Biochemical and Morphological Parameters of Inbred/Outbred Lines and DBCB Tetrahybrid Mouse in High-Sugar In Vivo Model of Metabolic Syndrome
Integral, biochemical, and morphological parameters and concentrations of vitamins, particularly lipid soluble vitamins, were analyzed in female mice of inbred DBA/2J line, outbred ICR-1 (CD-1) line, and DBCB tetrahybrid mice on the in vivo model of metabolic syndrome induced by consumption of 30% s...
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Published in | Bulletin of experimental biology and medicine Vol. 166; no. 1; pp. 96 - 101 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
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Springer US
01.11.2018
Springer Nature B.V |
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Abstract | Integral, biochemical, and morphological parameters and concentrations of vitamins, particularly lipid soluble vitamins, were analyzed in female mice of inbred DBA/2J line, outbred ICR-1 (CD-1) line, and DBCB tetrahybrid mice on the
in vivo
model of metabolic syndrome induced by consumption of 30% sucrose for 2 days. In contrast to inbred and outbred lines, DBCB tetrahybrid mice developed abdominal obesity, hypercholesterolemia, and pronounced morphological picture of fatty liver disease. The lipid-coupled transport of vitamin E to the liver is also enhanced in these animals, which compensated decreased supply of vitamin E to the liver under conditions of high-sugar ration. The observed interstrain differences can be related to genetic features of the used mouse lines and DBCB tetrahybrid mice and require further genomic, transcriptomic, proteomic, and morphological studies. The results of the study based on the
in vivo
model of metabolic syndrome allow identifying the key biomarkers for complex diagnostics and prognosis of metabolic syndrome complications, such as nonalcoholic steatosis of the liver. |
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AbstractList | Integral, biochemical, and morphological parameters and concentrations of vitamins, particularly lipid soluble vitamins, were analyzed in female mice of inbred DBA/2J line, outbred ICR-1 (CD-1) line, and DBCB tetrahybrid mice on the in vivo model of metabolic syndrome induced by consumption of 30% sucrose for 2 days. In contrast to inbred and outbred lines, DBCB tetrahybrid mice developed abdominal obesity, hypercholesterolemia, and pronounced morphological picture of fatty liver disease. The lipid-coupled transport of vitamin E to the liver is also enhanced in these animals, which compensated decreased supply of vitamin E to the liver under conditions of high-sugar ration. The observed interstrain differences can be related to genetic features of the used mouse lines and DBCB tetrahybrid mice and require further genomic, transcriptomic, proteomic, and morphological studies. The results of the study based on the in vivo model of metabolic syndrome allow identifying the key biomarkers for complex diagnostics and prognosis of metabolic syndrome complications, such as nonalcoholic steatosis of the liver. Integral, biochemical, and morphological parameters and concentrations of vitamins, particularly lipid soluble vitamins, were analyzed in female mice of inbred DBA/2J line, outbred ICR-1 (CD-1) line, and DBCB tetrahybrid mice on the in vivo model of metabolic syndrome induced by consumption of 30% sucrose for 2 days. In contrast to inbred and outbred lines, DBCB tetrahybrid mice developed abdominal obesity, hypercholesterolemia, and pronounced morphological picture of fatty liver disease. The lipid-coupled transport of vitamin E to the liver is also enhanced in these animals, which compensated decreased supply of vitamin E to the liver under conditions of high-sugar ration. The observed interstrain differences can be related to genetic features of the used mouse lines and DBCB tetrahybrid mice and require further genomic, transcriptomic, proteomic, and morphological studies. The results of the study based on the in vivo model of metabolic syndrome allow identifying the key biomarkers for complex diagnostics and prognosis of metabolic syndrome complications, such as nonalcoholic steatosis of the liver. |
Author | Trusov, N. V. Balakina, A. S. Apryatin, S. A. Nikityuk, D. B. Beketova, N. A. Kosheleva, O. V. Gmoshinskii, I. V. Mzhel’skaya, K. V. Soto, Kh. S. |
Author_xml | – sequence: 1 givenname: S. A. surname: Apryatin fullname: Apryatin, S. A. email: apryatin@mail.ru organization: Federal Research Center of Nutrition and Biotechnology – sequence: 2 givenname: K. V. surname: Mzhel’skaya fullname: Mzhel’skaya, K. V. organization: Federal Research Center of Nutrition and Biotechnology – sequence: 3 givenname: N. V. surname: Trusov fullname: Trusov, N. V. organization: Federal Research Center of Nutrition and Biotechnology – sequence: 4 givenname: A. S. surname: Balakina fullname: Balakina, A. S. organization: Federal Research Center of Nutrition and Biotechnology – sequence: 5 givenname: Kh. S. surname: Soto fullname: Soto, Kh. S. organization: Federal Research Center of Nutrition and Biotechnology – sequence: 6 givenname: N. A. surname: Beketova fullname: Beketova, N. A. organization: Federal Research Center of Nutrition and Biotechnology – sequence: 7 givenname: O. V. surname: Kosheleva fullname: Kosheleva, O. V. organization: Federal Research Center of Nutrition and Biotechnology – sequence: 8 givenname: I. V. surname: Gmoshinskii fullname: Gmoshinskii, I. V. organization: Federal Research Center of Nutrition and Biotechnology – sequence: 9 givenname: D. B. surname: Nikityuk fullname: Nikityuk, D. B. organization: Federal Research Center of Nutrition and Biotechnology |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30417297$$D View this record in MEDLINE/PubMed |
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CitedBy_id | crossref_primary_10_1007_s12011_021_02642_0 crossref_primary_10_1016_j_jnutbio_2020_108527 |
Cites_doi | 10.1186/1476-511X-9-42 10.1016/j.arr.2011.12.006 10.1371/journal.pone.0155163 10.1371/journal.pone.0107291 10.1371/journal.pone.0119784 10.1161/ATVBAHA.111.241919 10.1152/ajprenal.00233.2007 10.1186/s12986-016-0123-9 |
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SubjectTerms | Animals Biomedical and Life Sciences Biomedicine Cell Biology Disease Models, Animal Fatty liver Fatty Liver - metabolism Fatty Liver - pathology Female Hypercholesterolemia Inbreeding Internal Medicine Laboratory Medicine Liver Liver - metabolism Liver - pathology Liver diseases Male Metabolic syndrome Metabolic Syndrome - metabolism Mice Mice, Inbred BALB C Mice, Inbred C57BL Mice, Inbred DBA Morphology Morphology and Pathomorphology Pathology Proteomics Proteomics - methods Rodents Steatosis Sucrose Sucrose - adverse effects Sucrose - metabolism Sugar Vitamin E Vitamins |
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Title | Biochemical and Morphological Parameters of Inbred/Outbred Lines and DBCB Tetrahybrid Mouse in High-Sugar In Vivo Model of Metabolic Syndrome |
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