ÜNAL ISPIR

ÜNAL ISPIR

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Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 October 2006 in Pesticide Biochemistry and Physiology
Verified
Journal Article
Closed access
SKSibel Şimşek Köprücü
Sibel Şimşek Köprücü
KKKenan Köprücü
Kenan Köprücü
MUMEVLÜT ŞENER URAL
MEVLÜT ŞENER URAL
ÜIÜNAL ISPIR
ÜNAL ISPIR
MPMurat Pala
Murat Pala

1 January 2007 in Acta Veterinaria Brno
Verified
Journal Article
Open access
PDF file
ÜIÜNAL ISPIR
ÜNAL ISPIR
MYM. E. Yonar
M. E. Yonar
In this study, activation of phagocytic cells was examined in rainbow trout ( Oncorhynchus mykiss W.) exposed to 1, 5 and 10 μg ml -1 concentrations of levamisole solution. For this purpose, blood samples were taken from fish on days 1, 7 and 14 of exposure. Potential killing activity was determined by measuring oxidative radical production and phagocytic activity of neutrophils and superoxide anion production of phagocytic cells against Y. ruckeri . The activity of phagocytic cells in fish exposed to each of three concentrations was found higher than that in controls and the differences were statistically significant ( p < 0.05, p < 0.01). Although no activation in oxidative radical production, phagocytes and bactericidal killing activity in fish exposed to 5 and 10 μg ml -1 concentration of levamisole solution was determined on day 7, it was observed that all indicators increased on day 14 of exposure. The present results suggest that the application of levamisole in fish farms could increase non-specific immunity and resistance to infection of fish and offer economics benefits.

1 October 2014 in Research in Veterinary Science
Verified
Journal Article
Closed access
ÜIÜNAL ISPIR
ÜNAL ISPIR
MDMustafa Dorucu
Mustafa Dorucu

1 May 2016
Verified
Journal Article
Closed access
MYM. E. Yonar
M. E. Yonar
ÜIÜNAL ISPIR
ÜNAL ISPIR
SYSerpil Mişe Yonar
Serpil Mişe Yonar
MKMuammer KIRICI
Muammer KIRICI
The aim of this study was to evaluate antioxidant responses of rainbow trout (Oncorhynchus mykiss) exposed to different concentrations of copper sulphate (CuSO4). Fish were exposed to 0 (Group I-control), 5 (Group II), 15 (Group III) and 30 mu g/L (Group IV) concentrations of CuSO4 for 14 days. Liver and gills samples were collected at the end of the experiment, and analysed for their oxidant-antioxidant status, including the malondialdehyde (MDA) level, the catalase (CAT) and glutathione peroxidase (GSH-Px) activities as well as the reduced glutathione (GSH) concentration. Results obtained showed that the levels of MDA increased in tissues of fish. Compared to control, GSH level and GSH-Px and CAT activities were significantly reduced in the fish that were exposed to different concentrations of CuSO4. The result demonstrated that CuSO4 has an oxidative-stress-inducing potential in fish.

1 January 2009 in Acta Veterinaria Brno
Verified
Journal Article
Open access
PDF file
ÜIÜNAL ISPIR
ÜNAL ISPIR
HGH. Bayram Gokhan
H. Bayram Gokhan
MOMikail Ozcan
Mikail Ozcan
MDMustafa Dorucu
Mustafa Dorucu
NSNaim Sağlam
Naim Sağlam
In this study, effects of Yersinia ruckeri antigens on the immune mechanisms of rainbow trout ( Oncorhynchus mykiss ) were examined. The weight of the 120 fish used in this study was 20–30 g. After injecting 1 mg of formalin-inactivated whole cells (FKC) and O-antigen (Ag-O) intraperitoneally, blood was taken from the caudal vein of anaesthetized fish and metabolic activity of leukocytes (Nitroblue tetrazolium (NBT) activities), phagocytic activity (PA), phagocytic index (PI), serum protein and serum total immunoglobulin (TIg) levels were determined on day 30 after the first immunization. The same procedure was conducted in the control group. In all the experimental groups, considerable increases in the immune indicators were found and significant differences detected between the control and experimental groups ( p < 0.05). Metabolic activity of leukocytes decreased significantly ( p < 0.05) during the following treatment with antigens compared to the control fish group.