Differences in Intestinal Metabolism of Ginseng Between Normal and Immunosuppressed Rats
Autor: | Jin-Hao Zhu, Ming Kong, Jing Zhou, Qian Mao, Jin-Di Xu, Shan-Shan Zhou, Song-Lin Li, Xiao-Ya Zhang, He Zhu |
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Rok vydání: | 2020 |
Předmět: |
Male
Ginsenosides medicine.medical_treatment Panax Biology Gut flora Pharmacology 030226 pharmacology & pharmacy Rats Sprague-Dawley 03 medical and health sciences Ginseng chemistry.chemical_compound 0302 clinical medicine Immune Tolerance medicine Animals Pharmacology (medical) Eubacterium Intestinal Mucosa Cyclophosphamide Saline Bifidobacterium Plant Extracts Lachnospiraceae food and beverages biology.organism_classification Gastrointestinal Microbiome Rats chemistry Ginsenoside 030220 oncology & carcinogenesis Bacteroides Immunosuppressive Agents |
Zdroj: | European Journal of Drug Metabolism and Pharmacokinetics. 46:93-104 |
ISSN: | 2107-0180 0378-7966 |
DOI: | 10.1007/s13318-020-00645-1 |
Popis: | Ginseng is usually consumed as a dietary supplement for health care in the normal state or prescribed as a herbal medicine in pathologic conditions. Although metabolic studies of ginseng are commonly performed on healthy organisms, the metabolic characteristics in pathologic organisms remain unexplored. This study aimed to uncover the difference in intestinal metabolism of ginseng between normal and cyclophosphamide-induced immunosuppressed rats and further discuss the potential mechanisms involved. Twelve Sprague-Dawley rats (6–8 weeks old) were randomly divided into two groups: the normal group (NG) and immunosuppressed group (ISG). Rats in the NG and ISG groups were intraperitoneally administered normal saline and cyclophosphamide injections (40 mg/kg) on the 1st, 2nd, 3rd and 10th days; on the 12th day, all rats were intragastrically administered ginseng water extract (900 mg/kg). The difference in intestinal metabolism of ginseng was compared using an ultra-high-performance liquid chromatography coupled with quadruple time-of-flight mass spectrometry-based metabolomics approach, and the diversities of gut microbiota were analyzed by 16S rRNA gene sequencing between the two groups. The intestinal metabolomic characteristics of ginseng were significantly different between the normal and immunosuppressed rats, with the ginsenoside F2 (F2), 20S-ginsenoside Rg3 (20(S)-Rg3), pseudo-ginsenoside Rt5 (Pseudo-Rt5), ginsenoside Rd (Rd), ginsenoside Rh1 (Rh1), 20S-ginsenoside Rg1 (20(S)-Rg1), ginsenoside compound K (CK), ginsenoside Rg2 (Rg2) and 20S-panaxatriol (S-PPT) more abundant in immunosuppressed ones (P |
Databáze: | OpenAIRE |
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