DEVELOPMENTAL TOXICITY OF INHALED N-METHYLFORMAMIDE IN THE RAT

Citation
Lb. Rickard et al., DEVELOPMENTAL TOXICITY OF INHALED N-METHYLFORMAMIDE IN THE RAT, Fundamental and applied toxicology, 28(2), 1995, pp. 167-176
Citations number
24
Categorie Soggetti
Toxicology
ISSN journal
02720590
Volume
28
Issue
2
Year of publication
1995
Pages
167 - 176
Database
ISI
SICI code
0272-0590(1995)28:2<167:DTOINI>2.0.ZU;2-Z
Abstract
The developmental toxicity of N-methylformamide (MMF), an industrial c hemical intermediate used in the production of agrichemicals, was exam ined in pregnant rats. MMF was administered by nose-only inhalation, 6 hr daily on Days 7-16 of gestation (the day copulation was confirmed was termed Day 1 of gestation, Day 1G) at exposure concentrations of 0 , 15, 50, or 150 ppm. Darns were regularly monitored throughout gestat ion for body weight gain, feed consumption, and clinical signs. Cesare an sections were performed on Day 22G and the offspring were examined. Maternal toxicity was evident in dams exposed to 50 or 150 ppm; one d am exposed to 150 ppm died on Day 14G (considered to be treatment-rela ted) and darns in the 50 and 150 ppm groups exhibited concentration-re lated clinical findings. Clinical signs of wheezing and rattling were observed both during and after the exposure period. The 150 ppm group also showed significant decreases in weight gain and feed consumption. A significant increase in the mean number of resorptions per litter a t the 150 ppm level indicated an embryolethal effect. Developmental to xicity was apparent by a significant decrease in mean fetal body weigh t and increases in fetal malformations (subcutaneous cysts on the head , microphthalmia, anophthalmia, fused ribs and/or vertebra, and disten ded brain ventricles) and variations (misaligned and fused sternebrae) due to retarded development at 150 ppm. Significant fetal body weight decreases were also present at 50 ppm. Thus, in this study, the no-ob servable-adverse-effect level for both dam and fetus was 15 ppm MMF, i ndicating that for the parameters included in this study, the conceptu s is not uniquely sensitive to MMF. (C) 1995 Society of Toxicology