Tributyltin chloride induces renal dysfunction by inflammation and oxidative stress in female rats

被引:32
作者
Coutinho, Joao V. S. [1 ]
Freitas-Lima, Leandro C. [1 ]
Freitas, Frederico F. C. T. [2 ]
Freitas, Flavia P. S. [2 ]
Podratz, Priscila L. [1 ]
Magnago, Rafaella P. L. [1 ]
Porto, Marcella L. [2 ]
Meyrelles, Silvana S. [2 ]
Vasquez, Elisardo C. [2 ]
Brandao, Poliane A. A. [3 ]
Carneiro, Maria T. W. D. [3 ]
Paiva-Melo, Francisca D. [4 ]
Miranda-Alves, Leandro [4 ,5 ]
Silva, Ian V. [1 ]
Gava, Agata L. [2 ]
Graceli, Jones B. [1 ]
机构
[1] Univ Fed Espirito Santo, Dept Morphol, Goiabeiras, ES, Brazil
[2] Univ Fed Espirito Santo, Dept Physiol Sci, Goiabeiras, ES, Brazil
[3] Univ Fed Espirito Santo, Dept Chem, Goiabeiras, ES, Brazil
[4] Univ Fed Rio de Janeiro, Inst Biomed Sci, Expt Endocrinol Res Grp, BR-21941 Rio De Janeiro, Brazil
[5] Univ Fed Rio de Janeiro, Sch Med, Postgrad Program Endocrinol, BR-21941 Rio De Janeiro, Brazil
关键词
Tributyltin chloride; Renal function; Inflammation; Oxidative stress; Estrogen; MAST-CELL INFILTRATION; I COLLAGEN-SYNTHESIS; ESTROGEN-RECEPTOR; TUBULOINTERSTITIAL FIBROSIS; EXPRESSION; EXPOSURE; ACTIVATION; TOXICITY; PATHOGENESIS; LEADS;
D O I
10.1016/j.toxlet.2016.08.007
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Tributyltin chloride (TBT) is an organometallic pollutant that is used as a biocide in antifouling paints. TBT induces several toxic and endocrine-disrupting effects. However, studies evaluating the effects of TBT on renal function are rare. This study demonstrates that TBT exposure is responsible for improper renal function as well as the development of abnormal morphophysiology in mammalian kidneys. Female rats were treated with TBT, and their renal morphophysiology was assessed. Morphophysiological abnormalities such as decreased glomerular filtration rate and increased proteinuria levels were observed in TBT rats. In addition, increases in inflammation, collagen deposition and alpha-smooth muscle actin (alpha-SMA) protein expression were observed in TBT kidneys. A disrupted cellular redox balance and apoptosis in kidney tissue were also observed in TBT rats. TBT rats demonstrated reduced serum estrogen levels and estrogen receptor-alpha (ER alpha) protein expression in renal cortex. Together, these data provide in vivo evidence that TBT is toxic to normal renal function and that these effects may be associated with renal histopathology complications, such as inflammation and fibrosis. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:52 / 69
页数:18
相关论文
共 78 条
  • [1] How does proteinuria cause progressive renal damage?
    Abbate, Mauro
    Zoja, Carla
    Remuzzi, Giuseppe
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2006, 17 (11): : 2974 - 2984
  • [2] Omega-3 fatty acid supplementation attenuates oxidative stress, inflammation, and tubulointerstitial fibrosis in the remnant kidney
    An, Won Suk
    Kim, Hyun Ju
    Cho, Kyu-Hyang
    Vaziri, Nosratola D.
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2009, 297 (04) : F895 - F903
  • [3] Environmental levels, toxicity and human exposure to tributyltin (TBT)-contaminated marine environment. A review
    Antizar-Ladislao, Blanca
    [J]. ENVIRONMENT INTERNATIONAL, 2008, 34 (02) : 292 - 308
  • [4] Presence and quantification of mast cells in the gingiva of cats with tooth resorption, periodontitis and chronic stomatitis
    Arzi, Boaz
    Murphy, Brian
    Cox, Darren P.
    Vapniarsky, Natalia
    Kass, Philip H.
    Verstraete, Frank J. M.
    [J]. ARCHIVES OF ORAL BIOLOGY, 2010, 55 (02) : 148 - 154
  • [5] Do resident renal mast cells play a role in the pathogenesis of diabetic nephropathy?
    Balakumar, Pitchai
    Reddy, Jayarami
    Singh, Manjeet
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2009, 330 (1-2) : 187 - 192
  • [6] Bone Marrow Mononuclear Cells Attenuate Interstitial Fibrosis and Stimulate the Repair of Tubular Epithelial Cells after Unilateral Ureteral Obstruction
    Barreira, Andre L.
    Takiya, Christina M.
    Castiglione, Raquel C.
    Maron-Gutierrez, Tatiana
    Barbosa, Carolina M. L.
    Ornellas, Debora S.
    Verdoorn, Karine S.
    Pascarelli, Bernardo M.
    Borojevic, Radovan
    Einicker-Lamas, Marcelo
    Leite, Maurilo, Jr.
    Morales, Marcelo M.
    Vieyra, Adalberto
    [J]. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2009, 24 (5-6) : 585 - 594
  • [7] Tributyltin chloride leads to adiposity and impairs metabolic functions in the rat liver and pancreas
    Bertuloso, Bruno D.
    Podratz, Priscila L.
    Merlo, Eduardo
    de Araujo, Julia F. P.
    Lima, Leandro C. F.
    de Miguel, Emilio C.
    de Souza, Leticia N.
    Gava, Agata L.
    de Oliveira, Miriane
    Miranda-Alves, Leandro
    Carneiro, Maria T. W. D.
    Nogueira, Celia R.
    Graceli, Jones B.
    [J]. TOXICOLOGY LETTERS, 2015, 235 (01) : 45 - 59
  • [8] DNA Damage and Augmented Oxidative Stress in Bone Marrow Mononuclear Cells from Angiotensin-Dependent Hypertensive Mice
    Campagnaro, Bianca P.
    Tonini, Clarissa L.
    Nogueira, Breno V.
    Casarini, Dulce E.
    Vasquez, Elisardo C.
    Meyrelles, Silvana S.
    [J]. INTERNATIONAL JOURNAL OF HYPERTENSION, 2013, 2013
  • [9] Endogenous female sex hormones delay the development of renal dysfunction in apolipoprotein E-deficient mice
    Carneiro, Sonila S.
    Carminati, Raffaela Z.
    Freitas, Flavia P. S.
    Podratz, Priscila L.
    Balarini, Camille M.
    Graceli, Jones B.
    Meyrelles, Silvana S.
    Vasquez, Elisardo C.
    Gava, Agata L.
    [J]. LIPIDS IN HEALTH AND DISEASE, 2014, 13
  • [10] Bone Marrow-Derived Mononuclear Cells Promote Improvement in Glomerular Function in Rats with Early Diabetic Nephropathy
    Castiglione, Raquel C.
    Maron-Gutierrez, Tatiana
    Barbosa, Carolina M. L.
    Ornellas, Felipe M.
    Barreira, Andre Luis
    diBarros, Carolina B. A.
    Vasconcelos-dos-Santos, Andreia
    Paredes, Bruno Diaz
    Pascarelli, Bernardo M.
    Diaz, Bruno L.
    Rossi-Bergmann, Bartira
    Takiya, Christina M.
    Rocco, Patricia R. M.
    Souza-Menezes, Jackson
    Morales, Marcelo M.
    [J]. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2013, 32 (03) : 699 - 718