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Introduction Glucocorticoids (GCs) are a group of steroid drugs that exert strong anti-inflammatory and immunosuppressive effects. The synthetic GCs include dexamethasone and prednisolone, which are currently in clinical use for the treatment
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Introduction Dexamethasone (DEX) is one of the most commonly prescribed synthetic glucocorticoids with wide anti-inflammatory and immunosuppressive properties ( Overman et al . 2013 , Kumar et al . 2015 ). However, prolonged DEX treatment
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Department of Experimental Medicine, Sapienza University of Rome, Rome, Lazio, Italy
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Department of Biological and Medical Sciences, Oxford Brookes University, Oxford, Oxfordshire, UK
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Department of Biological and Medical Sciences, Oxford Brookes University, Oxford, Oxfordshire, UK
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. 2019 a ). Crucially, AKR1D1-002 is also implicated in drug metabolism, as it metabolises the synthetic glucocorticoids prednisolone and dexamethasone, with downstream decreases in glucocorticoid receptor activation ( Nikolaou et al. 2020 ). The
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signaling molecules and intracellular pathways. Our previous works demonstrated that treatment of human ovarian cancer cells with dexamethasone (DEX), a synthetic GC, significantly increases cellular adhesion to ECM and their resistance to apoptosis induced
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( Kassel & Herrlich 2007 , Biddie et al . 2012 ). Previously, we have shown that human endothelial sensitivity to dexamethasone (DEX) varied according to the levels of GRα protein degradation ( Mata-Greenwood et al . 2013 ). Human umbilical vein
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(Sigma). Differentiation was initiated 24 h after confluence by incubation for 2 days in a culture medium containing 0.25 μM dexamethasone (Dex), 0.5 mM 3-isobutyl-1-methyl-xanthine and 5 μg/ml insulin (Sigma). This was followed by maintenance in feeding
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Micro Biochip Center, Hanyang University, Ansan City 425-170, South Korea
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receiving an exposure to BMOV for 18 h and a brief insulin treatment for 15 min. Consequently, we have also checked whether treatment of dexamethasone which has been shown to increase the cellular content of IR in 3T3 fibroblasts and IM9 cells ( Fantus et
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dexamethasone (DEX)-induced augmented proteolysis ( Sacheck et al . 2004 ). Compared with mammals, the insulin cascade appears to be refractory in the muscle tissue of chickens ( Dupont et al . 2004 , 2008 ). However, the PI3K/AKT/MTOR pathway in chicken
Division of Nephrology and Immunology, RWTH Aachen University Hospital, Pauwelsstr. 30, D-52074 Aachen, Germany
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Division of Nephrology and Immunology, RWTH Aachen University Hospital, Pauwelsstr. 30, D-52074 Aachen, Germany
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Division of Nephrology and Immunology, RWTH Aachen University Hospital, Pauwelsstr. 30, D-52074 Aachen, Germany
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Division of Nephrology and Immunology, RWTH Aachen University Hospital, Pauwelsstr. 30, D-52074 Aachen, Germany
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Division of Nephrology and Immunology, RWTH Aachen University Hospital, Pauwelsstr. 30, D-52074 Aachen, Germany
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Division of Nephrology and Immunology, RWTH Aachen University Hospital, Pauwelsstr. 30, D-52074 Aachen, Germany
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Division of Nephrology and Immunology, RWTH Aachen University Hospital, Pauwelsstr. 30, D-52074 Aachen, Germany
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of inflammation. Our working hypothesis was that glucocorticoids may enhance Ahsg expression on the transcriptional level and may therefore be useful in up-regulating Ahsg during inflammation. We report that dexamethasone up-regulates Ahsg gene
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effect of long-term treatment (days) with dexamethasone (dex) on proTRH mRNA levels was first described in CA77 cells ( Tavianini et al. 1989 ), and later in rat anterior pituitary or in diencephalic primary cultures ( Bruhn et al. 1994 , Luo et al