Showing posts with label phenols. Show all posts
Showing posts with label phenols. Show all posts

Tuesday, December 17, 2013

Pistachio Phenols 90% Bioavailable. Phe, Leu, Glu & Trp - Four Satiating Aminos. Artificial Sweeteners Act as Anti- Convulsants. Dendrobium for Glucose, Lipids & Kidneys

Since I am a little pressed in time, I won't beat around the bush, but rather get to the meat of the matter of this Nutrition Quickie, right away... well, actually today's nutrition quickie has no item on meats, but is has one Dendrobium, which is actually rather a supplement - be that as it may, here you go:
  • Since you (hopefully ;-) haven't swallowed a bomb colorimeter, it's actually no wonder that your body can only access 75% and 95% of the energy this little oven can squeeze out of almonds and pistachios. If you went with the Atwood factor (which says fat = 9kcal/g) and simply added fats, proteins and carbs the discrepancy for almonds would even increase to ~35% (Nowotny. 2013)
    Almonds deliver 25% less calories that the nutritional label will tell you (Gebauer. 2013) -- At the FASEB meeting in April 2013, already, scientists from nowhere else than the mighty USDA, respectively the Beltsville Human Nutrition Research Center of the USDA presented the results of a human study that clearly shows that our tummies cannot squeeze out more than 75% of the nutrients a bomb calorimeter does. Nutrition Quickie: 25% Less Kcal in Almonds Than Label Says.

    The caloric value on both food labels and respective nutrient tables is thus off 25% too high. And the corrected energy content per 100g of almonds is 456kcal/100g not 575kcal/100g (nutritiondata.com), or even higher values you will find when you google  "almonds kcal" - I am curious if at least the nutrition labes will ever be updated.

    A similar but less pronounced mismatch has been found for pistachios by the same researchers earlier this year, already. According to a paper published in the January edition of the British Journal of Nutrition (Bear. 2013), the actual energy content of these heart healthy nuts 565kcal/100g, which is ~5% less than the currently established value. 

  • Bioavailability of pistachio polyphenols, xanthophylls, and tocopherols is very high - until you put them into a muffin (Mandalari. 2013) -- Bioavailability, i.e. the ratio of the total amount of a certain molecule that's in the food we eat in intact or at least active form in our bloodstream, can be a real issue for many of the good things the spectral analyzer of brainy scientists detects in our foodstuff.

    Table 1: Phenol, lutein and tocopherol content of the raw, roasted and salted pistacchios and regular and pistaccio (17g/100g) muffins (Madalari. 2013)
    In the upcoming January issue of Nutrition a group of researchers from the UK and Italy report the results of an investigation into the bioavailability of polyphenols, xanthophylls (lutein), and tocopherols (among them the rare gamma-variety) from raw pistachios, roasted salted pistachios, and muffins made with raw pistachios. You can see the original polyphenol, xanthophyll and tocopherol (mind the 90% gamma-tocopherol content, which has better chemoprotective effects than alpha-tocopherol; see "Vitamin(S!) E" post from 2011) content in table 1.

    Interestingly enough the availability of the tocopherols was almost identical for all three tested forms (raw, roasted, in muffins) and even the muffin reduced only the bioaccessability of protocatechuic acid (78%) and luteolin (36%), the rest of the phenols achieved the same ~90% Madalari et al. observed for the raw and roasted + salted pistachios in their million dollar model of the human digestive tract (click here for an article about this "artificial gut")

    • When the gut "tastes" phenylalanine (PHE), leucine (LEU), glutamate (GLUT) and tryptophane (TRP), satiety ensues (Daly. 2013) -- In their most recent paper Christin Daly et al. report on the cholecystokinin (CCK) release in the gut. According to the scientists from the University of Liverpool (UK) and the Kyushu University (Japan), the effect is mediated by interactions with the gastrointestinal bitter taste receptors. Since CCK inhibits food intake and reduces appetite, this provides another mechanistic explanation for the satiety promoting effects of high protein intakes. The effects was observed only for the L- and not the D-amino acids.

      Interestingly, the beneficial effects of  PHE, LEU and GLUT on CCK (but not the TRP-stimulated CCK secretion) were blunted in the presence of gurmarin. "Gurmarin?" Yeah, that's the rodent specific  sweet taste inhibitor in Gymnema sylvestre (note gurmarin does not work in humans; cf. Sigoillot. 2013), which is sold as an anti-diabetes supplement. Inosine, on the other hand increased the CCK release n response to all of the amino acids.

      How significant that is specifically for those who have a problem keeping their ravenous appetite in check is however questionable. After all the satiety response to CCK has been shown to be disturbed (at least in rodents; cf. Balaskó. 2013)

    • Table 2: Number of mice protected by the administered drug in the MES test (Talevi. 2013)
      Acesulfame potassium, cyclamate and saccharin are potential anti-convulsants (Talevi. 2013) -- It may sound counter-intuitive in view of all the bad stuff you have probably heard about artificial sweeteners, but it is their particular molecular structure and similarities between the T1R3 sweet taste receptor they are supposed to bind to ant several metabotropic glutamate receptors from different species that is probably behind the anticonvulsant effects a group of researchers from the Department of Biological Sciences at the Faculty of Exact Sciences of the National University of La Plata (UNLP) in Buenos Aires, Argentina.

      The overall effect size the scientists observed in their rodent model (see table 2) is yet far from earth shattering and generally more pronounced if the sweeteners had been ingested 4h instead of just 20 min before a Maximal Electroshock Seizure (MES) test. Whether this makes them worth "supplementing" is however more than questionable.

      Suggested additional reads:

    • Putting things into perspective: While the DPPH radical scavenging activity is not a really good measure of the in-vivo anti-oxidant potency of a given molecule it may yet still be worth mentioning that the one of Dendrobium (IC50 = 29.6 μg/mL) is more than 80% lower than that Areca catechuvar. Cinnamon cassia, Paeonia suffruticosa and Alpinia officinarum extracts which share IC50 values <6µg/mL (Lee. 2003). In other words, you need 80% more Dendrobium than cinnamon, for example, to neutralize the same amount H2O2 radicals.
      Dendrobium extract ameliorates renal fat accumulation, hyperglycemia and hyperlipidemia in rodents on "high fat" diet (Lee. 20012) -- While I cannot say if this is the same Dendrobium extract that's used in a pre-workout supplement that's "all the craze", these days, I can tell you that a group of researchers just published a paper on the renoprotective, hypoglycemic and hypolipidemic effects of an extract from Dendrobium moniliforme (a cursory search revealed that even within this genus of orchids there are at least 90 sub-types ranging from Aochidori to Yuten).

      Lee et al. administered the methanolic extract at dosages of 200mg/kg (HED ~16mg/kg) for nine weeks and reduced the elevated serum glucose, total cholesterol concentration and renal lipid accumulation in the HFD-fed mice. It also ameliorated renal dysfunction biomarkers including serum creatinine and renal collagen IV deposition. So that the scientists conclude that methanolic extracts from Dendrobium moniliforme exhibit pleiotropic effects on obesity induced parameters and exert renoprotective effect in HFD-fed mice.


    That's it for today,
    unless you are are interested in one of the following facebook news:
    • Crape ginger (Costus speciosus Koen) has significant anti-arthritic properties - at least in a rodent model (read more)
    • Ayurvedic polyherbal Unani formulation shows promising results in Acne vulgaris patients - 45 days, 45 subjects, significant improvements on Cook's acne scale (read more)
    • Endocannabinoids increase, leptin decreases a "sweet tooth" - And you can take this almost literally, since they do actually modulate sweet taste receptor sensitivity (read more)
        There are actually a couple more and they will "proliferate" *rofl* even before the next official SuppVersity  post will be published. Reason enough to check by from time to time, or simply "like" the SuppVersity on Facebook in order to keep up with the news.


        References:
        • Baer DJ, Gebauer SK, Novotny JA. Measured energy value of pistachios in the human diet. Br J Nutr. 2013 Jan;107(1):120-5.
        • Balaskó M, Soós S, Párniczky A, Koncsecskó-Gáspár M, Székely M, Pétervári E. Anorexic effect of peripheral cholecystokinin (CCK) varies with age and body composition (short communication). Acta Physiol Hung. 2013 Jun;99(2):166-72.
        • Gebauer SK, Novotny JA, Baer DJ. Macronutrient absorption from almonds: the measured energy value of almonds in the human diet. FASEB Journal. 2013;26:820.25.
        • Lee SE, Hwang HJ, Ha JS, Jeong HS, Kim JH. Screening of medicinal plant extracts for antioxidant activity. Life Sci. 2003 May 30;73(2):167-79.
        • Lee W, Eom DW, Jung Y, Yamabe N, Lee S, Jeon Y, Hwang YR, Lee JH, Kim YK, Kang KS, Kim SN. Dendrobium moniliforme Attenuates High-Fat Diet-Induced Renal Damage in Mice through the Regulation of Lipid-Induced Oxidative Stress. Am J Chin Med. 2013;40(6):1217-28.
        • Mandalari G, Bisignano C, Filocamo A, Chessa S, Sarò M, Torre G, Faulks RM, Dugo P. Bioaccessibility of pistachio polyphenols, xanthophylls, and tocopherols during simulated human digestion. Nutrition. 2013 Jan;29(1):338-44.
        • Novotny JA, Gebauer SK, Baer DJ. Discrepancy between the Atwater factor predicted and empirically measured energy values of almonds in human diets. Am J Clin Nutr. 2013 Aug;96(2):296-301. 
        • Sigoillot M, Brockhoff A, Meyerhof W, Briand L. Sweet-taste-suppressing compounds: current knowledge and perspectives of application. Appl Microbiol Biotechnol. 2013 Nov;96(3):619-30.
        • Talevi A, Enrique AV, Bruno-Blanch LE. Anticonvulsant activity of artificial sweeteners: a structural link between sweet-taste receptor T1R3 and brain glutamate receptors. Bioorg Med Chem Lett. 2013 Jun 15;22(12):4072-4.

        Wednesday, July 24, 2013

        Passionate Diabesity Prevention: Passion Fruit Rind Extract Halves Weight Gain & Quadruples HDL on Regular Diet

        Image 1: Looks like color matters! The yellow variety of Passiflora edulis is not just a particularly rich source of low-methoxyl pectin (dietary fiber), it's also packed with other bioactive substances which could keep you lean and healthy!
        The title of the paper Sandra Maria Barbalho and colleagues published in the Journal of Diabetes Research & Clinical Metabolism a couple of days ago is quite telling "Yellow passion fruit rind (Passiflora edulis): an industrial waste or an adjuvant in the maintenance of glycemia and prevention of dyslipidemia?", as it does imply that we could once again have missed an important part of the whole picture in our never-ending strive for ever maximal standardization, isolation and convenience: The waste that is generated from Brazil's 35,000 hectare passion fruit industry, more than 317,000 metric tons of fiber-, mineral., vitamin-, phenol- and flavenoid-laden flavedo (colored part of the rind) and albedo (white part of the rind) from Passiflora edulis.

        Passion Fruit Rind - Nothing in Nature is Wasted!

        If we dig somewhat deeper into the archives of the medical, chemical and even historico-cultural journals, it's not as if we could not have known about the potential health benefits of the putative "natural packaging" that protects the juicy kernel of the fruits of a plant which belongs to the family Passifloracea and originated in the tropical and subtropical regions of the American continent. Previous studies by Deng, Janebro and Ramos, for example, did already hint at the potent anxiolytic, antihyperglycemic and antihyperlipedemic effects of a fruit that has a longstanding tradition in traditional medicine (Ramos. 2007; Janebro. 2008; Deng. 2010). Against that background, it is almost surprising that the existent literature on the use of respective extracts is not exactly comprehensive.
        Figure 1: Changes in body weight (in g), absolute serum values (mg/mL) for glucose, triglycerides, cholesterol (total), HDL-C and LDL-C after 30 days of either regular or passion fruit bark powder solution (2x 1ml/kg body weight) supplemented diet in healthy Wistar rats (data adapted from Barbalho. 2013)
        Malicious gossip would probably have it that the surprisingly profound effects Barbalho et al. observed in healthy rodents in response to the twice-daily administration of 1ml/kg bodyweight of a quasi-homemade (see infobox on the right of the next paragraph for details), obviously non-patentable passion fruit extracts would hamper the sales of metformin, lipitor and the recently FDA-approved weight loss drug Belviq (a 5-HTC-2 serotonin receptor antagonist). After all, aside from the decrease in LDL, all the diabetes- and  CVD relevant changes in figure 1 were statistically highly significant (p<0.01); and what's more, the necessary raw material is not just looked down upon, as if it was a waste product, it is according to the authors also treated like any other industrial waste by Brazil's passion fruit juice industry who either dumps it on illegal landfills or has to pay money for its proper disposal (Barbalho. 2013).

        My GNC Does Not Have Passion Fruit Rind Extracts! Can I Make My Own?

        How to home-brew your own PFR extract ;-)
        1. dehydrate the rind on trays in a forced air circulation drying oven at 55ºC until a constant dry weight is reached
        2. ground 200g into powder in a multiprocessor for 6 minute (turn off the processor at 2 min intervals to stir the product)
        3. prepare a solution of 20 g of powdered rind and 500 mL of water
        4. beat solution in a blender for 12min 
        5. filtered through filter paper
        6. divide resulting solution into aliquots and stored in a freezer at -10ºC
        Ingest 2x10-14ml servings per day (standard HED calculation)
        Ecology and health aside, I bet that for (too) many people the -76% reduction in weight gain would constitute the most convincing argument to buy Passion-o-Lean(TM) or whatever stupid name the first company whose "product designer" reads the study will come up with ;-)

        Now, the good news is that we do actually have human data to confirm a statistically significant weight loss effect from passion fruit rind products: The nineteen 30-60 year-old, still normal-weight (BMI 24.8kg/m²) but hyperlipidemic (cholesterol > 200 mg/dL; went down by -18% as a result of supplementation) women in the aforementioned study by Ramos et al. lost 1.7 kg within one month (Ramos. 2007), but they did ingest 30g of passion flower rind flour per day and the weight loss stalled in the second month in the course of which they lost <300g, only - by no means as impressive as the weight loss, or, I should say, the absence of weight gain in the rodents from Barbalho study, right?

        Due to the fact that Ramos et al. don't disclose how the co-authoer Sabaasrur, who provided the flour, actually prepared it, we cannot definitely answer the question whether or not these differences could simply be a result of the different preparation methods and consequent yield of bioactive substances in the extract (Barbalho. 2013) and the flour (Ramos. 2007). It is however very unlikely that the production of the floor involved either low temperature drying (1), water extraction (3-5) or refrigeration to maintain the maximal vitamin and phenols content (see figure 2) as they were part of the manual extraction process that was used in the Barbalho study (for details on the preparation see box on the left).
        Figure 2: If you are more of a juicer, make sure to drink your juice right away to get the maximum amount of the good phenolic acids and avoid the potentially hazardous HMF (click to enlarge for more info; data based on Talcott. 2003)
        Implications: Despite the fact that the data in figure 2, though based on an analysis of passion fruit juice, would support the hypothesis that the handmade passion fruit rind extract in the Barbalho study was more than just one magnitude "stronger" than the flour that's been used with some success in the Ramos and the Janebro study, it is still questionable, whether the profound reductions in blood glucose, the  improvements in the triglyceride (1.3 vs. 4.3) and total cholesterol to HDL ratios (2.5 vs. 10.4) will translate 1:1, or even at all to human beings. After all, it could be partly mediated by the reduced weight gain... apropos, 'not gaining weight' is still very different from 'losing weight' and it is therefore not feasible to compare, the relatively mediocre weight loss in the Ramos study, of which the scientists assume that it was, just as the reduction in cholesterol, mediated by the high content of soluble fiber in the passion fruit flour (73% of the dry matter is fiber, 60% of it insoluble; Yapo. 2008), to the profound 'anti-obesity' effect in the Barbalho study.

        Moreover, in the absence of detailed information about the body composition of the lab animals and their energy intake, we could as well be dealing with the results of micronutrient malabsorption or anorexia as root causes of the reduced body weight in the passion fruit rind extract group of the Barbalho study.... although, with the twice daily bolus administration of only 2x 1ml of the PFR extract, both explanations, i.e. 'failure to thrive due to nutrient malabsorption' and 'anorexia in response to too much fiber', appear pretty unlikely, so that passion fruit rind extract would actually be a good candidate for a home-brew diabesity prevention potion... well, at least if you live next to one of those Brazilian dumping grounds where the passion fruit industry disposes of their hitherto unrecognized treasures ;-)

        References:
        • Barbalho SA, da Silva Soares de Souza M, de Paula e Silva J, Mendes CG, de Oliveira GA, Costa T, Farinazzi-Machado. Yellow passion fruit rind (Passiflora edulis): an industrial waste or an
          adjuvant in the maintenance of glycemia and prevention of dyslipidemia? FMV. Journal of Diabetes Research and Clinical Metabolism. 2013.
        • Deng J, Zhou Y, Bai M, Li H, Li L: Anxiolytic and sedative activities of  Passiflora edulis f. flavicarpa. J Ethnopharmacol  2010; 128;(1.);148-53.
        • Janebro D I, Queiroz M S R, Ramos A T, Sabaa-Srur A U O, Cunha MAL,  Diniz M F. Effect of the flour of the yellow passion fruit peel (Passiflora  edulis f. flavicarpa Deg.) in the glycemic and lipid levels of type 2 diabe- tes patients. Rev Bras Farmacog 2008;18: 723-732. 
        • Ramos AT, Cunha MAL, Sabaasrur AUO, Pires VCF, Cardoso AA et al. Use of Passiflora edulis f. flavicarpa on cholesterol reduction. Braz J Pharmacog 2007;17: 592-560.
        • Talcott ST, Percival SS, Pittet-Moore J, Celoria C. Phytochemical composition and antioxidant stability of fortified yellow passion fruit (Passiflora edulis). J Agric Food Chem. 2003 Feb 12;51(4):935-41.
        • Yapo BM, Koffi KL: Dietary fiber components in yellow passion fruit rind - a potential fiber source. J Agric Food Chem  2008; 56;(14.);5880-3. 

        Tuesday, July 23, 2013

        The Ergogenic Effect of Nonalcoholic Beer Front- & Back Loading + 15 Beerish Health Facts Everyone Should Know

        Image 1: Erdinger Weißbräu Alkoholfrei your first choice for peri workout isotonic carbohydrate supplementation!?
        Where else, if not from Germany, "The Land of Beer and Weißwurst" as it is falsely perceived by the average foreign Oktoberfest visitor, could the data for a study on the ergogenic effects of nonalcoholic beer originate from? In their recently published paper Johannes Scherr and his colleageas from the Department of Prevention and Sports Medicine at the Klinikum rechts der Isar of the Univerisity of Munich report that a 'forntload + post-supplementation' strategy (3 weeks before, 2 weeks after) with 1-1.5l/day of Erdinger Weißbräu Alkoholfrei led to statistically significant reductions in post-race total blood leukocyte counts (-9%) and interleukin-6 (-24%) and 66% lower incidence of upper-respiratory tract infections in the 58 beer-drinking subjects (age: 36-51y), when compared to their 63 peers(age:35-49y) who received an isocaloric control beverage, which differed from the beer only in terms of its polyphenol content (Scherr. 2013).

        It's not all about Erdinger Alkoholfrei  - 15 Beerish Health Facts You Should Know

        In fact, the ergogenic effects Scherr et al. observed in their most recent study are probably nothing but one of the manifold downstream effects of the nutrient dense non-alcoholic fraction of 'amber nectar', which consists of a whole host of bioactive ingredients with at least as many, mostly beneficial health effects (the following is in part based on Sohrabvandi. 2010; where other references were used, additional references are provided):
        How exactly is nonalcoholic beer produced?
        • Fermentation-free brewing and dilution procedures won't produce results European or US costumers will be happy with, therefore it is mostly used in Islamic countries
        • Alcohol removal by vacuum destillation, adsorptive alcohol removal, dialysis, reverse osmosis, or osmotic distillation
        • Restricted alcohol fermentation uses yeast that can only partially ferment the wort or represses or interrupts fermentation by applying different compositional and/or process procedures (interrupted fermentation technique)
        • Fermenting with GMO bacteria which lack the alcohol dehydrogenase (ADH) enzyme and produce no or minimal amonts of alcohol.
        • Reducing fermentable fractions / glucose content in wort by adjusting the concentration of sugar in the primary formulation so that no considerable sugar residue remains after the restricted fermentation period.
        • Heating or pressurizing the wort to inactivate yeast cells and inhibit the subsequent alcoholic fermentation, as soon as the desired flavor profile of the wort was achieved
        Note: The beer in the study at hand was brewed under tightly controlled temperature (the exact method is apparently a company secret, though).
        • has potentially blood pressure lowering effect due to high potassium to sodium ratio (typically 4:1) 
        • is relatively rich in magnesium and to less extent in phosphorous
        • contains glutathione precursors and co-factors zinc, copper, selenium and amino acids
        • features physiologically active immuno-modulatory peptides and proteins
        • has 35+ phenolic compounds (about 80–90% from malt and 10–20% from hops)
        • may prevent and improve obesity and type-2 diabetes, improve lipid metabolism, and suppress atherosclerosis due to beneficial health effects of the bitter substances in hops (Kondo. 2004)
        • has been shown to improve sleep and lactation in women; probably due to bioactive molecules from hops (Koletzko. 2000; Franco. 2013)
        • contains folate and glycine betaine which exert antimutagenic effects and reduce homocysteine
        • has up to 6.2g fiber per liter
        • its β-pseudouridine content may protect against radiation damage (Monobe. 2003)
        • contains silicic acid which increases renal excretion of aluminum (Aluminum has been associated with age related diseases and neurodegeneration; cf. Krewski. 2007)
        • is associated with higher hip mineral density in older men who drink 2 regular beers/day; probably due to its silicon content (Tucker. 2009)
        • provides more antioxidants per day than wine to the U.S. diet (Vinson. 2003)
        • exerts anti-oxidative effects on lipoproteins (=cholesterol) which are superior to that of its vitamin & antioxidants, alone (Vinson. 2003)
        • unfortunately, allegedly gluten-free barley based beers contain significant amounts of hordein (=gluten) and are not suitabe for patients with celiac disease (Colgrave. 2013)
        Now compare that to your average energy drink, which - as you should by now be aware of - may deliver zero fat calories and will still add 18g /day of body fat right to your frame, when consumed on a daily basis (cf. "Fat Content Per Energy Drink 0g, Body Fat Gain Per Energy Drink 18g!")
        Image 2 (FOX): Homer always knew what Schütze et al. confirmed in 2009: "Beer consumption leads to [waist circumference] gain [...] closely related to overall weight gain. This study does not support the common belief of a site-specific effect of beer on the abdomen."
        Implications: In view of the fact that carbohydrate supplementation is still common practice among endurance athletes, I don't see why a refreshing nonalcoholic beer (1.5l of Erdinger Weißbreu Alkoholfrei contain 375kcal and ~75g of carbohydrates)  that has been brewed according to the German purity law should not be at least as good as one of those sugar-laden electrolyte drinks or gels with artificial colorings and what not.

        Moreover, the relatively high phenolic content of the beer (~400 mg of gallic acid equivalents per day), of which Scherr et al. speculate that it was the underyling reason for the observed benefits, could render the use of other polyphenolic supplements obsolete, save you money and keep you healthy and sane, as only few people are like me don't like the taste of beer and can thus sit in the Biergarten with nothing but plain water, while their friends hoist brew after brew... although, when I come to think about it: Maybe I should order some Erdinger later today? *rofl*

        Note: The study was financed from a fund that was established by the Erdinger Weissbraeu, Werner Brombach GmbH. Contrary to some other researchers Scherr et al. do yet openly disclose the funding and state that "the funders had nodirect role in the study’s design, conduct, analysis, interpretation of data, and reporting" - and before you start lamenting, now, think about who finances and conducts the studies on pharmaceuticals...
        References:
        • Colgrave ML, Goswami H, Howitt CA, Tanner GJ. What is in a beer? Proteomic characterization and relative quantification of hordein (gluten) in beer. J Proteome Res. 2013 Jan 1;11(1):386-96.
        • Franco L, Sánchez C, Bravo R, Rodríguez AB, Barriga C, Romero E, Cubero J. The sedative effect of non-alcoholic beer in healthy female nurses. PLoS One. 2013;7(7):e37290. Epub 2013 Jul 18.
        • Koletzko B, Lehner F. Beer and breastfeeding. Adv Exp Med Biol. 2000;478:23-8. Review.
        • Kondo K. Beer and health: preventive effects of beer components on lifestyle-related diseases. Biofactors. 2004;22(1-4):303-10.
        • Krewski D, Yokel RA, Nieboer E, Borchelt D, Cohen J, Harry J, Kacew S, Lindsay J, Mahfouz AM, Rondeau V. Human health risk assessment for aluminium, aluminium oxide, and aluminium hydroxide. J Toxicol Environ Health B Crit Rev. 2007;10 Suppl 1:1-269.
        • Monobe M, Arimoto-Kobayashi S, Ando K. Beta-pseudouridine, a beer component, reduces radiation-induced chromosome aberrations in human lymphocytes. Mutat Res. 2003 Jul 8;538(1-2):93-9.
        • Scherr J, Nieman DC, Schuster T, Habermann J, Rank M, Braun S, Pressler A, Wolfarth B, Halle M. Nonalcoholic beer reduces inflammation and incidence of respiratory tract illness. Med Sci Sports Exerc. 2013 Jan;44(1):18-26.
        • Schütze M, Schulz M, Steffen A, Bergmann MM, Kroke A, Lissner L, Boeing H. Beer consumption and the 'beer belly': scientific basis or common belief? Eur J Clin Nutr. 2009 Sep;63(9):1143-9. Epub 2009 Jun 24.
        • Sohrabvandi S, Mousavi SM, Razavi SH, Mortazavian AM, Rezaei K. Alcohol-free Beer: Methods of Production, Sensorial Defects, and Healthful Effects, Food Reviews International. 2010;26:4, 335-352
        • Tucker KL, Jugdaohsingh R, Powell JJ, Qiao N, Hannan MT, Sripanyakorn S, Cupples LA, Kiel DP. Effects of beer, wine, and liquor intakes on bone mineral density in older men and women. Am J Clin Nutr. 2009 Apr;89(4):1188-96.
        • Vinson JA, Mandarano M, Hirst M, Trevithick JR, Bose P. Phenol antioxidant quantity and quality in foods: beers and the effect of two types of beer on an animal model of atherosclerosis. J Agric Food Chem. 2003 Aug 27;51(18):5528-33.