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. 2022 May 11;9:837222. doi: 10.3389/fmed.2022.837222

TABLE 3.

Compounds that inhibit the formation of advanced glycation end products (AGEs) and their mechanisms based on the categories of inhibitory pathways.

Category Inhibitory pathway Substance Inhibitory mechanism References
A Maintain and stabilise the protein structure Phytosterols Interacts with lysine residues of BSA (100)
Anthraquinones Interacts with amino acid residues in HSA to maintain protein structure (101)
Folic acid Binds to HSA and is stabilised by hydrophobic interactions and hydrogen bonding (102)
B Chelation of transition metals Pyridoxamine Binds metal ions to form complexes and inhibits oxidative degradation steps after the generation of Amadori products (105)
PTB, PMTB Chelated with Cu2+ ions (106)
C Capture and block dicarbonyl compounds Aminoguanidine Nucleophilic addition reaction captures carbonyl groups formed by oxidative cleavage of Amadori products and prevents rearrangement and degradation (109)
Phloridzin Capture MGO and GO via groups at the 3 and 5 positions of ring A (112)
ECG The hydroxyl group on the A ring traps MGO to form an ECG-MGO adduct (111)
Quercetin The C-6 and C-8 positions of the A ring trap MGO to scavenge dicarbonyl compounds (113)
Carnosine Reduces the contents of CML and pentoglycoside in skin by reducing the number of MGO reactive groups (110)
D Neutralise, inhibit and scavenge free radicals Lotus seedpod Antioxidant properties (116, 117)
Milk thistle Powerful antioxidant properties, reducing ROS formation (119)
Red maple leaf phenolic extract Reduces MGO-induced oxidative stress in HaCaT cells (120)
E Activation of the glyoxalase detoxification system Pterostilbene Increases the expression level of GLO-1 and increases the content of GSH to activate the glyoxalase defence system (121)
L. erythrorhizon root Upregulation of GLO-1 and GSH synthesis genes activates the glyoxalase system (122)
F Inhibition of AR Pumpkin polysaccharide Hydrogen bonds interact with residues on the enzyme side chains, and ionic bonds interact with the positively charged nicotinamide ring on the coenzyme (125)
Naringenin It binds to the NADPH binding site of AR to form a stable complex, and interacts with the key residues Trp20 and His 10 of AR to inhibit AR activity (126)
G Activation of the proteolytic system N. alba flower extract Removal and recycling of accumulated AGEs in the skin as an autophagy agonist (87)
H Regulation of AGE-RAGE signalling DNA aptamers Inhibits the binding of AGEs to RAGE and blocks AGE-RAGE signalling (131)
Resveratrol Significantly reduces RAGE expression by activating PPAR-γ and upregulates SR-A (132)
B. ceiba L. calyx Regulation of RAGE expression reduces oxidative stress (133)
Curcumin Inhibits ERK activity and upregulates PPAR-γ to induce AGE-R1 expression (136)
I Disrupt protein cross-links Chebulic acid (CA) Inhibit the cross-linking of AGEs with collagen and disrupts the collagen cross-linked structure (137)
Seaweed extract Fragmentation of AGEs and collagen cross-links (138)