Evidence map›Paper›PMID 33748503›Full record

ArticleHeliyon2021

Sleep deprivation induces oxidative stress in the liver and pancreas in young and aging rats.

Karina Hernández Santiago, Ana Laura López-López, Fausto Sánchez-Muñoz, José Luis Cortés Altamirano, Alfonso Alfaro-Rodríguez, Herlinda Bonilla-Jaime

Open access · goldAbstract read
In one paragraph

Article in Heliyon, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 24% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Cornelian Cherry (Biology · 2025
    Article
  4. Review
  5. Article
  6. Sleep Pattern Interference in the Cognitive Performance of Lusitano Horses.Animals : an open access journal from MDPI · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 4 institutions in 1 country.

Karina Hernández SantiagoMaestria en Biologia de la Reproducción, Universidad Autónoma Metropolitana-Iztapalapa, CP 09340, Ciudad de Mexico, Mexico.
Ana Laura López-LópezCINVESTAV sede sur, Departamento de Farmacología, Calz. de los Tenorios 235, Coapa, Rinconada de las Hadas, Tlalpan, Ciudad de México, 14330, México.
Fausto Sánchez-MuñozDepartamento de Inmunología, Instituto Nacional de Cardiología (Ignacio Chávez), Juan Badiano No. 1, Col. Sección XVI, Delegación Tlalpan, C.P. 14080, Ciudad de Mexico, Mexico.
José Luis Cortés AltamiranoDepartmento de Neurociencias, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra" (INR) Secretaría de Salud (SSA), Ciudad de México, México.
Alfonso Alfaro-RodríguezDepartmento de Neurociencias, Instituto Nacional de Rehabilitación "Luis Guillermo Ibarra Ibarra" (INR) Secretaría de Salud (SSA), Ciudad de México, México.
Herlinda Bonilla-JaimeDepartamento de Biología de la Reproducción, Área de Biología Conductual y Reproductiva, Universidad Autónoma Metropolitana-Iztapalapa, CP 09340, Ciudad de Mexico, Mexico.
Instituto Nacional de Rehabilitación · MXUniversidad Autónoma Metropolitana · MXCentro de Investigación y de Estudios Avanzados del Instituto Politécnico Nacional · MXInstituto Nacional de Cardiología · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aging process is characterized by a gradual impairment generally caused by oxidative stress and, more specifically, sleep deprivation, which induces oxidative stress in the brain. The objective of this study was to assess the effect of three types of paradoxical sleep deprivation (PSD): 96 h of PSD (96PSD group); 192 h of PSD (192PSD group); 192 h of PSD followed by a recovery period of 20 days (192PSD + Recovery group) on an oral glucose tolerance test (OGTT), lipid peroxidation (LPO), and superoxide dismutase (SOD) and catalase (CAT) activities in the liver and pancreas of young (3-month-old) and adult (14-month-old) rats. The 96PSD and 192PSD groups of young rats showed lower glucose levels on the OGTT than the control group. In the adult rats, only the 96PSD group had lower glucose levels than the control group. However, the areas under the curve for the young and adult 192 and 192PSD + Recovery groups showed significant differences. Both LPO and SOD increased in the 192PSD and 192PSD + Recovery groups, but CAT decreased in the liver of young rats in the 192PSD group. Regarding the pancreas, LPO and SOD levels increased after 96 h of PSD. In adult animals, CAT decreased in the liver after 96 and 192 h of PSD, while LPO and SOD increased in the pancreas of the 192PSD and PSD + Recovery groups. Differences in the SOD and CAT activities in the liver and SOD activities in the pancreas were also observed between the young and adult rats and maintained across all the PSD groups. In conclusion, PSD induced differential responses that appeared to depend on the duration of the induced condition, the animals' age, and the tissue analyzed. It was found that adult rats were more susceptible to the effects of PSD than young rats.

Indexed as

Aging processGlucoseLiverOxidative stressPancreasSleep deprivation

Identifiers

PMID33748503
PMCPMC7966994
OpenAlexW3133593543

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.