High Fructose Corn Syrup Accelerates Kidney Disease and Mortality in Obese Mice with Metabolic Syndrome

被引:9
作者
Andres-Hernando, Ana [1 ,2 ]
Orlicky, David J. [3 ]
Cicerchi, Christina [1 ]
Kuwabara, Masanari [4 ]
Garcia, Gabriela E. [1 ,5 ]
Nakagawa, Takahiko [6 ]
Sanchez-Lozada, Laura Gabriela [7 ]
Johnson, Richard J. [3 ,5 ]
Lanaspa, Miguel A. [1 ,2 ]
机构
[1] Univ Colorado, Div Endocrinol Metab & Diabet, Anschutz Med Campus, Aurora, CO 80045 USA
[2] Rocky Mt VA Med Ctr, Div Nephrol, Aurora, CO 80045 USA
[3] Univ Colorado, Dept Pathol, Anschutz Med Campus, Aurora, CO 80045 USA
[4] Toranomon Gen Hosp, Div Cardiovasc Dis, Tokyo 1058470, Japan
[5] Univ Colorado, Div Renal Dis & Hypertens, Anschutz Med Campus, Aurora, CO 80045 USA
[6] Shiga Univ Med Sci, Dept Regenerat Med Dev, Seta Tsukinowa cho, Otsu 5202192, Japan
[7] INC Ignacio Chavez, Dept Cardiorenal Physiopathol, Mexico City 14080, Mexico
关键词
metabolic syndrome; obesity; chronic kidney disease; fructose; high fructose corn syrup; URIC-ACID; FRUCTOKINASE; LEPTIN; SUGAR; ASSOCIATION; EXPRESSION; INJURY; LIVER; RATS;
D O I
10.3390/biom13050780
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
The presence of obesity and metabolic syndrome is strongly linked with chronic kidney disease (CKD), but the mechanisms responsible for the association are poorly understood. Here, we tested the hypothesis that mice with obesity and metabolic syndrome might have increased susceptibility to CKD from liquid high fructose corn syrup (HFCS) by favoring the absorption and utilization of fructose. We evaluated the pound mouse model of metabolic syndrome to determine if it showed baseline differences in fructose transport and metabolism and whether it was more susceptible to chronic kidney disease when administered HFCS. Pound mice have increased expression of fructose transporter (Glut5) and fructokinase (the limiting enzyme driving fructose metabolism) associated with enhanced fructose absorption. Pound mice receiving HFCS rapidly develop CKD with increased mortality rates associated with intrarenal mitochondria loss and oxidative stress. In pound mice lacking fructokinase, the effect of HFCS to cause CKD and early mortality was aborted, associated with reductions in oxidative stress and fewer mitochondria loss. Obesity and metabolic syndrome show increased susceptibility to fructose-containing sugars and increased risk for CKD and mortality. Lowering added sugar intake may be beneficial in reducing the risk for CKD in subjects with metabolic syndrome.
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页数:17
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  • [1] Leptin as an uremic toxin: Deleterious role of leptin in chronic kidney disease
    Alix, Pascaline M.
    Guebre-Egziabher, Fitsum
    Soulage, Christophe O.
    [J]. BIOCHIMIE, 2014, 105 : 12 - 21
  • [2] Vasopressin mediates fructose-induced metabolic syndrome by activating the V1b receptor
    Andres-Hernando, Ana
    Jensen, Thomas J.
    Kuwabara, Masanari
    Orlicky, David J.
    Cicerchi, Christina
    Li, Nanxing
    Roncal-Jimenez, Carlos A.
    Garcia, Gabriela E.
    Ishimoto, Takuji
    Maclean, Paul S.
    Bjornstad, Petter
    Sanchez-Lozada, Laura Gabriela
    Kanbay, Mehmet
    Nakagawa, Takahiko
    Johnson, Richard J.
    Lanaspa, Miguel A.
    [J]. JCI INSIGHT, 2021, 6 (01)
  • [3] Deletion of Fructokinase in the Liver or in the Intestine Reveals Differential Effects on Sugar-Induced Metabolic Dysfunction
    Andres-Hernando, Ana
    Orlicky, David J.
    Kuwabara, Masanari
    Ishimoto, Takuji
    Nakagawa, Takahiko
    Johnson, Richard J.
    Lanaspa, Miguel A.
    [J]. CELL METABOLISM, 2020, 32 (01) : 117 - +
  • [4] Obesity causes renal mitochondrial dysfunction and energy imbalance and accelerates chronic kidney disease in mice
    Andres-Hernando, Ana
    Lanaspa, Miguel A.
    Kuwabara, Masanari
    Orlicky, David J.
    Cicerchi, Christina
    Bales, Elise
    Garcia, Gabriela E.
    Roncal-Jimenez, Carlos A.
    Sato, Yuka
    Johnson, Richard J.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2019, 317 (04) : F941 - F948
  • [5] Protective role of fructokinase blockade in the pathogenesis of acute kidney injury in mice
    Andres-Hernando, Ana
    Li, Nanxing
    Cicerchi, Christina
    Inaba, Shinichiro
    Chen, Wei
    Roncal-Jimenez, Carlos
    Le, Myphuong T.
    Wempe, Michael F.
    Milagres, Tamara
    Ishimoto, Takuji
    Fini, Mehdi
    Nakagawa, Takahiko
    Johnson, Richard J.
    Lanaspa, Miguel A.
    [J]. NATURE COMMUNICATIONS, 2017, 8
  • [6] Hyperuricemia as a Mediator of the Proinflammatory Endocrine Imbalance in the Adipose Tissue in a Murine Model of the Metabolic Syndrome
    Baldwin, William
    McRae, Steven
    Marek, George
    Wymer, David
    Pannu, Varinderpal
    Baylis, Chris
    Johnson, Richard J.
    Sautin, Yuri Y.
    [J]. DIABETES, 2011, 60 (04) : 1258 - 1269
  • [7] Sugar-sweetened soda consumption, hyperuricemia, and kidney disease
    Bomback, Andrew S.
    Derebail, Vimal K.
    Shoham, David A.
    Anderson, Cheryl A.
    Steffen, Lyn M.
    Rosamond, Wayne D.
    Kshirsagar, Abhijit V.
    [J]. KIDNEY INTERNATIONAL, 2010, 77 (07) : 609 - 616
  • [8] Sugar-sweetened beverage consumption and mortality of chronic kidney disease: results from the US National Health and Nutrition Examination Survey, 1999-2014
    Cai, Xiao-Yu
    Zhang, Nan-Hui
    Cheng, Yi-Chun
    Ge, Shu-Wang
    Xu, Gang
    [J]. CLINICAL KIDNEY JOURNAL, 2022, 15 (04) : 718 - 726
  • [9] The metabolic syndrome and chronic kidney disease in US adults
    Chen, J
    Muntner, P
    Hamm, LL
    Jones, DW
    Batuman, V
    Fonseca, V
    Whelton, PK
    He, J
    [J]. ANNALS OF INTERNAL MEDICINE, 2004, 140 (03) : 167 - 174
  • [10] Fructose Promotes Leaky Gut, Endotoxemia, and Liver Fibrosis Through Ethanol-Inducible Cytochrome P450-2E1-Mediated Oxidative and Nitrative Stress
    Cho, Young-Eun
    Kim, Do-Kyun
    Seo, Wonhyo
    Gao, Bin
    Yoo, Seong-Ho
    Song, Byoung-Joon
    [J]. HEPATOLOGY, 2021, 73 (06) : 2180 - 2195