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The fruiting bodies of are renowned for their therapeutic properties, primarily due to their triterpenoid content. Variability in strains may influence the composition and abundance of triterpenoids. In this study, we explored the triterpenoid superiority in a newly developed strain (GL_V2) obtained through mutation breeding, and compared it to a widely cultivated strain (GL_V1). GL_V2 exhibited a 1.4-fold increase in total triterpenoid content and higher DPPH radical scavenging activity compared to GL_V1, while polysaccharide levels remained consistent. Using UPLC-Q-Orbitrap-MS and chemometric analyses, we identified 589 metabolites, including 86 triterpenoids. Multivariate statistical analyses revealed clear differences in overall metabolite profiles and triterpenoid compositions between the two strains. OPLS-DA identified 56 triterpenoids as key distinguishing markers with VIP values above 1.0. Notably, GL_V2 exhibited increased levels of seven ganoderic acids, two ganoderiols, three ganolucidic acids, and two ganosporelactones, while GL_V1 showed higher concentrations of six lucidenic acids. These results highlight the superior triterpenoid composition of GL_V2 and its potential for developing more potent -derived products. This study offers valuable insights into varietal differences in triterpenoid profiles and their implications for the cultivation and therapeutic use of . Additionally, the findings of this study suggest that GL_V2 holds significant potential for the development of more effective nutraceutical and pharmaceutical products derived from .
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http://dx.doi.org/10.3389/fnut.2025.1541162 | DOI Listing |
Discov Oncol
September 2025
Department of Oncology, LongHua Hospital, Shanghai University of Traditional Chinese Medicine, No. 725 Wanping South Road, Xuhui District, Shanghai, 200032, China.
Purpose: Ursolic Acid (UA), a triterpenoid extracted from Hedyotis Diffusa Willd. (HDW), is known for its anti-inflammatory, antioxidant, and antitumor effects. Nevertheless, the mechanisms underlying UA's anti-colorectal cancer (CRC) effects remain insufficiently understood.
View Article and Find Full Text PDFPlants (Basel)
August 2025
State Key Laboratory of Tree Genetics and Breeding, Nanjing Forestry University, Nanjing 210037, China.
To reveal the effects of genotype-herbivore interactions on leaf quality, foliar variations in phytochemicals, morphoanatomy, and herbivory damage ratio were investigated in a (Batalin) Iljinsk. (Juglandaceae) germplasm resources bank. Results showed less herbivory damage in genotypes with a higher leaf thickness, but more herbivory damage in genotypes with a higher leaf stomatal density.
View Article and Find Full Text PDFLiver Int
September 2025
Division of Gastroenterology and Hepatology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, NHC Key Laboratory of Digestive Diseases, Shanghai Research Center of Fatty Liver Disease, Shanghai, China.
Background And Aims: Steroids are the standard treatment for checkpoint inhibitor-induced liver injury (ChILI). However, concerns about their adverse effects and impacts on long-term outcomes highlight the need for alternative therapies. This study aims to evaluate the effectiveness of magnesium isoglycyrrhizinate (MgIG) in combination with steroids in ChILI.
View Article and Find Full Text PDFLangmuir
September 2025
College of Chemistry and Chemical Engineering, Qiqihar University, Wenhua Street No.42, Qiqihar, Heilongjiang 161006, China.
Hexavalent chromium (Cr(VI)) is an extremely poisonous heavy metal ion that poses a major risk to both human health and the environment. In this study, three types of amphipathic supramolecular hydrogels (C2-MUP, C2-MUBP, and C4-MUP) were prepared using ursolic acid (UA) as a substrate and covalently modified with pyridine (Pyr). The synergistic reduction and adsorption performances of these three hydrogels for the removal of Cr(VI) from water were then evaluated.
View Article and Find Full Text PDFCell Biol Int
August 2025
Instituto de Química, Universidade de São Paulo, São Paulo, São Paulo, Brazil.
Autophagy is a critical adaptive mechanism in tumor cells that promotes survival under stress, but when dysregulated, it may trigger programmed cell death. The pentacyclic triterpenoids betulinic acid (BA) and ursolic acid (UA) are structurally related compounds that modulate autophagy; however, comparative insights into their effects on nonmalignant and malignant cells, as well as model membranes, remain limited. Here, we investigated the distinct cellular outcomes induced by UA and BA in nonmalignant keratinocytes (HaCaT) and malignant cell lines (A549, HeLa, MCF7, MES-SA, PC3, SKMEL-25/28), as well as their interactions with mitochondrial membrane mimetics.
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