Nihat Dilsiz
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The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
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Research Interests
Nihat Dilsiz has a total of 5 co-authors. Here are the top co-authors by number of shared publications:
Ali Olcucu
Department of Chemistry, Faculty of Science, Firat University, Elaziǧ, Turkey
1 shared publicationAndreas Reichenbach
Paul-Flechsig-Institute for Brain Research, Department of Neurophysiology, University of Leipzig, Leipzig, Germany
1 shared publication- Ayse Sahaboglu
Institute for Ophthalmic Research, University of Tuebingen, Tuebingen, Germany
1 shared publication - Mehmet Zülfü Yıldız
Zoology Section, Department of Biology, Faculty of Engineering and Natural Sciences, Manisa Celal Bayar University, Şehit Prof. Dr. İlhan Varank Campus 45140 Yunusemre, Manisa, Türkiye
1 shared publication Mustafa Atas
Department of Ophthalmology, School of Medicine, Firat University, Elaziǧ, Turkey
1 shared publication
Latest Publications
- 5 October 2005
- Published by Springer Nature in Graefe's Archive for Clinical and Experimental Ophthalmology
- Vol. 244 (5) , 627-633
Protective effects of various antioxidants during ischemia-reperfusion in the rat retina
Background Oxidative stress during ischemia-reperfusion (I/R) is thought to be a major cause of retinal injury after I/R. The present study was aimed at investigating the protective role of antioxidant application. Methods Four commonly used antioxidants (vitamin E=alpha tocopherol, lutein, fenugreek=Trigonella foenum-graecum and germander=Teucrium multicaule) were applied in ischemia-reperfusion (I/R) injury of the right retinae of 51 adult pigmented rats. Each of the antioxidants was administered every 6 h, beginning 6 h before the ischemia. After 60 min ischemia and 24 h reperfusion, we assayed (1) oxidative damage by measuring malondialdehyde (MDA), (2) apoptosis by measuring activated caspase-3 (using immunoblots), and (3) intrinsic antioxidative capacity by measuring glutathione (GSH) levels in the retinae. Results In the order of lutein>Trigonella>vitamin E>Teucrium, all four compounds were effective in preventing retinal damage by I/R, as (1) they significantly decreased the formation of MDA (8.83, 16.48, 17.24, 18.5 nmol/100 mg tissue wet weight, respectively) compared with I/R without protection (23.29 nmol/100 mg tissue wet weight; controls: 8.0 nmol/100 mg tissue wet weight); (2) they significantly inhibited the activation of caspase-3 [0.01, 0.02, 0,02, and 0.04 arbitrary units (AU), respectively, versus control, 0.0, and I/R, 0.08 AU]; and (3) they significantly decelerated the loss of GSH (from control levels of 36.04 nmol/100 mg tissue wet weight) to 30.4, 15.98, 18.1, 15.02 nmol/100 mg tissue wet weight, respectively (lutein, Trigonella, vitamin E, Teucrium), compared with unprotected I/R (12.84 nmol/100 mg tissue wet weight). Conclusions Our study shows that lutein, Trigonella, Teucrium and vitamin E exert protection against in vivo retinal I/R injury in rats; this may recommend these compounds (in particular, lutein) for clinical use in patients with different types of ocular I/R injuries.
- 5 October 2005
- Published by Springer Nature in Graefe's Archive for Clinical and Experimental Ophthalmology
- Vol. 244 (5) , 627-633
Protective effects of various antioxidants during ischemia-reperfusion in the rat retina
Background Oxidative stress during ischemia-reperfusion (I/R) is thought to be a major cause of retinal injury after I/R. The present study was aimed at investigating the protective role of antioxidant application. Methods Four commonly used antioxidants (vitamin E=alpha tocopherol, lutein, fenugreek=Trigonella foenum-graecum and germander=Teucrium multicaule) were applied in ischemia-reperfusion (I/R) injury of the right retinae of 51 adult pigmented rats. Each of the antioxidants was administered every 6 h, beginning 6 h before the ischemia. After 60 min ischemia and 24 h reperfusion, we assayed (1) oxidative damage by measuring malondialdehyde (MDA), (2) apoptosis by measuring activated caspase-3 (using immunoblots), and (3) intrinsic antioxidative capacity by measuring glutathione (GSH) levels in the retinae. Results In the order of lutein>Trigonella>vitamin E>Teucrium, all four compounds were effective in preventing retinal damage by I/R, as (1) they significantly decreased the formation of MDA (8.83, 16.48, 17.24, 18.5 nmol/100 mg tissue wet weight, respectively) compared with I/R without protection (23.29 nmol/100 mg tissue wet weight; controls: 8.0 nmol/100 mg tissue wet weight); (2) they significantly inhibited the activation of caspase-3 [0.01, 0.02, 0,02, and 0.04 arbitrary units (AU), respectively, versus control, 0.0, and I/R, 0.08 AU]; and (3) they significantly decelerated the loss of GSH (from control levels of 36.04 nmol/100 mg tissue wet weight) to 30.4, 15.98, 18.1, 15.02 nmol/100 mg tissue wet weight, respectively (lutein, Trigonella, vitamin E, Teucrium), compared with unprotected I/R (12.84 nmol/100 mg tissue wet weight). Conclusions Our study shows that lutein, Trigonella, Teucrium and vitamin E exert protection against in vivo retinal I/R injury in rats; this may recommend these compounds (in particular, lutein) for clinical use in patients with different types of ocular I/R injuries.
- 1 December 2000
- Published by Wiley in Cell Biochemistry and Function
- Vol. 18 (4) , 259-262
Determination of calcium, sodium, potassium and magnesium concentrations in human senile cataractous lenses
Cataractous lenses have been found to have a distribution of the intracellular ionic environment, the concentrations of potassium and magnesium decreasing and the concentrations of sodium and calcium increasing relative to the cytosol of most cells. This arises as a result of changes to lens membrane characteristics causing an increase in lens membrane permeability. These changes have been found to be initiated as a result of normal ageing of the human lens. In this study, total Ca2+, K+, Na+ and Mg2+ contents have been determined in human normal and cataractous lenses using atomic absorption and flame emission spectroscopy. The normal human lens Ca2+ is between 0·15 and 0·5 μmol g‐1 fresh lens weight; in senile cataracts the value increased up to 9·31 μmol g‐1 ( p < 0·0001). The normal levels of Na+, Mg2+ and K+ are 20, 5·5 and 60 μmol g‐1 respectively; these changed to 136·10, 3·60 and 9·33 μmol g‐1, respectively in cataractous senile human lenses ( p < 0·002, p < 0·002 and p < 0·01). The remarkable differences in these elements may play some role in cataractogenesis. Copyright © 2000 John Wiley & Sons, Ltd.
- 1 December 2000
- Published by Wiley in Cell Biochemistry and Function
- Vol. 18 (4) , 259-262
Determination of calcium, sodium, potassium and magnesium concentrations in human senile cataractous lenses
Cataractous lenses have been found to have a distribution of the intracellular ionic environment, the concentrations of potassium and magnesium decreasing and the concentrations of sodium and calcium increasing relative to the cytosol of most cells. This arises as a result of changes to lens membrane characteristics causing an increase in lens membrane permeability. These changes have been found to be initiated as a result of normal ageing of the human lens. In this study, total Ca2+, K+, Na+ and Mg2+ contents have been determined in human normal and cataractous lenses using atomic absorption and flame emission spectroscopy. The normal human lens Ca2+ is between 0·15 and 0·5 μmol g‐1 fresh lens weight; in senile cataracts the value increased up to 9·31 μmol g‐1 ( p < 0·0001). The normal levels of Na+, Mg2+ and K+ are 20, 5·5 and 60 μmol g‐1 respectively; these changed to 136·10, 3·60 and 9·33 μmol g‐1, respectively in cataractous senile human lenses ( p < 0·002, p < 0·002 and p < 0·01). The remarkable differences in these elements may play some role in cataractogenesis. Copyright © 2000 John Wiley & Sons, Ltd.