PROTECTIVE EFFECTS OF SYSTEMIC PIRACETAM TREATMENT ON TESTICULAR TORSION/DETORSION DAMAGE IN RATS: A DOSE-RESPONSE STUDY

Year 2017, Volume: 19 Issue: 1, 8 - 16, 24.04.2017

Devrim Tuğlu Ercan Yuvanç Fatih Bal Erdal Yılmaz Pınar Atasoy Üçler Kısa Ertan Batislam

https://doi.org/10.24938/kutfd.286998

Abstract

Amaç:
Testiste iskemi/reperfüsyon (I/R) etkili ile oluşan oksidatif hasar üzereine
Pirasetam’ın koruyucu etkilerini araştırmak.

Gereç ve yöntemler: Ratlar rastgele 4 gruba ayrıldı. Grup 1 (sham, kontrol),
Grup 2 = I/R (iskemi/reperfüsyon), ilaç verilmedi. Grup 3 = I/R + Pirasetam 250
mg/kg (i.p) ve Grup 4 = I/R + Pirasetam 500 mg/kg (i.p). Pirasetam
intraperitoneal yolla testis torsiyonunu takiben 60. dakikada verilmiştir. Her
4 grupta işlemin başlangıcından 6 saat sonra ipsilateral sol testis ve
kontralateral sağ testisler çıkarılmıştır. 

Bulgular: Çalışmamızda, Pirasetam’ın artan dozlarda (250 - 500 mg/kg)
verilmesinin total antioksidan kapasiteyi (TAS) istatistiksel olarak anlamlı
arttırdığını, oksidan kapasite markırı olan total oksidan düzeyi (TOS)
istatistiksel açıdan anlamlı olmayan düzeyde arttırdığını ve oksidatif stres
indeks oranını (OSI) ise istatistiksel olarak anlamlı düzeyde azalttığını
belirledik. İpsilateral ve kontralateral testis grupları arasında Johnsen
skorlama sistemine göre istatistiksel farklılık saptamadık.

Sonuç: Bizim düşüncemize göre, Pirasetam tedavisi testis örneklerinde
antioksidan aktiviteyi arttırmış, oksidan aktiviteyi de baskılamıştır. Ancak,
histopatolojik incelemede ve spermatogenes skorlarında bir değişime neden
olmamıştır.

Keywords

Testis torsiyonu, detorsiyon, pirasetam

Ratlarda Sistemik Pirasetam Tedavisinin Testis Torsiyon/Detorsiyon Hasarında Koruyucu Etkileri: Doz Bağımlı Çalışma

Abstract

Objective: To research the
preventive effects of Piracetam on oxidative damage depending on ischemia /
reperfusion (I / R) in the testis. 

Material and methods: The rats indiscriminately separated into 4 groups. Group
1 was considered as control/sham, Group 2 = I/R (Ischemia/Reperfusion),
medicine was not administered to groups 1 and 2, Group 3 = Piracetam 250 mg/kg
(i.p) + I/R and finally Group 4 = Piracetam 500 mg/kg (i.p) + I/R. Piracetam
was given intraperitoneally (i.p) after 60 mins of testicular torsion. In all 4
groups, 6 hours after beginning of the method, the ipsilateral (Left testis)
(L) and contralateral testes (Right testis) (R) of rats were excised. 

Results: In our study, administration of increasing doses of piracetam (250 mg
/ kg - 500 mg / kg) statistically increases total antioxidant capacity (TAC)
and the oxidant capacity marker, total oxidant status (TOS) statistically but
non significant were increased and we have established statistically
significant decrease in the rate of oxidative stress index (OSI). There was no
difference statistically according to Johnsen’s scoring system between groups
in the ipsilateral or contralateral testes. 

Conclusion: In our opinion, piracetam therapy increased antioxidant activity
and decreased oxidative stres scores in testicular samples. However, it did not
cause alteration in histopathological examination and spermatogenesis scores.

Keywords

Testicular torsion, detorsion, piracetam

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