Dietary regulation of catabolic disposal of 4-hydroxynonenal analogs in rat liver

被引:19
作者
Li, Qingling [1 ]
Tomcik, Kristyen [1 ]
Zhang, Shenghui [1 ]
Puchowicz, Michelle A. [1 ]
Zhang, Guo-Fang [1 ]
机构
[1] Case Western Reserve Univ, Dept Nutr, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
4-Hydroxynonenal; 4-Oxononenal; 1,4-Dihydroxynonene; Diet; Rat liver; Metabolism; Lipid peroxidation; Mass isotopomer analysis; Free radicals; LIPID-PEROXIDATION PRODUCT; HIGH-FAT DIET; SPONTANEOUSLY HYPERTENSIVE-RATS; OXIDATIVE STRESS; INSULIN-RESISTANCE; MASS-SPECTROMETRY; CARBONYL STRESS; ACID OXIDATION; MALONYL-COA; ADDUCTS;
D O I
10.1016/j.freeradbiomed.2011.12.022
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
Our previous work in perfused rat livers has demonstrated that 4-hydroxynonenal (HNE) is catabolized predominantly via beta oxidation. Therefore, we hypothesized that perturbations in beta oxidation, such as diet-altered fatty acid oxidation activity, could lead to changes in HNE levels. To test our hypothesis, we (i) developed a simple and sensitive GC/MS method combined with mass isotopomer analysis to measure HNE and FINE analogs, 4-oxononenal (ONE) and 1,4-dihydroxynonene (DHN), and (ii) investigated the effects of four diets (standard, low-fat, ketogenic, and high-fat mix) on HNE, ONE, and DHN concentrations in rat livers. Our results showed that livers from rats fed the ketogenic diet or high-fat mix diet had high to omega-6 polyunsaturated fatty acid concentrations and markers of oxidative stress. However, high concentrations of HNE (1.6 +/- 0.5 nmol/g) and ONE (0.9 +/- 0.2 nmol/g) were found only in livers from rats fed the high-fat mix diet. Livers from rats fed the ketogenic diet had low HNE (0.8 +/- 0.1 nmol/g) and ONE (0.4 +/- 0.07 nmol/g), similar to rats fed the standard diet. A possible explanation is that the predominant pathway of FINE catabolism (i.e., beta oxidation) is activated in the liver by the ketogenic diet. This is consistent with a 10-fold decrease in malonyl-CoA in livers from rats fed a ketogenic diet compared to a standard diet. The accelerated catabolism of HNE lowers HNE and FINE analog concentrations in livers from rats fed the ketogenic diet. On the other hand, rats fed the high-fat mix diet had high rates of lipid synthesis and low rates of fatty acid oxidation, resulting in the slowing down of the catabolic disposal of HNE and HNE analogs. Thus, decreased HNE catabolism from a high-fat mix diet induces high concentrations of HNE and HNE analogs. The results of this work suggest a potential causal relationship to metabolic syndrome induced by Western diets (i.e., high-fat mix), as well as the effects of a ketogenic diet on the catabolism of lipid peroxidation products in liver. (C) 2011 Elsevier Inc. All rights reserved.
引用
收藏
页码:1043 / 1053
页数:11
相关论文
共 50 条
  • [1] Diabetes impairs the enzymatic disposal of 4-hydroxynonenal in rat liver
    Traverso, N
    Menini, S
    Odetti, P
    Pronzato, MA
    Cottalasso, D
    Marinari, UM
    FREE RADICAL BIOLOGY AND MEDICINE, 2002, 32 (04) : 350 - 359
  • [2] Cancer growth regulation by 4-hydroxynonenal
    Gasparovic, Ana Cipak
    Milkovic, Lidija
    Sunjic, Suzana Borovic
    Zarkovic, Neven
    FREE RADICAL BIOLOGY AND MEDICINE, 2017, 111 : 226 - 234
  • [3] Differential metabolism of 4-hydroxynonenal in liver, lung and brain of mice and rats
    Zheng, Ruijin
    Dragomir, Ana-Cristina
    Mishin, Vladimir
    Richardson, Jason R.
    Heck, Diane E.
    Laskin, Debra L.
    Laskin, Jeffrey D.
    TOXICOLOGY AND APPLIED PHARMACOLOGY, 2014, 279 (01) : 43 - 52
  • [4] 4-HYDROXYNONENAL IS DEGRADED TO MERCAPTURIC ACID CONJUGATE IN RAT-KIDNEY
    PETRAS, T
    SIEMS, WG
    GRUNE, T
    FREE RADICAL BIOLOGY AND MEDICINE, 1995, 19 (05) : 685 - 688
  • [5] Regulation of autophagy, mitochondrial dynamics, and cellular bioenergetics by 4-hydroxynonenal in primary neurons
    Dodson, Matthew
    Wani, Willayat Y.
    Redmann, Matthew
    Benavides, Gloria A.
    Johnson, Michelle S.
    Ouyang, Xiaosen
    Cofield, Stacey S.
    Mitra, Kasturi
    Darley-Usmar, Victor
    Zhang, Jianhua
    AUTOPHAGY, 2017, 13 (11) : 1828 - 1840
  • [6] Metabolism of 4-hydroxynonenal by rat Kupffer cells
    Luckey, SW
    Petersen, DR
    ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 2001, 389 (01) : 77 - 83
  • [7] Oxidation of 4-hydroxynonenal in rat brain slices
    Murphy, T
    Amarnath, V
    Picklo, MJ
    CHEMICO-BIOLOGICAL INTERACTIONS, 2003, 143 : 101 - 105
  • [8] Yeast Aquaporin Regulation by 4-Hydroxynonenal is Implicated in Oxidative Stress Response
    Rodrigues, Claudia
    Bujak, Ivana Tartaro
    Mihaljevic, Branka
    Soveral, Graca
    Gasparovic, Ana Cipak
    IUBMB LIFE, 2017, 69 (05) : 355 - 362
  • [9] 4-hydroxynonenal modifies IgA in rat intestine after lipopolysaccharide injection
    Kimura, Hiroko
    Mukaida, Masahiro
    Kuwabara, Kyoko
    Ito, Teruyo
    Hashino, Kimikazu
    Uchida, Koji
    Matsumoto, Kazuko
    Yoshida, Ken-ichi
    FREE RADICAL BIOLOGY AND MEDICINE, 2006, 41 (06) : 973 - 978
  • [10] 4-hydroxynonenal disrupts zinc export in primary rat cortical cells
    Smith, JL
    Xiong, S
    Lovell, MA
    NEUROTOXICOLOGY, 2006, 27 (01) : 1 - 5