Scientia Agricultura Sinica ›› 2026, Vol. 59 ›› Issue (13): 2933-2945.doi: 10.3864/j.issn.0578-1752.2026.13.014

• FOOD SCIENCE AND ENGINEERING • Previous Articles     Next Articles

Differential Absorption of Components in Buckwheat Polyphenols via MKN28/Caco-2 Continuous Transport Model and Their Lipid- Lowering Effects

YAO YiJun(), CHEN Yu, JU XingRong, WANG LiFeng()   

  1. College of Food Science and Engineering, Nanjing University of Finance and Economics/Collaborative Innovation Center for Modern Grain Circulation and Safety, Nanjing 210023
  • Received:2025-12-19 Accepted:2026-04-07 Online:2026-07-01 Published:2026-07-01
  • Contact: WANG LiFeng

Abstract:

【Background】 Polyphenolic compounds exhibit pronounced lipid-lowering effects, and their absorption in the human gastrointestinal tract varies considerably, which critically influences their bioavailability. Buckwheat, a natural food being rich in polyphenols, has been suggested to possess unique lipid-lowering potential. 【Objective】 This study aimed to investigate the differential absorption of buckwheat polyphenols using an MKN28/Caco-2 sequential transport model, and to systematically evaluate their lipid-lowering effects and underlying mechanisms through cellular assays and gut microbiota fermentation experiments.【Method】 Buckwheat polyphenol extract was characterized by ultra-high-performance liquid chromatography coupled with quadrupole Orbitrap mass spectrometry (UHPLC-Q-Orbitrap MS). Based on the MKN28/Caco-2 transport model, the extract was fractionated into readily absorbable and poorly absorbable components. The lipid-lowering effects of the absorbable fraction were assessed in adipocytes using Oil Red O staining and intracellular lipid quantification. In addition, the impact of the non-absorbable fraction on gut microbiota composition was evaluated in vitro fermentation.【Result】 Component analysis revealed that there are 23 kinds of polyphenolic compounds rutin and protocatechuic acid exhibited relatively high signal intensities. The absorbable fraction significantly reduced lipid accumulation in adipocytes, with triglyceride (TG), total cholesterol (TC), and low-density lipoprotein cholesterol (LDL-C) levels in 3T3-L1 cells decreased by 17.8%, 28.6%, and 15.2%, respectively. Furthermore, in vitro fermentation demonstrated that the poorly absorbable fraction (BWP-AP) modulated gut microbiota composition by increasing the relative abundance of Bacteroides and Bifidobacterium, while decreasing Escherichia-Shigella and Alistipes.【Conclusion】 Buckwheat polyphenol extract contained 23 identified phenolic compounds. The readily absorbable fraction exerted significant intracellular lipid-lowering effects, whereas the poorly absorbable fraction regulated metabolic homeostasis via modulation of gut microbiota. These findings revealed a dual-pathway mechanism involving direct host absorption and microbiota-mediated regulation, providing a theoretical basis for the development of functional foods based on buckwheat polyphenols.

Key words: buckwheat polyphenols, MKN28/Caco-2 continuous transport model, differential absorption, lipid-lowering effects, gut microbiota

Table 1

Receiving rate of ethanol extract of buckwheat and content of total phenols and flavonoids"

得率
Receiving rate (%)
总酚
Total phenolic content (mg GAE·g-1)
总黄酮
Total flavonoid content (mg RE·g-1)
苦荞 Tartary buckwheat 3.25±0.02 20.40±0.29 10.83±0.46
甜荞 Sweet buckwheat 2.50±0.04 13.24±0.54 7.30±0.62

Table 2

Composition and identification of polyphenols in tartary buckwheat extract by UHPLC-Q-Orbitrap MS"

序号
Number
保留时间
Retention
time
峰面积
Peak area
相对定量
Relative quantification (%)
分子量Molecular weight 误差
Error
value
分子式
Formula
注释源Annotation source 化合物
Compounds
测量值
Measured
value
理论值
Theoretical
value
mzCloud mzVault MassList
1 5.779 31520316066 95.31302115 610.1529 610.52 0.36715 C27H30O16 芦丁 Rutin
2 5.356 813686384.8 2.460473665 154.027 154.12 0.09301 C7H6O4 原儿茶酸 Protocatechuic acid
3 5.499 173675725.5 0.525171069 756.2135 756.66 0.44649 C33H40O20 山茶花苷A Camelliaside A
4 5.478 167558784.7 0.506674297 170.022 170.12 0.09805 C7H6O5 没食子酸 Gallic acid
5 5.685 110062044.7 0.332812208 390.132 390.38 0.24805 C20H22O8 虎杖苷 Polydatin
6 6.032 67686001.22 0.204672988 668.198 668.6 0.40199 C30H36O17 丹皮苷B
Tenuifoliside B
7 2.392 40018060.9 0.121009011 436.1357 436.41 0.27435 C21H24O10 根皮苷 Phlorizin
8 6.302 31067800.42 0.093944677 286.0482 286.236 0.18784 C15H10O6 木犀草素 Luteolin
9 6.179 30683750.47 0.092783364 346.0682 346.29 0.2218 C17H14O8 丁香苷 Syringetin
10 5.696 24698332.19 0.074684297 466.1122 466.39 0.27781 C21H22O12 车前草苷 Plantagoside
11 8.147 19850602.56 0.060025442 270.053 270.24 0.18705 C15H10O5 染料木黄酮 Genistein
12 5.903 16924242.75 0.05117654 194.0584 194.18 0.12162 C10H10O4 阿魏酸 Ferulic acid
13 9.826 13206999.01 0.039936115 770.2244 770.68 0.45556 C34H42O20 香蒲苷 Typhaneoside
14 5.652 12511802.1 0.037833937 304.0952 304.29 0.19482 C16H16O6 原苏木素B Protosappanin B
15 10.915 9320952.514 0.028185255 784.2782 784.75 0.47179 C36H48O19 安格洛苷C
Angoroside C
16 3.867 5294193.31 0.016008899 304.0581 304.25 0.19188 C15H12O7 二氢槲皮素 Taxifolin
17 6.305 3454208.941 0.010445044 166.0634 166.17 0.10657 C9H10O3 丹皮酚 Paeonol
18 5.464 3036822.242 0.009182925 492.1045 492.43 0.32549 C26H20O10 丹酚酸C
Salvianolic acid C
19 6.344 2796773.379 0.008457051 362.174 362.42 0.24605 C20H26O6 开环异落叶松树脂酚 Secoisolariciresinol
20 5.625 1966842.11 0.005947455 272.0901 272.25 0.15994 C12H16O7 熊果苷 Arbutin
21 5.599 1747962.418 0.005285594 582.1941 582.5505 0.35639 C27H34O14 柚皮苷
Naringin dihydrochalcone
22 11.716 631804.1539 0.001910487 578.1411 578.52 0.37889 C30H26O12 原花青素B2 Procyanidin B2
23 10.054 118564.9798 0.000358524 724.221 724.66 0.43898 C33H40O18 女贞苷 Ligustroflavone

Fig. 1

TEER values (A), fluorescein sodium permeability (B), and AKP activity on AP and BL sides (C) of MKN28 and Caco-2 cells"

Fig. 2

Schematic diagram of MKN28/Caco-2 continuous transport model and Caco-2/3T3-L1 adipocytes Co-culture model (A) and cultured cells (B) In Fig. B, a: MKN28 cell monolayer cultured for 21 days; b: Caco-2 cell monolayer cultured for 21 days; c: 3T3-L1 adipocytes cultured for 2 days; d: 3T3-L1 adipocytes cultured for 14 days (magnification: 200)"

Fig. 3

Western blotting analysis of related proteins in 3T3-L1 cells (A: Protein immunoblotting bands; B, C, and D: Gary value analysis)"

Fig. 4

The effect of different concentrations of BWP-BL on the expression of UCP-1 (A), PGC-1α (B) and PPAR-γ (C) genes in cells"

Fig. 5

Toxicity of sample solution on MKN28, Caco-2 cells, and 3T3-L1 adipocytes (A, values are the mean ± SD calculated from three independent experiments), Extraction results of 3T3-L1 cells by oil red O staining (B), Lipid lowering effects in TG, T-CHO and LDL-C (C)"

Fig. 6

The effect of BWP-AP on the human intestinal flora A: Venn diagram of species distribution; B: The relative abundance of bacteria at the phylum levels; C: The relative abundance of bacteria at the genus levels"

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