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六味地黄丸通过 YAP-自噬轴减轻骨髓间充质干细胞(BMSC)衰老来减轻去卵巢引起的骨丢失。

Liuwei Dihuang pills attenuate ovariectomy-induced bone loss by alleviating bone marrow mesenchymal stem cell (BMSC) senescence via the Yes-associated protein (YAP)-autophagy axis.

机构信息

Basic Medicine College, Chengdu University of Traditional Chinese Medicine, Chengdu, China.

出版信息

Pharm Biol. 2024 Dec;62(1):42-52. doi: 10.1080/13880209.2023.2291675. Epub 2023 Dec 19.

Abstract

CONTEXT

Liuwei Dihuang pill (LWDH) has been used to treat postmenopausal osteoporosis (PMOP).

OBJECTIVE

To explore the effects and mechanisms of action of LWDH in PMOP.

MATERIALS AND METHODS

Forty-eight female Sprague-Dawley rats were divided into four groups: sham-operated (SHAM), ovariectomized (OVX), LWDH high dose (LWDH-H, 1.6 g/kg/d) and LWDH low dose (LWDH-L, 0.8 g/kg/d); the doses were administered after ovariectomy via gavage for eight weeks. After eight weeks, the bone microarchitecture was evaluated. The effect of LWDH on the differentiation of bone marrow mesenchymal stem cells (BMSCs) was assessed via osteogenesis- and lipogenesis-induced BMSC differentiation. The senescence-related biological indices were also detected using senescence staining, cell cycle analysis, quantitative real-time polymerase chain reaction and western blotting. Finally, the expression levels of autophagy-related proteins and Yes-associated protein (YAP) were evaluated.

RESULTS

LWDH-L and LWDH-H significantly modified OVX-induced bone loss. LWDH promoted osteogenesis and inhibited adipogenesis in OVX-BMSCs. Additionally, LWDH decreased the positive ratio of senescence OVX-BMSCs and improved cell viability, cell cycle, and the mRNA and protein levels of p53 and p21. LWDH upregulated the expression of autophagy-related proteins, LC3, Beclin1 and YAP, in OVX-BMSCs and downregulated the expression of p62.

DISCUSSION AND CONCLUSIONS

LWDH improves osteoporosis by delaying the BMSC senescence through the YAP-autophagy axis.

摘要

背景

六味地黄丸(LWDH)已用于治疗绝经后骨质疏松症(PMOP)。

目的

探讨 LWDH 治疗 PMOP 的作用机制。

材料和方法

48 只雌性 Sprague-Dawley 大鼠分为 4 组:假手术(SHAM)组、去卵巢(OVX)组、LWDH 高剂量(LWDH-H,1.6g/kg/d)组和 LWDH 低剂量(LWDH-L,0.8g/kg/d)组;去卵巢后通过灌胃给药,持续 8 周。8 周后评估骨微结构。通过成骨和脂生成诱导 BMSC 分化来评估 LWDH 对骨髓间充质干细胞(BMSC)分化的影响。通过衰老染色、细胞周期分析、实时定量聚合酶链反应和蛋白质印迹检测衰老相关生物指标。最后,评估自噬相关蛋白和 Yes 相关蛋白(YAP)的表达水平。

结果

LWDH-L 和 LWDH-H 可显著改善 OVX 诱导的骨丢失。LWDH 促进 OVX-BMSCs 成骨和抑制脂生成。此外,LWDH 降低 OVX-BMSC 衰老的阳性率,提高细胞活力、细胞周期以及 p53 和 p21 的 mRNA 和蛋白水平。LWDH 上调 OVX-BMSCs 中自噬相关蛋白 LC3、Beclin1 和 YAP 的表达,下调 p62 的表达。

讨论和结论

LWDH 通过 YAP-自噬轴延缓 BMSC 衰老来改善骨质疏松症。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6901/11734888/fad0dd641fe6/IPHB_A_2291675_F0001_C.jpg

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