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排序方式: 共有275条查询结果,搜索用时 31 毫秒
11.
Rachael I. Scahill Nicola Z. Hobbs Miranda J. Say Natalie Bechtel Susie M.D. Henley Harpreet Hyare Douglas R. Langbehn Rebecca Jones Blair R. Leavitt Raymund A.C. Roos Alexandra Durr Hans Johnson Stéphane Lehéricy David Craufurd Christopher Kennard Stephen L. Hicks Julie C. Stout Ralf Reilmann Sarah J. Tabrizi the TRACK‐HD investigators 《Human brain mapping》2013,34(3):519-529
TRACK‐HD is a multicentre longitudinal observational study investigating the use of clinical assessments and 3‐Tesla magnetic resonance imaging as potential biomarkers for future therapeutic trials in Huntington's disease (HD). The cross‐sectional data from this large well‐characterized dataset provide the opportunity to improve our knowledge of how the underlying neuropathology of HD may contribute to the clinical manifestations of the disease across the spectrum of premanifest (PreHD) and early HD. Two hundred and thirty nine gene‐positive subjects (120 PreHD and 119 early HD) from the TRACK‐HD study were included. Using voxel‐based morphometry (VBM), grey and white matter volumes were correlated with performance in four domains: quantitative motor (tongue force, metronome tapping, and gait); oculomotor [anti‐saccade error rate (ASE)]; cognition (negative emotion recognition, spot the change and the University of Pennsylvania smell identification test) and neuropsychiatric measures (apathy, affect and irritability). After adjusting for estimated disease severity, regionally specific associations between structural loss and task performance were found (familywise error corrected, P < 0.05); impairment in tongue force, metronome tapping and ASE were all associated with striatal loss. Additionally, tongue force deficits and ASE were associated with volume reduction in the occipital lobe. Impaired recognition of negative emotions was associated with volumetric reductions in the precuneus and cuneus. Our study reveals specific associations between atrophy and decline in a range of clinical modalities, demonstrating the utility of VBM correlation analysis for investigating these relationships in HD. Hum Brain Mapp, 2013. © 2011 Wiley Periodicals, Inc. 相似文献
12.
Maternal administration of granulocyte colony-stimulating factor improves neonatal rat survival after a lethal group B streptococcal infection 总被引:2,自引:0,他引:2
Novales JS; Salva AM; Modanlou HD; Kaplan DL; del Castillo J; Andersen J; Medlock ES 《Blood》1993,81(4):923-927
Maternally administered recombinant human granulocyte colony- stimulating factor (rhG-CSF) has been shown to cross the placenta and induce a peripheral neutrophilia and increases in the marrow and spleen neutrophil storage pools in fetal and newborn rats. In the present study, we have used this model system to investigate the efficacy of prenatally administered rhG-CSF on neonatal defense to a lethal challenge with Group B-beta hemolytic Streptococcus (GBS). Pregnant rats were injected with rhG-CSF twice daily beginning 6 days before parturition. At birth, all pups were infected with a dose of GBS that is lethal for 90% of infected pups (LD90). Survival was monitored daily for 5 days. Survival of infected pups from saline-treated mothers beyond 60 hours after infection was 10%. No difference in survival was observed among pups from mothers treated 2 and 4 days before parturition. In contrast, we determined that survival was 82.5% among infected pups from mothers treated for 6 days before parturition with rhG-CSF. Our results demonstrate that maternal administration of rhG- CSF augments neonatal defenses against a lethal bacterial challenge. 相似文献
13.
M Storr P Born E Frimberger N Weigert T Rösch A Meining M Classen HD Allescher 《BMC gastroenterology》2002,2(1):19-8
Background
It has been suggested that intrasphincteric injection of botulinum toxin (BTX) may represent an alternative therapy to balloon dilatation in achalasia. The aim of the present study was to test the effectiveness of botulinum toxin injections in achalasia patients, as assessed using lower oesophageal sphincter pressure (LOSP) and symptom scores, and to compare the response in patients with different types of pretreatment (no previous treatment, balloon dilatation, myotomy, BTX injection). 相似文献14.
Patterns of cytokine gene expression in peripheral T-cell lymphoma of angioimmunoblastic lymphadenopathy type 总被引:3,自引:0,他引:3
Foss HD; Anagnostopoulos I; Herbst H; Grebe M; Ziemann K; Hummel M; Stein H 《Blood》1995,85(10):2862-2869
15.
von den Driesch P; Bhardwaj R; Flad HD; Neugebauer DC; Pielken HJ; Urbanitz D; Kolsch E 《Blood》1989,74(1):430-436
An immunoglobulin M (IgM)-positive cell line, Ms 28, apparently spontaneously transformed by Epstein-Barr virus (EBV) was established from peripheral blood cells of a patient with immature myeloblastic leukemia. It has been characterized according to phenotype, cytochemistry, and membrane antigen pattern. The cell line expresses lymphoid markers like CD 19, CD 22, and CD 30 and synthesizes and secretes IgM. Monocyte markers CD 11c, CD 14, and CD 15 are absent. Neither interleukin-1 (IL-1), nor tumor necrosis factor (TNF-alpha) are produced. But Ms 28 cells show strong phagocytic activity and engulf Latex particles and sheep RBCs (SRBCs) that need not to be opsonized. The phagocytic activity can be inhibited by chloroquine. Both phagocytosis and EBV nuclear-antigen (EBNA) expression can be observed in one and the same cell. Ms 28 cells might be useful to study immunologic activities like antigen processing and presentation. 相似文献
16.
Regionally selective atrophy of subcortical structures in prodromal HD as revealed by statistical shape analysis
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Laurent Younes J. Tilak Ratnanather Timothy Brown Elizabeth Aylward Peg Nopoulos Hans Johnson Vincent A. Magnotta Jane S. Paulsen Russell L. Margolis Roger L. Albin Michael I. Miller Christopher A. Ross PREDICT‐HD Investigators Coordinators of the Huntington Study Group 《Human brain mapping》2014,35(3):792-809
Huntington disease (HD) is a neurodegenerative disorder that involves preferential atrophy in the striatal complex and related subcortical nuclei. In this article, which is based on a dataset extracted from the PREDICT‐HD study, we use statistical shape analysis with deformation markers obtained through “Large Deformation Diffeomorphic Metric Mapping” of cortical surfaces to highlight specific atrophy patterns in the caudate, putamen, and globus pallidus, at different prodromal stages of the disease. On the basis of the relation to cortico‐basal ganglia circuitry, we propose that statistical shape analysis, along with other structural and functional imaging studies, may help expand our understanding of the brain circuitry affected and other aspects of the neurobiology of HD, and also guide the most effective strategies for intervention. Hum Brain Mapp 35:792–809, 2014. © 2012 Wiley Periodicals, Inc. 相似文献
17.
Large‐scale brain network abnormalities in Huntington's disease revealed by structural covariance
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Lora Minkova Simon B. Eickhoff Ahmed Abdulkadir Christoph P. Kaller Jessica Peter Elisa Scheller Jacob Lahr Raymund A. Roos Alexandra Durr Blair R. Leavitt Sarah J. Tabrizi Stefan Klöppel TRACK‐HD Investigators 《Human brain mapping》2016,37(1):67-80
Huntington's disease (HD) is a progressive neurodegenerative disorder that can be diagnosed with certainty decades before symptom onset. Studies using structural MRI have identified grey matter (GM) loss predominantly in the striatum, but also involving various cortical areas. So far, voxel‐based morphometric studies have examined each brain region in isolation and are thus unable to assess the changes in the interrelation of brain regions. Here, we examined the structural covariance in GM volumes in pre‐specified motor, working memory, cognitive flexibility, and social‐affective networks in 99 patients with manifest HD (mHD), 106 presymptomatic gene mutation carriers (pre‐HD), and 108 healthy controls (HC). After correction for global differences in brain volume, we found that increased GM volume in one region was associated with increased GM volume in another. When statistically comparing the groups, no differences between HC and pre‐HD were observed, but increased positive correlations were evident for mHD, relative to pre‐HD and HC. These findings could be explained by a HD‐related neuronal loss heterogeneously affecting the examined network at the pre‐HD stage, which starts to dominate structural covariance globally at the manifest stage. Follow‐up analyses identified structural connections between frontoparietal motor regions to be linearly modified by disease burden score (DBS). Moderator effects of disease load burden became significant at a DBS level typically associated with the onset of unequivocal HD motor signs. Together with existing findings from functional connectivity analyses, our data indicates a critical role of these frontoparietal regions for the onset of HD motor signs. Hum Brain Mapp 37:67–80, 2016. © 2015 Wiley Periodicals, Inc. 相似文献
18.
构建Loa22基因去信号肽片段原核重组表达载体 总被引:1,自引:0,他引:1
目的:构建赖型钩端螺旋体OmpA膜蛋白Loa22基因去信号肽片段的原核表达载体,并对其进行克隆表达。方法:实验于2004—12/2005—12在四川大学华西医学中心感染免疫研究室完成。以赖型钩端螺旋体017株基因组DNA为模板,PCR扩增Loa22基因去信号肽片段,亚克隆至原核表达载体pGEX-4T-1,经双酶切、PCR鉴定,筛选出阳性重组质粒克隆。经DNA测序正确后,转化大肠杆菌,利用IPTG进行诱导表达,通过SDS—PAGE鉴定表达产物。结果:PCR获得长516bp的片段。Loa22基因去信号肽片段与pGEX-4T-1的重组质粒构建成功。重组质粒经IPTG诱导后能在大肠杆菌中表达Mr45000的融合蛋白。结论:制备了Loa22基因去信号肽片段原核重组表达载体,为钩体新型疫苗的研究奠定基础。 相似文献
19.
SJ KANG HD WOO JY CHOI YJ LEE HW CHUNG 《中国药理学与毒理学杂志》2006,20(3):224-247
5-Flourouracil(5-FU) is one of well known anti-cancer drugs, but its toxicity in normal lymphocytes remains a major problem in chemotherapy. The eastern traditional drug, Bupleuri radix(BR), has been used for the treatment of liver diseases and contains series of triterpene saponins. 相似文献
20.
Dehydroepiandrosterone (DHEA) is an intermediate product in the synthesis
of male and female sex hormones in the adrenal cortex of man. In livers of
rats and mice DHEA increases the levels of cytochrome P450 IVA and
peroxisomal beta-oxidation enzymes associated with peroxisome
proliferation. Prolonged treatment of rats with DHEA induces liver tumors
that are more frequent in females arising mainly in the periportal regions
of the liver lobule (Metzger et al., Toxicol. Pathol. 23, 591-605, 1995).
Because of paucity of information on hepatic zonation of peroxisomal
response to DHEA and controversial reports on gender-specific differences
of its effects the present study was undertaken using qualitative
immunohistochemical and quantitative immunoelectron microscopical
techniques in addition to Western blotting. Rats were treated for 24 weeks
with 0.6% DHEA supplied with diet. Immunoblot analysis revealed marked
induction of peroxisomal beta- oxidation enzymes, which by quantitative
analysis was equally strong in male and female animals, whilst catalase and
urate-oxidase were not increased. Cytochrome P450 IVA, in contrast, was
induced significantly stronger in male than in female rats.
Immunohistochemistry confirmed the induction of cytochrome P450 IVA showing
a marked lobular gradient in female animals with strong induction in
pericentral and almost no induction in periportal regions of the liver
lobule. In male animals cytochrome P450 IVA was expressed more uniformly
across the liver lobule. A similar sex specific zone-dependent response was
observed for peroxisomes. DHEA induced in females a significant zonal
gradient with marked peroxisome proliferation and a strong induction of
peroxisomal hydratase/dehydrogenase in pericentral hepatocytes and a much
smaller response in periportal regions. Livers of male animals, in
contrast, showed a uniform peroxisomal proliferation to DHEA with only
slight zonal differences. The striking homologies of the induction patterns
of cytochrome P450 IVA and the peroxisome proliferation in both sexes
support the notion of a functional relationship. In view of the almost
exclusive periportal localization of DHEA-induced tumors in female rats in
contrast to the pericentral localization of the peroxisomal proliferation
shown by this study, it seems likely that other factors in addition to
peroxisome proliferation may contribute to the hepatocarcinogenic effect of
DHEA.
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