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- W2334706720 abstract "Neurodegeneration is a process that is characterized by the loss of neuronal structure and function and eventually ends with neuronal death. An elevated level of inducible nitric oxide synthase (iNOS) is suggested to accompany this process by inducing oxidative and nitrosative damage. Vitamin D is reported to protect glial cells against neurotoxicity via suppressing iNOS synthesis. Though there was no data about whether iNOS is regulated by vitamin D in hippocampal neurons. In this study our aim was to determine any alteration in iNOS expression of hippocampal neurons in response to vitamin D treatment.Twenty four and 48 hours of vitamin D treatments were performed on primary hippocampal neuron cultures that were prepared from Sprague dawley rat embryos (E18). The alterations in the iNOS mRNA expression were determined with quantative real time polymerase chain reaction (qRT-PCR). The cytotoxicity levels of each group were investigated by the measurement of lactate dehydrogenase (LDH) that is released to culture medium.No difference was observed between groups in 24 hours of treatment regarding the iNOS expression. Though the iNOS mRNA level of vitamin D treated group was significantly lower than that of control group on the 48th hours of treatment (p<.001). Vitamin D treatment also attenuated the LDH release which is an indicator of cytotoxicity (p<.001).Our results indicated that vitamin D has the potential to prevent oxidative damage by suppressing iNOS expression.Nörodejenerasyon, sinir hücrelerinin yapı ve fonksiyonlarını kaybetmesine bağlı olarak nöron ölümü ile sonuçlanan bir süreçtir. Bu süreçte artan indüklenebilir nitrik oksit sentaz (iNOS) seviyelerinin, hücrelerin oksidatif ve nitrozatif hasarına sebep olarak nörodejenerasyona eşlik ettiği düşünülmektedir. Vitamin D’nin ise glia hücrelerinde iNOS sentezini baskılayarak hücreleri nörotoksisiteye karşı koruduğu ileri sürülmektedir. Ancak iNOS’un hippokampal nöronlarda vitamin D tarafından düzenlenip düzenlenmediğini gösteren herhangi bir çalışma yoktur. Bu çalışmadaki amacımız, hippokampal nöronların vitamin D uygulamasına cevap olarak iNOS anlatımlarında bir değişiklik olup olmadığını belirlemektir.Sprague dawley cinsi sıçanların 18 günlük embriyolarının hippokampuslarından hazırlanan primer nöron kültürlerine 24 ve 48 saat süre ile vitamin D uygulandı. iNOS mRNA miktarlarındaki değişimler kantitatif gerçek zamanlı polimeraz zincir reaksiyonu (qRT-PCR) yöntemi ile belirlendi. Tüm grupların sitotoksisite seviyeleri kültür medyumuna salınan laktat dehidrogenazın (LDH) ölçülmesi ile belirlendi.Yirmi dört saat boyunca vitamin D uygulanan grupla diğer gruplar arasında herhangi bir iNOS anlatımı açısından bir fark gözlenmezken, 48 saat süreyle vitamin D uygulanan hippokampal nöronların iNOS mRNA seviyelerinin kontrol gruplarına kıyasla anlamlı derecede düştüğü saptandı (p<0,001). Ayrıca, vitamin D uygulamasının sitotoksiste belirteci olan LDH salınımını da azalttığı saptandı (p<0,001).Sonuçlarımız, vitamin D’nin iNOS anlatımındaki artışı engelleyerek, hippokampal nöronları oksidatif hasara karşı koruyabileceğini göstermektedir." @default.
- W2334706720 created "2016-06-24" @default.
- W2334706720 creator A5005616987 @default.
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- W2334706720 date "2014-06-05" @default.
- W2334706720 modified "2023-09-30" @default.
- W2334706720 title "Vitamin D Uygulamasının Primer Hippokampal Nöronlardaki İndüklenebilir Nitrik Oksit Sentaz (İNOS) Anlatımı Üzerine Etkileri" @default.
- W2334706720 cites W1481263059 @default.
- W2334706720 cites W1487935461 @default.
- W2334706720 cites W1546401588 @default.
- W2334706720 cites W1557365633 @default.
- W2334706720 cites W1559492976 @default.
- W2334706720 cites W1605832277 @default.
- W2334706720 cites W1668344921 @default.
- W2334706720 cites W1856438126 @default.
- W2334706720 cites W1966973649 @default.
- W2334706720 cites W1970809569 @default.
- W2334706720 cites W1975593226 @default.
- W2334706720 cites W1981032201 @default.
- W2334706720 cites W1984008481 @default.
- W2334706720 cites W1984214648 @default.
- W2334706720 cites W1988210470 @default.
- W2334706720 cites W2015351304 @default.
- W2334706720 cites W2025563134 @default.
- W2334706720 cites W2029205666 @default.
- W2334706720 cites W2035018742 @default.
- W2334706720 cites W2051073168 @default.
- W2334706720 cites W2052644645 @default.
- W2334706720 cites W2077261568 @default.
- W2334706720 cites W2079277269 @default.
- W2334706720 cites W2080845515 @default.
- W2334706720 cites W2082429191 @default.
- W2334706720 cites W2085006527 @default.
- W2334706720 cites W2087279936 @default.
- W2334706720 cites W2091590679 @default.
- W2334706720 cites W2094766497 @default.
- W2334706720 cites W2096410114 @default.
- W2334706720 cites W2099144303 @default.
- W2334706720 cites W2103734012 @default.
- W2334706720 cites W2105911160 @default.
- W2334706720 cites W2106494040 @default.
- W2334706720 cites W2109909789 @default.
- W2334706720 cites W2112674245 @default.
- W2334706720 cites W2116784956 @default.
- W2334706720 cites W2129199541 @default.
- W2334706720 cites W2144217189 @default.
- W2334706720 cites W2145731558 @default.
- W2334706720 cites W2145796722 @default.
- W2334706720 cites W2147180926 @default.
- W2334706720 cites W2149732522 @default.
- W2334706720 cites W2158094166 @default.
- W2334706720 cites W2159846383 @default.
- W2334706720 cites W2162612835 @default.
- W2334706720 cites W2163643313 @default.
- W2334706720 cites W2171998949 @default.
- W2334706720 cites W2313298280 @default.
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- W2334706720 doi "https://doi.org/10.4274/npa.y7089" @default.
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