SAGE Journals Online
Advertisement
Sign In to gain access to subscriptions and/or personal tools.

 

Advanced Search

Journal Navigation

Journal Home

Subscriptions

Archive

Contact Us

Table of Contents

Advertisement

Sign In to gain access to subscriptions and/or personal tools.
Vascular and Endovascular Surgery
This Article
Right arrow Full Text (PDF)
Right arrow References
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Alert me to new issues of the journal
Right arrow Add to Saved Citations
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Request Reprints
Right arrow Add to My Marked Citations
Citing Articles
Right arrow Citing Articles via Google Scholar
Right arrow Citing Articles via Scopus
Google Scholar
Right arrow Articles by Ikezawa, T.
Right arrow Articles by Oba, Y.
Right arrow Search for Related Content
PubMed
Right arrow Articles by Ikezawa, T.
Right arrow Articles by Oba, Y.
Social Bookmarking
 Add to CiteULike   Add to Complore   Add to Connotea   Add to Del.icio.us   Add to Digg   Add to Reddit   Add to Technorati   Add to Twitter  
What's this?

Lipid Peroxides in the Mechanism of Ischemia/Reperfusion Injury in Skeletal Muscle—Experimental Studies

T. Ikezawa

Nagoya University School of Medicine, Nagoya, Japan

N. Nishikimi

Nagoya University School of Medicine, Nagoya, Japan

Y. Oba

Nagoya University School of Medicine, Nagoya, Japan

Two sets of experiments were conducted to investigate whether oxygen-de rived free radicals are involved in the mechanism of ischemia/reperfusion (I/R) injury of skeletal muscle and vitamin E is effective in alleviating the injury.

In the first set of experiments, twenty adult mongrel dogs were divided into three groups: group 1 (n=7) control, group 2 (n = 6) I/R, and group 3 (n=7) I/R with 500 mg of vitamin E. Serum creatine phosphokinase (CPK) and lipid per oxides (LPO) were measured as markers of rhabdomyolysis and biomembrane injury due to oxygen-derived free radicals, respectively. CPK increased signifi cantly after reperfusion with a peak value of 38,000 ± 9,800 mU/mL in group 2, when compared with a peak value of 1,060 ± 290 mU/mL in group 3 (p < 0.02). LPO also significantly increased with a peak value of 20.4 ±3.7 nmol/mL in group 2, when compared with a peak value of 9.2 ± 2.2 nmol/mL in group 3 (p < 0.04).

In the second sets of experiments, 13 dogs were divided into two groups: group A (n=5) control and group B (n=8) I/R. Tissue LPO was measured eighteen hours after reperfusion in the gracilis muscle and gastrocnemius mus cle. The mean value of LPO in the gracilis muscle was 0.94 ± 0.46 nmol/mg protein in group A, compared with 1.13 ± 0.67 nmol/mg protein in group B. It was higher in group B, but there was no significant difference. Mean LPO in the gastrocnemius muscle was 0.85 ± 0.34 nmol/mg protein in group A, and 1.83 ± 0.71 nmol/mg protein in group B. There was a significant difference (p < 0.02).

Serum CPK and LPO were significantly higher in group 2 than in groups 1 and 3, and tissue LPO was also high in skeletal muscle after reperfusion. Serum CPK and LPO were effectively suppressed by administration of vitamin E be fore reperfusion.

These results show that oxygen-derived free radicals are involved in the mechanism of I/R injury in skeletal muscle and suggest that vitamin E is effec tive in alleviating the injury.

Vascular and Endovascular Surgery, Vol. 27, No. 3, 191-201 (1993)
DOI: 10.1177/153857449302700306


Add to CiteULike CiteULike   Add to Complore Complore   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter    What's this?




Advertisement