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Citations to this article

Unexpected inhibition of cholesterol 7 alpha-hydroxylase by cholesterol in New Zealand white and Watanabe heritable hyperlipidemic rabbits.
G Xu, … , T M Donnelly, G S Tint
G Xu, … , T M Donnelly, G S Tint
Published April 1, 1995
Citation Information: J Clin Invest. 1995;95(4):1497-1504. https://doi.org/10.1172/JCI117821.
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Research Article Article has an altmetric score of 3

Unexpected inhibition of cholesterol 7 alpha-hydroxylase by cholesterol in New Zealand white and Watanabe heritable hyperlipidemic rabbits.

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Abstract

We investigated the effect of cholesterol feeding on plasma cholesterol concentrations, hepatic activities and mRNA levels of HMG-CoA reductase and cholesterol 7 alpha-hydroxylase and hepatic LDL receptor function and mRNA levels in 23 New Zealand White (NZW) and 17 Watanabe heritable hyperlipidemic (WHHL) rabbits. Plasma cholesterol concentrations were 9.9 times greater in WHHL than NZW rabbits and rose significantly in both groups when cholesterol was fed. Baseline liver cholesterol levels were 50% higher but rose only 26% in WHHL as compared with 3.6-fold increase with the cholesterol diet in NZW rabbits. In both rabbit groups, hepatic total HMG-CoA reductase activity was similar and declined > 60% without changing enzyme mRNA levels after cholesterol was fed. In NZW rabbits, cholesterol feeding inhibited LDL receptor function but not mRNA levels. As expected, receptor-mediated LDL binding was reduced in WHHL rabbits. Hepatic cholesterol 7 alpha-hydroxylase activity and mRNA levels were 2.8 and 10.4 times greater in NZW than WHHL rabbits. Unexpectedly, cholesterol 7 alpha-hydroxylase activity was reduced 53% and mRNA levels were reduced 79% in NZW rabbits with 2% cholesterol feeding. These results demonstrate that WHHL as compared with NZW rabbits have markedly elevated plasma and higher liver cholesterol concentrations, less hepatic LDL receptor function, and very low hepatic cholesterol 7 alpha-hydroxylase activity and mRNA levels. Feeding cholesterol to NZW rabbits increased plasma and hepatic concentrations greatly, inhibited LDL receptor-mediated binding, and unexpectedly suppressed cholesterol 7 alpha-hydroxylase activity and mRNA to minimum levels similar to WHHL rabbits. Dietary cholesterol accumulates in the plasma of NZW rabbits, and WHHL rabbits are hypercholesterolemic because reduced LDL receptor function is combined with decreased catabolism of cholesterol to bile acids.

Authors

G Xu, G Salen, S Shefer, G C Ness, L B Nguyen, T S Parker, T S Chen, Z Zhao, T M Donnelly, G S Tint

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Total citations by year

Year: 2020 2017 2015 2012 2009 2008 2007 2005 2004 2003 2002 2001 2000 1999 1998 1997 1995 Total
Citations: 1 2 1 1 1 1 2 2 4 3 3 3 4 10 4 6 1 49
Citation information
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Citations to this article (49)

Title and authors Publication Year
Mammalian Sterols: Novel Biological Roles of Cholesterol Synthesis Intermediates, Oxysterols and Bile Acids
D Rozman, R Gebhardt
2020
Cholestyramine alters bile acid amounts and the expression of cholesterol-related genes in rabbit intestinal and hepatic tissues
DN Qiu, Q Shang, DY Sun, WQ Ding, ZG Luo, J Chen, WR Jiang, JP Huang, XY Jiang
Journal of Digestive Diseases 2017
Deficiency of Cholesteryl Ester Transfer Protein Protects Against Atherosclerosis in RabbitsHighlights
J Zhang, M Niimi, D Yang, J Liang, J Xu, T Kimura, AV Mathew, Y Guo, Y Fan, T Zhu, J Song, R Ackermann, Y Koike, A Schwendeman, L Lai, S Pennathur, M Garcia-Barrio, J Fan, YE Chen
Arteriosclerosis, thrombosis, and vascular biology 2017
New CETP inhibitor K-312 reduces PCSK9 expression: a potential effect on LDL cholesterol metabolism
K Miyosawa, Y Watanabe, K Murakami, T Murakami, H Shibata, M Iwashita, H Yamazaki, K Yamazaki, T Ohgiya, K Shibuya, K Mizuno, S Tanabe, SA Singh, M Aikawa
American journal of physiology. Endocrinology and metabolism 2015
The hypocholesterolemic activity of açaí (Euterpe oleracea Mart.) is mediated by the enhanced expression of the ATP-binding cassette, subfamily G transporters 5 and 8 and low-density lipoprotein receptor genes in the rat
MO de Souza, LS Silva, CL de Magalhães, BB de Figueiredo, DC Costa, ME Silva, ML Pedrosa
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Thyroid hormone β receptor activation has additive cholesterol lowering activity in combination with atorvastatin in rabbits, dogs and monkeys
BR Ito, BH Zhang, EE Cable, X Song, JM Fujitaki, DA MacKenna, CE Wilker, B Chi, PD van Poelje, DL Linemeyer, MD Erion
British Journal of Pharmacology 2009
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YK Lee, DR Schmidt, CL Cummins, M Choi, L Peng, Y Zhang, B Goodwin, RE Hammer, DJ Mangelsdorf, SA Kliewer
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F Gilardi, N Mitro, C Godio, E Scotti, D Caruso, M Crestani, ED Fabiani
Pharmacology & Therapeutics 2007
An overlapping binding site in the CYP7A1 promoter allows activation of FXR to override the stimulation by LXRα
Q Shang, L Pan, M Saumoy, JY Chiang, GS Tint, G Salen, G Xu
AJP Gastrointestinal and Liver Physiology 2007
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H Ando, S Tsuruoka, H Yamamoto, T Takamura, S Kaneko, A Fujimura
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Significance of plasma 7α-hydroxy-4-cholesten-3-one and 27-hydroxycholesterol concentrations as markers for hepatic bile acid synthesis in cholesterol-fed rabbits
A Honda, T Yoshida, G Xu, Y Matsuzaki, S Fukushima, N Tanaka, M Doy, S Shefer, G Salen
Metabolism 2004
Dietary cholesterol stimulates CYP7A1 in rats because farnesoid X receptor is not activated
G Xu, L Pan, H Li, Q Shang, A Honda, S Shefer, J Bollineni, Y Matsuzaki, GS Tint, G Salen
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Annual Review of Biochemistry 2003
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A Montoudis, S Boileau, L Simoneau, J Lafond
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T HE E NZYMES , R EGULATION , AND G ENETICSOF B ILE A CID S YNTHESIS
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Annual Review of Biochemistry 2003
Human Cholesterol 7alpha-Hydroxylase (CYP7A1) Deficiency has a Hypercholesterolemic Phenotype
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The Journal of biological chemistry 2002
Removal of the bile acid pool upregulates cholesterol 7α-hydroxylase by deactivating FXR in rabbits
G Xu, L Pan, SK Erickson, BM Forman, BL Shneider, M Ananthanarayanan, X Li, S Shefer, N Balasubramanian, L Ma, H Asaoka, SR Lear, LB Nguyen, I Dussault, FJ Suchy, GS Tint, G Salen
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