Red palm oil supplementation does not increase blood glucose or serum lipids levels in Wistar rats with different thyroid status
Language English Country Czech Republic Media print-electronic
Document type Journal Article
PubMed
29303614
DOI
10.33549/physiolres.933834
PII: 933834
Knihovny.cz E-resources
- MeSH
- Glutathione metabolism MeSH
- Thyroid Hormones blood MeSH
- Hyperthyroidism metabolism MeSH
- Hypothyroidism metabolism MeSH
- Mitochondria, Liver drug effects metabolism MeSH
- Liver drug effects metabolism MeSH
- Blood Glucose metabolism MeSH
- Rats MeSH
- Kidney drug effects metabolism MeSH
- Lipids blood MeSH
- Palm Oil pharmacology MeSH
- Rats, Wistar MeSH
- Dietary Supplements * MeSH
- Thyroid Gland metabolism MeSH
- Body Weight drug effects MeSH
- Organ Size drug effects MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Glutathione MeSH
- Thyroid Hormones MeSH
- Blood Glucose MeSH
- Lipids MeSH
- Palm Oil MeSH
Red palm oil (RPO) is a rich natural source of antioxidant vitamins, namely carotenes, tocopherols and tocotrienols. However, it contains approximately 50 % saturated fatty acids the regular consumption of which could negatively modify lipid profile. The aim of our study was to test whether 7 weeks of RPO supplementation (1 g/kg body weight/day) would affect blood glucose and lipid metabolism in adult male Wistar rats with altered thyroid status. We induced hypothyroidism and hyperthyroidism in rats by oral administration of either methimazole or mixture of thyroid hormones. Different thyroid status (EU - euthyroid, HY - hypothyroid and HT - hyperthyroid) was characterized by different serum thyroid hormones levels (total and free thyroxine and triiodothyronine), changes in the activity of a marker enzyme of thyroid status - liver mitochondrial glycerol-3-phosphate dehydrogenase, and altered absolute and relative heart weights. Fasting blood glucose levels were higher in HT rats in comparison with EU and HY rats, but the changes caused by RPO supplementation were not significant. The achievement of the HY status significantly increased serum levels of total cholesterol, as well as with high-density lipoprotein-cholesterol and low-density lipoprotein-cholesterol: 2.43+/-0.15, 1.48+/-0.09, 0.89+/-0.08 mmol/l, compared to EU: 1.14+/-0.06, 0.77+/-0.06, 0.34+/-0.05 mmol/l and HT: 1.01+/-0.06, 0.69+/-0.04, 0.20+/-0.03 mmol/l, respectively. RPO supplementation did not increase significantly levels of blood lipids but tended to increase glutathione levels in the liver. In conclusion, RPO supplementation did not induce the presumed deterioration of glucose and lipid metabolism in rats with three well-characterized alterations in thyroid status.
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