Abstract

Cells from neonatal rat cerebral hemispheres were disperesed by trypsin and cultured for 32 days. Histochemical, fluorescence, and electron microscopic analyses demonstrated that lipofucsion pigments increased in neuronal and non-neuronal cells in primary culture according to the lapse of time. When centrophenoxine (10 −4 or 5 × 10 −4 M) or chrolopromazine ((10 −6 or 10 −5 M) was added to the medium, the accumulation of lipofuscin pigments in neurons was significantly reduced. However, the effects of these agents were not detected in non-neuronal cells.

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