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Efficacy of leupeptin in treating ischemia in a rat hind limb model

Prolonged tourniquet use can lead to tissue ischemia and can cause progressive muscle and nerve injuries. Such injuries are accompanied by calpain activation and subsequent Wallerian‐like degeneration. Several known inhibitors, including leupeptin, are known to impede the activity of calpain and ass...

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Autores principales: Gurevich, Mikhail, Iocolano, Kari, Martin, Irene Nozal, Singh, Gurtej, Khan, Sami U., Bui, Duc T., Dagum, Alexander B., Komatsu, David E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350425/
https://www.ncbi.nlm.nih.gov/pubmed/35924300
http://dx.doi.org/10.14814/phy2.15411
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author Gurevich, Mikhail
Iocolano, Kari
Martin, Irene Nozal
Singh, Gurtej
Khan, Sami U.
Bui, Duc T.
Dagum, Alexander B.
Komatsu, David E.
author_facet Gurevich, Mikhail
Iocolano, Kari
Martin, Irene Nozal
Singh, Gurtej
Khan, Sami U.
Bui, Duc T.
Dagum, Alexander B.
Komatsu, David E.
author_sort Gurevich, Mikhail
collection PubMed
description Prolonged tourniquet use can lead to tissue ischemia and can cause progressive muscle and nerve injuries. Such injuries are accompanied by calpain activation and subsequent Wallerian‐like degeneration. Several known inhibitors, including leupeptin, are known to impede the activity of calpain and associated tissue damage. We hypothesize that employment of leupeptin in a rat model of prolonged hind limb ischemia can mitigate muscle and nerve injuries. Sprague–Dawley rats (n = 10) weighing between 300–400 g were employed in this study. Their left hind limbs were subjected to blood flow occlusion for a period of 2‐h using a neonatal blood pressure cuff. Five rats were given twice weekly intramuscular leupeptin injections, while the other five received saline. After 2 weeks, the animals were euthanized, their sciatic nerves and gastrocnemius muscles were harvested, fixed, stained, and analyzed using NIH Image J software. The administration of leupeptin resulted in larger gastrocnemius muscle fiber cross‐sectional areas for the right (non‐tourniquet applied) hindlimb as compared to that treated with the saline (p = 0.0110). However, no statistically significant differences were found between these two groups for the injured left hindlimb (p = 0.1440). With regards to the sciatic nerve cross‐sectional areas and sciatic functional index, no differences were detected between the leupeptin and control treated groups for both the healthy and injured hindlimbs. This research provides new insights on how to employ leupeptin to inhibit the degenerative effects of calpain and preserve tissues following ischemia resulting from orthopedic or plastic surgery procedures.
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spelling pubmed-93504252022-08-09 Efficacy of leupeptin in treating ischemia in a rat hind limb model Gurevich, Mikhail Iocolano, Kari Martin, Irene Nozal Singh, Gurtej Khan, Sami U. Bui, Duc T. Dagum, Alexander B. Komatsu, David E. Physiol Rep Original Articles Prolonged tourniquet use can lead to tissue ischemia and can cause progressive muscle and nerve injuries. Such injuries are accompanied by calpain activation and subsequent Wallerian‐like degeneration. Several known inhibitors, including leupeptin, are known to impede the activity of calpain and associated tissue damage. We hypothesize that employment of leupeptin in a rat model of prolonged hind limb ischemia can mitigate muscle and nerve injuries. Sprague–Dawley rats (n = 10) weighing between 300–400 g were employed in this study. Their left hind limbs were subjected to blood flow occlusion for a period of 2‐h using a neonatal blood pressure cuff. Five rats were given twice weekly intramuscular leupeptin injections, while the other five received saline. After 2 weeks, the animals were euthanized, their sciatic nerves and gastrocnemius muscles were harvested, fixed, stained, and analyzed using NIH Image J software. The administration of leupeptin resulted in larger gastrocnemius muscle fiber cross‐sectional areas for the right (non‐tourniquet applied) hindlimb as compared to that treated with the saline (p = 0.0110). However, no statistically significant differences were found between these two groups for the injured left hindlimb (p = 0.1440). With regards to the sciatic nerve cross‐sectional areas and sciatic functional index, no differences were detected between the leupeptin and control treated groups for both the healthy and injured hindlimbs. This research provides new insights on how to employ leupeptin to inhibit the degenerative effects of calpain and preserve tissues following ischemia resulting from orthopedic or plastic surgery procedures. John Wiley and Sons Inc. 2022-08-03 /pmc/articles/PMC9350425/ /pubmed/35924300 http://dx.doi.org/10.14814/phy2.15411 Text en © 2022 The Authors. Physiological Reports published by Wiley Periodicals LLC on behalf of The Physiological Society and the American Physiological Society. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Gurevich, Mikhail
Iocolano, Kari
Martin, Irene Nozal
Singh, Gurtej
Khan, Sami U.
Bui, Duc T.
Dagum, Alexander B.
Komatsu, David E.
Efficacy of leupeptin in treating ischemia in a rat hind limb model
title Efficacy of leupeptin in treating ischemia in a rat hind limb model
title_full Efficacy of leupeptin in treating ischemia in a rat hind limb model
title_fullStr Efficacy of leupeptin in treating ischemia in a rat hind limb model
title_full_unstemmed Efficacy of leupeptin in treating ischemia in a rat hind limb model
title_short Efficacy of leupeptin in treating ischemia in a rat hind limb model
title_sort efficacy of leupeptin in treating ischemia in a rat hind limb model
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9350425/
https://www.ncbi.nlm.nih.gov/pubmed/35924300
http://dx.doi.org/10.14814/phy2.15411
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