{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,19]],"date-time":"2026-09-19T00:02:14Z","timestamp":1789776134149,"version":"4.0.1"},"reference-count":44,"publisher":"SAGE Publications","issue":"11","license":[{"start":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T00:00:00Z","timestamp":1785369600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/journals.sagepub.com\/page\/policies\/text-and-data-mining-license"}],"content-domain":{"domain":["journals.sagepub.com"],"crossmark-restriction":true},"short-container-title":["Vector-Borne and Zoonotic Diseases"],"published-print":{"date-parts":[[2026,11,1]]},"abstract":"<jats:sec>\n                    <jats:title>Introduction:<\/jats:title>\n                    <jats:p>\n                      This investigation was conducted to assess the\n                      <jats:italic toggle=\"yes\">in\u00a0vivo<\/jats:italic>\n                      effects and potential mechanisms of action of phellandrene (PR) and pyrimethamine (PYM) combination therapy in the context of chronic cerebral toxoplasmosis in immunocompromised (ICM) murine models.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods:<\/jats:title>\n                    <jats:p>\n                      BALB\/c dexamethasone-induced ICM mice infected with the\n                      <jats:italic toggle=\"yes\">Toxoplasma gondii<\/jats:italic>\n                      ME49 strain were treated with PR (10 and 20 mg\/kg) alone or in combination with PYM for 2 weeks. The number and diameter of tissue cysts, oxidant\/antioxidant markers, cell-mediated immunity indicators (\n                      <jats:italic toggle=\"yes\">e.g.,<\/jats:italic>\n                      interferon\u2010gamma [\n                      <jats:italic toggle=\"yes\">IFN\u2010\u03b3<\/jats:italic>\n                      ], interleukin-12 [\n                      <jats:italic toggle=\"yes\">IL-12<\/jats:italic>\n                      ],\n                      <jats:italic toggle=\"yes\">IL-4<\/jats:italic>\n                      ), apoptosis-related genes (\n                      <jats:italic toggle=\"yes\">e.g., Caspase-3, BAX,<\/jats:italic>\n                      and\n                      <jats:italic toggle=\"yes\">Bcl-2<\/jats:italic>\n                      ), and pathogenesis-related genes (serine protease inhibitor [serpin A3k] and bradyzoite surface antigen 1 [BAG1]) were examined by qRT-PCR.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      PR, principally in combination with PYM, reduced the load (26.6 cysts) and size (23.4 \u00b5m) of tissue cysts, modulated lipid peroxidation (2.36 nmol\/mg tissue), glutathione peroxidase (5.31 U\/mg tissue), and superoxide dismutase (47.4 U\/mg tissue), and significantly elevated (\n                      <jats:italic toggle=\"yes\">p<\/jats:italic>\n                      &lt; 0.001) the expression levels of cytokines (\n                      <jats:italic toggle=\"yes\">IFN\u2010\u03b3<\/jats:italic>\n                      = 4.12-fold change,\n                      <jats:italic toggle=\"yes\">IL-12<\/jats:italic>\n                      = 3.91-fold change, and\n                      <jats:italic toggle=\"yes\">IL-4<\/jats:italic>\n                      = 1.24-fold change) and apoptosis genes (\n                      <jats:italic toggle=\"yes\">Caspase-3<\/jats:italic>\n                      = 3.1-fold change,\n                      <jats:italic toggle=\"yes\">BAX<\/jats:italic>\n                      = 3.89-fold change, and\n                      <jats:italic toggle=\"yes\">Bcl-2<\/jats:italic>\n                      = 1.17-fold change), while altering the expression of\n                      <jats:italic toggle=\"yes\">BAG1<\/jats:italic>\n                      (1.28-fold change) and serpin\n                      <jats:italic toggle=\"yes\">A3k<\/jats:italic>\n                      (3.46-fold change).\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>In summary, PR, particularly in combination with PYM, demonstrated significant therapeutic efficacy against chronic toxoplasmosis in ICM mice. This effect appears to be mediated through modulation of oxidative stress, enhancement of antioxidant defenses, regulation of apoptosis, and improvement of host immune responses. Importantly, no significant toxicity was observed in vital organs. These findings highlight PR as a promising adjunct candidate; however, further pharmacokinetic and clinical investigations are required to confirm its translational potential.<\/jats:p>\n                  <\/jats:sec>","DOI":"10.1177\/15303667261474977","type":"journal-article","created":{"date-parts":[[2026,7,30]],"date-time":"2026-07-30T10:21:59Z","timestamp":1785406919000},"page":"707-716","update-policy":"https:\/\/doi.org\/10.1177\/sage-journals-update-policy","source":"Crossref","is-referenced-by-count":0,"title":["Targeting Chronic Cerebral Toxoplasmosis in Immunocompromised Hosts:\n                    <i>In Vivo<\/i>\n                    Antiparasitic and Immuno-Apoptotic Effects of Phellandrene Combined with Pyrimethamine"],"prefix":"10.1177","volume":"26","author":[{"given":"Saeed M.N.","family":"Alasmari","sequence":"first","affiliation":[{"name":"Department of Biology, Faculty of Science and Arts, Najran University, Najran, Saudi Arabia."}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Aishah","family":"Alatawi","sequence":"additional","affiliation":[{"name":"Department of Biology, Faculty of Science, University of Tabuk, Tabuk, Saudi Arabia."}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"179","published-online":{"date-parts":[[2026,7,30]]},"reference":[{"key":"e_1_3_3_2_1","doi-asserted-by":"publisher","DOI":"10.3390\/ph16111574"},{"key":"e_1_3_3_3_1","doi-asserted-by":"publisher","DOI":"10.3390\/tropicalmed8070355"},{"key":"e_1_3_3_4_1","doi-asserted-by":"publisher","DOI":"10.1007\/s11686-021-00421-4"},{"key":"e_1_3_3_5_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.sjbs.2022.01.005"},{"key":"e_1_3_3_6_1","doi-asserted-by":"publisher","DOI":"10.1002\/jobm.202400039"},{"key":"e_1_3_3_7_1","doi-asserted-by":"publisher","DOI":"10.3390\/pathogens9030234"},{"key":"e_1_3_3_8_1","doi-asserted-by":"publisher","DOI":"10.1007\/s11686-020-00300-4"},{"key":"e_1_3_3_9_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.cbi.2021.109429"},{"key":"e_1_3_3_10_1","doi-asserted-by":"publisher","DOI":"10.1111\/neup.12263"},{"key":"e_1_3_3_11_1","doi-asserted-by":"publisher","DOI":"10.1017\/S0950268812001392"},{"key":"e_1_3_3_12_1","doi-asserted-by":"publisher","DOI":"10.1128\/CMR.00057-17"},{"key":"e_1_3_3_13_1","doi-asserted-by":"publisher","DOI":"10.21608\/puj.2021.75319.1120"},{"key":"e_1_3_3_14_1","doi-asserted-by":"publisher","DOI":"10.1016\/j.jtcms.2024.06.007"},{"key":"e_1_3_3_15_1","doi-asserted-by":"publisher","DOI":"10.1517\/14740338.7.2.107"},{"key":"e_1_3_3_16_1","doi-asserted-by":"publisher","DOI":"10.1891\/0730-0832.34.5.274"},{"key":"e_1_3_3_17_1","volume-title":"Pharmacological potential of selected natural compounds in the control of parasitic diseases","author":"Hrckova G","year":"2012","unstructured":"Hrckova G, , Velebny S. 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