Cranberry (Vaccinium macrocarpon) products are
widely available in North American food, juice, and dietary supplement
markets. The use of cranberry is popular for the prevention of urinary
tract infections (UTIs) and other reported health benefits. Preliminary
findings by our research group indicate that arabinoxyloglucan oligosaccharides
are present in cranberry products and may contribute to the antiadhesion
properties of urine produced after cranberry consumption, but relatively
little is known regarding the oligosaccharide components of cranberry.
This report describes the isolation from two cranberry sources and
the complete structure elucidation of two arabinoxyloglucan oligosaccharides
through the use of carbohydrate-specific NMR spectroscopic and chemical
derivatization methods. These compounds were identified as the heptasaccharide
β-d-glucopyranosyl-(1→4)-[α-d-xylopyranosyl-(1→6)]-β-d-glucopyranosyl-(1→4)-β-d-glucopyranosyl-(1→4)-[α-l-arabinofuranosyl-(1→2)-α-d-xylopyranosyl-(1→6)]-β-d-glucopyranose
(1) and the octasaccharide β-d-glucopyranosyl-(1→4)-[α-l-arabinofuranosyl-(1→2)-α-d-xylopyranosyl-(1→6)]-β-d-glucopyranosyl-(1→4)-β-d-glucopyranosyl-(1→4)-[α-l-arabinofuranosyl-(1→2)-α-d-xylopyranosyl-(1→6)]-β-d-glucopyranose (2). Selected fractions and the
isolated compounds were subjected to antimicrobial, cell viability,
and E. coli antiadhesion assays. Results indicated
that enriched fractions and purified compounds lacked antimicrobial
and cytotoxic effects, supporting the potential use of such compounds
for disease prevention without the risk for resistance development.
Preliminary antiadhesion results indicated that mixtures of oligosaccharides
exhibited greater antiadhesion properties than purified fractions
or pure compounds. The potential use of cranberry oligosaccharides
for the prevention of UTIs warrants continued investigations of this
complex compound series.
Purpose We studied the health benefits of low calorie cranberry beverage consumption on glucoregulation, oxidative damage, inflammation, and lipid metabolism in overweight but otherwise healthy humans. Methods 78 overweight or obese men and women (30-70 years; BMI 27-35 kg/m 2 ) with abdominal adiposity (waist: hip > 0.8 for women and > 0.9 for men; waist: height ≥ 0.5) consumed 450 mL placebo or low calorie, high polyphenol cranberry extract beverage (CEB) daily for 8 week in a randomized, double-blind, placebo-controlled, parallel design trial. Blood and urine samples were collected after overnight fast at baseline and after 8 weeks of daily beverage consumption. Blood and urine samples were also collected during 3 oral glucose tolerance test (OGTT) challenges: (1) pre-intervention without the test beverages, (2) following a single dose of placebo or CEB at baseline (week 0), and (3) following a single dose of placebo or CEB at 8 week. Results Compared to placebo, a single CEB dose at baseline lowered endothelin-1 and elevated nitric oxide and the reduced:oxidized glutathione ratio (P < 0.05). Interferon-γ was elevated (P < 0.05) after a single CEB dose at baseline; however, after 8 week of CEB intervention, fasting C-reactive protein was lower (P < 0.05). CEB consumption for 8 week also reduced serum insulin and increased HDL cholesterol compared to placebo (P < 0.05). Conclusions An acute dose of low calorie, high polyphenol cranberry beverage improved antioxidant status, while 8 week daily consumption reduced cardiovascular disease risk factors by improving glucoregulation, downregulating inflammatory biomarkers, and increasing HDL cholesterol.
A fluorometric microplate assay has been developed to determine Escherichia (E.) coli adhesion to uroepithelial cells (UEC). P-fimbriated E. coli were labeled with BacLight Green and preincubated 30 min with human urine or standard. Fluorescent-E. coli were added to UEC in mircoplates at a 400:1 ratio, incubated 1 h, and washed, and the fluorescence intensity was measured. Specific labeling and adherence were confirmed by flow cytometry. A myricetin (1) standard curve (0-30 μg/mL) was developed; the lower limit of detection was 0.1 μg/mL, and half-maximal inhibitory concentration was 0.88 μg/mL (intra- and interassay coefficients of variance were <10% and <15%, respectively). Vaccinium macrocarpon (cranberry) extracts, quercetin (2), and procyanidins B1 (3), B2 (4), and C1 (5) showed similar inhibition. Antiadhesion activity of urine samples from subjects (n = 12) consuming placebo or V. macrocarpon beverage determined using this assay was positively correlated (R(2) = 0.78; p < 0.01) with a radiolabeled-E. coli assay.
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