Literature DB >> 18296092

Oxidative stress and expression of chaperones in aging mollusks.

Anna V Ivanina1, Inna M Sokolova, Alexey A Sukhotin.   

Abstract

The mechanisms of aging are not well understood in animals with continuous growth such as fish, reptiles, amphibians and numerous invertebrates, including mollusks. We studied the effects of age on oxidative stress, cellular defense mechanisms (including two major antioxidant enzymes, superoxide dismutase (SOD) and catalase), and molecular chaperones in two mollusks--eastern oysters Crassostrea virginica and hard clams Mercenaria mercenaria. In order to detect the age-related changes in these parameters, correction for the effects of size was performed where appropriate to account for growth-related dilution. Fluorescent age pigments accumulated with age in both species. Protein carbonyls did not change with age or size indicating that they are not a good marker of aging in mollusks possibly due to the fast turnover and degradation of oxidized proteins in growing tissues. SOD did not show a compensatory increase with aging in either species, while catalase significantly decreased with age. Mitochondrial heat shock protein (HSP60) decreased with age in mollusks suggesting an age-related decline in mitochondrial chaperone protection. In contrast, changes in cytosolic chaperones were species-specific. HSP70 increased and HSP90 declined with age in clams, whereas in oysters HSP70 expression did not change, and HSP90 increased with aging.

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Year:  2008        PMID: 18296092     DOI: 10.1016/j.cbpb.2008.01.005

Source DB:  PubMed          Journal:  Comp Biochem Physiol B Biochem Mol Biol        ISSN: 1096-4959            Impact factor:   2.231


  5 in total

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Journal:  Cell Stress Chaperones       Date:  2015-12-18       Impact factor: 3.667

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4.  Regulation of global protein translation and protein degradation in aerobic dormancy.

Authors:  Christopher J Ramnanan; Marcus E Allan; Amy G Groom; Kenneth B Storey
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5.  Proteomic analyses reveal that ginsenoside Rg3(S) partially reverses cellular senescence in human dermal fibroblasts by inducing peroxiredoxin.

Authors:  Ik-Soon Jang; Eunbi Jo; Soo Jung Park; Su Jeong Baek; In-Hu Hwang; Hyun Mi Kang; Je-Ho Lee; Joseph Kwon; Junik Son; Ho Jeong Kwon; Jong-Soon Choi
Journal:  J Ginseng Res       Date:  2018-08-13       Impact factor: 6.060

  5 in total

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