Retinal metabolic events in preconditioning light stress as revealed by wide-spectrum targeted metabolomics.
Retinal metabolic events in preconditioning light stress as revealed by wide-spectrum targeted metabolomics.
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DOI：
10.1007/s11306-016-1156-9
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发表时间：
2017
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影响因子：
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通讯作者：
Valter K
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文献类型：
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作者：
de la Barca JMC;Huang NT;Jiao H;Tessier L;Gadras C;Simard G;Natoli R;Tcherkez G;Reynier P;Valter K
Light is the primary stimulus for vision, but may also cause damage to the retina. Pre-exposing the retina to sub-lethal amount of light (or preconditioning) improves chances for retinal cells to survive acute damaging light stress. This study aims at exploring the changes in retinal metabolome after mild light stress and identifying mechanisms that may be involved in preconditioning. Retinas from 12 rats exposed to mild light stress (1000 lux × for 12 h) and 12 controls were collected one and seven days after light stress (LS). One retina was used for targeted metabolomics analysis using the Biocrates p180 kit while the fellow retina was used for histological and immunohistochemistry analysis. Immunohistochemistry confirmed that in this experiment, a mild LS with retinal immune response and minimal photoreceptor loss occurred. Compared to controls, LS induced an increased concentration in phosphatidylcholines. The concentration in some amino acids and biogenic amines, particularly those related to the nitric oxide pathway (like asymmetric dimethylarginine (ADMA), arginine and citrulline) also increased 1 day after LS. 7 days after LS, the concentration in two sphingomyelins and phenylethylamine was found to be higher. We further found that in controls, retina metabolome was different between males and females: male retinas had an increased concentration in tyrosine, acetyl-ornithine, phosphatidylcholines and (acyl)-carnitines. Besides retinal sexual metabolic dimorphism, this study shows that preconditioning is mostly associated with re-organisation of lipid metabolism and changes in amino acid composition, likely reflecting the involvement of arginine-dependent NO signalling. The online version of this article (doi:10.1007/s11306-016-1156-9) contains supplementary material, which is available to authorized users.
