The heavy metal bismuth induces a new type of selective neuronal degen
eration that shares some common aspects with that seen following hypox
ia and ischemia. Continuous application of 3 mu m bismuth to organotyp
ic cultures of rat hippocampus resulted after 2-3 weeks in selective d
egeneration of CA1 pyramidal cells, while CA3 pyramidal cells, dentate
granule cells, and subicular neurons were resistant. With 10 mu m bis
muth, the majority of hippocampal neurons degenerated. The addition of
20 mu m MK-801, a noncompetitive NMDA-antagonist, during the entire c
ulturing period failed to prevent neuronal degeneration induced by 3 m
u m bismuth. GABA-immunoreactive interneurons were also affected by bi
smuth, but were generally less sensitive than CA1 pyramidal cells. Acu
te application of up to 100 mu m bismuth did not change the electrophy
siological properties of CA1 pyramidal cells. (C) 1994 Wiley-Liss, Inc
.