Literature DB >> 10598127

Potential downregulation of HMG-CoA reductase after prolonged administration of P-407 in C57BL/6 mice.

T P Johnston1, J C Baker, A S Jamal, D Hall, E E Emeson, W K Palmer.   

Abstract

This study investigated the potential alteration in the amount of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase messenger RNA (mRNA) and lipoprotein lipase (LPL) mRNA in the livers of C57BL/6 mice after long-term (200 days) treatment with the nonionic surfactant called poloxamer 407 (P-407). Previously, P-407 has been used to produce a dose-controlled hyperlipidemic state in C57BL/6 mice with subsequent formation of atherosclerotic lesions. Five groups of mice were studied; controls (C); mice fed a standard chow diet enriched with only cholic acid (CH); mice fed the high-cholesterol, high-fat Paigen diet (HF); mice treated with 0.5 g/kg P-407 every third day (P); and mice administered 0.5 g/kg P-407 every third day while consuming a diet identical to that of mice in group CH (PC). Neither a significant (p < 0.05) weight loss nor alteration in liver enzymes (AST and ALT) were observed for any group throughout the study when compared with the control mice. Total plasma cholesterol (CHOL) was significantly elevated compared with controls for mice in groups HF, P, and PC, whereas total plasma triglycerides (TG) were significantly increased for mice in only groups P and PC. Long-term ingestion of a high-fat diet or a diet enriched in cholic acid resulted in a significant (p < 0.05) reduction in HDL-CHOL when compared with controls. Plasma samples assayed at 200 days for mice in groups HF and P showed a shift in the lipoprotein fraction distribution primarily to VLDL-CHOL as compared with mice in group C in which, as expected, most of the CHOL was contained in the HDL fraction. The biologic activity of HMG-CoA reductase assayed in hepatic microsomal homogenates was significantly reduced for mice in groups CH (p < 0.01), HF (p < 0.01), and PC (p < 0.05), but not for mice in group P, when compared with control. A statistical analysis of the data demonstrated significant (p < 0.05) reductions in the HMG-CoA reductase mRNA levels in hepatic tissue for all treatment groups relative to mRNA levels determined for mice in group C. In contrast, no treatment group demonstrated a significant difference in hepatic LPL mRNA levels when compared with mRNA levels determined for control animals. These data demonstrate that P-407 administration to C57BL/6 mice significantly decreased the amount of HMG-CoA reductase mRNA detected in liver.

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Year:  1999        PMID: 10598127     DOI: 10.1097/00005344-199912000-00010

Source DB:  PubMed          Journal:  J Cardiovasc Pharmacol        ISSN: 0160-2446            Impact factor:   3.105


  10 in total

Review 1.  A review of poloxamer 407 pharmaceutical and pharmacological characteristics.

Authors:  Gilles Dumortier; Jean Louis Grossiord; Florence Agnely; Jean Claude Chaumeil
Journal:  Pharm Res       Date:  2006-11-11       Impact factor: 4.200

2.  Acute P-407 administration to mice causes hypercholesterolemia by inducing cholesterolgenesis and down-regulating low-density lipoprotein receptor expression.

Authors:  Carlos Leon; Kishor M Wasan; Kristina Sachs-Barrable; Thomas P Johnston
Journal:  Pharm Res       Date:  2006-06-21       Impact factor: 4.200

3.  Vascular anastomosis using controlled phase transitions in poloxamer gels.

Authors:  Edward I Chang; Michael G Galvez; Jason P Glotzbach; Cynthia D Hamou; Samyra El-ftesi; C Travis Rappleye; Kristin-Maria Sommer; Jayakumar Rajadas; Oscar J Abilez; Gerald G Fuller; Michael T Longaker; Geoffrey C Gurtner
Journal:  Nat Med       Date:  2011-08-28       Impact factor: 53.440

4.  The induction of atherogenic dyslipidaemia in poloxamer 407-treated mice is not mediated through PPARalpha.

Authors:  Thomas P Johnston; David J Waxman
Journal:  J Pharm Pharmacol       Date:  2008-06       Impact factor: 3.765

5.  Pluronic block copolymers inhibit low density lipoprotein self-association.

Authors:  Alexandra A Melnichenko; Denis V Aksenov; Veronika A Myasoedova; Oleg M Panasenko; Alexander A Yaroslavov; Igor A Sobenin; Yuri V Bobryshev; Alexander N Orekhov
Journal:  Lipids       Date:  2012-07-14       Impact factor: 1.880

6.  Hepatoprotective Effect of Camel Milk on Poloxamer 407 Induced Hyperlipidaemic Wistar Rats.

Authors:  Jibril Zuberu; Malajiya I A Saleh; Abdul Wahab Alhassan; Bello Y Adamu; Munira Aliyu; Bilkisu T Iliya
Journal:  Open Access Maced J Med Sci       Date:  2017-11-30

7.  Serum lysophospholipid levels are altered in dyslipidemic hamsters.

Authors:  Susana Suárez-García; Antoni Caimari; Josep Maria Del Bas; Manuel Suárez; Lluís Arola
Journal:  Sci Rep       Date:  2017-09-05       Impact factor: 4.379

8.  A triglyceride-rich lipoprotein environment exacerbates renal injury in the accelerated nephrotoxic nephritis model.

Authors:  M F Saja; H T Cook; M M Ruseva; M Szajna; M C Pickering; K J Woollard; M Botto
Journal:  Clin Exp Immunol       Date:  2018-03-09       Impact factor: 4.330

9.  Poloxamer 407-induced atherosclerosis in mice appears to be due to lipid derangements and not due to its direct effects on endothelial cells and macrophages.

Authors:  Thomas P Johnston; Yuai Li; Ahmed S Jamal; Daniel J Stechschulte; Kottarappat N Dileepan
Journal:  Mediators Inflamm       Date:  2003-06       Impact factor: 4.711

10.  In vitro evaluation of the inhibitory potential of pharmaceutical excipients on human carboxylesterase 1A and 2.

Authors:  Chengliang Zhang; Yanjiao Xu; Qiaoni Zhong; Xiping Li; Ping Gao; Chengyang Feng; Qian Chu; Yuan Chen; Dong Liu
Journal:  PLoS One       Date:  2014-04-03       Impact factor: 3.240

  10 in total

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