Message Board

Respected readers, authors and reviewers, you can add comments to this page on any questions about the contribution, review,        editing and publication of this journal. We will give you an answer as soon as possible. Thank you for your support!

Name
E-mail
Phone
Title
Content
Verification Code
x Close Forever Close
Volume 35 Issue 5
. 
Turn off MathJax
Article Contents
Article Navigation >  Journal of Pharmaceutical Practice and Service  > 2017  >  35(5): 402-406,426

QIAO Jin, CHEN Min, DOU Zhihua, XU Jiliang, WU Feng, MENG Guoliang. Mechanism of TGF-β1/Smad signaling pathway in rhein protected diabetic rat's kidney[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(5): 402-406,426. doi: 10.3969/j.issn.1006-0111.2017.05.004
Citation: QIAO Jin, CHEN Min, DOU Zhihua, XU Jiliang, WU Feng, MENG Guoliang. Mechanism of TGF-β1/Smad signaling pathway in rhein protected diabetic rat's kidney[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(5): 402-406,426. doi: 10.3969/j.issn.1006-0111.2017.05.004
shu

Mechanism of TGF-β1/Smad signaling pathway in rhein protected diabetic rat's kidney

doi: 10.3969/j.issn.1006-0111.2017.05.004
  • 1.

    Department of Pharmacy, Third Hospital Affiliated to Nantong University, Nantong 226006, China

  • 2.

    Department of Pharmacology, Medical College, Nantong University, Nantong 226001, China

  • Received Date: 2017-05-18
  • Rev Recd Date: 2017-06-26
  • Objective To study the protective effect of Rhein on the kidney of type 2 diabetic rats induced by high fat diet. Methods A rat model of type 2 diabetes was induced by high fat diet combined with low dose streptozotocin 35 mg/kg. The diabetic rats were randomly divided into diabetes group, Low, middle and high rhein dose groups (50,100,150 mg/kg), metformin group (300 mg/kg) and normal control group. Blood glucose and urine micro albumin were measured at 0, 2, 4 and 8 weeks respectively. Serum creatinine, urea nitrogen, total cholesterol and triglyceride were measured at 8 weeks. HE staining was used to observe the pathological changes of renal tissue. Effects of rhein on the expression of transforming growth factor-β1 and Smad3 protein in renal tissue of diabetic rats were detected with Western Blot. Results The blood glucose and urine micro albumin in model group were significantly higher than those in normal control group. Each rhein dose group exhibited reduced blood glucose and urinary micro albumin in diabetic rats. The high rhein dose group showed significant reduction of blood glucose and urine micro albumin in diabetic rats (P<0.05). Compared with model group, rhein reduced the serum Cr, BUN, TC and TG values in each dose group, most significantly in the high rhein dose group (P<0.05). The obvious pathological changes of renal tissue in model group were observed with most improved changes in the high rhein dose group. The expression of TGF-β1 and Smad3 protein in renal tissue of diabetic rats decreased significantly (P<0.05). Conclusion Rhein has preventive effect on diabetic nephropathy. The mechanism may relate to the improvement of renal function, regulation of blood lipid and down regulation of TGF-β1 and Smad3 protein expression in renal tissue.
  • [1] Sheng NP,Hui HZ,Ai XF,et al. Protection of rhein on IgA nephropathy mediated by inhibition of fibronectin expression in rats［J］. Indian J Pharmacol,2013,45(2):174-179.
    [2] Xu Y,Wang L,He J,et al. Prevalence and control of diabetes in Chinese adults［J］.JAMA,2013,310(9):948-959.
    [3] 陈才铭,张苗苗,胡利明.大黄酸对肥胖糖尿病大鼠肾皮质PPARγ_和TGF-β1表达的影响［J］.中药材,2015,38(4):810-812.
    [4] 吴影懿,段俗言,钱 军,等.大黄酸对糖尿病小鼠肾脏的保护作用［J］.江苏医药,2015,41 (16):1864-1866.
    [5] 陈卫东,常保超,张 燕,等.大黄酸增加2型糖尿病大鼠肾组织SIRT1的表达［J］.细胞与分子免疫学杂志,2015,31(5):615-619.
    [6] Geng CC,Chen GR,Wu QJ,et al.The molecular mechanism of rhein in diabetic nephropathy［J］.Evid Based Complement Alternat Med,2014,20(14):487-497.
    [7] 乔 进,窦志华,吴 锋,等.灵芝多糖联合二甲双胍对2型糖尿病大鼠心肌AGEs及CTGF的影响及其机制［J］.中国药理学通报,2014,30(4):536-541.
    [8] 乔 进,窦志华,吴 锋,等.灵芝多糖联合二甲双胍预防糖尿病大鼠主动脉病变及对VEGF表达的影响［J］.中国药理学通报,2014,30(8):1079-1084.
    [9] 乔 进,窦志华,吴 锋,等.灵芝多糖联合二甲双胍对2型糖尿病大鼠心肌结构及血流动力学的影响［J］.中国药理学通报,2016,32(7):1012-1016.
    [10] 陈 颖,刘竹影,周福兴,等.双丹口服液对大鼠糖尿病肾病的作用研究［J］.西北药学杂志,2016,31(1):56-61.
    [11] Chen Y,Liu Z Y,Zhou F X,et al. Effects of Shuangdan Oral Liquid on diabetic nephropathy rat models［J］.Northwest Pharm J,2016,31(1):56-61.
    [12] 李梦莹,谢春光,王晓灿.大黄酸治疗糖尿病肾病实验研究进展［J］.湖南中医杂志,2015,31(10):172-173.
    [13] Loeffler I,Hopfer U,Koczan D,et al. Type VIII collagen modulater TGF-β1- induced proliferation of mesangial cells［J］.J Am Soc Nephrol, 2011,22(4):649-663.
    [14] Overstreet JM,Samara Koon R,Meldrum KK,et al. Redox control of p53 in the transcriptional regulation of TGF-betal target genes through SMAD cooperativity ［J］.Cell Signal,2014,26(7):1427-1436.
    [15] Kim D,Lee AS,Jung YJ,et al. Tamoxifen ameliorates renal tubulointerstitial fibrosis by modulation of estrogen receptor alpha-mediated transforming growth factor-betal/Smad signaling pathway［J］.Nephrol Dial Transplant,2014,29(11):2043-2053.
    [16] Samarakoon R,Overstreet JM,Higgins PJ.TGF-beta signal in tissue fibrosis:redox controls,target genes and therapeutic opportunities［J］.Cell Signal,2013,25(1):264-268.
    [17] Zhang J,Zhang X,Xie F,et al.The regulation of TGF-beta/SMAD signaling by protein deubiquitination［J］.Protein Cell,2014,5(7):503-517.
    [18] Xie F,Zhang Z,van Dam H,et al. Regulation of TGF-beta superfamily signaling by SMAD mono-ubiquitination[j].Cells,2014,3(4):981-993.
  • 加载中
通讯作者: 陈斌, bchen63@163.com
  • 1. 

    沈阳化工大学材料科学与工程学院 沈阳 110142

  1. 本站搜索
  2. 百度学术搜索
  3. 万方数据库搜索
  4. CNKI搜索
Get Citation
PDF
XML

Article Metrics

Article views(4372) PDF downloads(1015) Cited by()

Related
Proportional views

Mechanism of TGF-β1/Smad signaling pathway in rhein protected diabetic rat's kidney

doi: 10.3969/j.issn.1006-0111.2017.05.004
  • 1. Department of Pharmacy, Third Hospital Affiliated to Nantong University, Nantong 226006, China
  • 2. Department of Pharmacology, Medical College, Nantong University, Nantong 226001, China
  • Received Date: 2017-05-18
  • Rev Recd Date: 2017-06-26

Abstract: Objective To study the protective effect of Rhein on the kidney of type 2 diabetic rats induced by high fat diet. Methods A rat model of type 2 diabetes was induced by high fat diet combined with low dose streptozotocin 35 mg/kg. The diabetic rats were randomly divided into diabetes group, Low, middle and high rhein dose groups (50,100,150 mg/kg), metformin group (300 mg/kg) and normal control group. Blood glucose and urine micro albumin were measured at 0, 2, 4 and 8 weeks respectively. Serum creatinine, urea nitrogen, total cholesterol and triglyceride were measured at 8 weeks. HE staining was used to observe the pathological changes of renal tissue. Effects of rhein on the expression of transforming growth factor-β1 and Smad3 protein in renal tissue of diabetic rats were detected with Western Blot. Results The blood glucose and urine micro albumin in model group were significantly higher than those in normal control group. Each rhein dose group exhibited reduced blood glucose and urinary micro albumin in diabetic rats. The high rhein dose group showed significant reduction of blood glucose and urine micro albumin in diabetic rats (P<0.05). Compared with model group, rhein reduced the serum Cr, BUN, TC and TG values in each dose group, most significantly in the high rhein dose group (P<0.05). The obvious pathological changes of renal tissue in model group were observed with most improved changes in the high rhein dose group. The expression of TGF-β1 and Smad3 protein in renal tissue of diabetic rats decreased significantly (P<0.05). Conclusion Rhein has preventive effect on diabetic nephropathy. The mechanism may relate to the improvement of renal function, regulation of blood lipid and down regulation of TGF-β1 and Smad3 protein expression in renal tissue.

QIAO Jin, CHEN Min, DOU Zhihua, XU Jiliang, WU Feng, MENG Guoliang. Mechanism of TGF-β1/Smad signaling pathway in rhein protected diabetic rat's kidney[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(5): 402-406,426. doi: 10.3969/j.issn.1006-0111.2017.05.004
Citation: QIAO Jin, CHEN Min, DOU Zhihua, XU Jiliang, WU Feng, MENG Guoliang. Mechanism of TGF-β1/Smad signaling pathway in rhein protected diabetic rat's kidney[J]. Journal of Pharmaceutical Practice and Service, 2017, 35(5): 402-406,426. doi: 10.3969/j.issn.1006-0111.2017.05.004
shu

    HTML

Reference (18)

Catalog

    版权所有：《药学实践与服务》编辑委员会

    Supervisor & Sponsors: Address: No 325 Guohe Road, ShanghaiPost Code: 200433

    Tel: （021）81871324,81871397 E-mail: yxsjzzs@163.com

    网站备案号 沪ICP备05003363号-1

    Supported by: Beijing Renhe Information Technology Co., Ltd.  

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return