Meta-analysis indicates that oxidative stress is both a constraint on and a cost of growth

被引:92
作者
Smith, Shona M. [1 ]
Nager, Ruedi G. [1 ]
Costantini, David [1 ,2 ]
机构
[1] Univ Glasgow, Inst Biodivers Anim Hlth & Comparat Med, Graham Kerr Bldg, Glasgow G12 8QQ, Lanark, Scotland
[2] Univ Antwerp, Dept Biol, B-2610 Antwerp, Belgium
来源
ECOLOGY AND EVOLUTION | 2016年 / 6卷 / 09期
基金
英国自然环境研究理事会;
关键词
Antioxidants; enzymes; growth rate; life-history theory; oxidative damage; reactive oxygen species; trade-offs; OXYGEN SPECIES PRODUCTION; TRANSGENIC COHO SALMON; CATCH-UP GROWTH; ANTIOXIDANT CAPACITY; LIPID-PEROXIDATION; METABOLIC-RATE; SHORT-TERM; LIFE-SPAN; DAMAGE; EVOLUTION;
D O I
10.1002/ece3.2080
中图分类号
Q14 [生态学(生物生态学)];
学科分类号
071012 ; 0713 ;
摘要
Oxidative stress (OS) as a proximate mechanism for life-history trade-offs is widespread in the literature. One such resource allocation trade-off involves growth rate, and theory suggests that OS might act as both a constraint on and a cost of growth, yet studies investigating this have produced conflicting results. Here, we use meta-analysis to investigate whether increased OS levels impact on growth (OS as a constraint on growth) and whether greater growth rates can increase OS (OS as a cost of growth). The role of OS as a constraint on growth was supported by the meta-analysis. Greater OS, in terms of either increased damage or reduced levels of antioxidants, was associated with reduced growth although the effect depended on the experimental manipulation used. Our results also support an oxidative cost of growth, at least in terms of increased oxidative damage, although faster growth was not associated with a change in antioxidant levels. These findings that OS can act as a constraint on growth support theoretical links between OS and animal life histories and provide evidence for a growth-self-maintenance trade-off. Furthermore, the apparent oxidative costs of growth imply individuals cannot alter this trade-off when faced with enhanced growth. We offer a starting platform for future research and recommend the use of oxidative damage biomarkers in nonlethal tissue to investigate the growth-OS relationship further.
引用
收藏
页码:2833 / 2842
页数:10
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