TY - JOUR
T1 - Therapeutic potential of omega-3 fatty acids supplementation in a mouse model of dry macular degeneration
AU - Prokopiou, Ekatherine
AU - Kolovos, Panagiotis
AU - Kalogerou, Maria
AU - Neokleous, Anastasia
AU - Papagregoriou, Gregory
AU - Deltas, Constantinos
AU - Malas, Stavros
AU - Georgiou, Tassos
N1 - Publisher Copyright:
© 2017 Article author(s) (or their employer(s) unless otherwise stated in the text of the article). All rights reserved. No commercial use is permitted unless otherwise expresSly granted.
PY - 2017/6/1
Y1 - 2017/6/1
N2 - Purpose To evaluate the therapeutic effects of omega-3 (ω-3) and omega-6 (ω-6) fatty acids in the CCL2-/- model of dry age-related macular degeneration (AMD). The blood level of eicosapentaenoic acid (EPA) and arachidonic acid (AA) served to adjust the treatment dosage (AA/EPA=1-1.5). Methods Nine-month-old animals were allocated to different groups: (A) C57BL/6 untreated, (B) CCL2-/- untreated, (C) CCL2-/- treated with ω-3+ω-6, and (D) CCL2-/- treated with ω-3. Treatment was daily administered by gavage for 3 months. Fatty acids analysis was performed and retinas were histologically examined. Three-month-old wild type mice were used for comparison purposes. Real-time PCR and Western blot were performed for retinal inflammatory mediators. Results Increased EPA and decreased AA levels were observed in both blood and retinas in the treatment groups. The outer nuclear layer thickness was increased in groups C (45.0±3.9 μm) and D (62.8±4.9 μm), compared with groups B (65.6±3.0 μm) and A (71.1±4.2 μm), and in younger mice, it was 98.0±3.9 μm. A decrease in NF-κB expression was noted in the treatment groups. Interleukin (IL) 18 protein levels demonstrated a significant reduction in the ω-3-treated group only. Conclusion Supplementation with ω-3+ω-6 or ω-3 alone (AA/EPA=1-1.5) suggests a protective mechanism in the CCL2-/- animal model of dry AMD, with a more beneficial effect when ω-3 are used alone. Our findings indicated that inflammation is not the only determining factor; perhaps a regenerative process might be involved following administration of ω-3 fatty acids.
AB - Purpose To evaluate the therapeutic effects of omega-3 (ω-3) and omega-6 (ω-6) fatty acids in the CCL2-/- model of dry age-related macular degeneration (AMD). The blood level of eicosapentaenoic acid (EPA) and arachidonic acid (AA) served to adjust the treatment dosage (AA/EPA=1-1.5). Methods Nine-month-old animals were allocated to different groups: (A) C57BL/6 untreated, (B) CCL2-/- untreated, (C) CCL2-/- treated with ω-3+ω-6, and (D) CCL2-/- treated with ω-3. Treatment was daily administered by gavage for 3 months. Fatty acids analysis was performed and retinas were histologically examined. Three-month-old wild type mice were used for comparison purposes. Real-time PCR and Western blot were performed for retinal inflammatory mediators. Results Increased EPA and decreased AA levels were observed in both blood and retinas in the treatment groups. The outer nuclear layer thickness was increased in groups C (45.0±3.9 μm) and D (62.8±4.9 μm), compared with groups B (65.6±3.0 μm) and A (71.1±4.2 μm), and in younger mice, it was 98.0±3.9 μm. A decrease in NF-κB expression was noted in the treatment groups. Interleukin (IL) 18 protein levels demonstrated a significant reduction in the ω-3-treated group only. Conclusion Supplementation with ω-3+ω-6 or ω-3 alone (AA/EPA=1-1.5) suggests a protective mechanism in the CCL2-/- animal model of dry AMD, with a more beneficial effect when ω-3 are used alone. Our findings indicated that inflammation is not the only determining factor; perhaps a regenerative process might be involved following administration of ω-3 fatty acids.
KW - inflammation
KW - macular degeneration
KW - omega-3 fatty acids
KW - photoreceptors.
KW - retina
UR - https://www.scopus.com/pages/publications/85038367582
U2 - 10.1136/bmjophth-2016-000056
DO - 10.1136/bmjophth-2016-000056
M3 - Article
C2 - 29354704
AN - SCOPUS:85038367582
SN - 2397-3269
VL - 1
JO - BMJ Open Ophthalmology
JF - BMJ Open Ophthalmology
IS - 1
M1 - e000056
ER -