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INTRODUCTION: One of the most significant clinical features of chronic kidney disease is renal interstitial fibrosis (RIF). This study aimed to investigate the role and mechanism of Shenqi Pill (SQP) on RIF. METHODS: RIF model was established by conducting unilateral ureteral obstruction (UUO) surgery on rat or stimulating human kidney-2 (HK-2) cell with transforming growth factor ß1 (TGFß1). After modeling, the rats in the SQP low dose group (SQP-L), SQP middle dose group (SQP-M) and SQP high dose group (SQP-H) were treated with SQP at 1.5, 3 or 6 g/kg/d, and the cells in the TGFß1+SQP-L/M/H were treated with 2.5%, 5%, 10% SQP-containing serum. In in vivo assays, serum creatinine (SCr) and blood urea nitrogen (BUN) content were measured, kidney histopathology was evaluated., and α-smooth muscle actin (α-SMA) expression was detected by immunohistochemistry. Interleukin-1ß (IL-1ß), interleukin-6 (IL-6) and tumor necrosis factor-α (TNF-α) content, inhibitor of kappa B alpha (IKBα) and P65 phosphorylation were assessed. Meanwhile, cell viability, inflammatory cytokines content, α-SMA expression, IKBα and P65 phosphorylation were detected in vitro experiment. Results. SQP exhibited reno-protective effect by decreasing SCr and BUN content, improving renal interstitial damage, blunting fibronectin (FN) and α-SMA expression in RIF rats. Similarly, after the treatment with SQP-containing serum, viability and α-SMA expression were remarkably decreased in TGFß1-stimulated HK-2 cell. Furthermore, SQP markedly down-regulated IL-1ß, IL-6, and TNF-α content, IKBα and RelA (P65) phosphorylation both in vivo and in vitro. Conclusion. SQP has a reno-protective effect against RIF in vivo and in vitro, and the effect is partly linked to nuclear factor-kappa B (NF-κB) pathway related inflammatory response, which indicates that SQP may be a candidate drug for RIF. DOI: 10.52547/ijkd.7546.
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Modelos Animales de Enfermedad , Medicamentos Herbarios Chinos , Fibrosis , Riñón , FN-kappa B , Animales , Humanos , Ratas , Actinas/metabolismo , Nitrógeno de la Urea Sanguínea , Línea Celular , Creatinina/sangre , Citocinas/metabolismo , Medicamentos Herbarios Chinos/farmacología , Fibrosis/tratamiento farmacológico , Fibrosis/metabolismo , Fibrosis/patología , Riñón/patología , Riñón/efectos de los fármacos , Riñón/metabolismo , FN-kappa B/efectos de los fármacos , FN-kappa B/metabolismo , Inhibidor NF-kappaB alfa/metabolismo , Ratas Sprague-Dawley , Insuficiencia Renal Crónica/metabolismo , Insuficiencia Renal Crónica/patología , Insuficiencia Renal Crónica/tratamiento farmacológico , Factor de Crecimiento Transformador beta1/metabolismo , Obstrucción Ureteral/patología , Obstrucción Ureteral/complicaciones , Obstrucción Ureteral/tratamiento farmacológicoRESUMEN
Objective: Shen Qi Wan (SQW) is the most classic prescription for the clinical therapy of chronic kidney disease in China. Nevertheless, the function of SQW in renal interstitial fibrosis (RIF) has not been clearly clarified. Our purpose was to explore the protective function of SQW on RIF. Methods: After intervention with SQW-containing serum alone at increasing concentrations (2.5, 5, and 10%) or in combination with siNotch1, the transforming growth factor-beta (TGF-ß)-induced HK-2 cell viability, extracellular matrix (ECM)-, epithelial-mesenchymal transition (EMT), and Notch1 pathway-associated protein expressions were assessed by cell counting kit-8, qRT-PCR, western blot, and immunofluorescence assays. Results: SQW-containing serum intensified the viability of TGF-ß-mediated HK-2 cells. Besides, it augmented the collagen II and E-cadherin levels, and weakened the fibronectin, α-SMA, vimentin, N-cadherin, and collagen I levels in HK-2 cells triggered by TGF-ß. Moreover, it is found that TGF-ß led to the upregulation of Notch1, Jag1, HEY1, HES1, and TGF-ß in HK-2 cells, which was partially offset by SQW-containing serum. Furthermore, cotreatment of SQW-containing serum and Notch1 knockdown further apparently alleviated the Notch1, vimentin, N-cadherin, collagen I, and fibronectin levels in HK-2 cells induced by TGF-ß. Conclusion: Collectively, these findings elucidated that SQW-containing serum attenuated RIF via restraining EMT through the repression of the Notch1 pathway.
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The in situ combustion (ISC) technique is promisingly applied in heavy oil recovery, whereas the operation inevitably causes high temperature and high pressure for a long duration in the thermal recovery well. As a critical component, oil casing, traditionally made of plain carbon steel in China, generally suffers from poor creep resistance and degraded remnant strength under such a harsh environment, which leads to frequent casing damage and inferior recovery efficiency. In this study, a strategy was adopted to tackle the issue by adding chromium (Cr) element into the plain carbon steel. We designed two types of novel steel with the respective addition of 1 wt.% and 13 wt.% Cr element into plain carbon steel for oil casing. Surprisingly, the trace addition of Cr element with 1 wt.% effectively lowered the creep rate in a creep test at 600 °C and 400 MPa and maintained high remnant tensile strength after creep. More significantly, prior creep history dramatically enhanced remnant strength when Cr element was added up to 13 wt.%. After a long-term creep time of 96 h, the samples were conferred by a stress increment of ~92.5 MPa (~11.0%) relative to the creep-free counterparts, whereas the value was reduced by ~158.4 MPa (~17.8%) for plain carbon steel under the same deformation conditions. Such superior mechanical performances in the Cr-doped steels are mainly ascribed to precipitation retardation of carbides and sluggish precipitate coarsening, which continuously favors a precipitation-strengthening effect in steel. These findings provide a fundamental understanding of precipitation response and creep behaviors and, more importantly, enable the development of high-performance steels used in the field of unconventional petroleum and gas resources.