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      【巖藻多糖快訊第十六期】《Scientific Reports》:巖藻多糖具有延緩慢性腎衰的活性

       中國生命營養(yǎng) 2019-10-22

      巖藻多糖快訊

      第十六期

      《Scientific Reports》:巖藻多糖具有延緩慢性腎衰的活性

      原標題:巖藻多糖通過抑制CD44信號通路抑制腎小管間質(zhì)纖維化

      ①巖藻多糖(fucoidan)是褐藻來源的以巖藻糖為主要組成單糖的一種硫酸化多糖,研究證明巖藻多糖具有治療糖尿病腎病及延緩慢性腎衰的活性;
      ②腎小管間質(zhì)纖維化是慢性腎炎的決定因素,本研究評價了巖藻多糖對腎小管間質(zhì)化的抑制作用;
      ③患有慢性腎炎的小鼠每天服用10-100mg/kg的巖藻多糖,持續(xù)六周,觀察小鼠的腎臟功能及腎炎病情。
      ④實驗結(jié)果:服用100mg/kg巖藻多糖的小鼠腎臟功能得到顯著改善,同時腎小管間質(zhì)化得到抑制,通過機理研究發(fā)現(xiàn),巖藻多糖能夠抑制CD44, β-catenin及TGF-β蛋白的表達,從而抑制間質(zhì)纖維化,改善慢性腎炎。
      ⑤結(jié)論:巖藻多糖具有治療糖尿病腎病及延緩慢性腎衰的活性。

      關(guān)鍵詞:巖藻多糖;腎衰;慢性腎炎;腎小管間質(zhì)纖維化

      延伸閱讀:

      Sci. Rep. 7, 40183; doi: 10.1038/srep40183 (2017).

      Oligo-fucoidan prevents renal tubulointerstitial fbrosis by inhibiting the CD44 signal pathway

      Abstract:

      Tubulointerstitial fbrosis is recognized as a key determinant of progressive chronic kidney disease (CKD). Fucoidan, a sulphated polysaccharide extracted from brown seaweed, exerts benefcial e?ects in some nephropathy models. The present study evaluated the inhibitory e?ect of oligo-fucoidan (800 Da) on renal tubulointerstitial fbrosis. We established a mouse CKD model by right nephrectomy with transient ischemic injury to the left kidney. Six weeks after the surgery, we fed the CKD mice oligo-fucoidan at 10, 20, and 100 mg/kg/d for 6 weeks and found that the oligo-fucoidan doses less than 100 mg/kg/d improved renal function and reduced renal tubulointerstitial fbrosis in CKD mice. Oligofucoidan also inhibited pressure-induced fbrotic responses and the expression of CD44, β-catenin, and TGF-β in rat renal tubular cells (NRK-52E). CD44 knockdown downregulated the expression of β-catenin and TGF-β in pressure-treated cells. Additional ligands for CD44 reduced the anti-fbrotic e?ect of oligofucoidan in NRK-52E cells. These data suggest that oligo-fucoidan at the particular dose prevents renal tubulointerstitial fbrosis in a CKD model. The anti-fbrotic e?ect of oligo-fucoidan may result from interfering with the interaction between CD44 and its extracellular ligands.

      First Authors:

      Cheng-Hsien Chen

      Correspondence:

      Tso-Hsiao Chen

      All Authors:

      Cheng-Hsien Chen, Yuh-Mou Sue, Chung-Yi Cheng, Yen-Cheng Chen, Chung-Te Liu, Yung-Ho Hsu, Pai-An Hwang, Nai-Jen Huang & Tso-Hsiao Chen

      2017-01-18 Article

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