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        <datestamp>2026-09-28T05:22:42Z</datestamp>
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          <dc:title>Subacute oral glyphosate induces dose-dependent renal injury in male mice (&lt;i&gt;Mus musculus&lt;/i&gt;)</dc:title>
          <dc:creator>Alaa Talal Qumsani (25119675)</dc:creator>
          <dc:creator>Mohamed E. Elbeeh (25119678)</dc:creator>
          <dc:subject>Biochemistry</dc:subject>
          <dc:subject>Medicine</dc:subject>
          <dc:subject>Cell Biology</dc:subject>
          <dc:subject>Neuroscience</dc:subject>
          <dc:subject>Physiology</dc:subject>
          <dc:subject>Pharmacology</dc:subject>
          <dc:subject>Biotechnology</dc:subject>
          <dc:subject>Environmental Sciences not elsewhere classified</dc:subject>
          <dc:subject>Immunology</dc:subject>
          <dc:subject>Developmental Biology</dc:subject>
          <dc:subject>Marine Biology</dc:subject>
          <dc:subject>Mental Health</dc:subject>
          <dc:subject>Glyphosate</dc:subject>
          <dc:subject>nephrotoxicity</dc:subject>
          <dc:subject>oxidative stress</dc:subject>
          <dc:subject>renal biomarkers</dc:subject>
          <dc:subject>lipid peroxidation</dc:subject>
          <dc:subject>dose–response</dc:subject>
          <dc:subject>risk assessment</dc:subject>
          <dc:subject>Mus musculus</dc:subject>
          <dc:description>&lt;p&gt;Glyphosate is the most heavily applied herbicide worldwide and human exposure is now near-ubiquitous, yet its renal toxicity at near-threshold doses remains incompletely characterized. We tested whether subacute oral glyphosate produces integrated, dose-dependent renal injury in male mice (&lt;i&gt;Mus musculus&lt;/i&gt;). Adult male mice (n = 10/group) received vehicle or technical-grade glyphosate at 10, 50 or 100 mg/kg/day by oral gavage for 28 days, with 50 mg/kg anchored near the chronic NOAEL. Serum renal-function markers, renal oxidative-stress markers (MDA, GSH, SOD, CAT) and hematoxylin–eosin histopathology were assessed in the same 40 animals. Glyphosate produced coherent, dose-dependent renal injury. At 100 mg/kg, serum urea, creatinine and uric acid rose by 63.5%, 46.9% and 84.7%, with hyponatraemia, hypochloraemia and hyperkalaemia; renal MDA increased 2.1-fold while GSH, SOD and CAT fell by 46–51%, and the composite lesion score rose from 0 to 9.5 (median). No endpoint differed from control at 10 mg/kg under the prespecified analysis (one heteroscedastic sensitivity test detected a low-dose MDA increase), whereas significant effects were present at 50 mg/kg. A monotone dose trend was confirmed for every endpoint tested (Jonckheere–Terpstra, FDR-adjusted p &lt; 0.001), and exploratory benchmark doses lay below the 50 mg/kg anchor. These findings indicate dose-dependent renal injury under subacute conditions and warrant duration-matched, both-sex confirmation. The doses studied lie far above realistic human intakes and characterize hazard rather than risk.&lt;/p&gt; &lt;p&gt;&lt;/p&gt;&lt;p&gt;Swiss albino mice received technical-grade glyphosate at 10, 50 or 100 mg/kg/day orally for 28 days.&lt;/p&gt;&lt;p&gt;Doses were anchored to the regulatory no-observed-adverse-effect level (NOAEL ≈ 50 mg/kg/day).&lt;/p&gt;&lt;p&gt;Renal function, oxidative-stress markers and histopathology were assessed jointly in the same animals (n = 10 per group).&lt;/p&gt;&lt;p&gt;Significant functional, redox and structural injury appeared from 50 mg/kg, whereas no statistically detectable adverse effect was observed at 10 mg/kg/day by the primary post-hoc analysis (with an isolated low-dose MDA signal on heteroscedastic sensitivity testing) under this 28-day male-mouse design.&lt;/p&gt;&lt;p&gt;A monotone dose trend was confirmed for every endpoint tested (Jonckheere–Terpstra, FDR-adjusted p &lt; 0.001; &lt;a target="_blank" href="10.1080/01480545.2026.2726183"&gt;Supplementary Table S4&lt;/a&gt;), consistent with nephrotoxicity of the active ingredient under the present conditions.&lt;/p&gt;&lt;p&gt;&lt;/p&gt; &lt;p&gt;Swiss albino mice received technical-grade glyphosate at 10, 50 or 100 mg/kg/day orally for 28 days.&lt;/p&gt; &lt;p&gt;Doses were anchored to the regulatory no-observed-adverse-effect level (NOAEL ≈ 50 mg/kg/day).&lt;/p&gt; &lt;p&gt;Renal function, oxidative-stress markers and histopathology were assessed jointly in the same animals (n = 10 per group).&lt;/p&gt; &lt;p&gt;Significant functional, redox and structural injury appeared from 50 mg/kg, whereas no statistically detectable adverse effect was observed at 10 mg/kg/day by the primary post-hoc analysis (with an isolated low-dose MDA signal on heteroscedastic sensitivity testing) under this 28-day male-mouse design.&lt;/p&gt; &lt;p&gt;A monotone dose trend was confirmed for every endpoint tested (Jonckheere–Terpstra, FDR-adjusted p &lt; 0.001; &lt;a target="_blank" href="10.1080/01480545.2026.2726183"&gt;Supplementary Table S4&lt;/a&gt;), consistent with nephrotoxicity of the active ingredient under the present conditions.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-28T05:22:42Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.6084/m9.figshare.34009059.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Subacute_oral_glyphosate_induces_dose-dependent_renal_injury_in_male_mice_i_Mus_musculus_i_/34009059</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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