AI Article Synopsis

  • The study aimed to assess how camel milk affects liver health by examining liver enzymes, total proteins, and liver tissue in hyperlipidaemic Wistar rats.
  • Thirty male Wistar rats were divided into groups receiving different treatments, including distilled water, poloxamer 407 (P407), atorvastatin, and varying doses of camel milk.
  • Results showed that camel milk significantly reduced certain liver enzymes and altered protein levels, suggesting it has protective effects on the liver in cases of induced hyperlipidemia.

Article Abstract

Aim: To investigate the effect of oral administration of camel milk on liver enzymes, total proteins and histology of poloxamer 407 induced hyperlipidaemic wistar rats.

Material And Methods: Thirty male wistar rats weighing between 150-200 g were randomly assigned into six groups of five each; group I: administered distilled water, group II: induced with P407, group III: induced with P407 and treated with atorvastatin (20 mg/kg) and groups IV, V and VI: induced with P407 and treated with camel milk 250 mg/kg, 500 mg/kg and 1000 mg/kg respectively. After three weeks, blood samples and liver tissues were collected for the determination of alkaline phospatase (ALP), alanine aminotransferase (ALT), aspartate aminotransferase (AST), total protein, albumin, globulin, albumin/globulin ratio and histological studies respectively.

Results: All camel milk treated groups showed significant (p < 0.05) decrease in ALT and AST. Camel milk treated groups; 250 mg/kg and 1000mg/kg showed significant (p < 0.05) decrease in total protein, globulin with all camel milk treated groups having significant (p < 0.05) increase in A/G ratio. Histological examination of liver tissues showed that camel milk at a dose of 250 mg/kg had slight adipocytes infiltration.

Conclusion: The results of our findings highlight the hepatoprotective effect of camel milk in poloxamer 407 induced hyperlipidaemic wistar rats.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5771285PMC
http://dx.doi.org/10.3889/oamjms.2017.158DOI Listing

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