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As exposure models (0.02, 0.1, or 0.5\u2009mg\/L As\n                    <jats:sub>2<\/jats:sub>\n                    O\n                    <jats:sub>3<\/jats:sub>\n                    ) were established for mice during pre\u2010pregnancy, gestation, and lactation. Meanwhile, the effects on the fertility of female mice, blood parameters, and pathological changes of the liver, kidneys, spleen, ovaries and uterus of the exposed mice were evaluated. Additionally, a marker of DNA\u2010strand break (\u03b3H2AX) and apoptosis (TUNEL) was assessed in the liver and kidney during gestation and lactation. The findings indicated that As exposure during these stages did not impair fertility in female mice. However, exposure to 0.5 mg\/L As\n                    <jats:sub>2<\/jats:sub>\n                    O\n                    <jats:sub>3<\/jats:sub>\n                    during gestation caused reductions in red blood cells (RBC), hemoglobins (HGB), and platelets (PLT). Meanwhile, hepatic lipid levels was increased in mice exposure to 0.1\u2009mg\/L As\n                    <jats:sub>2<\/jats:sub>\n                    O\n                    <jats:sub>3<\/jats:sub>\n                    during gestation, and mice exposed to 0.1\u2009mg\/L As\n                    <jats:sub>2<\/jats:sub>\n                    O\n                    <jats:sub>3<\/jats:sub>\n                    during lactation exhibited glomerular atrophy and hepatocyte vacuolization. In addition, mice exposed to 0.5\u2009mg\/L As\n                    <jats:sub>2<\/jats:sub>\n                    O\n                    <jats:sub>3<\/jats:sub>\n                    during both gestation and lactation exhibited varying degrees of inflammatory cell infiltration in both the liver and kidney. Notably, \u03b3H2AX was elevated in the kidneys at 0.1 and 0.5\u2009mg\/L As\n                    <jats:sub>2<\/jats:sub>\n                    O\n                    <jats:sub>3<\/jats:sub>\n                    during gestation and lactation, whereas no change was observed in the liver. TUNEL staining revealed no obvious alterations in either organ throughout this period. These observations suggest that females may be more vulnerable to As during gestation and lactation, with the liver and kidney serving as primary sites of toxicity accumulation.\n                  <\/jats:p>","DOI":"10.1002\/jat.70305","type":"journal-article","created":{"date-parts":[[2026,6,26]],"date-time":"2026-06-26T00:19:36Z","timestamp":1782433176000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Effects of Environmental Arsenic Exposure on the Morphology of Multiple Organs in Female Mice During Pre\u2010Pregnancy, Gestation, and Lactation"],"prefix":"10.1002","author":[{"ORCID":"https:\/\/orcid.org\/0009-0006-6394-6719","authenticated-orcid":false,"given":"Ying","family":"Xing","sequence":"first","affiliation":[{"name":"College of Veterinary Medicine Shanxi Agricultural University  Jinzhong Shanxi 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