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  1. Article ; Online: Rupatadine ameliorated ulcerative colitis in rats via modulation of platelet-activatiweng factor/interleukin-6/vascular endothelial growth factor signalling pathway.

    Ibrahim, Mohamed A / Abdelmonaem, Alyaa Abdelfattah / Abdel-Gaber, Seham A / Hafez, Heba M / Abdel Hafez, Sara Mohamed Naguib / Yehia Abdelzaher, Walaa

    The Journal of pharmacy and pharmacology

    2022  Volume 74, Issue 4, Page(s) 537–546

    Abstract: Objectives: This study aimed to analyse the potential effect of rupatadine (RUP) on ulcerative colitis (UC) induced by acetic acid (AA).: Methods: Forty male adult Wistar rats were divided into five groups: Control group: received vehicles for 14 ... ...

    Abstract Objectives: This study aimed to analyse the potential effect of rupatadine (RUP) on ulcerative colitis (UC) induced by acetic acid (AA).
    Methods: Forty male adult Wistar rats were divided into five groups: Control group: received vehicles for 14 days; AA model group: received AA at the 13th day; Sulfasalazine (SLZ) + AA group: received SLZ (250 mg/kg) for 14 days and AA at the 13th day; RUP-3 + AA group: received RUP (3 mg/kg/day) for 14 days and AA at the 13th day; and RUP-6 + AA group: received RUP (6 mg/kg/day) for 14 days and AA at the 13th day. Evidence of UC was assessed both macroscopically and microscopically. Oxidative stress markers (total antioxidant capacity and malondialdehyde), antioxidant enzyme (superoxide dismutase), histamine and platelet-activating factor (PAF) were determined. Immunohistochemical estimations of vascular endothelial growth factor (VEGF) and interleukin-6 (IL-6) were done.
    Key findings: The AA group showed evidence of UC that was associated with a significant increase in oxidative stress, histamine and PAF levels with significant elevation in colonic VEGF and IL-6 immuno-expressions. RUP, in a dose-dependent manner, significantly ameliorated UC.
    Conclusion: RUP protects against UC by reducing oxidative stress and by regulating the PAF/IL-6/VEGF pathway.
    MeSH term(s) Acetic Acid/pharmacology ; Animals ; Antioxidants/metabolism ; Antioxidants/pharmacology ; Colitis, Ulcerative/chemically induced ; Colitis, Ulcerative/drug therapy ; Colitis, Ulcerative/metabolism ; Colon ; Cyproheptadine/analogs & derivatives ; Histamine/metabolism ; Interleukin-6/metabolism ; Male ; Platelet Activating Factor/metabolism ; Rats ; Rats, Wistar ; Signal Transduction ; Vascular Endothelial Growth Factor A/metabolism
    Chemical Substances Antioxidants ; Interleukin-6 ; Platelet Activating Factor ; Vascular Endothelial Growth Factor A ; rupatadine (2AE8M83G3E) ; Cyproheptadine (2YHB6175DO) ; Histamine (820484N8I3) ; Acetic Acid (Q40Q9N063P)
    Language English
    Publishing date 2022-02-08
    Publishing country England
    Document type Journal Article
    ZDB-ID 3107-0
    ISSN 2042-7158 ; 0022-3573 ; 0373-1022
    ISSN (online) 2042-7158
    ISSN 0022-3573 ; 0373-1022
    DOI 10.1093/jpp/rgab170
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Empagliflozin Protects against Haloperidol Experimentally-Induced Ovarian Toxicity.

    Abdelzaher, Walaa Yehia / De Waard, Michel / Abdelmonaem, Alyaa Abdelfattah / Ali, Dalia Mohamed / El-Tahawy, Nashwa Fathy Gamal / Rifaai, Rehab Ahmed / Mohamed, Hatem A / Shaheen, Kareem / Zeen El-Din, Mohamed Ahmed / Welson, Nermeen N / Tawfeek, Shereen ELsayed / Batiha, Gaber El-Saber / Abdel-Aziz, Asmaa Mohamed

    Pharmaceuticals (Basel, Switzerland)

    2023  Volume 16, Issue 2

    Abstract: The present experiment aimed to identify the potential protective role of empagliflozin (EMPA) on haloperidol (HAL)-induced ovarian damage in female rats because of its anti-inflammatory, antioxidant, and antiapoptotic effects. EMPA was administered in ... ...

    Abstract The present experiment aimed to identify the potential protective role of empagliflozin (EMPA) on haloperidol (HAL)-induced ovarian damage in female rats because of its anti-inflammatory, antioxidant, and antiapoptotic effects. EMPA was administered in the presence and absence of HAL. Thirty-two adult female albino rats were divided into four groups. Control group, EMPA group: received EMPA (10 mg/kg/day) p.o., HAL group: received HAL (2 mg/kg/day) p.o., HAL + EMPA group: HAL (2 mg/kg/day) combined with EMPA for 28 days. Serum follicle-stimulating hormone (FSH), luteinizing hormone (LH), and anti-mullerian hormone (AMH) levels were measured. Ovarian oxidative stress parameters, besides inflammatory and apoptotic biomarkers, and ovarian Sirtuin-1 (Sirt-1) were evaluated. Ovarian histopathological examination and heat shock protein 70 (Hsp70) immunohistochemical study were performed. HAL significantly increased serum levels of FSH, LH, and ovarian inflammatory, apoptotic, and oxidative stress biomarkers and decreased serum AMH levels and Sirt-1 expression. Histopathological findings of ovarian damage and high Hsp70 immunoexpression were detected. EMPA significantly normalized the distributed hormonal levels, oxidative stress, inflammatory, and apoptotic biomarkers with a prompt improvement in the histopathological picture and a decrease in Hsp70 immunoexpression. Accordingly, EMPA protected against HAL-induced ovarian toxicity by modulating the Sirt-1/Hsp70/TNF-α/caspase-3 signaling pathway.
    Language English
    Publishing date 2023-01-23
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2193542-7
    ISSN 1424-8247
    ISSN 1424-8247
    DOI 10.3390/ph16020168
    Database MEDical Literature Analysis and Retrieval System OnLINE

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