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Astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats

BACKGROUND: There is emerging evidence that astaxanthin plays a significant role in protecting neuro-cells from apoptosis after central nervous system injury. Our study examined the effects of astaxanthin on neuro-cell apoptosis after spinal cord injury. METHODS: One hundred and forty-four healthy a...

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Autores principales: Li, Shuang, Gao, Xiaofan, Zhang, Qiushuang, Zhang, Xin, Lin, Wei, Ding, Wei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756234/
https://www.ncbi.nlm.nih.gov/pubmed/35071490
http://dx.doi.org/10.21037/atm-21-6356
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author Li, Shuang
Gao, Xiaofan
Zhang, Qiushuang
Zhang, Xin
Lin, Wei
Ding, Wei
author_facet Li, Shuang
Gao, Xiaofan
Zhang, Qiushuang
Zhang, Xin
Lin, Wei
Ding, Wei
author_sort Li, Shuang
collection PubMed
description BACKGROUND: There is emerging evidence that astaxanthin plays a significant role in protecting neuro-cells from apoptosis after central nervous system injury. Our study examined the effects of astaxanthin on neuro-cell apoptosis after spinal cord injury. METHODS: One hundred and forty-four healthy adult Sprague-Dawley rats were randomly divided into the experimental group, control group, and sham operation group (n=48). Spinal cord injury was induced using the modified Allen method in the control group and the experimental group; while in the sham operation group, the lamina was removed without spinal cord injury. The rats in the experimental group were given astaxanthin (75 mg/kg) by gavage immediately after the operation, and in the other groups were given the same amount of olive oil. Motor function was assessed by blood-brain barrier (BBB) scores. The malondialdehyde (MDA) content and the activity of superoxide dismutase (SOD) at 24 h was determined after the operation. The apoptosis index (AI) was determined at 6, 24, and 48 h after the operation. At 48 h after the operation, we calculated the water content of the spinal cord, the lesion ratio of the spinal cord, the ultrastructure of the spinal cord, and the ultrastructure score. RESULTS: The BBB scores of the control and experimental groups were significantly lower than the sham operation group at each postoperative time (P<0.05), and the BBB score of the experimental group was significantly higher than the control group at 1–4 weeks postoperatively (P<0.05). At 24 hours postoperatively, MDA content was highest in the control group and lowest in the sham operation group, while SOD activity was highest in the sham operation group and lowest in the control group (P<0.05). At each time point postoperatively, the sham operation group had the lowest AI and the control group had the highest AI (P<0.05). At 48 h after the operation, the water content and the lesion ratio of the spinal cord, and the ultrastructure score were the lowest in the sham operation group and the highest in the control group (P<0.05). CONCLUSIONS: Astaxanthin significantly improved the motor function of rats with spinal cord injury.
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spelling pubmed-87562342022-01-21 Astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats Li, Shuang Gao, Xiaofan Zhang, Qiushuang Zhang, Xin Lin, Wei Ding, Wei Ann Transl Med Original Article BACKGROUND: There is emerging evidence that astaxanthin plays a significant role in protecting neuro-cells from apoptosis after central nervous system injury. Our study examined the effects of astaxanthin on neuro-cell apoptosis after spinal cord injury. METHODS: One hundred and forty-four healthy adult Sprague-Dawley rats were randomly divided into the experimental group, control group, and sham operation group (n=48). Spinal cord injury was induced using the modified Allen method in the control group and the experimental group; while in the sham operation group, the lamina was removed without spinal cord injury. The rats in the experimental group were given astaxanthin (75 mg/kg) by gavage immediately after the operation, and in the other groups were given the same amount of olive oil. Motor function was assessed by blood-brain barrier (BBB) scores. The malondialdehyde (MDA) content and the activity of superoxide dismutase (SOD) at 24 h was determined after the operation. The apoptosis index (AI) was determined at 6, 24, and 48 h after the operation. At 48 h after the operation, we calculated the water content of the spinal cord, the lesion ratio of the spinal cord, the ultrastructure of the spinal cord, and the ultrastructure score. RESULTS: The BBB scores of the control and experimental groups were significantly lower than the sham operation group at each postoperative time (P<0.05), and the BBB score of the experimental group was significantly higher than the control group at 1–4 weeks postoperatively (P<0.05). At 24 hours postoperatively, MDA content was highest in the control group and lowest in the sham operation group, while SOD activity was highest in the sham operation group and lowest in the control group (P<0.05). At each time point postoperatively, the sham operation group had the lowest AI and the control group had the highest AI (P<0.05). At 48 h after the operation, the water content and the lesion ratio of the spinal cord, and the ultrastructure score were the lowest in the sham operation group and the highest in the control group (P<0.05). CONCLUSIONS: Astaxanthin significantly improved the motor function of rats with spinal cord injury. AME Publishing Company 2021-12 /pmc/articles/PMC8756234/ /pubmed/35071490 http://dx.doi.org/10.21037/atm-21-6356 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Li, Shuang
Gao, Xiaofan
Zhang, Qiushuang
Zhang, Xin
Lin, Wei
Ding, Wei
Astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats
title Astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats
title_full Astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats
title_fullStr Astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats
title_full_unstemmed Astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats
title_short Astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats
title_sort astaxanthin protects spinal cord tissues from apoptosis after spinal cord injury in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8756234/
https://www.ncbi.nlm.nih.gov/pubmed/35071490
http://dx.doi.org/10.21037/atm-21-6356
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