{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,9]],"date-time":"2026-09-09T05:07:50Z","timestamp":1788930470194,"version":"build-2803163510"},"reference-count":42,"publisher":"Wiley","license":[{"start":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T00:00:00Z","timestamp":1788825600000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"},{"start":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T00:00:00Z","timestamp":1788825600000},"content-version":"tdm","delay-in-days":0,"URL":"http:\/\/doi.wiley.com\/10.1002\/tdm_license_1.1"}],"content-domain":{"domain":["scijournals.onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["J Sci Food Agric"],"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:sec>\n                    <jats:title>BACKGROUND<\/jats:title>\n                    <jats:p>\n                      Liver injury represents a major global health burden, often initiated by oxidative stress, which subsequently triggers inflammatory cascades and apoptotic cell death. Polysaccharides from American ginseng (\n                      <jats:italic>Panax quinquefolius<\/jats:italic>\n                      L.) (AGPs) have demonstrated immunomodulatory and antioxidant properties. However, the hepatoprotective mechanisms of purified AGP fractions remain inadequately understood.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>RESULTS<\/jats:title>\n                    <jats:p>\n                      Two polysaccharide fractions, AGP\n                      <jats:sub>1<\/jats:sub>\n                      (&gt;100\u2009kDa) and AGP\n                      <jats:sub>2<\/jats:sub>\n                      (&lt;10\u2009kDa), were extracted, purified, and characterized. Neither fraction induced histopathological abnormalities in the major organs of healthy mice after daily intragastric administration at 200\u2009mg\u2009kg\n                      <jats:sup>\u22121<\/jats:sup>\n                      for 14 consecutive days. Their hepatoprotective efficacy was compared in a CCl\n                      <jats:sub>4<\/jats:sub>\n                      \u2010induced acute liver injury mouse model. Both fractions dose\u2010dependently reversed these alterations, with AGP\n                      <jats:sub>2<\/jats:sub>\n                      consistently outperforming AGP\n                      <jats:sub>1<\/jats:sub>\n                      at equivalent doses. Compared with the model group, high\u2010dose AGP\n                      <jats:sub>2<\/jats:sub>\n                      (200\u2009mg\u2009kg\n                      <jats:sup>\u22121<\/jats:sup>\n                      ) reduced serum aspartate aminotransferase and malondialdehyde by 36% and 45%, respectively, increased hepatic superoxide dismutase activity 1.3\u2010fold (to 585.4\u2009\u00b1\u200945.2\u2009U\u2009mg\n                      <jats:sup>\u22121<\/jats:sup>\n                      protein), and lowered serum TNF\u2010\n                      <jats:italic>\u03b1<\/jats:italic>\n                      and IL\u20106 by 39% and 38%, respectively (to 578.6\u2009\u00b1\u200922.8 and 112.5\u2009\u00b1\u20097.2\u2009pg\u2009mL\n                      <jats:sup>\u22121<\/jats:sup>\n                      ). These effects not only surpassed those of both low\u2010 and high\u2010dose AGP\n                      <jats:sub>1<\/jats:sub>\n                      but also approached the efficacy of silymarin. Mechanistically, AGP\n                      <jats:sub>2<\/jats:sub>\n                      produced 2.3\u2010 and 1.7\u2010fold increases in nuclear Nrf2 and HO\u20101, respectively, and 67% and 55% reductions in p38 MAPK phosphorylation and Bax expression compared to the model group, surpassing the effects of both low\u2010 and high\u2010dose AGP\n                      <jats:sub>1<\/jats:sub>\n                      .\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>CONCLUSION<\/jats:title>\n                    <jats:p>\n                      These findings identify AGP\n                      <jats:sub>2<\/jats:sub>\n                      as a promising low\u2010molecular\u2010weight polysaccharide candidate for liver protection and underscore the critical role of molecular weight in determining polysaccharide bioactivity. \u00a9 2026 Society of Chemical Industry.\n                    <\/jats:p>\n             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