Diterpenoid Alkaloids Isolated from Delphinium brunonianum and Their Inhibitory Effects on Hepatocytes Lipid Accumulation
This research aimed to excavate compounds with activity reducing hepatocytes lipid accumulation from . Four novel diterpenoid alkaloids, brunodelphinine B-E, were isolated from together with eleven known diterpenoid alkaloids through a phytochemical investigation. Their structures were elucidated by...
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Veröffentlicht in: | Molecules (Basel, Switzerland) Switzerland), 2022-03, Vol.27 (7), p.2257 |
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Hauptverfasser: | , , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | This research aimed to excavate compounds with activity reducing hepatocytes lipid accumulation from
. Four novel diterpenoid alkaloids, brunodelphinine B-E, were isolated from
together with eleven known diterpenoid alkaloids through a phytochemical investigation. Their structures were elucidated by comprehensive spectroscopy methods including HR-ESI-MS, NMR, IR, UV, CD, and single-crystal X-ray diffraction analysis. The inhibitory effects of a total of 15 diterpenoid alkaloids on hepatocytes lipid accumulation were evaluated using 0.5 mM FFA (oleate/palmitate 2:1 ratio) to induce buffalo rat liver (BRL) cells by measuring the levels of triglyceride (TG), total cholesterol (TC), alanine transaminase (ALT), aspartate transaminase (AST), and the staining of oil red O. The results show that five diterpenoid alkaloids-brunodelphinine E (
), delbruline (
), lycoctonine (
), delbrunine (
), and sharwuphinine A (
)-exhibited significant inhibitory effects on lipid accumulation in a dose-dependent manner and without cytotoxicity. Among them, sharwuphinine A (
) displayed the strongest inhibition of hepatocytes lipid accumulation in vitro. Our research increased the understanding on the chemical composition of
and provided experimental and theoretical evidence for the active ingredients screened from this herbal medicine in the treatment of the diseases related to lipid accumulation, such as non-alcoholic fatty liver disease and hyperlipidemia. |
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ISSN: | 1420-3049 1420-3049 |
DOI: | 10.3390/molecules27072257 |