Startseite Early-life stress altered pancreatic Krebs cycle-related enzyme activities in response to young adulthood physical and psychological stress in male rat offspring
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Early-life stress altered pancreatic Krebs cycle-related enzyme activities in response to young adulthood physical and psychological stress in male rat offspring

  • Mina Salimi , Forouzan Sadeghimahalli , Fatemeh Shaerzadeh , Fariba Khodagholi und Homeira Zardooz ORCID logo EMAIL logo
Veröffentlicht/Copyright: 10. Dezember 2020
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Abstract

Objectives

Early-life stress (ELS) increases the risk of metabolic disorders in later life. The present study investigated the ELS effect on pancreatic pyruvate dehydrogenase (PDH) protein level, α-ketoglutarate dehydrogenase (α-KGDH), and aconitase activities as metabolic enzymes in response to young adulthood stress in male rat offspring.

Methods

Male Wistar rats were divided into six groups: Control, early life stress (Early STR), young adult foot-shock stress (Y. adult F-SH STR), early + young adult foot-shock stress (Early + Y. adult F-SH STR), young adult psychological stress (Y. adult Psy STR) and early + young adult psychological stress (Early + Y. adult Psy STR). Stress was induced by a communication box at 2 weeks of age and young adulthood for five consecutive days. The blood samples were collected in young adult rats, then pancreases were removed to measure its PDH protein level and aconitase and α-KGDH activities.

Results

In ELS animals, applying foot-shock stress in young adulthood increased PDH protein level, decreased α-KGDH and aconitase activities, and increased plasma glucose, insulin, and corticosterone concentrations. However, exposure to young adulthood psychological stress only decreased α-KGDH and aconitase activities.

Conclusions

It seems that ELS altered metabolic response to young adulthood stress through changes of Krebs cycle-related enzymes activities, though the type of adulthood stress was determinant.


Corresponding author: Homeira Zardooz, PhD, Department of Physiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran; and Neurophysiology Research Center, Shahid Beheshti University of Medical Sciences, PO Box: 19615-1178 Tehran, Iran, Tel./Fax: (+9821) 22439971, E-mail:

This investigation has been carried out in Department of Physiology, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.


Funding source: Research Deputy of School of Medicine

Award Identifier / Grant number: 15314

Funding source: Shahid Beheshti University of Medical Sciences

  1. Research funding: This study was supported by a grant (No.:15314) from Research Deputy of School of Medicine, Shahid Beheshti University of Medical Sciences.

  2. Author contributions: All authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  3. Competing interests: The authors declare that they have no conflict of interest.

  4. Informed consent: Not applicable.

  5. Ethical approval: All procedures were approved by the Animal Care and Use Committee of the Neurophysiology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran (IR.SBMU.MSP.REC.1397.680).

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Received: 2020-09-15
Accepted: 2020-11-14
Published Online: 2020-12-10

© 2020 Walter de Gruyter GmbH, Berlin/Boston

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