W. Pierpaoli et W. Regelson, PINEAL CONTROL OF AGING - EFFECT OF MELATONIN AND PINEAL GRAFTING ON AGING MICE, Proceedings of the National Academy of Sciences of the United Statesof America, 91(2), 1994, pp. 787-791
Dark-cycle, night administration of the pineal hormone melatonin in dr
inking water to aging mice (15 months of age) prolongs survival of BAL
B/c females from 23.8 to 28.1 months and preserves aspects of their yo
uthful state. Similar results were seen in New Zealand Black females b
eginning at 5 months and C57BL/6 males beginning at 19 months. As mela
tonin is produced in circadian fashion from the pineal, we grafted pin
eals from young 3- to 4-month-old donors into the thymus of 20-month o
ld syngeneic C57BL/6 male recipients, and a 12% increase in survival w
as induced. Prolongation of survival was also seen on pineal transplan
t to the thymus in C57BL/6, BALB/cJ, and hybrid female mice at 16, 19,
and 22 months. In all studies, the endogenous pineal of grafted mice
was left in situ. Pineal grafted aged mice display a remarkable mainte
nance of thymic structure and cellularity. Preservation of T-cell-medi
ated function, despite age, as measured by response to oxazolone is se
en. Other evidence suggests that melatonin and/or pineal-related facto
rs could produce their effects through an influence on thyroid functio
n. These data indicate that pineal influences have a place in the phys
iologic regulation of aging.