• ثبت نام
    • ورود به سامانه
    مشاهده مورد 
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Avicenna Journal of Phytomedicine
    • Volume 8, Issue 2
    • مشاهده مورد
    •   صفحهٔ اصلی
    • نشریات انگلیسی
    • Avicenna Journal of Phytomedicine
    • Volume 8, Issue 2
    • مشاهده مورد
    JavaScript is disabled for your browser. Some features of this site may not work without it.

    Doxorubicin-induced renal inflammation in rats: Protective role of Plantago major

    (ندگان)پدیدآور
    Entezari Heravi, NazaninHosseinian, SaraNaji Ebrahimi Yazd, ZohrehShafei, Mohammad NaserEbrahimzadeh, AlirezaShahraki, SamiraSamadi, ZahraMotejadded, FatemehBeheshti, FarimahMohebbati, RezaParhizgar, SoghraKhajavirad, Abolfazl
    Thumbnail
    دریافت مدرک مشاهده
    FullText
    اندازه فایل: 
    848.2کیلوبایت
    نوع فايل (MIME): 
    PDF
    نوع مدرک
    Text
    Original Research Article
    زبان مدرک
    English
    نمایش کامل رکورد
    چکیده
    Objective: The aim of the present study was to evaluate the possible protective effect of Plantago major (P. major) extract against doxorubicin (DXR)-induced renal inflammation in rats. Materials and Methods: 80 male albino rats were randomly divided into 8 groups as follows: control, DXR, Ext (extract) 600, Ext1200, dexamethasone+DXR, vitamin E+DXR, Ext600+DXR, and Ext1200+DXR. Duration of the study was 35 days and DXR was intravenously injected on the 7th day of the experiment. Tumor necrosis factor-alpha (TNF-α) production and monocyte chemoattractant protein-1 (MCP-1) expression levels were assessed in the left kidney. Serum creatinine concentration and osmolarity were determined on the 1st, 14th, 21st, 28th and 35th days of the experiment. Results: DXR caused a significant increase in renal expression of MCP-1 and TNF-α production compared to control animals. Administration of dexamethasone, vitamin E and P. major extract significantly improved the expression of these inflammatory mediators compared to DXR group. Compared to day 1 in DXR group, serum osmolarity showed a significant increase on days 21, 28 and 35. Also, on these days, serum osmolarity in DXR group was significantly higher than that on the same days in control group. In Vit E+DXR and Ext 1200+DXR groups, there was no significant changes in serum osmolarity among different days of the study. However, in these groups, serum osmolarity on days 21, 28 and 35 showed a significant decrease compared to the same days in DXR group. Conclusion: Present results suggest that hydroethanolic extract of P. major protected renal tissue against DXR–induced renal inflammation.
    کلید واژگان
    Plantago major
    Doxorubicin
    Vitamin E
    Dexamethasone
    Inflammation
    urology-Kidney

    شماره نشریه
    2
    تاریخ نشر
    2018-02-01
    1396-11-12
    ناشر
    Mashhad University of Medical Sciences
    سازمان پدید آورنده
    Department of Physiology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iran
    Department of physiology, School of medicine, Mashhad University of Medical Sciences, Mashhad, Iran
    Department of Physiology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iran
    Division of Neurocognitive Sciences, Psychiatry and Behavioral Sciences Research Center, Mashhad University of Medical Sciences, Mashhad, Iran
    Department of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
    Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
    Department of Physiology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iran
    Department of Anatomy and Cell Biology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
    Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
    Department of Physiology, School of Medicine, Mashhad University of Medical Sciences, Iran
    Department of Physiology, School of Medicine, Mashhad University of Medical Sciences Mashhad, Iran
    Neurogenic Inflammation Research Center, Mashhad University of Medical Sciences, Mashhad, Iran

    شاپا
    2228-7930
    2228-7949
    URI
    https://dx.doi.org/10.22038/ajp.2018.10396
    http://ajp.mums.ac.ir/article_10396.html
    https://iranjournals.nlai.ir/handle/123456789/425514

    مرور

    همه جای سامانهپایگاه‌ها و مجموعه‌ها بر اساس تاریخ انتشارپدیدآورانعناوینموضوع‌‌هااین مجموعه بر اساس تاریخ انتشارپدیدآورانعناوینموضوع‌‌ها

    حساب من

    ورود به سامانهثبت نام

    آمار

    مشاهده آمار استفاده

    تازه ترین ها

    تازه ترین مدارک
    © کليه حقوق اين سامانه برای سازمان اسناد و کتابخانه ملی ایران محفوظ است
    تماس با ما | ارسال بازخورد
    قدرت یافته توسطسیناوب