Cargando…

Hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity

BACKGROUND: of the study: Hepatic encephalopathy (HE) is a complication in which brain ammonia (NH(4)(+)) levels reach critically high concentrations because of liver failure. HE could lead to a range of neurological complications from locomotor and behavioral disturbances to coma. Several tactics h...

Descripción completa

Detalles Bibliográficos
Autores principales: Niknahad, Hossein, Mobasheri, Ali, Arjmand, Abdollah, Rafiei, Elahe, Alidaee, Sepideh, Razavi, Hadi, Bagheri, Sara, Rezaei, Heresh, Sabouri, Samira, Najibi, Asma, Khodaei, Forouzan, Kashani, Seyyed Mohammad Amin, Ommati, Mohammad Mehdi, Heidari, Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551565/
https://www.ncbi.nlm.nih.gov/pubmed/37810869
http://dx.doi.org/10.1016/j.heliyon.2023.e20557
_version_ 1785115795917897728
author Niknahad, Hossein
Mobasheri, Ali
Arjmand, Abdollah
Rafiei, Elahe
Alidaee, Sepideh
Razavi, Hadi
Bagheri, Sara
Rezaei, Heresh
Sabouri, Samira
Najibi, Asma
Khodaei, Forouzan
Kashani, Seyyed Mohammad Amin
Ommati, Mohammad Mehdi
Heidari, Reza
author_facet Niknahad, Hossein
Mobasheri, Ali
Arjmand, Abdollah
Rafiei, Elahe
Alidaee, Sepideh
Razavi, Hadi
Bagheri, Sara
Rezaei, Heresh
Sabouri, Samira
Najibi, Asma
Khodaei, Forouzan
Kashani, Seyyed Mohammad Amin
Ommati, Mohammad Mehdi
Heidari, Reza
author_sort Niknahad, Hossein
collection PubMed
description BACKGROUND: of the study: Hepatic encephalopathy (HE) is a complication in which brain ammonia (NH(4)(+)) levels reach critically high concentrations because of liver failure. HE could lead to a range of neurological complications from locomotor and behavioral disturbances to coma. Several tactics have been established for subsiding blood and brain NH(4)(+). However, there is no precise intervention to mitigate the direct neurological complications of NH(4)(+). PURPOSE: It has been found that oxidative stress, mitochondrial damage, and neuro-inflammation play a fundamental role in NH(4)(+) neurotoxicity. Piracetam is a drug used clinically in neurological complications such as stroke and head trauma. Piracetam could significantly diminish oxidative stress and improve brain mitochondrial function. RESEARCH METHODS: In the current study, piracetam (100 and 500 mg/kg, oral) was used in a mice model of HE induced by thioacetamide (TA, 800 mg/kg, single dose, i.p). RESULTS: Significant disturbances in animals’ locomotor activity, along with increased oxidative stress biomarkers, including reactive oxygen species formation, protein carbonylation, lipid peroxidation, depleted tissue glutathione, and decreased antioxidant capacity, were evident in the brain of TA-treated mice. Meanwhile, mitochondrial permeabilization, mitochondrial depolarization, suppression of dehydrogenases activity, and decreased ATP levels were found in the brain of the TA group. The level of pro-inflammatory cytokines was also significantly high in the brain of HE animals. CONCLUSION: It was found that piracetam significantly enhanced mice's locomotor activity, blunted oxidative stress biomarkers, decreased inflammatory cytokines, and improved mitochondrial indices in hyperammonemic mice. These data suggest piracetam as a neuroprotective agent which could be repurposed for the management of HE.
format Online
Article
Text
id pubmed-10551565
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Elsevier
record_format MEDLINE/PubMed
spelling pubmed-105515652023-10-06 Hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity Niknahad, Hossein Mobasheri, Ali Arjmand, Abdollah Rafiei, Elahe Alidaee, Sepideh Razavi, Hadi Bagheri, Sara Rezaei, Heresh Sabouri, Samira Najibi, Asma Khodaei, Forouzan Kashani, Seyyed Mohammad Amin Ommati, Mohammad Mehdi Heidari, Reza Heliyon Research Article BACKGROUND: of the study: Hepatic encephalopathy (HE) is a complication in which brain ammonia (NH(4)(+)) levels reach critically high concentrations because of liver failure. HE could lead to a range of neurological complications from locomotor and behavioral disturbances to coma. Several tactics have been established for subsiding blood and brain NH(4)(+). However, there is no precise intervention to mitigate the direct neurological complications of NH(4)(+). PURPOSE: It has been found that oxidative stress, mitochondrial damage, and neuro-inflammation play a fundamental role in NH(4)(+) neurotoxicity. Piracetam is a drug used clinically in neurological complications such as stroke and head trauma. Piracetam could significantly diminish oxidative stress and improve brain mitochondrial function. RESEARCH METHODS: In the current study, piracetam (100 and 500 mg/kg, oral) was used in a mice model of HE induced by thioacetamide (TA, 800 mg/kg, single dose, i.p). RESULTS: Significant disturbances in animals’ locomotor activity, along with increased oxidative stress biomarkers, including reactive oxygen species formation, protein carbonylation, lipid peroxidation, depleted tissue glutathione, and decreased antioxidant capacity, were evident in the brain of TA-treated mice. Meanwhile, mitochondrial permeabilization, mitochondrial depolarization, suppression of dehydrogenases activity, and decreased ATP levels were found in the brain of the TA group. The level of pro-inflammatory cytokines was also significantly high in the brain of HE animals. CONCLUSION: It was found that piracetam significantly enhanced mice's locomotor activity, blunted oxidative stress biomarkers, decreased inflammatory cytokines, and improved mitochondrial indices in hyperammonemic mice. These data suggest piracetam as a neuroprotective agent which could be repurposed for the management of HE. Elsevier 2023-09-29 /pmc/articles/PMC10551565/ /pubmed/37810869 http://dx.doi.org/10.1016/j.heliyon.2023.e20557 Text en © 2023 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Niknahad, Hossein
Mobasheri, Ali
Arjmand, Abdollah
Rafiei, Elahe
Alidaee, Sepideh
Razavi, Hadi
Bagheri, Sara
Rezaei, Heresh
Sabouri, Samira
Najibi, Asma
Khodaei, Forouzan
Kashani, Seyyed Mohammad Amin
Ommati, Mohammad Mehdi
Heidari, Reza
Hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity
title Hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity
title_full Hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity
title_fullStr Hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity
title_full_unstemmed Hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity
title_short Hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity
title_sort hepatic encephalopathy complications are diminished by piracetam via the interaction between mitochondrial function, oxidative stress, inflammatory response, and locomotor activity
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10551565/
https://www.ncbi.nlm.nih.gov/pubmed/37810869
http://dx.doi.org/10.1016/j.heliyon.2023.e20557
work_keys_str_mv AT niknahadhossein hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT mobasheriali hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT arjmandabdollah hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT rafieielahe hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT alidaeesepideh hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT razavihadi hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT bagherisara hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT rezaeiheresh hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT sabourisamira hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT najibiasma hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT khodaeiforouzan hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT kashaniseyyedmohammadamin hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT ommatimohammadmehdi hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity
AT heidarireza hepaticencephalopathycomplicationsarediminishedbypiracetamviatheinteractionbetweenmitochondrialfunctionoxidativestressinflammatoryresponseandlocomotoractivity