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Rats were subjected to liver damage induced by intra\u2010peritoneal injection of thioacetamide (\n                    <jats:styled-content style=\"fixed-case\">TAA<\/jats:styled-content>\n                    ).\n                    <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>\n                    was tested first for its acute toxicity and then administered by oral gavage at doses 5, 10, and 50 mg\/kg to rats. At the end of the 8\n                    <jats:sup>th<\/jats:sup>\n                    week, livers from all rats were excised and evaluated\n                    <jats:italic>ex vivo<\/jats:italic>\n                    . Measurements included alkaline phosphatase (\n                    <jats:styled-content style=\"fixed-case\">AP<\/jats:styled-content>\n                    ), alanine transaminase (\n                    <jats:styled-content style=\"fixed-case\">ALT<\/jats:styled-content>\n                    ), aspartate transaminase (\n                    <jats:styled-content style=\"fixed-case\">AST<\/jats:styled-content>\n                    ) and gamma\u2010glutamyl transferase (\n                    <jats:styled-content style=\"fixed-case\">GGT<\/jats:styled-content>\n                    ), serum platelet\u2010derived growth factor (\n                    <jats:styled-content style=\"fixed-case\">PDGF<\/jats:styled-content>\n                    ) and transforming growth factor (\n                    <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\n                    \u2010\u03b21), and hepatic metalloproteinase enzyme (\n                    <jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>\n                    \u20102) and its inhibitor extracellular matrix protein (\n                    <jats:styled-content style=\"fixed-case\">TIMP<\/jats:styled-content>\n                    \u20101). Oxidative stress was measured by liver malondialdehyde (\n                    <jats:styled-content style=\"fixed-case\">MDA<\/jats:styled-content>\n                    ) and nitrotyrosine levels, urinary 8\u2010hydroxy 2\u2010 deoxyguanosine (8\u2010\n                    <jats:styled-content style=\"fixed-case\">OH<\/jats:styled-content>\n                    \u2010\n                    <jats:styled-content style=\"fixed-case\">dG<\/jats:styled-content>\n                    ), and hepatic antioxidant enzyme activities. The immunohistochemistry of\n                    <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\n                    \u2010\u03b2\n                    <jats:sub>1<\/jats:sub>\n                    was additionally performed.\n                    <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>\n                    revealed safe dose of 250 mg\/kg on experimental rats and positive effect on the liver. The results suggested reduced hepatic stellate cells (\n                    <jats:styled-content style=\"fixed-case\">HSC<\/jats:styled-content>\n                    s) activity as verified from the attenuation of serum\n                    <jats:styled-content style=\"fixed-case\">PDGF<\/jats:styled-content>\n                    and\n                    <jats:styled-content style=\"fixed-case\">TGF<\/jats:styled-content>\n                    \u2010\u03b21, hepatic\n                    <jats:styled-content style=\"fixed-case\">MMP<\/jats:styled-content>\n                    \u20102 and\n                    <jats:styled-content style=\"fixed-case\">TIMP<\/jats:styled-content>\n                    \u20101, and oxidative stress. The extensive data altogether conclude that\n                    <jats:styled-content style=\"fixed-case\">PA<\/jats:styled-content>\n                    treatment could protect the liver from the progression of cirrhosis through a possible mechanism inhibiting\n                    <jats:styled-content style=\"fixed-case\">HSC<\/jats:styled-content>\n                    s activity.\n                  <\/jats:p>","DOI":"10.1111\/apm.12878","type":"journal-article","created":{"date-parts":[[2018,7,29]],"date-time":"2018-07-29T21:29:41Z","timestamp":1532899781000},"page":"710-721","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":32,"title":["Hepatoprotectivity of Panduratin A against liver damage:\n                    <i>In vivo<\/i>\n                    demonstration with a rat model of cirrhosis induced by thioacetamide"],"prefix":"10.1111","volume":"126","author":[{"given":"Suzy M.","family":"Salama","sequence":"first","affiliation":[{"name":"Department of Biomedical Science Faculty of Medicine University of Malaya Kuala Lumpur Malaysia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ibrahim Abdel Aziz","family":"Ibrahim","sequence":"additional","affiliation":[{"name":"Department of Pharmacology and Toxicology Faculty of Medicine Umm Al\u2010Qura University Makkah Saudi Arabia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Naiyer","family":"Shahzad","sequence":"additional","affiliation":[{"name":"Department of Pharmacology and Toxicology Faculty of Medicine Umm Al\u2010Qura University Makkah Saudi Arabia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Saeed","family":"Al\u2010Ghamdi","sequence":"additional","affiliation":[{"name":"Department of Pharmacology and Toxicology Faculty of Medicine Umm Al\u2010Qura University Makkah Saudi 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