首页> 外文期刊>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-kappa B
【24h】

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-kappa B

机译:Lindera optusiLoba提取物阻断钙/磷酸盐诱导的血管平滑肌细胞的转染和钙化,并干扰基质金属蛋白酶-2和金属蛋白酶-9和NF-Kappa B.

获取原文
获取原文并翻译 | 示例
           

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-kappa B, 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:血管钙化承受心血管并发症的风险,慢性肾病患者具有高患病率。血管钙化的中央介质是血管平滑肌细胞(VSMC)。它们转化为合成/成骨细胞样表型,其由于损伤的矿物平衡而通过升高的钙和磷酸盐(CA / P)诱导。已知来自Lindera optusiLoba(LOE)的含水提取物施加抗纤维抗和抗肿瘤作用,或者干扰前脂肪细胞的分化。使用小鼠和大鼠VSMC细胞系,我们在这里研究了LOE是否保护VSMC免受CA / P诱导的钙化。实际上,LOE有效地阻断了VSMC的CA / P诱导的钙化,如下降的VSMC矿化和碱性磷酸酶分泌所示。同时,降低了钙化标记物和骨钙素的mRNA表达。反之亦然,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-α通过LOE救出。此外,LOE阻断的Ca / p诱导的MRNA表达和基质金属蛋白酶-2 / -9的分泌物和NF-Kappa B的活化,其是血管钙化的已知贡献者。总之,LOE干扰了VSMC的CA / P诱导的转染/钙化。因此,应进一步分析LOE,关于心血管疾病的潜在互补治疗选择,包括血管钙化。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号