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Abstract Supplements play a pivotal role in medicine especially fish consumption or supplementation with omega 3. Omega-3 and thyroid hormones are important in keeping some essential body functions working normally and alterations of thyroid hormones levels can result in many pathological states. Our study aimed to investigate whether omega-3 supplementation (1000 mg/day for 2 months given orally) would affect thyroid hormones and thyroid-stimulating hormone in healthy volunteers with normal thyroid status. Normal thyroid status of the experimental group was well defined by serum levels of triiodothyronine (T3), thyroxine (T4), and by thyroid-stimulating hormone. Thyroid hormones (T3 and T4) levels were increased insignificantly in treated volunteers compared to the same volunteers before consumption of omega-3 (2.20 ± 0.37 to 2.23 ± 0.39 and 89.87 ± 9.93 to 90.98 ± 11.85 nmol/L, respectively). On the other hand, thyroid-stimulating hormone significantly increased after 2 months of omega-3 consumption (1.46 ± 0.47 to 1.68 ± 0.39 μIu/L). In conclusion, supplementation of omega-3 in the present study did not significantly modify either T3 or T4 and bodyweight in healthy volunteers. These data reinforce recommendations that indicate consumption of omega-3 is considered safe as far as thyroid function is concerned in healthy human volunteers. These findings advocate continued investigation of omega-3 for more than 2 months and higher dose to confirm its safety. Keywords: Omega-3, thyroid stimulating hormone, triiodothyronine, thyroxine
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Developmental iodine deficiency (ID) leads to inadequate thyroid hormone that impairs learning and memory with an unclear mechanism. Here, we show that hippocampal neurogranin, calcium/calmodulin dependent protein kinase II (CaMKII), calmodulin (CaM) and calcineurin (CaN) are implicated in the brain impairment in lactational rat hippocampus following developmental ID and hypothyroidism. Three developmental rat models were created by administrating dam rats with either iodine-deficient diet or propylthiouracil (PTU, 5 ppm or 15 ppm)-added drinking water from gestational day (GD) 6 till postnatal day (PN) 21. Then, the neurogranin, CaMKII, CaM and CaN in the hippocampus were detected with immunohistochemistry and western blotting on PN14 and PN21. The iodine-deficient and hypothyroid pups showed significantly lower level of neurogranin, CaMKII and CaM and significantly increased CaN in hippocampal CA1 and CA3 regions than the controls on PN14 and PN21 (P<0.05, respectively). Data indicate that, in lactational rats, hippocampal neurogranin, CaMKII, CaM and CaN are involved in the brain impairment by developmental ID and hypothyroidism.
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Much evidence shows that the marine omega-3 fatty acids eicosapentaenoic acid and docosahexaenoic acid have beneficial effects in various cardiac disorders, and their use is recommended in guidelines for management of patients after myocardial infarction. However, questions have been raised about their usefulness alongside optimum medical therapies with agents proven to reduce risk of cardiac events in high-risk patients. Additionally, there is some evidence for a possible pro-arrhythmic effect in subsets of cardiac patients. Some uncertainly exists about the optimum dose needed to obtain beneficial effects and the relative merit of dietary intake of omega-3 polyunsaturated fatty acids versus supplements. We review evidence for the effects of omega-3 polyunsaturated fatty acids on various cardiac disorders and the risk factors for cardiac disease. We also assess areas of uncertainty needing further research.
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n-3 polyunsaturated fatty acids (PUFAs) present in fish oil (FO) potently decrease serum lipids, which is also an effect of thyroid hormones. Both PUFAs and thyroid hormones affect hepatic lipid metabolism, and here we hypothesized that a long-term diet rich in n-3 PUFAs would enhance thyroid hormone action in the liver. Female rats received isocaloric and normolipid diets containing either soybean oil (SO) or FO during lactation. Male offspring received the same diet as their dams since weaning until sacrifice when they were 11 weeks old. FO group, as compared to SO group, exhibited lower body weight since 5 weeks of age until sacrifice, with no alterations in food ingestion, lower retroperitoneal white fat mass and elevated inguinal fat mass relative to body weight, with unchanged water and lipid but reduced protein percentage in their carcasses. FO diet resulted in lower serum triglycerides and cholesterol. Serum total triiodothyronine, total thyroxine and thyrotropin were similar between groups. However, liver thyroid hormone receptor (TR) β1 protein expression was higher in the FO group and correlated negatively with serum lipids. Liver 5'-deiodinase activity, which converts thyroxine into triiodothyronine, was similar between groups. However, the activity of hepatic mitochondrial glycerophosphate dehydrogenase, the enzyme involved in thermogenesis and a well-characterized target stimulated by T3 via TRβ1, was higher in the FO group, suggesting enhancement of thyroid hormone action. These findings suggest that the increase in thyroid hormone signaling pathways in the liver may be one of the mechanisms by which n-3 PUFAs exert part of their effects on lipid metabolism.