Natural Plant Research Articles

TMT-Based Quantitative Proteomics Revealed the Antibacterial Mechanism of Cinnamaldehyde against MRSA.

Natural plant extracts have demonstrated significant potential in alternative antibiotic therapies. Cinnamaldehyde (CA) has garnered considerable attention as a natural antibacterial agent. In this study, Tandem mass tag (TMT) quantitative proteomics combined with Western blot and RT-qPCR methods were employed to explore the antibacterial mechanism of CA against Methicillin-Resistant Staphylococcus aureus (MRSA) at the protein level. The results showed that a total of 254 differentially expressed proteins (DEPs) were identified in the control group and CA treatment group, of which 161 were significantly upregulated and 93 were significantly downregulated. DEPs related to nucleotide synthesis, homeostasis of the internal environment, and protein biosynthesis were significantly upregulated, while DEPs involved in the cell wall, cell membrane, and virulence factors were significantly downregulated. The results of GO and KEGG enrichment analyses demonstrated that CA could exert its antibacterial effects by influencing pyruvate metabolism, the tricarboxylic acid (TCA) cycle, teichoic acid biosynthesis, and the Staphylococcus aureus (S. aureus) infection pathway in MRSA. CA significantly inhibited the expression of recombinant protein MgrA (p < 0.05), significantly reduced the mRNA transcription levels of mgrA, hla, and sdrD genes (p < 0.05), and thermostability migration assays demonstrated that CA can directly interact with MgrA protein, thereby inhibiting its activity. These findings suggest that CA exerts its antibacterial mechanism by regulating the expression of related proteins, providing a theoretical basis for further development of clinical applications of antimicrobial agents derived from natural plant essential oils in the treatment of dairy cow mastitis.

Network pharmacology-based strategy to reveal the mechanism of pinocembrin against ovarian cancer.

Ovarian cancer stands as the foremost cause of mortality among gynaecological diseases globally, characterized by high morbidity and mortality. Pinocembrin, a flavonoid from natural plant sources, exhibits diverse pharmacological properties. Despite its known pharmacological activities, its specific role in ovarian cancer treatment remains scarcely reported, and its precise molecular mechanism remains elusive. This study integrates network pharmacology and molecular docking techniques to explore pinocembrin's potential mechanism in ovarian cancer treatment. The targets of pinocembrin were compiled from the several online databases. Ovarian cancer targets were identified using the GeneCards database, with common target genes determined by data aggregation. Protein-protein interactions were analysed using the STRING platform. Subsequent Gene Ontology functional annotation and Kyoto Encyclopedia of Genes and Genomes pathway analyses were performed. Molecular docking assessed the binding affinity between potential targets and active compounds. Finally, target validity was verified through in vitro experiments. We identified 163 potential pinocembrin targets for ovarian cancer treatment. GO and KEGG analyses revealed pinocembrin's involvement in protein kinase activity, protein phosphorylation, protein kinase complexes and cancer pathways in ovarian cancer treatment. Molecular docking demonstrated strong binding affinity between pinocembrin and most potential target active sites. In vitro experiments suggested pinocembrin's potential to induce apoptosis in ovarian cancer cells through the AKT1-mTOR signalling pathway. This study comprehensively elucidates pinocembrin's potential targets and mechanisms against ovarian cancer, aiming to provide promising candidates for developing novel and effective alternative and/or complementary nutritional supplements for the clinical treatment of ovarian cancer.

Hybrid hydrogel loaded with natural plant extract accelerates diabetic wound healing via ROS scavenging and immunoregulation

Diabetic wound (DW) is often characterised by reactive oxygen species (ROS) accumulation, disordered inflammation, and macrophage polarisation abnormality. Herein, natural plant extract, Kunzea ericoides leaf extract (KELE), was loaded into Gelatin Methacryloyl (GelMA) to fabricate a hybrid hydrogel (referred to as KELE@Gel) as a multi-functional dressing to treat DW. Using the UHPLC-Q-Exactive Orbitrap MS/MS strategy aided by database analysis, multiple compounds with antioxidative and anti-inflammatory properties were identified in KELE. The optimal concentration of GelMA and KELE was determined based on the mechanical properties and biocompatibility evaluation to obtain an ideal hydrogel for wound application. Further in vitro investigations discovered that the KELE@Gel hydrogel possessed a superior cytocompatibility and ROS scavenging capacity on RAW 264.7 cell lines under hydrogen peroxide (H2O2) or lipopolysaccharides (LPS) stimulation. Meanwhile, the hybrid hydrogel inhibited expressions of several cytokines, such as interleukin (IL)-1β, IL-6, and tumour necrosis factor (TNF)-α and manipulated M1/M2 macrophage polarisation in an inflammatory microenvironment. The immunoregulatory mechanism of the hydrogel was investigated through mRNA-sequencing and transcriptomic bioinformatics analysis. Animal experiments also discovered that the KELE@Gel hydrogel significantly promoted DW healing with preferable re-epithelialisation, angiogenesis and collagen deposition by enhanced antioxidative, anti-inflammatory and immunoregulatory activities. Above all, the KELE@Gel hydrogel released bioactive components sustainably, achieving a moderate antioxidative, anti-inflammatory and immunoregulatory capacity alongside the whole course of DW healing. In conclusion, this naturally derived hybrid hydrogel ameliorated undesirable microenvironments in DW and showed great potential to serve as a multi-functional wound dressing in clinical practice.

Inhibition of polyphenol oxidase for preventing browning in edible mushrooms: A review.

Edible mushrooms are rich in nutrients and bioactive compounds, but their browning affects their quality and commercial value. This article reviews various methods to inhibit polyphenol oxidase (PPO)-induced browning in mushrooms. Physical methods such as heat treatment, low temperatures, irradiation, and ultrasound effectively reduce PPO activity but may affect mushroom texture and flavor. Chemical inhibitors, including synthetic chemicals and natural plant extracts, provide effective PPO inhibition but require careful monitoring of their content. Biological methods, including gene editing and microbial fermentation, show promise in targeting PPO genes and enhancing antioxidant production. Combining these methods offers a comprehensive strategy for preserving mushroom quality, extending shelf life, and maintaining nutritional value. PRACTICAL APPLICATION: These approaches can be applied in the food industry to improve post-harvest mushroom preservation, enhance product quality, and reduce waste, benefiting both producers and consumers. Further research and innovation are needed to optimize the practical application of these methods in large-scale processing and storage conditions.

Performance analysis of natural draft power plant cooling tower: Mathematical modeling of cross-flow type, application in capital cities of Iranian provinces

Cooling towers are heat exchangers that reduce the hot water temperature produced by process equipment through heat and mass transfer between water and air stream. This study investigates the performance of cross-flow cooling towers under various geometrical, physical, and environmental conditions. For this purpose, thermodynamic modeling of the cross-flow cooling tower was conducted, and the governing equations were numerically solved using the finite difference method. Unlike previous studies, the effects of water droplet deformation into an elliptical shape during its fall along the cooling tower were also considered. This deformation, which influences the drag coefficient, Reynolds number of the water droplets, droplet surface area, and its cross-section area, along with the incorporation of buoyancy force in the droplet momentum equation, led to an improvement in the results. Consequently, the maximum computational error in this case was reduced to 1.97 %, compared to the scenario where droplet deformation and buoyancy force were neglected. The change in geometrical parameters of the tower in Tehran and Rasht was investigated, revealing that increasing the outlet radius of the tower from 20 m to 22.5 m decreased the outlet water temperature by 1.21 °C and 0.67 °C and increased the thermal efficiency of the tower by 4.94 % and 2.88 % respectively, while increasing the tower height from 100 m to 120 m, only decreased the outlet water temperature by 0.47 °C and 0.26 °C, and increased the thermal efficiency of the tower by 1.89 % and 1.09 % respectively. Additionally, the cooling tower performance was assessed in the centers of different provinces .of Iran. Results showed that with an initial droplet radius of 1 mm and an inlet water temperature of 50 °C, the maximum and minimum temperature reductions occurred in Shahrekord by 20.16 °C and Bandarabbas by 12.37 °C, respectively.

Alkaloids as Additional Weapons in the Fight against Breast Cancer: A Review.

Breast carcinoma is among the most frequent cancerous tumour in females around the globe. The major modalities now employed in the therapeutic management of breast cancer include surgeries, chemotherapy, and specialized medicines. Despite their potential to help individuals' problems, they are also associated with many negative impacts. As a result, natural products are increasingly regarded to be a preferable alternative. Alkaloids are essential biochemical substances that can be used to develop new drugs. Numerous alkaloids that originate from natural plants have been shown in vitro and in vivo to have anti-proliferation and anti-metastasis actions on different kinds of carcinoma. According to the data collected in this study, the utilization of alkaloids as anti-tumor medicines appears to be extremely potent; nevertheless, extensive studies and clinical trials are required before utilizing individual alkaloids. In this overview, we provide a detailed and vital exploration of pre-existing alkaloids possessing anti-tumor activities due to bioactive compounds. This study also includes an overview of synthesized analogues and pharmacological characteristics that will be beneficial to scientists working on alkaloids for medicinal purposes. In a recent survey of the literature, alkaloids are an important component of plantderived antitumor medicines that hold great potential for the future development of cancer therapy and preventive therapies. We have also discussed structural analysis relationship (SAR) studies. Moreover, it covers clinical trial medications and FDA-approved medicines from the last five years that will be useful in further research.

Research Progress on Immunomodulatory Effects of Poly (Lactic-co- Glycolic Acid) Nanoparticles Loaded with Traditional Chinese Medicine Monomers.

Immunomodulatory mechanisms are indispensable and key factors in maintaining the balance of the environment in humans. When the immune function of the immune system is impaired, autoimmune diseases occur. Excessive body fatigue, natural aging of the human body, malnutrition, genetic factors and other reasons cause low immune function, due to which the body is prone to being infected by bacteria or cancer. Clinically, the existing therapeutic drugs still have problems such as high toxicity, long treatment cycle, drug resistance and high price, so we still need to explore and develop a high efficiency and low toxicity drug. Poly(lactic-co-glycolic acid) (PLGA) refers to a nontoxic polymer compound that exhibits excellent biocompatibility. Traditional Chinese medicine (TCM) monomers come from natural plants, and have the characteristics of high efficiency and low toxicity. Applying PLGA to TCM monomers can make up for the defects of traditional dosage forms, improve bioavailability, reduce the frequency and dosage of drug use, and reduce toxicity and side effects, thus having the characteristics of sustained release and targeting. Accordingly, PLGA nanoparticles loaded with TCM monomers have been the focus of development. The previous research on drug loading advantages, preparation methods, and immune regulation of TCM PLGA nanoparticles is summarized in the following sections.

Unveiling the antibacterial potential of anthocyanins - a comprehensive review on this natural plant extract.

With the gradual prohibition of antibiotic fungicides, it is of great significance to develop high-efficient, nontoxic and environmental-friendly antimicrobial agents. Anthocyanin is a natural plant polyphenol pigment which shows antibacterial, anti-inflammatory and antioxidant effects through inhibiting the synthesis of bacterial cell wall, interfering bacterial respiratory metabolism, and inducing bacterial autolysis. As a typical antibacterial agent, anthocyanins have been widely used in various fields, including biological pesticides or feed additives in agricultural production, anti-inflammatory and antibacterial wound dressings in medicine, etc. However, the structure of anthocyanins is unstable, which limits its practical application. In this article, the biological activity, antibacterial mechanism and stabilization strategy of anthocyanins as antibacterial agents were reviewed. The safety, application scope and methods of anthocyanins were discussed. In addition, the challenges and development prospects of anthocyanin extract antibacterial technology were also prospected. This will be the direction for researchers to further explore and better apply anthocyanins to practical production and application.

Experience in Monitoring Brazed Aluminium Heat Exchanger, after Major Repairs

Brazed Aluminium Heat Exchangers are fundamental for a natural gas liquid recovery plant. Refrigeration at cryogenic temperatures and the liquefaction process take advantages from their thermal hydraulic efficiency and compactness characteristics, making such units economically feasible. These exchangers are proprietary design, with only a few manufacturers around the world and limited knowledge about their maintenance. After two failures in the same equipment with possible thermal fatigue contributions, occurring only nine months apart, two complex repair procedures had to be carried out. To ensure operational safety, online monitoring through Acoustic Emission Technique has been performed. This monitoring led to discoveries of systems and routine maneuverer that triggered damage mechanisms. This allowed for the implementation of adjustments to mitigate the propagation of damage, thereby increasing the equipment's lifespan. The procedure applied in this type of equipment constitutes an innovative approach using the Acoustic Emission technique, which has resulted in a successful strategy of condition monitoring.

A novel numerical simulation approach for cryogenic CO2 frosting in binary mixture gas by integrating desublimation and gas-solid phase equilibrium models

Cryogenic CO2 separation from natural gas is a promising technology due to its environmental benefits and smaller spatial requirement. Nonetheless, the dynamics of CO2 desublimation and subsequent frost layer formation under cryogenic conditions for natural gas pre-treatment remain largely unexplored. Addressing this gap, this paper presents a novel numerical simulation approach by integrating desublimation phase change model and vapor-solid phase equilibrium model to investigate CO2 frost layer formation on the cold wall, revealing that both the cold wall temperature and the initial CO2 concentration significantly influence the thickness of the CO2 frost layer. Moreover, the study finds that the density of frost layer intensifies over time, with the highest density observed near the cold surface. Furthermore, increasing the cold wall temperature and the flow rate not only increases the average density of the CO2 frost layer but also affects the outlet CO2 concentration. To adhere to specific outlet CO2 concentration targets and desublimation duration, it is critical to adjust the cold wall temperature and the inlet flow velocity dynamically. Therefore, cryogenic CO2 removal methods, by reducing the spatial requirements of CO2 pre-treatment units, offer a practical and efficient solution for small-scale natural gas liquefaction plants. This approach not only facilitates operational efficiency but also contributes to the broader effort of mitigating greenhouse gas emissions, aligning with environmental sustainability objectives.

Bioactive Compounds in Phyllanthus Amarus Leaf Extract and its Toxicity in the Treatment of Newcastle Disease

Background: Using extracts from medicinal plants to cure sicknesses and enfeebling diseases remains a major practice for traditional healers and medical practitioners. This research aimed to elucidate the significance and potential composition of n-Hexane extract of Phyllanthus amarus leaf and also establish its safety for use in potential medicinal preparations. Methods: Bioactive compounds from an extract of Phyllanthus amarus leaf were used in the treatment of Newcastle Disease (ND) in broiler chickens. It was characterised using gas chromatography-mass spectrometry (GCMS) and its biosafety effect on selected biochemical markers in chickens was observed. Results: The results showed the presence of over 15 bioactive compounds including phytol, phenol, and vitamin E. The constituents did not have a toxic effect on the selected biochemical markers of the chickens. Conclusion: This study demonstrated that Phyllanthus amarus may be considered safe and contains numerous active constituents which could be further explored for probable novel drugs sourced from natural plants for the treatment of animal or human diseases.

Biodegradable antimicrobial films prepared in a continuous way by melt extrusion using plant extracts as effective components

Packaging plays an important role in delaying food spoilage. However, conventional packaging films do not have antimicrobial properties. Films with antimicrobial components are receiving growing research interest. However, many of the reported studies use conventional non-degradable polymers during film preparation, posing a significant threat to the environment and sustainable development. Furthermore, conventional inorganic antibacterial agents are commonly used during film preparation, posing a risk to food safety. In this study, antibacterial compounds were extracted from diverse plants, and then biodegradable antimicrobial films were prepared in a continuous way via the melt extrusion method. Especially, films prepared using Vernicia fordii and Phyllanthus urinaria extracts showed effective antibacterial activities against common foodborne pathogens. This study is the first to prepare antibacterial films in a continuous way using natural plant extracts as the effective components, and may shed new light on future research in preparing green antibacterial films via environment-friendly approaches.

Determination of ecological flow based on probability distributions of annual and monthly flows

ABSTRACT Developing scientifically sound ecological flow is crucial for protecting river ecosystems. However, most of the existing hydrological methods for determining ecological flow make it difficult to consider both inter-annual and intra-annual changes in runoff. To compensate for this shortcoming, this paper proposes an innovative ecological flow determination method based on the probability distributions of annual and monthly flows. Marginal distributions of annual and monthly flows are first fitted, and the Copula function is used to create joint probability distributions of annual and monthly flows. Conditional probabilities for different monthly flow sizes under different annual flow conditions are then calculated based on Bayesian inference. The conditional probabilities are combined with the flow–duration curve-–based method to finalize the ecological flow process considering both intra- and inter-annual runoff changes. A case study was conducted in Jinsha River, China. The results show that the total annual ecological water demand of the Jinsha River is 1.50, 1.25, and 1.04 × 1011 m3 under annual flow scenarios of high, medium, and low flows, respectively, which provide a red line for the development of water resources and hydro-energy resources of the Jinsha River, as well as for the better protection of the natural plant and animal species.

Eco-friendly corrosion inhibition of copper in NaCl media using Perseana americana extract: Insights from quantum and electrochemical studies

Corrosion of copper in saline environments, particularly in 3.5% sodium chloride (NaCl) solutions, poses significant challenges across various industries, leading to substantial economic losses and safety concerns. Traditional corrosion inhibitors, often synthetic and toxic, raise environmental issues that necessitate the exploration of sustainable alternatives. This study investigates the use of Perseana americana extract (PAE) as an eco-friendly inhibitor for copper corrosion, demonstrating an impressive inhibition efficiency of 96.53% at an optimal concentration of 300 mg/L. Electrochemical assessments, including potentiodynamic polarization (PDP) and electrochemical impedance spectroscopy (EIS), reveal that PAE functions as a mixed-type inhibitor, significantly reducing the corrosion current density (icorr) from 3.59 × 10⁻⁵ A/cm2 (without inhibitor) to 1.83 × 10⁻⁵ A/cm2 at 100 mg/L, and further to 0.12 × 10⁻⁵ A/cm2 at 300 mg/L. The adsorption behavior of PAE on the copper surface adheres to the Langmuir isotherm model, indicating monolayer adsorption with a Gibbs free energy of adsorption (ΔGads) of −18.84 kJ/mol, suggesting a predominantly physisorption mechanism. Additionally, Monte Carlo simulations confirm strong interactions between PAE molecules and the copper surface, with the highest adsorption energy recorded for phloretin at −3778.338 kcal/mol, highlighting the extract's potential as a green alternative to conventional inhibitors. This research underscores the viability of utilizing natural plant extracts for effective corrosion control, contributing to more sustainable practices in metal protection.

Preparation and Characterization of Anti-Microbial Wound Healing Materials from Natural Origins

Abstract Many types of polymers utilized as wound dressings, Polycaprolactone (PCL) displays high degree of biocompatibility as well as biodegradability, the mechanical strength states PCL in the foreground materials used in wound healing therapies. Current work aims to develop new types of wound plaster dressing, a multiple of natural and medical materials (aloe Vera, calendula and phenobarbital) were used to enhance the anti-microbial behavior as well as pain removal during wound healing period. Aloe Vera gels, Calendula extraction, with phenobarbital drug were precipitates on PCL layer in different percentage. Microstructure observation proves that polycaprolactone polymer is good base material supports dressing constituents, wound dressing homogeneity increased due to chemical reactions between the Aloe Vera and other materials. the main elements of dressing (carbon and oxygen) observed from chemical analysis (EDS) which is also showed that using combination of natural plants (aloe vera and Calendula) with phenobarbital medicine create wound plaster layer with wide range of active elements lead to therapeutic effects including antibacterial, In (FTIR) the results show using mixture of natural additives (aloe, calendula), medicine like phenobarbital in PCL lead to create wound plaster with high (OH) content acts to expedite the skin’s healing process by maintaining the natural level of minerals and hydration at wound area. Hydrophobicity of wound can minimized when adding some hydrophilic materials like Aloe Vera, phenobarbital and calendula, Aloe Vera gel, phenobarbital, as well as calendula decrease the contact angle value. Providing high adhesion between wound plaster and skin tissue. All prepared wound plaster has same and high resistance to Staphylococcus bacteria (40mm).

Investigation on the in vitro effects of resveratrol on peripheral blood mononuclear cells harvested from healthy and atopic dogs

Canine atopic dermatitis (AD) is a common skin disease. Many therapeutic options are available to decrease inflammation and ameliorate pruritus. However, those treatments are associated with side effects, a long lag phase for efficacy, or high expense. Natural plant extracts have been identified as possible, safer alternatives to traditional anti-inflammatory and antipruritic drugs. Resveratrol has been revisited as a new, possible alternative for its numerous beneficial properties. The purpose of this study was to evaluate the in vitro effects of resveratrol on peripheral blood mononuclear cells (PBMC) harvested from healthy and atopic privately-owned dogs.The PBMC harvested from nine healthy and 11 atopic dogs were isolated and exposed to four concentrations (1.5-9 μg/mL) of resveratrol both with or without phytohemagglutinin stimulation. After 24 h cytotoxicity, host defense peptides (HDPs), as well as oxidative stress (catalase and superoxide dismutase), and pro-inflammatory cytokines were assessed. Cytotoxicity was not observed in either group under any experimental conditions. An increase in catalase was only seen in healthy PBMC after exposure to low concentrations of resveratrol (p ≤ 0.03). Resveratrol did not show any effect on canine HDPs. Compared to baseline, there was a significant reduction in monocyte chemotactic protein-1 and interleukin-6 after exposure to 9 μg/mL of resveratrol in unstimulated healthy (p = 0.029) and stimulated atopic (p = 0.0075) PBMC. In conclusion, these data confirm the overall lack of cytotoxicity of resveratrol on healthy and atopic PBMC at the tested concentrations. However, at the concentrations tested, there was only a minimal effect of resveratrol on the secretion of HDPs and pro-inflammatory cytokines.

Anti-inflammatory, immuno-modulatory, and anti-proliferative effects of 5-mer Oligogalacturonides (OG DP5) from citrus pectin on different types of human cells. Perspectives for treatment of dermal diseases such as atopic dermatitis and psoriasis

BackgroundOligogalacturonides (OG) are natural plant cell wall pectin-derived products with different degrees of polymerisation (DP) and methylation (M). Their effects as stimulators of plant defence are well documented and they are also known for their potent effects on human health. PurposeHere, we investigated the anti-inflammatory effects of OG extracted from Citrus on different types of human cells and cell systems representative of several pathologies. Study designDifferent concentrations of 5-mer OG (DP5) with different methylation degrees (M: 0, 5, 30 and 70) were tested on cultured human peripheral blood mononuclear cells (PBMC) to see if there were able to decrease LPS-induced IL-1β release. Then, different human cell combination stimulated by specific agonists representative of several pathologies were used to test the effect of the most active OG DP5M0 (0 methylation). MethodsIL-1β was monitored in the PBMC culture medium with ELISA and effects on bio-markers typical of pathologies were studied using the BioMAP Diversity PLUS® method (Eurofins, France). ResultsDP5M0 dose-dependently reduced LPS-induced IL-1β release by cultured human peripheral blood mononuclear cells (PBMC). This was not observed for DP5M30 or DP5M70. DP5M0 was also more efficient than prednisolone when tested on 12 different human cell systems representative of known pathologies (BioMAP systems). The T BioMAP system, which consists in an equal combination of B cells and PBMC, shows the best response sensitivity to DP5M0. This latter induces a dose-dependent decrease of the biomarkers of inflammation and of those of immune responses (IL-6, IL-8, IL-2, IL-17A, IL-17F and TNF-α). ConclusionIn view that all these cytokines are involved in keratinocytes proliferation and differentiation, this model system fits with a possible beneficial effect of DP5M0 on atopic dermatitis and psoriasis. DP5M0 also showed anti-proliferative properties in 5 different cell systems. The comparison of the BioMAP profiles of DP5M0 and anti-inflammatory products prednisolone and diclofenac indicates that their modes of action are different. These data argue for a possible use of DP5M0 for treatments of psoriasis diseases as alternative strategy to other developed medicines when the patients do not tolerate them.

Apigenin Ameliorates H2O2-Induced Oxidative Damage in Melanocytes through Nuclear Factor-E2-Related Factor 2 (Nrf2) and Phosphatidylinositol 3-Kinase (PI3K)/Protein Kinase B (Akt)/Mammalian Target of Rapamycin (mTOR) Pathways and Reducing the Generation of Reactive Oxygen Species (ROS) in Zebrafish

Background: Apigenin is one of the natural flavonoids found mainly in natural plants, as well as some fruits and vegetables, with celery in particular being the most abundant. Apigenin has antioxidant, anti-tumor, anti-inflammatory, and anticancer effects. In this research, we attempted to further investigate the effects of apigenin on the mechanism of repairing oxidative cell damage. The present study hopes to provide a potential candidate for abnormal skin pigmentation disorders. Methods: We used 0.4 mM H2O2 to treat B16F10 cells for 12 h to establish a model of oxidative stress in melanocytes, and then we gave apigenin (0.1~5 μM) to B16F10 cells for 48 h, and detected the expression levels of melanin synthesis-related proteins, dendritic regulation-related proteins, antioxidant signaling pathway- and Nrf2 signaling pathway-related proteins, autophagy, and autophagy-regulated pathways by immunoblotting using Western blotting. The expression levels of PI3K/Akt/mTOR proteins were measured by β-galactosidase staining and Western blotting for cellular decay, JC-1 staining for mitochondrial membrane potential, and Western blotting for mitochondrial fusion- and mitochondrial autophagy-related proteins. Results: Apigenin exerts antioxidant effects by activating the Nrf2 pathway, and apigenin up-regulates the expression of melanin synthesis-related proteins Tyr, TRP1, TRP2, and gp100, which are reduced in melanocytes under oxidative stress. By inhibiting the expression of senescence-related proteins p53 and p21, and delaying cellular senescence, we detected the mitochondrial membrane potential using JC-1, and found that apigenin improved the reduction in mitochondrial membrane potential in melanocytes under oxidative stress, and maintained the normal function of mitochondria. In addition, we further detected the key regulatory proteins of mitochondrial fusion and division, MFF, p-DRP1 (S637), and p-DRP1 (S616), and found that apigenin inhibited the down-regulation of fusion-associated protein, p-DRP1 (S637), and the up-regulation of division-associated proteins, MFF and p-DRP1 (S616), due to oxidative stress in melanocytes, and promoted the mitochondrial fusion and ameliorated the imbalance between mitochondrial division and fusion. We further detected the expression of fusion-related proteins OPA1 and Mitofusion-1, and found that apigenin restored the expression of the above fusion proteins under oxidative stress, which further indicated that apigenin promoted mitochondrial fusion, improved the imbalance between mitochondrial division and fusion, and delayed the loss of mitochondrial membrane potential. Apigenin promotes the expression of melanocyte autophagy-related proteins and the key mitochondrial autophagy proteins BNIP3L/Nix under oxidative stress, and activates the PINK1/Parkin signaling pathway by up-regulating the expression of autophagy-related proteins, as well as the expression of PINK1 and Parkin proteins, to promote melanocyte autophagy and mitochondrial autophagy. Conclusions: Apigenin exerts anti-melanocyte premature aging and detachment effects by promoting melanin synthesis, autophagy, and mitochondrial autophagy in melanocytes, and inhibiting oxidative cell damage and senescence.

The potential of diallyl trisulfide for cancer prevention and treatment, with mechanism insights.

Cancer has become an important public health problem worldwide, and there is currently a lack of effective treatment and prevention strategies. Natural plant active ingredients have been proven to be a safe and highly promising method for preventing and treating cancer. It has been found that diallyl trisulfide have anticancer effects in multiple types of cancer via inhibiting cancer proliferation, enhancing chemotherapy sensitivity, inducing apoptosis/autophagy, suppressing invasion/migration, regulating microenvironment. With the deepening of research on new strategies for cancer prevention and treatment, the role of diallyl trisulfides in cancers occurrence, prognosis, and drug resistance is also receiving increasing attention. In order to better understand the relationship between diallyl trisulfides and various cancer, as well as the role and mechanism of diallyl trisulfides in cancer prevention and treatment, we briefly summarized the role and function of diallyl trisulfide in cancers.

Advances in Research on Semi-Synthesis, Biotransformation and Biological Activities of Novel Derivatives from Maslinic Acid

Since ancient times, humans have turned to medicinal plants for treating various ailments and curing specific diseases, as these natural plants serve as the primary source of a range of phytochemicals, including triterpenes. Maslinic acid (MA), also known as (2α,3β)-2,3-dihydroxyolean-12-en-28-oic acid, is a pentacyclic triterpene acid present in numerous plants including olive, known for its high safety profile in humans. Recent experimental data increasingly suggests that MA exhibits diverse biological properties and therapeutic effects on various organ diseases, highlighting its significant potential for clinical applications due to its diverse potential pharmacological activities that promote health and resist various diseases, such as hypoglycemic, neuroprotective, anti-tumor, anti-inflammatory, antioxidant and multiple other biological activities. However, the undesirable pharmacokinetic properties of MA, such as high lipophilicity, pose a limitation to its application and development, impacting its bioavailability. Consequently, extensive research spanning decades has focused on structurally modifying MA to overcome these limitations and enhance its pharmacokinetic and therapeutic characteristics, leading to the identification of several potential lead compounds. In this review, we focus on the progress of research in recent years on MA with interest to its chemical and enzymatic modifications as well as the relationships between the modified structures or derivatives and their biological activities.