Age-related effects of fenofibrate on the hepatic expression of sirtuin 1, sirtuin 3, and lipid metabolism-related genes

被引:0
作者
Zubrzycki, Adrian [1 ]
Wronska, Agata [1 ]
Wierzbicki, Piotr M. [1 ]
Kmiec, Zbigniew [1 ]
机构
[1] Med Univ Gdansk, Fac Med, Dept Histol, Gdansk, Poland
关键词
aging; liver; fenofibrate; sirtuin; lipid metabolism; PROLIFERATOR-ACTIVATED RECEPTOR; FATTY-ACID OXIDATION; PPAR-ALPHA AGONIST; INDUCED CD40 EXPRESSION; LIVER; INHIBITION; PROTECTS; GLUCOSE; HYPERACETYLATION; DEACETYLATION;
D O I
10.18388/abp.2020_6538
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
Background: Sirtuin 1 (Sirt1) and sirtuin 3 (Sirt3) par-ticipate in the regulation of lipid metabolism. Our aim was to investigate the effects of the hypolipemic drug fenofibrate (FN) on hepatic Sirt1 and Sirt3 expression, in relation to the expression of lipid metabolism-relat-ed genes and in the context of aging. Methods and Re-sults: Young and old male Wistar rats were fed standard chow or supplemented with 0.1% or 0.5% FN for 30 days (n=7-10 in each group). In young rats, 0.1% FN did not affect Sirt1 expression, however, 0.5% FN decreased Sirt1 and both doses reduced Sirt3 protein levels. In old rats, 0.5% FN decreased hepatic Sirt1 mRNA and both doses reduced Sirt1 protein levels, but not Sirt3 expression. Although hepatic Ppar alpha protein levels did not change, FN treatment of young rats induced Cpt1b expression, whereas Lcad, Acox1, Pmp70, and Hmgcs2 expression increased only after 0.1% FN, and Fas2 ex-pression decreased after 0.5% FN. In the liver of old rats, both doses increased Cpt1b and Lcad expression. Only 0.1% FN increased Pmp70 and Hmgcs2 expression, and only 0.5% FN increased Acox1 and Fas2 mRNA levels. Conclusions: Treatment with fenofibrate at low or high doses may downregulate the expression of Sirt1 and Sirt3 proteins in the rat liver. The dosage of FN af-fects molecular changes, and aging alters the response to 0.5% FN.
引用
收藏
页码:285 / 293
页数:9
相关论文
共 57 条
  • [1] Resveratrol and fenofibrate ameliorate fructose-induced nonalcoholic steatohepatitis by modulation of genes expression
    Abd El-Haleim, Enas A.
    Bahgat, Ashraf K.
    Saleh, Samira
    [J]. WORLD JOURNAL OF GASTROENTEROLOGY, 2016, 22 (10) : 2931 - 2948
  • [2] Badman MK, 2007, CELL METAB, V5, P426, DOI 10.1016/j.cmet.2007.05.002
  • [3] Molecular targets of fenofibrate in the cardiovascular-renal axis: A unifying perspective of its pleiotropic benefits
    Balakumar, Pitchai
    Sambathkumar, Ramanathan
    Mahadevan, Nanjaian
    Bin Muhsinah, Abdullatif
    Alsayari, Abdulrhman
    Venkateswaramurthy, Nallasamy
    Dhanaraj, Sokkalingam A.
    [J]. PHARMACOLOGICAL RESEARCH, 2019, 144 : 132 - 141
  • [4] Ligand-Regulated Heterodimerization of Peroxisome Proliferator-Activated Receptor α with Liver X Receptor α
    Balanarasimha, Madhumitha
    Davis, Andrea M.
    Soman, Frances L.
    Rider, S. Dean, Jr.
    Hostetler, Heather A.
    [J]. BIOCHEMISTRY, 2014, 53 (16) : 2632 - 2643
  • [5] ldentification of tissue-specific transcriptional markers of caloric restriction in the mouse and their use to evaluate caloric restriction mimetics
    Barger, Jamie L.
    Vann, James M.
    Cray, Nicole L.
    Pugh, Thomas D.
    Mastaloudis, Angela
    Hester, Shelly N.
    Wood, Steven M.
    Newton, Michael A.
    Weindruch, Richard
    Prolla, Tomas A.
    [J]. AGING CELL, 2017, 16 (04) : 750 - 760
  • [6] Hepatic sirtuin 1 is dispensable for fibrate- induced peroxisome proliferator-activated receptor-α function in vivo
    Bonzo, Jessica A.
    Brocker, Chad
    Jiang, Changtao
    Wang, Rui-Hong
    Deng, Chu-Xia
    Gonzalez, Frank J.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2014, 306 (07): : E824 - E837
  • [7] THE BIOCHEMICAL PHARMACOLOGY OF FENOFIBRATE
    CALDWELL, J
    [J]. CARDIOLOGY, 1989, 76 : 33 - 44
  • [8] Visualization and quantitation of peroxisomes using fluorescent nanocrystals: Treatment of rats and monkeys with fibrates and detection in the liver
    Colton, HM
    Falls, JG
    Ni, H
    Kwanyuen, P
    Creech, D
    McNeil, E
    Casey, WM
    Hamilton, G
    Cariello, NF
    [J]. TOXICOLOGICAL SCIENCES, 2004, 80 (01) : 183 - 192
  • [9] Sirt7 promotes adipogenesis in the mouse by inhibiting autocatalytic activation of Sirt1
    Fang, Jian
    Ianni, Alessandro
    Smolka, Christian
    Vakhrusheva, Olesya
    Nolte, Hendrik
    Kruger, Marcus
    Wietelmann, Astrid
    Simonet, Nicolas G.
    Adrian-Segarra, Juan M.
    Vaquero, Alejandro
    Braun, Thomas
    Bober, Eva
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2017, 114 (40) : E8352 - E8361
  • [10] Specific SIRT1 Activation Mimics Low Energy Levels and Protects against Diet-induced Metabolic Disorders by Enhancing Fat Oxidation
    Feige, Jerome N.
    Lagouge, Marie
    Canto, Carles
    Strehle, Axelle
    Houten, Sander M.
    Milne, Jill C.
    Lambert, Philip D.
    Mataki, Chikage
    Elliott, Peter J.
    Auwerx, Johan
    [J]. CELL METABOLISM, 2008, 8 (05) : 347 - 358