Pinealectomy-Induced Melatonin Deficiency Exerts Age-Specific Effects on Sphingolipid Turnover in Rats.

The existing body of literature, in conjunction with our recent studies, shows that melatonin dysfunction can accelerate the aging process, with this effect depending on the specific age of the subject. The present study aims to ascertain the impact of pinealectomy on sphingolipid (SL) turnover in young adult (3-month-old), middle-aged (14-month-old), and old (18-month-old) rats. Ceramide (Cer) levels, neutral (NSMase) and acid sphingomyelinase (ASMase), acid ceramidase (ASAH1), and sphingosine-1-phosphate (S1P) levels in hippocampus and/or plasma, were evaluated by enzyme-linked immunosorbent assay. The accumulation of Cer and its metabolite second messenger S1P in the hippocampus and plasma was associated with increased levels and activity of hippocampal NSMase in the hippocampus and plasma. However, no such association was observed for hippocampal ASMase, whose levels and activity were reduced in middle-aged and old rats compared to young adult rats. Pinealectomy-induced melatonin deficiency in young adult rats showed an increase in hippocampal Cer content compared to the sham group. However, in contrast to young adult rats, pinealectomy had an inverse effect on age-related changes in hippocampal Cer, NSMase, and ASMase in middle-aged rats. Furthermore, pinealectomy exacerbated the age-related increase in S1P in the hippocampus of 18-month-old rats. Collectively, the results of the present study suggest that melatonin deficiency may influence the aging process by modulating SL turnover in an age-specific manner.