Protective effect of whey proteins against nonalcoholic fatty liver in rats

被引:64
作者
Hamad, Essam M. [1 ]
Taha, Soad H. [1 ]
Abou Dawood, Abdel-Gawad I. [1 ]
Sitohy, Mahmoud Z. [2 ]
Abdel-Hamid, Mahmoud [1 ]
机构
[1] Cairo Univ, Dept Dairy Sci, Fac Agr, Cairo, Egypt
[2] Zagazig Univ, Fac Agr, Dept Biochem, Zagazig, Egypt
关键词
SUPPLEMENTATION; GLUTATHIONE; STEATOHEPATITIS; OBESITY; DISEASE;
D O I
10.1186/1476-511X-10-57
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Background: Nonalcoholic 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. Results: Oral 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. Conclusions: The 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.
引用
收藏
页数:7
相关论文
共 25 条
  • [1] Treatment of non-alcoholic fatty liver disease
    Adams, LA
    Angulo, P
    [J]. POSTGRADUATE MEDICAL JOURNAL, 2006, 82 (967) : 315 - 322
  • [2] [Anonymous], SPSS WIND REL 16 0 0
  • [3] Whey proteins influence hepatic glutathione after CCl4 intoxication
    Balbis, E.
    Patriarca, S.
    Furfaro, A. L.
    Millanta, S.
    Sukkar, S. G.
    Marinari, U. M.
    Pronzato, M. A.
    Cottalasso, D.
    Traverso, N.
    [J]. TOXICOLOGY AND INDUSTRIAL HEALTH, 2009, 25 (4-5) : 325 - 328
  • [4] Dietary cysteine alleviates sucrose-induced oxidative stress and insulin resistance
    Blouet, Clemence
    Mariotti, Francois
    Azzout-Marniche, Dalila
    Mathe, Veronique
    Mikogami, Takashi
    Tome, Daniel
    Huneau, Jean-Francois
    [J]. FREE RADICAL BIOLOGY AND MEDICINE, 2007, 42 (07) : 1089 - 1097
  • [5] Brunt EM, 1999, AM J GASTROENTEROL, V94, P2467, DOI 10.1111/j.1572-0241.1999.01377.x
  • [6] Resveratrol inhibits nonalcoholic fatty liver disease in rats
    Bujanda, Luis
    Hijona, Elizabeth
    Larzabal, Mikel
    Beraza, Marta
    Aldazabal, Pablo
    Garcia-Urkia, Nerea
    Sarasqueta, Cristina
    Cosme, Angel
    Irastorza, Belen
    Gonzalez, Alberto
    Arenas, Juan I., Jr.
    [J]. BMC GASTROENTEROLOGY, 2008, 8 (1)
  • [7] Open-labeled pilot study of cysteine-rich whey protein isolate supplementation for nonalcoholic steatohepatitis patients
    Chitapanarux, Taned
    Tienboon, Prasong
    Pojchamarnwiputh, Suwalee
    Leelarungrayub, Donrawee
    [J]. JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2009, 24 (06) : 1045 - 1050
  • [8] Dairy Protein Attenuates Weight Gain in Obese Rats Better Than Whey or Casein Alone
    Eller, Lindsay K.
    Reimer, Raylene A.
    [J]. OBESITY, 2010, 18 (04) : 704 - 711
  • [9] A whey-protein supplement increases fat loss and spares lean muscle in obese subjects: a randomized human clinical study
    Frestedt, Joy L.
    Zenk, John L.
    Kuskowski, Michael A.
    Ward, Loren S.
    Bastian, Eric D.
    [J]. NUTRITION & METABOLISM, 2008, 5 (1)
  • [10] Nonalcoholic fatty liver disease in severely obese subjects
    Gholam, Pierre M.
    Flancbaum, Louis
    Machan, Jason T.
    Charney, Douglas A.
    Kotler, Donald P.
    [J]. AMERICAN JOURNAL OF GASTROENTEROLOGY, 2007, 102 (02) : 399 - 408