Hematoxylin and Eosin‐stained images of kidney, lung, liver, and heart tissues from both male and female experimental groups. The images include control female group (a, f, k, p), tartrazine‐exposed female group (b, g, l, q), control male group (c, h, m, r), and tartrazine‐exposed male group (d, i, n, s). The magnification is set at 40× with a scale bar of 20 μm. In the kidney images, the yellow arrow indicates hemorrhage, the black arrow points to glomerular degeneration, the white arrow highlights vacuolization, and the blue arrow shows infiltration of inflammatory cells. For lung images, the yellow arrow signifies hemorrhage, while the blue arrow denotes inflammatory cell infiltration. The liver image showcases black arrows indicating apoptotic hepatocytes, and the heart image highlights irregular myocardial fibers. Histology score bar charts for kidney (e), lung (j), liver (o), and heart (t) are provided, expressed as ± SD. The statistical analysis conducted involves two‐way ANOVA and Tukey's multiple comparison tests denoted as follows: (a, α – p < .05 different from control female group), (b, β, μ, Ω – p < .05 different from tartrazine female group), and (c, γ, χ, ε – p < .05 different from control male group).

Hematoxylin and Eosin‐stained images of kidney, lung, liver, and heart tissues from both male and female experimental groups. The images include control female group (a, f, k, p), tartrazine‐exposed female group (b, g, l, q), control male group (c, h, m, r), and tartrazine‐exposed male group (d, i, n, s). The magnification is set at 40× with a scale bar of 20 μm. In the kidney images, the yellow arrow indicates hemorrhage, the black arrow points to glomerular degeneration, the white arrow highlights vacuolization, and the blue arrow shows infiltration of inflammatory cells. For lung images, the yellow arrow signifies hemorrhage, while the blue arrow denotes inflammatory cell infiltration. The liver image showcases black arrows indicating apoptotic hepatocytes, and the heart image highlights irregular myocardial fibers. Histology score bar charts for kidney (e), lung (j), liver (o), and heart (t) are provided, expressed as ± SD. The statistical analysis conducted involves two‐way ANOVA and Tukey's multiple comparison tests denoted as follows: (a, α – p < .05 different from control female group), (b, β, μ, Ω – p < .05 different from tartrazine female group), and (c, γ, χ, ε – p < .05 different from control male group).

Source publication
Article
Full-text available
Tartrazine, an azo dye prevalent in pharmaceuticals and food items, was investigated for its impact on fetal development, specifically examining visceral and skeletal abnormalities in rat offspring exposed to daily oral doses throughout pregnancy. Fourteen pregnant rats were randomly assigned to control and tartrazine groups (seven animals each), w...

Citations

Article
Purpose Existing research on the effects of azo dyes on human health is insufficient and often contradictory. Children are more exposed to the negative effects of food dyes than adults because they consume more foods and drinks containing food dyes. The research aimed to address the potential histopathological impacts of Sunset Yellow on the lungs and hearts of developing mice. Design/methodology/approach About36 adult male Swiss albino mice were separated into six groups (n: 6). The groups were created, including three treatment groups (four, eight and 10 weeks old) and three control groups. Sunset Yellow (a dose level of 30 mg/kg/bw) per week was administered orally for 28 days to the treatment groups, while the control groups were not treated. On the final day of the research, the mice were sacrificed by cervical dislocation, and their lungs and hearts were removed. The tissues were preserved in 10% formaldehyde and processed through a series of alcohol and xylene. Then they were dyed with hematoxylin-eosin and evaluated under light and electron microscopy. Findings Sunset Yellow caused significant increases in mean body weight ( p : 0.013), lung weight ( p : 0.011) and heart weight ( p : 0.049). Hemorrhage, inflammation and vacuole formation were detected in lung tissue, while severe hemorrhage, vacuoles and degenerated cells were observed in heart muscle tissue. Notably, the histopathological changes in lung and heart tissues were more pronounced during the weaning period. Sunset Yellow induced histopathological and physiological abnormalities in the lungs and hearts of mice, suggesting it may adversely affect lung and heart development during weaning and adolescence. Therefore, restricting the use of Sunset Yellow may be warranted in early life stages. Research limitations/implications Finally, as all studies have limitations, the research has limitations. The limitation of this study is the SY dose applied. Although the selected dose was determined based on the Acceptable Daily Intake (ADI) value used as a reference, investigating the effects of SY at different doses could be beneficial. Additionally, different analytical methods could be applied, and the results could be compared. In today’s society, challenges include a lack of knowledge about the effects of daily consumption of SY on health, limited and outdated resources on the subject and scarcity of field research. Originality/value Sunset Yellow may be especially harmful during adolescence and adulthood. Highlights • Sunset Yellow (SY) affected the lungs and hearts of mice developing. • SY caused a rise in the average bodyweight and relative organ weights. • Degeneration noted in lungs and hearts of all age groups of mice. • SY may be especially harmful during childhood and youth. Graphical abstract