Novel Flavonol Alkaloids in Green Tea: Synthesis, Detection, and Anti-Alzheimer's Disease Effect in a Transgenic CL4176 Model.

J Agric Food Chem

Natural Products Laboratory, International Joint Laboratory of Tea Chemistry and Healthy Effects, State Key Laboratory of Tea Plant Biology and Utilization, School of Tea and Food Science & Technology, Anhui Agricultural University, Hefei 230036, Anhui, China.

Published: February 2024

AI Article Synopsis

  • - The study synthesized novel flavonol alkaloids from green tea through thermal reactions of myricetin, quercetin, and kaempferol, identifying them in specific green tea cultivars using advanced chromatography and mass spectrometry techniques.
  • - The structural analysis of these compounds was conducted using 1D and 2D NMR spectroscopies, uncovering their potential therapeutic effects against Alzheimer's disease.
  • - One particular compound showed a strong binding affinity to amyloid β, significantly improving lifespan and neuroprotection in a transgenic worm model, indicating its potential health benefits.

Article Abstract

Novel -ethy-2-pyrrolidinone-substituted flavonols, myricetin alkaloids A-C (-), quercetin alkaloids A-C (, , and ), and kaempferol alkaloids A and B ( and ), were prepared from thermal reaction products of myricetin, quercetin, kaempferol─l-theanine, respectively. We used HPLC-ESI-HRMS/MS to detect - in 14 cultivars of green tea and found that they were all present in "Shuchazao," "Longjing 43", "Fudingdabai", and "Zhongcha 108" green teas. The structures of - and were determined by extensive 1D and 2D NMR spectroscopies. These flavonol alkaloids along with their skeletal flavonols were assessed for anti-Alzheimer's disease effect based on molecular docking, acetylcholinesterase inhibition, and the transgenic CL4176 model. Compound strongly binds to the protein amyloid β (Aβ) through hydrogen bonds (BE: -9.5 kcal/mol, : 114.3 nM). Compound (100 μM) is the strongest one in significantly extending the mean lifespan (13.4 ± 0.5 d, 43.0% promotion), delaying the Aβ-induced paralysis (PT: 40.7 ± 1.9 h, 17.1% promotion), enhancing the locomotion (140.0% promotion at 48 h), and alleviating glutamic acid (Glu)-induced neurotoxicity (153.5% promotion at 48 h) of CL4176 worms ( < 0.0001).

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Source
http://dx.doi.org/10.1021/acs.jafc.3c06608DOI Listing

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