Research Article

Protective Effects and Possible Mechanisms of Ergothioneine and Hispidin against Methylglyoxal-Induced Injuries in Rat Pheochromocytoma Cells

Table 1

Effects of ergothioneine, hispidin, and ergothioneine + hispidin on production of advanced glycated end products and receptor for advanced glycated end products in PC12 cells induced by glucose + methylglyoxal.

TreatmentsAGE (ng/mL)RAGE (ng/mL)
72 hIP %396 hIP %72 hIP %96 hIP %

CON191 ± 10a4302 ± 13bc2.8 ± 0.5a11.4 ± 1.0a
Mannitol230 ± 6bc308 ± 10bc24.9 ± 1.2b24.1 ± 0.5c
GLU + MGO1294 ± 18d411 ± 11d32.0 ± 1.6c43.0 ± 1.1e
 +EPA235 ± 11bc20.07299 ± 9bc27.2532.6 ± 1.3c−1.8825.1 ± 0.6c41.63
 +AMG202 ± 9a31.29269 ± 8b34.5529.9 ± 1.0c6.5620.7 ± 1.7b51.86
 +EGT264 ± 14c10.20275 ± 8b33.0926.9 ± 1.2b15.9420.3 ± 0.7b52.79
 +HIP296 ± 14d−0.68296 ± 10bc27.9831.7 ± 2.4c0.9428.6 ± 0.9d33.49
 +(EGT + HIP)231 ± 10bc21.43233 ± 14a43.3124.5 ± 2.6b23.4422.9 ± 1.5bc46.74

1GLU + MGO: 30 mM glucose (GLU) and 30 μM methylglyoxal (MGO); EPA: epalrestat; AMG: aminoguanidine. 2PC12 cells were pretreated with EPA, AMG, ETG, HIP, and EGT + HIP for 2 h and incubated with GLU + MGO for 72 h and 96 h. 3. 4Values (means ± SD of triplicate tests) without a superscript letter are significantly different ().