Literature DB >> 33868979

Liver functions in combined models of the gentamicin induced nephrotoxicity and metabolic syndrome induced by high fat or fructose diets: a comparative study.

Zaid O Ibraheem1, Sinan Subhi Farhan2, Ajwad Al Sumaidaee3, Layth Al Sufi4, Anas Bashir5,6, Anmar Balwa6, Rusliza Basir7.   

Abstract

Metabolic syndrome is one of the major risk factors that lead to various serious complications like cardiovascular abnormalities, hyperlipidemia and diabetes. Its co-incidence with other organs dysfunction results in further deterioration of the condition or precipitation of other dysfunctions. This study aimed at studying the changes in the hepatic functions after the co-incidence of the high fat or fructose diets induced metabolic syndrome along with the gentamicin induced nephrotoxicity. Briefly, six groups of male Sprague Daley rats (n = 10-12) were fed with different feeding protocols; viz; standard rodent's chow, an experimental high fat or high fructose diets feedings. For each, two groups were allocated that one of them was injected with normal saline and the other with 80 mg/kg/day I.P gentamicin during the last 24 days of the feeding period. The rats were monitored for changes in the metabolic data, glycemic control, lipid profile, renal and hepatic functions, oxidative stress and the inflammatory response. The study revealed stronger hepatic changes in the renal failure groups fed with the high fat diet rather than that in the groups fed with the high fructose diet. Although, the latter experienced a stronger deterioration in the glycemic control. The study suggests that the incidence of the hepatic changes is more linked to the incidence of the deterioration in the lipids profile that was observed after the high fat diet feeding. Overall, the co-incidence of the high fat diet induced metabolic syndrome along with the renal failure constitutes a risk factor for the hepatic dysfunction. © Korean Society of Toxicology 2020.

Entities:  

Keywords:  Fructose; High fat diet; Liver dysfunction and oxidative stress; Metabolic syndrome

Year:  2020        PMID: 33868979      PMCID: PMC8007678          DOI: 10.1007/s43188-020-00059-w

Source DB:  PubMed          Journal:  Toxicol Res        ISSN: 1976-8257


  29 in total

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Authors:  S Kacew
Journal:  J Pharmacol Exp Ther       Date:  1989-01       Impact factor: 4.030

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Journal:  Hum Exp Toxicol       Date:  1993-09       Impact factor: 2.903

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Review 10.  The Global Epidemic of the Metabolic Syndrome.

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