Figure 1.

(A) Immunofluorescence of high molecular weight neurofilament in cerebral cortex, (B) immunofluorescence of high molecular weight. neurofilaments in corpus striatum, (C) immunofluorescence of high molecular weight neurofilaments in hippocampus (Male albino rats (Wistar strain) exposed to 10 mg/(kg bw day), aluminum for a period of 12 weeks, smears were prepared from the three neuronal regions studied earlier, that is, cerebral cortex, corpus striatum, and hippocampus. These were initially stained with antineurofilament anti body followed by staining with FITC‐labeled secondary antibody. The slides were then observed under a fluorescence microscope) Toxicology 219 (2006) 1–10.