΎΠ²ΡƒΡŽ части. ОснованиСм для ΠΏΠΎΠ΄Π³ΠΎΡ‚ΠΎΠ²ΠΊΠΈ ΠΏΡ€ΠΎΠ΅ΠΊΡ‚Π° мСТСвания являСтся постановлСниС администрации Π“ΠΎΡ€ΠΎΠ΄Π° Вомска ΠΎΡ‚ 27.03.2017 Π³. β„–275-Π·.The boundary-setting plan is developed to the Tomsk’s non-residental quarter. An element of planning structure has its borders submitted by Kirova avenue, Kievskaya, Usova and Artyoma streets. Borders of quarter are defined by the city master plan and rules of land use and building of the city of Tomsk. The boundary-setting plan of quarter is prepared on the basis of the draft area plan of this territory for the purpose of land parcels borders establishment. The project consists of a graphic part and the text explanation. The basis for preparation of the project is the resolution of city administration of Tomsk

    Анализ ΠΏΡ€ΠΈΡ‡ΠΈΠ½ возникновСния Π΄Π΅Ρ„Π΅ΠΊΡ‚ΠΎΠ² Π² Ρ€Π΅Π·Π΅Ρ€Π²ΡƒΠ°Ρ€Π°Ρ… Π² процСссС ΠΈΡ… эксплуатации

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    ЦСль Ρ€Π°Π±ΠΎΡ‚Ρ‹ – ΠΏΡ€ΠΎΠ°Π½Π°Π»ΠΈΠ·ΠΈΡ€ΠΎΠ²Π°Ρ‚ΡŒ ΠΏΡ€ΠΈΡ‡ΠΈΠ½Ρ‹ возникновСния Π΄Π΅Ρ„Π΅ΠΊΡ‚ΠΎΠ² ΠΈ ΠΌΠ΅Ρ‚ΠΎΠ΄Ρ‹ ΠΈΡ… устранСния Ρ€Π΅Π·Π΅Ρ€Π²ΡƒΠ°Ρ€ΠΎΠ² Π²Π΅Ρ€Ρ‚ΠΈΠΊΠ°Π»ΡŒΠ½Ρ‹Ρ… ΡΡ‚Π°Π»ΡŒΠ½Ρ‹Ρ…. Π’ процСссС выполнСния выпускной ΠΊΠ²Π°Π»ΠΈΡ„ΠΈΠΊΠ°Ρ†ΠΈΠΎΠ½Π½ΠΎΠΉ Ρ€Π°Π±ΠΎΡ‚Ρ‹ Π±Ρ‹Π»ΠΈ ΠΏΡ€ΠΎΠ²Π΅Π΄Π΅Π½Ρ‹ ΡΠ»Π΅Π΄ΡƒΡŽΡ‰ΠΈΠ΅ расчСты: 1) ΠΎΠΏΡ€Π΅Π΄Π΅Π»Π΅Π½ΠΈΠ΅ гСомСтричСских ΠΏΠ°Ρ€Π°ΠΌΠ΅Ρ‚Ρ€ΠΎΠ² Ρ€Π΅Π·Π΅Ρ€Π²ΡƒΠ°Ρ€Π° 2)ΠΎΠΏΡ€Π΅Π΄Π΅Π»Π΅Π½ΠΈΠ΅ Ρ‚ΠΎΠ»Ρ‰ΠΈΠ½Ρ‹ всСх поясов стСнках Ρ€Π΅Π·Π΅Ρ€Π²ΡƒΠ°Ρ€Π° 3)расчСт стСнки Π½Π° ΡƒΡΡ‚ΠΎΠΉΡ‡ΠΈΠ²ΠΎΡΡ‚ΡŒ. ΠžΡΠ½ΠΎΠ²Π½Ρ‹Π΅ конструктивныС, тСхнологичСскиС ΠΈ Ρ‚Π΅Ρ…Π½ΠΈΠΊΠΎ- эксплуатационныС характСристики: выявлСниС Π΄Π΅Ρ„Π΅ΠΊΡ‚Π½Ρ‹Ρ… мСст, тСхнология ΠΈ организация выполнСния Ρ€Π΅ΠΌΠΎΠ½Ρ‚Π½Ρ‹Ρ… Ρ€Π°Π±ΠΎΡ‚, ΠΏΠΎΠ΄Π³ΠΎΡ‚ΠΎΠ²ΠΈΡ‚Π΅Π»ΡŒΠ½Ρ‹Π΅ Ρ€Π°Π±ΠΎΡ‚Ρ‹, ΠΌΠΎΠ½Ρ‚Π°ΠΆ Ρ€Π΅Π·Π΅Ρ€Π²ΡƒΠ°Ρ€Π°, сварочно-ΠΌΠΎΠ½Ρ‚Π°ΠΆΠ½Ρ‹Π΅ Ρ€Π°Π±ΠΎΡ‚Ρ‹ Ρ€Π΅Π·Π΅Ρ€Π²ΡƒΠ°Ρ€Π°, эксплуатационныС Ρ€Π°Π±ΠΎΡ‚Ρ‹ .The purpose of work - to analyze the causes of defects and remedies vertical steel tanks. During execution of final qualifying work following calculations were made: 1) determining the geometric parameters of the reservoir 2) determining the thickness of the walls of the reservoir zones 3) the calculation of the stability of the wall. The basic constructive, technological and technical and operational characteristics: the identification of defects, the technology and organization of repair work, the preparatory work, the tank assembly, welding and assembly works of the tank, maintenance work

    Hernia fibroblasts lack Ξ²-estradiol induced alterations of collagen gene expression

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    BACKGROUND: Estrogens are reported to increase type I and type III collagen deposition and to regulate Metalloproteinase 2 (MMP-2) expression. These proteins are reported to be dysregulated in incisional hernia formation resulting in a significantly decreased type I to III ratio. We aimed to evaluate the Ξ²-estradiol mediated regulation of type I and type III collagen genes as well as MMP-2 gene expression in fibroblasts derived from patients with or without history of recurrent incisional hernia disease. We compared primary fibroblast cultures from male/female subjects without/without incisional hernia disease. RESULTS: Incisional hernia fibroblasts (IHFs) revealed a decreased type I/III collagen mRNA ratio. Whereas fibroblasts from healthy female donors responded to Ξ²-estradiol, type I and type III gene transcription is not affected in fibroblasts from males or affected females. Furthermore Ξ²-estradiol had no influence on the impaired type I to III collagen ratio in fibroblasts from recurrent hernia patients. CONCLUSION: Our results suggest that Ξ²-estradiol does not restore the imbaired balance of type I/III collagen in incisional hernia fibroblasts. Furthermore, the individual was identified as an independent factor for the Ξ²-estradiol induced alterations of collagen gene expression. The observation of gender specific Ξ²-estradiol-dependent changes of collagen gene expression in vitro is of significance for future studies of cellular response
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