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  • Inhibitory effect of herbal medicines and their trapping abilities against methylglyoxal-derived advanced glycation end-products.

Inhibitory effect of herbal medicines and their trapping abilities against methylglyoxal-derived advanced glycation end-products.

BMC complementary and alternative medicine (2015-11-02)
Weerachat Sompong, Sirichai Adisakwattana
ABSTRACT

Methylglyoxal (MG) is one of the most reactive glycating agents, which result the formation of advanced glycation end-products (AGEs) that have been implicated in the progression of age-related diseases. Inhibition of MG-induced AGE formation is the imperative approach for alleviating diabetic complications. The objective of this study was to investigate the MG-trapping abilities of herbal medicines and their inhibitory activities on the formation of MG-derived AGEs. The aqueous extract of herbal medicines was measured for the content of total phenolic compounds and the antioxidant activity by Folin-Ciocalteu assay and the 1,1-diphenyl 2-picrylhydrazyl (DPPH) radical scavenging activity, respectively. The extracts were investigated the MG-trapping ability by high performance liquid chromatography (HPLC). The extracts were incubated with BSA and MG at 37 °C for 1 day. The formation of MG-derived AGEs was measured. Total phenolic compounds of eleven herbal medicines showed marked variations, ranging from 12.16 to 272.36 mg gallic acid equivalents/g extract. All extracts (1 mg/mL) markedly exhibited the DPPH radical scavenging activity (0.31-73.52%) and the MG-trapping abilities (13.97-58.97%). In addition, they also inhibited the formation of MG-derived AGEs by 4.01-79.98%. The results demonstrated that Rhinacanthus nasutus, Syzygium aromaticum, and Phyllanthus amarus were the potent inhibitors against the formation of MG-derived AGEs. The positive correlations between the contents of phenolics and % MG trapping (r = 0.912, p < 0.01) and % inhibition of MG-derived AGEs (r = 0.716, p < 0.01) were observed in the study. Furthermore, there was a moderate positive correlation between % MG trapping and % inhibition of MG-derived AGEs (r =0.584, p < 0.01). Rhinacanthus nasutus, Syzygium aromaticum, and Phyllanthus amarus could reduce the formation of MG-derived AGEs through their MG-trapping abilities. These findings are relevant for focusing on potential herbal medicines to prevent or ameliorate AGE-mediated diabetic complications.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
o-Phenylenediamine, Peroxidase substrate, ≥98.0%, powder
Sigma-Aldrich
o-Phenylenediamine, tablet, 20 mg substrate per tablet
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Pyruvaldehyde solution, 40 wt. % in H2O
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o-Phenylenediamine, flaked, 99.5%
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o-Phenylenediamine, sublimed, ≥99%
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2,2-Diphenyl-1-picrylhydrazyl
Sigma-Aldrich
Phenol, BioXtra, ≥99.5% (GC)
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Phenol solution, BioReagent, Equilibrated with 10 mM Tris HCl, pH 8.0, 1 mM EDTA, for molecular biology
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Phenol solution, BioReagent, Saturated with 0.01 M citrate buffer, pH 4.3 ± 0.2, for molecular biology
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Methylglyoxal solution, ~40% in H2O
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Phenol, puriss. p.a., ACS reagent, reag. Ph. Eur., 99.0-100.5%
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Phenol, ≥96.0% (calc. on dry substance, T)
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Phenol, puriss., meets analytical specification of Ph. Eur., BP, USP, 99.5-100.5% (GC)
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Phenol, unstabilized, purified by redistillation, ≥99%
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Phenol, unstabilized, ReagentPlus®, ≥99%
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5-Methylquinoxaline, 98%
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Phenol, ≥99%
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Phenol, BioUltra, for molecular biology, TE-saturated, ~73% (T)
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1,1-Diphenyl-2-picrylhydrazine, 97%
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Phenol, puriss., ≥99.5% (GC), meets analytical specification of Ph. Eur., BP, USP, crystalline (detached)
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Phenol, contains hypophosphorous as stabilizer, loose crystals, ACS reagent, ≥99.0%
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2-Methylquinoxaline, ≥97%
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Phenol, for molecular biology
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Gallic acid, 97.5-102.5% (titration)
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Liquified Phenol, ≥89.0%
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2-Methylquinoxaline, 97%
Supelco
Phenol solution, 5000 μg/mL in methanol, certified reference material
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5-Methylquinoxaline, ≥99%, FG
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