Evidence map›Paper›PMID 39669379›Full record

ArticleInternational journal of endocrinology2024

Efficacy of Local N-Acetylcysteine Administration in Mitigating OHSS Parameters: A Comparative Analysis With Dopaminergic Agonist in the OHSS Model.

Dulce Elena Letras-Luna, Nora Hilda Rosas-Murrieta, Nidia Gary Pazos-Salazar, Jorge Flores-Hernández, Francisco Castelán, Berenice Venegas, Alfonso Díaz, Samuel Treviño, Daniel Juárez-Serrano, Wendy Argelia García-Suastegui and 2 more

Abstract read
In one paragraph

Article in International journal of endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Minimising OHSS in women with PCOS.Frontiers in endocrinology · 2025
    Review
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

12 authors.

Dulce Elena Letras-LunaDepartment of Biology and Reproductive Toxicology, Institute of Sciences (ICUAP), Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0002-6866-2866
Nora Hilda Rosas-MurrietaBiochemistry and Molecular Biology Laboratory, Chemistry Center, Institute of Sciences (ICUAP), Benemérita Universidad Auténoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0002-4605-670X
Nidia Gary Pazos-SalazarDepartment of Microbiology, Faculty of Chemical Sciences, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0002-6451-1569
Jorge Flores-HernándezInstitute of Physiology, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0002-7394-3208
Francisco CastelánDepartment of Cell Biology and Physiology, Institute of Biomedical Research, Universidad Nacional Autónoma de México, Mexico City, Mexico.ORCID https://orcid.org/0000-0002-9835-3335
Berenice VenegasFaculty of Biological Science, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0001-9009-655X
Alfonso DíazInstitute of Physiology, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0003-4092-6636
Samuel TreviñoLaboratory of Metabolomics and Chronic Degenerative Diseases, Institute of Physiology, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0001-5679-1671
Daniel Juárez-SerranoDepartment of Biochemistry-Food Science, Faculty of Chemical Sciences, Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0002-2217-4891
Wendy Argelia García-SuasteguiDepartment of Biology and Reproductive Toxicology, Institute of Sciences (ICUAP), Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0001-5223-3189
Anabella Handal-SilvaDepartment of Biology and Reproductive Toxicology, Institute of Sciences (ICUAP), Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0002-6915-5655
José Luis Morán-PeralesDepartment of Biology and Reproductive Toxicology, Institute of Sciences (ICUAP), Benemérita Universidad Autónoma de Puebla, Puebla, Mexico.ORCID https://orcid.org/0000-0002-2823-2829

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we evaluated the effects of intrabursal administration of cabergoline and N-acetylcysteine on ovarian hyperstimulation syndrome (OHSS) in an immature rat model. The study assessed body, ovarian, and uterine weights, as well as the concentrations of vascular endothelial growth factor A (VEGF-A). Moreover, levels of MDA, 4-HDA, and nitrites were assessed in ovarian homogenates, and vascular permeability was quantified in the peritoneal cavity. Ovarian morphology was characterized using histology and hematoxylin-eosin staining, determining the count of ovarian follicles and corpus luteum. Our results demonstrated a significant increase in lipoperoxidation, nitrite levels, and VEGF-A concentrations in the OHSS group compared to the control group. These biochemical alterations corroborate the successful induction of OHSS in the experimental model. Direct injection into the ovarian bursa resulted in reduced vascular permeability and VEGF-A levels, suggesting that the effects of cabergoline are predominantly ovarian. Particularly, cabergoline did not significantly alter other parameters such as ovarian weight, lipoperoxidation, nitrite levels, or morphology. Conversely, low concentrations of N-acetylcysteine (25-50 µg/kg) significantly reduced ovarian and uterine weights, VEGF-A levels, and vascular permeability. Interestingly, this dose-response relationship was not observed at higher NAC concentrations (100-200 μg/kg), suggesting a potential threshold beyond which NAC loses efficacy in these specific parameters. Our results suggest that the localized administration of N-acetylcysteine shows promise as a therapeutic strategy for OHSS by modulating key parameters associated with the syndrome. These promising results warrant further investigation into its mechanisms and efficacy, potentially expanding therapeutic options for OHSS management.

Indexed as

antioxidantcabergolinedopamine agonistintrabursal injectionN-acetylcysteineovarian hyperstimulationoxidative stressVEGF

Identifiers

PMID39669379
PMCPMC11637629

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.