Effects of Chrysin Against Isoniazid-Induced Lung Injury in Rats

Year 2020, Volume: 13 Issue: 2, 161 - 171, 30.06.2020

Sefa Küçükler Selçuk Özdemir Selim Çomaklı Fatih Kandemir

https://doi.org/10.30607/kvj.709842

Cited By: 1

Abstract

The aim of the study was to investigate the effects of chrysin (CH), one of the natural flavonoids, against isoniazid lung damage caused by isoniazid (INH), which was widely used in the treatment of tuberculosis. Male Sprague-Dawley rats were randomly divided into five groups: a control group, INH-treated group, CH alone treated group 50 mg / kg, INH + CH 25 mg / kg treated group, and INH+ CH 50 mg / kg treated group. It was determined that INH caused oxidative damage by decreasing antioxidant enzyme activities such as glutathione peroxidase (GPx), superoxide dismutase (SOD), and catalase (CAT) and increasing lipid peroxidation (LPO). In addition, it was found that the administration of CH to INH-treated rats increased GSH level and antioxidant enzyme activities, and decreased lipid peroxidation. It was observed that the nuclear factor erythroid 2 related factor 2 (Nrf-2) and oxygenase-1 (HO-1) expression levels were up-regulated in the INH-treated group, and the expression of NF-κB increased in the INH-treated group in the immunohistochemical examination, and the CH administration, on the other hand, decreased the levels of these markers. Taken together, these results suggested that CH had beneficial effects in INH-induced lung toxicity by maintaining the oxidant-antioxidant balance and decreasing NF-κB, Nrf-2, and HO-1 expressions.

Keywords

Chrysin, Isoniazid, Lung, Oxidative Stress

Ratlarda İzoniazid Kaynaklı Akciğer Hasarına Karşı Krisinin Etkileri

Abstract

Bu çalışmanın amacı; tüberküloz tedavisinde yaygın olarak kullanılan izoniazid (İZN) kaynaklı akciğer hasarına karşı doğal flavonoidlerden olan krisin (KRS)’in etkilerinin araştırılmasıdır. Çalışmada Spraque Dawley cinsi 35 adet erkek rat rastgele 5 gruba ayrıldı: Kontrol grubu, İZN uygulanan grup, KRS 50 mg/kg uygulanan grup, İZN+ KRS 25 mg/kg uygulanan grup ve İZN+ KRS 50 mg/kg uygulanan grup. İZN’nin glutatyon peroksidaz (GPx), süperoksit dismutaz (SOD) ve katalaz (KAT) gibi antioksidan enzim aktivitelerini ve glutatyon (GSH) düzeylerini azaltıp, lipid peroksidasyonunu (LPO) artırarak oksidatif hasara neden olduğu belirlendi. Ayrıca İZN ile kombine uygulanan KRS uygulamasının GSH seviyesini ve antioksidan enzim aktivitelerini artırdığı, lipid peroksidasyonunu ise azalttığı ettiği tespit edildi. Çalışmada incelenen nükleer faktör eritroid 2 ile ilişkili faktör 2 (Nrf-2) ve hem oksijenaz-1 (HO-1) seviyelerinin İZN grubunda gen ekspresyonu düzeyinde, nükleer faktör kappa B (NF-κB) ekspresyonunu ise immunhistokimyasal incelemede arttığı tespit edilmiş, buna karşın KRS uygulamasının bu belirteçlerin düzeylerinde azalmaya neden olduğu gözlenmiştir. Birlikte ele alındığında, bu sonuçlar KRS'in oksidan-antioksidan dengesini koruyarak ve NF-κB, Nrf-2 ve HO-1 ekspresyonlarını azaltarak İZN’nin neden olduğu akciğer toksisitesinde faydalı etkilere sahip olduğunu düşündürmektedir.

Keywords

Akciğer, İzoniazid, Krisin, Oksidatif Stres

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