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Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation

Yıl 2025, Cilt: 34 Sayı: 3, 441 - 450, 30.12.2025
https://doi.org/10.34108/eujhs.1671907

Öz

This study aimed to evaluate the potential protective effects of octreotide, a somatostatin analogue, against acute liver injury induced by acetaminophen in rats. 28 male Wistar albino rats, aged 8–10 weeks, were randomly assigned into four experimental groups. Group 1 served as the control, and Group 2 received 1 g/kg of acetaminophen orally, Group 3 was administered 300 µg/kg of octreotide intraperitoneally, Group 4 was treated with both agents, where octreotide was given 30 minutes after acetaminophen administration. The experiment was terminated by taking liver tissue and blood samples under general anesthesia 24 hours after drug administration. Hematoxylin and Eosin staining was performed on the liver sections, and serum levels of aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase activities, as well as total antioxidant capacity, total oxidant capacity and malondialdehyde levelswere analyzed. Aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase activities, and total oxidant capacity were significantly higher in acetaminophen-treated rats compared to the other groups. Similarly, malondialdehyde levels were also higher, but these values were not statistically significant. Total antioxidant capacity were lower in the acetaminophen group compared to the other groups. In contrast, the treatment group showed a significant reduction in aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase activities and total oxidant capacitycompared to the acetaminophen group. Histological analysis revealed severe hepatic damage in the acetaminophen group, while less tissue damage was noted in the treatment group. Although malondialdehyde was lower in the treatment group on average, the difference was not statistically significant. These findings suggest that octreotide may offer partial protection against acetaminophen-induced liver injury. However, further investigation is required to elucidate its precise mechanism of action.

Etik Beyan

Ethics committee approval was received for this study from the Animal Experiments Ethics Committee of Pamukkale University (Date: 29.01.2019, Number: 2019/01). .

Destekleyen Kurum

This research supported by Pamukkale University Scientific Research Coordination Office as project number 2019SABE015. This research was produced from the master's thesis of MA.

Proje Numarası

2019/01

Kaynakça

  • Lin YH, Lin YC, Hou YT. Prospective application of tannic acid in acetaminophen (APAP)-induced acute liver failure. Int J Mol Sci. 2023;25(1):317. doi:10.3390/ijms25010317.
  • Golestan Jahromi M, Nabavizadeh F, Vahedian J, Nahrevanian H, Dehpour AR, Zare-Mehrjardi A. Protective effect of ghrelin on acetaminophen-induced liver injury in rat. Peptides. 2010;31(11):2114-2117. doi:10.1016/j.peptides.2010.08.009.
  • Koç A, Gazi M, Caner Sayar A, et al. Molecular mechanism of the protective effect of adenosine triphosphate against paracetamol-induced liver toxicity in rats. Gen Physiol Biophys. 2023;42(2):201-208. doi:10.4149/gpb_2022055.
  • Sabea AM, AlKhamas AJH, Sahib BS, Faris JK. Biochemical and Histopathological effects of acetaminophen and protective effects of naringin on liver rats. IJFMT. 2021;15(4): 794-801. doi:10.37506/ijfmt. v15i4.16801.
  • Al-Doaiss AA. Hepatotoxicity-induced by the therapeutic dose of acetaminophen and the ameliorative effect of oral co-administration of selenium/Tribulus terrestris extract in rats. Int J Morphol. 2020;38(5):1444-1454. doi:10.4067/S0717-95022020000501444.
  • AlWahsh M, Othman A, Hamadneh L, et al. Second exposure to acetaminophen overdose is associated with liver fibrosis in mice. EXCLIJ. 2019;18:51-62.
  • Ahmad ST, Arjumand W, Nafees S, et al. Hesperidin alleviates acetaminophen induced toxicity in Wistar rats by abrogation of oxidative stress, apoptosis and inflammation. Toxicol Lett. 2012;208(2):149-161. doi:10.1016/j.toxlet.2011.10.023.
  • Yan M, Huo Y, Yin S, Hu H. Mechanisms of acetaminophen-induced liver injury and its implications for therapeutic interventions. Red Biol. 2018;17:274-283 doi:10.1016/j.redox.2018.04.019.
  • Erfidan MA, Akkol EK, Sevimli A, Civelek T. Effects of pomegranate (Punica granatum L.) on paracetamol induced acute hepatic damage in mice. Kocatepe Vet J. 2016;9(4):273-280 doi:10.5578/kvj.28156.
  • Zhang J, Song Q, Han X, et al. Multi-targeted protection of acetaminophen-induced hepatotoxicity in mice by tannic acid. Int Immunopharmacol. 2017; 47:95-105. doi: 10.1016/j.intimp.2017.03.027.
  • Aziz NM, Ragy MM, Ahmed SM. Somatostatin analogue, Octreotide, improves restraint stress-induced liver injury by ameliorating oxidative stress, inflammatory response, and activation of hepatic stellate cells. Cell Stress Chaperones. 2018;23(6):1237-1245. doi:10.1007/s12192-018-0929-7.
  • Liao J, Lu Q, Li Z, Li J, Zhao Q, Li J. Acetaminophen-induced liver injury: Molecular mechanism and treatments from natural products. Front Pharmacol. 2023;14:1122632. doi:10.3389/fphar.2023.1122632.
  • European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Drug-induced liver injury. J Hepatol. 2019;70(6):1222-1261. doi:10.1016/j.jhep.2019.02.014.
  • Ntamo Y, Ziqubu K, Chellan N, et al. Drug-induced liver ınjury: clinical evidence of n-acetyl cysteine protective effects. Oxid Med Cell Longev. 2021;2021:3320325. doi:10.1155/2021/3320325.
  • Du K, Ramachandran A, Jaeschke H. Oxidative stress during acetaminophen hepatotoxicity: Sources, pathophysiological role and therapeutic potential. Redox Biol. 2016;10:148-156. doi:10.1016/j.redox.2016.10.001.
  • Hwang HJ, Kwon MJ, Kim IH, Nam TJ. Chemoprotective effects of a protein from the red algae Porphyra yezoensis on acetaminophen-induced liver injury in rats. Phytother Res. 2008;22(9):1149-1153. doi:10.1002/ptr.2368.
  • Almasi F, Khazaei M, Chehrei S, Ghanbari A. Hepatoprotective effects of Tribulus terrestris hydro-alcholic extract on nonalcoholic fatty liver- induced rats. Int J Morphol. 2017;35(1):345-350.
  • Wang L, Tang K, Zhang Q, et al. Somatostatin receptor-based molecular imaging and therapy for neuroendocrine tumors. Biomed Res Int. 2013;2013:102819. doi:10.1155/2013/102819.
  • Harvey M, Cave G. Octreotide may attenuate absorption and ameliorate toxicity following enteric drug overdose. Medical hypotheses. 2013;81(3):424-425. doi:10.1016/j.mehy.2013.05.036.
  • Sun H, Zou S, Candiotti KA, et al. Octreotide attenuates acute kidney ınjury after hepatic ıschemia and reperfusion by enhancing autophagy. Sci Rep. 2017;7:42701. doi:10.1038/srep42701.
  • Bhushan B, Apte U. Liver Regeneration after acetaminophen hepatotoxicity: mechanisms and therapeutic opportunities. Am J Pathol. 2019;189(4):719-729. doi:10.1016/j.ajpath.2018.12.006.
  • Yang J, Sun H, Takacs P, et al. The effect of octreotide on hepatic ischemia-reperfusion injury in a rabbit model. Transplant Proc. 2013;45(6):2433-2438. doi:10.1016/j.transproceed.2013.02.112.
  • Zou S, Sun H, Peng Y, Yang S, Yang J. Protective effect of octreotide against liver ıschemic reperfusion ınjury in rats. JBT. 2020;10(8):1115-1121.doi:10.1166/jbt.2020.2399.
  • Guo SB, Li Q, Duan ZJ, Wang QM, Zhou Q, Sun XY. Octreotide attenuates liver fibrosis by inhibiting hepatic heme oxygenase-1 expression. Mol Med Rep. 2015;11(1):83-90. doi:10.3892/mmr.2014.2735.
  • Zhang C, An R, Bao YW, et al. Inhibitory effects of octreotide on the progression of hepatic fibrosis via the regulation of Bcl-2/Bax and PI3K/AKT signaling pathways. Int Immunopharmacol. 2019;73:515-526. doi:10.1016/j.intimp.2019.05.055.
  • Du Z, Zhou Y, Lu X, et al. Octreotide prevents liver failure through upregulating 5'-methylthioadenosine in extended hepatectomized rats. Liver Int. 2016;36(2):212-222. doi:10.1111/liv.12863.
  • Elsayed MFE, Sabry AMM, El-lakany ABY. The potential effect of octreotide on liver fibrosis induced by alcohol in albino rats. IJNRLS. 2021;8(5):0-22.
  • Bessems JG, Vermeulen NP. Paracetamol (acetaminophen)-induced toxicity: molecular and biochemical mechanisms, analogues and protective approaches. Crit Rev Toxicol. 2001;31(1):55-138. doi:10.1080/20014091111677.
  • Aktas Senocak E, Utlu N, Kurt S, Kucukler S, Kandemir FM. Sodium pentaborate prevents acetaminophen-ınduced hepatorenal ınjury by suppressing oxidative stress, lipid peroxidation, apoptosis, and ınflammatory cytokines in rats. Biol Trace Elem Res. 2024;202(3):1164-1173. doi:10.1007/s12011-023-03755-4.
  • Konturek PC, Brzozowski T, Walter B, et al. Ghrelin-induced gastroprotection against ischemia-reperfusion injury involves an activation of sensory afferent nerves and hyperemia mediated by nitric oxide. Eur J Pharmacol. 2006;536(1-2):171-181. doi:10.1016/j.ejphar.2006.02.032.
  • Pederzoli P, Bassi C, Falconi M, Camboni MG. Efficacy of octreotide in the prevention of complications of elective pancreatic surgery. Italian Study Group. Br J Surg. 1994;81(2):265-269. doi:10.1002/bjs.1800810237.
  • Meier RF, Reichert MM. Octreotide: a clinical update. Saudi J Gastroenterol. 1998;4(3):147-155.
  • González-Castejón M, Visioli F, Rodriguez-Casado A. Diverse biological activities of dandelion. Nutr Rev. 2012;70(9):534-547. doi:10.1111/j.1753-4887.2012.00509. x.
  • Chen YH, Lin FY, Liu PL, et al. Antioxidative and hepatoprotective effects of magnolol on acetaminophen-induced liver damage in rats. Arch Pharm Res. 2009;32(2):221-228. doi:10.1007/s12272-009-1139-8.
  • Girish C, Koner BC, Jayanthi S, Rao KR, Rajesh B, Pradhan SC. Hepatoprotective activity of six polyherbal formulations in paracetamol induced liver toxicity in mice. Indian J Med Res. 2009;129(5):569-578.
  • Gutiérrezl RMP, Solís RV. Hepatoprotective and inhibition of oxidative stress in liver of prostechea michuacana. Rec Na Prod. 2009; 3:46-51.
  • Anantha KC, Siva RC, Manohar RA. Hepatoprotective effect of biherbal ethanolic extract against paracetamol-induced hepatic damage in albino rats. J Ayurveda Integr Med. 2012;3(4):198-203. doi:10.4103/0975-9476.104436.
  • Bhadauria M. Dose-dependent hepatoprotective effect of emodin against acetaminophen-induced acute damage in rats. Exp Toxicol Pathol. 2010;62(6):627-635. doi: 10.1016/j.etp.2009.08.006.
  • Igami K, Shimojo Y, Ito H, Miyazaki T, Kashiwada Y. Hepatoprotective effect of fermented ginseng and its major constituent compound K in a rat model of paracetamol (acetaminophen)-induced liver injury. J Pharm Pharmacol. 2015;67(4):565-572. doi:10.1111/jphp.12342.
  • Kamiş N, Karabağ Oban F. Investigation of Caffeic Acid Phenethly Ester Effect on Inflammation and Oxidative Stress in Paracetamol Induced Hepatotoxicity. AUJVS.2019;14(3):290-298. doi:10.17094/ataunivbd.552207.
  • Helal MG, Samra YA. Irbesartan mitigates acute liver injury, oxidative stress, and apoptosis induced by acetaminophen in mice. J Biochem Mol Toxicol. 2020;34(12): e22447. doi:10.1002/jbt.22447.
  • Xu J, Liu X, Koyama Y, et al. The types of hepatic myofibroblasts contributing to liver fibrosis of different etiologies. Front Pharmacol. 2014;5: 167.doi:10.3389/fphar.2014.00167.
  • Wang T, Zhou X, Liu H, et al. Fuzheng Huayu capsule as an adjuvant treatment for HBV-related cirrhosis: A systematic review and meta-analysis. Phytother Res. 2018;32(5):757-768. doi:10.1002/ptr.6009.
  • Kim JS, Koppula S, Yum MJ, et al. Anti-fibrotic effects of Cuscuta chinensis with in vitro hepatic stellate cells and a thioacetamide-induced experimental rat model. Pharm Biol. 2017;55(1):1909-1919. doi:10.1080/13880209.2017.1340965.
  • Paldır E. APAP ile oluşturulan karaciğer hasarında ozon ile L-karnitin tedavisinin kan ve doku antioksidan parametreleri ile biyokimyasal değerlere etkileri. Yüksek Lisans Tezi. Kafkas Üniversitesi Sağlık Bilimleri Enstitüsü, Kars, 2017, s.112.

Sıçanlarda Asetaminofen Kaynaklı Karaciğer Hasarına Oktreotidin Koruyucu Etkileri: Biyokimyasal ve Histopatolojik Değerlendirme

Yıl 2025, Cilt: 34 Sayı: 3, 441 - 450, 30.12.2025
https://doi.org/10.34108/eujhs.1671907

Öz

Bu araştırmanın amacı, somatostatin analoğu olan oktreotidin sıçanlarda asetaminofenle oluşturulan akut karaciğer hasarına karşı olası koruyucu etkilerini değerlendirmektir. Çalışmada, 8–10 haftalık toplam 28 yetişkin erkek Wistar albino sıçan rastgele dört gruba ayrıldı. Grup 1 kontrol olarak kullanıldı, Grup 2'ye 1 g/kg oral asetaminofen verildi, Grup 3'e 300 µg/kg intraperitoneal oktreotid uygulandı, Grup 4 her iki ajanla tedavi edildi, oktreotid asetaminofen uygulamasından 30 dakika sonra verildi. İlaç uygulamasından 24 saat sonra genel anestezi altında kan ve karaciğer dokusu örnekleri alındı. Karaciğer dokuları Hematoksilen-Eozin ile boyandı; serum örneklerinden aspartat aminotransferaz, alanin aminotransferaz, alkalin fosfataz, total antioksidan kapasite, total oksidan kapasitesi ve malondialdehid düzeyleri ölçüldü. Asetaminofen uygulanan sıçanlarda aspartat aminotransferaz, alanin aminotransferaz, alkalen fosfataz aktiviteleri ve toplam oksidan kapasitesi diğer gruplara göre anlamlı derecede yüksekti. Benzer şekilde, malondialdehit seviyeleri de daha yüksekti, ancak bu değerler istatistiksel olarak anlamlı değildi. Toplam antioksidan kapasite değerleri ise diğer guplara göre asetaminofen grubunda düşüktü. Tedavi grubunda ise aspartat aminotransferaz, alanin aminotransferaz, alkalin fosfataz ve total oksidan kapasitesi, yalnızca asetaminofen verilen gruba kıyasla anlamlı şekilde düşüktü. Histopatolojik değerlendirmede asetaminofen grubunda ciddi doku hasarı gözlenirken, tedavi grubunda daha az hasar tespit edildi. Malondialdehid düzeyleri tedavi grubunda daha düşük seyretse de bu fark istatistiksel olarak anlam kazanmadı. Elde edilen bulgular, oktreotidin asetaminofen kaynaklı karaciğer hasarını kısmen hafifletebileceğini göstermektedir. Ancak bu etkinin mekanizmasının daha iyi anlaşılabilmesi için ileri çalışmalara ihtiyaç vardır.

Etik Beyan

Bu çalışma için Pamukkale Üniversitesi Hayvan Deneyleri Etik Kurulu’ndan etik kurul onayı alınmıştır (Tarih: 29.01.2019, Sayı: 2019/01).

Destekleyen Kurum

Bu araştırma Pamukkale Üniversitesi Bilimsel Araştırma Koordinasyon Ofisi tarafından 2019SABE015 proje numarasıyla desteklenmiştir. Bu araştırma MA'nın yüksek lisans tezinden üretilmiştir.

Proje Numarası

2019/01

Kaynakça

  • Lin YH, Lin YC, Hou YT. Prospective application of tannic acid in acetaminophen (APAP)-induced acute liver failure. Int J Mol Sci. 2023;25(1):317. doi:10.3390/ijms25010317.
  • Golestan Jahromi M, Nabavizadeh F, Vahedian J, Nahrevanian H, Dehpour AR, Zare-Mehrjardi A. Protective effect of ghrelin on acetaminophen-induced liver injury in rat. Peptides. 2010;31(11):2114-2117. doi:10.1016/j.peptides.2010.08.009.
  • Koç A, Gazi M, Caner Sayar A, et al. Molecular mechanism of the protective effect of adenosine triphosphate against paracetamol-induced liver toxicity in rats. Gen Physiol Biophys. 2023;42(2):201-208. doi:10.4149/gpb_2022055.
  • Sabea AM, AlKhamas AJH, Sahib BS, Faris JK. Biochemical and Histopathological effects of acetaminophen and protective effects of naringin on liver rats. IJFMT. 2021;15(4): 794-801. doi:10.37506/ijfmt. v15i4.16801.
  • Al-Doaiss AA. Hepatotoxicity-induced by the therapeutic dose of acetaminophen and the ameliorative effect of oral co-administration of selenium/Tribulus terrestris extract in rats. Int J Morphol. 2020;38(5):1444-1454. doi:10.4067/S0717-95022020000501444.
  • AlWahsh M, Othman A, Hamadneh L, et al. Second exposure to acetaminophen overdose is associated with liver fibrosis in mice. EXCLIJ. 2019;18:51-62.
  • Ahmad ST, Arjumand W, Nafees S, et al. Hesperidin alleviates acetaminophen induced toxicity in Wistar rats by abrogation of oxidative stress, apoptosis and inflammation. Toxicol Lett. 2012;208(2):149-161. doi:10.1016/j.toxlet.2011.10.023.
  • Yan M, Huo Y, Yin S, Hu H. Mechanisms of acetaminophen-induced liver injury and its implications for therapeutic interventions. Red Biol. 2018;17:274-283 doi:10.1016/j.redox.2018.04.019.
  • Erfidan MA, Akkol EK, Sevimli A, Civelek T. Effects of pomegranate (Punica granatum L.) on paracetamol induced acute hepatic damage in mice. Kocatepe Vet J. 2016;9(4):273-280 doi:10.5578/kvj.28156.
  • Zhang J, Song Q, Han X, et al. Multi-targeted protection of acetaminophen-induced hepatotoxicity in mice by tannic acid. Int Immunopharmacol. 2017; 47:95-105. doi: 10.1016/j.intimp.2017.03.027.
  • Aziz NM, Ragy MM, Ahmed SM. Somatostatin analogue, Octreotide, improves restraint stress-induced liver injury by ameliorating oxidative stress, inflammatory response, and activation of hepatic stellate cells. Cell Stress Chaperones. 2018;23(6):1237-1245. doi:10.1007/s12192-018-0929-7.
  • Liao J, Lu Q, Li Z, Li J, Zhao Q, Li J. Acetaminophen-induced liver injury: Molecular mechanism and treatments from natural products. Front Pharmacol. 2023;14:1122632. doi:10.3389/fphar.2023.1122632.
  • European Association for the Study of the Liver. EASL Clinical Practice Guidelines: Drug-induced liver injury. J Hepatol. 2019;70(6):1222-1261. doi:10.1016/j.jhep.2019.02.014.
  • Ntamo Y, Ziqubu K, Chellan N, et al. Drug-induced liver ınjury: clinical evidence of n-acetyl cysteine protective effects. Oxid Med Cell Longev. 2021;2021:3320325. doi:10.1155/2021/3320325.
  • Du K, Ramachandran A, Jaeschke H. Oxidative stress during acetaminophen hepatotoxicity: Sources, pathophysiological role and therapeutic potential. Redox Biol. 2016;10:148-156. doi:10.1016/j.redox.2016.10.001.
  • Hwang HJ, Kwon MJ, Kim IH, Nam TJ. Chemoprotective effects of a protein from the red algae Porphyra yezoensis on acetaminophen-induced liver injury in rats. Phytother Res. 2008;22(9):1149-1153. doi:10.1002/ptr.2368.
  • Almasi F, Khazaei M, Chehrei S, Ghanbari A. Hepatoprotective effects of Tribulus terrestris hydro-alcholic extract on nonalcoholic fatty liver- induced rats. Int J Morphol. 2017;35(1):345-350.
  • Wang L, Tang K, Zhang Q, et al. Somatostatin receptor-based molecular imaging and therapy for neuroendocrine tumors. Biomed Res Int. 2013;2013:102819. doi:10.1155/2013/102819.
  • Harvey M, Cave G. Octreotide may attenuate absorption and ameliorate toxicity following enteric drug overdose. Medical hypotheses. 2013;81(3):424-425. doi:10.1016/j.mehy.2013.05.036.
  • Sun H, Zou S, Candiotti KA, et al. Octreotide attenuates acute kidney ınjury after hepatic ıschemia and reperfusion by enhancing autophagy. Sci Rep. 2017;7:42701. doi:10.1038/srep42701.
  • Bhushan B, Apte U. Liver Regeneration after acetaminophen hepatotoxicity: mechanisms and therapeutic opportunities. Am J Pathol. 2019;189(4):719-729. doi:10.1016/j.ajpath.2018.12.006.
  • Yang J, Sun H, Takacs P, et al. The effect of octreotide on hepatic ischemia-reperfusion injury in a rabbit model. Transplant Proc. 2013;45(6):2433-2438. doi:10.1016/j.transproceed.2013.02.112.
  • Zou S, Sun H, Peng Y, Yang S, Yang J. Protective effect of octreotide against liver ıschemic reperfusion ınjury in rats. JBT. 2020;10(8):1115-1121.doi:10.1166/jbt.2020.2399.
  • Guo SB, Li Q, Duan ZJ, Wang QM, Zhou Q, Sun XY. Octreotide attenuates liver fibrosis by inhibiting hepatic heme oxygenase-1 expression. Mol Med Rep. 2015;11(1):83-90. doi:10.3892/mmr.2014.2735.
  • Zhang C, An R, Bao YW, et al. Inhibitory effects of octreotide on the progression of hepatic fibrosis via the regulation of Bcl-2/Bax and PI3K/AKT signaling pathways. Int Immunopharmacol. 2019;73:515-526. doi:10.1016/j.intimp.2019.05.055.
  • Du Z, Zhou Y, Lu X, et al. Octreotide prevents liver failure through upregulating 5'-methylthioadenosine in extended hepatectomized rats. Liver Int. 2016;36(2):212-222. doi:10.1111/liv.12863.
  • Elsayed MFE, Sabry AMM, El-lakany ABY. The potential effect of octreotide on liver fibrosis induced by alcohol in albino rats. IJNRLS. 2021;8(5):0-22.
  • Bessems JG, Vermeulen NP. Paracetamol (acetaminophen)-induced toxicity: molecular and biochemical mechanisms, analogues and protective approaches. Crit Rev Toxicol. 2001;31(1):55-138. doi:10.1080/20014091111677.
  • Aktas Senocak E, Utlu N, Kurt S, Kucukler S, Kandemir FM. Sodium pentaborate prevents acetaminophen-ınduced hepatorenal ınjury by suppressing oxidative stress, lipid peroxidation, apoptosis, and ınflammatory cytokines in rats. Biol Trace Elem Res. 2024;202(3):1164-1173. doi:10.1007/s12011-023-03755-4.
  • Konturek PC, Brzozowski T, Walter B, et al. Ghrelin-induced gastroprotection against ischemia-reperfusion injury involves an activation of sensory afferent nerves and hyperemia mediated by nitric oxide. Eur J Pharmacol. 2006;536(1-2):171-181. doi:10.1016/j.ejphar.2006.02.032.
  • Pederzoli P, Bassi C, Falconi M, Camboni MG. Efficacy of octreotide in the prevention of complications of elective pancreatic surgery. Italian Study Group. Br J Surg. 1994;81(2):265-269. doi:10.1002/bjs.1800810237.
  • Meier RF, Reichert MM. Octreotide: a clinical update. Saudi J Gastroenterol. 1998;4(3):147-155.
  • González-Castejón M, Visioli F, Rodriguez-Casado A. Diverse biological activities of dandelion. Nutr Rev. 2012;70(9):534-547. doi:10.1111/j.1753-4887.2012.00509. x.
  • Chen YH, Lin FY, Liu PL, et al. Antioxidative and hepatoprotective effects of magnolol on acetaminophen-induced liver damage in rats. Arch Pharm Res. 2009;32(2):221-228. doi:10.1007/s12272-009-1139-8.
  • Girish C, Koner BC, Jayanthi S, Rao KR, Rajesh B, Pradhan SC. Hepatoprotective activity of six polyherbal formulations in paracetamol induced liver toxicity in mice. Indian J Med Res. 2009;129(5):569-578.
  • Gutiérrezl RMP, Solís RV. Hepatoprotective and inhibition of oxidative stress in liver of prostechea michuacana. Rec Na Prod. 2009; 3:46-51.
  • Anantha KC, Siva RC, Manohar RA. Hepatoprotective effect of biherbal ethanolic extract against paracetamol-induced hepatic damage in albino rats. J Ayurveda Integr Med. 2012;3(4):198-203. doi:10.4103/0975-9476.104436.
  • Bhadauria M. Dose-dependent hepatoprotective effect of emodin against acetaminophen-induced acute damage in rats. Exp Toxicol Pathol. 2010;62(6):627-635. doi: 10.1016/j.etp.2009.08.006.
  • Igami K, Shimojo Y, Ito H, Miyazaki T, Kashiwada Y. Hepatoprotective effect of fermented ginseng and its major constituent compound K in a rat model of paracetamol (acetaminophen)-induced liver injury. J Pharm Pharmacol. 2015;67(4):565-572. doi:10.1111/jphp.12342.
  • Kamiş N, Karabağ Oban F. Investigation of Caffeic Acid Phenethly Ester Effect on Inflammation and Oxidative Stress in Paracetamol Induced Hepatotoxicity. AUJVS.2019;14(3):290-298. doi:10.17094/ataunivbd.552207.
  • Helal MG, Samra YA. Irbesartan mitigates acute liver injury, oxidative stress, and apoptosis induced by acetaminophen in mice. J Biochem Mol Toxicol. 2020;34(12): e22447. doi:10.1002/jbt.22447.
  • Xu J, Liu X, Koyama Y, et al. The types of hepatic myofibroblasts contributing to liver fibrosis of different etiologies. Front Pharmacol. 2014;5: 167.doi:10.3389/fphar.2014.00167.
  • Wang T, Zhou X, Liu H, et al. Fuzheng Huayu capsule as an adjuvant treatment for HBV-related cirrhosis: A systematic review and meta-analysis. Phytother Res. 2018;32(5):757-768. doi:10.1002/ptr.6009.
  • Kim JS, Koppula S, Yum MJ, et al. Anti-fibrotic effects of Cuscuta chinensis with in vitro hepatic stellate cells and a thioacetamide-induced experimental rat model. Pharm Biol. 2017;55(1):1909-1919. doi:10.1080/13880209.2017.1340965.
  • Paldır E. APAP ile oluşturulan karaciğer hasarında ozon ile L-karnitin tedavisinin kan ve doku antioksidan parametreleri ile biyokimyasal değerlere etkileri. Yüksek Lisans Tezi. Kafkas Üniversitesi Sağlık Bilimleri Enstitüsü, Kars, 2017, s.112.
Toplam 45 adet kaynakça vardır.

Ayrıntılar

Birincil Dil İngilizce
Konular Histoloji ve Embriyoloji
Bölüm Araştırma Makalesi
Yazarlar

Murat Akbulut 0000-0002-5965-424X

Semih Tan 0000-0002-5609-9594

Hülya Çetin 0000-0001-8731-0631

Saim Özdamar 0000-0003-4440-5360

Proje Numarası 2019/01
Gönderilme Tarihi 13 Mayıs 2025
Kabul Tarihi 18 Kasım 2025
Yayımlanma Tarihi 30 Aralık 2025
Yayımlandığı Sayı Yıl 2025 Cilt: 34 Sayı: 3

Kaynak Göster

APA Akbulut, M., Tan, S., Çetin, H., Özdamar, S. (2025). Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation. Sağlık Bilimleri Dergisi, 34(3), 441-450. https://doi.org/10.34108/eujhs.1671907
AMA Akbulut M, Tan S, Çetin H, Özdamar S. Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation. JHS. Aralık 2025;34(3):441-450. doi:10.34108/eujhs.1671907
Chicago Akbulut, Murat, Semih Tan, Hülya Çetin, ve Saim Özdamar. “Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation”. Sağlık Bilimleri Dergisi 34, sy. 3 (Aralık 2025): 441-50. https://doi.org/10.34108/eujhs.1671907.
EndNote Akbulut M, Tan S, Çetin H, Özdamar S (01 Aralık 2025) Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation. Sağlık Bilimleri Dergisi 34 3 441–450.
IEEE M. Akbulut, S. Tan, H. Çetin, ve S. Özdamar, “Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation”, JHS, c. 34, sy. 3, ss. 441–450, 2025, doi: 10.34108/eujhs.1671907.
ISNAD Akbulut, Murat vd. “Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation”. Sağlık Bilimleri Dergisi 34/3 (Aralık2025), 441-450. https://doi.org/10.34108/eujhs.1671907.
JAMA Akbulut M, Tan S, Çetin H, Özdamar S. Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation. JHS. 2025;34:441–450.
MLA Akbulut, Murat vd. “Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation”. Sağlık Bilimleri Dergisi, c. 34, sy. 3, 2025, ss. 441-50, doi:10.34108/eujhs.1671907.
Vancouver Akbulut M, Tan S, Çetin H, Özdamar S. Protective Effects of Octreotide on Acetaminophen-Induced Liver Damage in Rats: Biochemical and Histopathological Evaluation. JHS. 2025;34(3):441-50.