4.6 Article

Diosmin Protects against Ethanol-Induced Gastric Injury in Rats: Novel Anti-Ulcer Actions

Journal

PLOS ONE
Volume 10, Issue 3, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0122417

Keywords

-

Ask authors/readers for more resources

Alcohol consumption has been commonly associated with gastric mucosal lesions including gastric ulcer. Diosmin (DIO) is a natural citrus flavone with remarkable antioxidant and anti-inflammatory features that underlay its protection against cardiac, hepatic and renal injuries. However, its impact on gastric ulcer has not yet been elucidated. Thus, the current study aimed to investigate the potential protective effects of DIO against ethanol-induced gastric injury in rats. Pretreatment with DIO (100 mg/kg p.o.) attenuated the severity of ethanol gastric mucosal damage as evidenced by lowering of ulcer index (UI) scores, area of gastric lesions, histopathologic aberrations and leukocyte invasion. These actions were analogous to those exerted by the reference antiulcer sucralfate. DIO suppressed gastric inflammation by curbing of myeloperoxidase (MPO) and tumor necrosis factor-alpha (TNF-alpha) levels along with nuclear factor kappa B (NF-kappa B) p65 expression. It also augmented the anti-inflammatory interleukin-10 (IL-10) levels. Meanwhile, DIO halted gastric oxidative stress via inhibition of lipid peroxides with concomitant enhancement of glutathione (GSH), glutathione peroxidase (GPx) and the total antioxidant capacity (TAC). With respect to gastric mucosal apoptosis, DIO suppressed caspase-3 activity and cytochrome C (Cyt C) with enhancement of the anti-apoptotic B cell lymphoma-2 (Bcl-2) in favor of cell survival. These favorable actions were associated with upregulation of the gastric cytoprotective prostaglandin E-2 (PGE(2)) and nitric oxide (NO). Together, these findings accentuate the gastroprotective actions of DIO in ethanol gastric injury which were mediated via concerted multi-pronged actions, including suppression of gastric inflammation, oxidative stress and apoptosis besides boosting of the antioxidant and the cytoprotective defenses.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Biochemistry & Molecular Biology

Phthalazone tethered 1,2,3-triazole conjugates: In silico molecular docking studies, synthesis, in vitro antiproliferative, and kinase inhibitory activities

Mohamed A. Abdelgawad, Syed Nasir Abbas Bukhari, Arafa Musa, Mohammed Elmowafy, AbdElAziz A. Nayl, Ahmed H. El-Ghorab, Mohamed Sadek Abdel-Bakky, Hany A. Omar, Nasser Hadal Alotaibi, Hossam M. Hassan, Mohammed M. Ghoneim, Rania B. Bakr

Summary: New phthalazone tethered 1,2,3-triazole derivatives 12-21 were synthesized through Cu(I)-catalyzed click reactions. The synthesized compounds were confirmed by spectroscopic tools and elemental analysis. The antiproliferative efficacy of compounds 12-21 against cancer cell lines was evaluated, and compound 16 showed potent activity and selectivity. In silico molecular docking confirmed stable protein-ligand interactions for the effective derivatives.

BIOORGANIC CHEMISTRY (2023)

Article Immunology

Edaravone alleviates methotrexate-induced testicular injury in rats: Implications on inflammation, steroidogenesis, and Akt/p53 signaling

Emad H. M. Hassanein, Wafaa R. Mohamed, Rasha M. Hussein, El-Shaimaa A. Arafa

Summary: Edaravone (ED) was found to have protective effects against methotrexate (MTX)-induced testicular damage by reducing oxidative stress, inflammation, and apoptosis. It also regulated the Akt/p53 signaling pathway and improved steroidogenesis. These findings highlight the potential of ED as a treatment for MTX-induced testicular damage.

INTERNATIONAL IMMUNOPHARMACOLOGY (2023)

Article Medicine, Research & Experimental

Targeting aldehyde dehydrogenase enzymes in combination with chemotherapy and immunotherapy: An approach to tackle resistance in cancer cells

Salma A. Al-Shamma, Dana M. Zaher, Fatema Hersi, Nour N. Abu Jayab, Hany A. Omar

Summary: Modern cancer chemotherapy has been limited by the resistance of cancer cells to therapy. One crucial factor in chemotherapy resistance is the overexpression of ALDH, which detoxifies toxic aldehydes and prevents the formation of reactive oxygen species. This review discusses the mechanisms of chemotherapy resistance promoted by ALDH and highlights its role in cancer stemness, metastasis, metabolism, and cell death. Targeting ALDH in combination with other treatments may be a potential therapeutic strategy to overcome resistance in various cancers.

LIFE SCIENCES (2023)

Article Chemistry, Medicinal

Targeting the Endoplasmic Reticulum Stress-Linked PERK/GRP78/CHOP Pathway with Magnesium Sulfate Attenuates Chronic-Restraint-Stress-Induced Depression-like Neuropathology in Rats

Hany H. Arab, Ali Khames, Shuruq E. Alsufyani, Azza A. K. El-Sheikh, Amany M. Gad

Summary: The study investigated the neuroprotective potential of magnesium sulfate in a rat model of chronic-restraint stress (CRS)-induced depression-like behavioral disturbance and the underlying molecular mechanisms. The results demonstrated that magnesium sulfate attenuated the depression-like behavioral outcomes and histopathological changes in the brain by dampening inflammation, ER stress, and the associated PERK/GRP78/CHOP pathway. These findings suggest the promising neuroprotective/antidepressant actions of magnesium sulfate in CRS.

PHARMACEUTICALS (2023)

Article Chemistry, Medicinal

Meloxicam Targets COX-2/NOX1/NOX4/Nrf2 Axis to Ameliorate the Depression-like Neuropathology Induced by Chronic Restraint Stress in Rats

Hany H. Arab, Ali Khames, Mostafa K. Mohammad, Shuruq E. Alsufyani, Ahmed M. Ashour, Azza A. K. El-Sheikh, Hany W. Darwish, Amany M. Gad

Summary: This study demonstrates the potential antidepressant effect of meloxicam in a chronic restraint stress model. Meloxicam improved depression-like behavior, neurohistopathological changes, and decreased neurotransmitter levels. These effects may be mediated through inhibition of the COX-2/NOX1/NOX4 pathway and activation of the Nrf2/HO-1 antioxidant pathway.

PHARMACEUTICALS (2023)

Article Chemistry, Medicinal

Targeting SIRT1/FoxO3a/Nrf2 and PI3K/AKT Pathways with Rebamipide Attenuates Acetic Acid-Induced Colitis in Rats

Maha M. Abdel-Fattah, Emad H. M. Hassanein, Ahmed M. Sayed, Shuruq E. Alsufyani, Azza A. K. El-Sheikh, Hany H. Arab, Wafaa R. Mohamed

Summary: The current study aimed to investigate the ameliorative effect of rebamipide in a rat model of acetic acid-evoked ulcerative colitis and the molecular mechanisms involved. The findings demonstrated that rebamipide significantly improved colonic injury by combating inflammation and oxidative stress, which may be mediated by regulating the SIRT1/FoxO3a/Nrf2 and PI3K/AKT pathways.

PHARMACEUTICALS (2023)

Article Pharmacology & Pharmacy

Intranasal Nanotransferosomal Gel for Quercetin Brain Targeting: II. Antidepressant Effect in an Experimental Animal Model

Mohammed H. Elkomy, Fatma I. Abo El-Ela, Randa Mohammed Zaki, Omar A. Alsaidan, Mohammed Elmowafy, Ameeduzzafar Zafar, Khaled Shalaby, Mohamed A. Abdelgawad, Hany A. Omar, Rania Salama, Hussein M. Eid

Summary: This study developed and optimized a drug-loaded thermosensitive gel for intranasal administration to combat depression. The results demonstrated that compared to other formulations, this thermosensitive gel significantly improved behavioral performance and alleviated neural tissue changes in depressed rats. Further research is needed to determine its effectiveness in humans.

PHARMACEUTICS (2023)

Article Chemistry, Medicinal

Stimulation of Autophagy by Dapagliflozin Mitigates Cadmium-Induced Testicular Dysfunction in Rats: The Role of AMPK/mTOR and SIRT1/Nrf2/HO-1 Pathways

Hany H. Arab, Ebtehal Mohammad Fikry, Shuruq E. Alsufyani, Ahmed M. Ashour, Azza A. K. El-Sheikh, Hany W. Darwish, Abdullah M. Al-Hossaini, Muhammed A. Saad, Muhammad Y. Al-Shorbagy, Ahmed H. Eid

Summary: The study demonstrated that dapagliflozin has a positive effect on Cd-induced testicular dysfunction by improving testicular weight, serum testosterone, and sperm count/motility, and reducing sperm abnormalities. It also showed antioxidative, anti-apoptotic, and pro-autophagic effects to mitigate testicular impairment and spermatogenesis disruption caused by Cd. Therefore, dapagliflozin could be a potential therapeutic tool for the management of Cd-induced testicular dysfunction.

PHARMACEUTICALS (2023)

Article Chemistry, Medicinal

Neuroprotective Impact of Linagliptin against Cadmium-Induced Cognitive Impairment and Neuropathological Aberrations: Targeting SIRT1/Nrf2 Axis, Apoptosis, and Autophagy

Hany H. Arab, Ahmed H. Eid, Shuruq E. Alsufyani, Ahmed M. Ashour, Azza A. K. El-Sheikh, Hany W. Darwish, Gehan S. Georgy

Summary: This study investigated the potential neuroprotective effect of linagliptin against cadmium-induced cognitive deficits in rats. The results showed that linagliptin improved learning and memory impairment caused by cadmium and reduced hippocampal neurodegeneration. Additionally, linagliptin regulated the signaling pathways in the hippocampus by inhibiting DPP-4 and increasing GLP-1 levels, resulting in a neuroprotective impact.

PHARMACEUTICALS (2023)

Article Chemistry, Medicinal

Dapagliflozin/Hesperidin Combination Mitigates Lipopolysaccharide-Induced Alzheimer's Disease in Rats

Maaly A. Abd Elmaaboud, Remon S. Estfanous, Aliaa Atef, Ahmed M. Kabel, Khalid A. Alnemari, Tamer M. Naguib, Shuruq E. Alsufyani, Hany W. Darwish, Hany H. Arab

Summary: In this study, the potential ameliorative effects of dapagliflozin and/or hesperidin on lipopolysaccharide-induced Alzheimer's disease (AD) were investigated. The results showed that both dapagliflozin and hesperidin improved the biochemical parameters, behavioral tests, and histopathological parameters in a rat model of AD. These favorable effects were significantly enhanced when the two agents were used in combination.

PHARMACEUTICALS (2023)

Article Chemistry, Medicinal

Targeting Autophagy, Apoptosis, and SIRT1/Nrf2 Axis with Topiramate Underlies Its Neuroprotective Effect against Cadmium-Evoked Cognitive Deficits in Rats

Hany H. Arab, Ahmed H. Eid, Rania Yahia, Shuruq E. Alsufyani, Ahmed M. Ashour, Azza A. K. El-Sheikh, Hany W. Darwish, Muhammed A. Saad, Muhammad Y. Al-Shorbagy, Marwa A. Masoud

Summary: The study found that topiramate has the potential to combat cadmium neurotoxicity and improve cognitive deficits. Topiramate is able to alleviate hippocampal oxidative damage, apoptosis, and autophagy induced by cadmium through multiple mechanisms, as well as increase hippocampal glutamate content and enhance acetylcholine and GABA neurotransmitters. These findings suggest that topiramate may be useful in mitigating cadmium-induced cognitive deficits.

PHARMACEUTICALS (2023)

Article Chemistry, Multidisciplinary

Design, synthesis, docking, ADMET and anticancer evaluations of N-alkyl substituted iodoquinazoline derivatives as dual VEGFR-2 and EGFR inhibitors

Marwa Alsulaimany, Khaled El-Adl, Ahmed K. B. Aljohani, Hussam Y. Alharbi, Omar M. Alatawi, Majed S. Aljohani, Ahmed El-morsy, Sara A. Almadani, Abdulrahman A. Alsimaree, Samir A. Salama, Doaa E. Keshek, Abeer A. Mohamed

Summary: Fifteen new 1-alkyl-6-iodoquinazoline derivatives were designed and synthesized, and their anticancer activities were evaluated against multiple cancer cell lines. Compound 9c showed the highest activity and exhibited excellent dual inhibition of EGFR and VEGFR-2.

RSC ADVANCES (2023)

Article Chemistry, Multidisciplinary

Five and six membered heterocyclic rings endowed with azobenzene as dual EGFRT790M and VEGFR-2 inhibitors: design, synthesis, in silico ADMET profile, molecular docking, dynamic simulation and anticancer evaluations

Kurls E. Anwer, Sanadelaslam S. A. El-Hddad, Nour E. A. Abd El-Sattar, Ahmed El-morsy, Fathalla Khedr, Samy Mohamady, Doaa E. Keshek, Samir A. Salama, Khaled El-Adl, Noura S. Hanafy

Summary: Novel azobenzene scaffold-joined heterocyclic isoxazole, pyrazole, triazole, and/or triazine derivatives were synthesized and tested for their growth inhibition effects on A549, MCF-7, HCT-116, and HepG2 cancer cells. The compounds showed dual targeting effects on VEGFR-2 and EGFR(T790M) enzymes. Molecular design and MD modeling revealed the binding mode of the compounds with the active sites. The compounds demonstrated significant inhibitory effects, particularly compound 14, which showed the highest activity on A549 cells.

RSC ADVANCES (2023)

Article Pharmacology & Pharmacy

Promising drug candidates for the treatment of polycystic ovary syndrome (PCOS) as alternatives to the classical medication metformin

Hanan S. Anbar, Nisha Yarifbhai Vahora, Hajra laghman Shah, Mariyam Mohammed Azam, Tamanna Islam, Fatima Hersi, Hany A. Omar, Wolfgang Dohle, Barry V. L. Potter, Mohammed I. El-Gamal

Summary: This study investigated the therapeutic potential of three drug candidates for the treatment of PCOS. The drug candidates showed promising effects on ovarian and uterine weight, lipid profile, hormone levels, and signaling pathways.

EUROPEAN JOURNAL OF PHARMACOLOGY (2023)

Article Chemistry, Multidisciplinary

In vitro and computational investigations of novel synthetic carboxamide-linked pyridopyrrolopyrimidines with potent activity as SARS-CoV-2-MPro inhibitors

Ateyatallah Aljuhani, Hany E. A. Ahmed, Saleh K. Ihmaid, Abdelsattar M. Omar, Sultan S. Althagfan, Yaser M. Alahmadi, Iqrar Ahmad, Harun Patel, Sahar Ahmed, Mohannad A. Almikhlafi, Ahmed M. El-Agrody, Mohamed F. Zayed, Safaa Abdulrahman Turkistani, Shorouk H. Abulkhair, Mohammed Almaghrabi, Samir A. Salama, Ahmed A. Al-Karmalawy, Hamada S. Abulkhair

Summary: A novel set of compounds was designed and evaluated for their antiviral activity against COVID-19 using in vitro assays and molecular docking simulations. The majority of these compounds showed potent antiviral activity with minimal cytotoxicity. Compounds 25 and 29 exhibited promising inhibitory activity and were stable in molecular dynamic simulations. These results suggest that compounds 25 and 29 are potential drug candidates for the treatment of SARS-CoV-2.

RSC ADVANCES (2022)

No Data Available