Liu Yunzhu, Yang Wanqiu, Yuan Rongli, Li Zimeng, Wang Tianyu, Yang Bin, Li Zhi, Wang Mengjing, Wu Jie
Department of Acupuncture and Moxibustion, Chengdu University of Traditional Chinese Medicine, No. 37 Shierqiao Road, Jinniu District, Chengdu, Sichuan, 610032, P.R. China.
Yibin Second Hospital of Traditional Chinese Medicine, No. 8 Longquan Road, Cuiping District, Yibin, Sichuan, 644000, P. R. China.
Comb Chem High Throughput Screen. 2025;28(8):1443-1457. doi: 10.2174/0113862073365843241223093834.
This study aimed to investigate the possible mechanism through which acupuncture protects ovaries with Poor Ovarian Response (POR) in rats based on microRNA (miRNA).
Thirty-six SPF SD female non-pregnant rats aged 8 weeks were randomly divided into the blank group, model group, and acupuncture group, with 12 rats in each group. According to the group, the rats were given gavage of Tripterygium wilfordii polyglycosides suspension for 14 days to establish the model of POR, and then the rats were treated with acupuncture for 2 weeks, once a day, for 20 minutes. Afterward, their hormone levels were measured, and HE staining was performed on the ovaries after the intervention. Three rats from each group were randomly selected for ovarian tissue miRNA sequencing, and differential miRNAs were subjected to Gene Ontology (GO) enrichment analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) signaling pathway analysis, and Quantitative Polymerase Chain Reaction (QPCR) verification. By using TargetScan to predict the target genes of differential miRNAs, we validated the results with a dual luciferase reporter gene assay.
Compared with the blank group, the estrus cycle of the model group was significantly prolonged (P<0.01). Anti-Müllerian Hormone (AMH) (P<0.01) and Estrogen (E2) were significantly decreased (P<0.05). Follicle-Stimulating Hormone (FSH) (P<0.05) and Luteinizing Hormone (LH) increased sharply (P<0.01). Compared with the model group, the estrus cycle was significantly shortened in the acupuncture group (P<0.01). AMH and E2 were markedly raised (P<0.05). FSH (P<0.05) and LH (P<0.01) were significantly declined. miRNA sequencing showed that there were 23 miRNAs significantly different between the model group and the blank group (P<0.05), and 30 miRNAs significantly different between the acupuncture group and the model group (P<0.05). GO demonstrated that the network was mainly involved in cellular components, cells, cellular metabolic processes, binding, and single biological processes; KEGG signaling pathway enrichment showed that it was mainly related to MAPK, adhesion junction, calcium signaling pathways, etc. Q-PCR results showed that after modeling, the expression rose, and after acupuncture, the expression of the following miRNA decreased: miR-154-5p (P<0.01), miR-300-5p (P < 0.05), miR-376c-5p (P<0.05). The dual luciferase reporter assay showed that the relative luciferase activity of the miR-300-5p mimics+MAP3K1-WT group was significantly lower than that of the NC+MAP3K1-WT group (P<0.01). HE results demonstrated that the number of primordial follicles and primary follicles in the model group was significantly lower than that in the blank group (P<0.05). Moreover, the morphology was poorer, and the granulosa cell layer was thinner. Compared with the model group, the number of primary follicles in the acupuncture group increased (P<0.05); the morphology and granulosa cell structure of the ovary were improved to different degrees, and mature follicles could be seen.
Acupuncture may improve the ovarian responsiveness of POR rats by regulating miR-154- 5p,miR-300-5p, and miR-376c-5p. Furthermore, miR-300-5p can specifically bind to the 3'-UTR of MAP3K1, and MAP3K1 may be the target of miR-300-5p.
本研究旨在基于微小RNA(miRNA)探讨针刺保护卵巢反应不良(POR)大鼠卵巢的可能机制。
将36只8周龄的SPF级SD雌性未孕大鼠随机分为空白组、模型组和针刺组,每组12只。按组给予大鼠灌胃雷公藤多苷混悬液14天以建立POR模型,然后对大鼠进行2周的针刺治疗,每天1次,每次20分钟。之后,检测其激素水平,并在干预后对卵巢进行苏木精-伊红(HE)染色。每组随机选取3只大鼠进行卵巢组织miRNA测序,对差异miRNA进行基因本体论(GO)富集分析、京都基因与基因组百科全书(KEGG)信号通路分析及定量聚合酶链反应(QPCR)验证。通过使用TargetScan预测差异miRNA的靶基因,并用双荧光素酶报告基因检测法验证结果。
与空白组相比,模型组的发情周期显著延长(P<0.01)。抗苗勒管激素(AMH)(P<0.01)和雌激素(E2)显著降低(P<0.05)。促卵泡生成素(FSH)(P<0.05)和促黄体生成素(LH)急剧升高(P<0.01)。与模型组相比,针刺组的发情周期显著缩短(P<0.01)。AMH和E2明显升高(P<0.05)。FSH(P<0.05)和LH(P<0.01)显著下降。miRNA测序显示,模型组与空白组之间有23种miRNA存在显著差异(P<0.05),针刺组与模型组之间有30种miRNA存在显著差异(P<0.05)。GO分析表明,该网络主要涉及细胞成分、细胞、细胞代谢过程、结合及单一生物学过程;KEGG信号通路富集显示,其主要与丝裂原活化蛋白激酶(MAPK)、黏附连接、钙信号通路等有关。QPCR结果显示,建模后以下miRNA的表达升高,针刺后表达降低:miR-154-5p(P<0.01)、miR-300-5p(P<0.05)、miR-376c-5p(P<0.05)。双荧光素酶报告基因检测显示,miR-300-5p模拟物+丝裂原活化蛋白激酶激酶激酶1(MAP3K1)野生型(WT)组的相对荧光素酶活性显著低于阴性对照(NC)+MAP3K1-WT组(P<0.01)。HE结果表明,模型组的原始卵泡和初级卵泡数量显著低于空白组(P<0.05)。此外,形态较差,颗粒细胞层较薄。与模型组相比,针刺组的初级卵泡数量增加(P<0.05);卵巢的形态和颗粒细胞结构有不同程度的改善,可见成熟卵泡。
针刺可能通过调节miR-154-5p、miR-300-5p和miR-376c-5p改善POR大鼠的卵巢反应性。此外,miR-300-5p可特异性结合MAP3K1的3'-非翻译区(UTR),MAP3K1可能是miR-300-5p的靶标。