January 1994
Volume 35, Issue 1
Articles  |   January 1994
Effect of dietary fish oil on acute light-induced photoreceptor damage in the rat retina.
Author Affiliations
  • C E Remé
    University Eye Clinic, Zürich, Switzerland.
  • A Malnoë
    University Eye Clinic, Zürich, Switzerland.
  • H H Jung
    University Eye Clinic, Zürich, Switzerland.
  • Q Wei
    University Eye Clinic, Zürich, Switzerland.
  • K Munz
    University Eye Clinic, Zürich, Switzerland.
Investigative Ophthalmology & Visual Science January 1994, Vol.35, 78-90. doi:
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      C E Remé, A Malnoë, H H Jung, Q Wei, K Munz; Effect of dietary fish oil on acute light-induced photoreceptor damage in the rat retina.. Invest. Ophthalmol. Vis. Sci. 1994;35(1):78-90.

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      © ARVO (1962-2015); The Authors (2016-present)

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PURPOSE: Previous studies have shown that ingestion of fish oil (FO) containing a high proportion of n-3 polyunsaturated fatty acids increases the susceptibility of cellular membranes to oxidative damage in various tissues. In the retina, lipid peroxidation is thought to be a major mechanism contributing to light-induced lesions. Therefore, we investigated the effect of FO on acute light-induced photoreceptor damage. METHODS: For 2 months, weanling rats were fed diets containing either soybean oil (SOY) or FO as main lipid component. RESULTS: Rats fed FO had significantly higher levels of eicosapentaenoic acid (EPA, 20:5n-3) and higher ratios of EPA to arachidonic acid (AA, 20:4n-6) in retinal phospholipids and diacylglycerols than rats fed SOY. The levels of docosahexaenoic acid (DHA, 22:6n-3) were similar in both dietary groups. The susceptibility to lipid peroxidation was enhanced in the isolated retina of FO-fed rats as shown by higher levels of thiobarbituric acid reactive substances after incubation of retinal membranes with Fe2+/ascorbate. The retinal content of alpha-tocopherol was similar in SOY- and FO-fed animals. Light damage consisting of acute rod outer segment (ROS) disruptions was induced by exposing dark-adapted animals to 600 to 700 lux (230 to 260 microW/cm2) of white fluorescent light for 30 minutes. Damage was quantitated using a computerized multifunctional image analysis of retinal thin sections. Although structural alterations of the ROS were present in both groups, FO-fed rats showed less damage at the base of the ROS. This occurred in spite of higher rhodopsin levels in FO-fed rats. There was no effect of diet on retinal morphology in dark-adapted rats. CONCLUSION: These results indicate that FO does not enhance the susceptibility to acute ROS disk disruptions in the rat retina. Our study further suggests that FO exerts a partial protective effect that may be related to changes in the formation of lipid mediators derived from EPA and AA in retinal phospholipids.


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