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1.
Biol Pharm Bull ; 37(6): 1003-13, 2014.
Article in English | MEDLINE | ID: mdl-24882411

ABSTRACT

We investigated whether body temperature (BT) regulatory mechanisms are influenced by dietary fatty acids (FA). Male Wistar rats were fed a high-fat diet containing fish oil (HFD), soybean oil (HSD) or lard (HLD). At the 20-week intervention, the BT of the HSD and HLD groups were lower than that of the normal diet (ND) group in the light and dark periods. The intracerebroventricular injections of interleukin-1ß and bombesin in the HSD group induced greater hyperthermia and weaker hypothermia, respectively, than in the ND group. The HSD differentially affected BT under both physiological and pharmacological conditions. In the hypothalamus, the ratio of n-6/n-3 FAs was higher in the HSD group compared with the ND group. DNA microarrays revealed increased expression of thyroid-stimulating hormone ß-subunit, and decreased expression of several genes in the hypothalamus of the HSD group compared with the ND group. The HSD feeding increased several adipokine concentrations in the plasma. However, there were no adipokines or gene expressions that changed in only the HSD and HLD groups showing significant hypothermia under the physiological condition. These findings suggested that long-term HSD intake produces abnormal BT regulation. It is less likely that adipokines or proteins/peptides are involved in abnormal BT regulation under the physiological conditions after HSD feeding.


Subject(s)
Body Temperature Regulation/drug effects , Diet, High-Fat , Soybean Oil/pharmacology , Adipokines/blood , Animals , Body Temperature/drug effects , Body Temperature Regulation/genetics , Body Weight/drug effects , Bombesin/pharmacology , Dietary Fats/administration & dosage , Dietary Fats/pharmacology , Energy Metabolism/drug effects , Fatty Acids/blood , Fatty Acids/metabolism , Fish Oils/administration & dosage , Fish Oils/pharmacology , Gene Expression/drug effects , Hypothalamus/drug effects , Hypothalamus/metabolism , Interleukin-1beta/pharmacology , Male , Motor Activity/drug effects , Photoperiod , Rats, Wistar , Soybean Oil/administration & dosage , Time Factors
2.
Lipids ; 48(8): 803-15, 2013 Aug.
Article in English | MEDLINE | ID: mdl-23807365

ABSTRACT

Epidemiologic and ecologic studies suggest that dietary fat plays an important role in the development of obesity. Certain Wistar rat strains do not become obese when fed high-fat diets unlike others. In a preliminary study, we confirmed that Slc:Wistar/ST rats did not become obese when fed high-fat diets. The mechanisms governing the response of hepatic lipid-metabolizing enzymes to large quantities of dietary lipids consumed by obesity-resistant animals are unknown. The aim of the present study is to examine how obesity-resistant animals metabolize various types of high-fat diets and why they do not become obese. For this purpose, male Slc:Wistar/ST rats were fed a control low-fat diet (LS) or a high-fat diet containing fish oil (HF), soybean oil (HS), or lard (HL) for 4 weeks. We observed their phenotypes and determined lipid profiles in plasma and liver as well as mRNA expression levels in liver of genes related to lipid and glucose metabolism using DNA microarray and quantitative reverse transcriptase polymerase chain analyses. The body weights of all dietary groups were similar due to isocaloric intakes, whereas the weight of white adipose tissues in the LS group was significantly lower. The HF diet lowered plasma lipid levels by accelerated lipolysis in the peroxisomes and suppressed levels of very-low-density lipoprotein (VLDL) secretion. The HS diet promoted hepatic lipid accumulation by suppressed lipolysis in the peroxisomes and normal levels of VLDL secretion. The lipid profiles of rats fed the LS or HL diet were similar. The HL diet accelerated lipid and glucose metabolism.


Subject(s)
Diet, High-Fat/adverse effects , Glucose/metabolism , Lipid Metabolism/drug effects , Adipose Tissue, White/drug effects , Animals , Body Weight/drug effects , Dietary Fats/analysis , Dietary Fats/metabolism , Dietary Fats/pharmacokinetics , Dietary Fats/pharmacology , Eating/drug effects , Energy Intake/drug effects , Fatty Acids/analysis , Fatty Acids/chemistry , Fish Oils/analysis , Fish Oils/pharmacology , Gene Expression Regulation/drug effects , Lipid Metabolism/genetics , Lipoproteins, VLDL/metabolism , Liver/drug effects , Liver/metabolism , Liver/physiology , Male , Obesity/metabolism , Rats , Rats, Wistar , Soybean Oil/analysis , Soybean Oil/pharmacology
3.
J Agric Food Chem ; 55(17): 7170-6, 2007 Aug 22.
Article in English | MEDLINE | ID: mdl-17661494

ABSTRACT

Recent reports have shown that dietary phosphatidylcholine (PC) has various beneficial biological effects. Omega 3 polyunsaturated fatty acids (omega3 PUFAs) have also been reported to have lipid-lowering effects in animal models and human studies. In the present study, we investigated the effect of omega3 PUFAs containing PC (omega3-PC) on obesity-related disorders in Otsuka Long-Evans Tokushima fatty (OLETF) rats. Rats were fed semisynthetic diets that contained either 5% corn oil and 2% egg-PC or 5% corn oil and 2% omega3-PC for 4 weeks. During this 4 week feeding of the omega3-PC, the OLEFT rats showed a decrease of omental white adipose tissue weight. In addition, the omega3-PC diet significantly decreased liver weight and hepatic lipid levels in OLETF rats. These changes were attributable to the significant suppression of fatty acid synthase activity and significant enhancement in the activities of carnitine palmitoyltransferase and peroxisomal beta-oxidation. Moreover, the omega3-PC diet reduced serum glucose levels concomitant with the increase of serum adiponectin levels. These results show that compared with egg-PC, omega3-PC can prevent or alleviate obesity-related disorders through the suppression of fatty acid synthesis, enhancement of fatty acid beta-oxidation, and increase of the serum adiponectin level in OLETF rats.


Subject(s)
Diet , Fatty Acids, Omega-3/administration & dosage , Obesity/complications , Phosphatidylcholines/administration & dosage , Adipose Tissue , Animals , Lipid Metabolism/genetics , Lipids/analysis , Liver/chemistry , Liver/enzymology , Male , Organ Size , RNA, Messenger/analysis , Rats , Rats, Inbred OLETF
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