Radiopharmaceutical model using 99mTc-DMSA to evaluate amifostine protection against cisplatin nephrotoxicity in rats

Çalışmanın amacı sisplatinin neden olduğu nefrotoksisiteye karşı amifostinin koruyucu etkisini bir in vivo radyofarmasötik model kullanarak araştırmaktı. Gereç ve Yöntemler: Erkek Wistar sıçanları her biri 6 hayvandan oluşan 4 gruba ayrıldı: 1) Serum fizyolojik (kontrol); 2) Amifostin (AMI; 200 mg /kg intraperitoneal); 3) Sisplatin (CIS; 5 mg/kg intraperitoneal); 4) Sisplatin artı amifostin (CIS + AMI). Grup 4’te amifostin sisplatinden 30 dakika once enjekte edildi. İlaçlar verildikten sonraki 72. saatte kuyruk veninden plazma BUN ve kreatinin düzeylerini belirlemek amacıyla kan örnekleri alındıktan sonra 7.4 MBq/0.2 ml 99mTc-DMSA enjekte edildi. Radyofarmasötiğin enjeksiyonundan 120 dakika sonra sıçanlar öldürüldü ve böbrekleri çıkarıldı. Her bir doku örneğindeki radyoaktivite RAD 501 tek kanallı analizörü olan bir Cd(Te) dedektörle sayıldı ve her bir böbrekteki aktivite enjekte edilen total aktivite ve organın kitlesine bölünerek bir %ID/gr aktivitesi hesaplandı. Bulgular: Kontrol ve AMI gruplarında %ID/g olarak 99mTc-DMSA uptake’i sırasıyla 8.9938 ± 1.5220 ve 6.4898 ± 1.4091 idi. Sisplatin uygulaması CIS grubunda %ID/g’de anlamlı azalmaya neden oldu (1.5913 ± 0.4566) (p

Sisplatin nefrotoksisitesine karşı amifostinin koruyuculuğunun değerlendirilmesinde 99mTc-DMSA radyofarmasötik modeli

Ob jec ti ve: The aim of our study was to use an in vi vo ra di op har ma ce u ti cal mo del to in ves - ti ga te the cytop ro tec ti ve ef fect of ami fos ti ne aga inst cisp la tin-in du ced nep hro to xi city. Ma te ri al and Met - hods: Ma le Wis tar rats we re di vi ded in to fo ur gro ups of six ani mals each: 1) Sa li ne (con trol); 2) Ami fos ti ne (AMI; 200 mg /kg in tra pe ri to ne ally); 3) Cisp la tin (CIS; 5 mg/kg in tra pe ri to ne ally); 4) Cisp la tin plus ami - fos ti ne (CIS + AMI). Ami fos ti ne was in jec ted 30 mi nu tes be fo re cisp la tin in Gro up 4. 99mTc-DMSA, 7.4 MBq/0.2 ml, was in jec ted thro ugh the ta il ve in 72 ho urs af ter the drug ad mi nis tra ti on. Blo od samp les we - re ob ta i ned for the as says of plas ma cre a ti ni ne and blo od ure a nit ro gen (BUN). Rats we re kil led and the kid neys we re re mo ved by dis sec ti on 120 mi nu tes af ter the in jec ti on of the ra di op har ma ce u ti cal. Ra di o - ac ti vity in each or gan samp le was co un ted using a Cd(Te) de tec tor equ ip ped with a RAD 501 sing lechan nel analy zer and a %ID/g ac ti vity was cal cu la ted by di vi ding the ac ti vity in each kid ney by the to tal ac ti vity in jec ted and the mass of the or gan. Re sults: 99mTc-DMSA up ta ke as %ID/g was 8.9938 ± 1.5220 and 6.4898 ± 1.4091 in the con trol and AMI gro ups res pec ti vely. Cisp la tin ad mi nis tra ti on re sul ted a sig - ni fi cant dec re a se in %ID/g (1.5913 ± 0.4566) (p<0.01). Ami fos ti ne ad mi nis tra ti on 30 mi nu tes be fo re cisp - la tin in jec ti on re sul ted a sig ni fi cant in cre a se in %ID/g (7.3670 ± 2.6090) com pa red to cisp la tin-tre a ted rats (p<0.002). A mar ked in cre a se in plas ma BUN and cre a ti ni ne in di ca ting nep hro to xi city and acu te re nal fa i lu re was ob ser ved in the cisp la tin-tre a ted gro up. Conc lu si on: The re sults sho wed that ami fos ti ne sig - ni fi cantly at te nu a ted cisp la tin-in du ced nep hro to xi city. We conc lu de that this ra di op har ma ce u ti cal mo - del is ab le to de mons tra te cisp la tin nep hro to xi city and ami fos ti ne pro tec ti on aga inst it.

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Turkish Journal of Nuclear Medicine (. Molecular Imaging and Radionuclide Therapy)-Cover
  • ISSN: 1304-1495
  • Yayın Aralığı: Yılda 4 Sayı
  • Başlangıç: 1992
  • Yayıncı: Ortadoğu Reklam Tanıtım Yayıncılık Turizm Eğitim İnşaat Sanayi ve Ticaret A.Ş.
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