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Panax ginseng exerts cardioprotective effect post myocardial infarction by attenuating myocardial fibrosis and inflammation through SIRT1 signaling pathways 人参通过SIRT1信号通路减轻心肌纤维化和炎症,发挥心肌梗死后心肌保护作用
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-11 DOI: 10.1016/j.jgr.2025.01.001
Honglin Xu , Mingjie Pang , Changlei Hu , Tong Xu , Guanghong Chen , Guoyong Zhang , Xin Han , Yue Hua , Yuting Wu , Jiayi Zhang , Yiming Bi , Bin Liu , Yingchun Zhou

Background

Myocardial fibrosis and inflammation induce adverse cardiac remodeling post-myocardial infarction (MI). Panax ginseng (P. ginseng) is beneficial for diverse cardiovascular diseases. However, the therapeutic effect and molecular mechanism underlying cardiac remodeling are largely unclear.

Methods

A MI mouse model was constructed through permanent left anterior descending (LAD) coronary artery ligation. Transforming growth factor-β1 (TGF-β1) or lipopolysaccharide (LPS) was used for stimulating cardiac fibroblasts (CFs) or RAW264.7 macrophages to construct the collagen synthesis and inflammation model in vitro. The cardiac structure and function were detected through hematoxylin-eosin staining, Masson staining, and echocardiography, while myocardial fibrosis and inflammation markers were determined by Western-blot, immunohistochemistry, RT-PCR, and ELISA. Additionally, the Silent information regulator 1 (SIRT1)/nuclear factor-κB (NF-κB) mediated NOD like receptor 3 (NLRP3) inflammasome and TGF-β receptor I (TGFBR1) signaling pathways were also evaluated. A SIRT1 selective inhibitor (EX-527) was used for confirming the pharmacological mechanism of P. ginseng.

Results

In vivo, P. ginseng alleviated ventricular remodeling, enhanced heart function, and ameliorated collagen I, collagen III, IL-1β, and IL-18 levels dose-dependently. Moreover, P. ginseng significantly suppressed NLRP3-caspase1 inflammasome and TGFBR1/Smads signaling in MI mice. In vitro, P. ginseng significantly suppressed collagen and inflammation markers, NLRP3 inflammasome and TGFBR1/Smads signaling in TGF-β1-induced CFs or LPS-stimulated RAW264.7 cells. Mechanistically, P. ginseng suppressed NF-κB activity while promoting SIRT1 expression. SIRT1 suppression by EX-527 partially abolished the protective effects of P. ginseng in TGF-β1-induced CFs.

Conclusion

P. ginseng protects from adverse cardiac remodeling by attenuating myocardial fibrosis and inflammation post-MI through the regulation of SIRT1 and its downstream signaling pathways.
心肌纤维化和炎症可诱导心肌梗死(MI)后不良的心脏重构。人参对多种心血管疾病有益。然而,心脏重构的治疗效果和分子机制在很大程度上尚不清楚。方法采用冠状动脉永久性左前降支结扎法建立心肌梗死小鼠模型。采用转化生长因子-β1 (TGF-β1)或脂多糖(LPS)刺激心肌成纤维细胞(CFs)或RAW264.7巨噬细胞构建体外胶原合成及炎症模型。采用苏木精-伊红染色、Masson染色、超声心动图检测心肌结构和功能,采用Western-blot、免疫组织化学、RT-PCR、ELISA检测心肌纤维化和炎症标志物。此外,沉默信息调节因子1 (SIRT1)/核因子-κB (NF-κB)介导的NOD样受体3 (NLRP3)炎性体和TGF-β受体1 (TGFBR1)信号通路也被评估。采用SIRT1选择性抑制剂EX-527对人参的药理机制进行了研究。结果在体内,人参可减轻心室重构,增强心功能,改善I型胶原、III型胶原、IL-1β和IL-18水平,呈剂量依赖性。此外,人参显著抑制心肌梗死小鼠NLRP3-caspase1炎性体和TGFBR1/Smads信号通路。在体外,人参显著抑制TGF-β1诱导的CFs或lps刺激的RAW264.7细胞中的胶原和炎症标志物、NLRP3炎性体和TGFBR1/Smads信号。机制上,人参抑制NF-κB活性,促进SIRT1表达。EX-527抑制SIRT1部分消除了人参对TGF-β1诱导的cfs的保护作用。人参通过调节SIRT1及其下游信号通路,减轻心肌梗死后心肌纤维化和炎症,从而保护心肌免受不良重构。
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引用次数: 0
Ginseng as a therapeutic target to alleviate gut and brain diseases via microbiome regulation 以人参为治疗靶标,通过调节微生物组缓解肠道和脑部疾病
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.04.005
Hamid Iqbal , Yihyo Kim , Mirim Jin , Dong-kwon Rhee
The human gut, which contains a diverse microbiome, plays an important role in maintaining physiological balance and preserving the immune system. The complex interplay between the central nervous system (CNS) and the gut microbiome has gained significant attention due to its profound implications for overall health, particularly for gut and brain disorders. There is emerging evidence that the gut-brain axis (GBA) represents a bidirectional communication system between the CNS and the gastrointestinal tract and plays a pivotal role in regulating many aspects of human health. Ginseng has shown potential to ameliorate conditions associated with dysbiosis, such as gut and CNS disorders by restoring microbial balance and enhancing gut barrier function. This comprehensive review provides valuable insights into the potential of ginseng as a herbal modulator of GBA as a therapeutic intervention for preventing and treating gut and neurological diseases via microbiota regulation to ultimately enhance overall health. Furthermore, we emphasize the therapeutic benefits of ginseng, its ability to enhance beneficial probiotics, such as Firmicutes, Bacteroides, Lactobacillus, Bifidobacterium, and Akkermansia while reducing pathogenic bacteria prevalence, such as Helicobacter, Clostridium, and Proteobacteria. Although the connection between ginseng regulation of microbial communities in response to the gut and neuropsychiatric disorders is lacking, additional investigations are warranted to elucidate the underlying mechanisms, optimize dosages, and explore the clinical relevance of ginseng in promoting GBA balance and ultimately overall health.
人体肠道含有多种微生物群,在维持生理平衡和保护免疫系统方面发挥着重要作用。中枢神经系统(CNS)和肠道微生物组之间复杂的相互作用对整体健康,尤其是肠道和大脑疾病有着深远的影响,因此受到了广泛关注。越来越多的证据表明,肠脑轴(GBA)是中枢神经系统和胃肠道之间的双向交流系统,在调节人体健康的许多方面发挥着关键作用。人参通过恢复微生物平衡和增强肠道屏障功能,具有改善与菌群失调相关的疾病(如肠道和中枢神经系统疾病)的潜力。本综述对人参作为 GBA 的草药调节剂,通过调节微生物群预防和治疗肠道和神经系统疾病,最终提高整体健康水平的潜力提供了宝贵的见解。此外,我们还强调了人参的治疗益处,它能够增强有益益生菌,如坚固菌、、、和,同时降低致病菌,如、和蛋白菌的流行率。虽然人参对肠道微生物群落的调节与神经精神疾病之间缺乏联系,但仍有必要进行更多研究,以阐明其潜在机制、优化剂量并探索人参在促进 GBA 平衡以及最终促进整体健康方面的临床意义。
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引用次数: 0
Corrigendum to “Panax notoginseng saponins promotes angiogenesis after cerebral ischemia-reperfusion injury”[J Ginseng Res 48(6), November 2024, 592–602] “三七皂苷促进脑缺血再灌注损伤后血管生成”的更正[J].人参杂志,2024,11(6),592-602。
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.12.001
Haiyan Xiao , Shusen Liu , Binyu Fang , Wenchao Zhang , Min Wang , Jingxue Ye , Tianxiao Huang , Li Cao , Xiaojun Zhang , Guibo Sun
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引用次数: 0
Ginsenoside-Re-rich ethanol extract of Panax ginseng berry enhances healthspan extension via mitostasis and NAD metabolism 人参皂苷乙醇提取物通过有丝分裂和NAD代谢促进寿命延长。
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.11.002
Minjeong Kim , Su Hwan Kim , Juewon Kim , Eun-Ju Jin , Shibo Wei , Yunju Jo , Chang-Myung Oh , Ki-Tae Ha , Jong-Hwa Roh , Wan-Gi Kim , Donghyun Cho , Young Jin Choi , Su Myung Jung , Dongryeol Ryu

Background

Ginseng Berry Concentrate (GBC) enhances exercise capacity in mice, but the effects of its key component, ginsenoside Re (G-Re), on aging and mitochondrial function are not well understood. This study investigates the impact of G-Re on mitophagy and its potential to promote healthy aging.

Methods

Experiments in C2C12 myocytes and HeLa-mitoKeima-PARKIN cells assessed GBC and G-Re's effects on mitophagy, supported by Gene Set Enrichment Analysis. G-Re was identified as the primary component of GBC via high-performance liquid chromatography. The influence of G-Re on lifespan and healthspan was examined in Caenorhabditis elegans, with a focus on mitophagy pathways.

Results

GBC and G-Re significantly induced mitophagy and enhanced mitochondrial gene expression, improving mitochondrial function. G-Re extended lifespan and healthspan in C. elegans, effects absent in mitophagy-impaired mutants.

Conclusion

G-Re enhances mitochondrial function and promotes healthy aging through mitophagy, suggesting its potential for mitigating age-related functional declines.
背景:人参浆果浓缩液(GBC)增强小鼠运动能力,但其关键成分人参皂苷Re (G-Re)对衰老和线粒体功能的影响尚不清楚。本研究探讨了G-Re对线粒体自噬的影响及其促进健康衰老的潜力。方法:在C2C12肌细胞和HeLa-mitoKeima-PARKIN细胞实验中,通过基因集富集分析,评估GBC和G-Re对线粒体自噬的影响。通过高效液相色谱法鉴定G-Re为GBC的主要成分。研究了G-Re对秀丽隐杆线虫寿命和健康寿命的影响,重点研究了有丝分裂途径。结果:GBC和G-Re可显著诱导线粒体自噬,增强线粒体基因表达,改善线粒体功能。G-Re延长了秀丽隐杆线虫的寿命和健康寿命,而在自噬受损的突变体中没有这种作用。结论:G-Re可增强线粒体功能,并通过线粒体自噬促进健康衰老,提示其具有减轻年龄相关功能衰退的潜力。
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引用次数: 0
Ethanol extract of lymphanax with gypenoside 17 and ginsenoside Re exerts anti-inflammatory properties by targeting the AKT/NF-κB pathway 含有刺五加甙 17 和人参皂苷 Re 的淋巴皂苷乙醇提取物通过靶向 AKT/NF-κB 通路发挥抗炎作用
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.08.003
Wooram Choi , Hyun Soo Kim , Donghyun Kim , Yong Deog Hong , Hyoung-June Kim , Ji Hye Kim , Jong-Hoon Kim , Jae Youl Cho

Background

Ginseng is processed into several types such as white ginseng, red ginseng, and black ginseng, according to the processing methods such as drying, steaming, and heating. These processing conditions can change the portion of the useful ingredients. Recently, new processing method was established to develop ‘lymphanax’, an aged fresh white ginseng prepared under anaerobic condition. This aging process was revealed to increase the content of gypenoside 17 (Gyp17) as well as ginsenoside Re, known to have anti-inflammatory effects. As the next step, therefore, we aimed to investigate the anti-inflammatory activity of lymphanax using its ethanol extract of lymphanax (Lymphanax-EE).

Methods

LC-MS/MS identified the ginsenoside content of lymphanax-EE. A nitric oxide (NO) assay revealed the anti-inflammatory activity of lymphanax-EE. Pro-inflammatory gene expression was analyzed by quantitative PCR. Finally, we identified the underlying mechanism for the anti-inflammatory activity of lymphanax-EE through luciferase analysis, Western blotting, and CETSA.

Results

The LC-MS/MS analysis revealed lymphanax-EE to contain more protopanaxatriol-type ginsenosides, and Gyp17 than fresh ginseng. Lymphanax-EE (0–200 μg/ml) suppressed NO release and mRNA levels of pro-inflammatory cytokines such as iNOS and COX-2 in LPS-treated RAW264.7 cells. Moreover, lymphanax-EE (200 μg/ml) reduced the activity of NF-κB and phosphorylation of NF-κB signal proteins such as p65, p50, IκBα, and IKKα/β. Finally, lymphanax-EE (200 μg/ml) decreased the phosphorylation of IKKα/β induced by AKT overexpression. Among the components of lymphanax-EE, ginsenoside Re and Gyp17 were found to suppress AKT1 activity.

Conclusions

Lymphanax-EE-containing ginsenosides and Gyp17 with anti-inflammatory properties suppressed LPS-induced inflammation by reducing the NF-κB signal.
根据烘干、蒸煮和加热等加工方法,人参被加工成多种类型,如白参、红参和黑参。这些加工条件会改变有用成分的比例。最近,人们建立了新的加工方法,开发出在厌氧条件下制备的陈年新鲜白参 "lymphanax"。研究发现,这种陈化过程增加了人参皂苷 17(Gyp17)和人参皂苷 Re 的含量,而人参皂苷 Re 具有抗炎作用。因此,我们下一步的目标是利用淋巴杉乙醇提取物(Lymphanax-EE)研究淋巴杉的抗炎活性。LC-MS/MS鉴定了Lymphanax-EE中的人参皂苷含量。一氧化氮(NO)测定显示了Lymphanax-EE的抗炎活性。通过定量 PCR 分析了促炎基因的表达。最后,我们通过荧光素酶分析、Western 印迹和 CETSA 确定了 lymphanax-EE 抗炎活性的内在机制。LC-MS/MS分析显示,与新鲜人参相比,淋巴-EE含有更多的原人参三醇型人参皂甙和Gyp17。Lymphanax-EE(0-200 μg/ml)可抑制LPS处理的RAW264.7细胞中NO的释放以及iNOS和COX-2等促炎细胞因子的mRNA水平。此外,lympanax-EE(200 μg/ml)还能降低NF-κB的活性以及NF-κB信号蛋白(如p65、p50、IκBα和IKKα/β)的磷酸化。最后,lympanax-EE(200 μg/ml)降低了AKT过表达诱导的IKKα/β磷酸化。在Lymphanax-EE的成分中,发现人参皂苷Re和Gyp17能抑制AKT1的活性。具有抗炎特性的人参皂苷和Gyp17通过减少NF-κB信号抑制了LPS诱导的炎症。
{"title":"Ethanol extract of lymphanax with gypenoside 17 and ginsenoside Re exerts anti-inflammatory properties by targeting the AKT/NF-κB pathway","authors":"Wooram Choi ,&nbsp;Hyun Soo Kim ,&nbsp;Donghyun Kim ,&nbsp;Yong Deog Hong ,&nbsp;Hyoung-June Kim ,&nbsp;Ji Hye Kim ,&nbsp;Jong-Hoon Kim ,&nbsp;Jae Youl Cho","doi":"10.1016/j.jgr.2024.08.003","DOIUrl":"10.1016/j.jgr.2024.08.003","url":null,"abstract":"<div><h3>Background</h3><div>Ginseng is processed into several types such as white ginseng, red ginseng, and black ginseng, according to the processing methods such as drying, steaming, and heating. These processing conditions can change the portion of the useful ingredients. Recently, new processing method was established to develop ‘lymphanax’, an aged fresh white ginseng prepared under anaerobic condition. This aging process was revealed to increase the content of gypenoside 17 (Gyp17) as well as ginsenoside Re, known to have anti-inflammatory effects. As the next step, therefore, we aimed to investigate the anti-inflammatory activity of lymphanax using its ethanol extract of lymphanax (Lymphanax-EE).</div></div><div><h3>Methods</h3><div>LC-MS/MS identified the ginsenoside content of lymphanax-EE. A nitric oxide (NO) assay revealed the anti-inflammatory activity of lymphanax-EE. Pro-inflammatory gene expression was analyzed by quantitative PCR. Finally, we identified the underlying mechanism for the anti-inflammatory activity of lymphanax-EE through luciferase analysis, Western blotting, and CETSA.</div></div><div><h3>Results</h3><div>The LC-MS/MS analysis revealed lymphanax-EE to contain more protopanaxatriol-type ginsenosides, and Gyp17 than fresh ginseng. Lymphanax-EE (0–200 μg/ml) suppressed NO release and mRNA levels of pro-inflammatory cytokines such as iNOS and COX-2 in LPS-treated RAW264.7 cells. Moreover, lymphanax-EE (200 μg/ml) reduced the activity of NF-κB and phosphorylation of NF-κB signal proteins such as p65, p50, IκBα, and IKKα/β. Finally, lymphanax-EE (200 μg/ml) decreased the phosphorylation of IKKα/β induced by AKT overexpression. Among the components of lymphanax-EE, ginsenoside Re and Gyp17 were found to suppress AKT1 activity.</div></div><div><h3>Conclusions</h3><div>Lymphanax-EE-containing ginsenosides and Gyp17 with anti-inflammatory properties suppressed LPS-induced inflammation by reducing the NF-κB signal.</div></div>","PeriodicalId":16035,"journal":{"name":"Journal of Ginseng Research","volume":"49 1","pages":"Pages 22-33"},"PeriodicalIF":6.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142178139","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Complex transcriptome network regulates the anthocyanin accumulation of four Panax ginseng cultivars in fruit 复杂转录组网络调控4个人参品种果实花青素积累
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.12.007
Jaewook Kim , Bae Young Choi , Donghwan Shim , Ick-Hyun Jo

Background

Panax ginseng fruit tissue is one of the richest sources of valuable constituents such as ginsenosides and anthocyanins. Although anthocyanins extracted from the fruit tissue of P. ginseng are utilized, it is uncertain how anthocyanin accumulation is regulated and which anthocyanin varieties are synthesized.

Methods

Fruits of four P. ginseng cultivars were collected for total RNA extraction and RNA-Seq analysis using the Illumina HiSeq X platform. Anthocyanins were extracted and analyzed by UPLC-DAD-QToF/MS to identify and quantify individual derivatives. Differentially expressed genes (DEGs) were identified, followed by functional annotation and network analysis to evaluate gene expression patterns.

Results

Comparative transcriptome analysis of four differently colored P. ginseng cultivars revealed that flavonoid biosynthetic genes associated with the karrikin response and jasmonate-responsive genes were upregulated in anthocyanin-rich fruits. Network analysis further revealed a putative regulatory complex consists of karrikin- and jasmonate-responsive genes along with flavonoid biosynthetic genes. Analyzing the UPLC-DAD extracts of the fruit of cv. Chunpoong found that the fruit tissue of P. ginseng is rich in pelargonidin.

Conclusion

Our research provides how anthocyanin is accumulated and which type is accumulated in fruit tissue of P. ginseng, including the original compound, pelargonidin 3-O-(2″-O-glucosyl)galactoside. We expect that our research will lead to improved breeding efficiency for the development of cultivars containing more flavonoid species that are beneficial to humans.
人参果实组织是人参皂苷和花青素等有价值成分最丰富的来源之一。虽然利用了从人参果实组织中提取的花青素,但花青素的积累是如何调控的以及哪些花青素品种是合成的还不清楚。方法采集4个人参品种的果实,采用Illumina HiSeq X平台进行总RNA提取和RNA- seq分析。提取花青素,采用UPLC-DAD-QToF/MS进行分析,对单个衍生物进行鉴定和定量。鉴定差异表达基因(deg),然后通过功能注释和网络分析来评估基因表达模式。结果4个不同颜色人参品种的转录组对比分析显示,花青素丰富的果实中,与卡里金反应相关的类黄酮生物合成基因和茉莉素反应相关的基因均上调。网络分析进一步揭示了一个假设的调控复合体,由卡瑞金和茉莉酸响应基因以及类黄酮生物合成基因组成。枸杞子UPLC-DAD提取物的分析。春蓬发现,人参果实组织中含有丰富的天竺葵苷。结论本研究揭示了花青素在人参果实组织中积累的途径和类型,包括其原始化合物花青素3-O-(2″- o -葡萄糖基)半乳糖苷。我们期望我们的研究将有助于提高育种效率,开发含有更多对人类有益的黄酮类化合物的品种。
{"title":"Complex transcriptome network regulates the anthocyanin accumulation of four Panax ginseng cultivars in fruit","authors":"Jaewook Kim ,&nbsp;Bae Young Choi ,&nbsp;Donghwan Shim ,&nbsp;Ick-Hyun Jo","doi":"10.1016/j.jgr.2024.12.007","DOIUrl":"10.1016/j.jgr.2024.12.007","url":null,"abstract":"<div><h3>Background</h3><div><em>Panax ginseng</em> fruit tissue is one of the richest sources of valuable constituents such as ginsenosides and anthocyanins. Although anthocyanins extracted from the fruit tissue of <em>P. ginseng</em> are utilized, it is uncertain how anthocyanin accumulation is regulated and which anthocyanin varieties are synthesized.</div></div><div><h3>Methods</h3><div>Fruits of four <em>P. ginseng</em> cultivars were collected for total RNA extraction and RNA-Seq analysis using the Illumina HiSeq X platform. Anthocyanins were extracted and analyzed by UPLC-DAD-QToF/MS to identify and quantify individual derivatives. Differentially expressed genes (DEGs) were identified, followed by functional annotation and network analysis to evaluate gene expression patterns.</div></div><div><h3>Results</h3><div>Comparative transcriptome analysis of four differently colored <em>P. ginseng</em> cultivars revealed that flavonoid biosynthetic genes associated with the karrikin response and jasmonate-responsive genes were upregulated in anthocyanin-rich fruits. Network analysis further revealed a putative regulatory complex consists of karrikin- and jasmonate-responsive genes along with flavonoid biosynthetic genes. Analyzing the UPLC-DAD extracts of the fruit of cv. Chunpoong found that the fruit tissue of <em>P. ginseng</em> is rich in pelargonidin.</div></div><div><h3>Conclusion</h3><div>Our research provides how anthocyanin is accumulated and which type is accumulated in fruit tissue of <em>P. ginseng,</em> including the original compound, pelargonidin 3-O-(2″-O-glucosyl)galactoside. We expect that our research will lead to improved breeding efficiency for the development of cultivars containing more flavonoid species that are beneficial to humans.</div></div>","PeriodicalId":16035,"journal":{"name":"Journal of Ginseng Research","volume":"49 3","pages":"Pages 315-325"},"PeriodicalIF":6.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143870382","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Enhancement of skin regeneration through activation of TGF-β/SMAD signaling pathway by Panax ginseng meyer non-edible callus-derived extracellular vesicles 三七麦芽非食用茧源性细胞外囊泡通过激活 TGF-β/SMAD 信号通路促进皮肤再生
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.08.002
Ha Young Park , Min Ho Kang , Guewha Lee , Jin Woo Kim

Background

This study aimed to investigate the effects of ginseng non-edible callus-derived extracellular vesicle (GNEV) on skin regeneration, particularly focusing on its impact on proliferation and migration in human dermal fibroblast (HDF).

Methods

GNEV was isolated from ginseng non-edible callus using sequential filtration and size exclusion chromatography (SEC). The extracellular vesicle was characterized using nanoparticle tracking analysis (NTA). HDF was treated with various concentrations of GNEV, and cell viability, proliferation, and migration were assessed using MTT and scratch wound healing assays. Gene expression related to collagen synthesis (TGF-β, SMAD-2, SMAD-3, COL1A1) was measured using RT-PCR.

Results

Treatment of HDF with GNEV resulted in a significant 2.5-fold increase in cell migration compared to the non-treated group. Furthermore, GNEV demonstrated the upregulation of collagen synthesis genes, specifically TGF-β, SMAD-2, SMAD-3, and COL1A1, by 41.7 %, 59.4 %, 60.2 %, and 21.8 %, respectively. These findings indicated that GNEV activates the TGF-β/SMAD signaling pathway, showcasing its potential to induce skin regeneration.

Conclusions

In conclusion, GNEV exhibits a notable ability to enhance skin regeneration through its stimulatory effects on cell migration and the upregulation of key collagen synthesis genes. The activation of the TGF-β/SMAD signaling pathway further suggests the potential of GNEV as a promising candidate for drug delivery systems in the fields of cosmetics and pharmaceuticals, opening avenues for further research and application in skincare and dermatology.
本研究旨在探讨人参非食用胼胝体衍生的细胞外囊泡(GNEV)对皮肤再生的影响,尤其是对人真皮成纤维细胞(HDF)增殖和迁移的影响。利用顺序过滤和尺寸排阻色谱法(SEC)从人参非食用胼胝体中分离出细胞外囊泡。利用纳米粒子跟踪分析(NTA)对细胞外囊泡进行了表征。用不同浓度的 GNEV 处理 HDF,并用 MTT 和划痕伤口愈合试验评估细胞活力、增殖和迁移。采用 RT-PCR 技术测定了与胶原合成()相关的基因表达。用 GNEV 处理 HDF 后,细胞迁移率比未处理组显著增加了 2.5 倍。此外,GNEV 还能上调胶原合成基因,特别是 、 和 ,上调幅度分别为 41.7%、59.4%、60.2% 和 21.8%。这些发现表明,GNEV 激活了信号通路,展示了其诱导皮肤再生的潜力。总之,GNEV 通过刺激细胞迁移和上调关键胶原合成基因,表现出显著的促进皮肤再生的能力。信号通路的激活进一步表明,GNEV 有潜力成为化妆品和药品领域药物输送系统的候选物质,为护肤品和皮肤病学的进一步研究和应用开辟了道路。
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引用次数: 0
Targeting the DNA damage response (DDR) of cancer cells with natural compounds derived from Panax ginseng and other plants 利用从三七和其他植物中提取的天然化合物靶向癌细胞的 DNA 损伤反应(DDR)
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.04.001
SeokGyeong Choi , Minwook Shin , Woo-Young Kim
DNA damage is a driver of cancer formation, leading to the impairment of repair mechanisms in cancer cells and rendering them susceptible to DNA-damaging therapeutic approaches. The concept of “synthetic lethality” in cancer clinics has emerged, particularly with the use of PARP inhibitors and the identification of DNA damage response (DDR) mutation biomarkers, emphasizing the significance of targeting DDR in cancer therapy. Novel approaches aimed at genome maintenance machinery are under development to further enhance the efficacy of cancer treatments. Natural compounds from traditional medicine, renowned for their anti-aging and anticarcinogenic properties, have garnered attention. Ginseng-derived compounds, in particular, exhibit anti-carcinogenic effects by suppressing reactive oxygen species (ROS) and protecting cells from DNA damage-induced carcinogenesis. However, the anticancer therapeutic effect of ginseng compounds has also been demonstrated by inducing DNA damage and blocking DDR. This review concentrates on the biphasic effects of ginseng compounds on DNA mutations—both inhibiting mutation accumulation and impairing DNA repair. Additionally, it explores other natural compounds targeting DDR directly, providing potential insights into enhancing cancer therapy efficacy.
DNA 损伤是癌症形成的驱动因素,它导致癌细胞修复机制受损,使癌细胞易受 DNA 损伤治疗方法的影响。癌症临床中出现了 "合成致死 "的概念,特别是随着 PARP 抑制剂的使用和 DNA 损伤反应(DDR)突变生物标志物的确定,强调了在癌症治疗中靶向 DDR 的重要性。目前正在开发针对基因组维护机制的新方法,以进一步提高癌症治疗的疗效。传统医药中的天然化合物以其抗衰老和抗癌特性而闻名,已引起人们的关注。特别是人参提取物,通过抑制活性氧(ROS)和保护细胞免受 DNA 损伤诱发的癌变,显示出抗癌作用。然而,人参化合物的抗癌治疗效果也通过诱导 DNA 损伤和阻断 DDR 得到了证实。本综述集中探讨了人参化合物对 DNA 变异的双相作用--既抑制突变积累,又损害 DNA 修复。此外,它还探讨了其他直接针对 DDR 的天然化合物,为提高癌症治疗效果提供了潜在的见解。
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引用次数: 0
Compositional changes and physiological activities of fresh ginseng extracts prepared at various temperatures in subcritical water 人参鲜提液在亚临界水中不同温度下的成分变化及生理活性。
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.09.007
Jong Won Lee , Mi-Yeon Lee , SangYoon Lee , Geun-Pyo Hong

Background

Subcritical water (SW) is regarded as an effective conversion technology for lignocellulosic biomass. The effect of SW on ginseng are limited to evaluate the ginsenoside composition of red ginseng, and there is little information on the effects of SW on fresh ginseng.

Methods

The general characteristics of ginseng extracts (GE) prepared with SW were evaluated in terms of brix, reducing sugar and residual solid content, and compositions of GE was estimated using chromatography. For utilization of GE as a bioactive food, the ginsenoside composition, antioxidative activity, angiotensin-converting enzyme (ACE) inhibitory activity, prebiotic potential and taste attributes were measured.

Results

Increasing SW temperature decreased residual solid content of ginseng and the soluble compounds of GE were yielded by SW at 250 °C. Despite that ginsenoside content decreased with SW temperature, a steep increase in Rg5 was observed at 200 °C. The SW at 200–250 °C manifested the highest antioxidant activities and ACE inhibitory activity of GE. However, the GE prepared at greater than 250 °C completely lost prebiotic potentials. Based on electronic-tongue, umami taste was enhanced by SW at 200 °C, but sweetness and bitterness were dominated at 250–300 °C.

Conclusion

The results demonstrated that SW has a potential application to convert lignocellulosic wastes generated from ginseng roots into bioactive food resource, and SW at ∼200 °C can be potentially used to enhance the physiological activities of GE.
背景:亚临界水(SW)被认为是一种有效的木质纤维素生物质转化技术。SW对人参的影响仅限于对红参人参皂苷成分的评价,对于SW对鲜参的影响研究甚少。方法:从白度、还原糖和残留固形物含量等方面评价人参提取物的一般特性,并采用色谱法对人参提取物的成分进行鉴定。为了利用转基因作为生物活性食品,测定了其人参皂苷组成、抗氧化活性、血管紧张素转换酶(ACE)抑制活性、益生元潜力和风味特性。结果:随着SW温度的升高,人参的残固含量降低,且在250℃下SW可获得GE的可溶性化合物。尽管人参皂苷含量随SW温度的升高而降低,但Rg5在200℃时急剧升高。在200 ~ 250℃的SW中,GE的抗氧化活性和ACE抑制活性最高。然而,在高于250°C时制备的GE完全失去了益生元潜力。以电子舌为基础,在200°C时,SW对鲜味有增强作用,而在250 ~ 300°C时,SW对甜味和苦味有增强作用。结论:SW具有将人参根产生的木质纤维素废物转化为具有生物活性的食物资源的潜在应用价值,并且SW在~ 200°C下可以潜在地用于增强GE的生理活性。
{"title":"Compositional changes and physiological activities of fresh ginseng extracts prepared at various temperatures in subcritical water","authors":"Jong Won Lee ,&nbsp;Mi-Yeon Lee ,&nbsp;SangYoon Lee ,&nbsp;Geun-Pyo Hong","doi":"10.1016/j.jgr.2024.09.007","DOIUrl":"10.1016/j.jgr.2024.09.007","url":null,"abstract":"<div><h3>Background</h3><div>Subcritical water (SW) is regarded as an effective conversion technology for lignocellulosic biomass. The effect of SW on ginseng are limited to evaluate the ginsenoside composition of red ginseng, and there is little information on the effects of SW on fresh ginseng.</div></div><div><h3>Methods</h3><div>The general characteristics of ginseng extracts (GE) prepared with SW were evaluated in terms of brix, reducing sugar and residual solid content, and compositions of GE was estimated using chromatography. For utilization of GE as a bioactive food, the ginsenoside composition, antioxidative activity, angiotensin-converting enzyme (ACE) inhibitory activity, prebiotic potential and taste attributes were measured.</div></div><div><h3>Results</h3><div>Increasing SW temperature decreased residual solid content of ginseng and the soluble compounds of GE were yielded by SW at 250 °C. Despite that ginsenoside content decreased with SW temperature, a steep increase in Rg5 was observed at 200 °C. The SW at 200–250 °C manifested the highest antioxidant activities and ACE inhibitory activity of GE. However, the GE prepared at greater than 250 °C completely lost prebiotic potentials. Based on electronic-tongue, umami taste was enhanced by SW at 200 °C, but sweetness and bitterness were dominated at 250–300 °C.</div></div><div><h3>Conclusion</h3><div>The results demonstrated that SW has a potential application to convert lignocellulosic wastes generated from ginseng roots into bioactive food resource, and SW at ∼200 °C can be potentially used to enhance the physiological activities of GE.</div></div>","PeriodicalId":16035,"journal":{"name":"Journal of Ginseng Research","volume":"49 1","pages":"Pages 64-70"},"PeriodicalIF":6.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11770229/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143052881","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Effects of Korean red ginseng on auditory, cognitive, and liver functions in a naturally aged mouse model 红参对自然衰老小鼠听觉、认知和肝功能的影响。
IF 6.8 2区 医学 Q1 CHEMISTRY, MEDICINAL Pub Date : 2025-01-01 DOI: 10.1016/j.jgr.2024.10.001
Sung Woo Shin , Ji Heon Shim , Youn Hee Nam , Na Woo Kim , Gyeong Jin Seo , Murughanantham Nevedita , Pandian Subha , Quy-Hoai Nguyen , Yong Su Jeong , Bin Na Hong , Tong Ho Kang

Background

Korean Red Ginseng and ginsenosides have been studied for their efficacy against various diseases, including those related to aging. However, most aging studies use D-galactose to induce aging, which often does not accurately represent natural aging. This study aimed to verify improvements in auditory, cognitive, and liver function through administering red ginseng to an 18-month-old naturally aging mouse model.

Methods

Auditory function was assessed using Auditory Brainstem Response (ABR) and Auditory Middle Latency Response (AMLR). Cognitive function was evaluated electrophysiologically with P300 and mismatch negativity (MMN), and behaviorally using the Y-maze. Additionally, biochemical tests and histological analysis were conducted to assess liver function. The effects of red ginseng on gene expression regulation were also examined in the cochlea, auditory cortex, and liver, focusing on age-related disease processes.

Results

Red ginseng significantly decreased hearing thresholds and improved central auditory function. It also enhanced cognitive behavior and function in response to external stimulation. Furthermore, red ginseng regulated alkaline phosphatase (ALP), albumin (Alb), and total protein (TP) levels, notably decreasing aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels. Hematoxylin and eosin (H&E) staining of liver tissue showed significant improvement in fat droplets. These effects appear to be mediated by the regulation of aging-related genes Dec, c-Jun, Stat5b, and Lims2.

Conclusion

These results suggest that red ginseng improves auditory, cognitive, and liver functions in a naturally aged mouse model.
背景:韩国红参和人参皂苷已被研究其对各种疾病的功效,包括与衰老有关的疾病。然而,大多数衰老研究使用d -半乳糖诱导衰老,这往往不能准确地代表自然衰老。这项研究旨在通过给18个月大的自然衰老小鼠模型服用红参来验证听觉、认知和肝功能的改善。方法:采用听觉脑干反应(ABR)和听觉中潜伏期反应(AMLR)评价听觉功能。认知功能电生理评价采用P300和失配负性(MMN),行为学评价采用y型迷宫。此外,进行生化试验和组织学分析以评估肝功能。红参对耳蜗、听觉皮层和肝脏基因表达调控的影响也被研究,重点是与年龄相关的疾病过程。结果:红参能明显降低听力阈值,改善中枢听觉功能。它还增强了对外界刺激的认知行为和功能。红参还能调节碱性磷酸酶(ALP)、白蛋白(Alb)和总蛋白(TP)水平,显著降低天冬氨酸转氨酶(AST)和丙氨酸转氨酶(ALT)水平。肝组织苏木精和伊红(H&E)染色显示脂肪滴明显改善。这些影响似乎是由衰老相关基因Dec、c-Jun、Stat5b和Lims2的调控介导的。结论:红参对自然衰老小鼠的听觉、认知和肝功能有改善作用。
{"title":"Effects of Korean red ginseng on auditory, cognitive, and liver functions in a naturally aged mouse model","authors":"Sung Woo Shin ,&nbsp;Ji Heon Shim ,&nbsp;Youn Hee Nam ,&nbsp;Na Woo Kim ,&nbsp;Gyeong Jin Seo ,&nbsp;Murughanantham Nevedita ,&nbsp;Pandian Subha ,&nbsp;Quy-Hoai Nguyen ,&nbsp;Yong Su Jeong ,&nbsp;Bin Na Hong ,&nbsp;Tong Ho Kang","doi":"10.1016/j.jgr.2024.10.001","DOIUrl":"10.1016/j.jgr.2024.10.001","url":null,"abstract":"<div><h3>Background</h3><div>Korean Red Ginseng and ginsenosides have been studied for their efficacy against various diseases, including those related to aging. However, most aging studies use D-galactose to induce aging, which often does not accurately represent natural aging. This study aimed to verify improvements in auditory, cognitive, and liver function through administering red ginseng to an 18-month-old naturally aging mouse model.</div></div><div><h3>Methods</h3><div>Auditory function was assessed using Auditory Brainstem Response (ABR) and Auditory Middle Latency Response (AMLR). Cognitive function was evaluated electrophysiologically with P300 and mismatch negativity (MMN), and behaviorally using the Y-maze. Additionally, biochemical tests and histological analysis were conducted to assess liver function. The effects of red ginseng on gene expression regulation were also examined in the cochlea, auditory cortex, and liver, focusing on age-related disease processes.</div></div><div><h3>Results</h3><div>Red ginseng significantly decreased hearing thresholds and improved central auditory function. It also enhanced cognitive behavior and function in response to external stimulation. Furthermore, red ginseng regulated alkaline phosphatase (ALP), albumin (Alb), and total protein (TP) levels, notably decreasing aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels. Hematoxylin and eosin (H&amp;E) staining of liver tissue showed significant improvement in fat droplets. These effects appear to be mediated by the regulation of aging-related genes <em>Dec</em>, <em>c-Jun</em>, <em>Stat5b</em>, and <em>Lims2</em>.</div></div><div><h3>Conclusion</h3><div>These results suggest that red ginseng improves auditory, cognitive, and liver functions in a naturally aged mouse model.</div></div>","PeriodicalId":16035,"journal":{"name":"Journal of Ginseng Research","volume":"49 1","pages":"Pages 71-79"},"PeriodicalIF":6.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11764134/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143052888","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Ginseng Research
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