The effects of strontium chloride on viability of mouse connective tissue fibroblast cells

Amaç. Stronsiyum tuzları yanma, batma ya da kaşıntıyla birlikteki kimyasal olarak uyarılmışsensoryal irritasyon için etkili ve seçici antiirritanlardır. Bu çalışmanın amacı fibroblast hücrekültürü üzerine stronsiyum kloridin sitotoksik ve/veya proliferatif etkilerini belirlemekti. Yöntem.Fare konnektif doku fibroblast hücrelerinin kültürü (L929 (ATCC cell line, NCTC clone 929) )yapıldı. Fibroblast kültürü %20, %10, %5, %2,5 , %1,25 ve %0,6 ve %0,3 (w/v)konsantrasyonlarda stronsiyum klorid heksahidrat ile muamele edildi. Proliferasyon düzeneğindeXTT işaretli reagen kullanılarak kültür ortamına eklenen tetrazolyum tuzlarının klivajı yoluylacanlı hücre sayısı analiz edildi. Örneklerin optik dansitesi kontrol grubuyla karşılaştırıldı ve şuformül kullanıldı: Hücre canlılığı (%)=[(OD450 (örnek)/OD450 (negatif kontrol))×100].Bulgular. Stronsiyum klorid heksahidrat sitotoksisite açısından kontrol grubuna göre farklılıkgöstermemiştir (p>0.05). %1.25 konsantrasyonda canlı hücre sayısı diğer konsantrasyonlardandaha fazlaydı (p

Fare konnektif doku f ibroblast hücre canlılığı üzerine stronsiy um kloridin etkileri

Aim. Strontium salts are effective and selective anti-irritants for chemically induced sensoryirritation associated with stinging, burning, or itching. The aim of the present study was todetermine the cytotoxic and/or proliferative effects of strontium chloride on fibroblast cell culture.Method. A mouse connective tissue fibroblast cell line, L929 (ATCC cell line, NCTC clone 929)was cultured. Fibroblast cell lines were examined with 20%, 10%, 5%, 2.5%, 1.25%, 0.6%, and0.3% (w/v) concentrations of Strontium chloride hexahydrate (SrCl2.6H2O). The proliferationassay analyzed the number of viable cells by the cleavage of tetrazolium salts added to the culturemedium, using the XTT labeling reagent. The optical density of the samples was compared withthat of the control to obtain the percentage viability, as follows: cell viability (%)=[(OD450(sample)/OD450 negative control))×100]. Results. The cytotoxicity value of strontium chloridefor all concentrations (w/v) was compared with that of the control, and cytotoxicity levels were nothigher than those of the controls (p>0.05). The level of viable cell was higher at 1.25% (w/v) than2.5% (w/v) (p

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