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Numan KARAARSLAN1*, Ibrahim YILMAZ2,
Mehmet ISYAR3, Hanefi OZBEK4, Yener AKYUVA5,
Duygu YASAR SIRIN6, Mehmet Sabri GURBUZ7,
Tezcan CALISKAN1, Necati KAPLAN8, Yasin
Emre KAYA9, Bulent BILIR10, Mahir
MAHIROGULLARI11 and Ozkan ATES12 |
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1Assist.
Prof. M.D.; Namik Kemal University School of Medicine,
Department of Neurosurgery, 59100, Tekirdag, Turkey
2Medical pharmacologist, pharmacist; Istanbul Medipol
University School of Medicine, Department of Medical
Pharmacology, 34810, Istanbul, Turkey
3Assoc. Prof. M.D., Acibadem Kadikoy Hospital,
Department of Orthopaedic and Traumatology, 34517, Istanbul,
Turkey.
4Prof. M.D., Ph.D., Istanbul Medipol University
School of Medicine, Department of Medical Pharmacology, 34810,
Istanbul, Turkey
5M.D.; Gaziosmanpasa Taksim Training and Research
Hospital, Department of Neurosurgery, 34433, Istanbul, Turkey.
6Assist. Prof. Ph.D., Namik Kemal University, Faculty
of Arts and Sciences, Department of Molecular Biology and
Genetics, 59100, Tekirdag, Turkey.
7Assist. Prof. M.D., Istanbul Medeniyet University
School of Medicine, Department of Neurosurgery, 34000, Istanbul,
Turkey
8Assist. Prof. M.D.; Department of Neurosurgery,
Istanbul Rumeli University, Corlu Reyap Hospital, 59680,
Tekirdag, Turkey
9Assist. Prof. M.D., Department of Orthoaedic and
Traumatology, Abant Izzet Baysal University School of Medicine,
14000, Bolu, Turkey
10Assist. Prof. M.D., Namik Kemal University School
of Medicine, Department of Internal Mecicine, 59100, Tekirdag,
Turkey
11Prof. M.D., Memorial Health Group, Department of
Orthopaedic and Traumatology, 34384, Istanbul, Turkey
12Prof. M.D., Istanbul Esenyurt University, Esencan
Hospital, Department of Neurosurgery, 34517, Istanbul, Turkey
*Corresponding Author’s É-mail: numikara@yahoo.com
Pbx: +9028 2250 5500
Accepted December 13, 2017 |
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In the
experimental models, it was observed that osteoarthritis-related
clinical and histologic findings could be inhibited with nitric
oxide synthase inhibitors. The aim of the present study was to
investigate the effects of NO, MMP-9, MMP-13, TIMP-1 and TNF-α
on the viability and proliferation of chondrocytes. Primary
chondrocyte cultures were obtained from the tissues of patients
undergoing osteoarthritis surgery. Cell surface antigens were
examined via flow cytometric analyses. Chondrocyte cultures were
evaluated for cell viability and proliferation before and after
the administration of 7-NI, AG, and L-ARG were added, either
alone or with TGF-β1. Cell surface morphologies were examined
via inverted light and environmental scanning electron
microscopy. In all groups, TNF-α, MMP-9, MMP-13, TIMP-1 and NO
were measured spectrophotometrically using commercial kits.
Obtained data were analyzed statistically andalpha<0.05 was
considered assignificant. Locally administered neuronal nitric
oxide synthase inhibitors as 7-nitroindazole were shown to
selectively inhibit nitric oxide release, and increase
chondrocyte proliferation significantly more than the group to
which inducible nitric oxide synthase inhibitors were
applied.Injecting the aforementioned medications into the knee
reduces the side-effects of nitric oxide-related biochemical
mechanisms to the minimum, suggesting that these medication
molecules may be effective in repairing cartilage damage or
decreasing cartilage degeneration?
Keywords: Aminoguanidine, L-arginine, Nitric oxide
synthase, 7-nitroindazole, osteoarthritic chondrocyte, primary
cell culture
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