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Aging Is Associated With Impaired Activation of Protein Homeostasis-Related Pathways After Cardiac Arrest in Mice.

Publication ,  Journal Article
Shen, Y; Yan, B; Zhao, Q; Wang, Z; Wu, J; Ren, J; Wang, W; Yu, S; Sheng, H; Crowley, SD; Ding, F; Paschen, W; Yang, W
Published in: J Am Heart Assoc
September 4, 2018

Background The mechanisms underlying worse outcome at advanced age after cardiac arrest ( CA ) and resuscitation are not well understood. Because protein homeostasis (proteostasis) is essential for cellular and organismal health, but is impaired after CA , we investigated the effects of age on proteostasis-related prosurvival pathways activated after CA . Methods and Results Young (2-3 months old) and aged (21-22 months old) male C57Bl/6 mice were subjected to CA and cardiopulmonary resuscitation ( CPR ). Functional outcome and organ damage were evaluated by assessing neurologic deficits, histological features, and creatinine level. CA / CPR -related changes in small ubiquitin-like modifier conjugation, ubiquitination, and the unfolded protein response were analyzed by measuring mRNA and protein levels in the brain, kidney, and spinal cord. Thiamet-G was used to increase O-linked β-N-acetylglucosamine modification. After CA / CPR , aged mice had trended lower survival rates, more severe tissue damage in the brain and kidney, and poorer recovery of neurologic function compared with young mice. Furthermore, small ubiquitin-like modifier conjugation, ubiquitination, unfolded protein response, and O-linked β-N-acetylglucosamine modification were activated after CA / CPR in young mice, but their activation was impaired in aged mice. Finally, pharmacologically increasing O-linked β-N-acetylglucosamine modification after CA improved outcome. Conclusions Results suggest that impaired activation of prosurvival pathways contributes to worse outcome after CA / CPR in aged mice because restoration of proteostasis is critical to the survival of cells stressed by ischemia. Therefore, a pharmacologic intervention that targets aging-related impairment of proteostasis-related pathways after CA / CPR may represent a promising therapeutic strategy.

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Published In

J Am Heart Assoc

DOI

EISSN

2047-9980

Publication Date

September 4, 2018

Volume

7

Issue

17

Start / End Page

e009634

Location

England

Related Subject Headings

  • Unfolded Protein Response
  • Ubiquitination
  • Spinal Cord
  • Small Ubiquitin-Related Modifier Proteins
  • Recovery of Function
  • Proteostasis
  • Mice
  • Kidney
  • Heart Arrest
  • Cardiopulmonary Resuscitation
 

Citation

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Shen, Y., Yan, B., Zhao, Q., Wang, Z., Wu, J., Ren, J., … Yang, W. (2018). Aging Is Associated With Impaired Activation of Protein Homeostasis-Related Pathways After Cardiac Arrest in Mice. J Am Heart Assoc, 7(17), e009634. https://doi.org/10.1161/JAHA.118.009634
Shen, Yuntian, Baihui Yan, Qiang Zhao, Zhuoran Wang, Jiangbo Wu, Jiafa Ren, Wei Wang, et al. “Aging Is Associated With Impaired Activation of Protein Homeostasis-Related Pathways After Cardiac Arrest in Mice.J Am Heart Assoc 7, no. 17 (September 4, 2018): e009634. https://doi.org/10.1161/JAHA.118.009634.
Shen Y, Yan B, Zhao Q, Wang Z, Wu J, Ren J, et al. Aging Is Associated With Impaired Activation of Protein Homeostasis-Related Pathways After Cardiac Arrest in Mice. J Am Heart Assoc. 2018 Sep 4;7(17):e009634.
Shen, Yuntian, et al. “Aging Is Associated With Impaired Activation of Protein Homeostasis-Related Pathways After Cardiac Arrest in Mice.J Am Heart Assoc, vol. 7, no. 17, Sept. 2018, p. e009634. Pubmed, doi:10.1161/JAHA.118.009634.
Shen Y, Yan B, Zhao Q, Wang Z, Wu J, Ren J, Wang W, Yu S, Sheng H, Crowley SD, Ding F, Paschen W, Yang W. Aging Is Associated With Impaired Activation of Protein Homeostasis-Related Pathways After Cardiac Arrest in Mice. J Am Heart Assoc. 2018 Sep 4;7(17):e009634.
Journal cover image

Published In

J Am Heart Assoc

DOI

EISSN

2047-9980

Publication Date

September 4, 2018

Volume

7

Issue

17

Start / End Page

e009634

Location

England

Related Subject Headings

  • Unfolded Protein Response
  • Ubiquitination
  • Spinal Cord
  • Small Ubiquitin-Related Modifier Proteins
  • Recovery of Function
  • Proteostasis
  • Mice
  • Kidney
  • Heart Arrest
  • Cardiopulmonary Resuscitation