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1.
Can J Physiol Pharmacol ; 95(12): 1414-1425, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-28800398

RESUMO

An open-label, randomized, exploratory study of 44 healthy overweight subjects with cardio-metabolic syndrome (CMS) risk factors was conducted to assess the safety, tolerability, and efficacy of a proprietary lifestyle modification program without (DIET) and with (PROG) targeted nutraceutical supplementation, including phytosterols, antioxidants, probiotics, fish oil, berberine, and soy, pea, and whey proteins over 13 weeks. Key metrics were recorded at baseline and weeks 9 and 13. For the DIET and PROG groups, compliance was 85% and 86%, respectively, with no adverse events related to the diet or supplements. Twelve subjects discontinued participation before week 9 for reasons unrelated to the study. PROG subjects experienced greater decreases (p < 0.05) than DIET in body mass, fat mass, total cholesterol, LDL cholesterol, TG, cholesterol / HDL ratio, TG/HDL ratio, apolipoprotein B / apolipoprotein A1 ratio, and hs-CRP. The Framingham 10-year cardiovascular disease risk score decreased by 40% (p < 0.01) in the PROG arm versus no change for the DIET arm. As a pilot study, it was not possible to state whether the observed effects were the result of nutraceutical supplementation alone or the result of additive or synergistic interactions among diet, lifestyle modifications, and nutraceutical supplementation. Moreover, individuals with CMS risk factors following a lifestyle modification program received additional health benefits from targeted nutraceutical supplementation.


Assuntos
Peso Corporal/efeitos dos fármacos , Proteínas Alimentares/farmacologia , Suplementos Nutricionais , Carga Glicêmica , Estilo de Vida , Adulto , Apolipoproteínas/sangue , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Fatores de Risco , Segurança , Fatores de Tempo , Circunferência da Cintura/efeitos dos fármacos
2.
Can J Physiol Pharmacol ; 94(12): 1257-1266, 2016 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-27463949

RESUMO

We examined the clinical safety and efficacy of F105 in 11 subjects with moderate dyslipidemia. F105 is a combination of bergamot fruit extract (Citrus bergamia, BFE) and 9 phytoextracts selected for their ability to improve the antioxidant and anti-inflammatory activity of BFE. In vitro F105 exhibited a synergistic inhibition of oxygen radical absorbing capacity, peroxynitrite formation, and myeloperoxidase activity. Following 12 weeks of F105 daily, no treatment-related adverse events or changes in body mass were seen. Statistically significant changes were noted in total cholesterol (-7.3%), LDL-cholesterol (-10%), non-HDL cholesterol (-7.1%), cholesterol/HDL (-26%), and apolipoprotein B (-2.8%). A post hoc analysis of 8 subjects with HbA1c > 5.4 and HOMA-IR score > 2 or elevated triglycerides revealed additional statistically significant changes in addition to those previously observed in all subjects including triglycerides (-27%), oxLDL (-19%), LDL/HDL (-25%), triglycerides/HDL (-27%), oxLDL/HDL (-25%), and PAI-1 (-37%). A follow-up case report of a 70-year-old female patient, nonresponsive to statin therapy and placed on F105 daily, demonstrated improved cardiometabolic variables over 12 weeks similar to the subgroup. In summary, F105 was clinically well-tolerated and effective for ameliorating dyslipidemia in subjects with moderate cardiometabolic risk factors, particularly in the individuals with HbA1c > 5.4%.


Assuntos
Antioxidantes/uso terapêutico , Citrus , Dislipidemias/tratamento farmacológico , Doenças Metabólicas/prevenção & controle , Compostos Fitoquímicos/uso terapêutico , Extratos Vegetais/uso terapêutico , Adulto , Idoso , Antioxidantes/química , Antioxidantes/isolamento & purificação , Composição de Medicamentos , Sinergismo Farmacológico , Dislipidemias/diagnóstico , Dislipidemias/metabolismo , Feminino , Humanos , Masculino , Doenças Metabólicas/metabolismo , Pessoa de Meia-Idade , Compostos Fitoquímicos/química , Compostos Fitoquímicos/isolamento & purificação , Projetos Piloto , Extratos Vegetais/isolamento & purificação , Extratos Vegetais/farmacologia , Fatores de Risco
3.
J Sep Sci ; 35(9): 1183-9, 2012 May.
Artigo em Inglês | MEDLINE | ID: mdl-22689494

RESUMO

Commercially available hops (Humulus lupulus L.) bitter acid extracts contain a mixture of three major congeners (co-, n-, and ad-) in addition to cis/trans diastereomers for each congener. Individual isomerized α-acids were obtained by the consecutive application of two separate countercurrent chromatography methods. First, individual isomerized α-acid congeners as a mixture of cis/trans diastereomers were obtained using a solvent system consisting of hexane and aqueous buffer. The second purification, capable of separating cis/trans diastereomers, was accomplished using a quaternary solvent system; an alternative procedure using ß-cyclodextrin followed by countercurrent chromatography was also investigated. The NaBH(4) reduction of the purified isomerized α-acid compounds followed by countercurrent chromatography purification resulted in individual ρ iso α-acids (>95%). Similarly, catalytic hydrogenation of the purified isomerized α-acid compounds followed by countercurrent chromatography purification produced individual tetrahydro isomerized α-acids (>95%). Reported herein is a widely applicable approach that focuses on three critical variables--solvent system composition, pH, and buffer-to-sample ratio--that enable the efficient purification of individual bitter acids (≥95%) from commercially available hops extracts.


Assuntos
Ácidos/isolamento & purificação , Distribuição Contracorrente/métodos , Humulus/química , Extratos Vegetais/isolamento & purificação , Ácidos/química , Isomerismo , Extratos Vegetais/química
4.
J Med Food ; 22(5): 479-489, 2019 May.
Artigo em Inglês | MEDLINE | ID: mdl-31084538

RESUMO

Among the comorbidities of high body mass index, cardiovascular disease continued to be the leading cause of death and disability globally in 2015, while type 2 diabetes remained second. The primary objectives of this observational study were to confirm the safety, tolerability, and efficacy of our calorie-restricted Mediterranean diet with targeted dietary supplementation (PROG1) using globally recognized dietary supplementation. Fifty healthy overweight and obese subjects with cardiometabolic risk factors were assigned a modified Mediterranean diet, including protein shakes and targeted supplementation (PROG2), providing ∼68-76% of subject estimated calorie requirements. Salivary nitrite was assessed weekly and key cardiometabolic metrics were recorded at baseline and weeks 9 and 13. PROG2 was well tolerated with 86% compliance. The most common adverse effects were bloating, flatulence, and constipation, which were self-limiting. Subjects exhibited decreases (P < .01) from baseline of 12% in body weight, 18% in body fat, and 8.8% in waist circumference. Total cholesterol (TC), low-density lipoprotein (LDL) cholesterol, and triglycerides (TG) were reduced (P < .01), respectively, 19%, 22%, and 40%. Lipid ratios of TC/high-density lipoprotein (HDL), TG/HDL, and oxidized LDL (oxLDL)/HDL were decreased 15% (P < .01), 35% (P < .01), and 13% (P < .05), respectively. Inflammation biomarkers, oxLDL and high-sensitivity C-reactive protein, were reduced 17% (P < .01) and 30% (P < .05), respectively. Reductions of 9.0% for systolic (P < .01) and 12% (P < .01) for diastolic blood pressure were noted. In concert, the nitrogen dioxide salivary biomarker for nitric oxide was increased relative to baseline. PROG2 produced a dramatic 50% reduction in subjects meeting cardiometabolic syndrome criteria and a 38% decrease in Framingham 10-year cardiovascular risk. These results confirmed our previous findings that the addition of targeted nutraceutical supplementation to a calorie-restricted Mediterranean diet with lifestyle modifications improves multiple longevity risk factors more effectively than diet and lifestyle modification alone.


Assuntos
Dieta Mediterrânea , Miocárdio/metabolismo , Sobrepeso/dietoterapia , Extratos Vegetais/administração & dosagem , Probióticos/administração & dosagem , Adulto , Biomarcadores/metabolismo , Peso Corporal/efeitos dos fármacos , Proteína C-Reativa/metabolismo , Estudos de Casos e Controles , Colesterol/metabolismo , Suplementos Nutricionais/análise , Feminino , Índice Glicêmico , Coração/efeitos dos fármacos , Coração/fisiopatologia , Humanos , Estilo de Vida , Longevidade/efeitos dos fármacos , Masculino , Pessoa de Meia-Idade , Sobrepeso/tratamento farmacológico , Sobrepeso/fisiopatologia , Sobrepeso/psicologia , Triglicerídeos/metabolismo
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