Volume 40, Issue 11 pp. 1002-1010

Effects of acetyl-L-carnitine and oxfenicine on aorta stiffness in diabetic rats

Kuo-Chu Chang

Kuo-Chu Chang

Department of Physiology, College of Medicine, National Taiwan University, Taipei, Taiwan

Search for more papers by this author
Chuen-Den Tseng

Chuen-Den Tseng

Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan

Search for more papers by this author
Shao-Chun Lu

Shao-Chun Lu

Institute of Biochemistry and Molecular Biology, College of Medicine, National Taiwan University, Taipei, Taiwan

Search for more papers by this author
Jin-Tung Liang

Jin-Tung Liang

Department of Surgery, National Taiwan University Hospital, Taipei, Taiwan

Search for more papers by this author
Ming-Shiou Wu

Ming-Shiou Wu

Department of Internal Medicine, National Taiwan University Hospital, Taipei, Taiwan

Search for more papers by this author
Ming-Shian Tsai

Ming-Shian Tsai

Department of Surgery, E-Da Hospital, Kaohsiung, Taiwan

Search for more papers by this author
Kwan-Lih Hsu

Kwan-Lih Hsu

Department of Internal Medicine, E-Da Hospital and Department of Nursing, I-Shou University, Kaohsiung, Taiwan

Search for more papers by this author
First published: 29 July 2010
Citations: 6
Kuo-Chu Chang, PhD, Department of Physiology, College of Medicine, National Taiwan University, No. 1, Sec. 1, Jen-Ai Road, Taipei, Taiwan.Tel.: +886-2-2312-3456, ext. 88243; fax: +886-2-2396-4350; e-mail: [email protected]

Abstract

Eur J Clin Invest 2010; 40 (11): 1002–1010

Background We compared the haemodynamic and metabolic effects of acetyl-L-carnitine (one of the carnitine derivatives) and of oxfenicine (a carnitine palmitoyltransferase-1 inhibitor) in streptozotocin-induced diabetes in male Wistar rats.

Materials and methods Diabetes was induced by a single tail vein injection of 55 mg kg−1 streptozotocin. The diabetic animals daily treated with either acetyl-L-carnitine (150 mg kg−1 in drinking water) or oxfenicine (150 mg kg−1 by oral gavage) for 8 weeks,were compared with the untreated age-matched diabetic controls. Arterial wave reflection was derived using the impulse response function of the filtered aortic input impedance spectra. Thiobarbituric acid reactive substances (TBARS) measurement was used to estimate malondialdehyde (MDA) content.

Results Oxfenicine, but not acetyl-L-carnitine, increased total peripheral resistance in diabetes, which paralleled its elevation in plasma levels of free fatty acids. By contrast, acetyl-L-carnitine, but not oxfenicine, resulted in a significant increase in wave transit time and a decrease in wave reflection factor, suggesting that acetyl-L-carnitine may attenuate the diabetes-induced deterioration in systolic loading condition for the left ventricle. This was in parallel with its lowering of MDA/TBARS content in plasma and aortic walls in diabetes. Acetyl-L-carnitine therapy also prevented the diabetes-related cardiac hypertrophy, as evidenced by the reduction in ratio of the left ventricular weight to body weight.

Conclusion Acetyl-L-carnitine, but not oxfenicine, attenuates aortic stiffening and cardiac hypertrophy, possibly through its decrease of lipid oxidation-derived MDA/TBARS in the rats with insulin deficiency.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.