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In Vitro Intestinal Transepithelial Transport, Safety, and Bioactivity Evaluation of Milk Peptides 乳肽的体外肠上皮转运、安全性和生物活性评价
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-18 DOI: 10.1155/jfbc/3531386
Melissa Fanzaga, Gilda Aiello, Lorenza D’Adduzio, Giulia Ranaldi, Giovanna Boschin, Anna Arnoldi, Carlotta Bollati, Carmen Lammi

This study aimed to evaluate the bioaccessibility, stability to brush border peptidases, bioavailability, intestinal safety, and bioactivity of low molecular weight (LMW)-milk protein hydrolysate on intestinal Caco-2 and STC-1 cellular models. Milk proteins were first subjected to simulated gastrointestinal digestion, and the resulting peptide mixture was analyzed for intestinal absorption using differentiated human Caco-2 cells. Using high-performance liquid chromatography-mass spectrometry (HPLC-MS), 82 peptides from casein and 16 peptides from β-lactoglobulin were identified as bioaccessible and stable, with some peptides already known to circulate in human plasma. Notably, 47% of apical peptides successfully crossed the epithelial barrier to the basolateral side. Importantly, the peptide mixtures preserved the intestinal monolayer integrity as shown by unchanged transepithelial electrical resistance (TEER) values at 5 mg/mL and demonstrated the intestinal safety through the absence of cytotoxicity in 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) viability experiment in differentiated Caco-2 cells. Moreover, the bioactivity of the LMW-milk protein hydrolysate was assessed through in vitro and cell-based assays. Antioxidant potential was assessed using the 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt (ABTS) and ferric reducing antioxidant power (FRAP) assays, revealing a strong radical scavenging effect (up to 72.6%) and a FRAP increase of 3864% at 2.5 mg/mL. In addition, LMW hydrolysate significantly inhibited dipeptidyl peptidase-IV (DPP-IV) activity by 70.1% in vitro and 20.9% in Caco-2 cells at 10 mg/mL and stimulated glucagon-like peptide-1 (GLP-1) secretion in STC-1 cells by up to 122.4%. Finally, angiotensin-converting enzyme (ACE) inhibition reached 23% at 6.67 mg/mL in a dose-dependent manner. These findings demonstrate that LMW-milk peptides are safe, bioavailable, and exert multifunctional biological activities antioxidant, hypoglycemic, and hypotensive, supporting their potential application in functional food development.

本研究旨在评价低分子量(LMW)牛奶蛋白水解物在肠道Caco-2和STC-1细胞模型上的生物可及性、对刷边肽酶的稳定性、生物利用度、肠道安全性和生物活性。首先对牛奶蛋白进行模拟胃肠道消化,并利用分化的人Caco-2细胞对所得多肽混合物进行肠道吸收分析。利用高效液相色谱-质谱(HPLC-MS)技术,鉴定了82个酪蛋白肽段和16个β-乳球蛋白肽段具有生物可及性和稳定性,其中一些肽段已知可在人血浆中循环。值得注意的是,47%的根尖肽成功地穿过上皮屏障到达基底外侧。重要的是,肽混合物在5mg /mL时保持了肠道单层的完整性,经上皮电阻(TEER)值不变,并且在分化的cco -2细胞的3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)活力实验中,通过无细胞毒性证明了肠道安全性。此外,通过体外和细胞实验对低分子量牛奶蛋白水解物的生物活性进行了评估。采用2,2 ' -氮基-双(3-乙基苯并噻唑-6-磺酸)二铵盐(ABTS)和铁还原抗氧化能力(FRAP)试验评估其抗氧化能力,结果表明,在2.5 mg/mL浓度下,其自由基清除能力达到72.6%,FRAP提高3864%。此外,LMW水解液在10 mg/mL浓度下显著抑制二肽基肽酶- iv (DPP-IV)在体外的活性为70.1%,在cco -2细胞中的活性为20.9%,刺激STC-1细胞中胰高血糖素样肽-1 (GLP-1)的分泌高达122.4%。最后,血管紧张素转换酶(ACE)抑制率在6.67 mg/mL时达到23%,呈剂量依赖性。这些研究结果表明,低分子量乳肽具有安全、生物利用度高、抗氧化、降糖、降血压等多种生物活性,在功能食品开发中具有潜在的应用前景。
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引用次数: 0
The Effect of the Emulsion of Echinophora cinerea Boiss. on Paraquat-Induced Lung Fibrosis in Male Rats 棘球虱乳剂的抑菌效果。百草枯致雄性大鼠肺纤维化的研究
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-18 DOI: 10.1155/jfbc/8342085
Naser Pajouhi, Arash Heydari Ariya, Marzieh Rashidipour, Hadis Jamshidvand, Ali Pajouhi, Raheleh Assaei

Introduction: Paraquat (PQ) induces pulmonary fibrosis through mechanisms involving oxidative stress, inflammatory responses, and fibrotic reactions. During this process, the overexpression of alpha-smooth muscle actin (α-SMA) promotes the differentiation of fibroblasts into myofibroblasts, leading to excessive protein accumulation in the extracellular matrix (ECM). Echinophora cinerea Boiss. (E. cinerea) is an herb known for its antioxidant effects. The goal of this study is to assess the protective effects of E. cinerea in PQ-induced lung injury.

Methods: Fifty adult male Sprague Dawley rats, weighing 220–250 g, were randomly assigned to five groups: (1) Sham received daily gavage of Tween 20, 3% for 6 weeks, along with inhalation of nebulized sterile distilled water (10 mg/m3 for 30 min, three times a week) during Weeks 3 and 4 of treatment. (2) PQ was administered via inhalation of nebulized PQ in sterile distilled water at a concentration of 10 mg/m3 for 30 min, three times a week, during Weeks 3 and 4 of treatment. (3) PQ and emulsion 100 were administered via daily gavage at a dosage of 100 mg/kg emulsion in a 3% Tween 20 solution for 6 weeks, alongside inhalation of PQ, similar to Group 2. The animals in Groups 4 (PQ + E200) and 5 (PQ + E400) were administered with higher doses of emulsion. At the end of the study period, the animals’ lungs were excised for histological analysis.

Results: PQ exposure caused lung injury and an elevation in α-SMA relative to the sham group. The administration of emulsion at doses of 400 and 200 mg/kg, along with PQ, reduced lung injury and α-SMA levels relative to the PQ group. No significant differences were observed in the protective effects of the emulsion at doses of 400 and 200 mg/kg.

Conclusion: Echinophora cinerea essence emulsion attenuates PQ toxicity and mitigates lung injury, with more studies needed to confirm these effects further.

简介:百草枯(PQ)通过氧化应激、炎症反应和纤维化反应等机制诱导肺纤维化。在此过程中,α-平滑肌肌动蛋白(α-SMA)的过度表达促进成纤维细胞向肌成纤维细胞分化,导致细胞外基质(ECM)中蛋白质的过度积累。棘球绦虫。(E. cinerea)是一种以抗氧化作用闻名的草药。本研究的目的是评估灰绿杆菌对pq诱导的肺损伤的保护作用。方法:选取体重220 ~ 250 g的成年雄性Sprague Dawley大鼠50只,随机分为5组:(1)在给药第3、4周,每天灌胃20,3 %的Tween,连续6周,同时雾化吸入无菌蒸馏水(10 mg/m3,连续30 min,每周3次)。(2)在治疗的第3周和第4周,将PQ雾化吸入浓度为10 mg/m3的无菌蒸馏水中,持续30分钟,每周3次。(3) PQ和乳剂100以100 mg/kg乳剂在3% Tween 20溶液中每日灌胃,连续6周,同时吸入PQ,与2组相似。第4组(PQ + E200)和第5组(PQ + E400)给予较高剂量的乳剂。在研究期结束时,切除动物的肺进行组织学分析。结果:与假手术组相比,PQ暴露导致大鼠肺损伤,α-SMA升高。与PQ组相比,乳状液剂量分别为400和200 mg/kg和PQ组肺损伤和α-SMA水平均有所降低。在400 mg/kg和200 mg/kg剂量下,乳剂的保护作用无显著差异。结论:棘球蚴精油乳剂具有减轻PQ毒性和减轻肺损伤的作用,这些作用有待进一步的研究证实。
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引用次数: 0
Eco-Friendly Extraction and Characterization of Terpenoids From Plants as Functional Food Ingredients: A Review 植物功能性食品成分中萜类化合物的生态友好提取与表征研究进展
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-16 DOI: 10.1155/jfbc/9746960
Ameen Hammed, Nushrat Yeasmen, Valérie Orsat

Terpenoids have emerged as essential ingredients in the functional food industry due to their diverse bioactivities and potential health benefits. This review examines recent advances in green extraction techniques and characterization methods for terpenoids from plants, with further focus on their applications as functional food ingredients. The study explores novel extraction methods, including supercritical fluid, ultrasound-assisted, high-pressure, and microwave-assisted extraction, detailing their underlying extraction mechanisms, operating conditions, and compatibility for extracting terpenoids. It also evaluates various qualitative and quantitative characterization techniques, including chromatographic, spectroscopic, and computational methods. Additionally, the review discusses the current and potential applications of terpenoids in functional foods, highlighting their roles in food preservation, flavoring, coloring, packaging, and health promotion. By synthesizing recent research, this work offers insights into the efficient extraction, accurate characterization, and innovative utilization of terpenoids in the functional food sector.

萜类化合物由于具有多种生物活性和潜在的健康益处,已成为功能性食品工业的重要成分。本文综述了植物中萜类化合物的绿色提取技术和表征方法的最新进展,并重点介绍了其在功能性食品成分中的应用。本研究探讨了超临界流体萃取、超声萃取、高压萃取、微波萃取等新型萃取方法,详细介绍了它们的萃取机理、操作条件和萃取萜类化合物的相容性。它还评估了各种定性和定量表征技术,包括色谱,光谱和计算方法。此外,本文还讨论了萜类化合物在功能性食品中的应用现状和潜力,重点介绍了它们在食品保鲜、调味、着色、包装和健康促进方面的作用。通过综合最近的研究,本工作为功能性食品部门中萜类化合物的高效提取、准确表征和创新利用提供了见解。
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引用次数: 0
Analysis of the Differences Between Different Fruit Colors of Amomum tsao-ko Based on Widely Targeted Metabolomics and Network Pharmacology 基于广泛靶向代谢组学和网络药理学的砂砂果不同颜色差异分析
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-16 DOI: 10.1155/jfbc/3869156
Tao Chen, Meiquan Yang, Tianmei Yang, Weize Yang, Jinyu Zhang

Amomum tsao-ko (AT) is an important medicinal and edible plant. Its fruit has various colors, commonly available in green, red and dark red colors. There may be significant differences in chemical composition and pharmacological activity among ATs with different fruit colors. In this study, we systematically analyzed the metabolite composition of ATs of different fruit colors and their potential pharmacological mechanisms of action using a combination of widely targeted metabolomics and network pharmacology. Through widely targeted metabolomics techniques, we identified and quantified a variety of metabolites in ATs, including flavonoids, phenolic acids, terpenes, and alkaloids. The results showed that there were significant differences in metabolite composition among AT with different fruit colors, especially in the contents of flavonoids and phenolic acids. Among them, flavonoid components such as kaempferol, isorhamnetin derivatives, and epigallocatechin analogs play a major role in the color formation of ATs. Furthermore, through the network pharmacological analysis, we constructed the metabolite-target-disease network of AT and revealed the potential pharmacological mechanism of AT with different fruit color. Five compounds, ent-Epicatechin, (4e_(6e))-1,ent-Epicatechin(4-hydroxyphenyl)hepta-4,6-dien-3-one, beta-daucosterol_qt, (−)-catechin and quercetin, which are effective in the treatment of tumor, were obtained by screening. They had good docking ability to the protein target of tumor. After screening the metabolites of four kinds of fruit color, quercetin was the common component of four kinds of fruit color AT, but the other four compounds could not be detected. In terms of the relative content of the detected compounds, light red AT > dark red AT > red AT > green AT; generally speaking, the content is relatively high, the more potential biological activity, so in theory, the light red AT is more effective in the treatment of tumor, but further pharmacological verification is needed.

This study not only provides a new scientific basis for the chemical differences and pharmacological effects of different fruit colors, but also provides theoretical support.

砂木(Amomum tsao-ko, AT)是一种重要的药用和食用植物。它的果实有各种各样的颜色,常见的有绿色、红色和深红色。不同果实颜色的ATs在化学成分和药理活性上可能存在显著差异。本研究采用广泛靶向代谢组学和网络药理学相结合的方法,系统分析了不同水果颜色ATs的代谢物组成及其潜在的药理作用机制。通过广泛靶向代谢组学技术,我们鉴定和量化了ATs中的多种代谢物,包括黄酮类、酚酸、萜烯和生物碱。结果表明,不同果色的山楂代谢物组成差异显著,其中黄酮类和酚酸含量差异最大。其中,山奈酚、异鼠李素衍生物和表没食子儿茶素类似物等类黄酮成分在ATs的颜色形成中起主要作用。进一步,通过网络药理分析,构建了AT的代谢物-靶点-疾病网络,揭示了不同果色AT的潜在药理机制。筛选得到5个有效治疗肿瘤的化合物,(4e_(6e))-1, (4e_(6e))-1, (4-hydroxyphenyl)hepta-4,6-dien-3-one, β -daucosterol_qt,(−)-儿茶素和槲皮素。它们与肿瘤蛋白靶点有良好的对接能力。筛选4种果色的代谢物后发现,槲皮素是4种果色AT的共同成分,其余4种化合物均未检出。检测到的化合物相对含量为:浅红色AT >;深红色AT >;红色AT >;一般来说,含量越高,潜在的生物活性越强,因此理论上,浅红色AT治疗肿瘤更有效,但还需要进一步的药理学验证。本研究不仅为不同水果颜色的化学差异和药理作用提供了新的科学依据,也提供了理论支持。
{"title":"Analysis of the Differences Between Different Fruit Colors of Amomum tsao-ko Based on Widely Targeted Metabolomics and Network Pharmacology","authors":"Tao Chen,&nbsp;Meiquan Yang,&nbsp;Tianmei Yang,&nbsp;Weize Yang,&nbsp;Jinyu Zhang","doi":"10.1155/jfbc/3869156","DOIUrl":"https://doi.org/10.1155/jfbc/3869156","url":null,"abstract":"<p><i>Amomum tsao-ko</i> (AT) is an important medicinal and edible plant. Its fruit has various colors, commonly available in green, red and dark red colors. There may be significant differences in chemical composition and pharmacological activity among ATs with different fruit colors. In this study, we systematically analyzed the metabolite composition of ATs of different fruit colors and their potential pharmacological mechanisms of action using a combination of widely targeted metabolomics and network pharmacology. Through widely targeted metabolomics techniques, we identified and quantified a variety of metabolites in ATs, including flavonoids, phenolic acids, terpenes, and alkaloids. The results showed that there were significant differences in metabolite composition among AT with different fruit colors, especially in the contents of flavonoids and phenolic acids. Among them, flavonoid components such as kaempferol, isorhamnetin derivatives, and epigallocatechin analogs play a major role in the color formation of ATs. Furthermore, through the network pharmacological analysis, we constructed the metabolite-target-disease network of AT and revealed the potential pharmacological mechanism of AT with different fruit color. Five compounds, ent-Epicatechin, (4e_(6e))-1,ent-Epicatechin(4-hydroxyphenyl)hepta-4,6-dien-3-one, beta-daucosterol_qt, (−)-catechin and quercetin, which are effective in the treatment of tumor, were obtained by screening. They had good docking ability to the protein target of tumor. After screening the metabolites of four kinds of fruit color, quercetin was the common component of four kinds of fruit color AT, but the other four compounds could not be detected. In terms of the relative content of the detected compounds, light red AT &gt; dark red AT &gt; red AT &gt; green AT; generally speaking, the content is relatively high, the more potential biological activity, so in theory, the light red AT is more effective in the treatment of tumor, but further pharmacological verification is needed.</p><p>This study not only provides a new scientific basis for the chemical differences and pharmacological effects of different fruit colors, but also provides theoretical support.</p>","PeriodicalId":15802,"journal":{"name":"Journal of Food Biochemistry","volume":"2025 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jfbc/3869156","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145101594","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Lycopene Ameliorates Hepatic Ischemia-Reperfusion Injury in Rats by Suppressing HRD1 E3 Ubiquitin Ligase to Restore Nrf2 Signaling 番茄红素通过抑制HRD1 E3泛素连接酶恢复Nrf2信号通路改善大鼠肝缺血再灌注损伤
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-16 DOI: 10.1155/jfbc/6651066
Li Li, Hui Zhang, Yuchao Sun

Background: Hepatic ischemia-reperfusion injury (HIRI) is a critical clinical challenge, and lycopene, a natural carotenoid with antioxidant properties, has shown potential in mitigating organ damage. This research evaluated the therapeutic potential and mechanistic basis of lycopene against HIRI utilizing in vivo and in vitro approaches.

Methods: A rat HIRI model and AML-12 cell models (H2O2-induced oxidative stress and hypoxia/reoxygenation [H/R]) were established.

Results: Lycopene significantly alleviated HIRI in rats, evidenced by improved hepatic histopathology (HE staining), restored antioxidant enzyme activities (SOD1 and GSH), and reduced proinflammatory cytokines (TNF-α, IL-6, and IL-1β). Notably, HRD1, an E3 ubiquitin ligase, exhibited dynamic temporal expression: In mild HIRI (30 min ischemia/6 h reperfusion), HRD1 initially increased adaptively but declined thereafter, whereas severe ischemia (60 min) caused persistent HRD1 upregulation during reperfusion, exacerbating apoptosis and liver dysfunction. Lycopene treatment normalized HRD1 levels, reducing apoptosis markers (Bax, Cleaved-Caspase-3) and enhancing antiapoptotic Bcl-2. In vitro, lycopene attenuated H2O2- and H/R-induced oxidative stress, inflammation, and apoptosis. Mechanistically, genetic manipulation of HRD1 (silencing or overexpression) confirmed that it targets Nrf2, the central regulator of antioxidant defense, for degradation. Lycopene suppressed HRD1-mediated Nrf2 ubiquitination, thereby stabilizing Nrf2 and activating downstream antioxidant genes (HO-1 and NQO1).

Conclusions: These findings demonstrate that lycopene ameliorates HIRI by modulating the HRD1-Nrf2 axis, highlighting its therapeutic potential via dual antioxidant and antiapoptotic mechanisms. This study provides novel insights into HRD1’s context-dependent roles in HIRI and positions lycopene as a promising candidate for clinical translation.

背景:肝缺血再灌注损伤(HIRI)是一个重要的临床挑战,番茄红素是一种具有抗氧化特性的天然类胡萝卜素,已显示出减轻器官损伤的潜力。本研究利用体内和体外方法评估了番茄红素对HIRI的治疗潜力和机制基础。方法:建立大鼠HIRI模型和AML-12细胞模型(h2o2诱导的氧化应激和缺氧/再氧化[H/R])。结果:番茄红素显著缓解大鼠HIRI,改善肝脏组织病理学(HE染色),恢复抗氧化酶(SOD1和GSH)活性,降低促炎因子(TNF-α、IL-6和IL-1β)。值得注意的是,E3泛素连接酶HRD1表现出动态的时间表达:在轻度HIRI(缺血30分钟/再灌注6小时)中,HRD1最初适应性升高,但随后下降,而严重缺血(60分钟)导致HRD1在再灌注期间持续上调,加剧细胞凋亡和肝功能障碍。番茄红素处理使HRD1水平正常化,降低凋亡标志物(Bax, Cleaved-Caspase-3),增强抗凋亡Bcl-2。在体外,番茄红素可减弱H2O2-和H/ r诱导的氧化应激、炎症和细胞凋亡。从机制上讲,HRD1的基因操作(沉默或过表达)证实了它针对Nrf2(抗氧化防御的中心调节因子)进行降解。番茄红素抑制hrd1介导的Nrf2泛素化,从而稳定Nrf2并激活下游抗氧化基因(HO-1和NQO1)。结论:这些研究结果表明,番茄红素通过调节HRD1-Nrf2轴改善HIRI,突出了其通过双重抗氧化和抗凋亡机制的治疗潜力。这项研究为HRD1在HIRI中的环境依赖性作用提供了新的见解,并将番茄红素定位为临床翻译的有希望的候选者。
{"title":"Lycopene Ameliorates Hepatic Ischemia-Reperfusion Injury in Rats by Suppressing HRD1 E3 Ubiquitin Ligase to Restore Nrf2 Signaling","authors":"Li Li,&nbsp;Hui Zhang,&nbsp;Yuchao Sun","doi":"10.1155/jfbc/6651066","DOIUrl":"https://doi.org/10.1155/jfbc/6651066","url":null,"abstract":"<p><b>Background:</b> Hepatic ischemia-reperfusion injury (HIRI) is a critical clinical challenge, and lycopene, a natural carotenoid with antioxidant properties, has shown potential in mitigating organ damage. This research evaluated the therapeutic potential and mechanistic basis of lycopene against HIRI utilizing in vivo and in vitro approaches.</p><p><b>Methods:</b> A rat HIRI model and AML-12 cell models (H<sub>2</sub>O<sub>2</sub>-induced oxidative stress and hypoxia/reoxygenation [H/R]) were established.</p><p><b>Results:</b> Lycopene significantly alleviated HIRI in rats, evidenced by improved hepatic histopathology (HE staining), restored antioxidant enzyme activities (SOD1 and GSH), and reduced proinflammatory cytokines (TNF-α, IL-6, and IL-1β). Notably, HRD1, an E3 ubiquitin ligase, exhibited dynamic temporal expression: In mild HIRI (30 min ischemia/6 h reperfusion), HRD1 initially increased adaptively but declined thereafter, whereas severe ischemia (60 min) caused persistent HRD1 upregulation during reperfusion, exacerbating apoptosis and liver dysfunction. Lycopene treatment normalized HRD1 levels, reducing apoptosis markers (Bax, Cleaved-Caspase-3) and enhancing antiapoptotic Bcl-2. In vitro, lycopene attenuated H<sub>2</sub>O<sub>2</sub>- and H/R-induced oxidative stress, inflammation, and apoptosis. Mechanistically, genetic manipulation of HRD1 (silencing or overexpression) confirmed that it targets Nrf2, the central regulator of antioxidant defense, for degradation. Lycopene suppressed HRD1-mediated Nrf2 ubiquitination, thereby stabilizing Nrf2 and activating downstream antioxidant genes (HO-1 and NQO1).</p><p><b>Conclusions:</b> These findings demonstrate that lycopene ameliorates HIRI by modulating the HRD1-Nrf2 axis, highlighting its therapeutic potential via dual antioxidant and antiapoptotic mechanisms. This study provides novel insights into HRD1’s context-dependent roles in HIRI and positions lycopene as a promising candidate for clinical translation.</p>","PeriodicalId":15802,"journal":{"name":"Journal of Food Biochemistry","volume":"2025 1","pages":""},"PeriodicalIF":4.2,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1155/jfbc/6651066","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145101269","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Anti-Diabetes Mellitus Potential of MTHP-2-a Purified and Identified by Mass Spectrometry and NMR Technology MTHP-2-a抗糖尿病潜能的质谱和核磁共振技术纯化和鉴定
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-15 DOI: 10.1155/jfbc/9999211
Rong Li, Changyi Wu, Dongmei Wang, Cheng Tan, Muhammad Fattah Fazel, Huani Chen, Weiyun Chew, Venkata Sathya Saiappala Raju Velaga, Li Qian

Murraya tetramera Huang (MTH) is a traditional medicinal plant in western Guangxi and southeastern Yunnan, China. Residents commonly use it as tea. Preliminary experiments conducted by our research team revealed that the Murraya tetramera Huang polysaccharides (MTHPs) exhibit significant inhibitory effects on alpha-glucosidase (α-glucosidase) and alpha-amylase (α-amylase). In this study, MTHPs were purified using diethylaminoethyl cellulose-52 (DEAE-52) anion-exchange chromatography and Sephadex G-75 gel chromatography, resulting in a homogeneous polysaccharide named MTHP-2-a. Structural analysis indicates that MTHP-2-a has a weight-average molecular weight (Mw) of 62.25 kDa. It primarily consists of rhamnose (Rha), arabinose (Ara), galactose (Gal), and glucose (Glc). The backbone fragments include Araf-(1 ⟶, ⟶ 3)-Rhap-(1 ⟶, ⟶ 3)-Araf-(1 ⟶, ⟶ 5)-Araf-(1 ⟶, Glcp-(1 ⟶, ⟶ 2)-Araf-(1 ⟶, ⟶ 2,5)-Araf-(1 ⟶, Galp-(1 ⟶, ⟶ 4)-Galp-(1 ⟶, ⟶ 3)-Galp-(1 ⟶, ⟶ 6)-Glcp-(1 ⟶, ⟶ 6)-Galp-(1 ⟶, and ⟶ 3,6)-Galp-(1 ⟶. In vitro antidiabetic activity assays demonstrate that MTHP-2-a effectively inhibits α-amylase and α-glucosidase, with IC50 values of 1.24 ± 0.02 and 0.32 ± 0.004 mg/mL, respectively. For comparison, the well-known antidiabetic drug acarbose exhibited similar inhibitory effects, with IC50 values of 1.80 ± 0.06 mg/mL for α-amylase and 0.21 ± 0.006 mg/mL for α-glucosidase. These results suggest that MTHP-2-a exhibits comparable inhibitory potency to acarbose, a widely used antidiabetic agent. Furthermore, through both in vitro and in vivo experiments, MTHP-2-a can significantly exhibit hypoglycemic effects. The molecular structure and sugar composition of MTHP-2-a were purified and elucidated for the first time, revealing its strong potential for antihyperglycemic activity. These findings provide new insights into the pharmacological properties of MTHP and lay the foundation for its future development as an antidiabetic drug, supporting further pharmacological studies and preclinical trials.

黄木(Murraya tetramera Huang, MTH)是广西西部和云南东南部的传统药用植物。当地居民通常把它当茶喝。本课题组初步实验发现,Murraya tetramera Huang多糖(MTHPs)对α-葡萄糖苷酶(α-葡萄糖苷酶)和α-淀粉酶(α-淀粉酶)具有显著的抑制作用。本研究采用DEAE-52阴离子交换层析和Sephadex G-75凝胶层析纯化MTHPs,得到均质多糖MTHP-2-a。结构分析表明,MTHP-2-a的分子量为62.25 kDa。它主要由鼠李糖(Rha)、阿拉伯糖(Ara)、半乳糖(Gal)和葡萄糖(Glc)组成。骨干片段包括Araf -(1⟶⟶3)世行(1⟶⟶3)-Araf -(1⟶⟶5)-Araf -(1⟶Glcp(1⟶⟶2)-Araf -(1⟶⟶2、5)-Araf -(1⟶Galp(1⟶⟶4)Galp -(1⟶⟶3)Galp -(1⟶⟶6)-Glcp -(1⟶⟶6)Galp(1⟶,⟶3、6)Galp -(1⟶。体外抗糖尿病活性实验表明,MTHP-2-a能有效抑制α-淀粉酶和α-葡萄糖苷酶,IC50值分别为1.24±0.02和0.32±0.004 mg/mL。相比之下,众所周知的降糖药阿卡波糖表现出类似的抑制作用,α-淀粉酶的IC50值为1.80±0.06 mg/mL, α-葡萄糖苷酶的IC50值为0.21±0.006 mg/mL。这些结果表明MTHP-2-a具有与阿卡波糖相当的抑制效力,阿卡波糖是一种广泛使用的降糖药。此外,在体外和体内实验中,MTHP-2-a均能表现出明显的降糖作用。首次纯化并阐明了MTHP-2-a的分子结构和糖组成,揭示了其强大的降糖活性潜力。这些发现为MTHP的药理特性提供了新的认识,并为其作为抗糖尿病药物的未来发展奠定了基础,为进一步的药理研究和临床前试验提供了支持。
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引用次数: 0
Impact of a Green Cabbage-Based Diet on Selected Proinflammatory Cytokines and Hormones in Pre-Eclamptic Rats 以大白菜为基础的饮食对子痫前期大鼠选定的促炎细胞因子和激素的影响
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-15 DOI: 10.1155/jfbc/9923156
Omolola Mary Omosebi, Fehintoluwa Joy Femi-Olabisi, Jesukorede Chisom Aluko

The growing interest in functional foods has led to the utilization of various vegetables for their nutritional benefits. This study focused on the development and evaluation of a green cabbage-enriched meal and the investigation of the impact of the enriched cookies on selected proinflammatory cytokines and hormones in pre-eclamptic Wistar rats. A cabbage-based diet was formulated and assessed for proximate composition and sensory qualities. In vivo studies were carried out with thirty-five female rats, which were completely randomized into 7 groups. The effect of continued feeding with the diet on immunological parameters was observed. The data obtained from the results were subjected to statistical analysis using analysis of variance (ANOVA). The proximate composition results indicated that the cabbage-based diet exhibited the highest ash content (2.47%–3.6%) and fiber content (2.40%–4.03%). Additionally, the cabbage-based diet exhibited a lower fat content of 9.00%. However, the pre-eclampsia (PE) + cabbage diet group demonstrated TNF-α and IL-6 levels comparable to control groups, showing the anti-inflammatory potential of cabbage, likely due to its sulforaphane content. Similarly, the PE + amlodipine group exhibited reduced cytokine levels, reinforcing the anti-inflammatory effects of the antihypertensive drug. Hormonal analysis revealed significantly lower progesterone levels in pre-eclamptic rats, aligning with impaired placental function and increased vascular resistance. However, the cabbage-based diet appeared to mitigate these hormonal disruptions. These findings suggest that dietary interventions, particularly harnessing bioactive compounds in vegetables, have the potential to serve as a complementary approach to managing inflammation and hormonal imbalances in PE.

随着人们对功能性食品的兴趣日益浓厚,人们开始利用各种蔬菜来获取其营养价值。本研究的重点是开发和评估一种青菜强化餐,并研究强化饼干对子痫前期Wistar大鼠选定的促炎细胞因子和激素的影响。制定了以卷心菜为基础的饮食,并对其近似成分和感官品质进行了评估。实验采用35只雌性大鼠进行体内实验,随机分为7组。观察连续饲喂对免疫指标的影响。从结果中获得的数据采用方差分析(ANOVA)进行统计分析。近似组成结果表明,以白菜为基础的日粮灰分含量最高(2.47% ~ 3.6%),纤维含量最高(2.40% ~ 4.03%)。此外,以卷心菜为基础的日粮脂肪含量较低,为9.00%。然而,子痫前期(PE) +白菜饮食组的TNF-α和IL-6水平与对照组相当,显示出白菜的抗炎潜力,可能是由于其萝卜硫素含量。同样,PE +氨氯地平组细胞因子水平降低,增强了抗高血压药物的抗炎作用。激素分析显示,子痫前期大鼠的孕酮水平显著降低,与胎盘功能受损和血管阻力增加一致。然而,以卷心菜为基础的饮食似乎减轻了这些激素的干扰。这些发现表明,饮食干预,特别是利用蔬菜中的生物活性化合物,有可能作为一种补充方法来管理PE中的炎症和激素失衡。
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引用次数: 0
Enhancement of Bioactivities in Sorghum and Italian Millet Through Household Thermal Processing: Antioxidant Capacity and Lipid Accumulation Inhibition 通过家庭热处理提高高粱和意大利谷子的生物活性:抗氧化能力和抑制脂质积累
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-11 DOI: 10.1155/jfbc/5592006
Narae Han, Jin Young Lee, Yu-Young Lee, Hana Lee, Junsoo Lee, Hyun-Joo Kim

The aim of this study was to investigate the effects of common household thermal processing methods, such as steaming, pressure rice cooking, and roasting, on the enhancement of bioactivities in sorghum and Italian millet, with a focus on nonalcoholic fatty liver disease (NAFLD)–related functionality. The total phenolic and flavonoid contents, antioxidant activities, lipase inhibitory activity, and lipid accumulation in HepG2 cells were evaluated. In sorghum, pressure rice cooking resulted in the highest total phenolic (110.90 mg GAE/g) and flavonoid (46.83 mg CE/g) contents, whereas both pressure rice cooking and steaming improved antioxidant activities across all assays. However, steaming was the most effective in NAFLD-related functionality, showing the most pronounced lipase inhibition (35.66%) and the greatest reduction in lipid accumulation in HepG2 cells (84.67%) under free fatty acid (FFA)–induced conditions. Although Italian millet showed lower baseline activity than sorghum, steaming consistently resulted in the highest phenolic content (ranging from 19.06 to 26.16 mg GAE/g), improved antioxidant activities, and enhanced lipase inhibition (from 8.00% to 9.70%) compared to all other treatments. Lipid accumulation inhibition was observed only in the steaming group, where lipid levels were reduced to 94.15% of those in the FFA-induced control. Thermal treatments led to functional improvements that were associated with increases in bioactive compounds, such as arginine, branched-chain amino acids, and sulfur-containing amino acids, which have been associated with the regulation of lipid metabolism and hepatic function. These findings highlight the effectiveness of simple steaming for enhancing the health-promoting properties of cereal grains, suggesting the potential of this method for application in the development of functional food ingredients aimed at NAFLD prevention.

本研究的目的是研究常见的家庭热加工方法,如蒸、压米和烤,对提高高粱和意大利小米生物活性的影响,重点关注非酒精性脂肪性肝病(NAFLD)相关功能。测定HepG2细胞总酚和类黄酮含量、抗氧化活性、脂肪酶抑制活性和脂质积累。在高粱中,压力蒸煮的总酚(110.90 mg GAE/g)和类黄酮(46.83 mg CE/g)含量最高,而压力蒸煮和蒸煮均能提高抗氧化活性。然而,蒸对nafld相关功能最有效,在游离脂肪酸(FFA)诱导的条件下,显示出最明显的脂肪酶抑制(35.66%)和最大的HepG2细胞脂堆积减少(84.67%)。尽管意大利谷子的基线活性低于高粱,但与其他处理相比,蒸谷子的酚含量最高(19.06 ~ 26.16 mg GAE/g),抗氧化活性提高,脂肪酶抑制能力增强(8.00% ~ 9.70%)。脂质积累抑制仅在蒸组中观察到,其中脂质水平降低到ffa诱导对照组的94.15%。热处理导致功能的改善,与生物活性化合物的增加有关,如精氨酸、支链氨基酸和含硫氨基酸,这些化合物与脂质代谢和肝功能的调节有关。这些发现强调了简单蒸煮对增强谷物健康促进特性的有效性,表明该方法在开发旨在预防NAFLD的功能性食品成分方面具有潜力。
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引用次数: 0
Understanding the Mechanisms of Lipid Metabolism Reprogramming and Ferroptosis in Diabetic Kidney Disease Progression 了解糖尿病肾病进展中脂质代谢重编程和铁下垂的机制
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-10 DOI: 10.1155/jfbc/8388326
Yi Zhen Han, Xing Yu Zhu, Yang Zhi Yuan Wang, Bo Xuan Du, Yun Qiao Zhou, Xue Qin Zhang, Yao Xian Wang, Hui Juan Zheng, Wei Jing Liu

Diabetic kidney disease (DKD) is a common complication of diabetes. The primary mechanism by which renal damage affects renal cells, including podocytes and renal tubular epithelial cells in DKD patients, is lipid metabolism reprogramming. These changes result in a metabolic stress response, including oxidative stress, energy stress in mitochondria, lysosomal stress, endoplasmic reticulum stress, and other stress reactions. Altered lipid metabolism, including abnormalities in proteins and enzymes related to lipid absorption, synthesis, and breakdown, may result in lipid peroxidation and the generation of reactive oxygen species derived from lipids, ultimately initiating ferroptosis in kidney cells. Ferroptosis is a crucial form of programmed cell death in DKD, marked by the buildup of toxic lipid peroxides dependent on iron. It plays a significant role in the progression of kidney-related tissue damage. The discussion also touches on the potential of reducing ferroptosis treatment in DKD by targeting lipid metabolism reprogramming and the metabolic stress response.

糖尿病肾病(DKD)是糖尿病的常见并发症。DKD患者肾损伤影响肾细胞(包括足细胞和肾小管上皮细胞)的主要机制是脂质代谢重编程。这些变化导致代谢应激反应,包括氧化应激、线粒体能量应激、溶酶体应激、内质网应激和其他应激反应。脂质代谢的改变,包括与脂质吸收、合成和分解相关的蛋白质和酶的异常,可能导致脂质过氧化和源自脂质的活性氧的产生,最终引发肾细胞的铁死亡。铁凋亡是DKD中程序性细胞死亡的一种重要形式,其特征是依赖铁的有毒脂质过氧化物的积累。它在肾脏相关组织损伤的进展中起着重要作用。讨论还涉及到通过靶向脂质代谢重编程和代谢应激反应来减少DKD中铁下垂治疗的潜力。
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引用次数: 0
Effect of Slurry Ice With Chlorine Dioxide or Ozone on Chicken Meat Quality During Prechilling 二氧化氯或臭氧对预冷鸡肉品质的影响
IF 4.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Pub Date : 2025-09-10 DOI: 10.1155/jfbc/4435996
Yue Zhang, Yating Zhao, Fang Wang, Xiaona Chu, Hong Zeng, Jigang Yao, Shulai Liu, Yuting Ding, Shiliang Jia, Xuxia Zhou

The study investigated the effects of slurry ice (SI), different concentrations of chlorine dioxide (20, 40, 60 mg/L) or ozone (1, 2, and 3 mg/L) in SI on the microorganisms, physicochemical properties, and lipid and protein oxidation of prechilled chicken. The total viable counts (TVCs) and dominant spoilage bacteria in treated groups were significantly lower than in untreated chicken, and the effect of reducing bacteria was significantly improved with the increase of chlorine dioxide or ozone concentration in SI. Additionally, color, texture, TBARS, total sulfhydryl content, SDS-PAGE, histology, and transmission electron microscopy (TEM) results showed that high concentrations of chlorine dioxide or ozone accelerated the oxidation of proteins and lipids to some extent. Based on the results, 40 mg/L of chlorine dioxide-SI (SI-40) or 3 mg/L of ozone-SI (SI-3) was recommended to treat the chicken carcass. These findings will provide a theoretical basis for the rapid chilling and preservation of whole chicken in the future.

研究了冰浆、二氧化氯浓度(20、40、60 mg/L)和臭氧浓度(1、2、3 mg/L)对预冷鸡肉微生物、理化性质及脂质和蛋白质氧化的影响。处理组的总活菌数(tvc)和优势腐败菌数显著低于未处理组,且随着SI中二氧化氯或臭氧浓度的增加,还原菌的效果显著提高。此外,颜色、质地、TBARS、总巯基含量、SDS-PAGE、组织学和透射电镜(TEM)结果表明,高浓度二氧化氯或臭氧在一定程度上加速了蛋白质和脂质的氧化。根据试验结果,推荐用40 mg/L二氧化氯- si (SI-40)或3 mg/L臭氧- si (SI-3)处理鸡胴体。这些研究结果将为今后全鸡的快速冷藏和保鲜提供理论依据。
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引用次数: 0
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Journal of Food Biochemistry
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