Background: Lead had been known as a human health hazard for a long time. In particular, damages to brain and nervous system are the main issue in the lead toxicites. The goal of this study is to investigate the brain metabolism using a 3 T magnetic resonance spectroscopy (MRS) in a group of chronic lead-exposed workers in comparison with the matched non-exposed control group. Materials and Methods: The lead-exposed subjects were from a lead paint manufactory, total of 22 workers is included. They did not show any clinical syndromes. Eighteen age and sex matched non-exposed healthy people as control group were voluntarily participated. Blood samples were send to KMU hospital for blood lead concentrations and other biochemistry tests. Bone lead levels were measured by a KXRF equipment. A 3T MRS was used to measure their brain N-acetyl aspartate (NAA), Choline (Cho), and creatine (Cr) levels. In addition, a structural questionnaire was used to collect their working and health histories, as well as smoking, alcohol consumptions. Results: In comparisons of NAA/Cr, the frontal gray, subcortical, and white matters of Lead-exposed group had significantly lower NAA/Cr ratio, comparing to the non-exposed group. In the occipital lobe, only NAA/Cr ratio of white matter in the lead-exposed group was significant lower than those of non-exposed group. The NAA/Cr ratio of basal ganglions were also lower in the exposed group than those of non-exposed group. Similarly, in comparison of Cho/Cr ratio, the data of frontal gray, white matters in exposed group were lower than those of non-exposed. In occipital lobe, all the gray, subcortical, and white matters in the exposed group had lower Cho/Cr ratio than those of non-exposed ones. Discussion: The lead toxicity to human brain is complex, and not well recognized. However, this study found that brain metabolism, especially NAA/Cr and Cho/Cr, may be disturbed by lead. Brain NAA and choline were negative correlated to blood and bone lead levels, which may mean that lead may induce a neuronal and axonal damage or loss.