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101.
102.
We analyzed the effect of the PAF receptor antagonist (+)-cis-3,5-dimethyl-2-(3-pyridyl) thiazolidin-4-one hydrochloride (SM-12502) on the release of leukotriene B4 and IL-8 from human leukocytes. Peripheral blood from healthy donors was separated in two different fractions: polymorphonuclear leukocytes (PMN) and a lymphocyte, monocyte and basophil granulocyte cell fraction (LMB). After incubation of the cell population with different concentrations of SM-12502 the cells were subsequently stimulated with either the Ca ionophore A23187, the bacterial derived peptide fMLP, or with an activator of heterotrimetric G-proteins, the sodium fluoride (NaF, in the presence of Al3+). The PAF receptor antagonist led to a concentration and time dependent inhibition of LTB4 formation and IL-8 release from PMN and LMB. Our data clearly indicate an inhibitory effect of the PAF receptor antagonist SM-12502 on the formation of mediators of the lipoxygenase pathway and on the release of IL-8. 相似文献
103.
M. A. Pfaller A. L. Barry P. C. Fuchs E. H. Gerlach D. J. Hardy J. C. McLaughlin 《European journal of clinical microbiology & infectious diseases》1993,12(5):356-362
Ampicillin combined with sulbactam was tested at both fixed ratio (2:1 and 1:1) and fixed sulbactam concentrations (4 µg/ml, 8 µg/ml and 16 µg/ml) against 2440 consecutively isolated gram-negative bacilli. Sulbactam significantly enhanced the spectrum of ampicillin activity. Overall, at 8 µg/ml ampicillin inhibited 50 % of theEnterobacteriaceae isolates, whereas 69 % to 84 % of the isolates were inhibited by the various sulbactam combinations. The widest spectrum of activity for ampicillin/sulbactam was achieved by testing at a fixed sulbactam concentration of 16 µg/ml, followed by the 1:1 ratio and the fixed 8 µg/ml (84 %, 76 % and 74 % inhibited, respectively). The amount of sulbactam at the susceptible breakpoint concentrations of ampicillin markedly affected the percentage of susceptible strains. Combinations that include 8 µg/ml of sulbactam are suggested for consideration. 相似文献
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105.
The cyclization equilibria constant Kx is evaluated for the formation of cyclic poly(ethylene terephthalate)s (PET) in the range of degree of polymerization 2 ≤ x ≤ 10 on the basis of an elaborated form of the Jacobson-Stockmayer theory. According to this theory, Kx = W( 0 )·2Γ0(1)/(σcx NA), where W( r ) is the probability density function for the chain vector r ; Γ0(γ) is the probability distribution, when r = 0 of γ = cos Δθ; Δθ being the deviation of the bond angle formed by cyclization from its unconstrained value; σcx corresponds to the symmetry number of the ring; NA is Avogadro's number. The evaluation of W( r ) is performed in different approximations. The required configurational averages for computing the density distribution W( r ) and the angular correlation factor Γ0(1) are obtained by Monte Carlo techniques. The density W( 0 ) of chain vectors at r = 0 is overestimated by the Gaussian approximation. Values of W( 0 ) calculated in higher approximation lower Kx for x < 10. By taking into account the oriental correlation between terminal bonds of the x-meric acyclic sequence, Kx is lowered additionally by factors of ca. 2,2, 1,3 and 1,1 for x = 4, 5 and 6, respectively. Similar to other polymer chains treated so far, Kx is lowered for medium sized chain lengths by taking into account the deviation from Gaussian distribution and angular correlations of chain ends. This result is in contradiction to experimental data, which yield even higher Kx-values than expected by the classical Jacobson-Stockmayer theory for medium sized chain lengths. The inclusion of cis-ester residues into the all trans-ester PET chain only slightly reduces this discrepancy. Structural modifications of the PET chain during cyclization experiments are discussed as a rationale for the deviations from the present theory. 相似文献
106.
Silviu-Alin Bacanu Cynthia M Bulik Kelly L Klump Manfred M Fichter Katherine A Halmi Pamela Keel Allan S Kaplan James E Mitchell Alessandro Rotondo Michael Strober Janet Treasure D Blake Woodside Vibhor A Sonpar Weiting Xie Andrew W Bergen Wade H Berrettini Walter H Kaye Bernie Devlin 《American journal of medical genetics. Part B, Neuropsychiatric genetics》2005,(1):61-68
To increase the likelihood of finding genetic variation conferring liability to eating disorders, we measured over 100 attributes thought to be related to liability to eating disorders on affected individuals from multiplex families and two cohorts: one recruited through a proband with anorexia nervosa (AN; AN cohort); the other recruited through a proband with bulimia nervosa (BN; BN cohort). By a multilayer decision process based on expert evaluation and statistical analysis, six traits were selected for linkage analysis (1): obsessionality (OBS), age at menarche (MENAR), and anxiety (ANX) for quantitative trait locus (QTL) linkage analysis; and lifetime minimum body mass index (BMI), concern over mistakes (CM), and food-related obsessions (OBF) for covariate-based linkage analysis. The BN cohort produced the largest linkage signals: for QTL linkage analysis, four suggestive signals: (for MENAR, at 10p13; for ANX, at 1q31.1, 4q35.2, and 8q13.1); for covariate-based linkage analyses, both significant and suggestive linkages (for BMI, one significant [4q21.1] and three suggestive [3p23, 10p13, 5p15.3]; for CM, two significant [16p13.3, 14q21.1] and three suggestive [4p15.33, 8q11.23, 10p11.21]; and for OBF, one significant [14q21.1] and five suggestive [4p16.1, 10p13.1, 8q11.23, 16p13.3, 18p11.31]). Results from the AN cohort were far less compelling: for QTL linkage analysis, two suggestive signals (for OBS at 6q21 and for ANX at 9p21.3); for covariate-based linkage analysis, five suggestive signals (for BMI at 4q13.1, for CM at 11p11.2 and 17q25.1, and for OBF at 17q25.1 and 15q26.2). Overlap between the two cohorts was minimal for substantial linkage signals. 相似文献
107.
108.
Manfred Mller Vladimir V. Tsukruk Jürgen Wendling Joachim H. Wendorff Holger Bengs Helmut Ringsdorf 《Macromolecular chemistry and physics.》1992,193(10):2659-2668
The synthesis and the results of the structural study of two copolysiloxanes with laterally fixed trinitrofluorenone (TNF) units is reported. The two copolysiloxanes having 2,4 ( 1a ) and 5,3 ( 1b ) dimethylsiloxane comonomer units per TNF side group differ significantly in their phase behaviour as evident from optical microscopy, differential scanning calorimetry and X-ray scattering: 1b shows a nematic mesophase whereas 1a is an amorphous material. The different phase behaviour is discussed in terms of microphase separation between the siloxane backbone and TNF side groups. 相似文献
109.
Defective peroxisomal catabolism of branched fatty acyl coenzyme A in mice lacking the sterol carrier protein-2/sterol carrier protein-x gene function 下载免费PDF全文
Udo Seedorf Martin Raabe Peter Ellinghaus Frank Kannenberg Manfred Fobker Thomas Engel Simone Denis Fred Wouters Karel W.A. Wirtz Ronald J.A. Wanders Nobuyo Maeda Gerd Assmann 《Genes & development》1998,12(8):1189-1201
Gene targeting in mice was used to investigate the unknown function of Scp2, encoding sterol carrier protein-2 (SCP2; a peroxisomal lipid carrier) and sterol carrier protein-x (SCPx; a fusion protein between SCP2 and a peroxisomal thiolase). Complete deficiency of SCP2 and SCPx was associated with marked alterations in gene expression, peroxisome proliferation, hypolipidemia, impaired body weight control, and neuropathy. Along with these abnormalities, catabolism of methyl-branched fatty acyl CoAs was impaired. The defect became evident from up to 10-fold accumulation of the tetramethyl-branched fatty acid phytanic acid in Scp2(−/−) mice. Further characterization supported that the gene disruption led to inefficient import of phytanoyl-CoA into peroxisomes and to defective thiolytic cleavage of 3-ketopristanoyl-CoA. These results corresponded to high-affinity binding of phytanoyl-CoA to the recombinant rat SCP2 protein, as well as high 3-ketopristanoyl-CoA thiolase activity of the recombinant rat SCPx protein. 相似文献
110.
Differential pulse polarography (DPP) and cyclovoltammetry (CV) were conducted to study the redox behaviour of poly(p-phenylenevinylene) (PPV; E = 0,76 V; E = ?1,74 V) as well as of three insoluble PPV-derivatives and four soluble aryl-substituted PPV's. Oxidation studies of DP-PPV, DMOP-PPV and DPOP-PPV in comparison with two series of the oligomeric model compounds 1a–e and 2a–d lead to the conclusion that for DMOP-PPV (E = 0,98, 1,24,1,31 V) and DPOP-PPV (E = 1,10, 1,29, 1,44 V) three distinct oxidation stages exist, which are reversibly occupied and represent 1/2, 1 and 2 positive charges per repeating unit. In DP-PPV two oxidation stages representing 1/2 and 1 positive charges were found to be reversibly occupied (E = 1,17, 1,69 V), whereas at higher potentials irreversible dehydrocyclization occurred. 相似文献