Lactate Dehydrogenase-Inhibitors Isolated from Ethyl Acetate Extract of


Journal

Frontiers in bioscience (Landmark edition)
ISSN: 2768-6698
Titre abrégé: Front Biosci (Landmark Ed)
Pays: Singapore
ID NLM: 101612996

Informations de publication

Date de publication:
26 07 2022
Historique:
received: 20 05 2022
revised: 17 06 2022
accepted: 13 07 2022
entrez: 30 8 2022
pubmed: 31 8 2022
medline: 3 9 2022
Statut: ppublish

Résumé

Lactate dehydrogenase (LDH) is one of the important enzyme systems for glycolysis and gluconeogenesis. It can catalyze the reduction and oxidation reaction between propionic acid and L-lactic acid, which is usually overexpressed in cancer cells. Therefore, inhibiting the activity of LDH is a promising way for the treatment of cancer. In this study, an effective method based on ligand fishing and ultra performance liquid chromatography-mass spectrum (UPLC-MS) was established to screen and identify active ingredients from Firstly, LDH was immobilized on the magnetic nanoparticles (MNPs), three immobilization parameters including LDH concentration, immobilization time and pH were optimized by single factor and response surface methodology for maximum (max) immobilization yield. Then, a mixed model of galloflavin and chlorogenic acid (inhibitors and non-inhibitors of LDH) was used to verify the specificity of immobilized LDH ligand fishing, and the conditions of ligand fishing were further optimized. Finally, combined with UPLC-MS, immobilized LDH was used to simultaneously screen and identify potential LDH inhibitors from the ethyl acetate extract of The prepared fishing material was comprehensively characterized by scanning electron microscopy (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD) and fourier transform infrared spectrometer (FT-IR). The optimal immobilization conditions were obtained as LDH concentration of 0.7 mg/mL, pH value of 4.5, and immobilization time of 3.5 h. Under these conditions, the max immobilization yield was (3.79 ± 0.08) × 103 U/g. The specificity analysis showed that immobilized LDH could recognize and capture ligands, and the optimal ligand fishing conditions included that the incubation time was 30 min, the elution time was 20 min, and the concentration of methanol as eluent was 80%. Finally, two LDH inhibitors, amentoflavone and robustaflavone, were screened by immobilized LDH from the ethyl acetate extract of The study provided a meaningful evidence for discovering the bioactive constituents in ethyl acetate extract of

Sections du résumé

BACKGROUND
Lactate dehydrogenase (LDH) is one of the important enzyme systems for glycolysis and gluconeogenesis. It can catalyze the reduction and oxidation reaction between propionic acid and L-lactic acid, which is usually overexpressed in cancer cells. Therefore, inhibiting the activity of LDH is a promising way for the treatment of cancer. In this study, an effective method based on ligand fishing and ultra performance liquid chromatography-mass spectrum (UPLC-MS) was established to screen and identify active ingredients from
METHODS
Firstly, LDH was immobilized on the magnetic nanoparticles (MNPs), three immobilization parameters including LDH concentration, immobilization time and pH were optimized by single factor and response surface methodology for maximum (max) immobilization yield. Then, a mixed model of galloflavin and chlorogenic acid (inhibitors and non-inhibitors of LDH) was used to verify the specificity of immobilized LDH ligand fishing, and the conditions of ligand fishing were further optimized. Finally, combined with UPLC-MS, immobilized LDH was used to simultaneously screen and identify potential LDH inhibitors from the ethyl acetate extract of
RESULTS
The prepared fishing material was comprehensively characterized by scanning electron microscopy (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD) and fourier transform infrared spectrometer (FT-IR). The optimal immobilization conditions were obtained as LDH concentration of 0.7 mg/mL, pH value of 4.5, and immobilization time of 3.5 h. Under these conditions, the max immobilization yield was (3.79 ± 0.08) × 103 U/g. The specificity analysis showed that immobilized LDH could recognize and capture ligands, and the optimal ligand fishing conditions included that the incubation time was 30 min, the elution time was 20 min, and the concentration of methanol as eluent was 80%. Finally, two LDH inhibitors, amentoflavone and robustaflavone, were screened by immobilized LDH from the ethyl acetate extract of
CONCLUSIONS
The study provided a meaningful evidence for discovering the bioactive constituents in ethyl acetate extract of

Identifiants

pubmed: 36042169
pii: S2768-6701(22)00591-3
doi: 10.31083/j.fbl2708229
doi:

Substances chimiques

Acetates 0
Ligands 0
Magnetite Nanoparticles 0
Plant Extracts 0
ethyl acetate 76845O8NMZ
L-Lactate Dehydrogenase EC 1.1.1.27

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

229

Informations de copyright

© 2022 The Author(s). Published by IMR Press.

Déclaration de conflit d'intérêts

The authors declare no conflict of interest.

Auteurs

Feng Zhang (F)

School of Pharmacy, Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Huiyun Li (H)

School of Pharmacy, Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Chao Liu (C)

School of Pharmacy, Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Kun Fang (K)

School of Pharmacy, Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Yongmei Jiang (Y)

School of Pharmacy, Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Mingjiang Wu (M)

Department of Pharmacy, Zunyi Medical and Pharmaceutical College, 563000 Zunyi, Guizhou, China.

Shiji Xiao (S)

School of Pharmacy, Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Lei Zhu (L)

School of Pharmacy, Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Jiaqi Yu (J)

Department of Pharmacy, The Third Affiliated Hospital of Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Shenge Li (S)

Department of Pharmacy, The Third Affiliated Hospital of Zunyi Medical University, 563000 Zunyi, Guizhou, China.

Gang Wang (G)

School of Pharmacy, Zunyi Medical University, 563000 Zunyi, Guizhou, China.

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Classifications MeSH