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1.
Biosci Biotechnol Biochem ; 83(7): 1329-1335, 2019 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-30912732

RESUMEN

Difructose anhydride III (DFAIII) is a prebiotic involved in the reduction of secondary bile acids (BAs). We investigated whether DFAIII modulates BA metabolism, including enterohepatic circulation, in the rats fed with a diet supplemented with cholic acid (CA), one of the 12α-hydroxylated BAs. After acclimation, the rats were fed with a control diet or a diet supplemented with DFAIII. After 2 weeks, each group was further divided into two groups and was fed diet with or without CA supplementation at 0.5 g/kg diet. BA levels were analyzed in aortic and portal plasma, liver, intestinal content, and feces. As a result, DFAIII ingestion reduced the fecal deoxycholic acid level via the partial suppression of deconjugation and 7α-dehydroxylation of BAs following CA supplementation. These results suggest that DFAIII suppresses production of deoxycholic acid in conditions of high concentrations of 12α-hydroxylated BAs in enterohepatic circulation, such as obesity or excess energy intake. Abbreviation: BA: bile acid; BSH: bile salt hydrolase; CA: cholic acid; DCA: deoxycholic acid; DFAIII: difructose anhydride III; MCA: muricholic acid; MS: mass spectrometry; NCDs: non-communicable diseases; LC: liquid chromatography; SCFA: short-chain fatty acid; TCA: taurocholic acid; TCDCA: taurochenodeoxycholic acid; TDCA: taurodeoxycholic acid; TUDCA: tauroursodeoxychlic acid; TαMCA: tauro-α-muricholic acid; TßMCA: tauro-ß-muricholic acid; TωMCA: tauro-ω-muricholic acid.


Asunto(s)
Ácidos y Sales Biliares/metabolismo , Ácido Cólico/administración & dosificación , Suplementos Dietéticos , Disacáridos/farmacología , Animales , Ácidos y Sales Biliares/sangre , Disacáridos/administración & dosificación , Heces/química , Contenido Digestivo , Hidroxilación , Masculino , Ratas , Ratas Wistar , Espectrofotometría Atómica
2.
Biosci Biotechnol Biochem ; 82(3): 489-496, 2018 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-29383988

RESUMEN

The effect of a combination of inulin (INU) and polyphenol-containing adzuki bean extract (AE) on intestinal fermentation was examined in vitro using fermenters for 48 h and in vivo using rats for 28 d. The total short-chain fatty acid concentrations in the fermenters were decreased by a combination of INU and AE, but the concentration in the INU + AE group was higher than the cellulose (CEL) and CEL + AE groups. The cecal propionate concentration was increased by a combination of INU and AE compared with their single supplement. The ammonia-nitrogen concentration in the fermenters and rat cecum was decreased by INU and AE. Cecal mucin levels were increased by INU and AE respectively. Therefore, our observations suggested that the combination of INU and AE might be a material of functional food that includes several healthy effects through intestinal fermentation.


Asunto(s)
Fermentación/efectos de los fármacos , Intestinos/efectos de los fármacos , Inulina/farmacología , Extractos Vegetales/química , Extractos Vegetales/farmacología , Polifenoles/química , Vigna/química , Animales , Peso Corporal/efectos de los fármacos , Colon/efectos de los fármacos , Colon/metabolismo , Interacciones Farmacológicas , Ingestión de Alimentos/efectos de los fármacos , Ácidos Grasos/química , Ácidos Grasos/metabolismo , Heces/microbiología , Humanos , Concentración de Iones de Hidrógeno , Mucosa Intestinal/metabolismo , Masculino , Ratas , Porcinos
3.
Biosci Biotechnol Biochem ; 81(11): 2186-2194, 2017 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-28950751

RESUMEN

We investigated the effects of dietary supplementation of difructose anhydride III (DFA III), raffinose (Raf), and fructooligosaccharides (FOS) on diet-induced obesity development. Male rats were fed normal or high-fat and high-sucrose (HFS) diet, with or without supplementing (3%) DFA III, Raf, or FOS, for 8 or 5 weeks. Supplementing DFA III to the HFS diet decreased energy intake compared to the non-supplemented HFS diet. Accordingly, body weight gain and fat accumulation reduced in DFA III-fed rats. Cecal acetate production and plasma glucagon-like peptide-1 (GLP-1) and peptide-YY (PYY) were elevated in DFA III-fed rats, while Raf and FOS partially affected these parameters. These results demonstrate that DFA III has suppressive effect on excessive energy intake driven by the palatable obesogenic diet, possibly due to combined effects of increased anorexigenic factors such as cecal acetate production and GLP-1/PYY secretion.


Asunto(s)
Ciego/efectos de los fármacos , Dieta Alta en Grasa/efectos adversos , Sacarosa en la Dieta/efectos adversos , Ingestión de Energía/efectos de los fármacos , Fermentación/efectos de los fármacos , Hormonas/metabolismo , Oligosacáridos/farmacología , Animales , Ciego/metabolismo , Ciego/microbiología , Disacáridos/farmacología , Masculino , Rafinosa/farmacología , Ratas , Ratas Sprague-Dawley
4.
Metabolites ; 14(7)2024 Jul 18.
Artículo en Inglés | MEDLINE | ID: mdl-39057713

RESUMEN

Supplementation of betaine is associated with improved cardiac health, potentially due to its function in re-methylation of homocysteine, an independent risk factor for cardiovascular diseases. We investigated the effects of oral betaine supplementation on blood pressure homeostasis in spontaneously hypertensive (SHR) rats and Wistar Kyoto (WKY) rats in an 8 week-feeding trial with control (SHR-con and WKY-con) and 1% betaine supplemented (SHR-b and WKY-b) diets. Systolic, diastolic, and mean blood pressure in the SHR-b group were significantly lower at week 8 (p = 0.013, p = 0.011, p = 0.010, respectively). Furthermore, serum nitric oxide (NO) levels were significantly (p < 0.05) improved in the WKY-b and SHR-b groups, suggesting a healthy endothelial function. Additionally, the serum angiotensin I converting enzyme level in SHR-b rats was also significantly lowered, which may have been another reason for lower blood pressure. A significantly higher non-HDL level in the SHR-b group might reflect enhanced lipid secretion into the circulation in the form of very-low-density lipoprotein (VLDL). Betaine is known for its effect on the synthesis of phosphatidylcholine, a key component of VLDL. However, the long-term net outcomes of both blood pressure lowering and serum lipid increment should be further studied.

5.
Dig Dis Sci ; 58(8): 2177-86, 2013 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23606109

RESUMEN

BACKGROUND: Inulin-type fructan ameliorates metabolic diseases associated with obesity in animals. However, relatively little information is available on the comparative effects of inulins with different degree of polymerization (DP) on the lipid or glucose metabolism. AIM: The objective of this study was to investigate the effect of inulins with various DP on metabolic disorders associated with obesity in rats fed a high-fat diet under food restriction. METHODS: Rats were fed a high-fat diet supplemented with 5 % inulin-GR (Raftiline GR), inulin-Tokachi (Tokachi), or inulin-HP (Raftiline HP) without cellulose for 28 days at normal energy intakes or 14.5 % energy restriction. RESULTS: Under food restriction, the dietary inulin-Tokachi (mean DP 15) and -HP (mean DP 24), but not -GR (mean DP 10), reduced (p < 0.05) the serum cholesterol and triglyceride levels, and liver triglyceride concentration in rats, compared to the control diet. The cecal neutral steroid, bile acid, and propionate concentrations in the Tokachi and HP groups were higher (p < 0.05) than in the CONT group, and the cecal Bifidobacterium count in the Tokachi group was higher (p < 0.05) than in the other groups. CONCLUSIONS: Findings suggest that, depending on DP, dietary supplementation with inulin (DP 15 or DP 24) in rats fed a high-fat diet, regardless of food intake, positively modulates lipid metabolism and fecal microbiota but not glucose metabolism.


Asunto(s)
Grasas de la Dieta/administración & dosificación , Ingestión de Energía , Fructanos/química , Fructanos/farmacología , Glucosa/metabolismo , Metabolismo de los Lípidos/efectos de los fármacos , Animales , Aterosclerosis/patología , Aterosclerosis/prevención & control , Glucemia/efectos de los fármacos , Grasas de la Dieta/efectos adversos , Esquema de Medicación , Metabolismo de los Lípidos/fisiología , Lípidos/sangre , Polímeros , Ratas
6.
Biosci Biotechnol Biochem ; 75(7): 1335-41, 2011.
Artículo en Inglés | MEDLINE | ID: mdl-21737928

RESUMEN

The effects of betaine supplementation on D-galactosamine-induced liver injury were examined in terms of hepatic and serum enzyme activities and of the levels of glutathione and betaine-derived intermediates. The rats induced with liver injury showed marked increases in serum enzyme activity, but those receiving dietary supplementation of 1% betaine showed enzyme activity levels similar to a control group without liver injury. Administration of betaine also increased both hepatic and serum glutathione levels, even following D-galactosamine injection. The activity of glutathione-related enzymes was markedly decreased following injection of D-galactosamine, but remained comparable to that of the control group in rats receiving 1% betaine. The concentrations of hepatic S-adenosyl methionine and cysteine showed similar trends to that observed for hepatic glutathione levels. These results indicate that 1% betaine has a hepatoprotective effect by increasing hepatic and serum glutathione levels along with glutathione-related enzyme activities in rats.


Asunto(s)
Beta vulgaris/química , Betaína/administración & dosificación , Enfermedad Hepática Inducida por Sustancias y Drogas/tratamiento farmacológico , Glutatión/metabolismo , Hígado/efectos de los fármacos , Adenosilhomocisteinasa/efectos de los fármacos , Adenosilhomocisteinasa/metabolismo , Alanina Transaminasa/efectos de los fármacos , Alanina Transaminasa/metabolismo , Fosfatasa Alcalina/efectos de los fármacos , Fosfatasa Alcalina/metabolismo , Animales , Aspartato Aminotransferasas/efectos de los fármacos , Aspartato Aminotransferasas/metabolismo , Beta vulgaris/metabolismo , Suplementos Dietéticos , Galactosamina , Glutatión/efectos de los fármacos , Glutatión Peroxidasa/efectos de los fármacos , Glutatión Peroxidasa/metabolismo , Glutatión Transferasa/efectos de los fármacos , Glutatión Transferasa/metabolismo , L-Lactato Deshidrogenasa/efectos de los fármacos , L-Lactato Deshidrogenasa/metabolismo , Masculino , Melaza , Ratas , S-Adenosilmetionina/efectos de los fármacos , S-Adenosilmetionina/metabolismo
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