Melatonin as antioxidant, geroprotector and anticarcinogen
(2006) In Biochimica et Biophysica Acta - Bioenergetics 1757(5-6). p.573-589- Abstract
- The effect of the pineal indole hormone melatonin on the life span of mice, rats and fruit flies has been studied using various approaches. It has been observed that in female CBA, SHR, SAM and transgenic HER-2/neu mice long-term administration of melatonin was followed by an increase in the mean life span. In rats, melatonin treatment increased survival of male and female rats. In D. melanogaster, supplementation of melatonin to nutrient medium during developmental stages produced contradictory results, but and increase in the longevity of fruit flies has been observed when melatonin was added to food throughout the life span. In mice and rats, melatonin is a potent antioxidant both in vitro and in vivo. Melatonin alone turned out neither... (More)
- The effect of the pineal indole hormone melatonin on the life span of mice, rats and fruit flies has been studied using various approaches. It has been observed that in female CBA, SHR, SAM and transgenic HER-2/neu mice long-term administration of melatonin was followed by an increase in the mean life span. In rats, melatonin treatment increased survival of male and female rats. In D. melanogaster, supplementation of melatonin to nutrient medium during developmental stages produced contradictory results, but and increase in the longevity of fruit flies has been observed when melatonin was added to food throughout the life span. In mice and rats, melatonin is a potent antioxidant both in vitro and in vivo. Melatonin alone turned out neither toxic nor mutagenic in the Ames test and revealed clastogenic activity at high concentration in the COMET assay. Melatonin has inhibited mutagenesis and clastogenic effect of a number of indirect chemical mutagens. Melatonin inhibits the development of spontaneous and 7-12-dimethlbenz(a)anthracene (DMBA)- or N-nitrosomethylurea-induced mammary carcinogenesis in rodents; colon carcinogenesis induced by 1,2-dimethylhydrazine in rats, N-diethyl nitrosamine-induced hepatocarcinogenesis in rats, DMBA-induced carcinogenesis of the uterine cervix and vagina in mice; benzo(a)pyrene-induced soft tissue carcinogenesis and lung carcinogenesis induced by urethan in mice. To identify molecular events regulated by melatonin, gene expression profiles were studied in the heart and brain of melatonin-treated CBA mice using cDNA gene expression arrays (15,247 and 16,897 cDNA clone sets, respectively). It was shown that genes controlling the cell cycle, cell/organism defense, protein expression and transport are the primary effectors for melatonin. Melatonin also increased the expression of some mitochondrial genes (16S, cytochrome c oxidases I and 3 (COX I and COX3), and NADH dehydrogenases I and 4 (ND1 and ND4)), which agrees with its ability to inhibit free radical processes. Of great interest is the effect of melatonin upon the expression of a large number of genes related to calcium exchange, such as Cu15, Dcamk11 and Kcnn4; a significant effect of melatonin on the expression of some oncogenesis-related genes was also detected. Thus, we believe that melatonin may be used for the prevention of premature aging and carcinogenesis. (c) 2006 Elsevier B.V. All rights reserved. (Less)
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https://lup.lub.lu.se/record/399231
- author
- Anisimov, Vladimir N. ; Popovich, Irina G. ; Zabezhinski, Mark A. ; Anisimov, Sergey LU ; Vesnushkin, Georgy M. and Vinogradova, Irina A.
- organization
- publishing date
- 2006
- type
- Contribution to journal
- publication status
- published
- subject
- keywords
- mouse, fruit fly, rat, tumorigenesis, longevity, life span, mutagenesis, gene activity, melatonin, free radicals
- in
- Biochimica et Biophysica Acta - Bioenergetics
- volume
- 1757
- issue
- 5-6
- pages
- 573 - 589
- publisher
- Elsevier
- external identifiers
-
- wos:000239481800037
- scopus:33745610430
- ISSN
- 0005-2728
- DOI
- 10.1016/j.bbabio.2006.03.012
- language
- English
- LU publication?
- yes
- additional info
- The information about affiliations in this record was updated in December 2015. The record was previously connected to the following departments: Neuronal Survival (013212041)
- id
- f1c2c0e0-d245-4c48-9f4a-9290390c6f6e (old id 399231)
- date added to LUP
- 2016-04-01 15:17:15
- date last changed
- 2022-04-14 21:24:42
@article{f1c2c0e0-d245-4c48-9f4a-9290390c6f6e,
abstract = {{The effect of the pineal indole hormone melatonin on the life span of mice, rats and fruit flies has been studied using various approaches. It has been observed that in female CBA, SHR, SAM and transgenic HER-2/neu mice long-term administration of melatonin was followed by an increase in the mean life span. In rats, melatonin treatment increased survival of male and female rats. In D. melanogaster, supplementation of melatonin to nutrient medium during developmental stages produced contradictory results, but and increase in the longevity of fruit flies has been observed when melatonin was added to food throughout the life span. In mice and rats, melatonin is a potent antioxidant both in vitro and in vivo. Melatonin alone turned out neither toxic nor mutagenic in the Ames test and revealed clastogenic activity at high concentration in the COMET assay. Melatonin has inhibited mutagenesis and clastogenic effect of a number of indirect chemical mutagens. Melatonin inhibits the development of spontaneous and 7-12-dimethlbenz(a)anthracene (DMBA)- or N-nitrosomethylurea-induced mammary carcinogenesis in rodents; colon carcinogenesis induced by 1,2-dimethylhydrazine in rats, N-diethyl nitrosamine-induced hepatocarcinogenesis in rats, DMBA-induced carcinogenesis of the uterine cervix and vagina in mice; benzo(a)pyrene-induced soft tissue carcinogenesis and lung carcinogenesis induced by urethan in mice. To identify molecular events regulated by melatonin, gene expression profiles were studied in the heart and brain of melatonin-treated CBA mice using cDNA gene expression arrays (15,247 and 16,897 cDNA clone sets, respectively). It was shown that genes controlling the cell cycle, cell/organism defense, protein expression and transport are the primary effectors for melatonin. Melatonin also increased the expression of some mitochondrial genes (16S, cytochrome c oxidases I and 3 (COX I and COX3), and NADH dehydrogenases I and 4 (ND1 and ND4)), which agrees with its ability to inhibit free radical processes. Of great interest is the effect of melatonin upon the expression of a large number of genes related to calcium exchange, such as Cu15, Dcamk11 and Kcnn4; a significant effect of melatonin on the expression of some oncogenesis-related genes was also detected. Thus, we believe that melatonin may be used for the prevention of premature aging and carcinogenesis. (c) 2006 Elsevier B.V. All rights reserved.}},
author = {{Anisimov, Vladimir N. and Popovich, Irina G. and Zabezhinski, Mark A. and Anisimov, Sergey and Vesnushkin, Georgy M. and Vinogradova, Irina A.}},
issn = {{0005-2728}},
keywords = {{mouse; fruit fly; rat; tumorigenesis; longevity; life span; mutagenesis; gene activity; melatonin; free radicals}},
language = {{eng}},
number = {{5-6}},
pages = {{573--589}},
publisher = {{Elsevier}},
series = {{Biochimica et Biophysica Acta - Bioenergetics}},
title = {{Melatonin as antioxidant, geroprotector and anticarcinogen}},
url = {{http://dx.doi.org/10.1016/j.bbabio.2006.03.012}},
doi = {{10.1016/j.bbabio.2006.03.012}},
volume = {{1757}},
year = {{2006}},
}