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1.
Phytochem Anal ; 34(5): 606-616, 2023 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-37226258

RESUMO

INTRODUCTION: Standardizing the planting process is an effective way to control the quality stability of herbal resources, which are susceptible to external environmental factors (e.g., moisture, soil, etc.). However, how to scientifically and comprehensively assess the effects of standardized planting on plant quality and quickly test unknown samples has not been addressed. OBJECTIVE: The aim of this study was to determine and compare the metabolite levels of herbs before and after standardized planting, to quickly distinguish their sources, and to evaluate their quality, using the typical herb Astragali Radix (AR) as an example. METHODS: In this study, an efficient strategy using liquid chromatography-mass spectrometry (LC-MS) based on plant metabolomics combined with extreme learning machine (ELM) has been developed to efficiently distinguish and predict AR after standardized planting. Moreover, a comprehensive multi-index scoring method has been developed for the comprehensive evaluation of the quality of AR. RESULTS: The results confirmed that AR after standardized planting was significantly differentiated, with a relatively stable content of 43 differential metabolites, mainly including flavonoids. An ELM model was established based on LC-MS data, and the accuracy in predicting unknown samples could reach more than 90%. As expected, higher total scores were obtained for AR after standardized planting, indicating much better quality. CONCLUSION: A dual system for evaluating the impact of standardized planting on the quality of plant resources has been established, which will significantly contribute to innovation in the quality evaluation of medicinal herbs and support the selection of optimal planting conditions.


Assuntos
Astrágalo , Medicamentos de Ervas Chinesas , Astragalus propinquus/química , Medicamentos de Ervas Chinesas/química , Astrágalo/química , Cromatografia Líquida , Metabolômica , Cromatografia Líquida de Alta Pressão/métodos
2.
Chem Biodivers ; 16(6): e1900062, 2019 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-30983116

RESUMO

Seven new polyhydroxypregnane glycosides, named cynotophyllosides P-V, together with three known analogs were isolated from the roots of Cynanchum otophyllum C.K.Schneid. Their structures were elucidated by a variety of spectroscopic techniques, as well as acid-catalyzed hydrolysis. All isolates were tested for their immunological activities in vitro against Con A- and LPS-induced proliferation of mice splenocytes. Immunoenhancing (for 1, 9) and immunosuppressive (for 2) activities were observed. Furthermore, cynotophylloside R (3) showed immunomodulatory as it enhanced the proliferation of splenocytes in low concentration and suppressed immune cells in concentration more than 1.0 µg/ml.


Assuntos
Cynanchum/química , Glicosídeos/química , Pregnanos/química , Animais , Proliferação de Células/efeitos dos fármacos , Cynanchum/metabolismo , Glicosídeos/isolamento & purificação , Glicosídeos/farmacologia , Lipopolissacarídeos/farmacologia , Masculino , Camundongos , Camundongos Endogâmicos BALB C , Conformação Molecular , Raízes de Plantas/química , Raízes de Plantas/metabolismo , Baço/citologia , Baço/efeitos dos fármacos , Baço/metabolismo
3.
Fitoterapia ; 158: 105142, 2022 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-35124161

RESUMO

This is the first phytochemical investigation of Schisandra tomentella A. C. Smith. 11 lignans and 8 sesquiterpenoids, were isolated from the stems of S. tomentella, including two undescribed lignans, tomentaschinins A-B (1-2), and two new sesquiterpenoids, tomentaschinnes A-B (3-4). Their structures were elucidated based on the interpretation of their spectroscopic data. Cytotoxicity and MDR reversal effect of these compounds were screened on multidrug resistance cancer cell line MCF-7/ADR, and results showed gomisin M2 (7) could promote the efficacy of adriamycin against MCF-7/ADR.


Assuntos
Lignanas , Schisandra , Sesquiterpenos , Lignanas/química , Lignanas/farmacologia , Estrutura Molecular , Schisandra/química , Sesquiterpenos/química , Sesquiterpenos/farmacologia
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