Irisin Protects Against Hind Limb Ischemia Reperfusion Injury
The aim of this study was to evaluate the effects of irisin in a murine model of hind limb ischemia reperfusion (I/R). The mice were divided into four groups (n = 6 in each group): control, irisin, ischemia reperfusion (I/R), and irisin-ischemia reperfusion (I-I/R). Irisin (0.5 µg.g , intraperitonea...
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Published in: | Drug design, development and therapy Vol. 15; pp. 361 - 368 |
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Main Authors: | , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
New Zealand
Dove Medical Press Limited
01-01-2021
Taylor & Francis Ltd Dove Dove Medical Press |
Subjects: | |
Online Access: | Get full text |
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Summary: | The aim of this study was to evaluate the effects of irisin in a murine model of hind limb ischemia reperfusion (I/R).
The mice were divided into four groups (n = 6 in each group): control, irisin, ischemia reperfusion (I/R), and irisin-ischemia reperfusion (I-I/R). Irisin (0.5 µg.g
, intraperitoneally [i.p.]) was administered 30 min before the I/R procedure. After 2 h of ischemia and 2.5 h of reperfusion, blood and tissue samples were taken for biochemical and histopathological analysis. The results were analyzed by Kruskal-Wallis and Mann-Whitney
-tests.
There was a statistically significant difference in the total antioxidant status (TAS) and total oxidant status (TOS) levels in all the groups. The TAS level in the I/R group was significantly lower than that in the control, irisin, and I-I/R groups, whereas the TOS level was significantly higher in the I/R group as compared with that in the other groups. Caspase-3 activity and caspase-8 activity, indicators of inflammation, were significantly higher in the I/R and I-I/R groups as compared with those in the control and irisin groups.
Irisin may have protective effects in skeletal muscle ischemia reperfusion injury. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 These authors contributed equally to this work |
ISSN: | 1177-8881 1177-8881 |
DOI: | 10.2147/DDDT.S279318 |