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Effect of Vitamin E on Vascular Integrity in Cholesterol‐Fed Guinea Pigs

 

作者: Yan Qiao,   Munehiro Yokoyama,   Kohji Kameyama,   Goro Asano,  

 

期刊: Arteriosclerosis and Thrombosis: A Journal of Vascular Biology  (OVID Available online 1993)
卷期: Volume 13, issue 12  

页码: 1885-1892

 

ISSN:1049-8834

 

年代: 1993

 

出版商: OVID

 

关键词: hypercholesterolemia;atherosclerosis;vascular permeability;proteoglycans;vitamin E

 

数据来源: OVID

 

摘要:

This study was designed to clarify the effects of vitamin E on the alterations in proteoglycan distribution and vascular permeability, which were examined by immunohistochemical and ultrastructural techniques in the aortas of cholesterol-fed guinea pigs. The animals were divided into three groups: a control group, a cholesterol group, and a vitamin E group. Serum levels of cholesterol, triglyceride, low-density lipoprotein, high-density lipoprotein, and thiobarbituric acid-reactive substances were measured. An increase in thiobarbituric acid-reactive substances was observed in the cholesterol group compared with control and vitamin E groups. Intimal atheromatous lesions of the aorta were significantly decreased in the vitamin E group compared with the cholesterol group. Histochemically, an increased distribution of proteoglycans such as chondroitin, dermatan, and heparan sulfates and ruthenium red reaction products in the intima; decreased glycocalyx on the endothelial surface; and increased permeability to horseradish peroxidase were revealed in the cholesterol group compared with the vitamin E group. Hypercholesterolemia, resulting in superoxide production, may have contributed to the endothelial damage and increased permeability to plasma proteins and lipids in the vascular wall of the cholesterol group. However, vitamin E administration inhibited lipid deposition and development of this abnormal permeability associated with an irregular distribution of proteoglycan. These results suggest that vitamin E preserves the morphological and functional integrity of the vascular wall and may contribute to the inhibition of atherogenesis in cholesterol-fed guinea pigs.

 

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