2014
DOI: 10.1016/j.jss.2013.09.031
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The effects of iloprost on ischemia-reperfusion injury in skeletal muscles in a rodent model

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Cited by 11 publications
(14 citation statements)
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“…Similarly, some other studies also found decreased serum and tissue SOD activities in models of I/R injury. [15,19] In the present study, the serum SOD activity was numerically lower in the I/R and solvent groups, but significantly higher in the edaravone group compared to the I/R group. The SOD activity in the renal tissue was numerically lower in the I/R group than in the control group and numerically higher in the edaravone group than in the I/R group; however, none of these differences were significant.…”
Section: Discussionsupporting
confidence: 39%
“…Similarly, some other studies also found decreased serum and tissue SOD activities in models of I/R injury. [15,19] In the present study, the serum SOD activity was numerically lower in the I/R and solvent groups, but significantly higher in the edaravone group compared to the I/R group. The SOD activity in the renal tissue was numerically lower in the I/R group than in the control group and numerically higher in the edaravone group than in the I/R group; however, none of these differences were significant.…”
Section: Discussionsupporting
confidence: 39%
“…Second, skeletal muscle have longer endurance to IR injury than other susceptible organs. Drugs such as silibinin [24], iloprost [25], and dextran sulfate [26], which can attenuate the heart, renal, and brain IR injury have little effect in skeletal muscle injury. Finally, some drugs like hydrogen sulfide [2] and carbon monoxide [21], which are effective in physiologic dosage might be poisonous in moderate or high doses.…”
Section: Discussionmentioning
confidence: 99%
“…It is less toxic and expands blood vessels through different mechanisms. It can change the concentration of biomarkeroactive substances in patients with biomarkercular endothelial dysfunction …”
Section: Discussionmentioning
confidence: 99%
“…Iloprost, a vasodilator, is commonly used in treating patients with PAH. It is also a synthetic analogue of prostacyclin with few systemic adverse effects but with the additional advantages such as simple delivery, minimal toxicity, and dilation of the pulmonary artery through different cellular mechanisms …”
Section: Introductionmentioning
confidence: 99%