We investigated the influence of the polyunsaturated docosahexaenoic acid (22:6n-3; DHA) on the constitutive expression of choline acetyltransferase (ChAT) in native and induced expression in differentiated cholinergic cells NG108-15 grown in serum-free medium. Elimination of serum-derived trophic support resulted in growth arrest and a strong decrease of ChAT activity. In either conditions, DHA largely rescued general indicators of cell growth and function, and partially prevented the decrease of ChAT activity. However, the maximal effect on general cell state in native and differentiated cells, and ChAT activity in native cells, was reached at or below 10 mumol/l of DHA. In contrast, maximal induction of ChAT activity in differentiated cells required about six times higher concentrations of DHA. These data thus demonstrate stimulatory effect of DHA on ChAT activity that is independent of its general cell protective properties.

• MeSH
• Cell Division drug effects   MeSH
• Cell Line MeSH
• Choline O-Acetyltransferase metabolism   MeSH
• Culture Media, Serum-Free MeSH
• Docosahexaenoic Acids pharmacology   MeSH
• Humans MeSH
• Oxidative Stress MeSH
• Check Tag
• Humans MeSH
• Publication type
• Journal Article MeSH
• Research Support, Non-U.S. Gov't MeSH
• Names of Substances
• Choline O-Acetyltransferase MeSH
• Culture Media, Serum-Free MeSH
• Docosahexaenoic Acids MeSH