Review Article

Bioactivity of Polyphenols: Preventive and Adjuvant Strategies toward Reducing Inflammatory Bowel Diseases—Promises, Perspectives, and Pitfalls

Table 3

Human intervention trials suggesting health benefits of polyphenol intake with respect to IBD—an overview.

Aspects studiedDosing and timeEffects foundMechanism proposed and criticsReference

Effect of curcumin on CD patients in a RCT study89 patients with UC, 45 given 2 g curcumin/d for 6 monthsCurcumin improved both clinical activity index & endoscopic indexCurcumin suppressed morbidity associated with UC[75]

Effect of different dietary interventions, prospective trial22 CD subjects receiving semivegetarian versus omnivorous diet for 2 y Semivegetarian diet more successful in maintaining remission over 2 y versus omnivorous diet (94 versus 33%)Effects of fiber & polyphenols?[76]

Effect of cacao drink on gut bacteria22 healthy adults receiving 494 mg or () cocoa
flavanols/d for 4 weeks
Significant reductions in plasma TG & CRP in group receiving high flavonol drink Flavonol rich drink sign. increased Bifidobacteria & Lactobacilli populations, sign. decreasing Clostridia counts[77]

Effect of pycnogenol in subjects with CD15 children with CD receiving 2 mg/kg bw. for 12 weeks. 15 control children with no interventionCompared to baseline, improved lipoperoxides, improved SOD, reduced AOPP Oxidative stress related markers improved following PP consumption[78]

Effect of red wine consumption on plasma LPS & gut bacteria10 volunteers, 20 d, 272 mL of red wine (RW) with/without alcohol (DRW), or 100 mL ginNo significant differences in the change in LPS or LBP conc. between chronic RW, DRW, & gin consumption Bifidobacterium & Prevotella amounts were significantly increased by RW & correlated negatively with LPS concentrations[79]

Effect of blueberry beverage (bb) on healthy subjects20 subjects, either consuming bb (375 mg ACNs & 128 mg CA) for 6 weeks versus placeboBb enhanced Bifidobacteria counts compared to placebo Prebiotic effect of polyphenols[80]

Effect of apple products on inflammation & gut microbiota5 × 4 weeks crossover, whole apples (550 g/d), apple pomace (22 g/d), clear & cloudy apple juices (500 mL/d), none, healthy adults, 75–240 mg PP/d No effect on HDL-cholesterol, TAG, weight, waist-to-hip ratio, blood pressure, CRP, gut microbiota, insulin, IGF1, lower serum LDL for whole apples & pomaceToo high variation of bacterial changes such as Bifidobacteria, already health subjects, too short intervention period?[81]

Effect of red wine on fecal markers of inflammation34 healthy subjects drinking RW (1.76 g/L PP) for 4 weeksIn a subgroup of 6 subjects, TNF-, IL-6, & IFN- in feces were sign. reduced Reduced inflammation via NF-κB?[82]

Effect of red wine PP on gut bacteria of obese subjects10 obese & 10 normal subjects receiving 272 mL RW over 30 dPP sign. increased fecal Bifidobacteria & Lactobacillus & butyrate producers (Faecalibacterium prausnitzii & Roseburia) at expense of undesired bacteria, for example, LPS producers (E. coli & Enterobacter cloacae)Intestinal barrier protection & SCFA production[83]

ACNs: anthocyanins; AMPK: adenosine monophosphate kinase; AOPP: advanced oxidation protein end-products; Bcl-xl: B-cell lymphoma-extra large; bcrp: breast cancer cell resistance protein; bw: body weight; CA: chlorogenic acid; CAT: catalase; ccl2: chemokine (C-C motif) ligand 2; CINC1: cytokine-induced neutrophil chemoattractant-1; CYP1A1: cytochrome P450, family 1, member 1A1; CD: Crohn’s disease; COX-2: cyclooxygenase 2; CRP: c-reactive protein; CXCL1: chemokine (C-X-C motif) ligand, neutrophil activating; DAI: disease activity index; DSS: dextran sodium sulphate; DRW: dealcoholized wine; EA: ellagic acid; EGCG: epigallocatechin gallate; EP: evening primrose (Oenothera paradoxa) pomace; GAE: gallic acid equivalents; GM-CSF: granulocyte macrophage colony stimulating factor; FRAP: ferric reducing antioxidant power assay; GR: glutathione reductase; Gred: reduced glutathione; GrTP: green tea extract; GPx: glutathione peroxidase; GSH: glutathione (reduced); GSP: grape seed polyphenols; GSTT2: glutathione-S-transferase theta 2; ICAM: Intercellular adhesion molecule 1; IFN: interferon; IL: interleukin; iNOS: inducible nitric oxide synthase; LBP: LPS binding protein; LPS: lipopolysaccharides; Mcp-1: monocyte chemoattractant protein-1; Mdr1a (−/−): multidrug resistance targeted mutation; MDA: malondialdehyde; MPO: myeloperoxidase; MIP2: macrophage inflammatory protein 2; MRP: multidrug resistance protein; OHdG: 8-hydroxy-2′-deoxyguanosine; NF-B: nuclear factor kappa B; Nrf-2: nuclear factor (erythroid-derived 2)-like 2; NQO1: NAD(P)H dehydrogenase [quinone-1] 1; PCAM-1: platelet endothelial cell adhesion molecule; PGE2: prostaglandin-E2; P-gp: P-glycoprotein; PP: polyphenols; PRDX-6: peroxiredoxin-6; PPAR: peroxisome proliferator-activated receptor; RCT: randomized control trial; RW: red wine; SAA: serum amyloid α; SAPK: stress activated protein kinase; SCFAs: short chain fatty acids; SOD: superoxide dismutase; STAT1: signal transducer and activator of transcription 1; TAC: total antioxidant capacity; TBNS: 2,4,6-trinitrobenzenesulfonic acid; TBARS: thiobarbituric acid reactive substances; TG: triglycerides; TNF-α: tumor necrosis factor alpha; TXNRD-1: thioredoxin reductase-1; UGT1A1: UDP-glucuronosyltransferase family 1 member A1; UTR: untranslated; VCAM-1: vascular cell adhesion protein 1; WB: Western blot.