Dergiler / Turkish Journal of Medical Sciences / 2021 / Cilt: 51 - Sayı: 4

The role of anakinra in the modulation of intestinal cell apoptosis and inflammatory response during ischemia/reperfusion

Sayfa
2177–2184
Yayın Tarihi
2022-11-03
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Histopathologically, anakinra better preserved the villous structure of the small intestine at a dose of 100 mg/kg than 50 mg/kg.Conclusion: Anakinra decreased the intestinal damage caused by ischemia-reperfusion and a dose of 100 mg/kg was found to be histopathologically more effective.Key words: Ischemia reperfusion injury, interleukin-1 receptor antagonist, anakinra

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Background/aim: Even though interleukin-1 receptor antagonist, IL-1Ra, is used in certain inflammatory diseases, its effect on ischemia-reperfusion injury is a current research topic.
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Temel Bulgular & Veri:We aimed to investigate the protective effects of anakinra, an IL-1Ra, on the I/R induced intestinal injury.
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Sonuç & Katkı:Histopathologically, anakinra better preserved the villous structure of the small intestine at a dose of 100 mg/kg than 50 mg/kg.Conclusion: Anakinra decreased the intestinal damage caused by ischemia-reperfusion and a dose of 100 mg/kg was found to be histopathologically more effective.Key words: Ischemia reperfusion injury, interleukin-1 receptor antagonist, anakinra
🔬Tür:Modelleme & Sayısal Simülasyon
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Background/aim: Even though interleukin-1 receptor antagonist, IL-1Ra, is used in certain inflammatory diseases, its effect on ischemia-reperfusion injury is a current research topic. We aimed to investigate the protective effects of anakinra, an IL-1Ra, on the I/R induced intestinal injury. Materials and methods: The rat model of intestinal ischemia-reperfusion was induced. Rats were randomized into 4 groups: (group 1) control group, (group 2) I/R group, (group 3 and 4) treatment groups (50 mg/kg and 100 mg/kg, respectively). Gene expressions of caspase-3, TNF-α, IL-1α, IL-6, and apoptotic cells in tissue samples were evaluated by PCR and TUNEL methods, respectively. Plasma levels of superoxide dismutase (SOD), catalase (CAT), and malondialdehyde (MDA) were studied by the ELISA method and tissue samples were examined histopathologically as well. Results: Anakinra inhibited the expression of IL-1α, IL-6, and TNF-α and decreased the SOD, CAT, and MDA caused by ischemiareperfusion injury in both treatment groups. Caspase-3 expression and TUNEL-positive cell number in treatment groups were also less. Histopathologically, anakinra better preserved the villous structure of the small intestine at a dose of 100 mg/kg than 50 mg/kg.Conclusion: Anakinra decreased the intestinal damage caused by ischemia-reperfusion and a dose of 100 mg/kg was found to be histopathologically more effective.Key words: Ischemia reperfusion injury, interleukin-1 receptor antagonist, anakinra

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Bu Makaleye Atıf Yap

YAŞAR, N. F., AYKANAT, N. E. B., KANDEMİR, M., ÖZKURT, M., ÖZYURT, R., ERKASAP, N. (2022). The role of anakinra in the modulation of intestinal cell apoptosis and inflammatory response during ischemia/reperfusion. Turkish Journal of Medical Sciences, Cilt: 51 - Sayı: 4, 2177–2184. https://ajindex.com/articles/609311

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Kaynakça (13)

  1. Ueda T, Takagi T, Katada K, Iida T, Mizushima K et al. The protective effect of orally administered redox nanoparticle on intestinal ischemia-reperfusion injury in mice. Biochemical and Biophysical Research Communications 2018
  2. 495 (2): 2044-2049. doi: 10.1016/j.bbrc.2017.11.204 2. Cvetkovic RS, Keating G. Anakinra. BioDrugs 2002
  3. 16 (4): 303-311. doi: 10.2165/00063030-200216040-00005 3. Anaya-Prado R, Toledo-Pereyra LH, Lentsch AB, Ward PA. Ischemia/reperfusion injury. Journal of Surgical Research 2002
  4. 105 (2): 248-258. doi: 10.1006/jsre.2002.6385 4. Vivo V, Zini I, Cantoni AM, Grandi A, Tognolini M et al. Protection by the Eph-ephrin system against mesenteric ischemia-reperfusion injury. Shock 2017
  5. 48 (6): 681-689. doi: 10.1097/SHK.0000000000000890 5. Kalogeris T, Baines CP, Krenz M, Korthuis RJ. Ischemia/ reperfusion. Comprehensive Physiology 2016
  6. 7(1): 113-170. doi: 10.1002/cphy.c160006 6. Kaneko N, Kurata M, Yamamoto T, Morikawa S, Masumoto J. The role of interleukin-1 in general pathology. Inflammation and Regeneration 2019
  7. doi: 10.1186/s41232-019-0101-5 7. Pradillo JM, Murray KN, Coutts GA, Moraga A, Oroz-Gonjar F et al. Reparative effects of interleukin-1 receptor antagonist in young and aged/co-morbid rodents after cerebral ischemia. Brain, Behavior and Immunity 2017
  8. doi: 10.1016/j.bbi.2016.11.013 8. Nayki UA, Nayki C, Cetin N, Cimen FK, Coban A et al. Effect of Kineret® on ovarian ischemia reperfusion injury in a rat model. Journal of Obstetrics and Gynaecology Research 2016
  9. 42 (11): 1525-1533. doi: 10.1111/jog.13095 9. Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Analytical Biochemistry 1979
  10. 95 (2): 351-358. doi: 10.1016/0003-2697(79)90738-3 10. Aebi H. Catalase in vitro. Methods in Enzymology. 1984
  11. doi: 10.1016/s0076-6879(84)05016-3 11. Guneli E, Cavdar Z, Islekel H, Sarioglu S, Erbayraktar S et al. Erythropoietin protects the intestine against ischemia/ reperfusion injury in rats. Molecular Medicine 2007
  12. 13 (9-10): 509-517. doi: 10.2119/2007-00032 12. Marshall JC. The gut as a potential trigger of exercise-induced inflammatory responses. Canadian Journal of Physiology and Pharmacology 1998
  13. 76 (5): 479-484. doi: 10.1139/cjpp-76-5-479 13. Zhang DD, Zou MJ, Zhang YT, Fu WL, Xu T et al. A novel IL-1RA-PEP fusion protein with enhanced brain penetration ameliorates cerebral ischemia-reperfusion injury by inhibition of oxidative stress and neur