Effect of uremia on HDL composition, vascular inflammation, and atherosclerosis in wild-type mice
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Effect of uremia on HDL composition, vascular inflammation, and atherosclerosis in wild-type mice. / Bang, Christian A; Bro, Susanne; Bartels, Emil D; Pedersen, Tanja X; Nielsen, Lars B.
I: American Journal of Physiology - Renal Physiology, Bind 293, Nr. 4, 2007, s. F1325-31.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Effect of uremia on HDL composition, vascular inflammation, and atherosclerosis in wild-type mice
AU - Bang, Christian A
AU - Bro, Susanne
AU - Bartels, Emil D
AU - Pedersen, Tanja X
AU - Nielsen, Lars B
N1 - Keywords: Animals; Aorta, Thoracic; Apolipoprotein A-I; Apolipoproteins B; Atherosclerosis; Cholesterol, Dietary; Cholic Acid; Intercellular Adhesion Molecule-1; Kidney; Lipoproteins, HDL; Liver; Mice; Mice, Inbred C57BL; Nephrectomy; RNA, Messenger; Serum Amyloid A Protein; Uremia; Vascular Cell Adhesion Molecule-1; Vasculitis
PY - 2007
Y1 - 2007
N2 - Wild-type mice normally do not develop atherosclerosis, unless fed cholic acid. Uremia is proinflammatory and increases atherosclerosis 6- to 10-fold in apolipoprotein E-deficient mice. This study examined the effect of uremia on lipoproteins, vascular inflammation, and atherosclerosis in wild-type C57BL/6J mice. Uremia was induced by nephrectomy (NX) and increased plasma urea and creatinine concentrations 2.5- to 4.5-fold; control mice were sham operated. After NX, mice were fed a Western-type diet or the same diet with 0.5% cholic acid. Cholic acid-fed NX mice did not thrive and were killed. In NX mice fed the Western-type diet (n = 7), the total plasma cholesterol concentration was similar to that in sham mice (n = 11), but on gel filtration the LDL/HDL cholesterol ratio was increased. HDL from NX mice contained more serum amyloid A and triglycerides and less cholesterol than HDL from sham mice. Plasma concentrations of sICAM-1 and sVCAM-1 and aortic mRNA expression of ICAM-1 and VCAM-1 did not differ between NX and sham mice. Twenty-six weeks after NX, the average oil red O-stained area of the aortic root was similar in NX and sham mice fed the Western-type diet, while it was increased in cholic acid-fed sham mice. The results suggest that moderate uremia neither induces aortic inflammation nor atherosclerosis in C57BL/6J mice despite increased LDL/HDL cholesterol ratio and altered HDL composition.
AB - Wild-type mice normally do not develop atherosclerosis, unless fed cholic acid. Uremia is proinflammatory and increases atherosclerosis 6- to 10-fold in apolipoprotein E-deficient mice. This study examined the effect of uremia on lipoproteins, vascular inflammation, and atherosclerosis in wild-type C57BL/6J mice. Uremia was induced by nephrectomy (NX) and increased plasma urea and creatinine concentrations 2.5- to 4.5-fold; control mice were sham operated. After NX, mice were fed a Western-type diet or the same diet with 0.5% cholic acid. Cholic acid-fed NX mice did not thrive and were killed. In NX mice fed the Western-type diet (n = 7), the total plasma cholesterol concentration was similar to that in sham mice (n = 11), but on gel filtration the LDL/HDL cholesterol ratio was increased. HDL from NX mice contained more serum amyloid A and triglycerides and less cholesterol than HDL from sham mice. Plasma concentrations of sICAM-1 and sVCAM-1 and aortic mRNA expression of ICAM-1 and VCAM-1 did not differ between NX and sham mice. Twenty-six weeks after NX, the average oil red O-stained area of the aortic root was similar in NX and sham mice fed the Western-type diet, while it was increased in cholic acid-fed sham mice. The results suggest that moderate uremia neither induces aortic inflammation nor atherosclerosis in C57BL/6J mice despite increased LDL/HDL cholesterol ratio and altered HDL composition.
U2 - 10.1152/ajprenal.00039.2007
DO - 10.1152/ajprenal.00039.2007
M3 - Journal article
C2 - 17686960
VL - 293
SP - F1325-31
JO - American Journal of Physiology - Renal Fluid and Electrolyte Physiology
JF - American Journal of Physiology - Renal Fluid and Electrolyte Physiology
SN - 1931-857X
IS - 4
ER -
ID: 17343401