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1.
Nutrients ; 14(1)2022 Jan 03.
Article in English | MEDLINE | ID: mdl-35011083

ABSTRACT

Obesity is a major health problem that is caused by body fat accumulation and that can lead to metabolic diseases. Owing to several side effects of the currently used antiobesity drugs, natural plants have risen as safe and potential candidates to alleviate obesity. We have previously reported the antiobesity effect of Hydrangea serrata (Thunb.) Ser. leaves extract (WHS) and its underlying mechanisms. As an extension of our preclinical studies, this study aimed to investigate the effect of WHS on body weight and body fat reduction in overweight or obese humans. A total of 93 healthy overweight or obese males and females, aged 19-65 years, with body mass indexes (BMIs) ≥ 25 and <32 kg/m2, were recruited and received either an oral administration of 600 mg of WHS, or placebo tablets for 12 weeks. Daily supplementation with WHS decreased body weights, body fat masses, and BMIs compared with the placebo-treated group. The hip circumferences, visceral fat areas, abdominal fat areas, and visceral-to-subcutaneous ratios decreased after WHS supplementation. No significant side effects were observed during or after the 12 weeks of WHS intake. In conclusion, WHS, which has beneficial effects on body weight and body fat reduction, could be a promising antiobesity supplement that does not produce any side effects.


Subject(s)
Adipose Tissue/drug effects , Body Weight/drug effects , Hydrangea/chemistry , Overweight/drug therapy , Plant Extracts/administration & dosage , Plant Leaves/chemistry , Abdominal Fat/drug effects , Adult , Aged , Anti-Obesity Agents , Body Composition/drug effects , Body Mass Index , Double-Blind Method , Humans , Intra-Abdominal Fat/drug effects , Male , Middle Aged , Obesity/drug therapy , Obesity/physiopathology , Overweight/physiopathology , Placebos
2.
Mar Drugs ; 19(5)2021 May 11.
Article in English | MEDLINE | ID: mdl-34064922

ABSTRACT

Metabolic syndrome-related diseases affect millions of people worldwide. It is well established that changes in nutritional habits and lifestyle can improve or prevent metabolic-related pathologies such as type-2 diabetes and obesity. Previous reports have shown that nutritional supplements have the capacity to limit glucose intolerance and suppress diabetes development. In this study, we investigated the effect of dietary supplementation with fish-derived extracts on obesity and type 2 diabetes and their impact on gut microbial composition. We showed that nutritional supplements containing Fish Complex (FC), Fish Complex combined with Cod Powder (FC + CP), or Cod Powder combined with Collagen (CP + C) improved glucose intolerance, independent of abdominal fat accumulation, in a mouse model of diet-induced obesity and type 2 diabetes. In addition, collagen-containing supplements distinctly modulate the gut microbiome in high-fat induced obesity in mice. Our results suggest that fish-derived supplements suppress diet-induced type 2 diabetes, which may be partly mediated through changes in the gut microbiome. Thus, fish-derived supplements and particularly the ones containing fish collagen have potential beneficial properties as dietary supplements in managing type 2 diabetes and metabolic syndrome via modulation of the gut microbiome.


Subject(s)
Diabetes Mellitus, Type 2/drug therapy , Dietary Supplements , Fishes , Gastrointestinal Microbiome/drug effects , Hypoglycemic Agents/pharmacology , Obesity , Tissue Extracts/pharmacology , Abdominal Fat/drug effects , Animals , Body Weight/drug effects , Diabetes Mellitus, Type 2/chemically induced , Diabetes Mellitus, Type 2/complications , Diet, High-Fat/adverse effects , Dietary Supplements/microbiology , Disease Models, Animal , Female , Glucose Intolerance/drug therapy , Hypoglycemic Agents/therapeutic use , Insulin Resistance , Leptin/metabolism , Mice, Inbred C57BL , Obesity/chemically induced , Obesity/complications , Tissue Extracts/isolation & purification , Tissue Extracts/therapeutic use
3.
Int J Biochem Cell Biol ; 133: 105932, 2021 04.
Article in English | MEDLINE | ID: mdl-33529717

ABSTRACT

OBJECTIVE: Obesity is now a worldwide disease and is mainly attributable to increased body fat deposition. In a growing number of epidemiological studies, lutein has been revealed to have different degrees of anti-obesity properties, but the potential underlying mechanisms that have been reported are limited. Therefore, we aimed to clarify the protective effects of lutein against excessive lipid accumulation, and we explored the role of SIRT1 and SIRT1-mediated pathways both in abdominal adipose tissue and mature 3T3-L1 cells during lutein administration. METHODS: In our design, male Sprague-Dawley rats were fed either control or high-fat diets with or without 25 mg/kg·bw/day lutein for 5 weeks. Additionally, differentiated 3T3-L1 cells were incubated with 40 µM lutein or 10 µM Ex527 for 24 h. RESULTS: Lutein supplementation decreased the body weight, abdominal fat index ratio, frequency and mean area of larger adipocytes in HE staining induced by the high-fat diet and then activated the expression of SIRT1 and thus upregulated FoxO1, ATGL, and HSL expression and downregulated SREBP-1, FAS, and ACC expression both in abdominal adipose tissue and differentiated 3T3-L1 cells. However, coincubation with Ex527 and lutein suppressed the activation of SIRT1 and reversed the expression of FoxO1, ATGL, HSL, SREBP-1, FAS, and ACC in comparison to those in the Lut group. CONCLUSIONS: Overall, we suggest that the effects of lutein on attenuating excessive lipid accumulation are dependent on the SIRT1-mediated pathway in vivo and in vitro, which indicates that lutein administration may be a potential strategy for preventing excessive lipid accumulation and obesity.


Subject(s)
Abdominal Fat/drug effects , Body Weight , Lipid Metabolism , Lipids/analysis , Lutein/pharmacology , Obesity/drug therapy , Sirtuin 1/metabolism , 3T3-L1 Cells , Abdominal Fat/metabolism , Abdominal Fat/pathology , Animals , Cell Differentiation , Diet, High-Fat , Male , Mice , Obesity/etiology , Obesity/pathology , Rats , Rats, Sprague-Dawley , Sirtuin 1/genetics
4.
Int J Mol Sci ; 22(2)2021 Jan 14.
Article in English | MEDLINE | ID: mdl-33466647

ABSTRACT

While exercise training (ET) is an efficient strategy to manage obesity, it is recommended with a dietary plan to maximize the antiobesity functions owing to a compensational increase in energy intake. Capsiate is a notable bioactive compound for managing obesity owing to its capacity to increase energy expenditure. We aimed to examine whether the antiobesity effects of ET can be further enhanced by capsiate intake (CI) and determine its effects on resting energy expenditure and metabolic molecules. Mice were randomly divided into four groups (n = 8 per group) and fed high-fat diet. Mild-intensity treadmill ET was conducted five times/week; capsiate (10 mg/kg) was orally administered daily. After 8 weeks, resting metabolic rate and metabolic molecules were analyzed. ET with CI additively reduced the abdominal fat rate by 18% and solely upregulated beta-3-adrenoceptors in adipose tissue (p = 0.013) but did not affect the metabolic molecules in skeletal muscles. Surprisingly, CI without ET significantly increased the abdominal fat rate (p = 0.001) and reduced energy expenditure by 9%. Therefore, capsiate could be a candidate compound for maximizing the antiobesity effects of ET by upregulating beta-3-adrenoceptors in adipose tissue, but CI without ET may not be beneficial in managing obesity.


Subject(s)
Abdominal Fat/metabolism , Anti-Obesity Agents/therapeutic use , Capsaicin/analogs & derivatives , Exercise Therapy , Obesity/therapy , Abdominal Fat/drug effects , Animals , Basal Metabolism/drug effects , Capsaicin/therapeutic use , Diet, High-Fat/adverse effects , Male , Mice , Mice, Inbred ICR , Obesity/etiology , Obesity/metabolism , Physical Conditioning, Animal
5.
Poult Sci ; 99(11): 5827-5837, 2020 Nov.
Article in English | MEDLINE | ID: mdl-33142500

ABSTRACT

This study investigated the effects of dietary corn-resistant starch on lipid metabolism of broilers and its potential relationship with cecal microbiota modulation. A total of three hundred twenty 1-day-old male broilers were randomly assigned into 5 dietary treatments: 1 normal corn-soybean (NC) diet, 1 corn-soybean-based diet supplementation with 20% corn starch (CS), and 3 corn-soybean-based diets supplementation with 4, 8, and 12% corn resistant starch (RS) (identified as 4%RS, 8%RS, and 12%RS, respectively). Each group had 8 replicates with 8 broilers per replicate. The experiment lasted 21 d. The results showed that the abdominal fat percentage were lower in birds from 8%RS and 12%RS groups (0.75 and 0.58%, respectively) than those from NC and CS groups (1.20 and 1.28%, respectively; P < 0.05). The birds from 8%RS and 12%RS groups exhibited lower concentrations of blood triglyceride and nonestesterified fatty acid than those in the NC and CS groups (P < 0.05). Moreover, birds fed diets supplementation with 12% RS decreased the relative mRNA expressions of peroxisome proliferator-activated receptor gamma, ATP citrate-lyase, fatty acid synthase, and acetyl-CoA carboxylase in liver, and glycerol-3-phosphate acyltransferase in abdominal adipose tissue (P < 0.05). Microbiota analysis revealed that birds fed diets supplementation with 8 and 12% RS decreased the abundance of cecal Firmicutes by 23.08 and 20.47% and increased the proportion of Bacteroidetes by 24.33 and 21.92%, respectively, compared with the NC group (P < 0.05). In addition, correlation analysis revealed that many Firmicutes members had highly positive relationship with blood lipid levels and fat storage capacity, which might contribute to the lower abdominal fat phenotype. Overall, broilers receiving diets containing a higher concentration of RS harbor less Firmicutes, which decreased liver fatty acid synthesis and suppress abdominal fat deposition of birds during the starter phase. These findings provide a profound understanding about the relationship between gut microbial composition and lipid metabolism in broilers.


Subject(s)
Abdominal Fat , Dietary Supplements , Resistant Starch , Zea mays , Abdominal Fat/drug effects , Animal Feed/analysis , Animal Nutritional Physiological Phenomena , Animals , Chickens , Diet/veterinary , Firmicutes/drug effects , Male , Random Allocation , Resistant Starch/pharmacology , Zea mays/chemistry
6.
Oxid Med Cell Longev ; 2020: 8686248, 2020.
Article in English | MEDLINE | ID: mdl-33014279

ABSTRACT

This study is aimed at evaluating the regulatory mechanism of quercetin on lipid metabolism in the ileum of broilers to better understand these pathways decreasing abdominal fat. 480 chickens were randomly divided into 4 groups (control, 0.02% quercetin, 0.04% quercetin, and 0.06% quercetin). Breast muscle, thigh muscle, and abdominal fat pad were removed and weighed at 42 d of age. Serum was obtained by centrifuging blood samples from the jugular vein (10 ml) to determine high-density lipoprotein (HDL), total cholesterol (TC), low-density lipoprotein (LDL), triglyceride (TG), leptin, and adiponectin using ELISA. About 5 g of the ileum was harvested and immediately frozen in liquid nitrogen for RNA-seq. Then, the confirmation of RNA-seq results by the Real-Time Quantitative PCR (RT-qPCR) method was evaluated using Pearson's correlation. Compared with control, abdominal fat percentage was significantly decreased with increasing quercetin supplementation, and the best result was obtained at 0.06% dietary quercetin supplementation (P < 0.01). Breast muscle percentage was significantly decreased at 0.02% quercetin (P < 0.01), and thigh muscle percentage tended to increase (P = 0.078). Meanwhile, 0.04% and 0.06% quercetin significantly decreased TG (P < 0.01), TC (P < 0.01), and LDL content (P < 0.05) in serum. Serum leptin and adiponectin contents were significantly increased by 0.04% and 0.06% dietary quercetin supplementation, compared with the control (P < 0.01). Analyses of Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) database were used to identify differently expressed genes and lipid metabolism pathways. Quercetin decreased abdominal fat percentage through regulating fat digestion and absorption, glycerophospholipid metabolism, AMPK signaling pathway, fatty acid degradation, and cholesterol metabolism.


Subject(s)
Ileum/metabolism , Lipid Metabolism/drug effects , Quercetin/pharmacology , AMP-Activated Protein Kinases/metabolism , Abdominal Fat/drug effects , Abdominal Fat/metabolism , Abdominal Fat/physiology , Animals , Chickens , Dietary Supplements , Gene Expression Regulation/drug effects , Gene Ontology , Glycerophospholipids/metabolism , Intestinal Mucosa/metabolism , Lipid Metabolism/genetics , Lipoproteins, HDL/blood , Muscle, Skeletal/drug effects , Muscle, Skeletal/physiology , Signal Transduction/drug effects , Triglycerides/blood
7.
Molecules ; 25(17)2020 Aug 27.
Article in English | MEDLINE | ID: mdl-32867219

ABSTRACT

Several studies have shown that binge drinking of alcoholic beverages leads to non-desirable outcomes, which have become a serious threat to public health. However, the bioactive compounds in some alcohol-containing beverages might mitigate the negative effects of alcohol. In beer, the variety and concentration of bioactive compounds in the non-alcoholic fraction suggests that its consumption at moderate levels may not only be harmless but could also positively contribute to an improvement of certain physiological states and be also useful in the prevention of different chronic diseases. The present review focuses on the effects of non-alcoholic components of beer on abdominal fat, osteoporosis, and body hydration in women, conditions selected for their relevance to health and aging. Although beer drinking is commonly believed to cause abdominal fat deposition, the available literature indicates this outcome is inconsistent in women. Additionally, the non-alcoholic beer fraction might improve bone health in postmenopausal women, and the effects of beer on body hydration, although still unconfirmed seem promising. Most of the health benefits of beer are due to its bioactive compounds, mainly polyphenols, which are the most studied. As alcohol-free beer also contains these compounds, it may well offer a healthy alternative to beer consumers.


Subject(s)
Abdominal Fat/drug effects , Beer , Minerals/pharmacology , Phytoestrogens/pharmacology , Polyphenols/pharmacology , Adult , Aged , Aged, 80 and over , Aging/drug effects , Beer/adverse effects , Beer/analysis , Female , Humans , Middle Aged , Organism Hydration Status/drug effects , Osteoporosis , Postmenopause , Young Adult
8.
Biol Pharm Bull ; 43(3): 440-449, 2020.
Article in English | MEDLINE | ID: mdl-32115502

ABSTRACT

There is significant cultivation of persimmon (Diospyros kaki) in East Asia, a plant whose fruit has abundant nutrients, including vitamins, polyphenols, and dietary fiber. Persimmon dietary supplements can benefit health by amelioration of diabetes, cardiovascular disease, and obesity. There are also persimmon-based beverages produced via fermentation, such as wines and vinegars, and increasing consumption of these products in East Asia. Although there is great interest in functional foods, the health effects of fermented persimmon extract (FPE) are completely unknown. We examined the effects of FPE on the metabolic parameters of mice fed a high-fat diet (HFD). Our results indicated that FPE supplementation led to an approx. 15% reduction of body weight, reduced abdominal and liver fat, and reduced serum levels of triglycerides, total cholesterol, and glucose. FPE also blocked the differentiation of murine 3T3-L1 pre-adipocyte cells into mature adipocytes. We suggest that gallic acid is a major bioactive component of FPE, and that AMP-activated protein kinase mediates the beneficial effects of FPE and gallic acid.


Subject(s)
AMP-Activated Protein Kinases/metabolism , Diospyros/chemistry , Obesity/diet therapy , Obesity/metabolism , Plant Extracts/pharmacology , 3T3-L1 Cells/metabolism , Abdominal Fat/drug effects , Adipocytes/drug effects , Adipocytes/metabolism , Animals , Blood Glucose , Body Weight/drug effects , Fermentation , Fruit , Gallic Acid/pharmacology , Intra-Abdominal Fat/drug effects , Lipids/blood , Male , Mice , Mice, Inbred C57BL , Plant Extracts/chemistry
9.
Anim Biotechnol ; 31(6): 483-490, 2020 Dec.
Article in English | MEDLINE | ID: mdl-31230524

ABSTRACT

A total of 270 one-d-old Ross 308 broiler chicks were randomly allotted to 9 experimental diets (3 replicates of 10 birds each), including three types of supplemental lipotropic factors (control, 0.1% or 0.2% choline and 0.5% or 1% lecithin) in a 3 × 3 factorial arrangement. Supplementation of lecithin improved FCR values during 1-21 days of age. Although no differences were noticed for mortality index among different diets, the group supplemented with a combination of choline (0.1) and lecithin (0.5) showed the highest (P < 0.0001) production index. Choline (0.1% or 0.2%) significantly decreased serum total cholesterol by 11%, triglycerides by 21%, low-density lipoprotein (LDL) by 20%, and very low-density lipoprotein (VLDL) by 20%, while increased the glucose and high-density lipoprotein (HDL) values by 11% and 6%, respectively. On the other hand, lecithin significantly increased glucose, total cholesterol, triglycerides, HDL, LDL and VLDL by 4%, 9%, 7%, 24%, and 25%, respectively. Choline supplementation decreased the aspartate amino transferase (AST), alanine amino transferase (ALT), and alkaline phosphatase (AP); however, the lecithin addition increased their respective proportions. This study concluded that the combinations of 0.1% choline and 0.5% lecithin is the best among all other treatments because of the highest production index and least mortality.


Subject(s)
Abdominal Fat/drug effects , Animal Feed , Chickens , Choline , Lecithins , Animals , Chickens/growth & development , Chickens/physiology , Cholesterol/blood , Choline/administration & dosage , Choline/pharmacology , Diet/veterinary , Enzymes/blood , Lecithins/administration & dosage , Lecithins/pharmacology , Male , Stress, Physiological/drug effects
10.
J Am Coll Nutr ; 39(3): 206-215, 2020.
Article in English | MEDLINE | ID: mdl-31368861

ABSTRACT

Objective: The aim of the study is to investigate the effect of Jeju steamed onion (ONIRO) on body fat and metabolic profiles in overweight subjects.Methods: This randomized, double-blind, placebo-controlled clinical intervention was conducted and completed at one clinical research site. The subjects (n = 70) were randomly divided into placebo or test group and were instructed to take before each meal either the placebo or ONIRO capsule for 12 weeks. Anthropometric as well as serum and metabolic parameters, including triglycerides, cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, leptin, adiponectin, C-peptide, and aspartate aminotransferase (AST) were measured at baseline and after 12 weeks. Body composition was also measured by dual-energy x-ray absorptiometry (DEXA) and computed tomography (CT). This trial is registered under the trial registration code clinicaltrials.gov: NCT03645382 (https://register.clinicaltrials.gov).Results: Compared to the placebo, ONIRO supplementation for significantly reduced the percentage of body fat and fat mass as measured by DEXA (p = 0.028 and 0.022, respectively) with no significant effects on lean body mass. CT analyses at the L1 level showed a significant decrease in the areas of whole fat, visceral fat, and subcutaneous fat (p = 0.009, p = 0.039, p = 0.020, respectively), while CT scan of L4 resulted in a significant reduction of whole fat area and subcutaneous area (p = 0.006 and p = 0.012, respectively). The levels of triglycerides (TG) and C-peptide were significantly lower after 12 weeks of ONIRO treatment.Conclusions: These findings suggest that ONIRO supplementation reduces total body fat, notably abdominal visceral fat, with positive changes of the clinically relevant metabolic parameters serum TG and C-peptide.


Subject(s)
Body Composition/drug effects , Metabolome/drug effects , Onions/chemistry , Overweight/drug therapy , Plant Extracts/therapeutic use , Abdominal Fat/drug effects , Adiponectin/blood , Adult , C-Peptide/blood , Dietary Supplements , Double-Blind Method , Female , Humans , Leptin/blood , Lipids/blood , Male , Middle Aged , Phytotherapy , Placebos , Republic of Korea , Triglycerides/blood
11.
BMC Complement Altern Med ; 19(1): 232, 2019 Aug 28.
Article in English | MEDLINE | ID: mdl-31462242

ABSTRACT

BACKGROUND: Metabolic syndrome is a non-communicable disease inclusive of risk factors such as central obesity, hypertension, hyperglycaemia and dyslipidaemia. In this present study, we investigated the ability of Pandanus amaryllifolius (PA) leaf water extract to reverse the cluster of diseases in an established rat model induced by fructose in drinking water. METHODS: Thirty healthy adult male Wistar rats (150-180 g) were randomly divided into three groups which included control (C; n = 6), PA extract (PAE; n = 6) and Metabolic Syndrome (MetS; n = 18). Food and fluid were given ad libitum for 8 weeks. These groups differed in fluid intake whereby rats received tap water, 10% of PA leaf water extracts and 20% of fructose in drinking water in group C, PAE and MetS, respectively. After 8 weeks, the MetS group was further subdivided into three subgroups namely MetS1 (n = 6), MetS2 (n = 6) and MetS3 (n = 6). The C, PAE and MetS1 were sacrificed. MetS1 group was sacrificed as the control for metabolic syndrome. MetS2 and MetS3 groups were treated with only tap water and 10% of PA leaf water extract respectively for another 8 weeks. The parameters for physiological and metabolic changes such as obesity, hypertension, hyperglycaemia, dyslipidaemia, and inflammatory biomarkers (NFκß p65, TNFα, leptin and adiponectin) were measured. RESULTS: The intake of 20% of fructose in drinking water induced full blown of metabolic syndrome symptoms, including obesity, hypertension, dyslipidaemia and hyperglycaemia in male Wistar rats. Subsequently, treatment with PA leaf water extract improved obesity parameters including BMI, abdominal adipose tissue deposition and adipocytes size, systolic and diastolic blood pressures, fasting plasma glucose, triglycerides, high density lipoprotein with neutral effects on inflammatory biomarkers. CONCLUSIONS: Administration of PA in metabolic syndrome rat model attenuates most of the metabolic syndrome symptoms as well as improves obesity. Therefore, PA which is rich in total flavonoids and total phenolic acids can be suggested as a useful dietary supplement to improve metabolic syndrome components induces by fructose.


Subject(s)
Fructose/adverse effects , Metabolic Syndrome , Pandanaceae/chemistry , Plant Extracts/pharmacology , Abdominal Fat/drug effects , Animals , Blood Glucose/drug effects , Blood Pressure/drug effects , Disease Models, Animal , Lipids/blood , Male , Metabolic Syndrome/chemically induced , Metabolic Syndrome/metabolism , Plant Extracts/chemistry , Plant Leaves/chemistry , Rats , Rats, Wistar
12.
J Dairy Res ; 86(3): 296-302, 2019 Aug.
Article in English | MEDLINE | ID: mdl-31409432

ABSTRACT

This research paper addresses the hypothesis that in times of negative energy balance around parturition in dairy cattle, lipids stored in adipocytes are mobilised in a more intensive manner out of the abdominal depots than out of the subcutaneous adipose tissues. Furthermore, the impact of niacin supplementation and energy density of the ration on adipose tissue mass gain and loss was assessed. Absolute masses of subcutaneous (SCAT), retroperitoneal (RPAT), omental (OMAT), mesenterial (MAT) and abdominal adipose tissue as a whole (AAT) were estimated by ultrasonography at -42, 3, 21 and 100 DIM. Absolute and relative daily gain during dry period (-42 to 3 DIM) and loss in fresh cow period (3 to 21 DIM) and early lactation period (22 to 100 DIM) were calculated. Feeding regime neither by niacin nor by energy density exerted any effect on adipose tissue masses. The AAT was always bigger than SCAT, but RPAT, OMAT and MAT did not differ amongst each other. All depot masses showed similar patterns with an increase during dry period and a decrease after calving. In fresh cow period AAT absolutely and relatively lost more mass than SCAT. This confirms that AAT is more intensively mobilised than SCAT during that time span. Further absolute daily gain during dry period was strongly negatively correlated with absolute daily loss during fresh cow period. This underlines the impact of individual body condition on adipose mobilisation in periparturient dairy cows. According to these results, it has to be taken into account that the largest amount of fat mobilised in the fresh cow period origins from AAT. This might impact the pattern of adipose derived metabolites and metabolic effectors interacting in physiological and deregulated adaptation to negative energy balance.


Subject(s)
Abdominal Fat/physiology , Cattle/physiology , Energy Metabolism/physiology , Subcutaneous Fat/physiology , Abdominal Fat/diagnostic imaging , Abdominal Fat/drug effects , Animals , Body Composition , Diet/veterinary , Dietary Supplements , Female , Germany , Lactation , Niacin/administration & dosage , Parturition , Postpartum Period , Pregnancy , Reproduction , Subcutaneous Fat/diagnostic imaging , Subcutaneous Fat/drug effects , Ultrasonography/veterinary
13.
Nutrients ; 11(7)2019 Jul 16.
Article in English | MEDLINE | ID: mdl-31315279

ABSTRACT

The components of roasted or green coffee beans that promote abdominal fat reduction are not clear. We investigated the effects of daily consumption of coffee enriched in chlorogenic acids (CGA) on abdominal fat area in a randomized, double-blind, parallel controlled trial. Healthy, overweight men and women (n = 150, body mass index (BMI) ≥25 to <30 kg/m2) were randomly allocated to high-CGA (369 mg CGA/serving) or control (35 mg CGA/serving) coffee groups. Instant coffee was consumed once daily for 12 weeks, with four-week pre- and post-observation periods. Abdominal fat area and anthropometric measurements were analyzed at baseline and at four, eight, and 12 weeks, and 142 subjects completed the trial. Visceral fat area (VFA), total abdominal fat area (TFA), body weight, and waist circumference significantly decreased in the CGA group compared with the control group, with a group × time interaction (p < 0.001, p = 0.001, p = 0.025, and p = 0.001, respectively). Changes in VFA and TFA from baseline to 12 weeks were significantly greater in the CGA group than in the control group (-9.0 ± 13.9 cm2 vs. -1.0 ± 14.3 cm2, p < 0.001; -13.8 ± 22.9 cm2 vs. -2.0 ± 16.2 cm2, p < 0.001). No severe adverse events occurred. Consumption of high-CGA coffee for 12 weeks by overweight adults might lower VFA, TFA, BMI, and waist circumference.


Subject(s)
Abdominal Fat/drug effects , Chlorogenic Acid/administration & dosage , Chlorogenic Acid/chemistry , Coffee/chemistry , Overweight , Adult , Double-Blind Method , Female , Humans , Male , Middle Aged
14.
Int J Mol Sci ; 20(12)2019 Jun 12.
Article in English | MEDLINE | ID: mdl-31212773

ABSTRACT

Numerous Foods with Function Claims that contain the extract of Pueraria flower (kudzu) isoflavones (PFI) are available in the Japanese market. These are labelled with function claims of reducing visceral fat. However, these foods have not undergone proper safety assessment such as the evaluation of their oestrogenic activity and effects on drug-metabolising enzymes (cytochrome P-450: CYP) in the liver. This study evaluated the estrogenic effect and the hepatic CYP activity and mRNA expression in normal female mice as a safety assessment of PFI (Experiment 1). In addition, the bone mineral density and visceral fat weight in ovariectomised mice (OVX) compared to soy isoflavones (SI) was evaluated to assess the efficacy of PFI (Experiment 2). OVX control fed a control diet, OVX fed a PFI diet (the recommended human intake of PFI), OVX fed a PFI20 diet (20- times the recommended PFI), OVX fed an SI diet (the recommended human intake of SI), and OVX fed an SI20 diet (20 -times the recommended intake of SI) for 28 days in Experiment 2. Body, liver, and visceral fat weights were not affected by the PFI, PFI20, SI, or SI20 diets. The hepatic CYP1A and CYP3A activities were elevated by the SI20 treatment. Ovariectomy-induced bone loss was inhibited by the SI20 treatment, but not by the PFI20 treatment. These results suggest that (1) PFI intake in human doses had no oestrogenic properties and did not affect CYP activity in the liver; (2) there was no evidence that PFI affects the amount of visceral fat in OVX mice.


Subject(s)
Flowers/chemistry , Isoflavones/chemistry , Isoflavones/pharmacology , Plant Extracts/chemistry , Plant Extracts/pharmacology , Pueraria/chemistry , Abdominal Fat/drug effects , Abdominal Fat/metabolism , Animals , Biomarkers , Bone Density/drug effects , Cytochrome P-450 Enzyme System/metabolism , Enzyme Activation/drug effects , Female , Gene Expression Regulation/drug effects , Liver/drug effects , Liver/metabolism , Mice , Models, Animal , Osteogenesis/drug effects , Ovariectomy
15.
J Anim Physiol Anim Nutr (Berl) ; 103(4): 1090-1098, 2019 Jul.
Article in English | MEDLINE | ID: mdl-31012184

ABSTRACT

This study investigated effect of increasing level of dietary sodium using sodium bicarbonate or sodium chloride on growth performance, mortality, characteristics of carcass, organs and tibia, calcium and phosphorus of serum in broilers reared in a high-altitude area (1,700 m above sea level). A total of 588 Ross 308 male broiler chicks were used in seven treatments, six replicates per treatment of 14 birds per each from 1 to 38 d of age. Seven dietary treatments consisted of a basal diet (with 0.16% sodium and 0.23% chloride), top-dressed for six diets to give three supplementary levels of sodium (0.07%, 0.14% and 0.21%) from sodium bicarbonate (respectively by 0.26%, 0.52% and 0.78%) or sodium chloride (respectively by 0.18%, 0.36% and 0.54%), resulting in seven diets with total sodium and chloride levels of 0.16% and 0.23%, 0.23% and 0.23%, 0.30% and 0.23%, 0.37% and 0.23%, 0.23% and 0.33%, 0.30% and 0.44%, 0.37% and 0.55% respectively. Increasing sodium level improved feed conversion ratio (FCR) linearly and quadratically. However, when FCR was calculated without adjusting for feed intake of mortalities, the enhanced sodium level did not improve this parameter. Increasing sodium level via sodium chloride enhanced ascites mortality, total mortality, relative weight of heart and right ventricle linearly. Increasing sodium level reduced serum calcium and enhanced serum phosphorus linearly; however, there was a linear tendency to increase tibia ash when sodium level was enhanced by sodium bicarbonate (p = 0.08) or sodium chloride (p = 0.07). Increasing sodium level via sodium bicarbonate tended (p = 0.08) to reduce tibia strength linearly. In conclusion, a diet with 0.16% sodium and 0.23% chloride is enough for broiler chicken reared in a high-altitude area, and increasing dietary sodium level via sodium chloride has detrimental effect on survivability of broiler in such condition.


Subject(s)
Altitude , Animal Feed/analysis , Chickens , Diet/veterinary , Sodium Chloride, Dietary/administration & dosage , Abdominal Fat/anatomy & histology , Abdominal Fat/drug effects , Animal Nutritional Physiological Phenomena , Animals , Bone Density/drug effects , Heart/anatomy & histology , Heart/drug effects , Intestines/anatomy & histology , Intestines/drug effects , Liver/anatomy & histology , Liver/drug effects , Male , Organ Size , Pancreas/anatomy & histology , Pancreas/drug effects , Sodium Bicarbonate/administration & dosage
16.
Br Poult Sci ; 59(1): 121-127, 2018 Feb.
Article in English | MEDLINE | ID: mdl-29094608

ABSTRACT

1. This study was carried out to investigate the effects of liquidambar essential oils (LEO) isolated from Turkish sweet gum (Liquidambar orientalis Mill.) leaves on growth performance, carcass, edible inner organs (EIO), gastrointestinal traits (gut), some blood metabolites and jejunum microbiota in broilers. 2. A total of 375 one-d-old male broilers (Ross 308) were randomly allocated to 5 treatments with 5 pens with 15 birds. The birds were fed on diets without antibiotics (CONT), with antibiotic (50 mg per kg, AB), with LEOs at 0.0405 (0.04LEO), 0.0811 (0.08LEO) or 0.1622 (0.16LEO) g/kg feed up to 42 d of age. The levels of LEOs included to diets were determined according to in vitro antimicrobial activity. 3. From d 1 to 42, the 0.08LEO treatment had higher live weight gain (LWG) compared to others. The 0.08LEO treatment increased feed intake (FI) compared to the CONT, AB and 0.04LEO. However, the feed conversion ratio (FCR) of these birds was lower than those in the AB and 0.16LEO treatments. From 1 to 42 d of age for LWG, the effects were quadratic and cubic, while those for FI and FCR were cubic and quadratic, respectively. Birds that fed 0.08LEO and AB diets had higher and lower carcass weights (CW) than those that fed other diets. The effect of LEO levels was cubic on the CW. The 0.08LEO and 0.16LEO decreased abdominal fat (AF) weight compared to the AB. The blood cholesterol decreased by the 0.04LEO and 0.08LEO treatments compared to the CONT. For the blood cholesterol, the effects of LEO levels were cubic. The 0.08LEO treatments decreased Escherichia coli counts in jejunum compared to the CONT and 0.16LEO. 4. Feeding a diet with LEO at 0.0811 g/kg might increase the LWG, FI and weights of carcass and AF, whereas it might decrease blood cholesterol and E. coli counts without affecting blood high-density lipoprotein, low-density lipoprotein, triglyceride, glucose, aspartate transaminase and alanine transaminase concentrations.


Subject(s)
Chickens/growth & development , Diet/veterinary , Dietary Supplements/analysis , Gastrointestinal Microbiome/drug effects , Liquidambar/chemistry , Oils, Volatile/pharmacology , Abdominal Fat/drug effects , Animal Feed/analysis , Animal Nutritional Physiological Phenomena/drug effects , Animals , Anti-Bacterial Agents/pharmacology , Chickens/metabolism , Cholesterol/blood , Escherichia coli/drug effects , Male , Weight Gain/drug effects
17.
PLoS One ; 12(10): e0187061, 2017.
Article in English | MEDLINE | ID: mdl-29073281

ABSTRACT

Our previous results showed that green tea polyphenols (GTPs) significantly altered the expression of lipid-metabolizing genes in the liver of chickens. However, the underlying mechanism was not elucidated. In this study, we further characterized how GTPs influence AMP-activated protein kinase (AMPK) in the regulation of hepatic fat metabolism. Thirty-six male chickens were fed GTPs at a daily dose of 0, 80 or 160 mg/kg of body weight for 4 weeks. The results demonstrated that oral administration of GTPs significantly reduced hepatic lipid content and abdominal fat mass, enhanced the phosphorylation levels of AMPKα and ACACA, and altered the mRNA levels and enzymatic activities of lipid-metabolizing enzymes in the liver. These results suggested that the activation of AMPK is a potential mechanism by which GTPs regulate hepatic lipid metabolism in such a way that lipid synthesis is reduced and fat oxidation is stimulated.


Subject(s)
AMP-Activated Protein Kinases/metabolism , Lipid Metabolism/drug effects , Liver/drug effects , Polyphenols/pharmacology , Tea/chemistry , Abdominal Fat/drug effects , Animals , Body Weight/drug effects , Chickens , Liver/enzymology , Liver/metabolism , Male , Organ Size/drug effects , Phosphorylation , Polyphenols/administration & dosage , Real-Time Polymerase Chain Reaction
18.
Mol Nutr Food Res ; 61(12)2017 12.
Article in English | MEDLINE | ID: mdl-28940752

ABSTRACT

SCOPE: Nonalcoholic fatty liver disease is the most common cause of liver disease, for which there is no validated drug therapy at present time. In this respect, the PUFA docosahexaenoic acid (DHA; C22:6 n-3) modulate lipid metabolism in the liver, and extra virgin olive oil (EVOO) has hepatoprotective effects. METHODS AND RESULTS: The effect of combined DHA (C22:6 n-3) and EVOO administration to mice on oxidative stress and metabolic disturbances induced by high-fat diet (HFD) is evaluated. Male C57BL/6J mice are fed with a control diet (10% fat, 20% protein, and 70% carbohydrates) or an HFD (60% fat, 20% protein, and 20% carbohydrates) for 12 weeks. Animals are supplemented with DHA (50 mg/kg/day), EVOO (50 mg/kg/day), or DHA + EVOO through oral route. DHA + EVOO cosupplementation results in greater protection (p < 0.05) over that elicited by DHA or EVOO supply alone, when compared to the damage induced by HFD. DHA + EVOO significantly reduces hepatic steatosis, oxidative stress, systemic inflammation, and insulin resistance. CONCLUSION: Synergistic beneficial effects of DHA + EVOO supplementation are associated with the activation/inactivation of key transcription factors involved in the above-mentioned processes. Data presented indicate that dietary supplementation with DHA + EVOO drastically reduces the development of nonalcoholic fatty liver disease.


Subject(s)
Docosahexaenoic Acids/pharmacology , Liver/drug effects , Non-alcoholic Fatty Liver Disease/prevention & control , Olive Oil/pharmacology , Abdominal Fat/drug effects , Animals , Diet, High-Fat/adverse effects , Dietary Supplements , Down-Regulation/drug effects , Fatty Acids/metabolism , Liver/metabolism , Liver/pathology , Male , Mice, Inbred C57BL , NF-E2-Related Factor 2/metabolism , NF-kappa B/metabolism , Non-alcoholic Fatty Liver Disease/etiology , Oxidative Stress/drug effects , PPAR alpha/metabolism , Sterol Regulatory Element Binding Protein 1/metabolism
19.
Lipids Health Dis ; 16(1): 151, 2017 Aug 14.
Article in English | MEDLINE | ID: mdl-28806968

ABSTRACT

BACKGROUND: Cardamom is a well-known spice in Indian subcontinent, used in culinary and traditional medicine practices since ancient times. The current investigation was untaken to evaluate the potential benefit of cardamom powder supplementation in high carbohydrate high fat (HCHF) diet induced obese rats. METHOD: Male Wistar rats (28 rats) were divided into four different groups such as Control, Control + cardamom, HCHF, HCHF + cardamom. High carbohydrate and high fat (HCHF) diet was prepared in our laboratory. Oral glucose tolerance test, organs wet weight measurements and oxidative stress parameters analysis as well as liver marker enzymes such as alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP) activities were assayed on the tissues collected from the rats. Plasma lipids profiles were also measured in all groups of animals. Moreover, histological staining was also performed to evaluate inflammatory cells infiltration and fibrosis in liver. RESULTS: The current investigation showed that, HCHF diet feeding in rats developed glucose intolerance and increased peritoneal fat deposition compared to control rats. Cardamom powder supplementation improved the glucose intolerance significantly (p > 0.05) and prevented the abdominal fat deposition in HCHF diet fed rats. HCHF diet feeding in rats also developed dyslipidemia, increased fat deposition and inflammation in liver compared to control rats. Cardamom powder supplementation significantly prevented the rise of lipid parameters (p > 0.05) in HCHF diet fed rats. Histological assessments confirmed that HCHF diet increased the fat deposition and inflammatory cells infiltration in liver which was normalized by cardamom powder supplementation in HCHF diet fed rats. Furthermore, HCHF diet increased lipid peroxidation, decreased antioxidant enzymes activities and increased advanced protein oxidation product level significantly (p > 0.05) both in plasma and liver tissue which were modulated by cardamom powder supplementation in HCHF diet fed rats. HCHF diet feeding in rats also increased the ALT, AST and ALP enzyme activities in plasma which were also normalized by cardamom powder supplementation in HCHF diet fed rats. Moreover, cardamom powder supplementation ameliorated the fibrosis in liver of HCHF diet fed rats. CONCLUSION: This study suggests that, cardamom powder supplementation can prevent dyslipidemia, oxidative stress and hepatic damage in HCHF diet fed rats.


Subject(s)
Antioxidants/pharmacology , Dyslipidemias/diet therapy , Elettaria/chemistry , Liver Cirrhosis/prevention & control , Obesity/diet therapy , Plant Extracts/pharmacology , Abdominal Fat/drug effects , Abdominal Fat/metabolism , Abdominal Fat/pathology , Alanine Transaminase/metabolism , Alkaline Phosphatase/metabolism , Animals , Aspartate Aminotransferases/metabolism , Diet, High-Fat/adverse effects , Dietary Carbohydrates/adverse effects , Disease Models, Animal , Dyslipidemias/etiology , Dyslipidemias/metabolism , Dyslipidemias/physiopathology , Glucose/metabolism , Glucose Intolerance , Glucose Tolerance Test , Glycation End Products, Advanced/blood , Lipid Peroxidation/drug effects , Liver Cirrhosis/etiology , Liver Cirrhosis/metabolism , Liver Cirrhosis/physiopathology , Male , Obesity/etiology , Obesity/metabolism , Obesity/physiopathology , Oxidative Stress , Powders , Rats , Rats, Wistar
20.
Exp Physiol ; 102(11): 1474-1485, 2017 11 01.
Article in English | MEDLINE | ID: mdl-28786140

ABSTRACT

NEW FINDINGS: What is the central question of this study? We investigated whether 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR) could prevent acute increases in body fat and changes in omental and subcutaneous adipose tissue following the sudden transition from physical activity to physical inactivity. What is the main finding and its importance? AICAR prevented fat gains following the transition from physical activity to inactivity to levels comparable to rats that remained physically active. AICAR and continuous physical activity produced depot-specific changes in cyclin A1 mRNA and protein that were associated with the prevention of fat gain. These findings suggest that targeting AMP-activated protein kinase signalling could oppose rapid adipose mass growth. The transition from physical activity to inactivity is associated with drastic increases in 'catch-up' fat that in turn foster the development of many obesity-associated maladies. We tested whether 5-aminoimidazole-4-carboxamide-1-beta-D-ribofuranoside (AICAR) treatment would prevent gains in body fat following the sudden transition from a physically active state to an inactive state by locking a voluntary running wheel. Male Wistar rats were either sedentary (SED) or given wheel access for 4 weeks, at which time rats with wheels continued running (RUN), had their wheel locked (WL) or had WL with daily AICAR injection (WL + AICAR) for 1 week. RUN and WL + AICAR prevented gains in body fat compared with SED and WL (P < 0.001). Cyclin A1 mRNA, a marker of cell proliferation, was decreased in omental, but not subcutaneous adipose tissue, in RUN and WL + AICAR compared with SED and WL groups (P < 0.05). Both cyclin A1 mRNA and protein were positively associated with gains in fat mass (P < 0.05). Cyclin A1 mRNA in omental, but not subcutaneous, adipose tissue was negatively correlated with p-AMPK levels (P < 0.05). Differences in fat gain and omental mRNA and protein levels were independent of changes in food intake and in differences in select hypothalamic mRNAs. These findings suggest that AICAR treatment prevents acute gains in adipose tissue following physical inactivity to levels of rats that continuously run, and that together, continuous physical activity and AICAR could, at least initially in these conditions, exert similar inhibitory effects on adipogenesis in a depot-specific manner.


Subject(s)
Abdominal Fat/drug effects , Adipogenesis/drug effects , Adiposity/drug effects , Aminoimidazole Carboxamide/analogs & derivatives , Anti-Obesity Agents/pharmacology , Physical Conditioning, Animal/methods , Ribonucleotides/pharmacology , Sedentary Behavior , Subcutaneous Fat/drug effects , Weight Gain/drug effects , AMP-Activated Protein Kinases/metabolism , Abdominal Fat/metabolism , Aminoimidazole Carboxamide/pharmacology , Animals , Cyclin A1/genetics , Cyclin A1/metabolism , Enzyme Activation , Enzyme Activators/pharmacology , Hypothalamus/drug effects , Hypothalamus/metabolism , Male , Phosphorylation , Physical Exertion , Rats, Wistar , Running , Subcutaneous Fat/metabolism , Time Factors , Volition
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