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Potentilla reptans L. postconditioning protects reperfusion injury via the RISK/SAFE pathways in an isolated rat heart

BACKGROUND: Our previous study indicated that Potentilla reptans root has a preconditioning effect by its antioxidant and anti-apoptotic effects in an isolated rat heart ischemia/reperfusion (IR) model. In the present study, we investigated the post-conditioning cardio-protective effects of Potentil...

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Autores principales: Enayati, Ayesheh, Salehi, Aref, Alilou, Mostafa, Stuppner, Hermann, Polshekan, Mirali, Rajaei, Maryam, Pourabouk, Mona, Jabbari, Ali, Mazaheri, Zohreh, Yassa, Narguess, Moheimani, Hamid Reza, Khori, Vahid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620719/
https://www.ncbi.nlm.nih.gov/pubmed/34823510
http://dx.doi.org/10.1186/s12906-021-03456-2
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author Enayati, Ayesheh
Salehi, Aref
Alilou, Mostafa
Stuppner, Hermann
Polshekan, Mirali
Rajaei, Maryam
Pourabouk, Mona
Jabbari, Ali
Mazaheri, Zohreh
Yassa, Narguess
Moheimani, Hamid Reza
Khori, Vahid
author_facet Enayati, Ayesheh
Salehi, Aref
Alilou, Mostafa
Stuppner, Hermann
Polshekan, Mirali
Rajaei, Maryam
Pourabouk, Mona
Jabbari, Ali
Mazaheri, Zohreh
Yassa, Narguess
Moheimani, Hamid Reza
Khori, Vahid
author_sort Enayati, Ayesheh
collection PubMed
description BACKGROUND: Our previous study indicated that Potentilla reptans root has a preconditioning effect by its antioxidant and anti-apoptotic effects in an isolated rat heart ischemia/reperfusion (IR) model. In the present study, we investigated the post-conditioning cardio-protective effects of Potentilla reptans and its active substances. METHODS: The ethyl acetate fraction of P. reptans root (Et) was subjected to an IR model under 30 min of ischemia and 100 min of reperfusion. To investigate the postconditioning effect, Et was perfused for 15 min at the early phase of reperfusion. RISK/SAFE pathway inhibitors, 5HD and L-NAME, were applied individually 10 min before the ischemia, either alone or in combination with Et during the early reperfusion phase. The hemodynamic factors and ventricular arrhythmia were calculated during the reperfusion. Oxidative stress, apoptosis markers, GSK-3β and SGK1 proteins were assessed at the end of experiments. RESULTS: Et postconditioning (Etpost) significantly reduced the infarct size, arrhythmia score, ventricular fibrillation incidence, and enhanced the hemodynamic parameters by decreasing the MDA level and increasing expression of Nrf2, SOD and CAT activities. Meanwhile, Etpost increased the BCl-2/BAX ratio and decreased Caspase-3 expression. The cardioprotective effect of Etpost was abrogated by L-NAME, Wortmannin (a PI3K/Akt inhibitor), and AG490 (a JAK/STAT3 inhibitor). Finally, Etpost reduced the expression of GSK-3β and SGK1 proteins pertaining to the IR group. CONCLUSION: P. reptans reveals the post-conditioning effects via the Nrf2 pathway, NO release, and the RISK/SAFE pathway. Also, Etpost decreased apoptotic indexes by inhibiting GSK-3β and SGK1 expressions. Hence, our data suggest that Etpost can be a suitable natural candidate to protect cardiomyocytes during reperfusion injury. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-021-03456-2.
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spelling pubmed-86207192021-11-29 Potentilla reptans L. postconditioning protects reperfusion injury via the RISK/SAFE pathways in an isolated rat heart Enayati, Ayesheh Salehi, Aref Alilou, Mostafa Stuppner, Hermann Polshekan, Mirali Rajaei, Maryam Pourabouk, Mona Jabbari, Ali Mazaheri, Zohreh Yassa, Narguess Moheimani, Hamid Reza Khori, Vahid BMC Complement Med Ther Research BACKGROUND: Our previous study indicated that Potentilla reptans root has a preconditioning effect by its antioxidant and anti-apoptotic effects in an isolated rat heart ischemia/reperfusion (IR) model. In the present study, we investigated the post-conditioning cardio-protective effects of Potentilla reptans and its active substances. METHODS: The ethyl acetate fraction of P. reptans root (Et) was subjected to an IR model under 30 min of ischemia and 100 min of reperfusion. To investigate the postconditioning effect, Et was perfused for 15 min at the early phase of reperfusion. RISK/SAFE pathway inhibitors, 5HD and L-NAME, were applied individually 10 min before the ischemia, either alone or in combination with Et during the early reperfusion phase. The hemodynamic factors and ventricular arrhythmia were calculated during the reperfusion. Oxidative stress, apoptosis markers, GSK-3β and SGK1 proteins were assessed at the end of experiments. RESULTS: Et postconditioning (Etpost) significantly reduced the infarct size, arrhythmia score, ventricular fibrillation incidence, and enhanced the hemodynamic parameters by decreasing the MDA level and increasing expression of Nrf2, SOD and CAT activities. Meanwhile, Etpost increased the BCl-2/BAX ratio and decreased Caspase-3 expression. The cardioprotective effect of Etpost was abrogated by L-NAME, Wortmannin (a PI3K/Akt inhibitor), and AG490 (a JAK/STAT3 inhibitor). Finally, Etpost reduced the expression of GSK-3β and SGK1 proteins pertaining to the IR group. CONCLUSION: P. reptans reveals the post-conditioning effects via the Nrf2 pathway, NO release, and the RISK/SAFE pathway. Also, Etpost decreased apoptotic indexes by inhibiting GSK-3β and SGK1 expressions. Hence, our data suggest that Etpost can be a suitable natural candidate to protect cardiomyocytes during reperfusion injury. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12906-021-03456-2. BioMed Central 2021-11-26 /pmc/articles/PMC8620719/ /pubmed/34823510 http://dx.doi.org/10.1186/s12906-021-03456-2 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Enayati, Ayesheh
Salehi, Aref
Alilou, Mostafa
Stuppner, Hermann
Polshekan, Mirali
Rajaei, Maryam
Pourabouk, Mona
Jabbari, Ali
Mazaheri, Zohreh
Yassa, Narguess
Moheimani, Hamid Reza
Khori, Vahid
Potentilla reptans L. postconditioning protects reperfusion injury via the RISK/SAFE pathways in an isolated rat heart
title Potentilla reptans L. postconditioning protects reperfusion injury via the RISK/SAFE pathways in an isolated rat heart
title_full Potentilla reptans L. postconditioning protects reperfusion injury via the RISK/SAFE pathways in an isolated rat heart
title_fullStr Potentilla reptans L. postconditioning protects reperfusion injury via the RISK/SAFE pathways in an isolated rat heart
title_full_unstemmed Potentilla reptans L. postconditioning protects reperfusion injury via the RISK/SAFE pathways in an isolated rat heart
title_short Potentilla reptans L. postconditioning protects reperfusion injury via the RISK/SAFE pathways in an isolated rat heart
title_sort potentilla reptans l. postconditioning protects reperfusion injury via the risk/safe pathways in an isolated rat heart
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8620719/
https://www.ncbi.nlm.nih.gov/pubmed/34823510
http://dx.doi.org/10.1186/s12906-021-03456-2
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