TY - JOUR
T1 - The impact of sugar-sweetened beverage consumption on the liver
T2 - A proteomics-based analysis
AU - Benade, Janina
AU - Sher, Lucien
AU - De Klerk, Sheneez
AU - Deshpande, Gaurang
AU - Bester, Dirk
AU - Marnewick, Jeanine L.
AU - Sieck, Gary
AU - Laher, Ismail
AU - Essop, M. Faadiel
N1 - Funding Information:
Funding: This study was funded by grants from the South African National Research Foundation (IFR150119112480) and Stellenbosch University (to MFE).
Funding Information:
This study was funded by grants from the South African National Research Foundation (IFR150119112480) and Stellenbosch University (to MFE).
Publisher Copyright:
© 2020 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2020/7
Y1 - 2020/7
N2 - Cardiometabolic complications such as the metabolic syndrome and Type 2 Diabetes Mellitus (T2DM) are major causes of global morbidity and mortality. As sugar-sweetened beverages (SSBs) are implicated in this process, this study aimed to obtain greater mechanistic insights. Male Wistar rats (~200 g) were gavaged with a local SSB every day for a period of six months while the control group was gavaged with an iso-volumetric amount of water. Experimental dosages were calculated according to the surface area-to-volume ratio and were equivalent to 125 mL/day (in human terms). A proteomic analysis was performed on isolated liver samples and thereafter, markers of endoplasmic reticulum (ER) stress, antioxidant/oxidant capacity, calcium regulation, and mitochondrial functionality were assessed. These data show that SSB consumption resulted in (a) the induction of mild hepatic ER stress; (b) altered hepatic mitochondrial dynamics; and (c) perturbed calcium handling across mitochondria-associated ER membranes. Despite significant changes in markers of ER stress, the antioxidant response and calcium handling (proteomics data), the liver is able to initiate adaptive responses to counteract such stressors. However, the mitochondrial data showed increased fission and decreased fusion that may put the organism at risk for developing insulin resistance and T2DM in the longer term.
AB - Cardiometabolic complications such as the metabolic syndrome and Type 2 Diabetes Mellitus (T2DM) are major causes of global morbidity and mortality. As sugar-sweetened beverages (SSBs) are implicated in this process, this study aimed to obtain greater mechanistic insights. Male Wistar rats (~200 g) were gavaged with a local SSB every day for a period of six months while the control group was gavaged with an iso-volumetric amount of water. Experimental dosages were calculated according to the surface area-to-volume ratio and were equivalent to 125 mL/day (in human terms). A proteomic analysis was performed on isolated liver samples and thereafter, markers of endoplasmic reticulum (ER) stress, antioxidant/oxidant capacity, calcium regulation, and mitochondrial functionality were assessed. These data show that SSB consumption resulted in (a) the induction of mild hepatic ER stress; (b) altered hepatic mitochondrial dynamics; and (c) perturbed calcium handling across mitochondria-associated ER membranes. Despite significant changes in markers of ER stress, the antioxidant response and calcium handling (proteomics data), the liver is able to initiate adaptive responses to counteract such stressors. However, the mitochondrial data showed increased fission and decreased fusion that may put the organism at risk for developing insulin resistance and T2DM in the longer term.
KW - Antioxidant capacity
KW - Calcium homeostasis
KW - Endoplasmic reticulum stress
KW - Metabolic syndrome
KW - Mitochondrial dysfunction
KW - Mitochondrial fission and fusion
KW - Sugar-sweetened beverages
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U2 - 10.3390/antiox9070569
DO - 10.3390/antiox9070569
M3 - Article
AN - SCOPUS:85087421394
SN - 2076-3921
VL - 9
SP - 1
EP - 17
JO - Antioxidants
JF - Antioxidants
IS - 7
M1 - 569
ER -