首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >A Lindera obtusiloba Extract Blocks Calcium-/Phosphate-Induced Transdifferentiation and Calcification of Vascular Smooth Muscle Cells and Interferes with Matrix Metalloproteinase-2 and Metalloproteinase-9 and NF-κB
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A Lindera obtusiloba Extract Blocks Calcium-/Phosphate-Induced Transdifferentiation and Calcification of Vascular Smooth Muscle Cells and Interferes with Matrix Metalloproteinase-2 and Metalloproteinase-9 and NF-κB

机译:tusLindera obtusiloba提取物可阻止钙/磷酸盐诱导的血管平滑肌细胞的转分化和钙化并干扰基质金属蛋白酶-2金属蛋白酶9和NF-κB

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摘要

Vascular calcifications bear the risk for cardiovascular complications and have a high prevalence among patients with chronic kidney disease. Central mediators of vascular calcifications are vascular smooth muscle cells (VSMC). They transdifferentiate into a synthetic/osteoblast-like phenotype, which is induced, for example, by elevated levels of calcium and phosphate (Ca/P) due to a disturbed mineral balance. An aqueous extract from Lindera obtusiloba (LOE) is known to exert antifibrotic and antitumor effects or to interfere with the differentiation of preadipocytes. Using murine and rat VSMC cell lines, we here investigated whether LOE also protects VSMC from Ca/P-induced calcification. Indeed, LOE effectively blocked Ca/P-induced calcification of VSMC as shown by decreased VSMC mineralization and secretion of alkaline phosphatase. In parallel, mRNA expression of the calcification markers osterix and osteocalcin was reduced. Vice versa, the Ca/P-induced loss of the VSMC differentiation markers alpha smooth muscle actin and smooth muscle protein 22-alpha was rescued by LOE. Further, LOE blocked Ca/P-induced mRNA expressions and secretions of matrix metalloproteinases-2/-9 and activation of NF-κB, which are known contributors to vascular calcification. In conclusion, LOE interferes with the Ca/P-induced transdifferentiation/calcification of VSMC. Thus, LOE should be further analysed regarding a potential complementary treatment option for cardiovascular diseases including vascular calcifications.
机译:血管钙化具有心血管并发症的风险,并且在慢性肾脏病患者中患病率很高。血管钙化的主要介质是血管平滑肌细胞(VSMC)。它们转分化为合成/成骨细胞样表型,例如由于矿物质平衡失调而引起的钙和磷酸盐(Ca / P)水平升高所诱导。众所周知,Lindera obtusiloba(LOE)的水提物具有抗纤维化和抗肿瘤作用,或干扰前脂肪细胞的分化。使用鼠类和大鼠VSMC细胞系,我们在这里研究LOE是否也保护VSMC免受Ca / P诱导的钙化的影响。实际上,LOE有效地阻止了Ca / P诱导的VSMC钙化,如VSMC矿化减少和碱性磷酸酶分泌减少所表明。平行地,钙化标志物osterix和骨钙素的mRNA表达降低。反之亦然,LOE挽救了Ca / P诱导的VSMC分化标志物α平滑肌肌动蛋白和平滑肌蛋白22-alpha的丧失。此外,LOE阻断了Ca / P诱导的mRNA表达和基质金属蛋白酶-2 / -9的分泌以及NF-κB的激活,这是导致血管钙化的已知因素。总之,LOE会干扰Ca / P诱导的VSMC转分化/钙化。因此,应就包括血管钙化在内的心血管疾病的潜在补充治疗方案进一步分析LOE。

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