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排序方式: 共有270条查询结果,搜索用时 15 毫秒
41.
Fibrin-induced release of platelet serotonin 总被引:1,自引:0,他引:1
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Platelet activation by circulating levels of hormones: a possible link in coronary heart disease 总被引:4,自引:0,他引:4
Blood platelets participating in the formation of haemostatic plugs or thrombi are likely to be exposed to combinations of several agonists. We have found that platelet aggregation and the release reaction are enhanced by combinations of the hormones adrenaline, noradrenaline, vasopressin and 5 hydroxytryptamine acting synergistically at levels obtained in circulating blood for three of these hormones. If surges of adrenaline and other hormones sensitize platelets this may provide a link between some of the risk factors and coronary heart disease. 相似文献
44.
4-甲氧羰基-4-N-丙酰苯胺基哌啶1位衍生物的合成及其镇痛作用 总被引:2,自引:0,他引:2
本文报道了一系列N-[-1(2-苯乙基-4-甲氧羰基-4-哌啶基]-N-丙酰苯胺(4-甲氧羰基芬太尼)哌啶环1位取代衍生物的合成及其镇痛活性;讨论了结构与镇痛活性之间的关系。药理试验结果表明,大部分化合物具有典型的吗啡样镇痛活性,是一类作用极强的麻醉性镇痛剂。特别是哌啶环1位β-苯环被取代乙烯基替代的化合物具有相当或接近子母体化合物的镇痛活性。其代表物1321的镇痛活性(ED_(50)=0.005mg/kg ip,小鼠,热板法)略强于4-甲氧羰基芬太尼(ED_(50)=0.0063 mg/kg)。 相似文献
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V Nimmrich KG Reymann M Strassburger UH Sch?der G Gross A Hahn H Schoemaker K Wicke A M?ller 《British journal of pharmacology》2010,159(7):1523-1531
Background and purpose:
Alzheimer''s disease (AD) is a multifactorial, neurodegenerative disease, which is in part caused by an impairment of synaptic function, probably mediated by oligomeric forms of amyloid-β (Aβ). While the Aβ pathology mainly affects the physiology of neurotransmission, neuronal decline is caused by excitotoxic cell death, which is mediated by the NMDA receptor. A comprehensive therapeutic approach should address both Aβ-induced synaptic deficits, as well as NMDA receptor-mediated neurodegeneration, via one molecular target. This study was designed to test whether calpain could be involved in both pathological pathways, which would offer a promising avenue for new treatments.Experimental approach:
Application of the specific, water-soluble calpain inhibitor A-705253 was used to inhibit calpain in hippocampal slice cultures. We examined whether inhibition of calpain would prevent Aβ-induced deficits in neurotransmission in CA1, as well as NMDA-induced neuronal cell death.Key results:
A-705253 dose-dependently prevented excitotoxicity-induced neurodegeneration at low nanomolar concentrations, determined by propidium iodide histochemistry. Inhibition of the NMDA receptor similarly protected from neuronal damage. Caspase staining indicated that calpain inhibition was protective by reducing apoptosis. Electrophysiological analysis revealed that inhibition of calpain by A-705253 also fully prevented Aβ oligomer-induced deficits in neurotransmission. The protective effect of calpain was compared to the clinically available NMDA receptor antagonist memantine, which was also effective in this model.Conclusions and implications:
We suggest that inhibition of calpain exhibits a promising strategy to address several aspects of the pathology of AD that may go beyond the available therapeutic intervention by memantine. 相似文献47.
The functional -169T-->C single-nucleotide polymorphism in FCRL3 is not associated with rheumatoid arthritis in white North Americans 总被引:1,自引:0,他引:1
48.
Monica Chang Randall K. Saiki Joseph J. Cantanese David Lew Annette H. M. van der Helm‐van Mil Rene E. M. Toes Thomas W. J. Huizinga Kristin G. Ardlie Lindsey A. Criswell Michael F. Seldin Christopher I. Amos Daniel L. Kastner Peter K. Gregersen Steven J. Schrodi Ann B. Begovich 《Arthritis \u0026amp; Rheumatology》2008,58(6):1877-1881
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