Search Results (4,324)

Backgrouınd/Objectives: Edible fungi are increasingly regarded as important natural reservoirs of secondary metabolites exhibiting a wide range of biological activities. The present study aimed to molecularly identify Rhizopogon roseolus collected from Türkiye and to systematically evaluate its bioactive properties. Methods: The antimicrobial and antioxidant activities of methanolic, ethanolic, and aqueous extracts were evaluated. The phenolic profile and the fatty acid composition of the species were characterized using HPLC-DAD and GC–MS respectively. Results: All extracts showed noticeable antimicrobial activity against several pathogenic microorganisms, including Bacillus subtilis, Micrococcus luteus, Bacillus cereus and Pseudomonas aeruginosa. In addition, the extracts displayed remarkable antioxidant potential. The methanolic extract of R. roseolus demonstrated DPPH and ABTS radical scavenging activities of 651.44 ± 15.02 mg TE/g and 162.71 ± 8.11 mg TE/g, respectively. Its ferric reducing antioxidant power was determined as 724.33 ± 12.23 mg AAE/g DW, while the cupric reducing antioxidant capacity reached 952.45 ± 4.35 mg TE/g DW. These strong antioxidant effects were closely associated with the high phenolic content (9.89 ± 0.08 mg GAE/g DW) of the extracts. GC–MS analysis indicated that palmitoleic, oleic, and linoleic acids were the major fatty acids, while HPLC-DAD revealed that gallic acid and pyrocatechol were major phenolic compounds present in R. roseolus, suggesting a nutritionally beneficial metabolite composition. Conclusions: Taken together, the findings demonstrate that R. roseolus represents a promising natural source of antimicrobial and antioxidant compounds with potential applications. Full article

This study examined the evolution of volatile and non-volatile compounds of a Cypriot monovarietal cultivar Maratheftiko red wine over a span of six years (2019–2024). Several physicochemical properties of the wines were evaluated. Alcohol content and volatile acidity remained stable; acidity and malic acid are the main differentiating factors among vintages. In addition, bioactive molecules in the wines showed a distinct vintage effect, with the 2024 vintage exhibiting significantly higher concentrations. For instance, the high concentration of polyphenols (3877.86 mg gallic acid equivalents per L), tannins (688.43 mg of catechin equivalents per L), flavonoids (506.90 mg of rutin equivalents per L), and anthocyanins (413.74 mg of cyanidin equivalents per L) contributed to the high antioxidant capacity of the specific vintage, as FRAP and DPPH assays were measured at 44.60 and 29.91 mmol of ascorbic acid equivalents per L, respectively. Furthermore, the intense crimson color of this red wine could be attributed to the high concentration of the abundant anthocyanin malvidin-3-O-glucoside in this vintage (21.62 mg/L). On the other hand, it was observed that the latest vintage showed high polyphenol concentration but low volatile compound concentration. This pattern was ascertained through correlation analyses and could be attributed to an unsatisfactory level of the aging process. Correlation analysis (Pearson’s r) confirmed inverse relationships between polyphenol concentration and volatile compounds (r = −0.62, p < 0.05). Principal component analysis (PCA) further highlighted the 2024 as an outlier vintage, distinguished by elevated phenolic and antioxidant profiles. Full article

Inter-row mulching with reflective film (RF) has been increasingly adopted in cool-climate vineyards to improve light availability and promote grape ripening. This study investigated the effects of ground-reflected light on the flavoromic profiles of wine grape berries (Vitis vinifera L.) over two consecutive vintages (2020–2021) in the Beijing Fangshan region of Eastern China, an area characterized by high precipitation and limited sunlight during ripening. Physicochemical analyses showed that RF treatment significantly increased total soluble solids (TSSs) and decreased titratable acidity (TA) at harvest. Targeted metabolomic analyses using HPLC–MS and GC–MS identified 21 flavonoids and 35 volatile compounds responsive to altered light conditions. RF treatment markedly enhanced the accumulation of anthocyanins and flavonols, especially malvidin-based derivatives, and increased terpene and norisoprenoid concentrations, while C₆/C₉ compounds were more abundant in control berries. Multivariate analysis revealed that PC1 was mainly associated with anthocyanin accumulation, clearly separating RF-treated samples, whereas PC2 reflected differences in flavonols and flavan-3-ols, with higher flavonols under RF and higher skin- and seed-derived flavan-3-ols in controls. Overall, these findings demonstrate that ground-reflected light plays a critical role in modulating grape flavor composition and provides practical guidance for improving fruit quality in suboptimal climatic regions. Full article

Background: In this study, we aimed to compare metabolomic profiles, biodistribution, and detoxification patterns of the novel SN-38 derivative NMe with irinotecan (IR), and to identify NMe-specific metabolites to evaluate its preclinical pharmacokinetic advantages. Methods: In vivo ADME studies were conducted for NMe, a 9-aminomethyl SN-38 derivative, and IR following a single intraperitoneal dose of 40 mg/kg in mice. Additionally, ADMET properties were predicted using ADMETlab and SwissADME tools for comparison. Levels of NMe and irinotecan absorbed into plasma, distributed to tissues, and metabolized were monitored in liver, lung, spleen, kidney, and stool samples at 15, 30, and 60 min post-administration. Tissue extracts were analysed using high-performance liquid chromatography (HPLC), liquid chromatography–electrospray ionization quadrupole time-of-flight-tandem mass spectrometry (LC-ESI-QTOF-MS), and nuclear magnetic resonance (NMR) techniques after lyophilization and reconstitution. We compared the metabolomic profiles of irinotecan and NMe. Results: We identified and confirmed NMe-specific metabolites, including 9-CH₂-S-cysteine conjugate, 9-CH₂OH, and NMe-formyl. Notably, novel irinotecan metabolites (IR-OH and IR-ΔE) were detected in small amounts in kidney samples. In some cases, two literature-known photodegradation products of irinotecan were present. NMe was found to quickly metabolize with different distribution to tissues, significantly greater to kidney and liver. Two SN-38 glucuronides, SN-38G(α) and SN-38G(β), were detected corresponding to α- and β-anomers. Where it was possible, NMe, IR and SN-38 were quantified using external calibration curves. In IR group, controlled and prolonged release of SN-38 was confirmed in all samples, yet SN-38G was observed in minority only in plasma, kidney, or lungs. In NMe groups, great relative amounts of SN-38 and SN-38G were detected. Greater content of SN-38G in NMe group than in irinotecan is expected to contribute to modulation and alleviation of some side effects in irinotecan-involved therapies, such as gastrointestinal toxicities (GIT). Conclusions: NMe shows a distinct metabolic profile characterized by rapid biotransformation, higher systemic glucuronidation of SN-38, and formation of unique metabolites, suggesting a potentially wider therapeutic window and reduced toxicity compared with IR. Full article

Epilepsy remains one of the most prevalent neurological disorders, characterised by complex aetiology encompassing genetic, structural, metabolic, and inflammatory factors. Despite advances in neuroimaging and neurophysiological diagnostics, there is a persistent lack of sensitive and specific biomarkers to enable early diagnosis, risk stratification, and monitoring of therapeutic efficacy. Key epilepsy biomarkers include neurotransmitters, energy–related compounds, tryptophan pathway metabolites, and choline derivatives. Their determination employs liquid chromatography coupled with tandem mass spectrometry (LC–MS/MS), high–performance liquid chromatography (HPLC) with electrochemical or fluorescence detection, gas chromatography with tandem mass spectrometry (GC–MS/MS), high–resolution mass spectrometry (HRMS), and proton nuclear magnetic resonance (¹H–NMR) spectroscopy, revealing metabolic disturbances in neurotransmission, energy metabolism, and oxidative stress associated with epileptogenesis. Among these techniques, LC–MS/MS currently provides the highest analytical sensitivity and specificity for quantifying low–abundance epilepsy–related metabolites, while HPLC with conventional detection remains a simpler and more cost–effective alternative for routine clinical laboratories. This review presents the current state of knowledge regarding chromatographic techniques applied to the analysis of mentioned metabolites, as well as therapeutic drug monitoring of antiepileptic drugs. Key sample preparation stages are also discussed. Various biological matrices–plasma, serum, urine, cerebrospinal fluid (CSF), dried blood spots (DBSs), and brain tissue—are evaluated. Novel approaches are also presented, including hair samples, microsampling techniques, and headspace analysis of volatile metabolites. Chromatographic techniques constitute the foundation of contemporary metabolomic research in epileptology, enabling biomarker identification and supporting personalised medicine. Further standardisation and translational validation remain necessary, as current evidence is insufficient for routine clinical implementation. Full article

Plant-based egg analogs often fail to develop characteristic egg aroma, which limits their sensory acceptance. While the pronounced differences in key aroma compounds between chicken egg and vegan egg products have been identified, the precursor-driven mechanisms underlying these differences remain unclear. The HPLC-MS technique was used to measure the free amino acids of scrambled chicken eggs and a commercial plant-based egg product before and after cooking. This first comparative analysis revealed pronounced deficits in key free amino acids involved in egg aroma chemistry, particularly methionine, cysteine, glutamic acid, and aspartic acid, in the plant-based matrix. To address this gap, 23 plant-derived raw materials were analyzed for their free amino acid composition, generating a targeted comparative dataset that links naturally occurring free amino acids in plant ingredients to egg-relevant aroma precursors. Oyster mushroom, yeast extract, cucumber, and celery root were identified as the most effective contributors to the missing precursor pool. These findings were translated into three prototype formulations designed to restore precursor availability. Consumer test results (n = 58) reported that the prototype enriched with celery root and dried cucumber powder achieved improved overall liking, odor, and taste compared with the original product. This study introduces the first precursor-guided formulation strategy that enables in situ egg-like aroma generation in vegan eggs during cooking, hence providing a mechanistic basis for future flavor- and taste-focused research. Full article

Current treatments for ulcerative colitis (UC) often fail to adequately address its multifactorial pathogenesis, which involves oxidative stress, barrier dysfunction, and gut microbiota dysbiosis. This study evaluated the therapeutic potential and multi-targeting mechanism of a ginseng, salvia root, and notoginseng oral solution (GSNS) in a mouse model of colitis induced by dextran sulfate sodium (DSS). Based on high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) technology, 25 major bioactive components were identified. Following the induction of colitis with 3.5% DSS in C57BL/6J mice, the animals were treated with the GSNS (40, 80, or 160 mg/kg/day) or 5-Amino Salicylic Acid (5-ASA). The therapeutic efficacy was assessed via disease activity, histopathological staining, cytokines and oxidative stress analysis, and a barrier integrity test. Combined data from Western blot, qPCR, immunohistochemistry, electron microscopy, and 16S rRNA sequencing indicate that the therapeutic effect of the GSNS against colitis is attributable to its dual role in dampening pro-inflammatory cytokines and potentiating antioxidant defenses via the Nrf2/HO-1 signaling pathway. It also upregulated Occludin expression, repaired tight junctions, and was associated with beneficial alterations in the gut microbiota, as evidenced by increased Prevotellaceae and suppressing Escherichia-Shigella. These findings demonstrated that the GSNS exerts a multi-target effect against colitis by synergistically enhancing antioxidant defense, repairing the intestinal barrier, and modulating microbial ecology, supporting its potential as a promising natural compound-based candidate for DSS-induced colitis treatment. Full article

Background: Traditionally, wild jujube (Ziziphus jujuba Mill. var. spinosa (Bunge) Hu ex H. F. Chou) has been used to nourish the heart, calm the spirit, and arrest spontaneous sweating. Modern research confirms its broad pharmacological activities, including antioxidant, anti-inflammatory, neuroprotective, and cognitive-enhancing effects. This study aims to isolate and characterize the structure of jujube polysaccharides and evaluate their protective effects against oxidative stress damage in neural stem cells (NSCs). Methods: We successfully isolated and purified a novel pectin polysaccharide (ZJP-2) from wild jujube. Its structure was characterized in detail using high-performance liquid chromatography coupled with multi-angle laser light scattering and refractive index detection (HPLC-MALS-RI), high-performance anion exchange chromatography (HPAEC), gas chromatography–mass spectrometry (GC-MS), and nuclear magnetic resonance (NMR) spectroscopy. Results: Structural analysis revealed that ZJP-2 is a pectin heteropolysaccharide with a molecular weight of approximately 67.93 kDa. Its monosaccharide composition primarily includes galac-turonic acid (GalA), arabinose (Ara), rhamnose (Rha), galactose (Gal), and glucose (Glc). The backbone consists of α-GalA and rhamnose-galacturonic acid-I (RG-I) domains linked by (1→4)-glycosidic bonds. NMR spectroscopy further confirmed its glycosidic bond types. In activity assessment, our study demonstrated that ZJP-2 significantly alleviated DMNQ-induced oxidative stress damage in C17.2 neural stem cells. Its protective effect was achieved by reducing intracellular reactive oxygen species (ROS) levels and upregulating the mRNA expression of antioxidant genes associated with the signaling axis (p < 0.05). Moreover, ZJP-2 suppressed DMNQ-induced overexpression of Nestin and NeuN (p < 0.05), contributing to the maintenance of NSCs’ undifferentiated state and functional homeostasis. Conclusions: In conclusion, ZJP-2 possesses distinct structural characteristics and significant neuroprotective potential, supporting its development as a natural functional food or dietary supplement for preventing oxidative stress-related neural damage. Full article

(1) Background: Bioactive peptides from marine and plant sources show neuroprotective potential, yet how their combination ratios affect memory regulation via the gut–brain axis remains unclear. This study investigated the effects of different ratios of marine peptide QMDDQ (Glutamine-Methionine-Aspartate-Aspartate-Glutamine) and plant peptide AGLPM (Alanine-Glycine-Leucine-Proline-Methionine) on scopolamine-induced memory impairment in mice. (2) Methods: Cognitive function was assessed using the Morris water maze and novel object recognition tests. Nissl staining, microplate-based assays for acetylcholine (ACh) content and acetylcholinesterase (AChE) activity, Western blotting for neurotrophic factors, LC-MS/MS-based intestinal peptide profiling, and HPLC-based brain amino acid analysis were performed. (3) Results: The 1:1 ratio most effectively restored learning and memory, regulated hippocampal cholinergic function, mitigated neuronal damage, and elevated BDNF, NGF, and NTF-3 expression. In the gut, peptides were hydrolyzed into glutamate- and proline-rich fragments, which influenced brain amino acid balance by elevating glutamate and proline levels while reducing NH₃-related signaling. (4) Conclusions: These results highlight the ratio-dependent efficacy of QMDDQ-AGLPM combinations and provide evidence for a gut peptide remodeling-brain metabolic link relevant to cognitive impairment. Full article

This study aims to evaluate the interspecific variation in polyphenolic profiles and biological activities of acorn flours from three native Tunisian Quercus L. species (Q. ilex L., Q. suber L., and Q. canariensis Willd.). Q. canariensis extracts are the richest in total phenolic, flavonoid and hydrolysable tannin contents. Six phenolic compounds were identified by HPLC-DAD analysis. Chlorogenic acid was the dominant compound in Q. canariensis and Q. ilex acorns. Whereas in Q. suber, caffeic acid was the main component and, along with trans-ferulic acid, was exclusive to this species. Hyperoside was notably identified in Q. canariensis. The UHPLC-DAD-MS analysis of hydrolysable tannins revealed twelve compounds. Acorns of Q. canariensis and Q. suber were dominated by ellagitannins, whereas Q. ilex contained mainly gallotannins. To our knowledge, these compounds are identified for the first time in Tunisian acorns. Q. canariensis exhibited the strongest antioxidant potential with DPPH, ABTS and FRAP assays, as well as the highest antibiofilm and anti-α-amylase activities. All extracts inhibited ATCC pathogenic bacterial strains while largely sparing the beneficial probiotic Limosilactobacillus fermentum. This result indicates a selective antibacterial effect not previously reported for Quercus acorns. Q. canariensis may represent a potential source of functional food ingredient, nutraceuticals, and pharmaceuticals, which remains to be confirmed through in vivo investigations. Full article

Objectives: The aim of the work was to present a method for routine determination of antiarrhythmic drugs, propafenone (PPF), its two metabolites, 5-hydroxypropafenone (5OHPPF) and N-depropylpropafenone (NDPPF), mexiletine (MEX), amiodarone (AD) and desethylamiodarone (DEAD) in serum. Methods: A simple isocratic HPLC-UV system with a manual injector was applied. The separations were performed at ambient temperature on Supelcosil LC-CN column (150 × 4.6 mm, 5 μm). Two analytical procedures (A and B) were used: (A) for AD and (B) for PPF/MEX. The mobile phase for (A) was a mixture of: CH₃OH:CH₃CN:H₂O:0.5M KH₂PO₄ (200:100:194:6 v/v + 0.1 mL 85% H₃PO₄ per 500 mL). The slightly acidified serum sample was extracted with hexane and the analytes were detected at 240 nm. The mobile phase for (B) was a mixture of: CH₃CN:H₂O:0.5M KH₂PO₄ (185:310:5 v/v + 0.1 mL 85% H₃PO₄ per 500 mL). The alkalized serum sample was extracted with diisopropyl ether, then back extracted into 0.01M HCl and finally the analytes were detected at 210 nm. Results: The method was calibrated with adequate selectivity and specificity in the range of 20–4000 ng/mL for AD, DEAD and MEX, 10–4000 ng/mL for PPF and 10–500 ng/mL for 5OHPPF and NDPPF. For all analytes, precision and accuracy fulfilled EMA requirements, i.e., ≤15% (≤20% for LLOQ), ensuring the reliability of the measurements. Conclusions: The method can be suitable for laboratories equipped with basic HPLC apparatus as an economical alternative to the LC-MS/MS technique. Full article

Background: Mangrove fungi are a prolific source of structurally diverse natural products. Among these, natural peptides with varied biological activities hold high commercial value and have been successfully developed into drugs for treating numerous diseases. Methods: Following rice solid-state fermentation of the strain, extracellular metabolites were extracted from the culture filtrate to obtain a crude extract. Cyclic depsipeptides were isolated from the crude extract by silica gel vacuum liquid chromatography for preliminary fractionation and enrichment, followed by high-performance liquid chromatography (HPLC) purification. The structures of the compounds were determined based on extensive spectroscopic analysis (1D and 2D NMR, ESI-MS-MS analysis) and Marfey’s method for amino acid configuration assignment. Results: Ultimately, two new compounds, aspertides F (1) and G (2), and three known compounds, aspertides C, D, and A (3−5), were identified. The bioassays indicated that these compounds exhibited weak activity against acetylcholinesterase and neuraminidase. Conclusions: The research findings on this strain have not only enriched the metabolic resource library of mangrove fungi but also highlighted their diverse biological activities and significant application potential. Full article

Elderberry (Sambucus nigra L.) and linden (Tilia cordata Mill.) flower extracts are known for their pro-healthy properties. Various extraction methods, both conventional (Soxhlet) and advanced (ultrasound assisted extraction, UAE, accelerated solvent extraction, ASE, and matrix solid phase dispersion, MSPD), were applied to obtain ethanol–water extracts from the plants. The biological profiles, the total polyphenol content (TPC) and total flavonoid content (TFC) in the extracts were determined spectrophotometrically. Almost 40 compounds were identified in extracts by means of HPLC-MS/MS. The contents of the chosen phenolic acids (chlorogenic, p-coumaric, protocatechuic, and gallic) and flavonoids (rutin, catechin, quercetin, kaempferol, apigenin, and naringenin) were determined by HPLC-DAD. It was observed that the elderflower extracts contained higher levels of the compounds investigated than did the linden extracts. Chlorogenic acid was the main phenolic acid in the majority of extracts form the elderberry flower, whereas in the linden extracts, it was protocatechuic acid. Nevertheless, rutin was the main component of both plant extracts. The cytotoxicity of the elderberry and linden flower extracts against VERO, FaDu, H1HeLa, and RKO cell lines were subsequently examined. The elderflower extracts exerted no cytotoxicity, whereas linden extracts showed selective cytotoxicity against FaDu and RKO cells with CC₅₀ of 54.35 and 46.27 µg/mL, respectively. The antiviral potential of the extracts against HHV-1, CVB3, and HRV14 were also examined. The results demonstrate antiviral activity against HHV-1, particularly for linden flower extract in concentration of 62.5 µg/mL. Full article

Microscopic green algae are active producers of beneficial compounds, particularly those containing nitrogen. However, the metabolism of nitrogen-containing compounds is diverse and depends on the conditions of the nitrogen source. As a result, the approach to studying the metabolism of nitrogen-containing compounds becomes more complicated. This work demonstrates the metabolic changes in the high-productive green algae Neochlorella semenenkoi IPPAS C-1210 under conditions of nitrogen starvation and subsequent reintake, using high-performance liquid chromatography–mass spectrometry (HPLC–MS) with ¹⁵N isotopic labeling. The presented results include semi-quantitative chromatography–mass spectrometric analysis for 17 amino acids, a metabolomic profile of over 40 isotopically labeled compounds, an assessment of metabolic flux via isotopic incorporation, and an analysis of cellular lipid composition under varying growth conditions. The findings indicate that this strain can utilize ammonium acetate as a nitrogen source, consuming nitrogen in the ammonium form. The degree of isotopic labeling in compounds often diverged significantly from their quantitative changes (concentrations and chromatographic peak areas), suggesting that isotopic analysis may offer advantages over purely quantitative analysis for biological systems. Furthermore, in vivo biological isotopic labeling is shown to assist in identifying compounds absent from standard mass spectrometric databases. Full article

Background/Objectives: Trimethylamine N-oxide (TMAO) is a gut microbiota-derived metabolite increasingly recognized as a pro-atherogenic factor and a biomarker of cardiometabolic risk. Dietary patterns and adiposity are key modulators of circulating TMAO levels; however, evidence on the impact of very-low-energy ketogenic therapy (VLEKT) on TMAO metabolism, particularly in women with obesity, remains limited. This study aimed to investigate the effects of VLEKT on circulating TMAO concentrations, with specific focus on treatment duration and body composition (BC) changes. Methods: This study included 43 adult women with obesity eligible for VLEKT based on meal replacements. Anthropometric measurements and BC were assessed using standardized protocols and bioelectrical impedance analysis at baseline and post-intervention. Serum TMAO concentrations were quantified by validated HPLC–ESI–MS/MS. Results: After VLEKT, participants exhibited significant reductions in body weight, BMI, waist girth, fat mass (FM), and circulating TMAO levels. Greater reductions in TMAO were observed in women with longer ketogenic exposure and more pronounced FM loss. Changes in TMAO levels correlated negatively with VLEKT duration and positively with FM variations. In multivariate models, treatment duration and FM reduction emerged as independent predictors of TMAO decrease. A Receiver Operating Characteristic (ROC) analysis identified a FM reduction ≥14.25% as the optimal threshold associated with clinically relevant TMAO lowering. Conclusions: VLEKT reduces circulating TMAO levels in women with obesity. This effect appears to be primarily driven by the duration of ketogenic exposure and the magnitude of FM loss, rather than total weight reduction alone, highlighting the relevance of BC-targeted interventions in modulating gut microbiota-derived cardiometabolic risk markers. Full article