Research Article
BibTex RIS Cite

Zerdeçalın (Kurkumın) Albino Wistar Sıçanlarda Kronik Asetaminofen Kaynaklı Karaciğer Hasarı Üzerindeki Hepatoprotektif Etkisi

Year 2026, Volume: 21 Issue: 1 , 111 - 122 , 30.03.2026
https://doi.org/10.55525/tjst.1729061
https://izlik.org/JA83HE88DW

Abstract

Asetaminofen yaygın olarak kullanılan bir analjezik ve antipiretik olup, özellikle yüksek dozlarda hepatotoksik etkileriyle de bilinmektedir. Bu çalışmanın amacı, kurkuminin parasetamol (asetaminofen) kaynaklı hepatotoksisiteye karşı hepatoprotektif bir ajan olarak etkinliğini değerlendirmektir. Bu çalışmada, 130–150 g ağırlığında, her iki cinsiyetten 30 albino Wistar sıçan kullanılmış ve hayvanlar beş gruba ayrılmıştır. Bu gruplara (1–5) farklı uygulamalar yapılmıştır: standart kemirgen yemi (kontrol), asetaminofen, kurkumin ve asetaminofen ile kurkuminin hem eş zamanlı hem de ardışık kombinasyonları. Kurkuminin biyoyararlanımını artırmak amacıyla intraperitoneal uygulama yöntemi kullanılmıştır. Her iki ajanın uygulanması 6 hafta (42 gün) sürmüştür. AST, ALT ve ALP serum düzeyleri dahil olmak üzere biyokimyasal parametreler ölçülmüştür. Karaciğer dokuları, karaciğer hasarını ve kurkuminin koruyucu etkilerini değerlendirmek amacıyla histopatolojik olarak incelenmiştir. Özellikle asetaminofen uygulanan gruplarda karaciğer enzim düzeylerinde artış gözlenmiştir. Kurkumin uygulanan gruplarda ALT düzeyinde anlamlı bir azalma (p<0.05), ayrıca AST ve ALP düzeylerinde de azalma (p>0.05) saptanmıştır. Histopatolojik analiz, kurkumin uygulanan gruplarda daha az karaciğer hasarı ve iyileşmiş karaciğer yapısı göstermiştir. Kurkuminin, oksidatif stresi azaltarak ve mitokondriyal fonksiyonu koruyarak asetaminofen kaynaklı karaciğer hasarını azaltma yeteneğine sahip olduğu, hem biyokimyasal hem de histopatolojik bulgularla desteklenmiştir.

References

  • Vaja R, Rana M. Drugs and the liver. Anaesth. Intensive Care Med. 2020;21(10):517–523.
  • Rani J, Dhull SB, Rose PK, Kidwai MK. Drug-induced liver injury and anti-hepatotoxic effect of herbal compounds: a metabolic mechanism perspective. Phytomedicine 2024;122:155142.
  • Yan M, Huo Y, Yin S, Hu H. Mechanisms of acetaminophen-induced liver injury and its implications for therapeutic interventions. Redox Biol. 2018;17:274–283.
  • Zhou Y, Wang J, Zhang D, Liu J, Wu Q, Chen J, Tan P, Xing B, Han Y, Zhang P, Xiao X, Pei J. Mechanism of drug-induced liver injury and hepatoprotective effects of natural drugs. Chin. Med. 2021; 16(1): 2–3.
  • Yaghi C, Assaf A. Acetaminophen toxicity at therapeutic doses. Intern. Med. Rev. 2017; 3(11): 1–13.
  • Khan H, Ullah H, Nabavi SM. Mechanistic insights of hepatoprotective effects of curcumin: Therapeutic updates and future prospects. Food Chem. Toxicol. 2019; 124: 182–191.
  • Aziziaram Z, Bilal I, Zhong Y, Mahmod AK, Roshandel MR. Protective effects of curcumin against naproxen-induced mitochondrial dysfunction in rat kidney tissue. Cell. Mol. Biomed. Rep. 2021; 1(1): 23–32.
  • John OC, Kalu AN, Christopher OO, Amarachi OC. Phytochemical composition and toxicological profiling of Curcuma longa (turmeric) root extract in rats. Int. J. Biochem. Res. Rev. 2024; 33(1): 1–12.
  • Zubaidah E, Susanti I, Sujuti H, Martati E, Rahayu AP, Srianta I, Tewfik I. The distinctive hepatoprotective activity of turmeric kombucha (Curcuma longa) induced by diethylnitrosamine in Balb/C mice. Food Biosci. 2023; 55: 103043.
  • Stanić Z. Curcumin, a compound from natural sources, a true scientific challenge – A review. Plant Foods Hum. Nutr. 2017; 72(1): 1–12.
  • Hewlings S, Kalman D. Curcumin: A review of its effects on human health. Foods 2017; 6(10): 92.
  • Kocaadam B, Şanlier N. Curcumin, an active component of turmeric (Curcuma longa), and its effects on health. Crit. Rev. Food Sci. Nutr. 2017; 57(13): 2889–2895.
  • Prasad S, Tyagi AK, Aggarwal BB. Recent developments in delivery, bioavailability, absorption and metabolism of curcumin: The golden pigment from golden spice. Cancer Res. Treat. 2014; 46(1): 2–18.
  • Bertoncini-Silva C, Vlad A, Ricciarelli R, Fassini PG, Suen VMM, Zingg JM. Enhancing the bioavailability and bioactivity of curcumin for disease prevention and treatment. Antioxidants 2024; 13(3): 331.
  • Ozturk NB, Uskudar E, Toruner M, Simsek C, Gurakar A. Drug-induced liver injury: Diagnosis, management and the role of liver transplantation. Hepatol. Forum 2024; 5(4): 1–6.
  • Sigma-Aldrich. Trichrome stains. 2015. Available from: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/204/644/ht15.pdf (Accessed 20 Nov 2024).
  • Ochei JO, Kolhatkar AA. Medical Laboratory Science: Theory and Practice. New Delhi: Tata McGraw-Hill Publishing Company; 2003. p. 152–169.
  • Ullah N, Khan MN. Curcumin: A review of its effects on human health. J. Clin. Med. Res. 2017; 9(7): 524–533.
  • Bektur NE, Sahin E, Baycu C, Unver G. Protective effects of silymarin against acetaminophen-induced hepatotoxicity and nephrotoxicity in mice. Toxicol. Ind. Health 2016; 32(4): 589–600.
  • El-Fadil HA, Edress N, Khorshid N, Amin N. Protective impact of curcumin against paracetamol-induced hepatotoxicity in rats. Int. J. Pharm. Res. Allied Sci. 2019; 8(1): 45–49.
  • 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.
  • Eassawy MMT, Salem AA, Ismail AFM. Biochemical study on the protective effect of curcumin on acetaminophen and gamma‐irradiation induced hepatic toxicity in rats. Environ. Toxicol. 2021; 36(5): 748–763.
  • Chen X, Tian F, Lun P, Feng Y. Curcumin inhibits HGF-induced EMT by regulating c-MET-dependent PI3K/Akt/mTOR signaling pathways in meningioma. Evid. Based Complement. Alternat. Med. 2021; 2021: 5574555. https://doi.org/10.1155/2021/5574555.
  • Jagetia GC, Rajanikant GK. Curcumin stimulates the antioxidant mechanisms in mouse skin exposed to fractionated γ-irradiation. Antioxidants 2015; 4(1): 25–41.
  • Cao W, Zhang Y, Li A, Yu P, Song L, Liang J, Cao N, Gao J, Xu R, Ma Y, Tang X. Curcumin reverses hepatic epithelial mesenchymal transition induced by trichloroethylene by inhibiting IL-6R/STAT3. Toxicol. Mech. Methods 2021; 31(8): 589–599.
  • Bayomy NA, Elshafey SH, Mosaed MM, Hegazy AM. Protective effect of curcumin versus N-acetylcysteine on acetaminophen-induced hepatotoxicity in adult albino rats. J. Cytol. Histol. 2015; S3: 2–8.
  • Chidiac AS, Buckley NA, Noghrehchi F, Cairns R. Paracetamol (acetaminophen) overdose and hepatotoxicity: mechanism, treatment, prevention measures, and estimates of burden of disease. Expert Opin. Drug Metab. Toxicol. 2023; 19(5): 297–317.
  • Tung BT, Hai NT, Son PK. Hepatoprotective effect of phytosome curcumin against paracetamol-induced liver toxicity in mice. Braz. J. Pharm. Sci. 2017; 53(1): e16136. https://doi.org/10.1590/s2175-97902017000116136.
  • Jaeschke H, Akakpo JY, Umbaugh DS, Ramachandran A. Novel therapeutic approaches against acetaminophen-induced liver injury and acute liver failure. Toxicol. Sci. 2020; 174(2): 159–167.
  • Ahmad MM, Rezk NA, Fawzy A, Sabry M. Protective effects of curcumin and silymarin against paracetamol-induced hepatotoxicity in adult male albino rats. Gene 2019; 712: 143966.
  • Bai Q, Yan H, Sheng Y, Jin Y, Shi L, Ji L, Wang Z. Long-term acetaminophen treatment induced liver fibrosis in mice and the involvement of Egr-1. Toxicology 2017; 382: 47–58.

Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats

Year 2026, Volume: 21 Issue: 1 , 111 - 122 , 30.03.2026
https://doi.org/10.55525/tjst.1729061
https://izlik.org/JA83HE88DW

Abstract

Acetaminophen is a widely used analgesic and antipyretic, but it is also known for its hepatotoxic effects, particularly at overdose level. The aim of this study was to evaluate the efficacy of curcumin as a hepatoprotective agent against paracetamol (acetaminophen) induced hepatotoxicity. This study used 30 albino Wistar rats (both males and females) weighing 130-150g, divided into five groups. These groups were administered various treatments; standard rodent feed (control), acetaminophen, curcumin, and combinations of acetaminophen and curcumin both simultaneously and sequentially. Intra-peritoneal administration was employed to enhance curcumin’s bioavailability. The administration of both agents lasted 6 weeks (42 days). Biochemical parameters, including serum levels of AST, ALT, and ALP, were measured, and liver tissues were examined histopathologically to assess liver damage and the protective effects of curcumin. Elevated liver enzyme levels were observed, particularly in the groups treated with acetaminophen. The curcumin-treated groups showed a significant decrease in ALT (p<0.05), as well as in AST and ALP (p>0.05). Histopathological analysis revealed less hepatic damage and improved liver structure in curcumin-treated groups. Curcumin demonstrated the ability to reduce acetaminophen-induced liver damage by mitigating oxidative stress and preserving mitochondrial function, as supported by both biochemical and histopathological findings.

Ethical Statement

The protocol for this study was approved by University Of Ibadan Animal Care and Use Research Ethics Committee (UI-ACUREC), Ibadan, Oyo state. Reference number: UI-ACUREC/070-0524/23.

Supporting Institution

THE STUDY WAS CARRIED OUT IN UNIVERSITY OF IBADAN, IBADAN CITY, NIGERIA

References

  • Vaja R, Rana M. Drugs and the liver. Anaesth. Intensive Care Med. 2020;21(10):517–523.
  • Rani J, Dhull SB, Rose PK, Kidwai MK. Drug-induced liver injury and anti-hepatotoxic effect of herbal compounds: a metabolic mechanism perspective. Phytomedicine 2024;122:155142.
  • Yan M, Huo Y, Yin S, Hu H. Mechanisms of acetaminophen-induced liver injury and its implications for therapeutic interventions. Redox Biol. 2018;17:274–283.
  • Zhou Y, Wang J, Zhang D, Liu J, Wu Q, Chen J, Tan P, Xing B, Han Y, Zhang P, Xiao X, Pei J. Mechanism of drug-induced liver injury and hepatoprotective effects of natural drugs. Chin. Med. 2021; 16(1): 2–3.
  • Yaghi C, Assaf A. Acetaminophen toxicity at therapeutic doses. Intern. Med. Rev. 2017; 3(11): 1–13.
  • Khan H, Ullah H, Nabavi SM. Mechanistic insights of hepatoprotective effects of curcumin: Therapeutic updates and future prospects. Food Chem. Toxicol. 2019; 124: 182–191.
  • Aziziaram Z, Bilal I, Zhong Y, Mahmod AK, Roshandel MR. Protective effects of curcumin against naproxen-induced mitochondrial dysfunction in rat kidney tissue. Cell. Mol. Biomed. Rep. 2021; 1(1): 23–32.
  • John OC, Kalu AN, Christopher OO, Amarachi OC. Phytochemical composition and toxicological profiling of Curcuma longa (turmeric) root extract in rats. Int. J. Biochem. Res. Rev. 2024; 33(1): 1–12.
  • Zubaidah E, Susanti I, Sujuti H, Martati E, Rahayu AP, Srianta I, Tewfik I. The distinctive hepatoprotective activity of turmeric kombucha (Curcuma longa) induced by diethylnitrosamine in Balb/C mice. Food Biosci. 2023; 55: 103043.
  • Stanić Z. Curcumin, a compound from natural sources, a true scientific challenge – A review. Plant Foods Hum. Nutr. 2017; 72(1): 1–12.
  • Hewlings S, Kalman D. Curcumin: A review of its effects on human health. Foods 2017; 6(10): 92.
  • Kocaadam B, Şanlier N. Curcumin, an active component of turmeric (Curcuma longa), and its effects on health. Crit. Rev. Food Sci. Nutr. 2017; 57(13): 2889–2895.
  • Prasad S, Tyagi AK, Aggarwal BB. Recent developments in delivery, bioavailability, absorption and metabolism of curcumin: The golden pigment from golden spice. Cancer Res. Treat. 2014; 46(1): 2–18.
  • Bertoncini-Silva C, Vlad A, Ricciarelli R, Fassini PG, Suen VMM, Zingg JM. Enhancing the bioavailability and bioactivity of curcumin for disease prevention and treatment. Antioxidants 2024; 13(3): 331.
  • Ozturk NB, Uskudar E, Toruner M, Simsek C, Gurakar A. Drug-induced liver injury: Diagnosis, management and the role of liver transplantation. Hepatol. Forum 2024; 5(4): 1–6.
  • Sigma-Aldrich. Trichrome stains. 2015. Available from: https://www.sigmaaldrich.com/deepweb/assets/sigmaaldrich/product/documents/204/644/ht15.pdf (Accessed 20 Nov 2024).
  • Ochei JO, Kolhatkar AA. Medical Laboratory Science: Theory and Practice. New Delhi: Tata McGraw-Hill Publishing Company; 2003. p. 152–169.
  • Ullah N, Khan MN. Curcumin: A review of its effects on human health. J. Clin. Med. Res. 2017; 9(7): 524–533.
  • Bektur NE, Sahin E, Baycu C, Unver G. Protective effects of silymarin against acetaminophen-induced hepatotoxicity and nephrotoxicity in mice. Toxicol. Ind. Health 2016; 32(4): 589–600.
  • El-Fadil HA, Edress N, Khorshid N, Amin N. Protective impact of curcumin against paracetamol-induced hepatotoxicity in rats. Int. J. Pharm. Res. Allied Sci. 2019; 8(1): 45–49.
  • 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.
  • Eassawy MMT, Salem AA, Ismail AFM. Biochemical study on the protective effect of curcumin on acetaminophen and gamma‐irradiation induced hepatic toxicity in rats. Environ. Toxicol. 2021; 36(5): 748–763.
  • Chen X, Tian F, Lun P, Feng Y. Curcumin inhibits HGF-induced EMT by regulating c-MET-dependent PI3K/Akt/mTOR signaling pathways in meningioma. Evid. Based Complement. Alternat. Med. 2021; 2021: 5574555. https://doi.org/10.1155/2021/5574555.
  • Jagetia GC, Rajanikant GK. Curcumin stimulates the antioxidant mechanisms in mouse skin exposed to fractionated γ-irradiation. Antioxidants 2015; 4(1): 25–41.
  • Cao W, Zhang Y, Li A, Yu P, Song L, Liang J, Cao N, Gao J, Xu R, Ma Y, Tang X. Curcumin reverses hepatic epithelial mesenchymal transition induced by trichloroethylene by inhibiting IL-6R/STAT3. Toxicol. Mech. Methods 2021; 31(8): 589–599.
  • Bayomy NA, Elshafey SH, Mosaed MM, Hegazy AM. Protective effect of curcumin versus N-acetylcysteine on acetaminophen-induced hepatotoxicity in adult albino rats. J. Cytol. Histol. 2015; S3: 2–8.
  • Chidiac AS, Buckley NA, Noghrehchi F, Cairns R. Paracetamol (acetaminophen) overdose and hepatotoxicity: mechanism, treatment, prevention measures, and estimates of burden of disease. Expert Opin. Drug Metab. Toxicol. 2023; 19(5): 297–317.
  • Tung BT, Hai NT, Son PK. Hepatoprotective effect of phytosome curcumin against paracetamol-induced liver toxicity in mice. Braz. J. Pharm. Sci. 2017; 53(1): e16136. https://doi.org/10.1590/s2175-97902017000116136.
  • Jaeschke H, Akakpo JY, Umbaugh DS, Ramachandran A. Novel therapeutic approaches against acetaminophen-induced liver injury and acute liver failure. Toxicol. Sci. 2020; 174(2): 159–167.
  • Ahmad MM, Rezk NA, Fawzy A, Sabry M. Protective effects of curcumin and silymarin against paracetamol-induced hepatotoxicity in adult male albino rats. Gene 2019; 712: 143966.
  • Bai Q, Yan H, Sheng Y, Jin Y, Shi L, Ji L, Wang Z. Long-term acetaminophen treatment induced liver fibrosis in mice and the involvement of Egr-1. Toxicology 2017; 382: 47–58.
There are 31 citations in total.

Details

Primary Language English
Subjects Enzymes, Systems Biology
Journal Section Research Article
Authors

Ayodeji Ajileye 0000-0002-1576-6207

Tobiloba Cole This is me 0009-0003-6560-3099

Submission Date June 27, 2025
Acceptance Date February 7, 2026
Publication Date March 30, 2026
DOI https://doi.org/10.55525/tjst.1729061
IZ https://izlik.org/JA83HE88DW
Published in Issue Year 2026 Volume: 21 Issue: 1

Cite

APA Ajileye, A., & Cole, T. (2026). Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats. Turkish Journal of Science and Technology, 21(1), 111-122. https://doi.org/10.55525/tjst.1729061
AMA 1.Ajileye A, Cole T. Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats. TJST. 2026;21(1):111-122. doi:10.55525/tjst.1729061
Chicago Ajileye, Ayodeji, and Tobiloba Cole. 2026. “Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats”. Turkish Journal of Science and Technology 21 (1): 111-22. https://doi.org/10.55525/tjst.1729061.
EndNote Ajileye A, Cole T (March 1, 2026) Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats. Turkish Journal of Science and Technology 21 1 111–122.
IEEE [1]A. Ajileye and T. Cole, “Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats”, TJST, vol. 21, no. 1, pp. 111–122, Mar. 2026, doi: 10.55525/tjst.1729061.
ISNAD Ajileye, Ayodeji - Cole, Tobiloba. “Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats”. Turkish Journal of Science and Technology 21/1 (March 1, 2026): 111-122. https://doi.org/10.55525/tjst.1729061.
JAMA 1.Ajileye A, Cole T. Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats. TJST. 2026;21:111–122.
MLA Ajileye, Ayodeji, and Tobiloba Cole. “Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats”. Turkish Journal of Science and Technology, vol. 21, no. 1, Mar. 2026, pp. 111-22, doi:10.55525/tjst.1729061.
Vancouver 1.Ayodeji Ajileye, Tobiloba Cole. Hepatoprotectıve Property Of Turmeric (Curcumin) Administration On Chronic Acetaminophen Induced Liver Damage In Albino Wistar Rats. TJST. 2026 Mar. 1;21(1):111-22. doi:10.55525/tjst.1729061