Evidence map›Paper›PMID 38133142›Full record

ArticlePathophysiology : the official journal of the International Society for Pathophysiology2023

Combination Therapy with Enalapril and Paricalcitol Ameliorates Streptozotocin Diabetes-Induced Testicular Dysfunction in Rats via Mitigation of Inflammation, Apoptosis, and Oxidative Stress.

Magdy Y Elsaeed, Osama Mahmoud Mehanna, Ezz-Eldin E Abd-Allah, Mohamed Gaber Hassan, Walid Mostafa Said Ahmed, Abd El Ghany A Moustafa, Gaber E Eldesoky, Amal M Hammad, Usama Bahgat Elgazzar, Mohamed R Elnady and 8 more

Open access · goldAbstract read
In one paragraph

Article in Pathophysiology : the official journal of the International Society for Pathophysiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.8field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 3 citations in OpenAlex.

  1. CanInternational journal of molecular sciences · 2026
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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

18 authors at 4 institutions in 3 countries.

Magdy Y ElsaeedDepartment of Physiology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Osama Mahmoud MehannaDepartment of Physiology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Ezz-Eldin E Abd-AllahDepartment of Histology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Mohamed Gaber HassanDepartment of Physiology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Walid Mostafa Said AhmedDepartment of Physiology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Abd El Ghany A MoustafaDepartment of Histology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Gaber E EldesokyDepartment of Chemistry, College of Science, King Saud University, P.O. Box 2455, Riyadh 11451, Saudi Arabia.
Amal M HammadDepartment of Biochemistry, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Usama Bahgat ElgazzarDepartment of Biochemistry, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Mohamed R ElnadyDepartment of Physiology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Fatma M Abd-AllahDepartment of Histology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Walaa M ShiplDepartment of Biochemistry and Molecular Biology, Faculty of Medicine for Girls, Al-Azhar University, Cairo 11765, Egypt.
Amr Mohamed YounesDepartment of Basic Dental Sciences, Faculty of Dentistry, Applied Science Private University, Al-Arab Street, Amman 11196, Jordan.
Mostafa Rizk MagarDepartment of Restorative Dentistry and Basic Medical Sciences, Faculty of Dentistry, University of Petra, Amman 11196, Jordan.
Ahmed E AmerDepartment of Anatomy and Embryology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Mohamed Ali Mahmoud AbbasDepartment of Physiology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Khaled Saleh Ali ElhamakyDepartment of Physiology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Mohammed Hussien Mohammed HassanDepartment of Anatomy and Embryology, Damietta Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt.
Al-Azhar University · EGDamietta University · EGKing Saud University · SAPetra University · JO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs the impacts of diabetes-induced reproductive damage are now evident in young people, we are now in urgent need to devise new ways to protect and enhance the reproductive health of diabetic people. The present study aimed to evaluate the protective effects of enalapril (an ACE inhibitor) and paricalcitol (a vitamin D analog), individually or in combination, on streptozotocin (STZ)-diabetes-induced testicular dysfunction in rats and to identify the possible mechanisms for this protection. MATERIAL AND

methodsThis study was carried out on 50 male Sprague-Dawley rats; 10 normal rats were allocated as a non-diabetic control group. A total of 40 rats developed diabetes after receiving a single dose of STZ; then, the diabetic rats were divided into four groups of equivalent numbers assigned as diabetic control, enalapril-treated, paricalcitol-treated, and combined enalapril-and-paricalcitol-treated groups. The effects of mono and combined therapy with paricalcitol and enalapril on testicular functions, sperm activity, glycemic state oxidative stress, and inflammatory parameters, as well as histopathological examinations, were assessed in comparison with the normal and diabetic control rats.

resultsAs a result of diabetes induction, epididymal sperm count, sperm motility, serum levels of testosterone, follicle-stimulating hormone (FSH) as well as luteinizing hormone (LH), and the antioxidant enzyme activities, were significantly decreased, while abnormal sperm (%), insulin resistance, nitric oxide (NO), malondialdehyde (MDA), interleukin-6 (IL-6), and tumor necrosis factor-α (TNF-α) were significantly increased, along with severe distortion of the testicular structure. Interestingly, treatment with paricalcitol and enalapril, either alone or in combination, significantly improved the sperm parameters, increased antioxidant enzyme activities in addition to serum levels of testosterone, FSH, and LH, reduced insulin resistance, IL-6, and TNF-α levels, and finally ameliorated the diabetes-induced testicular oxidative stress and histopathological damage, with somewhat superior effect for paricalcitol monotherapy and combined therapy with both drugs compared to monotherapy with enalapril alone.

conclusionsMonotherapy with paricalcitol and its combination therapy with enalapril has a somewhat superior effect in improving diabetes-induced testicular dysfunction (most probably as a result of their hypoglycemic, antioxidant, anti-inflammatory, and anti-apoptotic properties) compared with monotherapy with enalapril alone in male rats, recommending a synergistic impact of both drugs.

Indexed as

diabetesenalapriloxidative stressparicalcitoltesticular dysfunction

Identifiers

PMID38133142
PMCPMC10747062
OpenAlexW4389200712

What OpenQuestion 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 OpenQuestion graph.