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Dietary polyphenols reduced the allergenicity of β-lactoglobulin via non-covalent interactions: a study on the structure-allergenicity relationship 膳食多酚通过非共价相互作用降低了β-乳球蛋白的致敏性:关于结构-致敏性关系的研究
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250210
Studies showed that complexation of polyphenols with milk allergens reduced their immunogenic potential. However, the relationship between structures of polyphenols and their hypoallergenic effects on milk allergens in association with physiological and conformational changes of the complexes remain unclear. In this study, polyphenols from eight botanical sources were extracted to prepare non-covalent complexes with β-lactoglobulin (β-LG), a major allergen in milk. The dominant phenolic compounds bound to β-LG with a diminished allergenicity were identified to investigate their respective role on the structural and allergenic properties of β-LG. Extracts from Vaccinium fruits and black soybeans were found to have great inhibitory effects on the IgE- and IgG-binding abilities of β-LG. Among the fourteen structure-related phenolic compounds, flavonoids and tannins with larger MWs and multi-hydroxyl substituents, notably rutin, EGCG, and ellagitannins were more potent to elicit changes on the conformational structures of β-LG to decrease the allergenicity of complexed β-LG. Correlation analysis further demonstrated that a destabilized secondary structure and protein depolymerization caused by polyphenol-binding were closely related to the allergenicity property of formed complexes. This study provides insights into the understanding of structure-allergenicity relationship of β-LG-polyphenol interactions and would benefit the development of polyphenol-fortified matrices with hypoallergenic potential.
研究表明,多酚与牛奶过敏原的复合物可降低其免疫原性。然而,多酚的结构及其对牛奶过敏原的低过敏效应与复合物的生理和构象变化之间的关系仍不清楚。本研究从八种植物中提取多酚,制备与牛奶中主要过敏原 β-乳球蛋白(β-LG)的非共价复合物。研究人员确定了与β-LG结合后过敏性降低的主要酚类化合物,以研究它们各自对β-LG的结构和过敏特性所起的作用。研究发现,从越橘果实和黑大豆中提取的提取物对 β-LG 的 IgE 和 IgG 结合能力有很大的抑制作用。在 14 种结构相关的酚类化合物中,具有较大分子量和多羟基取代基的黄酮类和单宁类化合物,尤其是芦丁、EGCG 和鞣花丹宁类化合物,能更有效地引起 β-LG 构象结构的变化,从而降低与 β-LG 复合物的致敏性。相关分析进一步表明,多酚结合导致的二级结构不稳定和蛋白质解聚与形成的复合物的致敏性密切相关。这项研究为了解β-LG-多酚相互作用的结构-致敏性关系提供了深入的见解,有利于开发具有低致敏潜力的多酚强化基质。
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引用次数: 0
Application and prospects of proteomic technology in inflammation: a review 蛋白质组技术在炎症中的应用与前景:综述
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250248
Senye Wang , Yanhai Chu , Jiajia Yuan , Yiqi Li , Zhenhua Liu , Xiaoyu Chen , Wenyi Kang
Proteomics is a new technology that has been widely applied in the field of life and health science. It effectively addresses issues related to the impact of dietary structure on organs, tissues, and cells, as well as the changes in proteins in various organs, tissues, and cells under disease conditions. The differential proteins identified through proteomics can serve as disease biomarkers and target proteins affecting health and can be used for disease diagnosis and health regulation. In this paper, the application of proteomics in the field of inflammation in recent years was summarized, especially in the therapeutic target and mechanism of action, which opens up a new way for more effective prevention, diagnosis, and treatment of inflammation, and provides medical protection for human life and health.
蛋白质组学是生命与健康科学领域广泛应用的一项新技术。它能有效解决饮食结构对器官、组织和细胞的影响,以及疾病条件下各种器官、组织和细胞中蛋白质的变化等相关问题。通过蛋白质组学发现的差异蛋白质可作为疾病生物标志物和影响健康的靶蛋白,可用于疾病诊断和健康调控。本文总结了近年来蛋白质组学在炎症领域的应用,尤其是在治疗靶点和作用机制方面的应用,为更有效地预防、诊断和治疗炎症开辟了新途径,为人类生命健康提供医学保障。
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引用次数: 0
Effect of exogenous free Nε-(carboxymethyl)lysine on diabetes-associated cognitive dysfunction: neuroinflammation, and metabolic disorders 外源性游离 Nε-(羧甲基)赖氨酸对糖尿病相关认知功能障碍、神经炎症和代谢紊乱的影响
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250240
Diabetes-associated cognitive dysfunction has already been attracted considerable attention. Advanced glycation end products (AGEs) from daily diets are thought to be a vital contributor to the development of this diseases. However, the effect of one of the best-characterized exogenous AGEs Nε-(carboxymethyl)lysine (CML) on cognitive function is not fully reported. In the present study, diabetical Goto-Kakizaki (GK) rats were treated with free CML for 8-weeks. It was found that oral consumption of exogenous CML significantly aggravated diabetes-associated cognitive dysfunction in behavioral test. In details, exogenous CML increased levels of oxidative stress, promoted the activation of glial cells in the brain, up-regulated the release of inflammatory cytokines interleukin-6, inhibited the protein expression of the brain-derived neurotrophic factor and thus led to neuroinflammation. Furthermore, exogenous CML promoted the amyloidogenesis in the brain of GK rats, and inhibited the expression of GLUT4. Additionally, several tricarboxylic acid cycle and glutamate-glutamine/γ-aminobutyric acid cycle intermediates including pyruvate, succinic acid, glutamine, glutamate were significantly changed in brain of GK rats treated with exogenous free CML. In conclusion, exogenous free CML is a potentially noxious compounds led to aggravated diabetes-associated cognitive dysfunction which could be possibly explained by its effects on neuroinflammation, energy and neurotransmitter amino acid homeostasis.
与糖尿病相关的认知功能障碍已经引起了广泛关注。日常饮食中的高级糖化终产物(AGEs)被认为是导致这种疾病发生的重要因素。然而,关于外源性 AGEs Nε-(羧甲基)赖氨酸(CML)对认知功能的影响,目前还没有充分的报道。在本研究中,糖尿病后藤柿崎(GK)大鼠接受了为期 8 周的游离 CML 治疗。结果发现,在行为测试中,口服外源性 CML 会明显加重糖尿病相关的认知功能障碍。具体而言,外源性 CML 增加了氧化应激水平,促进了脑胶质细胞的活化,上调了炎症细胞因子白细胞介素-6 的释放,抑制了脑源性神经营养因子的蛋白表达,从而导致神经炎症。此外,外源性 CML 会促进 GK 大鼠脑内淀粉样蛋白的生成,并抑制 GLUT4 的表达。此外,用外源性游离 CML 处理的 GK 大鼠脑中的一些三羧酸循环和谷氨酸-谷氨酰胺/γ-氨基丁酸循环中间产物(包括丙酮酸、琥珀酸、谷氨酰胺、谷氨酸)发生了显著变化。总之,外源性游离 CML 是一种可能导致糖尿病相关认知功能障碍加重的有毒化合物,这可能是由于它对神经炎症、能量和神经递质氨基酸平衡的影响。
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引用次数: 0
Anti-biofilm and anti-virulence potential of cell free supernatant of Akkermansia muciniphila against Salmonella Akkermansia muciniphila 细胞游离上清液对沙门氏菌的抗生物膜和抗病毒潜力
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250215
Akkermansia muciniphila is one of the commensals residing within the mammalian gut and co-evolving with the host. Numerous studies have demonstrated the benefits of A. muciniphila in ameliorating metabolic disorders, while little is known about the antimicrobial potential of A. muciniphila against pathogens. Here, we examined the antimicrobial and anti-virulence properties of cell free supernatant (CFS) of A. muciniphila against Salmonella Typhimurium. CFS retarded bacterial growth and inhibited the motility of S. Typhimurium SL1344 and S. Typhimurium 14028. CFS dose-dependently reduced cell hydrophobicity and auto-aggregation of both strains. Also, CFS from A. muciniphila significantly attenuated biofilm formation. Compared with untreated bacteria, CFS-treated bacteria significantly decreased adhesion and invasion to Caco-2 cells, and reduced intracellular survival in macrophages. CFS maintained antimicrobial properties after treatment with high temperatures and various proteases, while it lost its antimicrobial activity after pH neutralization. Gas chromatography-mass spectrometry (GC-MS) confirmed that A. muciniphila produced a certain amount of acetate and propionate, and ultra-high-performance liquid chromatography-mass spectrometry (UHPLC-MS) identified other organic acids and metabolites in CFS. In summary, CFS from A. muciniphila exhibited anti-biofilm and anti-virulence properties against Salmonella and could be potentially utilized in the food industry for controlling Salmonella contamination and reducing infection.
Akkermansia muciniphila 是哺乳动物肠道内的共生菌之一,与宿主共同进化。大量研究表明,粘多糖对改善代谢紊乱有好处,但对粘多糖针对病原体的抗菌潜力却知之甚少。在这里,我们研究了粘菌素细胞游离上清液(CFS)对鼠伤寒沙门氏菌的抗菌和抗病毒特性。CFS 可延缓细菌生长并抑制鼠伤寒沙门氏菌 SL1344 和鼠伤寒沙门氏菌 14028 的运动。CFS剂量依赖性地降低了这两种菌株的细胞疏水性和自动聚集性。此外,来自 A. muciniphila 的 CFS 能显著减少生物膜的形成。与未经处理的细菌相比,经 CFS 处理的细菌能明显减少对 Caco-2 细胞的粘附和侵袭,并降低巨噬细胞的细胞内存活率。CFS 在经过高温和各种蛋白酶处理后仍能保持抗菌特性,而在 pH 中和后则失去了抗菌活性。气相色谱-质谱法(GC-MS)证实,A. muciniphila 产生了一定量的乙酸盐和丙酸盐,超高效液相色谱-质谱法(UHPLC-MS)鉴定出了 CFS 中的其他有机酸和代谢物。总之,粘液虹彩菌的 CFS 具有抗沙门氏菌生物膜和抗沙门氏菌病毒的特性,可用于食品工业控制沙门氏菌污染和减少感染。
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引用次数: 0
Mechanisms and active substances of targeting lipid peroxidation in ferroptosis regulation 以脂质过氧化为目标调控铁变态反应的机制和活性物质
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250204
Ferroptosis is a novel form of cell death driven by iron-dependent lipid peroxidation and it is implicated in various diseases, such as liver disease, acute kidney injury, cardiovascular disease, neurodegenerative disease and cancer. Lipid-based reactive oxygen species (ROS), particularly lipid hydroperoxides in the cellular membrane can lead to membrane disruption and cell death mediated by ferroptosis. There are three necessary stages involving in the process of lipid peroxidation regulation in ferroptosis, including the synthesis of membrane phospholipids, initiation of lipid peroxidation and clearance of lipid peroxides. In this review, we summarized the molecular modulation mechanisms of lipid peroxidation in ferroptosis from the above three stages, as well as various ferroptosis modulators targeting lipid peroxidation, including commonly used products, natural bioactive compounds and selenocompounds. Collectively, these findings suggest the vital role of lipid peroxidation in ferroptosis, and targeting lipid peroxidation in ferroptosis is potential to treat ferroptosis-associated diseases.
铁变态反应是由铁依赖性脂质过氧化驱动的一种新型细胞死亡形式,与肝病、急性肾损伤、心血管疾病、神经退行性疾病和癌症等多种疾病有关。以脂质为基础的活性氧(ROS),特别是细胞膜上的脂质氢过氧化物,可导致膜破坏,并在铁氧化作用的介导下导致细胞死亡。铁变态反应中的脂质过氧化调节过程涉及三个必要阶段,包括膜磷脂的合成、脂质过氧化的启动和脂质过氧化物的清除。在这篇综述中,我们从上述三个阶段总结了铁变态反应中脂质过氧化的分子调节机制,以及针对脂质过氧化的各种铁变态反应调节剂,包括常用产品、天然生物活性化合物和硒化合物。总之,这些研究结果表明脂质过氧化在铁变态反应中的重要作用,而针对铁变态反应中的脂质过氧化具有治疗铁变态反应相关疾病的潜力。
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引用次数: 0
Structural characteristics of phenylboronic acid-modified astaxanthin ester and its effect on DSS-induced ulcerative colitis by blocking reactive oxygen species and maintaining intestinal homeostasis 苯硼酸改性虾青素酯的结构特征及其通过阻断活性氧和维持肠道稳态对 DSS 诱导的溃疡性结肠炎的影响
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250223
A novel and reactive oxygen species (ROS) responsive astaxanthin phenylboronic acid derivative (AstaD-PBA) was constructed by grafting phenylboronic acid (PBA) onto astaxanthin succinate diester (AstaD), and its chemical structure and physicochemical property were identified. AstaD-PBA could effectively improve the ROS quenching ability in the lipopolysaccharide (LPS)-induced RAW264.7 cell inflammation model. Then, the bioactivity of AstaD-PBA was studied by 4 zebrafish ROS-responsive inflammatory models induced by LPS, copper (Cu2+), high-fat diet, and dextran sodium sulfate (DSS). The results suggest that AstaD-PBA might have high biosafety and the best effect on ulcerative colitis (UC) induced by DSS. Furtherly, AstaD-PBA significantly alleviated and treated weight loss and colonic shrinkage, inhibited inflammatory cytokines, and maintained microbiota homeostasis to improve UC in C57BL/6J mice. Alistipes and Oscillibacter were expected to be considered UC marker flora according to the Metastats analysis and Pearson correlation Mantel test (P < 0.01) of 16S rRNA gene sequencing data. In conclusion, AstaD-PBA has been promised to be a functional compound to improve UC and maintain intestinal microbiota homeostasis.
通过将苯硼酸(PBA)接枝到虾青素琥珀酸二酯(AstaD)上,构建了一种新型的活性氧(ROS)反应性虾青素苯硼酸衍生物(AstaD-PBA),并鉴定了其化学结构和理化性质。在脂多糖(LPS)诱导的RAW264.7细胞炎症模型中,AstaD-PBA能有效提高ROS淬灭能力。随后,通过LPS、铜(Cu2+)、高脂饮食和右旋糖酐硫酸钠(DSS)诱导的4种斑马鱼ROS反应性炎症模型研究了AstaD-PBA的生物活性。结果表明,AstaD-PBA 可能具有较高的生物安全性,对 DSS 诱导的溃疡性结肠炎(UC)具有最佳效果。此外,AstaD-PBA 还能显著缓解和治疗 C57BL/6J 小鼠的体重减轻和结肠萎缩,抑制炎症细胞因子,维持微生物群平衡,从而改善 UC。根据 16S rRNA 基因测序数据的 Metastats 分析和 Pearson 相关性 Mantel 检验(P < 0.01),Alistipes 和 Oscillibacter 被认为是 UC 标志菌群。总之,AstaD-PBA有望成为改善UC和维持肠道微生物群平衡的功能性化合物。
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引用次数: 0
Transcriptomic analysis of molecular mechanisms underlying the biodegradation of organophosphorus pesticide chlorpyrifos by Lactobacillus delbrueckii ssp. bulgaricus in skimmed milk 脱脂乳中的保加利亚乳杆菌生物降解有机磷农药毒死蜱的分子机制转录组分析
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250244
Bioremediation of organophosphorus pesticides in contaminated foodstuffs using probiotics has been increasingly under the spotlight in recent years, though the biodegradation mechanism and derived intermediate products remain unclear. This study aimed to help fill this knowledge gap and examined the degradation mechanism of organophosphorus pesticide, chlorpyrifos, in milk by Lactobacillus delbrueckii ssp. bulgaricus using gas chromatography- tandem mass spectrometry (GC-MS/MS) combined with transcriptome analysis. After the strain was cultured for 20 h in the presence of chlorpyrifos, differential expressions of 383 genes were detected, including genes probably implicated during chlorpyrifos degradation such as those related to hydrolase, phosphoesterase, diphosphatase, oxidoreductase, dehydratase, as well as membrane transporters. GC-MS/MS analysis revealed the changes of secondary metabolites in L. bulgaricus during milk fermentation due to chlorpyrifos stress. 6-Methylhexahydro-2H-azepin-2-one, 2,6-dihydroxypyridine and methyl 2-aminooxy-4-methylpentanoate as intermediates, along with the proposed pathways, might be involved in chlorpyrifos biodegradation by L. bulgaricus.
近年来,利用益生菌对受污染食品中的有机磷农药进行生物修复日益受到关注,但其生物降解机制和衍生的中间产物仍不清楚。本研究旨在填补这一知识空白,采用气相色谱-串联质谱法(GC-MS/MS)结合转录组分析,研究了保加利亚乳杆菌对牛奶中有机磷农药毒死蜱的降解机制。在毒死蜱存在下培养该菌株 20 小时后,检测到 383 个基因有不同的表达,其中包括可能与毒死蜱降解有关的基因,如与水解酶、磷酸酯酶、二磷酸酶、氧化还原酶、脱水酶以及膜转运体有关的基因。气相色谱-质谱/质谱分析表明,在牛奶发酵过程中,由于毒死蜱胁迫,保加利亚鹅膏菌中的次生代谢物发生了变化。作为中间产物的 6-甲基六氢-2H-氮杂卓-2-酮、2,6-二羟基吡啶和 2-氨基氧基-4-甲基戊酸甲酯以及所提出的途径可能参与了保加利亚酵母菌对毒死蜱的生物降解。
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引用次数: 0
Curcumin delivery nanoparticles based on Maillard reaction of Haematococcus pluvialis protein/galactose for alleviating acute alcoholic liver damage 基于血球菌蛋白/半乳糖的马氏反应的姜黄素递送纳米颗粒,用于缓解急性酒精性肝损伤
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250211
The aim of this study is to investigate the feasibility of Maillard reaction products of Haematococcus pluvialis protein and galactose (HPP-GAL) for improving the bioactivities of curcumin (CUR) for alleviating alcoholic liver damage. CUR was embedded into HPP-GAL nanoparticles by the self-assembly of hydrogen bonding and hydrophobic interaction with the particle size around 200 nm. HPP-GAL enhanced the encapsulation efficiency and loading amount of CUR with the value of (89.21 ± 0.33)% and (0.500 ± 0.004)%, respectively. The stabilities of CUR under strong acid, salt ion stability and ultraviolet irradiation conditions were improved by the encapsulation. HPP-GAL-CUR nanoparticles exhibited excellent concentration-dependent in vitro antioxidant activities including DPPH and ABTS scavenging rates, and better protective effect on CUR against gastric acid environment as well as longer release of CUR in simulated intestinal fluid. In addition, the HPP-GAL-CUR delivery system possessed liver targeting property due to the existence of GAL, which could effectively alleviate the alcohol-induced liver damage and the inflammation indexes by inhibiting the oxidative stress. Therefore, HPP-GAL-CUR nanoparticles might be a potential candidate system for the prevention of alcoholic liver damage in the future.
本研究旨在探讨血球菌蛋白与半乳糖的马氏反应产物(HPP-GAL)改善姜黄素(CUR)生物活性以减轻酒精性肝损伤的可行性。通过氢键和疏水作用的自组装,姜黄素被嵌入 HPP-GAL 纳米粒子,粒径约为 200 nm。HPP-GAL提高了CUR的包封效率和负载量,其值分别为(89.21 ± 0.33)%和(0.500 ± 0.004)%。封装后的 CUR 在强酸、盐离子稳定性和紫外线照射条件下的稳定性都得到了改善。HPP-GAL-CUR 纳米粒子具有优异的浓度依赖性体外抗氧化活性,包括 DPPH 和 ABTS 清除率,对 CUR 在胃酸环境中具有更好的保护作用,在模拟肠液中的释放时间更长。此外,由于 GAL 的存在,HPP-GAL-CUR 给药系统具有肝脏靶向性,可通过抑制氧化应激有效缓解酒精引起的肝损伤和炎症指标。因此,HPP-GAL-CUR纳米颗粒可能是未来预防酒精性肝损伤的潜在候选系统。
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引用次数: 0
Antiglycating effects of citrus flavonoids and associated mechanisms 柑橘类黄酮的抗糖化作用及相关机制
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250247
Yunli Xiao , Junfeng Shen , Jianfeng Zhan , Limin Guo , Chi-Tang Ho , Shiming Li
Glycation of proteins and DNA forms advanced glycation end products (AGEs) causing cell and tissue dysfunction and subsequent various chronic diseases, in particular, metabolic and age-related diseases. Targeted AGE inhibition includes scavengers of reactive carbonyl species (RCS) such as methylglyoxal (MG), glyoxalase-1 enhancers, Nrf2/ARE pathway activators, AGE/RAGE formation inhibitors and other antiglycatng agents. Citrus flavonoids have demonstrated antioxidant and anti-inflammatory effects and are also found to be effective antiglycating agents. Herein, we reviewed the up to date progress of the antiglycation effects of citrus flavonoids and associated mechanisms. Major citrus flavonoids, hesperedin and its aglycone, hesperetin, inhibited glycation by scavenging MG forming mono- or di-flavonoid adducts with MG, enhanced the activity of glyoxase-1, activated Akt/Nrf2 signal pathway while inhibiting AGE/RAGE/NF-κB pathway, reduced the formation of Nε-(carboxylmethyl)lysine (CML) and pentosidine, inhibited aldol reductase activity and decreased the levels of fructosamine. The antiglycating activity and mechanisms of other flavonoids was also summarized in this review. In conclusion, citrus flavonoids possess effective antiglycating activity via different mechanisms, yet there are many challenging questions remaining to be studied in the near future such as in vivo testing and human study of citrus flavonoids for efficacy, effectiveness and adverse effects of citrus flavonoids as a functional food in managing high levels of AGEs and controlling AGE-induced chronic diseases, diabetic complications in particular.
蛋白质和 DNA 的糖化会形成高级糖化终产物(AGEs),导致细胞和组织功能障碍,进而引发各种慢性疾病,尤其是代谢性疾病和与年龄有关的疾病。有针对性的 AGE 抑制剂包括甲基乙二醛(MG)等活性羰基(RCS)清除剂、乙醛缩醛酶-1 增强剂、Nrf2/ARE 途径激活剂、AGE/RAGE 形成抑制剂和其他抗糖化剂。柑橘类黄酮具有抗氧化和抗炎作用,也是有效的抗糖化剂。在此,我们回顾了柑橘类黄酮抗糖化作用及相关机制的最新进展。主要的柑橘类黄酮、橙皮素及其苷元橙皮素通过清除与 MG 形成单或双黄酮加合物的 MG 来抑制糖化,增强糖化酶-1 的活性、激活 Akt/Nrf2 信号通路,同时抑制 AGE/RAGE/NF-κB 通路,减少 Nε-(羧甲基)赖氨酸(CML)和喷托糖苷的形成,抑制醛醇还原酶的活性,降低果糖胺的水平。本综述还总结了其他黄酮类化合物的抗糖化活性和机制。总之,柑橘类黄酮通过不同的机制具有有效的抗糖化活性,但在不久的将来仍有许多具有挑战性的问题有待研究,如柑橘类黄酮的体内试验和人体研究,以了解柑橘类黄酮作为功能食品在控制高浓度 AGEs 和控制 AGE 引起的慢性疾病(尤其是糖尿病并发症)方面的功效、有效性和不良影响。
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引用次数: 0
Fufang E’jiao Jiang’s effect on immunity, hematopoiesis, and angiogenesis via a systematic “compound-effect-target” analysis 通过系统的 "复合效应-靶标 "分析,了解扶芳二条姜对免疫、造血和血管生成的影响
IF 5.6 1区 农林科学 Q1 FOOD SCIENCE & TECHNOLOGY Pub Date : 2024-09-01 DOI: 10.26599/FSHW.2022.9250228
Fufang Ejiao Jiang (FEJ) as a healthy food consisting of medicine food homology materials approved by China’s Ministry of Health has been extensively applied to replenish qi and nourish blood, and it has a positive impact on women’s health. To find out the material basis and mechanism of FEJ, a systematic “compound-effect-target” analysis including chemical composition resolution, zebrafish, network pharmacology, molecular docking, transcriptome, and bibliometric analysis was adopted. 124 chemical components including ginsenosides, and phenylethanoid glycosides in FEJ were discovered, and effects of FEJ on promoting the generation of immune cells, erythropoiesis and angiogenesis in zebrafish were exhibited. Based on network pharmacology, molecular docking and in vivo activity assay, 6 compounds including jionoside A1, isoacteoside, echinacoside, acteoside, lobetyolin, and rehmannioside D were identified as active components of FEJ. Transcriptome data showed that several pathways such as complement and coagulation cascades, ECM-receptor interaction, and PI3K-Akt signaling pathway were associated with proangiogenic effect of FEJ. 19 common targets were obtained through combined analysis of network pharmacology and transcriptomics, and 5 targets of them were verified by PCR. The bibliometric analysis of these common targets revealed that FEJ was related to energy metabolism, pathway in cancer, etc., which was consistent with the results of network pharmacology and transcriptome. The studies suggested that FEJ could replenish qi and nourish blood through multi-compound and multi-targets.
馥芳娥娇姜作为中国卫生部批准的药食同源健康食品,在补气养血方面得到了广泛应用,对女性健康产生了积极影响。为探明人参皂苷的物质基础和作用机理,采用了化学成分解析、斑马鱼、网络药理学、分子对接、转录组和文献计量学等系统的 "化合物-效应-靶标 "分析方法。发现了 FEJ 中包括人参皂苷、苯乙醇苷在内的 124 种化学成分,并展示了 FEJ 促进斑马鱼免疫细胞生成、红细胞生成和血管生成的作用。基于网络药理学、分子对接和体内活性检测,6 个化合物,包括琼瑶苷 A1、异内酯苷、棘鲷苷、放线菌苷、龙脑香苷和雷曼薯蓣皂苷 D 被鉴定为 FEJ 的活性成分。转录组数据显示,补体和凝血级联、ECM-受体相互作用和 PI3K-Akt 信号通路等多个通路与 FEJ 的促血管生成作用有关。通过网络药理学和转录组学的联合分析,获得了19个共同靶点,并对其中的5个靶点进行了PCR验证。对这些共同靶点的文献计量分析表明,FEJ与能量代谢、癌症通路等有关,这与网络药理学和转录组学的结果一致。这些研究表明,FEJ 可通过多化合物和多靶点来补气养血。
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引用次数: 0
期刊
Food Science and Human Wellness
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