Literature DB >> 24200942

Altered fatty acid profile in the liver and serum of stroke-prone spontaneously hypertensive rats: reduced proportion of cis-vaccenic acid.

Shizuyo Tanaka1, Chiho Kojiguchi, Tohru Yamazaki, Atsushi Mitsumoto, Daisuke Kobayashi, Naomi Kudo, Yoichi Kawashima.   

Abstract

Stroke-prone spontaneously hypertensive rats (SHRSP) are utilized as models for study of the pathogenesis of not only stroke and cardiovascular disorders but also atherosclerosis and metabolic syndrome. Basic information on the profiles of fatty acids and lipid classes in the liver is indispensable to use SHRSP as a model of disorder of lipid metabolism; nevertheless, detailed information on the metabolism of triacylglycerols (TAGs) and fatty acids in the liver of SHRSP is lacking. This study aimed to characterize profiles of lipid classes and fatty acids and to explore the mechanism underlying the characteristic alterations in metabolism of TAGs and fatty acids in the liver of SHRSP, in comparison with spontaneously hypertensive rats (SHR). The characteristic changes observed in SHRSP were (1) markedly lower hepatic TAG contents; (2) altered expressions of genes encoding three enzymes responsible for the control of TAG level, namely, adipose triglyceride lipase (for TAG degradation; up-regulated), carnitine palmitoyltransferase 1a (for fatty acid β-oxidation; up-regulated) and long-chain acyl-CoA synthetase 3 (for glycerolipid synthesis; down-regulated); (3) evidently lower contents and proportions of monounsaturated fatty acids, in particular cis-vaccenic acid (18:1n-7), in the liver and serum; and (4) down-regulation of palmitoleoyl-CoA chain elongase, which is necessary for the biosynthesis of 18:1n-7, in the liver. From the above observations, we concluded that there are significant differences in profiles of lipid classes and fatty acids between SHRSP and SHR, and that altered characteristics in SHRSP are likely responsible for increases in TAG hydrolysis and β-oxidation, and decreases in TAG synthesis and 18:1n-7 synthesis.

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Year:  2013        PMID: 24200942     DOI: 10.5650/jos.62.933

Source DB:  PubMed          Journal:  J Oleo Sci        ISSN: 1345-8957            Impact factor:   1.601


  4 in total

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Journal:  Toxicology       Date:  2017-09-07       Impact factor: 4.221

3.  Fully hydrogenated canola oil extends lifespan in stroke-prone spontaneously hypertensive rats.

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Journal:  Lipids Health Dis       Date:  2021-09-12       Impact factor: 3.876

4.  Rapeseed (canola) oil aggravates metabolic syndrome-like conditions in male but not in female stroke-prone spontaneously hypertensive rats (SHRSP).

Authors:  Mai Nishikawa; Naoki Ohara; Yukiko Naito; Yoshiaki Saito; Chihiro Amma; Kenjiro Tatematsu; Jinhua Baoyindugurong; Daisuke Miyazawa; Yoko Hashimoto; Harumi Okuyama
Journal:  Toxicol Rep       Date:  2022-02-07
  4 in total

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