Research Article
BibTex RIS Cite

SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats

Year 2020, Volume: 10 Issue: 2, 189 - 197, 08.06.2020

Abstract

ÖZET
Amaç: Bu çalışmada, Beta Glukan, fukoksantin ve kombinasyonlarının serulein kaynaklı akut pankreatit (AP)
sıçan modelindeki etkileri araştırıldı.
Gereç ve Yöntem: Sıçanlar kontrol ve AP gruplarına ayrıldı. AP bir saat arayla dört kez serulein (20 ug/kg/
ip) enjeksiyonuyla oluşturuldu. Serulein enjeksiyonundan 3 gün önce AP gruplarına günde 1 kez taşıyıcı,
Beta Glukan (BG;40 mg/kg/po), fukoksantin (Fuko;40 mg/kg/po) veya Beta Glukan (BG;40 mg/kg/po)
+fukoksantin (Fuko;40 mg/kg/po) uygulandı. Son enjeksiyondan sonraki 8. saatte ötenazi gerçekleştirildi.
Serumda amilaz ve lipaz, pankreas dokusunda interlökin-1β (IL-1β), interlökin-6 (IL-6), interlökin-10 (IL-
10), lucigenin kemilüminesans (CL), malondialdehit (MDA), miyeloperoksidaz (MPO) enzim aktivitesi ve
Hematoksilen&Eosin (H&E), Siklooksijenaz-2 (COX-2), nükleer faktör kappa B (NF-κB) histopatolojik incelemeleri
yapıldı. İstatistiksel analizler için tek yönlü ANOVA ve Bonferroni post-hoc testi uygulandı.
Bulgular: Taşıyıcı grubunda; amilaz, lipaz, lusigenin, IL-1β ve IL-6 düzeyleri kontrole göre (p <0,01-0,0001)
yükselirken, GSH ve IL-10 düzeyleri azaldı (p<0,0001). Lipaz ve amilaz düzeyleri; BG, Fuko ve BG+Fuko tedavileri
ile taşıyıcıya göre azaldı (p<0,05-0,001). IL-6 düzeyleri, Fuko ve BG+Fuko grubunda taşıyıcıya göre
azaldı (p <0,01). IL-1β düzeyleri; BG, Fuko ve BG+Fuko gruplarında taşıyıcı grubuna göre azaldı (p<0,001-
0.0001). IL-10 düzeyi yalnızca BG grubunda taşıyıcı grubuna göre arttı (p<0,01). H&E, COX-2 skorları taşıyıcı
grubunda kontrole göre artarken (p<0,0001); BG, Fuko ve BG+Fuko tedavileri ile azalma gözlendi (p<0,05-
0,001). Taşıyıcı grubunda artan NF-κB skorları (p<0,0001), BG tedavisi ile azaldı (p<0,01). Taşıyıcı grubundaki
artan lusigenin kemiluminesans, MPO ve MDA düzeyleri (p <0,01-0,0001) tüm tedavilerle azaldı (p <0,01-
0,0001).
Sonuç: Beta Glukan ve fukoksantin tedavisi pro-inflamatuvar sitokinleri, COX-2 düzeyini ve oksidatif belirteçleri
azaltarak anti-inflamatuvar sitokin düzeyini arttırarak AP gelişimini hafifletmiştir.
Anahtar sözcükler: Beta glukan; fukoksantin; COX-2; oksidatif stres
ABSTRACT
Aim: This study aims to investigate the effects of Beta Glucan, fucoxanthin and their combinations in acute
pancreatitis (AP) rat model.
Material and Methods: Rats were divided into control and AP groups. The AP was induced by injection of
cerulein (20 μg/kg/ip) four times with an hour interval. Vehicle, Beta Glucan (BG;40 mg/kg/po), fucoxanthin
(Fuco;40 mg/kg/po) or Beta Glucan (BG;40 mg/kg/+ fucoxanthin (Fuco;40 mg/kg/po) were administered
3 days before cerulein injection. Euthanasia was performed at the 8th hour after the last injection. Serum
and pancreatic tissue collected for biochemical and histopathological examinations. One-way ANOVA and
Bonferroni post-hoc test was used for statistical analysis.
Results: Amylase, lipase, lucigenin, interleukin-1β, and interleukin-6 levels are significantly elevated in the
vehicle-treated AP groups (p<0.01-0.0001) while IL-10 was decreased (p<0.0001). Lipase and amylase levels
decreased in the BG, Fuco and BG+Fuco groups compared to vehicle group (p<0.05-0.001). IL-6 levels,
decreased in the fuco and BG+Fuco group (p <0.01). IL-1β levels decreased in BG, Fuco and BG+Fuco groups
compared to vehicle group (p<0,001-0.0001). IL-10 levels increased in BG group compared to the vehicle
group (p<0.01). H&E and COX-2 scores increased in the vehicle groups, compared to the control group
(p<0.0001). All treatments decreased that scores (p<0.05-0.001). Increased NF-κB scores with vehicle
(p<0.0001), decreased with BG treatment (p<0.01). Increased lucigenin, MPO and MDA levels (p<0.01-
0.0001), decreased with BG, Fuco and BG+Fuco treatments (p<0.01-0.0001).
Conclusion: Treatment of Beta Glucan and fucoxanthin alleviated AP development by decreasing proinflammatory
cytokines, COX-2 and oxidative markers and increasing anti-inflammatory cytokine.
Keywords: Beta glucan; fucoxanthine; COX-2; Oxidative stress

References

  • 1. Su KH, Cuthbertson C, Christophi C. Review of experimental animal models of acute pancreatitis. HPB (Oxford). 2006; 8(4):264–286. doi:10.1080/13651820500467358 2. Escobar J, Pereda J, Arduini A, Sandoval J, Sabater L, Aparisi L, et al. Cross-Talk between Oxidative Stress and Pro-Inflammatory Cytokines in Acute Pancreatitis: A Key Role for Protein Phosphatases. Current Pharmaceutical Design. 2009; 15(26), 3027–3042. doi:10.2174/138161209789058075 3. Lin ZS, Ku CF, Guan YF, Xiao HT, Shi XK, Wang HQ, et al. Dihydro-Resveratrol Ameliorates Lung Injury in Rats with Cerulein-Induced Acute Pancreatitis. Phytother Res. 2016 ;30(4):663-70. doi: 10.1002/ptr.5576. 4. Rakonczay Jr Z, Hegyi P, Taka´cs T, McCarroll J, Saluja AK. The role of NF-kB activation in the pathogenesis of acute pancreatitis. Gut. 2008; 57:259–267. doi:10.1136/gut.2007.124115 5. Xiong J, Wang K, Yuan C, Xing R, Ni J, Hu G, et al. Luteolin protects mice from severe acute pancreatitis by exerting HO-1-mediated anti-inflammatory and antioxidant effects. Int J Mol Med. 2017; 39(1): 113–125. 6. Altavilla D, Famulari C, Passaniti M, Campo GM, Macrì A, Seminara P, et al. Lipid peroxidation inhibition reduces NF-kappaB activation and attenuates cerulein-induced pancreatitis. Free Radic Res. 2003; 37:425–35. 7. de Almeida JL, Jukemura J, Coelho AM, Patzina RA, Machado MC, da Cunha JE. Inhibition of cyclooxygenase-2 in experimental severe acute pancreatitis. Clinics (Sao Paulo). 2006;61(4):301-6. doi:10.1590/s1807-59322006000400005 8. Song AM, Bhagat L, Singh VP, Van Acker GGD, Steer ML, Saluja AK. Inhibition of cyclooxygenase-2 ameliorates the severity of pancreatitis and associated lung injury. Am J Physiol Gastrointest Liver Physiol. 2002; 283:1166-74. 9. Raposo MF, de Morais AM, de Morais RM. Carotenoids from Marine Microalgae: A Valuable Natural Source for the Prevention of Chronic Diseases. Mar Drugs. 2015; 13(8):5128–5155. 10. Heo SJ, Ko SC, Kang SM, Kang HS, Kim JP, Kim SH, et al. Cytoprotective effect of fucoxanthin isolated from brown algae Sargassum siliquastrum against H2O2-induced cell damage. Eur. Food Res. Technol. 2008; 228:145–151. doi: 10.1007/s00217-008-0918-7.
Year 2020, Volume: 10 Issue: 2, 189 - 197, 08.06.2020

Abstract

References

  • 1. Su KH, Cuthbertson C, Christophi C. Review of experimental animal models of acute pancreatitis. HPB (Oxford). 2006; 8(4):264–286. doi:10.1080/13651820500467358 2. Escobar J, Pereda J, Arduini A, Sandoval J, Sabater L, Aparisi L, et al. Cross-Talk between Oxidative Stress and Pro-Inflammatory Cytokines in Acute Pancreatitis: A Key Role for Protein Phosphatases. Current Pharmaceutical Design. 2009; 15(26), 3027–3042. doi:10.2174/138161209789058075 3. Lin ZS, Ku CF, Guan YF, Xiao HT, Shi XK, Wang HQ, et al. Dihydro-Resveratrol Ameliorates Lung Injury in Rats with Cerulein-Induced Acute Pancreatitis. Phytother Res. 2016 ;30(4):663-70. doi: 10.1002/ptr.5576. 4. Rakonczay Jr Z, Hegyi P, Taka´cs T, McCarroll J, Saluja AK. The role of NF-kB activation in the pathogenesis of acute pancreatitis. Gut. 2008; 57:259–267. doi:10.1136/gut.2007.124115 5. Xiong J, Wang K, Yuan C, Xing R, Ni J, Hu G, et al. Luteolin protects mice from severe acute pancreatitis by exerting HO-1-mediated anti-inflammatory and antioxidant effects. Int J Mol Med. 2017; 39(1): 113–125. 6. Altavilla D, Famulari C, Passaniti M, Campo GM, Macrì A, Seminara P, et al. Lipid peroxidation inhibition reduces NF-kappaB activation and attenuates cerulein-induced pancreatitis. Free Radic Res. 2003; 37:425–35. 7. de Almeida JL, Jukemura J, Coelho AM, Patzina RA, Machado MC, da Cunha JE. Inhibition of cyclooxygenase-2 in experimental severe acute pancreatitis. Clinics (Sao Paulo). 2006;61(4):301-6. doi:10.1590/s1807-59322006000400005 8. Song AM, Bhagat L, Singh VP, Van Acker GGD, Steer ML, Saluja AK. Inhibition of cyclooxygenase-2 ameliorates the severity of pancreatitis and associated lung injury. Am J Physiol Gastrointest Liver Physiol. 2002; 283:1166-74. 9. Raposo MF, de Morais AM, de Morais RM. Carotenoids from Marine Microalgae: A Valuable Natural Source for the Prevention of Chronic Diseases. Mar Drugs. 2015; 13(8):5128–5155. 10. Heo SJ, Ko SC, Kang SM, Kang HS, Kim JP, Kim SH, et al. Cytoprotective effect of fucoxanthin isolated from brown algae Sargassum siliquastrum against H2O2-induced cell damage. Eur. Food Res. Technol. 2008; 228:145–151. doi: 10.1007/s00217-008-0918-7.
There are 1 citations in total.

Details

Primary Language Turkish
Subjects Health Care Administration
Journal Section Original Research
Authors

Dilek Özbeyli This is me

Özlem Tuğçe Çilingir Kaya This is me

Aslı Aykaç This is me

Sezgin Aydemir This is me

Esra Bihter Gürler This is me

Meral Yüksel This is me

Publication Date June 8, 2020
Published in Issue Year 2020 Volume: 10 Issue: 2

Cite

APA Özbeyli, D., Kaya, Ö. T. Ç., Aykaç, A., Aydemir, S., et al. (2020). SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats. Bozok Tıp Dergisi, 10(2), 189-197.
AMA Özbeyli D, Kaya ÖTÇ, Aykaç A, Aydemir S, Gürler EB, Yüksel M. SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats. Bozok Tıp Dergisi. June 2020;10(2):189-197.
Chicago Özbeyli, Dilek, Özlem Tuğçe Çilingir Kaya, Aslı Aykaç, Sezgin Aydemir, Esra Bihter Gürler, and Meral Yüksel. “SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats”. Bozok Tıp Dergisi 10, no. 2 (June 2020): 189-97.
EndNote Özbeyli D, Kaya ÖTÇ, Aykaç A, Aydemir S, Gürler EB, Yüksel M (June 1, 2020) SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats. Bozok Tıp Dergisi 10 2 189–197.
IEEE D. Özbeyli, Ö. T. Ç. Kaya, A. Aykaç, S. Aydemir, E. B. Gürler, and M. Yüksel, “SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats”, Bozok Tıp Dergisi, vol. 10, no. 2, pp. 189–197, 2020.
ISNAD Özbeyli, Dilek et al. “SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats”. Bozok Tıp Dergisi 10/2 (June 2020), 189-197.
JAMA Özbeyli D, Kaya ÖTÇ, Aykaç A, Aydemir S, Gürler EB, Yüksel M. SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats. Bozok Tıp Dergisi. 2020;10:189–197.
MLA Özbeyli, Dilek et al. “SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats”. Bozok Tıp Dergisi, vol. 10, no. 2, 2020, pp. 189-97.
Vancouver Özbeyli D, Kaya ÖTÇ, Aykaç A, Aydemir S, Gürler EB, Yüksel M. SERULEİNLE OLUŞTURULMUŞ SIÇAN AKUT PANKREATİT MODELINDE BETA GLUKAN VE FUKOKSANTİNİN ETKİSİ The Effect of Beta Glucan and Fucoxanthine in a Serulein- Induced Acute Pancreatitis in Rats. Bozok Tıp Dergisi. 2020;10(2):189-97.
Copyright © BOZOK Üniversitesi - Tıp Fakültesi