Evidence map›Paper›PMID 38322160›Full record

ArticleIranian journal of medical sciences2024

Effect of Aromatase Inhibitor Letrozole on the Placenta of Adult Albino Rats: A Histopathological, Immunohistochemical, and Biochemical Study.

Mohamed Ali Alabiad, Ibtesam Elhasadi, Sulaiman Mohammed Alnasser, Mohammed Alorini, Ahmed Baker A Alshaikh, Fatima A Jaber, Amany Mohamed Shalaby, Walaa Samy, Ahmed Ismail Heraiz, Khalid Mohammed Mohammed Albakoush and 1 more

Abstract read
In one paragraph

Article in Iranian journal of medical sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

11 authors.

Mohamed Ali AlabiadDepartment of Pathology, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Ibtesam ElhasadiDepartment of Pathology, Faculty of Medicine, University of Benghazi, Benghazi, Libya.
Sulaiman Mohammed AlnasserDepartment of Pharmacology and Toxicology, Unaizah College of Pharmacy, Qassim, University, Buraydah, Saudi Arabia.
Mohammed AloriniDepartment of Basic Medical Sciences, Unaizah College of Medicine and Medical Sciences, Qassim University, Unaizah, Kingdom of Saudi Arabia.
Ahmed Baker A AlshaikhDepartment of Obstetrics and Gynecology, College of Medicine, Jouf University, Sakaka, Kingdom of Saudi Arabia.
Fatima A JaberDepartment of Biology, College of Science, University of Jeddah, Jeddah, Kingdom of Saudi Arabia.
Amany Mohamed ShalabyDepartment of Histology and Cell Biology, School of Medicine, Tanta University, Tanta, Egypt.
Walaa SamyDepartment of Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Zagazig University, Zagazig, Egypt.
Ahmed Ismail HeraizDepartment of Gynecology and Obstetrics, School of Medicine, Zagazig University, Zagazig, Egypt.
Khalid Mohammed Mohammed AlbakoushDepartment of Anatomy and Embryology, Faculty of Medicine, Alasmarya Islamic University, Zliten, Libya.
Dina Ahmed KhairyDepartment of Pathology, School of Medicine, Beni-Suef University, Beni-Suef, Egypt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Letrozole, an aromatase inhibitor, has recently been introduced as the preferred treatment option for ectopic pregnancy. To date, no study has investigated the effect of letrozole alone on placental tissue. The present study aimed to evaluate the effect of different doses of letrozole on the placenta of rats and to clarify the underlying mechanism. Methods: Sixty pregnant female rats were equally divided into three groups, namely the control group (GI), low-dose (0.5 mg/Kg/day) letrozole group (GII), which is equivalent to the human daily dose (HED) of 5 mg, and high-dose (1 mg/Kg/day) letrozole group (GIII), equivalent to the HED of 10 mg. Letrozole was administered by oral gavage daily from day 6 to 16 of gestation. Data were analyzed using a one-way analysis of variance followed by Tukey's Results: Compared to the GI and GII groups, high-dose letrozole significantly increased embryonic mortality with a high post-implantation loss rate (P<0.001) and significantly reduced the number of viable fetuses (P<0.001) and placental weight (P<0.001) of pregnant rats. Moreover, it significantly reduced placental estrogen receptor (ER) and progesterone receptor (PR) (P<0.001) and the expression of vascular endothelial growth factor (P<0.001), while increasing the apoptotic index of cleaved caspase-3 (P<0.001). Conclusion: Letrozole inhibited the expression of ER and PR in rat placenta. It interrupted stimulatory vascular signals causing significant apoptosis and placental vascular dysfunction. Letrozole in an equivalent human daily dose of 10 mg caused a high post-implantation loss rate without imposing severe side effects.

Indexed as

Aromatase InhibitorsLetrozolePlacentaAnimalsFemalePregnancyRatsReceptors, EstrogenVascular Endothelial Growth Factor AAromatase InhibitorsLetrozoleReceptors, EstrogenVascular Endothelial Growth Factor ACaspaseEstrogenLetrozolePlacentaProgesteroneReceptorsVascular endothelial growth factor

Identifiers

PMID38322160
PMCPMC10839141

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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.