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21.
Douglas McHugh Sherry SJ Hu Neta Rimmerman Ana Juknat Zvi Vogel J Michael Walker Heather B Bradshaw 《BMC neuroscience》2010,11(1):44
Background
Microglia provide continuous immune surveillance of the CNS and upon activation rapidly change phenotype to express receptors that respond to chemoattractants during CNS damage or infection. These activated microglia undergo directed migration towards affected tissue. Importantly, the molecular species of chemoattractant encountered determines if microglia respond with pro- or anti-inflammatory behaviour, yet the signaling molecules that trigger migration remain poorly understood. The endogenous cannabinoid system regulates microglial migration via CB2 receptors and an as yet unidentified GPCR termed the 'abnormal cannabidiol' (Abn-CBD) receptor. Abn-CBD is a synthetic isomer of the phytocannabinoid cannabidiol (CBD) and is inactive at CB1 or CB2 receptors, but functions as a selective agonist at this Gi/o-coupled GPCR. N-arachidonoyl glycine (NAGly) is an endogenous metabolite of the endocannabinoid anandamide and acts as an efficacious agonist at GPR18. Here, we investigate the relationship between NAGly, Abn-CBD, the unidentified 'Abn-CBD' receptor, GPR18, and BV-2 microglial migration. 相似文献22.
Stilbenes and zeranol are nonsteroidal estrogenic growth promoters which are banned in the European Union (EU) for use in
food-producing animals by Council Directive 96/22/EC. A liquid chromatography–tandem mass spectrometry (LC-MS/MS) method was
developed for the screening and confirmation of stilbenes (diethylstilbestrol, dienestrol, hexestrol) and resorcylic acid
lactones (zeranol and its metabolites taleranol and zearalanone as well as the mycotoxins α-zearalenol, β-zearalenol and zearalenone)
in bovine urine. The method permits the confirmation and quantification of stilbenes and resorcylic acid lactones at levels
below 1 μg L−1 and 1.5 μg L−1, respectively. The validation was carried out according to Commission Decision 2002/657/EC, Chap. 3.1.3 “alternative validation”
by a matrix-comprehensive in-house validation concept. Decision limit CCα, detection capability CCβ, recovery, repeatabiliy,
within-laboratory reproducibility and the uncertainty of measurement were calculated. Furthermore, a factorial effect analysis
was carried out to identify factors that have a significant influence on the method. Factors considered to be relevant for
the method in routine analysis (e.g. operator, matrix condition, storage duration of the extracts before measurement, different
cartridge lots, hydrolysis conditions) were systematically varied on two levels. The factorial analysis showed that different
cartridge lots, storage durations and matrix conditions can exert a relevant influence on the method. 相似文献
23.
The presented multi-method was developed for the confirmation of 37 antibiotic substances from the six antibiotic groups: macrolides, lincosamides, quinolones, tetracyclines, pleuromutilines and diamino-pyrimidine derivatives. All substances were analysed simultaneously in a single analytical run with the same procedure, including an extraction with buffer, a clean-up by solid-phase extraction, and the measurement by liquid chromatography tandem mass spectrometry in ESI+ mode. The method was validated on the basis of an in-house validation concept with factorial design by combination of seven factors to check the robustness in a concentration range of 5-50 μg kg(-1). The honeys used were of different types with regard to colour and origin. The values calculated for the validation parameters-decision limit CCα (range, 7.5-12.9 μg kg(-1)), detection capability CCβ (range, 9.4-19.9 μg kg(-1)), within-laboratory reproducibility RSD(wR) (<20% except for tulathromycin with 23.5% and tylvalosin with 21.4 %), repeatability RSD(r) (<20% except for tylvalosin with 21.1%), and recovery (range, 92-106%)-were acceptable and in agreement with the criteria of Commission Decision 2002/657/EC. The validation results showed that the method was applicable for the residue analysis of antibiotics in honey to substances with and without recommended concentrations, although some changes had been tested during validation to determine the robustness of the method. 相似文献
24.
Olaf Elsholz Carsten Frank Birgit Matyschok Frank Steiner Oliver Wurl Burkhard Stachel Heinrich Reincke Manfred Schulze Ralf Ebinghaus Maximilian Hempel 《Analytical and bioanalytical chemistry》2000,366(2):196-199
A monitor is described which provides the on-line determination of mercury in river water at concentrations from 20 to 1000 ng/L. The measurement includes an on-line digestion with Br–/BrO3 – and UV-radiation. Each determination is controlled by an on-line addition of 50 and 100 ng/L mercury carried out by pre-dilution of a 500 and 1000 ng/L stock solution using sequential injection analysis (SIA). One cycle of analysis takes 20 min and results in nine signals. A five days stand-alone operation has been performed successfully. Details are also published at web page: “http/www.rzbd.fh-hamburg.de/¶~prmercol” 相似文献
25.
B. Bassalleck P. Braun-Munzinger W. Cleland G. David A. Farooq M. Fatyga A. Gavron V. Greene J. Hall R. Heifetz M. Herman H. Kent D. Kraus D. Lissauer W. Llope T. Ludlam Z. Moroz E. O'Brien L. Olsen D. Sarantites T. Semkow B. Shivakumar J. E. Simon J. Stachel H. Takai T. Throwe L. Waters J. Wojtkowska K. Wolf D. Wolfe E Collaboration 《Zeitschrift fur Physik C Particles and Fields》1988,38(1):45-49
Transverse energy distributions have been measured for collisions of 10 GeV/nucleon Si with targets of Al, Cu and Pb using a combination of a NaI wall and a uranium based sampling calorimeter. The measured cross sectionsdσ/dE T anddE T /dη are consistent with full stopping and an increase, with increasing values ofE T , of energy flow into large angles. 相似文献
26.
Hans-Dietrich Stachel Bruno Wiesend Christine Kreiner 《Journal of heterocyclic chemistry》1985,22(5):1413-1418
The epimeric bromoghydrins 13/14 as well as their ethers 5/6 rearrange in the presence of silver ions to the 5-hydroxypyridones 15 or their ketals 9 respectively. with the bromohydrin ethers 5/6a and b this transformation is effected also with sodium methoxide. Under these reaction conditions the ring expansion is presumend ot proceed via bicyclic aziridines of which 7 could be issolated, The N-methylated compounds 5c/6c which cannot react likewise, form with sodium methoxide the 6-methoxypyridone 12 . 相似文献
27.
P. Schong R. Stumper K. Quandel J. L. Hague H. A. Bright E. T. Allen E. G. Zies L. F. Rader W. L. Hill W. Fischer und F. Stachel 《Fresenius' Journal of Analytical Chemistry》1942,123(5-6):209-215
Ohne Zusammenfassung 相似文献
28.
Barrette J Bellwied R Braun-Munzinger P Cleland WE David G Duek E Fatyga M Fox D Gavron A Greene SV Hall J Hemmick TK Heifetz R Herman M Herrmann N Hogue RW Ingold G Jayananda K Kraus D Lissauer D Llope WJ Legault A Ludlam T Majka R Makowiecki D Mark SK Mitchell JT Muthuswamy M O'Brien E Olsen L Polychronakos V Rawool-Sullivan M Rotondo F Sandweiss J Shivakumar B Simon J Sonnadara U Sullivan JP Stachel J Sunier J Takai H Throwe T Van Hecke H Waters L Woody C Wolf K Wolfe D 《Physical review letters》1990,64(11):1219-1222
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