The addition of aluminum-maltol complex to PC12D cells induced a time-depen
dent and concentration-dependent growth inhibition as well as cell death, w
hereas aluminum chloride or maltol alone did not affect the viability of PC
12D cells. Apoptosis of differentiated PC12D cells was assessed by using te
rminal deoxynucleotidyltransferase-mediated 2'-deoxyuridine-5'-triphosphate
nick end labeling (TUNEL) technique to detect DNA strand breaks in situ. T
he number of TUNEL-positive cells treated with aluminum-maltol increased wi
th time in the treatment cultures. The ability of aluminum ion to elevate i
ntracellular reactive oxygen species was determined by fluorescence in PC12
D cells loaded with the oxidant-sensitive dye 2',7'-dichlorofluorescin diac
etate. Aluminum ion incorporated to PC12D cells causes apoptotic cell death
by enhancing the generation of reactive oxygen species.