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Current Aging Science

Editor-in-Chief

ISSN (Print): 1874-6098
ISSN (Online): 1874-6128

Research Article

Physiological and Biochemical Mechanisms of Lifespan Regulation in Rats Kept Under Various Light Conditions

Author(s): Evgeniy A. Khizhkin, Victor A. Ilukha, Irina A. Vinogradova, Lyudmila B. Uzenbaeva, Tatiana N. Ilyina, Victoria D. Yunash, Artem V. Morozov and Vladimir N. Anisimov

Volume 10, Issue 1, 2017

Page: [49 - 55] Pages: 7

DOI: 10.2174/1874609809666160921115550

Price: $65

Abstract

Background: The present study was aimed to identify how age-related changes in some physiological and biochemical systems are related to changes in the life span of rats with long-term pineal gland hypo- and hyperfunction induced by constant light and constant darkness, respectively.

Methods: At the age of 25 days the rats were randomly divided into 3 groups: standard light/dark regimen (LD), constant light (LL) and constant darkness (DD). Age-related Antioxidant System (AOS) changes in liver tissues, alteration of immunoreactivity in blood smears were investigated, pubescence and lifespan of the animals were determined.

Results: Modification of the level of melatonin synthesis induced by constant light results in interrelated rearrangements in the functioning of the investigated physiological systems. Elevated activity of the antioxidant system extends the lifespan, while at the same time slowing down pubescence and altering the morpho-functional properties of leukocytes in blood.

Conclusion: The absence of light/dark alternation (constant light and constant darkness) affects only those physiological indices that follow the organism’s circadian rhythms (Activity of Antioxidant Enzymes (AOE), levels of individual immune system cell types), whereas changes in the parameters not governed by circadian fluctuations (vitamin concentrations, pubescence, and aging) depend on the level of melatonin produced by the pineal gland.

Keywords: Antioxidant system, constant darkness, constant light, leucocytes, life span, melatonin, pineal gland, pubescence.

Graphical Abstract

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