Chronic nicotine exposure exacerbates acute renal ischemic injury

被引:67
作者
Arany, Istvan [1 ]
Grifoni, Samira [2 ]
Clark, Jeb S. [1 ]
Csongradi, Eva [2 ,4 ,5 ]
Maric, Christine [2 ]
Juncos, Luis A. [2 ,3 ]
机构
[1] Univ Mississippi, Dept Pediat, Div Pediat Nephrol, Med Ctr, Jackson, MS 39216 USA
[2] Univ Mississippi, Dept Physiol & Biophys, Med Ctr, Jackson, MS 39216 USA
[3] Univ Mississippi, Dept Med, Med Ctr, Div Nephrol, Jackson, MS 39216 USA
[4] Univ Debrecen, Hlth Sci Ctr, Debrecen, Hungary
[5] Univ Debrecen, Dept Internal Med 1, Debrecen, Hungary
关键词
smoking; oxidative stress; JNK/AP-1; activation; PROXIMAL TUBULE CELLS; N-ACETYL CYSTEINE; CIGARETTE-SMOKE; OXIDATIVE INJURY; EPITHELIAL-CELLS; KIDNEY-DISEASE; RAT-KIDNEY; REPERFUSION INJURY; URINARY-EXCRETION; RISK-FACTOR;
D O I
10.1152/ajprenal.00041.2011
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Arany I, Grifoni S, Clark JS, Csongradi E, Maric C, Juncos LA. Chronic nicotine exposure exacerbates acute renal ischemic injury. Am J Physiol Renal Physiol 301: F125-F133, 2011. First published April 20, 2011; doi: 10.1152/ajprenal.00041.2011.-Recent epidemiological reports showed that smoking has a negative impact on renal function and elevates the renal risk not only in the renal patient but perhaps also in the healthy population. Studies suggested that nicotine, a major tobacco alkaloid, links smoking to renal dysfunction. While several studies showed that smoking/chronic nicotine exposure exacerbates the progression of chronic renal diseases, its impact on acute kidney injury is virtually unknown. Here, we studied the effects of chronic nicotine exposure on acute renal ischemic injury. We found that chronic nicotine exposure increased the extent of renal injury induced by warm ischemia-reperfusion as evidenced by morphological changes, increase in plasma creatinine level, and kidney injury molecule-1 expression. We also found that chronic nicotine exposure elevated markers of oxidative stress such as nitrotyrosine as well as malondialdehyde. Interestingly, chronic nicotine exposure alone increased oxidative stress and injury in the kidney without morphological alterations. Chronic nicotine treatment not only increased reactive oxygen species (ROS) production and injury but also exacerbated oxidative stress-induced ROS generation through NADPH oxidase and mitochondria in cultured renal proximal tubule cells. The resultant oxidative stress provoked injury through JNK-mediated activation of the activator protein (AP)-1 transcription factor in vitro. This mechanism might exist in vivo as phosphorylation of JNK and its downstream target c-jun, a component of the AP-1 transcription factor, is elevated in the ischemic kidneys exposed to chronic nicotine. Our results imply that smoking may sensitize the kidney to ischemic insults and perhaps facilitates progression of acute kidney injury to chronic kidney injury.
引用
收藏
页码:F125 / F133
页数:9
相关论文
共 51 条
  • [1] Activation of ERK or inhibition of JNK ameliorates H2O2 cytotoxicity in mouse renal proximal tubule cells
    Arany, I
    Megyesi, JK
    Kaneto, H
    Tanaka, S
    Safirstein, RL
    [J]. KIDNEY INTERNATIONAL, 2004, 65 (04) : 1231 - 1239
  • [2] p66shc inhibits pro-survival epidermal growth factor receptor/ERK signaling during severe oxidative stress in mouse renal proximal tubule cells
    Arany, Istvan
    Faisal, Amir
    Nagamine, Yoshikuni
    Safirstein, Robert L.
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (10) : 6110 - 6117
  • [3] p66SHC-mediated mitochondrial dysfunction in renal proximal tubule cells during oxidative injury
    Arany, Istvan
    Faisal, Amir
    Clark, Jeb S.
    Vera, Trinity
    Baliga, Radhakrishna
    Nagamine, Yoshikuni
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2010, 298 (05) : F1214 - F1221
  • [4] Recent advances in the pathophysiology of ischemic acute renal failure
    Bonventre, JV
    Weinberg, JM
    [J]. JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (08): : 2199 - 2210
  • [5] Smoking is associated with renal impairment and proteinuria in the normal population: The AusDiab kidney study
    Briganti, EM
    Branley, P
    Chadban, SJ
    Shaw, JE
    McNeil, JJ
    Welborn, TA
    Atkins, RC
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2002, 40 (04) : 704 - 712
  • [6] In vivo nicotine treatment regulates mesocorticolimbic CREB and ERK signaling in C57Bl/6J mice
    Brunzell, DH
    Russell, DS
    Picciotto, MR
    [J]. JOURNAL OF NEUROCHEMISTRY, 2003, 84 (06) : 1431 - 1441
  • [7] Tempol, a membrane-permeable radical scavenger, reduces oxidant stress-mediated renal dysfunction and injury in the rat
    Chatterjee, PK
    Cuzzocrea, S
    Brown, PAJ
    Zacharowski, K
    Stewart, KN
    Mota-Filipe, H
    Thiemermann, C
    [J]. KIDNEY INTERNATIONAL, 2000, 58 (02) : 658 - 673
  • [8] The effects of chronic exposure to ethanol and cigarette smoke on the level of reduced glutathione and malondialdehyde in rat kidney
    Cigremis, Y
    Turkoz, Y
    Akgoz, M
    Sozmen, M
    [J]. UROLOGICAL RESEARCH, 2004, 32 (03): : 213 - 218
  • [9] The effects of chronic exposure to ethanol and cigarette smoke on the formation of peroxynitrite, level of nitric oxide, xanthine oxidase and myeloperoxidase activities in rat kidney
    Cigremis, Yilmaz
    Turkoz, Yusuf
    Tuzcu, Mehmet
    Ozen, Hasan
    Kart, Asim
    Gaffaroglu, Muhammet
    Erdogan, Kenan
    Akgoz, Muslum
    Ozugurlu, Fikret
    [J]. MOLECULAR AND CELLULAR BIOCHEMISTRY, 2006, 291 (1-2) : 127 - 138
  • [10] The effect of inhaling thinner and/or cigarette smoke on rat kidneys
    Cobanoglu, Bengu
    Ozercan, Ibrahim H.
    Ozercan, M. Resat
    Yalcin, Orhan
    [J]. INHALATION TOXICOLOGY, 2007, 19 (03) : 303 - 308