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10.1016/j.biopha.2017.11.028

http://scihub22266oqcxt.onion/10.1016/j.biopha.2017.11.028
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29156525!ä!29156525

suck abstract from ncbi


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pmid29156525      Biomed+Pharmacother 2018 ; 97 (ä): 1356-1365
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  • Esomeprazole ameliorates CCl(4) induced liver fibrosis in rats via modulating oxidative stress, inflammatory, fibrogenic and apoptotic markers #MMPMID29156525
  • Eltahir HM; Nazmy MH
  • Biomed Pharmacother 2018[Jan]; 97 (ä): 1356-1365 PMID29156525show ga
  • BACKGROUND: Hepatic fibrosis is a major health problem that requires further medical attention. Proton pump inhibitors are proven to possess other therapeutic potentials apart of their acid anti-secretory actions. AIM OF THE WORK: To test possible anti-fibrotic effect of esomeprazole magnesium trihydrate in management of liver fibrosis compared to silymarin, the well-known hepatoprotective agent. MATERIALS & METHODS: 40 male albino rats were divided into 4 groups: normal control group; CCl(4)-treated group (1 mL/kg 40% CCl(4), diluted in olive oil) I.P twice weekly for 6 weeks; esomeprazole-treated group (30 mg/kg body weight); and Silymarin-treated group (100 mg/kg body weight). Both esomeprazole and silymarin were given orally daily for two weeks after the last CCl(4) dose. Serum and tissue samples were assessed for histopathological and biochemical analyses. RESULTS: Esomeprazole reversed hepatocellular damage, improved liver integrity, corrected major histopathological disturbances induced by CCl(4) and lowered fibrosis scoring. It also improved anti-oxidant capacity and attenuated lipid peroxidation. Esomeprazole treatment resulted in down-regulation of hepatic pro-apoptotic Bax and up-regulation of anti-apoptotic Bcl2 protein expressions. In addition, it resulted in inhibition of TNF-alpha, TGF-beta and IL-6 -mediated inflammatory responses, and retrieval of the epithelial marker e-cadherin. CONCLUSION: Esomeprazole confers significant anti-fibrotic actions. Further study is needed to elucidate other probable mechanisms for this effect and to test their anti-fibrotic potential clinically.
  • |Administration, Oral[MESH]
  • |Animals[MESH]
  • |Antioxidants/metabolism[MESH]
  • |Apoptosis/drug effects[MESH]
  • |Carbon Tetrachloride/toxicity[MESH]
  • |Disease Models, Animal[MESH]
  • |Down-Regulation/drug effects[MESH]
  • |Esomeprazole/administration & dosage/*pharmacology[MESH]
  • |Inflammation/drug therapy/pathology[MESH]
  • |Lipid Peroxidation/drug effects[MESH]
  • |Liver Cirrhosis/*prevention & control[MESH]
  • |Male[MESH]
  • |Oxidative Stress/*drug effects[MESH]
  • |Protective Agents/administration & dosage/pharmacology[MESH]
  • |Proton Pump Inhibitors/administration & dosage/pharmacology[MESH]
  • |Rats[MESH]
  • |Silymarin/administration & dosage/*pharmacology[MESH]


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