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101.
Julie A. Eclov Qingwen Qian Rebecca Redetzke Quanhai Chen Steven C. Wu Chastity L. Healy Steven B. Ortmeier Erin Harmon Gregory C. Shearer Timothy D. O’Connell 《Journal of lipid research》2015,56(12):2297-2308
Heart failure with preserved ejection fraction (HFpEF) is half of all HF, but standard HF therapies are ineffective. Diastolic dysfunction, often secondary to interstitial fibrosis, is common in HFpEF. Previously, we found that supra-physiologic levels of ω3-PUFAs produced by 12 weeks of ω3-dietary supplementation prevented fibrosis and contractile dysfunction following pressure overload [transverse aortic constriction (TAC)], a model that resembles aspects of remodeling in HFpEF. This raised several questions regarding ω3-concentration-dependent cardioprotection, the specific role of EPA and DHA, and the relationship between prevention of fibrosis and contractile dysfunction. To achieve more clinically relevant ω3-levels and test individual ω3-PUFAs, we shortened the ω3-diet regimen and used EPA- and DHA-specific diets to examine remodeling following TAC. The shorter diet regimen produced ω3-PUFA levels closer to Western clinics. Further, EPA, but not DHA, prevented fibrosis following TAC. However, neither ω3-PUFA prevented contractile dysfunction, perhaps due to reduced uptake of ω3-PUFA. Interestingly, EPA did not accumulate in cardiac fibroblasts. However, FFA receptor 4, a G protein-coupled receptor for ω3-PUFAs, was sufficient and required to block transforming growth factor β1-fibrotic signaling in cultured cardiac fibroblasts, suggesting a novel mechanism for EPA. In summary, EPA-mediated prevention of fibrosis could represent a novel therapy for HFpEF. 相似文献
102.
103.
Anne F Mannion Stephane Kämpfen Urs Munzinger Ines Kramers-de Quervain 《Arthritis research & therapy》2009,11(5):R139-13
Introduction
Patient's expectations are variably reported to influence self-rated outcome and satisfaction after medical treatment; this prospective study examined which of the following was the most important unique determinant of global outcome/satisfaction after total knee arthroplasty (TKA): baseline expectations; fulfilment of expectations; or current symptoms and function. 相似文献104.
Tamar F Brionez Shervin Assassi John D Reveille Thomas J Learch Laura Diekman Michael M Ward John C Davis Jr Michael H Weisman Perry Nicassio 《Arthritis research & therapy》2009,11(6):R182-9
Introduction
Functional status is an integral component of health-related quality of life in patients with ankylosing spondylitis (AS). The purpose of this study was to investigate the role of psychological variables in self-reported functional limitation in patients with AS, while controlling for demographic and medical variables. 相似文献105.
Christelle Boileau Johanne Martel-Pelletier Judith Caron Philippe Msika Georges B Guillou Caroline Baudouin Jean-Pierre Pelletier 《Arthritis research & therapy》2009,11(2):R41-9
Introduction
The aims of this study were, first, to investigate the in vivo effects of treatment with avocado/soybean unsaponifiables on the development of osteoarthritic structural changes in the anterior cruciate ligament dog model and, second, to explore their mode of action. 相似文献106.
107.
F. L. Laksmana P. J. A. Hartman Kok H. Vromans H. W. Frijlink K. Van der Voort Maarschalk 《AAPS PharmSciTech》2009,10(3):732-742
Next to the coating formulation, process conditions play important roles in determining coating quality. This study aims to
develop an operational window that separates layering from agglomeration regimes and, furthermore, the one that leads to the
best coating quality in a fluidized bed coater. The bed relative humidity and the droplet size of the coating aerosol were
predicted using a set of engineering models. The coating quality was characterized using a quantitative image analysis method,
which measures the coating thickness distribution, the total porosity, and the pore size in the coating. The layering regime
can be achieved by performing the coating process at a certain excess of the viscous Stokes number (ΔSt
v). This excess is dependent on the given bed relative humidity and droplet size. The higher the bed relative humidity, the
higher is the ΔSt
v required to keep the process in the layering regime. Further, it is shown that using bed relative humidity and droplet size
alone is not enough to obtain constant coating quality. The changes in bed relative humidity and droplet size have been identified
to correlate to the fractional area of particles sprayed per unit of time. This parameter can effectively serve as an additional
parameter to be considered for a better control on the coating quality. High coating quality is shown to be achieved by performing
the process close to saturation and spraying droplets small enough to obtain high spraying rate, but not too small to cause
incomplete coverage of the core particles. 相似文献
108.
David A. Dik Daniel R. Marous Jed F. Fisher 《Critical reviews in biochemistry and molecular biology》2017,52(5):503-542
The lytic transglycosylases (LTs) are bacterial enzymes that catalyze the non-hydrolytic cleavage of the peptidoglycan structures of the bacterial cell wall. They are not catalysts of glycan synthesis as might be surmised from their name. Notwithstanding the seemingly mundane reaction catalyzed by the LTs, their lytic reactions serve bacteria for a series of astonishingly diverse purposes. These purposes include cell-wall synthesis, remodeling, and degradation; for the detection of cell-wall-acting antibiotics; for the expression of the mechanism of cell-wall-acting antibiotics; for the insertion of secretion systems and flagellar assemblies into the cell wall; as a virulence mechanism during infection by certain Gram-negative bacteria; and in the sporulation and germination of Gram-positive spores. Significant advances in the mechanistic understanding of each of these processes have coincided with the successive discovery of new LTs structures. In this review, we provide a systematic perspective on what is known on the structure–function correlations for the LTs, while simultaneously identifying numerous opportunities for the future study of these enigmatic enzymes. 相似文献
109.
C. A. Kreikemeier T. B. Engle K. L. Lucot S. D. Kachman T. E. Burkey D. C. Ciobanu 《Animal genetics》2015,46(2):205-208
Tumor necrosis factor alpha (TNF‐α) is a pro‐inflammatory cytokine with a role in activating adaptive immunity to viral infections. By inhibiting the capacity of plasmacytoid dendritic cells to produce interferon‐α and TNF‐α, porcine circovirus 2 (PCV2) limits the maturation of myeloid dendritic cells and impairs their ability to recognize viral and bacterial antigens. Previously, we reported QTL for viremia and immune response in PCV2‐infected pigs. In this study, we analyzed phenotypic and genetic relationships between TNF‐α protein levels, a potential indicator of predisposition to PCV2 co‐infection, and PCV2 susceptibility. Following experimental challenge with PCV2b, TNF‐α reached the peak at 21 days post‐infection (dpi), at which time a difference was observed between pigs that expressed extreme variation in viremia and growth (P < 0.10). A genome‐wide association study (n = 297) revealed that genotypes of 56 433 SNPs explained 73.9% of the variation in TNF‐α at 21 dpi. Major SNPs were identified on SSC8, SSC10 and SSC14. Haplotypes based on SNPs from a SSC8 (9 Mb) 1‐Mb window were associated with variation in TNF‐α (P < 0.02), IgG (P = 0.05) and IgM (P < 0.13) levels at 21 dpi. Potential overlap of regulatory mechanisms was supported by the correlations between genomic prediction values of TNF‐α and PCV2 antibodies (21 dpi, r > 0.22), viremia (14–21 dpi, P > 0.29) and viral load (r = 0.31, P < 0.0001). Characterization of the QTL regions uncovered genes that could influence variation in TNF‐α levels as well as T‐ and B‐cell development, which can affect disease susceptibility. 相似文献
110.
Daw-Yang Hwang Stefan Kohl Xueping Fan Asaf Vivante Stefanie Chan Gabriel C. Dworschak Julian Schulz Albertien M. van Eerde Alina C. Hilger Heon Yung Gee Tracie Pennimpede Bernhard G. Herrmann Glenn van de Hoek Kirsten Y. Renkema Christoph Schell Tobias B. Huber Heiko M. Reutter Neveen A. Soliman Natasa Stajic Radovan Bogdanovic Elijah O. Kehinde Richard P. Lifton Velibor Tasic Weining Lu Friedhelm Hildebrandt 《Human genetics》2015,134(8):905-916