No abstract

No abstract

BackgroundNonalcoholic fatty liver disease (NAFLD) is the hepatic manifestation of the metabolic syndrome and can vary from hepatic steatosis to end-stage liver disease. It is the most common liver disease and its prevalence is increasing worldwide. In the present study, the effect of whey proteins on some parameters of NAFLD was investigated.ResultsOral administration of the studied whey proteins products reduced the final body weight of rats. There was a significant reduction effect (P < 0.05) of the tested proteins on hepatic triglycerides, liver enzymes (ALT and AST), lipid peroxidation (malondialdehyde level) and serum glucose. Feeding on whey proteins caused an increase in the reduced glutathione. Hepatic content of reduced glutathione was not affected by any of the used whey proteins, but it showed an increasing tendency (P > 0.05). Liver histology showed an improvement of fatty infiltration in hepatocytes from whey protein groups and gives the histology of liver a normal appearance.ConclusionsThe obtained results indicate a possible role for oral administration of whey proteins in the regulation of liver biochemistries in a rat's model of NAFLD. This regulatory effect of whey proteins was accompanied by an improvement in fatty infiltration in hepatocytes and a reduction of oxidative stress parameters.

No abstract

To meet the increased consumer demand for yogurt with reduced fat content, various efforts have been made to improve the quality of reduced-fat variants that still is regarded as having inferior quality. As an alternative, a yogurt was produced from buffalo skim milk with the addition of microbial transglutaminase (TG; 1 U.g −1 protein) and buttermilk powder (BMP; 1 and 2% "w/w"). For comparison, a fat-free variant without TG or BMP and a full-fat yogurt were studied. Monitoring the pH drop during incubation time revealed that TG did not interfere with the pH reduction, while BMP addition accelerated the decline in pH. TG treatment or BMP addition substantially improved the water holding capacity functionality of the yogurt gel. Electrophoretic analysis revealed that the addition of BMP enhanced the reactivity of TG as indicated by the appearance of high molecular weight protein polymer bands. These results were confirmed by scanning electron microscope analysis. The addition of TG and BMP, either individually or in combination, showed a marked impact on gel network, resulting in a more compact and dense gel structure accompanied by irregular agglomerated clusters of protein aggregates. Fat-free yogurts of individually BMP addition exhibited the most desirable organoleptic attributes as indicated by a sensory panel and were perceived as similar to the fullfat yogurt perception. Overall, the addition of TG or BMP appeared to have potential as a valuable alternative in fat-free yogurt production, and BMP can be used as a source of extra protein, which in turn offers promising option to develop innovative functional fat-free yogurt.

No abstract

Kefir is a functional beverage that contains lactic and acetic acid bacteria (LAB, AAB) and yeasts. This work’s aim was to study the chemical, microbial, and functional characteristics of kefir produced from cow’s milk and soy milk. After fermentation, free amino acids were 20.92 mg 100 mL−1 and 36.20 mg 100 mL−1 for cow’s milk and soy milk kefir, respectively. Glutamic acid was majority in both, suggesting that microbial proteolysis leads to an increase in free amino acids including glutamic acid. 108–109 CFU mL−1 LAB, 106–107 CFU mL−1 AAB, and 106–107 CFU mL−1 yeasts were counted in cow’s milk kefir, whereas soy milk kefir contained greatly lower yeasts and AAB. Lactococcus lactis, Kazachstania unispora, and Saccharomyces cerevisiae were isolated as major microorganisms in both kefirs. Acetobacter orientalis only existed in cow’s milk kefir. Cow’s milk and soy milk showed ACE inhibitory activity, which significantly increased after fermentation. Both kefirs also exhibited antioxidant activity and bactericidal activity against Escherichia coli, Salmonella Typhimurium, and Staphylococcus aureus.

No abstract