Department of Pharmaceutics and Industrial Pharmacy, Faculty of Pharmaceutical Sciences, Chulalongkorn University, Bangkok, 10330, Thailand.
Center of Excellence in Biomaterial Engineering in Medical and Health, Chulalongkorn University, Bangkok, 10330, Thailand.
Sci Rep. 2023 Aug 29;13(1):14102. doi: 10.1038/s41598-023-41388-8.
Asiatic acid (AA) and asiaticoside, pentacyclic triterpenoid compounds derived from Centella asiatica, are known for their biological effects in promoting type I collagen synthesis and inducing osteogenesis of stem cells. However, their applications in regenerative medicine are limited due to their low potency and poor aqueous solubility. This work aimed to evaluate the osteogenic induction activity of AA derivatives in human periodontal ligament stem cells (hPDLSCs) in vitro. Four compounds were synthesised, namely 501, 502, 503, and 506. AA was used as the control. The 502 exhibited low water solubility, while the 506 compound showed the highest. The cytotoxicity analysis demonstrated that 503 caused significant deterioration in cell viability, while other derivatives showed no harmful effect on hPDLSCs. The dimethyl aminopropyl amine derivative of AA, compound 506, demonstrated a relatively high potency in inducing osteogenic differentiation. An elevated mRNA expression of osteogenic-related genes, BMP2, WNT3A, ALP, OSX and IBSP was observed with 506. Additionally, the expression of BMP-2 protein was enhanced with increasing dose of 506, and the effect was pronounced when the Erk signalling molecule was inhibited. The 506 derivative was proposed for the promotion of osteogenic differentiation in hPDLSCs by upregulating BMP2 via the Erk signalling pathway. The 506 molecule showed promise in bone tissue regeneration.
积雪草酸(AA)和积雪草苷,是来源于积雪草的五环三萜类化合物,具有促进 I 型胶原合成和诱导干细胞成骨的生物学效应。然而,由于其效力低和水溶性差,其在再生医学中的应用受到限制。本研究旨在评估 AA 衍生物在人牙周膜干细胞(hPDLSCs)中的体外成骨诱导活性。合成了 4 种化合物,分别为 501、502、503 和 506。AA 用作对照。502 表现出低水溶性,而 506 化合物表现出最高的水溶性。细胞毒性分析表明 503 导致细胞活力显著恶化,而其他衍生物对 hPDLSCs 没有不良影响。AA 的二甲氨基丙基胺衍生物,化合物 506,在诱导成骨分化方面表现出相对较高的效力。与 506 一起观察到成骨相关基因 BMP2、WNT3A、ALP、OSX 和 IBSP 的 mRNA 表达升高。此外,随着 506 剂量的增加,BMP-2 蛋白的表达增强,当抑制 Erk 信号分子时,效果更为明显。506 衍生物通过上调 Erk 信号通路中的 BMP2 促进 hPDLSCs 的成骨分化。506 分子在骨组织再生方面具有潜力。