Journal: Neurochemical Research

Article Title: Characterization and Selective Antiglioma Activity of a Standardized Hydroalcoholic Extract from Yellow Psidium cattleianum Fruits

doi: 10.1007/s11064-026-04907-3

Figure Lengend Snippet: Effect of hydroalcoholic extract from yellow Psidium cattleianum fruits on cell viability A – C and cell proliferation D – F in C6 rat glioma cells at 72 h A and D , 48 h B and E , and 24 h C and F . Data are expressed as mean ± standard error and analyzed by one-way ANOVA with Tukey’s post-hoc test. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 significantly different from the control. Three independent experiments were performed in triplicate

Article Snippet: Cell lines used were C6 (rat glioma), U87MG (human glioma), L929 (mouse fibroblast), and MRC5 (human fibroblast), all purchased from the American Type Culture Collection (ATCC, USA).

Techniques: Control

Journal: Neurochemical Research

Article Title: Characterization and Selective Antiglioma Activity of a Standardized Hydroalcoholic Extract from Yellow Psidium cattleianum Fruits

doi: 10.1007/s11064-026-04907-3

Figure Lengend Snippet: Clonogenic assay of C6 rat glioma cells: untreated A and treated with hydroalcoholic extract from yellow Psidium cattleianum fruits (1500 µg/mL) for 48 h B . Graphic representation of colony number C and colony size D . Data are expressed as mean ± standard error and analyzed by Student’s t-test. * p < 0.05 significantly different from the control. Three independent experiments were performed in triplicate

Article Snippet: Cell lines used were C6 (rat glioma), U87MG (human glioma), L929 (mouse fibroblast), and MRC5 (human fibroblast), all purchased from the American Type Culture Collection (ATCC, USA).

Techniques: Clonogenic Assay, Control

Journal: Neurochemical Research

Article Title: Characterization and Selective Antiglioma Activity of a Standardized Hydroalcoholic Extract from Yellow Psidium cattleianum Fruits

doi: 10.1007/s11064-026-04907-3

Figure Lengend Snippet: Effect of hydroalcoholic extract from yellow Psidium cattleianum fruits (750 µg/mL) on the migration of C6 rat glioma cells at 0, 2, 4, 6, and 24 h A and B . Data are expressed as mean ± standard error and analyzed by two-way ANOVA with Bonferroni’s post-hoc test. ** p ˂ 0.01, **** p < 0.0001 significantly different from the control. Three independent experiments were performed in triplicate

Article Snippet: Cell lines used were C6 (rat glioma), U87MG (human glioma), L929 (mouse fibroblast), and MRC5 (human fibroblast), all purchased from the American Type Culture Collection (ATCC, USA).

Techniques: Migration, Control

Journal: Neurochemical Research

Article Title: Characterization and Selective Antiglioma Activity of a Standardized Hydroalcoholic Extract from Yellow Psidium cattleianum Fruits

doi: 10.1007/s11064-026-04907-3

Figure Lengend Snippet: Effect of hydroalcoholic extract from yellow Psidium cattleianum fruits (750–2000 µg/mL) on cell death in C6 rat glioma cell line at 72 h. Data are expressed as mean ± standard error and analyzed by two-way ANOVA with Tukey’s post-hoc test. ** p ˂ 0.01, *** p ˂ 0.001, **** p < 0.0001 significantly different from the control. Three independent experiments were performed in triplicate

Article Snippet: Cell lines used were C6 (rat glioma), U87MG (human glioma), L929 (mouse fibroblast), and MRC5 (human fibroblast), all purchased from the American Type Culture Collection (ATCC, USA).

Techniques: Control

Journal: Neurochemical Research

Article Title: Characterization and Selective Antiglioma Activity of a Standardized Hydroalcoholic Extract from Yellow Psidium cattleianum Fruits

doi: 10.1007/s11064-026-04907-3

Figure Lengend Snippet: Effect of hydroalcoholic extract from yellow Psidium cattleianum fruits (500–2000 µg/mL) on redox equilibrium parameters in C6 rat glioma cell line after 48 h. A Reactive oxygen species levels (ROS); B superoxide dismutase activity (SOD); C catalase activity (CAT); D glutathione peroxidase (GPx). Data are expressed as mean ± standard error and analyzed by one-way ANOVA with Tukey’s post-hoc test. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001 significantly different from the control. Three independent experiments were performed in triplicate

Article Snippet: Cell lines used were C6 (rat glioma), U87MG (human glioma), L929 (mouse fibroblast), and MRC5 (human fibroblast), all purchased from the American Type Culture Collection (ATCC, USA).

Techniques: Activity Assay, Control

Journal: Frontiers in Cell and Developmental Biology

Article Title: Integrated re-analysis of bulk and single-cell transcriptomic data reveals limited ferroptosis and neuroinflammation signatures after sevoflurane exposure in the aged rat hippocampus and human prefrontal cortex cells

doi: 10.3389/fcell.2026.1938601

Figure Lengend Snippet: qRT-PCR analysis of ferroptosis-related gene expression after sevoflurane and H 2 O 2 exposure. Relative expression of GPX4, SLC7A11, ACSL4, and PTGS2 in Control, Sevo (3.3% for 6 h), H 2 O 2 (200 μM for 24 h), and Sevo + H 2 O 2 groups in C6 glioma cells and HA astrocytes. *P < 0.05 versus Control; significant comparisons are displayed with a single asterisk. Data represent mean ± SEM from three independent experiments. Two-way ANOVA (sevoflurane × H 2 O 2 ) was followed by Dunnett’s multiple-comparisons test against Control.

Article Snippet: To examine regulation of key ferroptosis-related genes identified in the transcriptomic analyses, quantitative RT-PCR was performed in C6 rat glioma cells (ATCC CRL-2309) and HA human astrocytes (ATCC CRL-3050).

Techniques: Quantitative RT-PCR, Analysis, Gene Expression, Expressing, Control