Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Jul 22:2022:5059761.
doi: 10.1155/2022/5059761. eCollection 2022.

Seventy-Day Toxicity Study in Juvenile Sprague-Dawley Rats with Semicarbazide (SEM) from Weaning to Sexual Maturity

Affiliations

Seventy-Day Toxicity Study in Juvenile Sprague-Dawley Rats with Semicarbazide (SEM) from Weaning to Sexual Maturity

Vijaykumar Malashetty et al. J Toxicol. .

Abstract

The study was conducted to evaluate the toxicological effects, functional observation battery tests, and sexual maturity of semicarbazide oral gavage administration to juvenile Sprague-Dawley rats for 70 days at 0, 15, 30, and 60 mg/kg/day weaning to sexual maturity. At 60 mg/kg/day, there was a delay in mean age at acquisition of balano-preputial and vaginal patency and a decrease in body weight and food consumption in males. Treatment increased reticulocyte count, aspartate aminotransferase, and alanine aminotransferase levels in both sexes and decreased hematocrit and protein in males. Increased absolute and relative liver and spleen weight in both sexes were observed. Male rats had lower thymus and testes weights, whereas female rats had lower uterine weights. Semicarbazide caused significant changes in sperm motility, sperm count, and sperm abnormality. Histopathologically, semicarbazide caused cortical hypertrophy in adrenals and increased extramedullary hematopoiesis in the spleen; hepatocellular hypertrophy, follicular epithelial hypertrophy in the thyroid, and degeneration of seminiferous tubules in the testis were observed at 60 mg/kg/day when compared to control. Results suggest that 60 mg/kg/day of semicarbazide can exert systemic toxicity in juvenile rats. The no observed adverse effect level (NOAEL) of semicarbazide for juvenile Sprague-Dawley rats was estimated to be 30 mg/kg/day.

PubMed Disclaimer

Conflict of interest statement

The authors declare that they have no conflicts of interest.

Figures

Figure 1
Figure 1
Body weight of male rats treated with SEM.
Figure 2
Figure 2
Body weight of female rats treated with SEM.
Figure 3
Figure 3
Food consumption of male rats treated with SEM.
Figure 4
Figure 4
Food consumption of female rats treated with SEM.

References

    1. Dorgan H. N., Duran A., Yemini E. Synthesis and anti-bacterial activity of 1-(3-hydroxy-2-naphthoyl)-4-substitutedthiosemicarbazides. Drug Metabolism and Drug Interactions . 1999;15:187–195. - PubMed
    1. Singhal M., Paul A. Anti-bacterial evaluation of synthesized methyl semicarbazone derivative. International Journal of Pharmaceutical Sciences and Research . 2011;2
    1. Pandeya S. N., Yogeeswari P., Stables J. P. Synthesis and anticonvulsant activity of 4-bromophenyl substituted aryl semicarbazones. European Journal of Medicinal Chemistry . 2000;35 doi: 10.1016/s0223-5234(00)01169-7. - DOI - PubMed
    1. Sriram D., Yogeeswari P. Thirumurugan antitubercular activity of arylsemicarbazone derivative. Bioorganic and Medicinal Chemistry Letters . 2000;14
    1. Singhal M., Paul A. Anti-oxidant activity of synthesized methyl semicarbazone derivative by DPPH scavenging assay. Global Journal of Pharmacology . 2011;5:60–66.

LinkOut - more resources