Premium
Supplemental melatonin increases clonal lifespan in the protozoan Paramecium tetraurelia
Author(s) -
Thomas John N.,
SmithSonneborn Joan
Publication year - 1997
Publication title -
journal of pineal research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.881
H-Index - 131
eISSN - 1600-079X
pISSN - 0742-3098
DOI - 10.1111/j.1600-079x.1997.tb00344.x
Subject(s) - melatonin , biology , paramecium , incubation , protozoa , longevity , andrology , endocrinology , genetics , microbiology and biotechnology , biochemistry , medicine
Thomas JN, Smith‐Sonneborn J. Supplemental melatonin increases clonal lifespan in the protozoan Paramecium tetraurelia . J. Pineal Res. 1997; 23:123–130. © Munksgaard, Copenhagen Abstract The hypothesis that melatonin supplementation can increase the lifespan of a single‐celled organism was tested by the administration of melatonin to the ciliated protozoan Paramecium tetraurelia . Melatonin supplementation in dim red light at a dose of 0.043 mM (10 mg/L) of nutrient media (bacterized Cerophyl) per day, followed by incubation for 23 hr in darkness, increased the mean clonal lifespan of Paramecium tetraurelia in days by percentages ranging from 20.8% ( P < 0.01, two‐tailed t‐test) to 24.2% ( P < 0.01, ANOVA) over controls. Maximum clonal lifespan in days was also increased in melatonin‐supplemented cells, from 14.8% to 24.0% over controls. Mean clonal lifespan in fissions was not significantly greater in melatonin‐supplemented cells, with values ranging from 6.0% to 15.5% over controls. Maximum clonal lifespan in fissions did not differ appreciably, with values ranging from 1.0% to 9.1 % over controls, except in the case of cells selected for rapid division rates, in which melatonin‐supplemented cells (393 fissions) lived 20.9% longer than controls (325 fissions) in terms of cumulative cell doublings during the clonal lifespan. The finding that melatonin supplementation increased clonal lifespan in Paramecium tetraurelia , an aerobic, single‐celled organism, suggests that the mechanism of melatonin's longevity‐promoting effects may be intracellular.