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Glycyrrhizinate reduces portal hypertension in isolated perfused rat livers with chronic hepatitis.
World J Gastroenterol. 2013 Sep 28; 19(36):6069-76.WJ

Abstract

AIM

To investigate the effects of diammonium glycyrrhizinate (Gly) on portal hypertension (PHT) in isolated portal perfused rat liver (IPPRL) with carbon tetrachloride (CCl₄)-induced chronic hepatitis.

METHODS

PHT model was replicated with CCl₄ in rats for 84 d. Model was identified by measuring the ascetic amounts, hepatic function, portal pressure in vivo, splenic index, and pathological alterations. Inducible nitric oxide synthase (iNOS) in liver was assessed by immunohistochemistry. IPPRLs were performed at d₀, d₂₈, d₅₆, and d₈₄. After phenylephrine-induced constriction, Gly was geometrically used to reduce PHT. Gly action was expressed as median effective concentration (EC₅₀) and area under the curve (AUC). Underlying mechanism was exploited by linear correlation between AUC values of Gly and existed iNOS in portal triads.

RESULTS

PHT model was confirmed with ascites, splenomegaly, serum biomarkers of hepatic injury, and elevated portal pressure. Pathological findings had shown normal hepatic structure at d₀, degenerations at d₂₈, fibrosis at d₅₆, cirrhosis at d₈₄ in PHT rats. Pseudo lobule ratios decreased and collagen ratios increased progressively along with PHT development. Gly does dose-dependently reduce PHT in IPPRLs with CCl₄-induced chronic hepatitis. Gly potencies were increased gradually along with PHT development, characterized with its EC₅₀ at 2.80 × 10⁻¹⁰, 3.03 × 10⁻¹¹, 3.77 × 10⁻¹¹ and 4.65×10⁻¹¹ mol/L at d₀, d₂₈, d₅₆ and d₈₄, respectively. Existed iNOS was located at hepatocyte at d₀, stellate cells at d₂₈, stellate cells and macrophages at d₅₆, and macrophages in portal triads at d₈₄. Macrophages infiltrated more into portal triads and expressed more iNOS along with PHT development. AUC values of Gly were positively correlated with existed iNOS levels in portal triads.

CONCLUSION

Gly reduces indirectly PHT in IPPRL with CCl₄-induced chronic hepatitis. The underlying mechanisms may relate to rescue NO bioavailability from macrophage-derived peroxynitrite in portal triads.

Authors+Show Affiliations

Xin Zhao, Bo Deng, Xue-Yan Xu, Shi-Jun Yang, Tao Zhang, Da-Yong Cai, Institute of Medicinal Plant Development, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100193, China.No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

24106408

Citation

Zhao, Xin, et al. "Glycyrrhizinate Reduces Portal Hypertension in Isolated Perfused Rat Livers With Chronic Hepatitis." World Journal of Gastroenterology, vol. 19, no. 36, 2013, pp. 6069-76.
Zhao X, Deng B, Xu XY, et al. Glycyrrhizinate reduces portal hypertension in isolated perfused rat livers with chronic hepatitis. World J Gastroenterol. 2013;19(36):6069-76.
Zhao, X., Deng, B., Xu, X. Y., Yang, S. J., Zhang, T., Song, Y. J., Liu, X. T., Wang, Y. Q., & Cai, D. Y. (2013). Glycyrrhizinate reduces portal hypertension in isolated perfused rat livers with chronic hepatitis. World Journal of Gastroenterology, 19(36), 6069-76. https://doi.org/10.3748/wjg.v19.i36.6069
Zhao X, et al. Glycyrrhizinate Reduces Portal Hypertension in Isolated Perfused Rat Livers With Chronic Hepatitis. World J Gastroenterol. 2013 Sep 28;19(36):6069-76. PubMed PMID: 24106408.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Glycyrrhizinate reduces portal hypertension in isolated perfused rat livers with chronic hepatitis. AU - Zhao,Xin, AU - Deng,Bo, AU - Xu,Xue-Yan, AU - Yang,Shi-Jun, AU - Zhang,Tao, AU - Song,Yi-Jun, AU - Liu,Xiao-Ting, AU - Wang,Yue-Qi, AU - Cai,Da-Yong, PY - 2012/03/16/received PY - 2012/05/30/revised PY - 2012/06/08/accepted PY - 2013/10/10/entrez PY - 2013/10/10/pubmed PY - 2014/3/14/medline KW - Chronic hepatitis KW - Diammonium glycyrrhizinate KW - Inducible nitric oxide synthase KW - Isolated portal perfused rat liver KW - Portal hypertension SP - 6069 EP - 76 JF - World journal of gastroenterology JO - World J Gastroenterol VL - 19 IS - 36 N2 - AIM: To investigate the effects of diammonium glycyrrhizinate (Gly) on portal hypertension (PHT) in isolated portal perfused rat liver (IPPRL) with carbon tetrachloride (CCl₄)-induced chronic hepatitis. METHODS: PHT model was replicated with CCl₄ in rats for 84 d. Model was identified by measuring the ascetic amounts, hepatic function, portal pressure in vivo, splenic index, and pathological alterations. Inducible nitric oxide synthase (iNOS) in liver was assessed by immunohistochemistry. IPPRLs were performed at d₀, d₂₈, d₅₆, and d₈₄. After phenylephrine-induced constriction, Gly was geometrically used to reduce PHT. Gly action was expressed as median effective concentration (EC₅₀) and area under the curve (AUC). Underlying mechanism was exploited by linear correlation between AUC values of Gly and existed iNOS in portal triads. RESULTS: PHT model was confirmed with ascites, splenomegaly, serum biomarkers of hepatic injury, and elevated portal pressure. Pathological findings had shown normal hepatic structure at d₀, degenerations at d₂₈, fibrosis at d₅₆, cirrhosis at d₈₄ in PHT rats. Pseudo lobule ratios decreased and collagen ratios increased progressively along with PHT development. Gly does dose-dependently reduce PHT in IPPRLs with CCl₄-induced chronic hepatitis. Gly potencies were increased gradually along with PHT development, characterized with its EC₅₀ at 2.80 × 10⁻¹⁰, 3.03 × 10⁻¹¹, 3.77 × 10⁻¹¹ and 4.65×10⁻¹¹ mol/L at d₀, d₂₈, d₅₆ and d₈₄, respectively. Existed iNOS was located at hepatocyte at d₀, stellate cells at d₂₈, stellate cells and macrophages at d₅₆, and macrophages in portal triads at d₈₄. Macrophages infiltrated more into portal triads and expressed more iNOS along with PHT development. AUC values of Gly were positively correlated with existed iNOS levels in portal triads. CONCLUSION: Gly reduces indirectly PHT in IPPRL with CCl₄-induced chronic hepatitis. The underlying mechanisms may relate to rescue NO bioavailability from macrophage-derived peroxynitrite in portal triads. SN - 2219-2840 UR - https://www.unboundmedicine.com/medline/citation/24106408/Glycyrrhizinate_reduces_portal_hypertension_in_isolated_perfused_rat_livers_with_chronic_hepatitis_ L2 - https://www.wjgnet.com/1007-9327/full/v19/i36/6069.htm DB - PRIME DP - Unbound Medicine ER -