Research Article
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Year 2022, Volume: 12 Issue: 3, 653 - 658, 28.09.2022
https://doi.org/10.33808/clinexphealthsci.1008534

Abstract

References

  • Chapelle T, Op de Beeck B, Driessen A, Roeyen G, Bracke B, Hartman V, Huyghe I, Morrison S, Ysebaert D, Francque S. Estimation of the future remnant liver function is a better tool to predict post-hepatectomy liver failure than platelet-based liver scores. Eur J Surg Oncol. 2017;43(12):2277-2284.
  • Asencio J.M, Vaquero J, Olmedilla L, Garcia Sabrido JL: “Smallfor-flow” syndrome: shifting the “size” paradigm. Med Hypotheses 2013;80(5):573-537.
  • Clavien PA. Liver regeneration: A spotlight on the novel role of platelets and serotonin. Swiss Med Wkly. 2008; 138(25-26): 361-370.
  • Thorgeirsson SS: Hepatic stem cells in liver regeneration. FASEB J. 1996; September 10(11):1249-56.
  • Michalopoulos GK. Liver regeneration after partial hepatectomy: Critical analysis of mechanistic dilemmas. The American Journal of Pathology 2010; 176 (1): 2-13
  • Naseem S, Hussain T, Manzoor S. Interleukin-6: A promising cytokine to support liver regeneration and adaptive immunity in liverpathologies. Cytokine Growth Factor Rev. 2018;39:36-45.
  • Salekzamani S, Mameghani ME, Rezazadeh K. The antioxidant activity of artichoke (Cynara scolymus): A systematic review and meta-analysis of animal studies. Phytother Res. 2019;33(1):55-71.
  • Colak E, Ustuner MC, Tekin N, Colak E, Burukoglu D, Degirmenci I, Guney HV. The hepatocurative effects of Cynara scolymus. Leaf extract on carbon tetrachlorideinducedoxidative stress and hepatic injury in rats. Springerplus. 2016;5:216.
  • Pérez-García F, Adzet T, Cañigueral S. Activity of artichoke leaf extract on reactive oxygen species in human leukocytes. Free Radic Res. 2000;33(5):661–665.
  • Kinra P, Malik A. Ki 67: Are we counting it right?. Indian J Pathol Microbiol 2020;63:98-99.
  • Matsuo K, Murakami T, Kawaguchi D, Hiroshima Y, Koda K, Yamazaki K, Ishida Y, Tanaka K. Histologic features after surgery associating liver partition and portal vein ligation for staged hepatectomy versus those after hepatectomy with portal vein embolization. Surgery. 2016;159(5):1289-1298.
  • Lauterio, A. , Di Sandro S, Concone G, De Carlis R, Giacomoni A, De Carlis L. Current status and perspectives in split liver transplantation. World J. Gastroenterol. 2015; 21: 11003–11015.
  • Ren, W. Wang X, Zhang A, Li C, Chen G, Ge X, Pan K, Dong JH. Selective bowel decontamination improves the survival of 90% hepatectomy in rats. J. Surg. Res. 2015,195: 454–464.
  • M Ninomiya, K Shirabe, T Terashi, H Ijichi, Y Yonemura, N Harada, Soejima Y, Taketomi A, Shimada M, Maehara Y. Deceleration of regenerative response improves the outcome of rat with massive hepatectomy. Am. J. Transplant.2010; 10:1580–1587.
  • Ben Salem M, Affes H, Ksouda K, Dhouibi R, Sahnoun Z, Hammami S, Zeghal KM. Pharmacological Studies of artichoke leaf extract and their health benefits. Plant Foods Hum Nutr. 2015;70(4):441-453.
  • Ahmadi A, Heidarian E, Ghatreh-Samani K. Modulatory effects of artichoke (Cynara scolymus L.) leaf extract against oxidative stress and hepatic TNF-α gene expression in acute diazinoninduced liver injury in rats. J Basic Clin Physiol Pharmacol. 2019;30(5):/j/jbcpp.2019.30.
  • Sümer E, Senturk GE, Demirel ÖU, Yesilada E. Comparative biochemical and histopathological evaluations proved that receptacle is the most effective part of Cynara scolymus against liver and kidney damages. J Ethnopharmacol. 2020;249:112458.
  • Michalopoulos, G. K. & DeFrances, M. C. Liver regeneration. Science 1997; 276: 60–66.
  • Michalopoulos, G. K. Liver regeneration. J. Cell. Physiol. 2007; 213: 286–300.
  • Dusabineza AC, Van Hul NK, Quinones JA, Starkel P, Najimi M, Leclercq IA. Participation of liver progenitor cells in liver regeneration: lack of evidence in the AAF/PH rat model. Lab. Invest. 2012; 92: 72–81.
  • Miyaoka Y, Ebato K, Kato H, Arakawa S, Shimizu S, Miyajima A. Hypertrophy and unconventional cell division of hepatocytes underlie liver regeneration. Curr Biol. 2012;22(13):1166-1175.
  • Miyaoka Y, Miyajima A. To divide or not to divide: revisiting liver regeneration. Cell Div. 2013;8(1):8.
  • Akçan A, Kucuk C, Ok E, Canoz O, Muhtaroglu S, Yilmaz N, Yilmaz Z. The effect of amrinone on liver regeneration in experimental hepatic resection model. J Surg Res. 2006;130:66–72.
  • Wan HF, Li JX, Liao HT, Liao MH, Luo L, Xu L, Yuan KF, Zeng Y. Nicotinamide induces liver regeneration and improves liver function by activating SIRT1. Mol Med Rep. 2019;19(1):555 562.
  • Lattanzio V, Paul AK, Lansalta V, Cardinali A. Globe artichoke: a functional food and source of nutraceutical ingredients. J Funct Foods. 2009; 1:131–144.
  • Gebhardt, Fausel M. Antioxydant and hepatoprotective effects of artichoke extracts and constituents in cultured rat hepatocytes. Toxicol In Vitro. 1997; 144:279–286.
  • Kraft K. Artichoke leaf extract–recent findings reflecting effects on lipid metabolism, liver, and gastrointestinal tracts. Phytomedicine. 1997; 43:69–78.

Cynara Scolymus (Artichoke) Improves Liver Regeneration after Partial Liver Resection in Rats

Year 2022, Volume: 12 Issue: 3, 653 - 658, 28.09.2022
https://doi.org/10.33808/clinexphealthsci.1008534

Abstract

Objective: Liver regeneration is necessary to restore hepatic mass and functional capacity after partial hepatectomy (PH). Cynara scolymus (CS) is a pharmacologically important plant that contains phenolic acids and flavonoids, and experimental studies have indicated that it has antioxidant and hepatoprotective effects. The aim of this study was to investigate the role of CS in liver regeneration after PH in rats.
Methods: A total of 36 Wistar albino rats weighing 280.5 ± 18.6 g were used. CS leaf extract was administered after partial hepatectomy. The rats were sacrificed at postoperative day 14, and the histological changes were assessed. The mitotic index (MI), nucleus size, hepatocyte size, and binucleation rate (BR) of hepatocytes were assessed using hematoxylin-eosin (H&E) staining.
Results: The rats that received CS extract had significant differences in liver regeneration markers, including the hepatocyte size, mitotic index, and Ki-67 proliferation index (p<0.05). The average increase in liver mass in 14 days was higher in the CS group, but the differences between the groups were not significant (1.70±0.2 g in sham group versus 2±0.8 g in CS group, p=0.75).
Conclusions: The results indicate that CS leaf extract promoted hepatocellular proliferation and hypertrophy, which resulted in accelerated liver regeneration.

References

  • Chapelle T, Op de Beeck B, Driessen A, Roeyen G, Bracke B, Hartman V, Huyghe I, Morrison S, Ysebaert D, Francque S. Estimation of the future remnant liver function is a better tool to predict post-hepatectomy liver failure than platelet-based liver scores. Eur J Surg Oncol. 2017;43(12):2277-2284.
  • Asencio J.M, Vaquero J, Olmedilla L, Garcia Sabrido JL: “Smallfor-flow” syndrome: shifting the “size” paradigm. Med Hypotheses 2013;80(5):573-537.
  • Clavien PA. Liver regeneration: A spotlight on the novel role of platelets and serotonin. Swiss Med Wkly. 2008; 138(25-26): 361-370.
  • Thorgeirsson SS: Hepatic stem cells in liver regeneration. FASEB J. 1996; September 10(11):1249-56.
  • Michalopoulos GK. Liver regeneration after partial hepatectomy: Critical analysis of mechanistic dilemmas. The American Journal of Pathology 2010; 176 (1): 2-13
  • Naseem S, Hussain T, Manzoor S. Interleukin-6: A promising cytokine to support liver regeneration and adaptive immunity in liverpathologies. Cytokine Growth Factor Rev. 2018;39:36-45.
  • Salekzamani S, Mameghani ME, Rezazadeh K. The antioxidant activity of artichoke (Cynara scolymus): A systematic review and meta-analysis of animal studies. Phytother Res. 2019;33(1):55-71.
  • Colak E, Ustuner MC, Tekin N, Colak E, Burukoglu D, Degirmenci I, Guney HV. The hepatocurative effects of Cynara scolymus. Leaf extract on carbon tetrachlorideinducedoxidative stress and hepatic injury in rats. Springerplus. 2016;5:216.
  • Pérez-García F, Adzet T, Cañigueral S. Activity of artichoke leaf extract on reactive oxygen species in human leukocytes. Free Radic Res. 2000;33(5):661–665.
  • Kinra P, Malik A. Ki 67: Are we counting it right?. Indian J Pathol Microbiol 2020;63:98-99.
  • Matsuo K, Murakami T, Kawaguchi D, Hiroshima Y, Koda K, Yamazaki K, Ishida Y, Tanaka K. Histologic features after surgery associating liver partition and portal vein ligation for staged hepatectomy versus those after hepatectomy with portal vein embolization. Surgery. 2016;159(5):1289-1298.
  • Lauterio, A. , Di Sandro S, Concone G, De Carlis R, Giacomoni A, De Carlis L. Current status and perspectives in split liver transplantation. World J. Gastroenterol. 2015; 21: 11003–11015.
  • Ren, W. Wang X, Zhang A, Li C, Chen G, Ge X, Pan K, Dong JH. Selective bowel decontamination improves the survival of 90% hepatectomy in rats. J. Surg. Res. 2015,195: 454–464.
  • M Ninomiya, K Shirabe, T Terashi, H Ijichi, Y Yonemura, N Harada, Soejima Y, Taketomi A, Shimada M, Maehara Y. Deceleration of regenerative response improves the outcome of rat with massive hepatectomy. Am. J. Transplant.2010; 10:1580–1587.
  • Ben Salem M, Affes H, Ksouda K, Dhouibi R, Sahnoun Z, Hammami S, Zeghal KM. Pharmacological Studies of artichoke leaf extract and their health benefits. Plant Foods Hum Nutr. 2015;70(4):441-453.
  • Ahmadi A, Heidarian E, Ghatreh-Samani K. Modulatory effects of artichoke (Cynara scolymus L.) leaf extract against oxidative stress and hepatic TNF-α gene expression in acute diazinoninduced liver injury in rats. J Basic Clin Physiol Pharmacol. 2019;30(5):/j/jbcpp.2019.30.
  • Sümer E, Senturk GE, Demirel ÖU, Yesilada E. Comparative biochemical and histopathological evaluations proved that receptacle is the most effective part of Cynara scolymus against liver and kidney damages. J Ethnopharmacol. 2020;249:112458.
  • Michalopoulos, G. K. & DeFrances, M. C. Liver regeneration. Science 1997; 276: 60–66.
  • Michalopoulos, G. K. Liver regeneration. J. Cell. Physiol. 2007; 213: 286–300.
  • Dusabineza AC, Van Hul NK, Quinones JA, Starkel P, Najimi M, Leclercq IA. Participation of liver progenitor cells in liver regeneration: lack of evidence in the AAF/PH rat model. Lab. Invest. 2012; 92: 72–81.
  • Miyaoka Y, Ebato K, Kato H, Arakawa S, Shimizu S, Miyajima A. Hypertrophy and unconventional cell division of hepatocytes underlie liver regeneration. Curr Biol. 2012;22(13):1166-1175.
  • Miyaoka Y, Miyajima A. To divide or not to divide: revisiting liver regeneration. Cell Div. 2013;8(1):8.
  • Akçan A, Kucuk C, Ok E, Canoz O, Muhtaroglu S, Yilmaz N, Yilmaz Z. The effect of amrinone on liver regeneration in experimental hepatic resection model. J Surg Res. 2006;130:66–72.
  • Wan HF, Li JX, Liao HT, Liao MH, Luo L, Xu L, Yuan KF, Zeng Y. Nicotinamide induces liver regeneration and improves liver function by activating SIRT1. Mol Med Rep. 2019;19(1):555 562.
  • Lattanzio V, Paul AK, Lansalta V, Cardinali A. Globe artichoke: a functional food and source of nutraceutical ingredients. J Funct Foods. 2009; 1:131–144.
  • Gebhardt, Fausel M. Antioxydant and hepatoprotective effects of artichoke extracts and constituents in cultured rat hepatocytes. Toxicol In Vitro. 1997; 144:279–286.
  • Kraft K. Artichoke leaf extract–recent findings reflecting effects on lipid metabolism, liver, and gastrointestinal tracts. Phytomedicine. 1997; 43:69–78.
There are 27 citations in total.

Details

Primary Language English
Subjects Health Care Administration
Journal Section Articles
Authors

Yusuf Gunay 0000-0002-6518-9997

Esin Kaymaz 0000-0003-4127-6559

Publication Date September 28, 2022
Submission Date October 12, 2021
Published in Issue Year 2022 Volume: 12 Issue: 3

Cite

APA Gunay, Y., & Kaymaz, E. (2022). Cynara Scolymus (Artichoke) Improves Liver Regeneration after Partial Liver Resection in Rats. Clinical and Experimental Health Sciences, 12(3), 653-658. https://doi.org/10.33808/clinexphealthsci.1008534
AMA Gunay Y, Kaymaz E. Cynara Scolymus (Artichoke) Improves Liver Regeneration after Partial Liver Resection in Rats. Clinical and Experimental Health Sciences. September 2022;12(3):653-658. doi:10.33808/clinexphealthsci.1008534
Chicago Gunay, Yusuf, and Esin Kaymaz. “Cynara Scolymus (Artichoke) Improves Liver Regeneration After Partial Liver Resection in Rats”. Clinical and Experimental Health Sciences 12, no. 3 (September 2022): 653-58. https://doi.org/10.33808/clinexphealthsci.1008534.
EndNote Gunay Y, Kaymaz E (September 1, 2022) Cynara Scolymus (Artichoke) Improves Liver Regeneration after Partial Liver Resection in Rats. Clinical and Experimental Health Sciences 12 3 653–658.
IEEE Y. Gunay and E. Kaymaz, “Cynara Scolymus (Artichoke) Improves Liver Regeneration after Partial Liver Resection in Rats”, Clinical and Experimental Health Sciences, vol. 12, no. 3, pp. 653–658, 2022, doi: 10.33808/clinexphealthsci.1008534.
ISNAD Gunay, Yusuf - Kaymaz, Esin. “Cynara Scolymus (Artichoke) Improves Liver Regeneration After Partial Liver Resection in Rats”. Clinical and Experimental Health Sciences 12/3 (September 2022), 653-658. https://doi.org/10.33808/clinexphealthsci.1008534.
JAMA Gunay Y, Kaymaz E. Cynara Scolymus (Artichoke) Improves Liver Regeneration after Partial Liver Resection in Rats. Clinical and Experimental Health Sciences. 2022;12:653–658.
MLA Gunay, Yusuf and Esin Kaymaz. “Cynara Scolymus (Artichoke) Improves Liver Regeneration After Partial Liver Resection in Rats”. Clinical and Experimental Health Sciences, vol. 12, no. 3, 2022, pp. 653-8, doi:10.33808/clinexphealthsci.1008534.
Vancouver Gunay Y, Kaymaz E. Cynara Scolymus (Artichoke) Improves Liver Regeneration after Partial Liver Resection in Rats. Clinical and Experimental Health Sciences. 2022;12(3):653-8.

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