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基于生物化学计量学的方法从果实中发现苯丙素类化合物作为体外破骨细胞形成的抑制剂。

Biochemometry-Based Discovery of Phenylpropanoids from Fruits as Inhibitors of In Vitro Osteoclast Formation.

机构信息

Division of Pharmacognosy, Department of Pharmaceutical Sciences, University of Vienna, Josef-Holaubek-Platz 2, 1090 Vienna, Austria.

Division of Pharmacology and Toxicology, Department of Pharmaceutical Sciences, University of Vienna, Josef-Holaubek-Platz 2, 1090 Vienna, Austria.

出版信息

Molecules. 2022 Jun 4;27(11):3611. doi: 10.3390/molecules27113611.

DOI:10.3390/molecules27113611
PMID:35684547
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9182001/
Abstract

(1) Background: Inhibition of osteoclast differentiation is the key approach in treating osteoporosis. However, using state-of-the-art treatments such as bisphosphonates and estrogen-based therapy is usually accompanied by many side effects. As opposed to this, the use of natural products as an osteoporotic remedy delivers promising outcomes with minimal side effects. (2) Methods: In the present study, we implemented a biochemometric workflow comprising (i) chemometric approaches using NMR and mass spectrometry and (ii) cell biological approaches using an osteoclast cytochemical marker (TRAP). The workflow serves as a screening tool to pursue potential in vitro osteoclast inhibitors. (3) Results: The workflow allowed for the selective isolation of two phenylpropanoids (coniferyl alcohol and sinapyl alcohol) from the fruits of neem tree (). These two isolated phenylpropanoids showed a very promising dose-dependent inhibition of osteoclast differentiation with negligible effects in terms of cell viability. (4) Conclusion: The presented workflow is an effective tool in the discovery of potential candidates for osteoclast inhibition from complex extracts. The used biochemometric approach saves time, effort and costs while delivering precise hints to selectively isolate bioactive constituents.

摘要

(1) 背景:抑制破骨细胞分化是治疗骨质疏松症的关键方法。然而,使用最新的治疗方法,如双磷酸盐和雌激素为基础的治疗,通常伴随着许多副作用。相比之下,使用天然产物作为骨质疏松症的治疗方法,具有最小的副作用,可带来有前景的结果。

(2) 方法:在本研究中,我们实施了一个生物化学计量学工作流程,包括(i)使用 NMR 和质谱的化学计量方法,以及(ii)使用破骨细胞细胞化学标志物(TRAP)的细胞生物学方法。该工作流程可作为一种筛选工具,以寻找潜在的体外破骨细胞抑制剂。

(3) 结果:该工作流程允许从楝树果实中选择性地分离出两种苯丙烷类化合物(松柏醇和芥子醇)。这两种分离出的苯丙烷类化合物对破骨细胞分化具有非常有前途的剂量依赖性抑制作用,对细胞活力几乎没有影响。

(4) 结论:所提出的工作流程是从复杂提取物中发现潜在的破骨细胞抑制剂候选物的有效工具。所使用的生物化学计量方法节省了时间、精力和成本,同时提供了选择性分离生物活性成分的精确提示。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/bae61c7603db/molecules-27-03611-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/32d4c8f81ddb/molecules-27-03611-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/72682ec3272a/molecules-27-03611-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/3c7464d327ad/molecules-27-03611-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/2f27e553a052/molecules-27-03611-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/4f3c71629fe7/molecules-27-03611-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/0e9eb2edfd9b/molecules-27-03611-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/704328cf600d/molecules-27-03611-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/bae61c7603db/molecules-27-03611-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/32d4c8f81ddb/molecules-27-03611-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/72682ec3272a/molecules-27-03611-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/3c7464d327ad/molecules-27-03611-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/2f27e553a052/molecules-27-03611-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/4f3c71629fe7/molecules-27-03611-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/0e9eb2edfd9b/molecules-27-03611-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/704328cf600d/molecules-27-03611-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf84/9182001/bae61c7603db/molecules-27-03611-g008.jpg

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