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提取液促进人原代成骨细胞的体外分化和功能。

Extract Promotes In Vitro Differentiation and Functionality of Human Primary Osteoblasts.

机构信息

Dipartimento di Biotecnologie, Chimica e Farmacia (Dipartimento di Eccellenza 2018-2022), Università degli Studi di Siena, via Aldo Moro 2, 53100 Siena, Italy.

Institute of Cellular Pharmacology (ICP Ltd.), F24, Triq Valletta, Mosta Technopark, Mosta MST 3000, Malta.

出版信息

Mar Drugs. 2019 Aug 15;17(8):473. doi: 10.3390/md17080473.

DOI:10.3390/md17080473
PMID:31443264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6724011/
Abstract

Marine algae have gained much importance in the development of nutraceutical products due to their high content of bioactive compounds. In this work, we investigated the activity of with the aim to demonstrate the pro-osteogenic ability of its extract on human primary osteoblast (HOb). Our data indicated that the acetonic extract of (EPP) is a safe product as it did not show any effect on osteoblast viability. At the same time, EPP showed to possess a beneficial effect on HOb functionality, triggering their differentiation and mineralization abilities. In particular EPP enhanced the expression of the earlier differentiation stage markers: a 5.4-fold increase in collagen type I alpha 1 chain (COL1A1), and a 2.3-fold increase in alkaline phosphatase (ALPL), as well as those involved in the late differentiation stage: a 3.7-fold increase in osteocalcin (BGLAP) expression and a 2.8-fold in osteoprotegerin (TNFRSF11B). These findings were corroborated by the enhancement in ALPL enzymatic activity (1.7-fold increase) and by the reduction of receptor activator of nuclear factor-B ligand (RANKL) and osteoprotegerin (OPG) ratio (0.6-fold decrease). Moreover, EPP demonstrated the capacity to enhance the bone nodules formation by 3.2-fold in 4 weeks treated HOb. Therefore, EPP showed a significant capability of promoting osteoblast phenotype. Given its positive effect on bone homeostasis, EPP could be used as a useful nutraceutical product that, in addition to a healthy lifestyle and diet, can be able to contrast and prevent bone diseases, especially those connected with ageing, such as osteoporosis (OP).

摘要

海洋藻类因其生物活性化合物含量高,在营养保健品的开发中受到了极大的重视。在这项工作中,我们研究了 的活性,旨在证明其提取物对人原代成骨细胞(HOb)的促成骨能力。我们的数据表明, 的丙酮提取物(EPP)是一种安全的产品,因为它对成骨细胞活力没有任何影响。同时,EPP 显示对 HOb 功能具有有益的影响,触发其分化和矿化能力。特别是,EPP 增强了早期分化阶段标志物的表达:COL1A1 增加了 5.4 倍,碱性磷酸酶(ALPL)增加了 2.3 倍,以及那些涉及晚期分化阶段的标志物:骨钙素(BGLAP)表达增加了 3.7 倍,骨保护素(TNFRSF11B)增加了 2.8 倍。这些发现得到了增强的 ALPL 酶活性(增加 1.7 倍)和核因子-B 配体受体激活剂(RANKL)和骨保护素(OPG)比值降低(降低 0.6 倍)的证实。此外,EPP 显示出在 4 周处理的 HOb 中增强骨结节形成的能力增加了 3.2 倍。因此,EPP 表现出显著促进成骨细胞表型的能力。鉴于其对骨稳态的积极影响,EPP 可用作一种有用的营养保健品,除了健康的生活方式和饮食外,还可以能够对抗和预防骨骼疾病,特别是与衰老相关的骨骼疾病,如骨质疏松症(OP)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/25c4801a772b/marinedrugs-17-00473-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/4e9aedccbccb/marinedrugs-17-00473-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/2624a8099b59/marinedrugs-17-00473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/a3038efc71f6/marinedrugs-17-00473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/a4562e9a5f69/marinedrugs-17-00473-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/39306756d567/marinedrugs-17-00473-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/651a1ec00502/marinedrugs-17-00473-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/620c42a51a6c/marinedrugs-17-00473-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/bf133bfb3cc9/marinedrugs-17-00473-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/c562a2de9267/marinedrugs-17-00473-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/dd1612fd7a2e/marinedrugs-17-00473-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/25c4801a772b/marinedrugs-17-00473-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/4e9aedccbccb/marinedrugs-17-00473-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/2624a8099b59/marinedrugs-17-00473-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/a3038efc71f6/marinedrugs-17-00473-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/a4562e9a5f69/marinedrugs-17-00473-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/39306756d567/marinedrugs-17-00473-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/651a1ec00502/marinedrugs-17-00473-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/620c42a51a6c/marinedrugs-17-00473-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/bf133bfb3cc9/marinedrugs-17-00473-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/c562a2de9267/marinedrugs-17-00473-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/dd1612fd7a2e/marinedrugs-17-00473-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f634/6724011/25c4801a772b/marinedrugs-17-00473-g011.jpg

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