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Title: | Investigation of neuroprotective effects of cyclooxygenase inhibitors in the 6-hydroxydopamine induced rat Parkinson model |
Authors: | Uludağ Üniversitesi/Tıp Fakültesi/Fizyoloji Anabilim Dalı. Uludağ Üniversitesi/Tıp Fakültesi/Histoloji ve Embriyoloji Anabilim Dalı. Uludağ Üniversitesi/Tıp Fakültesi/Nöroloji Anabilim Dalı. Uludağ Üniversitesi/Tıp Fakültesi/Nöroşirürji Anabilim Dalı. 0000-0001-5757-8450 Gören, Bülent Mimbay, Zehra Bilici, Nebahat Zarifoğlu, Mehmet Oğul, Erhan Korfalı, Ender AAH-1718-2021 ABC-1475-2020 6602543716 35092977400 35092119200 6603411305 6603268541 7004641343 |
Keywords: | 6-OHDA NSAID Parkinson model Rat Induced dopaminergic neurotoxicity In-vivo microdialysis Mptp-mouse model Nf-kappa-b Sodium-salicylate Antiinflammatory drugs 7-nitroindazole protects Induced degeneration Disease Aspirin Neurosciences & neurology Surgery |
Issue Date: | Jul-2009 |
Publisher: | Türk Nöroşurji Derneği |
Citation: | Gören, B. vd. (2009). "Investigation of neuroprotective effects of cyclooxygenase inhibitors in the 6-hydroxydopamine induced rat Parkinson model". Turkish Neurosurgery, 19(3), 230-236. |
Abstract: | AIM: Recent experimental and clinical studies on Parkinson's disease point out the pivotal role of inflammation in the pathogenesis of neurodegeneration and the possible positive effects of nonsteroidal anti-inflammatory drug therapies. Our aim in this study was to investigate the preventive effects of nonsteroidal anti-inflammatory drugs in the 6-hydroxydopamine (6-OHDA) induced rat model of Parkinson's disease. MATERIAL and METHODS: Twenty-one female Wistar-Albino rats (200-250g) were used in this study. The rats were divided in three groups: Saline group (n: 7, 2 ml), Acetylsalicylic acid group (n: 7, 100 mg/kg), and Meloxicam group (n: 7, 50 mg/kg). An hour after administration, the rats received a unilateral intranigral injection of 6-OHDA to produce the Parkinson model lesion. Rotational tests were performed two weeks later as follow-up. Immunohistochemical tests were performed in all groups to determine the severity of the lesion in the substantia nigra. RESULTS: Administration of drugs an hour before the lesions were created did not protect the degeneration of dopaminergic neurons in the substantia nigra. CONCLUSION: Oral usage of low repeated doses of nonsteroidal anfi-inflammatory drugs may possibly slow down the progression of the disease. |
URI: | http://hdl.handle.net/11452/23987 |
ISSN: | 1019-5149 |
Appears in Collections: | Scopus TrDizin Web of Science |
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