Literature DB >> 7661876

Comparative effects of HMG-CoA reductase inhibitors on apo B production in the casein-fed rabbit: atorvastatin versus lovastatin.

B J Auerbach1, B R Krause, C L Bisgaier, R S Newton.   

Abstract

Rabbits fed a diet enriched in casein develop an endogenous hypercholesterolemia (EH) due both to an increased low density lipoprotein (LDL) synthetic rate and decreased LDL receptor activity. Pre-established EH in this model was used to assess the ability and mechanism by which atorvastatin lowers total plasma cholesterol (TPC) compared to the reference agent lovastatin. Rabbits were fed a casein diet for 6 weeks, obtaining average TPC levels above 200 mg/dl. To ensure equivalent mean cholesterol concentrations, animals were randomized into treatment groups based on the 6-week TPC levels, and fed the casein diet alone or in combination with either atorvastatin or lovastatin for an additional 6 weeks. Under these conditions, new steady-state cholesterol values were established. Lipoprotein concentrations and distributions were determined at this point. Compared to pretreatment values, TPC were similar in untreated animals. Atorvastatin, however, significantly reduced TPC by 38%, 45%, and 54% at the 1, 3, and 10 mg/kg doses, respectively. Statistically significant lowering of TPC (35%) by lovastatin was only achieved at the 10 mg/kg dose. To determine the mechanism by which atorvastatin lowered TPC in the EH rabbits, kinetic studies using human [125I]-LDL were performed in a subset of animals maintained on the casein diet alone (n = 5), or those treated with 3 mg/kg of atorvastatin (n = 5) or lovastatin (n = 7). In this set of studies, atorvastatin significantly lowered TPC compared to control and lovastatin-treated rabbits by 57% and 46%, respectively. Lovastatin treatment resulted in a 20% decrease in TPC as compared to untreated controls.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7661876     DOI: 10.1016/0021-9150(94)05508-g

Source DB:  PubMed          Journal:  Atherosclerosis        ISSN: 0021-9150            Impact factor:   5.162


  7 in total

1.  Atorvastatin and simvastatin have distinct effects on hydroxy methylglutaryl-CoA reductase activity and mRNA abundance in the guinea pig.

Authors:  K Conde; S Roy; H C Freake; R S Newton; M L Fernandez
Journal:  Lipids       Date:  1999-12       Impact factor: 1.880

2.  Different effect of simvastatin and atorvastatin on key enzymes involved in VLDL synthesis and catabolism in high fat/cholesterol fed rabbits.

Authors:  J C Verd; C Peris; M Alegret; C Díaz; G Hernández; M Vázquez; T Adzet; J C Laguna; R M Sánchez
Journal:  Br J Pharmacol       Date:  1999-07       Impact factor: 8.739

3.  The role of the LDL receptor in apolipoprotein B secretion.

Authors:  J Twisk; D L Gillian-Daniel; A Tebon; L Wang; P H Barrett; A D Attie
Journal:  J Clin Invest       Date:  2000-02       Impact factor: 14.808

Review 4.  Atorvastatin: an updated review of its pharmacological properties and use in dyslipidaemia.

Authors:  H S Malhotra; K L Goa
Journal:  Drugs       Date:  2001       Impact factor: 9.546

Review 5.  Atorvastatin. A review of its pharmacology and therapeutic potential in the management of hyperlipidaemias.

Authors:  A P Lea; D McTavish
Journal:  Drugs       Date:  1997-05       Impact factor: 9.546

6.  Reduced intimal hyperplasia in rabbits via medical therapy after carotid venous bypass.

Authors:  Semih Yucel; Muzaffer Bahcivan; Mehmet Kamil Gol; Behice H Erenler; Fersat Kolbakir; Hasan T Keceligil
Journal:  Tex Heart Inst J       Date:  2009

7.  Effect of Atorvastatin versus Simvastatin on Lipid Profile and Plasma Fibrinogen in Patients with Hypercholesterolaemia: A Pilot, Randomised, Double-Blind, Dose-Titrating Study.

Authors:  V G Athyros; A A Papageorgiou; H A Hatzikonstandinou; V V Athyrou; A G Kontopoulos
Journal:  Clin Drug Investig       Date:  1998       Impact factor: 2.859

  7 in total

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