Nitric oxide and oxidative stress is associated with severity of diabetic retinopathy and retinal structural alterations

被引:64
作者
Sharma, Shashi [1 ]
Saxena, Sandeep [1 ]
Srivastav, Khushboo [1 ]
Shukla, Rajendra K. [2 ]
Mishra, Nibha [1 ]
Meyer, Carsten H. [3 ]
Kruzliak, Peter [4 ,5 ]
Khanna, Vinay K. [2 ]
机构
[1] King Georges Med Univ, Dept Ophthalmol, Retina Serv, Lucknow 226003, Uttar Pradesh, India
[2] Indian Inst Toxicol & Res, Dev Toxicol Div, Lucknow, Uttar Pradesh, India
[3] Pallas Klin, Dept Ophthalmol, Olten, Switzerland
[4] St Annes Univ Hosp, Int Clin Res Ctr, Dept Cardiovasc Dis, Brno 65691, Czech Republic
[5] Masaryk Univ, Brno 65691, Czech Republic
关键词
diabetic retinopathy; nitric oxide; nitrosative stress; oxidative stress; spectral domain optical coherence tomography; ENDOTHELIAL GROWTH-FACTOR; VISUAL-ACUITY; PHOTORECEPTOR STATUS; MACULAR EDEMA; PEROXYNITRITE; PLASMA; BLOOD; COMPLICATIONS; PREVALENCE; EXPRESSION;
D O I
10.1111/ceo.12506
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
BackgroundThe aim of the study was to determine plasma nitric oxide (NO) and lipid peroxide (LPO) levels in diabetic retinopathy and its association with severity of disease. DesignProspective observational study. ParticipantsA total of 60 consecutive cases and 20 healthy controls were included. MethodsSeverity of retinopathy was graded according to early treatment diabetic retinopathy study (ETDRS) classification. Photoreceptor inner segment ellipsoid band (ISel) disruption and retinal pigment epithelium (RPE) alteration were graded using spectral domain optical coherence tomography. Data were statistically analyzed. Main Outcome MeasuresPlasma thiobarbituric acid reactive substances, NO assay and reduced glutathione (GSH) were measured using standard protocol. ResultsIncreased severity of diabetic retinopathy was significantly associated with increase in plasma levels of LPO (P<0.05), NO (P<0.001) and decrease in plasma levels of GSH (P<0.0001), ISel disruption (P<0.001) and RPE topographic alteration (P<0.01). ConclusionIncreased plasma NO levels are associated with increased severity of diabetic retinopathy. For the first time, it has been demonstrated that increased plasma LPO, NO and decreased GSH levels are associated with in vivo structural changes in inner segment ellipsoid and RPE.
引用
收藏
页码:429 / 436
页数:8
相关论文
共 45 条
  • [1] ROLE OF OXIDATIVE STRESS IN DEVELOPMENT OF COMPLICATIONS IN DIABETES
    BAYNES, JW
    [J]. DIABETES, 1991, 40 (04) : 405 - 412
  • [2] NITRIC-OXIDE DECREASES IN-VITRO PHAGOCYTOSIS OF PHOTORECEPTOR OUTER SEGMENTS BY BOVINE RETINAL PIGMENTED EPITHELIAL-CELLS
    BECQUET, F
    COURTOIS, Y
    GOUREAU, O
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 1994, 159 (02) : 256 - 262
  • [3] Bell E. T., 1906, Anatomischer Anzeiger, V29
  • [4] Optical coherence tomography in unilateral resolved central serous chorioretinopathy
    Eandi, CM
    Chung, JE
    Cardillo-Piccolino, F
    Spaide, RF
    [J]. RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2005, 25 (04): : 417 - 421
  • [5] Experimental diabetes causes breakdown of the blood-retina barrier by a mechanism involving tyrosine nitration and increases in expression of vascular endothelial growth factor and urokinase plasminogen activator receptor
    El-Remessy, AB
    Behzadian, MA
    Abou-Mohamed, G
    Franklin, T
    Caldwell, RW
    Caldwell, RB
    [J]. AMERICAN JOURNAL OF PATHOLOGY, 2003, 162 (06) : 1995 - 2004
  • [6] Oxidative stress and diabetic neuropathy: a new understanding of an old problem
    Feldman, EL
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (04) : 431 - 433
  • [7] RELATIONSHIP BETWEEN PHOTORECEPTOR OUTER SEGMENT LENGTH AND VISUAL ACUITY IN DIABETIC MACULAR EDEMA
    Forooghian, Farzin
    Stetson, Paul F.
    Meyer, Scott A.
    Chew, Emily Y.
    Wong, Wai T.
    Cukras, Catherine
    Meyerle, Catherine B.
    Ferris, Frederick L., III
    [J]. RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2010, 30 (01): : 63 - 70
  • [8] FROESCH ER, 1956, DIABETES, V5, P1
  • [9] Nitric oxide: A review of its role in retinal function and disease
    Goldstein, IM
    Ostwald, P
    Roth, S
    [J]. VISION RESEARCH, 1996, 36 (18) : 2979 - 2994
  • [10] Hamann S, 1998, AM J PHYSIOL, V274, P1332