Evidence map›Paper›PMID 40108916›Full record

ArticleCurrent medicinal chemistry2026

The Protective Effects of

Roja Rahimi, Nazila Heidari, Yekta Ghane, Maryam Baeeri, Ozra Tabatabaei-Malazy, Mahdi Gholami, Nahal Obeidi, Roham Foroumadi, Amirhossein Heidari, Mohammad Abdollahi

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Article in Current medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

10 authors.

Roja RahimiDepartment of Traditional Pharmacy, School of Persian Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Nazila HeidariSchool of Medicine, Iran University of Medical Sciences, Tehran, Iran.ORCID 0000-0001-7259-4926
Yekta GhaneSchool of Medicine, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0002-7309-4066
Maryam BaeeriToxicology and Diseases Group (TDG), Pharmaceutical Sciences Research Center (PSRC), The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences (TUMS), Tehran, Iran.ORCID 0000-0002-5018-7438
Ozra Tabatabaei-MalazyNon-Communicable Diseases Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-0188-9721
Mahdi GholamiDepartment of Toxicology & Pharmacology, Faculty of Pharmacy; Toxicology and Poisoning Research Centre, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-3886-398X
Nahal ObeidiDepartment of Clinical Sciences, Faculty of Veterinary Medicine, Islamic Azad University, Karaj, Iran.ORCID 0009-0000-6973-7105
Roham ForoumadiToxicology and Diseases Group (TDG), Pharmaceutical Sciences Research Center (PSRC), The Institute of Pharmaceutical Sciences (TIPS), Tehran University of Medical Sciences (TUMS), Tehran, Iran.ORCID 0000-0002-1415-0371
Amirhossein HeidariFaculty of Medicine, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Mohammad AbdollahiFaculty of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran.ORCID 0000-0003-0123-1209

Funding

Tehran University of Medical Sciences & Health Services 99-3-221-51388
6 · The paper itself

Abstract

backgroundFerula assa-foetida L. has traditionally been used to treat various diseases, including infections, asthma, stomach aches, and flatulence. Previous studies have highlighted its anti-inflammatory, anti-oxidative, anti-diabetic, neuroprotective, and nerve-stimulating properties.

objectiveThis study aimed to evaluate the therapeutic effects and molecular mechanisms of action of the oleo-gum resin from Ferula assa-foetida L. in an animal model of diabetic neuropathy (DN).

methodsThe essential oil of oleo-gum resin from Ferula assa-foetida L. was analyzed using Gas Chromatography-Mass Spectrometric Analysis. Forty-two male Wistar rats were included in the study, with diabetes induced via streptozotocin (STZ) injection. The rats were randomly assigned to seven groups (n=6 per group) and treated with different doses of Ferula assa-foetida L. extract (100, 200 mg/kg/day) or oil (10, 20 mg/kg/day), alongside appropriate control groups. After a five-week treatment period, samples of dorsal root ganglia (DRG), pancreatic tissue, and blood were collected. Key parameters assessed included blood glucose and insulin levels, motor function tests, oxidative stress protein generation, pro-inflammatory cytokine gene expression, and histopathological analyses.

resultsTreatment with various doses of Ferula assa-foetida L. extract or oil, as well as gabapentin, led to significant improvements. These included reduced blood sugar levels, increased insulin levels, and improved glycemic control. Motor function was enhanced, while the expression of pro-inflammatory cytokines and oxidative stress markers was significantly reduced.

conclusionThese findings indicate a promising therapeutic approach for managing DN. Further studies are warranted to elucidate the underlying mechanisms of Ferula assa-foetida L.'s beneficial effects in DN.

Indexed as

Diabetes Mellitus, ExperimentalDiabetic NeuropathiesFerulaHypoglycemic AgentsResins, PlantAnimalsBlood GlucoseDisease Models, AnimalMaleOils, VolatileOxidative StressRatsRats, WistarStreptozocinBlood GlucoseHypoglycemic AgentsOils, VolatileResins, PlantStreptozocinanti-oxidativeDiabetes mellitusdiabetic neuropathyFerula assa-foetida Loleo-gum resinstreptozotocin

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Registered trials

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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.