Uncovering the effect and mechanism of Panax notoginseng saponins on metabolic syndrome by network pharmacology strategy (Record no. 53888)

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fixed length control field 03416nam a2200301Ia 4500
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control field MX-MdCICY
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20250625162436.0
040 ## - CATALOGING SOURCE
Transcribing agency CICY
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) B-19769
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245 10 - TITLE STATEMENT
Title Uncovering the effect and mechanism of Panax notoginseng saponins on metabolic syndrome by network pharmacology strategy
490 0# - SERIES STATEMENT
Volume/sequential designation Journal of EthnoPharmacology, 300, p.115680, 2023
520 3# - SUMMARY, ETC.
Summary, etc. Ethnopharmacological relevance: Metabolic syndrome (MetS)is a cluster of disease centered on obesity, which is the result of stagnation of liver qi according to traditional Chinese medicine. Panax notoginseng is a traditional Chinese herbal medicine, entering liver and stomach meridians and dissipating blood stasis, in which panax notoginseng saponins (PNS)are the main active components. However, its effects and mechanism on metabolic syndrome has not been revealed yet. Aim of study: To evaluate the anti-MetS effect of PNS, including body weight and adiposity, glucose metabolism and non-alcoholic fatty liver disease (NAFLD), as well as to explore the mechanism and signaling pathway of PNS on MetS effect. Materials and methods: HPLC was utilized to affirm the percentages of saponins in PNS. In vivo, normal C57BL/6J mice and high-fat diet (HFD)-induced MetS mice were used to evaluate anti-MetS effect of PNS. Body weight, food and water intake were recorded. NMR imager was used for NMR imaging and lipid-water analysis. Blood glucose detection, glucose and insulin tolerance test were performed to evaluate glucose metabolism. Biochemical indexes analysis and histopathological staining were used to evaluate the effect on NAFLD. The expressions of mRNA and proteins related to thermogenesis in adipose tissue were determined using real-time PCR and Western blot. In silico, network pharmacology was utilized to predict potential mechanism. In vitro, matured 3T3-L1 adipocyte was used as subject to confirm the signaling pathway by Western blot. Results: We determined the content of PNS component by HPLC. In vivo, PNS could improve metabolic syndrome with weight loss, reduction of adiposity, improvement of adipose distribution, correction of glucose metabolism disorder and attenuation of NAFLD. Mechanismly, PNS boosted energy exhaustion and dramatically enhanced thermogenesis in brown adipose tissue (BAT), induced white adipose tissue (WAT)browning. In silico, utilizing network pharmacology strategy, we identified 307 candidate targets which were enriched in MAPK signaling pathway specifically in liver tissue and adipocyte. In vitro validation confirmed ERK and p38MAPK mediated anti-MetS effects of PNS, not JNK signaling pathway. Conclusion: PNS exerted protective effect on metabolic syndrome through MAPK-mediated adipose thermogenic activation, which may serve as a prospective therapeutic drug for metabolic syndrome.
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element PANAX NOTOGINSENG SAPONINS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element METABOLIC SÍNDROME
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element ADIPOSE THERMOGENESIS
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element BROWNING
650 14 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element MAPK SIGNALING PATHWAY
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Wang, Y.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Ma, P.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Wang, Z.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Sun, M.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Hou, B.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Xu, T.
700 12 - ADDED ENTRY--PERSONAL NAME
Personal name Qiang, G.
856 40 - ELECTRONIC LOCATION AND ACCESS
Uniform Resource Identifier <a href="https://drive.google.com/file/d/1Vq-IzUFFMao8R6BxUB9h6rFI71XkoQJU/view?usp=drivesdk">https://drive.google.com/file/d/1Vq-IzUFFMao8R6BxUB9h6rFI71XkoQJU/view?usp=drivesdk</a>
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Source of classification or shelving scheme Clasificación local
Koha item type Documentos solicitados
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  Clasificación local     Ref1 CICY CICY Documento préstamo interbibliotecario 25.06.2025   B-19769 25.06.2025 25.06.2025 Documentos solicitados