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Nasiona kakaowca (Cacao semen) to znany od starożytności surowiec roślinny, szeroko wykorzystywany w celach spożywczych i farmaceutycznych. Przetwory nasion kakaowca, takie jak czekolada i wyroby czekoladowe są jednymi z najchętniej spożywanych rodzajów słodyczy. Rosnąca świadomość zdrowotna konsumentów sprawia, że coraz większą popularność zyskują czekolady gorzkie oraz inne produkty z wysoką zawartością kakao. Ich efekty prozdrowotne, wynikające ze zwyczajowego spożycia, warunkowane są zawartością miazgi (masy) kakaowej, w której występują związki biologicznie aktywne. W nasionach kakao i jego przetworach zidentyfikowano liczne polifenole, jak procyjanidyny, flawanole i flawonole; metyloksantyny, a także aminy, amidy i in. Wykazują one korzystny wpływ na układ sercowo-naczyniowy, obniżając ryzyko występowania incydentów kardiologicznych poprzez działanie antyoksydacyjne, przeciwzapalne, naczyniorozszerzające, poprawę funkcjonowania śródbłonka naczyniowego, obniżenie aktywności płytek krwi i ciśnienia tętniczego oraz regulację gospodarki lipidowej. Umiarkowane spożycie czekolady związane jest także z mniejszym ryzykiem zachorowania na cukrzycę, w wyniku zwiększenia wrażliwości tkanek na insulinę, poprawę glikemii i profilu lipidowego. W ostatnich latach pojawił się nowy kierunek badań nad wpływem czekolady i kakao na nastrój, funkcje poznawcze i pamięć epizodyczną. Wskazuje się również na zależność między spożyciem czekolady, a obniżoną śmiertelnością z powodu choroby Alzheimera. Ze względu na obecność metyloksantyn i działanie poprawiające nastrój czekolada zaliczana jest do produktów typu „mood food”. Obecnie sugeruje się, że czekolada, wcześniej kojarzona z nadwagą i otyłością, może wykazywać korzystne działanie w regulacji apetytu, a regularna konsumpcja gorzkiej czekolady w umiarkowanych ilościach związana jest z obniżeniem masy ciała i wskaźnika BMI. Przytoczone prozdrowotne efekty składników nasion kakaowca, kakao oraz czekolady mogą potencjalnie znaleźć zastosowanie w prewencji oraz wspomaganiu terapii pacjentów z chorobami kardiometabolicznymi i zaburzeniami funkcji kognitywnych.

Aspalathus linearis (Burman f.) R. Dahlgren is a shrub of the Fabaceae family, growing endemically in southern Africa. Aspalathus linearis has transformed from a wild plant to a cultivated crop. Now it is commercially available as fermented (red) rooibos and the less common unfermented (green) rooibos. This article aimed to review the literature on the redbush with a focus on its health-promoting properties. Numerous laboratory investigations of extracts and infusions of A. linearis have shown that rooibos is a rich source of biologically active compounds, especially polyphenols. The active compounds present in redbush infusions and extracts include flavonoids, phenolic acids, and minute amounts of procyanidins, coumarins, lignans, phenylethanoids, and phenylpropanoids. The characteristic active compounds of rooibos are the C-glucosyl dihydrochalcone - aspalathin and notofagin. An important active compound found in the infusion is also PPAG (Z-2-(beta-D-glucopyranosyloxy)-3-phenylpropenoic acid), which significantly determines the sensory quality of the infusion and its hypoglycaemic properties. Rooibos is also a source of minerals. Studies in both experimental models and healthy volunteers have confirmed the multiple effects of the redbush. The antioxidant properties of A. linearis were especially well studied. The greater antioxidant activity has been reported for aspalathin-rich green rooibos. The consumption of redbush infusions has been reported to have beneficial effects on the parameters like total plasma antioxidant capacity, lipid peroxidation index, and blood glutathione levels. Rooibos has also been shown to alleviate the inflammatory process induced by lipopolysaccharides or that associated with colitis. This is underlined by reduced expression of pro-inflammatory factors, as well as antioxidant properties. Redbush may be used in supporting the treatment of glucose and lipid metabolism disorders, endocrine disorders, and metabolic syndrome. It has been proven to stimulate pancreatic cells to secrete insulin, regulate the expression of genes responsible for glucose metabolism, and affect the amount of glucose transporter protein type 4 (GLUT-4). Other health properties of rooibos may include antimutagenic and hepatoprotective properties and acceleration of skin healing. The bioavailability of redbush flavonoids and the interaction of rooibos ingredients with drugs were also investigated. Studying the mechanism of absorption of flavonoids contained in the redbush and their interactions with drugs will allow determining the appropriate dosage of the extracts. Precise recognition of the chemical composition and health-promoting properties of the redbush will enable its utilization as pharmacotherapy support.

Various mint taxa are widely cultivated and are used not only for medicinal purposes but also in cosmetic and industrial applications. The development of new varieties or cultivars of mint generates difficulties in their correct identification and safe use. Volatile organic compounds (VOCs) from the leaves of seven different taxa of the genus Mentha obtained by hydrodistillation (HD) and headspace solid-phase microextraction (HS-SPME) were analyzed using gas chromatography–mass spectrometry (GC-MS). Principal component analysis (PCA) was also performed. Comparative GC-MS analysis of the obtained extracts showed similarity in the major compounds. PCA data allowed the separation of two groups of chemotypes among the analyzed mints, characterized by the abundance of piperitenone oxide and carvone. Two out of seven analyzed taxa were not previously examined for VOC profile, one was examined only for patent application purposes, and six out of seven were investigated for the first time using the HS-SPME technique. The presented analysis provides new data on the abundance and qualitative characterization of VOCs in the studied mint plants and on the safety of their use, related to the possibility of the presence of potentially toxic components. HS-SPME is a valuable method to extend the characterization of the VOC profile obtained by hydrodistillation.

Strawberry leaves are considered a valuable waste material; so far, mainly due to their antioxidant properties. Since the annual production of this crop is high, our study aimed to thoroughly examine the chemical composition and antidiabetes-related bioactivity of Fragaria × ananassa leaf of its popular and productive cultivar Senga Sengana. Leaves from three different seasons, collected after fruiting, were extensively analyzed (UHPLC-qTOF-MS/MS, HPLC-DAD). Some individual components were isolated and quantified, including specific flavonol diglycosides (e.g., 3-O-[β-xylosyl(1‴→2″)]-β-glucuronosides). The separated quercetin glycosides were tested in an antiglycation assay, and their methylglyoxal uptake capacity was measured. In addition, the biodegradable polyester precursor 2-pyrone-4,6-dicarboxylic acid (PDC) was confirmed at relatively high levels, providing further opportunity for strawberry leaf utilization. We want to bring to the attention of the food, pharmaceutical, and cosmetic industries the Senga Sengana strawberry leaf as a new botanical raw material. It is rich in PDC, ellagitannins, and flavonols—potent glycation inhibitors.

The most significant reactive α-dicarbonyl RCS involved in the pathomechanism of glycation and related diseases is methylglyoxal (MGO). Hyperglycemia promotes the generation of MGO and leads to the formation of advanced glycation end products (AGEs). Therefore, MGO trapping and glycation inhibition appear to be important therapeutic targets in prediabetes, diabetes, and in the early prevention of hyperglycemic complications. Peppermint leaf is commonly used as herbal tea, rich in polyphenols. Eriocitrin, its predominant component, in a double-blind, randomized controlled study reversed the prediabetic condition in patients. However, the antiglycation activity of this plant material and its polyphenols has not been characterized to date. Therefore, the aim of this study was to evaluate the ability of a peppermint leaf dry extract and its polyphenols to inhibit non-enzymatic protein glycation in a model with bovine serum albumin (BSA) and MGO as a glycation agent. Peppermint polyphenols were also evaluated for their potential to trap MGO in vitro, and the resulting adducts were analyzed by UHPLC-ESI-MS. To relate chemical composition to glycation inhibitory activity, the obtained peppermint extract was subjected to qualitative and quantitative analysis. The capability of peppermint leaf polyphenols to inhibit glycation (27.3–77.2%) and form adducts with MGO was confirmed. In the case of flavone aglycones, mono- and di-adducts with MGO were observed, while eriodictyol and eriocitrin effectively produced only mono-adducts. Rosmarinic acid and luteolin-7-O-glycosides did not reveal this action. IC50 of the peppermint leaf dry extract was calculated at 2 mg/mL, equivalent to a concentration of 1.8 μM/mL of polyphenols, including ~1.4 μM/mL of flavonoids and ~0.4 μM/mL of phenolic acids. The contribution of the four major components to the anti-AGE activity of the extract was estimated at 86%, including eriocitrin 35.4%, rosmarinic acid 25.6%, luteolin-7-O-rutinoside 16.9%, luteolin-7-O-β-glucuronoside 8.1%, and others 14%. The effect of peppermint dry extract and polyphenols in inhibiting MGO-induced glycation in vitro was comparable to that of metformin used as a positive control.

One of the modern nutritional trends is to enthusiastically look for natural products that can be considered functional food and be a source of ingredients with a health-promoting effect. Today, many food manufacturers offer Cistus × incanus leaves to prepare common self-preparations (e.g., infusions) or as ready-to-use dietary supplements. Cistus × incanus (rock rose, pink rock-rose, hoary rock-rose), belonging to the family Cistaceae, is widespread in Mediterranean countries. For many years, cistus extracts and its aromatic resin have been used in traditional Middle East medicine to treat, among others, colds, fever, stomach problems, and skin wounds. In past years, this plant was rediscovered by the public. Due to the growing popularity of Cistus products, the most recent scientific literature on this subject is reviewed here. This article aims to present the latest research results on the phytochemical composition of Cistus × incanus and the impact of its consumption on human health. Particular emphasis is put on antioxidant, anti-inflammatory, antibacterial, antiviral, and antiproliferative activities and support of digestive system functions. Studies have shown that the main active ingredients of Cistus × incanus are flavonoid compounds, including flavonol glycosides (myricetin, quercetin, kaempferol), flavan-3-ols, and tannins. It was demonstrated that the presence of these compounds determines the therapeutic and health-promoting properties of cistus leaves and its products. That applies primarily to a strong antioxidant effect, which may reduce the risk of noncommunicable diseases, including cardiovascular diseases, neurodegenerative diseases, and cancer. Cistus preparations are also recommended as immunostimulants, supporting the treatment of bacterial and viral infections. Labdanum oleoresin and essential oil are a valuable source of substances with strong antibacterial and anti-inflammatory properties, which can be used in the future in the production of pharmaceutical and cosmetic preparations, and also serve as a natural food preservative.

Reactive oxygen and carbonyl species promote oxidative and carbonyl stress, and the development of diabetes, metabolic syndrome, cardiovascular diseases, and others. The traditional herb Cistus × incanus is known for its antioxidant properties; therefore, the current study aimed to assess how the chemical composition of a C. incanus water infusion corresponds with its antioxidative and antiglycative effects in vitro. The composition of infusions prepared from commercial products was analyzed with UHPLC-ESI-qTOF-MS. Total phenolics, flavonoids, and non-flavonoid polyphenols were determined. Antioxidant activity of infusions and selected polyphenols was investigated using DPPH, ABTS, and FRAP. Fluorometric measurements and methylglyoxal capture were performed to investigate the antiglycation activity. PCA and PLS-DA models were applied to explore the correlation between chemical and antioxidant results. The principal flavonoids in C. incanus were flavonols. In vitro tests revealed that a stronger antioxidant effect was demonstrated by plant material from Turkey rich in flavonoids, followed by Albania and Greece. Flavonols and ellagic acid displayed stronger antiradical and reducing power than EA-derived urolithins. Hyperoside was the most potent inhibitor of glycation. The results indicate that flavonoids are primarily responsible for rock rose antioxidant and antiglycation properties. PLS-DA modeling can be used to identify the origin of plant material with sensitivity and specificity exceeding 86%.

Apple fruits (Malus x domestica Borkh.) are considered one of the most important agricultural products in the world, both economically and culturally. Their key significance is indicated, among others, by the number of registered apple varieties, which in recent years has been estimated at around 10,000. Apples are a valuable component of the fruit and vegetable diet due to their taste and aroma, and mainly due to their favorable health-promoting properties, such as gastrointestinal, weight reduction promoting, anti-diabetic, antiatherosclerotic and reducing the risk of cardiovascular diseases or cancer. Recently, many articles have been published regarding the impact of apple consumption on various aspects of human health. The Scopus database alone lists over 2,300 articles about the impact of apples on different types of influence of the fruits on the human wholesomeness in the years 1993-2019. Thus, due to the significant number of publications available in the literature, it was considered appropriate to prepare this review. The article aims to present the latest research results on the phytochemical composition of apples and the impact of their consumption on human health, with particular emphasis on antioxidant, anti-inflammatory , hypoglycaemic, hypocholesterolemic, vasoprotective, antiproliferativeactivity, as well as supporting digestive system functions. The results presented in the review allow us to conclude that apple fruits, as well as preparations derived from them, can be considered as a valuable source of biologically active ingredients in the human diet. Studies have shown that they are mainly polysaccharides (dietary fiber) and polyphenols such as: chlorogenic acid, phlori(d)zin, quercetin glycosides, catechin, epicatechin and procyanidins. Their consumption results in a lower risk of many non-communicable diseases, in particular chronic diseases of the cardiovascular system, type 2 diabetes, gastrointestinal diseases and some types of cancer. Therefore, it is believed that M. domestica fruit should be a regular part of the daily diet.

Peppermint leaf, sage leaf, thyme herb, and their preparations are common components of herbal medicinal products (HMPs). According to the European Pharmacopoeia guidelines, the above-mentioned plant substances are standardized for the content of essential oils, omitting polyphenols, which also have a significant impact on their activities. The aim of this study was to evaluate the stability of the predominant polyphenols—rosmarinic acid, luteolin-7-O-β-glucuronide, and eriocitrin—in selected commercial liquid HMPs containing thyme, sage, and peppermint under long-term, intermediate, and accelerated testing conditions. Qualitative and quantitative analyses of these polyphenols were performed by the previously optimized and validated HPLC-DAD method. Rosmarinic acid stability was better in hydroethanolic than in an aqueous solution. The effect of the solvent on the stability of luteolin-7-O-β-glucuronide and eriocitrin could not be determined and requires further investigation. The present study is the first to analyze the stability of these compounds in commercial herbal medicinal products. The expiration dates proposed by the manufacturers of the tested HMPs did not guarantee stable levels of all analyzed polyphenols throughout the stated period. However, this study is preliminary and requires continuation on a larger number of medicinal products.

Cistus is a plant that has been used in natural medicine for hundreds of years; it works primarily as an antioxidant and cleansing agent. Cistus × incanus leaves or herb can be an attractive source of polyphenols and flavonoids. The official protocols of active compound analysis relies on the extraction of compounds of interest from plant matter, which makes their determination long and costly. An analysis of plant material in its native state can be performed using vibrational spectroscopy. This paper presents a comparison of Raman spectroscopy, attenuated total reflection in mid-infrared and diffuse reflectance technique in the near-infrared region for the simultaneous quantification of total polyphenols (TPC) and flavonoids (TF) content, as well as the determination of FRAP antioxidant activity of C. incanus material. Utilizing vibrational spectra and using partial least squares algorithm, TPC and TF were quantified with the RSEPVAL errors in the 2.7–5.4% range, while FRAP antioxidant activity for validation sets was determined with relative errors ranged from 5.2 to 9.3%. For the analyzed parameters, the lowest errors of predictions were computed for models constructed using Raman data. The developed models allow for fast and precise quantification of the studied active compounds in C. incanus material without any chemical sample treatment.

Galega officinalis L. has been known for centuries as an herbal medicine used to alleviate the symptoms of diabetes, but its comprehensive chemical composition and pharmacological activity are still insufficiently known. The current study involved the qualitative and quantitative phytochemical analysis and in vitro evaluation of the antioxidative and methylglyoxal (MGO) trapping properties of galega herb. Ultra high-performance liquid chromatography coupled with both the electrospray ionization mass spectrometer and diode-array detector (UHPLC-ESI-MS and UHPLC-DAD) were used to investigate the composition and evaluate the anti-MGO capability of extracts and their components. Hot water and aqueous methanol extracts, as well as individual compounds representing phytochemical groups, were also assessed for antioxidant activity using DPPH (2,2-diphenyl-1-(2,4,6-trinitrophenyl)hydrazyl) and ABTS (2,2&prime, azino-bis(3-ethylbenz-thiazoline-6-sulfonic acid) assays. Quercetin and metformin were used as a positive control. We confirmed the presence of tricyclic quinazoline alkaloids, guanidines, flavonoids, and hydroxycinnamic acids (HCAs) in galega extracts. The polyphenolic fraction was dominated by mono-, di-, and triglycosylated flavonols, as well as monocaffeoylhexaric acids. The in vitro tests indicated which G. officinalis components exhibit beneficial antioxidative and MGO trapping effects. For galega extracts, flavonols, and HCAs, a potent antiradical activity was observed. The ability to trap MGO was noted for guanidines and flavonoids, whereas HCA esters and quinazoline alkaloids were ineffective. The formation of mono-MGO adducts of galegine, hydroxygalegine, and rutin in the examined water infusion was observed.

The stone of Cornus mas L. remains the least known morphological part of this plant, whereas the fruit is appreciated for both consumption purposes and biological activity. The stone is considered to be a byproduct of fruit processing and very little is known about its phytochemical composition and biological properties. In this study, the complete qualitative determination of hydrolyzable tannins, their quantitative analysis, total polyphenolic content, and antioxidant properties of the stone of C. mas are presented for the first time. The 37 identified compounds included the following: various gallotannins (11), monomeric ellagitannins (7), dimeric ellagitannins (10), and trimeric ellagitannins (7). The presence of free gallic acid and ellagic acid was also reported. Our results demonstrate that C. mas stone is a source of various bioactive hydrolyzable tannins and shows high antioxidant activity which could allow potential utilization of this raw material for recovery of valuable pharmaceutical or nutraceutical substances. The principal novelty of our findings is that hydrolyzable tannins, unlike other polyphenols, have been earlier omitted in the evaluation of the biological activities of C. mas. Additionally, the potential recovery of these bioactive chemicals from the byproduct is in line with the ideas of green chemistry and sustainable production.

Thymol (2-isopropyl-5-methylphenol) belongs to the phenolic monoterpenes and mostly occurs in thyme species. It is one of the main compounds of thyme essential oil. Both thymol and thyme essential oil have long been used in traditional medicine as expectorant, anti-inflammatory, antiviral, antibacterial, and antiseptic agents, mainly in the treatment of the upper respiratory system. The current search for new directions of biological or therapeutic activities of natural plant substances with known structures includes thyme essential oil and thymol. Novel studies have demonstrated their antibiofilm, antifungal, antileishmanial, antiviral, and anticancer properties. Also, their new therapeutic formulations, such as nanocapsules containing these constituents, can be beneficial in medicinal practice and create opportunities for their extensive use. Extensive application of thymol and thyme essential oil in the healthcare sector is very promising but requires further research and analysis.

The purpose of this study was to investigate the composition of leaf extracts from Aronia melanocarpa, Chaenomeles superba, and Cornus mas, and their antimicrobial activity against typical spoilage-causing and pathogenic bacteria found in meat and meat products. The highest total phenolic content (TPC) was detected in C. superba extract, followed by C. mas and A. melanocarpa extracts. The antioxidant capacity of the extracts was measured by DPPH and ABTS assays. The lowest IC50 values were found for C. superba extract, followed by C. mas and A. melanocarpa extracts. LC-MS and HPLC analysis revealed that A. melanocarpa and C. superba extracts contained hydroxycinnamic acid derivatives and flavonoids (mainly flavonols). Hydroxycinnamic acid derivatives were detected in the C. mas extract, as well as flavonols, ellagitannins, and iridoids. The antibacterial activity of the plant extracts was tested against Gram-negative bacteria (Moraxella osloensis, Pseudomonas fragi, Acinetobacter baumanii, Escherichia coli, Enterobacter aerogenes, Salmonella enterica) and Gram-positive bacteria (Enterococcus faecium, Staphylococcus aureus, Brochothrix thermosphacta, Lactobacillus sakei, Listeria monocytogenes) using the microculture method. The extracts acted as bacteriostatic agents, decreasing the growth rate (&micro, max) and extending the lag phase (tlag). C. mas showed most potent antibacterial activity, as confirmed by principal component analysis (PCA).

Hyperglycemia and oxidative stress may be observed in different diseases as important factors connected with their development. They often occur simultaneously and are considered together as one process: Glycoxidation. This can influence the function or structure of many macromolecules, for example albumin, by changing their physiological properties. This disturbs the homeostasis of the organism, so the search for natural compounds able to inhibit the glycoxidation process is a current and important issue. The aim of this study was the examination of the antiglycoxidative capacity of 16 selected phenolic compounds, belonging to three phenolic groups, as potential therapeutic agents. Their antiglycoxidative ability, in two concentrations (2 and 20 &micro, M), were examined by in vitro study. The inhibition of the formation of both glycoxidative products (advanced glycation end products (AGEs) and advanced oxidation protein products (AOPPs)) were assayed. Stronger antiglycoxidative action toward the formation of both AOPPs and AGEs was observed for homoprotocatechuic and ferulic acids in lower concentrations, as well as catechin, quercetin, and 8-O-methylurolithin A in higher concentrations. Homoprotocatechuic acid demonstrated the highest antiglycoxidative capacity in both examined concentrations and amongst all of them. A strong, significant correlation between the percentage of AOPPs and AGEs inhibition by compounds from all phenolic groups, in both examined concentrations, was observed. The obtained results give an insight into the antiglycoxidative potential of phenolic compounds and indicate homoprotocatechuic acid to be the most promising antiglycoxidative agent, but further biological and pharmacological studies are needed.

Iridoid and polyphenol profiles of 30 different honeysuckle berry cultivars and genotypes were studied. Compounds were identified by ultra-performance liquid chromatography coupled with electrospray ionization mass spectrometry (UPLC-ESI-qTOF-MS/MS) in positive and negative ion modes and quantified by HPLC-PDA. The 50 identified compounds included 15 iridoids, 6 anthocyanins, 9 flavonols, 2 flavanonols (dihydroflavonols), 5 flavones, 6 flavan-3-ols, and 7 phenolic acids. 8-epi-Loganic acid, pentosyl-loganic acid, taxifolin 7-O-dihexoside, and taxifolin 7-O-hexoside were identified in honeysuckle berries for the first time. Iridoids and anthocyanins were the major groups of bioactive compounds of honeysuckle constituents. The total content of quantified iridoids and anthocyanins was between 128.42 mg/100 g fresh weight (fw) (‘Dlinnoplodnaya’) and 372 mg/100 g fw (‘Kuvshinovidnaya’) and between 150.04 mg/100 g fw (‘Karina’) and 653.95 mg/100 g fw (‘Amur’), respectively. Among iridoids, loganic acid was the dominant compound, and it represented between 22% and 73% of the total amount of quantified iridoids in honeysuckle berry. A very strong correlation was observed between the antioxidant potential and the quantity of anthocyanins. High content of iridoids in honeysuckle berries can complement antioxidant properties of phenolic compounds.

Iridoid profiles of honeysuckle berry were studied. Compounds were identified by ultra-performance liquid chromatography coupled with electrospray ionization mass spectrometry UPLC-ESI-qTOF-MS/MS in positive and negative ions mode. The MS fragmentation pathways of detected iridoid glycosides were also studied in both modes. In the negative ESI mass spectra, iridoids with a methyl ester or lactone structure have preferentially produced adduct [M + HCOOH - H](-) ions. However, protonated ions of molecular fragments, which were released by glycosidic bond cleavage and following fragmentation of aglycone rings, were more usable for iridoid structure analysis. In addition, the neutral losses of H₂O, CO, CO₂, CH₃OH, acetylene, ethenone and cyclopropynone have provided data confirming the presence of functional substituents in the aglycone. Among the 13 iridoids, 11 were identified in honeysuckle berries for the first time: pentosides of loganic acid (two isomers), pentosides of loganin (three isomers), pentosyl sweroside, and additionally 7-epi-loganic acid, 7-epi-loganin, sweroside, secologanin, and secoxyloganin. The five pentoside derivatives of loganic acid and loganin have not been previously detected in the analyzed species. Honeysuckle berries are a source of iridoids with different structures, compounds that are rarely present in fruits.