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Kinetics of [35S]dATPalphaS (2'deoxyadenosine-5'-[alpha-35S]-thiotriphosphate) interaction with rat brain membrane fragments was studied at 25 degrees C and at radioligand concentrations from 2 to 250 nM. At least two different ways of [35S]dATPalphaS interaction with the membranes were distinguished on the basis of radioligand on-rate. Firstly, the binding sites characterized by 'fast' on-rate can be observed. Secondly, the 'slow' binding sites were kinetically identified and quantified. As in both cases the bound radioligand could be displaced by excess of ATP, all these binding sites can be defined as 'specific sites'. In the 'slow' binding sites isomerization of the receptor-ligand complex was observed, as is typical for interaction of antagonists with G-protein coupled receptors, and the kinetic parameters for this interaction were similar with the appropriate data for the hP2Y1 receptors expressed in 1321N1 astrocytoma cells Therefore these sites could be assigned to the same receptor subtype in brain membranes while the 'fast' binding sites belong to other membrane-bound proteins, also interacting with ATP and its analogues. The kinetic properties of the latter sites were not analysed in detail. 相似文献
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Objective This study aimed to investigate the importance of cytochrome P450
enzymes for the reported interaction between tramadol and warfarin.Materials and methods Cases of suspected interaction between tramadol and warfarin resulting in International Normalised Ratios increases that were reported to the Swedish Adverse Drug Reactions Advisory Committee until March 2003 were included. Ten cases had been genotyped for known polymorphisms of CYP2D6, CYP2C9 and CYP2C19.Results Seven of ten patients carried defective CYP2D6 alleles (population prevalence 42.2%) (one-sided binomial test,
P=0.07). A further patient received concomitant drug treatments that may have resulted in CYP2D6 enzyme inhibition.Conclusion The liability to an interaction between tramadol and warfarin may be related to the CYP2D6 activity. 相似文献
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Lindh JD Lundgren S Holm L Alfredsson L Rane A 《Clinical pharmacology and therapeutics》2005,78(5):540-550
OBJECTIVE: Our objective was to prospectively study the impact of CYP2C9 polymorphism (*2 and *3) on the risk of overanticoagulation during the induction phase of warfarin therapy. METHODS: Blood samples for genotyping were collected from 219 patients requiring warfarin therapy, and clinical data were prospectively collected during the first 3 weeks of medication. Patients were divided into 3 groups according to CYP2C9 genotype, as follows: *1 (homozygous), *2 (*1/*2 and *2/*2), and *3 (any genotype containing the *3 allele). RESULTS: During the first week of treatment, the relative risk of achieving at least 1 international normalized ratio (INR) value above the therapeutic interval (2-3) was 2.8 (95% confidence interval, 1.2-6.7) and 6.1 (2.7-13.6) in the *2 and *3 groups, respectively (with *1 used as control). During the second week, the corresponding values were 2.1 (1.2-3.7) and 3.5 (2.1-5.8), respectively. By the third week, the genetic impact was no longer evident, presumably as a result of successful dose individualization. Increased INR levels (compared with the *1 group) were already demonstrated in the *2 group on the fourth treatment day. CONCLUSIONS: The CYP2C9*2 and *3 single-nucleotide polymorphisms significantly increase the risk of overanticoagulation during the first 2 weeks of warfarin treatment, with increased INR levels evident after only 4 days' treatment in *2 carriers. Our prospective data are consistent with results from previous retrospective studies and indicate that CYP2C9 genotyping may be a means of improving safety during warfarin induction. 相似文献
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Although the development of an effective HIV‐1 vaccine has proved very challenging for more than two decades, it remains the best hope to control the HIV pandemic. Since Brazil has particular epidemiological features, as well as adequate policies and infrastructure, the country has been an interesting site for HIV vaccine trials. Since 1995, eight trials were performed in Brazil enrolling over 2000 subjects. Peptide vaccine candidates were initially designed to elicit neutralising antibodies as an attempt to provide sterilising immunity against HIV‐1. This strategy, however, has proved extremely difficult, and candidates were poorly immunogenic. Therefore, the next vaccine candidates focused mainly on the induction of cell mediated immune responses that would limit AIDS progression and transmission by suppressing viremia. Such candidates were naked DNA or viral vectors in either prophylactic or therapeutic approaches. Even though several candidates were immunogenic, protective immune responses against HIV‐1 remain to be achieved. However, several studies with non‐human primates and human elite controllers demonstrate that effective immune responses against HIV‐1 may be elicited, supporting the belief that an HIV‐1 vaccine is possible. Much has been learned, and now the development of an effective HIV‐1 vaccine requires resetting priorities with focus on basic research, considering the merits of neutralising antibodies and CMI, as well as the role of innate immunity on HIV‐1 protection. In this new perspective, large‐scale trials should be replaced by smaller preliminary efficacy studies. Copyright © 2009 John Wiley & Sons, Ltd. 相似文献
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Carsten?Reidies?Bjarkam Thomas?J.?Corydon Inger?Marie?L.?Olsen Jonatan?Pallesen Mette?Nyegaard Tue?Fryland Ole?Mors Anders?D.?B?rglum 《Brain structure & function》2009,214(1):37-47
We have recently shown that the gene BRD1 is associated with schizophrenia and bipolar affective disorder and that the BRD1 protein (BRD1) which is expressed in neurons may occur in a short and a long variant. The aim of the study was to generate
polyclonal antibodies against new BRD1 epitopes enabling discrimination between the long and short BRD1 variants, and elucidate
the BRD1 distribution in several human tissues, including the CNS. Polyclonal rabbit antibodies were raised against three
different BRD1 epitopes. One (67) was specific for the long BRD1 variant, whereas the two others (63/64 and 65/66) like the
original monoclonal mouse antibody (K22) were predicted to stain both variants. Immunohistochemical staining procedures were
subsequently performed on paraffin-embedded human cerebral cortex and microarray slides containing 30 different human tissues.
Western blotting confirmed the predicted specificity of the developed antibodies. K22, 63/64 and 65/66 displayed a similar
neuronal staining pattern characterized by a distinct but weak nuclear staining, while the surrounding cytoplasm and proximal
dendrites were more intensely stained. Interestingly, staining with 67 generated in contrast primarily an intense nuclear
staining. The new antibodies resulted, furthermore, in a prominent neuroglial reaction characterized by staining of cell bodies,
nuclei and glial processes. The tissue microarray analysis revealed that BRD1 was widely distributed in human tissues. The
particular expression profile, e.g., the degree of nuclear and/or cytoplasmatic staining, seemed, however, to be highly tissue
dependent. These results suggest a general role of BRD1 in the cell and stress that the two BRD1 variants may play different
roles in the etiology of psychiatric disease. 相似文献
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Margarita Pérez Jonatan R. Ruiz María Fernández del Valle Gisela Nogales-Gadea Antoni L. Andreu Joaquín Arenas Alejandro Lucía 《Neuromuscular disorders : NMD》2009,19(6):403-405
We investigated the phenomenon of second wind in four patients with McArdle’s disease: a brother and sister (aged 4 and 12 years respectively) and two unrelated patients, a boy of 14 and a 17-year-old girl. We also studied the siblings’ healthy 6-year-old sister. Each patient performed a 15-min exercise test at a constant workload and a subsequent graded exercise test until exhaustion. Overall the healthy girl and the youngest McArdle’s patient, the 4-year-old boy, did not show a second wind phenomenon. Further, the peak cardio-respiratory capacity of the young McArdle’s boy was normal for his age (32.3mL02/kg/min) and he did not report any function limitations during physical education classes. 相似文献
29.
Vicente-Rodríguez G Urzanqui A Mesana MI Ortega FB Ruiz JR Ezquerra J Casajús JA Blay G Blay VA Gonzalez-Gross M Moreno LA;AVENA-Zaragoza Study Group 《Journal of bone and mineral metabolism》2008,26(3):288-294
We studied 278 adolescents (169 females) aged 13.0–18.5 years to elucidate whether an independent effect of physical fitness
and lean mass in the differences between male and female bones can be detected. Lean and fat masses and bone mineral content
(BMC) were measured with DXA. Physical fitness was evaluated with six different tests included in the EUROFIT test battery
(flexibility, isometric, dynamic and endurance strength, speed, and cardiovascular fitness). To test the independent relationship
between physical fitness and bone mass, multiple regression analysis was applied, including lean mass, age, and Tanner development
as covariates. The males had a 43% lower fat mass and 40% and 16% higher lean mass and total BMC compared with the females
(all P < 0.05). After adjustment for differences in body size and lean mass, the females exhibited a 7.4% higher BMC than the males
(P < 0.05). The multiple regression analysis showed that lean mass had an independent relationship with bone mass (P < 0.001), explaining 67% of the total variance in whole-body BMC. In males, change in R
2 was 0.658 for hand grip and 0.035–0.151 for the rest of physical fitness-related variables; but 0.019–0.042 in females (all
P–0.001); however, the independent relationships between physical fitness and bone disappeared after controlling for lean mass.
In conclusion, it is likely the differences between male and female in bone mass could be explained by differences in lean
mass and physical fitness. 相似文献
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Marta González-Freire Gabriel Rodríguez-Romo Catalina Santiago Natalia Bustamante-Ara Thomas Yvert Félix Gómez-Gallego José A. Serra Rexach Jonatan R. Ruiz Alejandro Lucia 《Age (Dordrecht, Netherlands)》2010,32(3):405-409
We studied the A55T, E164K, I225T, K153R and P198A variants in the myostatin (GDF8) gene, muscle strength and mass, and physical function during daily living in 41 nonagenarians [33 women, age range, 90,
97]. No participant carried a mutant allele of the aforementioned variants, except three participants (all women), who carried
the R allele of the K153R polymorphism, with one of them (woman aged 96 years) being homozygous. Overall, in KR women muscle
phenotype values (1RM leg press and estimated muscle mass) were low-to-normal compared to the whole group (∼25th–50th percentile),
and their functional capacity (Barthel and Tinetti tests) was normal. In the woman bearing the RR genotype, values of muscle
mass and functional capacity were below the 25th percentile. She is the first RR Caucasian whose phenotype has been characterised
specifically. In summary, heterozygosity for the GDF8 K153R polymorphism does not seem to exert a negative influence on the muscle phenotypes of women who are at the end of the
human lifespan, yet homozygosity might do so. More research on larger cohorts of nonagenarians is needed to corroborate the
present findings. 相似文献