Kevser EROL, Çiğdem ÇENGELLİ ÜNEL, Mahsum AYAZ, Enes YEŞİLTUNA, Ezgi DEMİR, Hamza DALÇINAR, Bengihan ÖZCAN

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Dipiron’un Analjezik Aktivitesi Üzerine H2S’in Etkilerinin Sıçanlarda Araştırılması

Dipiron antipiretik, analjezik ve antiinflamatuvar etkileri olan pirazolon türevi bir ilaçtır. Postoperatif ağrı, kanser ağrısı, kolik ağrıları ve migren tedavisinde kullanılmaktadır. Analjezik etkisinin santral ve periferik yolla olduğu bilinmektedir. İstenmeyen ciddi yan etkileri olabilir. Hidrojen sülfür (H2S) aktif-radikal bir gazdır. Somatik, nöropatik ve viseral ağrı üzerine etkisi olduğu, inflamasyonu azalttığı gözlenmiştir. Dipironun santral ve periferik antinosiseptif etkileri ve bu etkilerde H2S’in katkısı değerlendirilmiştir. Otuz adet erkek Sprague-Dawley sıçan kullanılmıştır. İlaç uygulamasından 30 dakika önce tail clip ve hot plate test ölçümleri alınıp, kontrol grubuna serum fizyolojik, diğer gruplara Dipiron (50-100 mg/kg, i.p); NaHS (5mg/kg, i.p); NaHS (5mg/kg, i.p) + Dipiron (50mg/kg, i.p) verilmiştir. Uygulamadan bir saat sonra ölçümler tekrarlanmış, %0.6 asetik asid 60 mg/kg ip verildikten 5 dakika sonra kıvranma sayıları 10 dakika boyunca kaydedilmiştir. Latens, %MPE (olası maksimal etki) ve kıvranma sayısı kaydedilmiştir. İki ve tek yönlü ANOVA testi kullanılmıştır. 
Anahtar Kelimeler:

Antinosiseptif etki, dipiron

The Effects of H2S on The Analgesic Activity of Dipyrone in Rats

Dipyrone is an analgesic, antipyretic and antiinflammatory drug that has been used for treating postopertive, colic, cancer pain, and migraine. It has some adverse effects such as of bone morrow suppression, sodium and water retention, and gastroenteropathy. Hydrogen sulfide (H2S) is a active-radical gas. The precursors of H2S were reported to overcome some drug side-effects. H2S was also shown to have activity against several pain-related situations. Study aimed to evaluate the contribution of H2S on central and peripheral antinociceptive activity of dipyrone. Male six weeks old Sprague Dawley rats were divided into five groups (n=6): Control (Saline, ip); dipyrone (50 or 100 mg/kg i.p); NaHS (5mg/kg i.p); NaHS (5mg/kg) + dipyrone (50 mg/kg). Tail clip and hot plate tests were applied to the animals 30 minutes before and one hour after the drug injections. Five minutes after the injection of 60 mg/kg acetic acid (%0,6), stretching number was counted for ten minutes. The results were expressed as mean±SEM of latency, %MPE (maximal possible effect) and stretching number. One way and two way ANOVA tests were used for statistical analysis. P<0.05 was accepted as significant. Both doses of dipyrone did not have a significant activity on tail clip test, but 100 mg/kg dipyrone showed significant antinociceptive activity on hot plate and stretching tests. NaHS (5 mg/kg) was increased latency only on hot plate test. But the combination of NaHS with dipyrone has significant antinociceptive activity. It seems that H2S increased the antinociceptive activity of dipyrone both central and peripherally.
Keywords:

Antinociceptive activity, dipyrone,

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Türk Tıp Öğrencileri Araştırma Dergisi-Cover
  • ISSN: 2667-8969
  • Başlangıç: 2019
  • Yayıncı: Eskişehir Osmangazi Üniversitesi
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