HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Mechanism of Developmental Effects in Rats Caused by an N-Phenylimide Herbicide: Transient Fetal Anemia and Sequelae during Mid-to-Late Gestation.

AbstractBACKGROUND:
Rat developmental toxicity including embryolethality and teratogenicity (mainly ventricular septal defects [VSDs] and wavy ribs) was produced by an N-phenylimide herbicide that inhibits protoporphyrinogen oxidase (PPO) common to chlorophyll and heme biosynthesis. Major characteristics of the developmental toxicity included species difference between rats and rabbits, compound-specific difference among structurally similar herbicides, and sensitive period. Protoporphyrin accumulation in treated fetuses closely correlated with the major characteristics. Iron deposits in erythroblastic mitochondria and degeneration of erythroblasts were observed in treated rat fetuses. In this study we investigated fetal anemia and subsequent developmental effects in rats, and inhibition of PPO in rats, rabbits, and humans by the herbicides in vitro.
METHODS:
Fetuses were treated on gestational day (GD) 12 and removed on GDs 13 through 20. All litters were examined externally. One half of litters were examined for blood and skeletal development, and the other half for interventricular foramen closure. Effects on PPO were determined in mitochondria from embryos and adult livers.
RESULTS:
Fetal anemia in rats was evident on GDs 13 through 16. Subsequently, enlarged heart, delayed closure of the foramen, reduced serum protein, and retarded rib ossification were observed. In vitro PPO inhibition exhibited species- and compound-specific differences corresponding to the developmental toxicity.
CONCLUSION:
We propose that developmental toxicity results from PPO inhibition in primitive erythroblasts, causing transient fetal anemia followed by death. Compensatory enlargement of the fetal heart results in failure of interventricular foramen closure and VSD. Reduced serum protein leads to delayed ossification and wavy ribs.
AuthorsSatoshi Kawamura, Takafumi Yoshioka, Nobuaki Mito, Noriyuki Kishimoto, Masanao Nakaoka, Alan G Fantel
JournalBirth defects research. Part B, Developmental and reproductive toxicology (Birth Defects Res B Dev Reprod Toxicol) Vol. 107 Issue 1 Pg. 45-59 (Feb 2016) ISSN: 1542-9741 [Electronic] United States
PMID26865470 (Publication Type: Journal Article)
Copyright© 2016 Wiley Periodicals, Inc.
Chemical References
  • Benzoxazines
  • Blood Proteins
  • Hemoglobins
  • Herbicides
  • Imides
  • Phthalimides
  • Heme
  • Protoporphyrinogen Oxidase
  • flumioxazin
Topics
  • Anemia (embryology, pathology)
  • Animals
  • Benzoxazines (pharmacology)
  • Blood Proteins (metabolism)
  • Erythrocyte Count
  • Female
  • Fetal Mortality
  • Fetus (abnormalities, drug effects, embryology, pathology)
  • Heart (drug effects, embryology)
  • Heme (biosynthesis)
  • Hemoglobins (metabolism)
  • Herbicides (chemistry, toxicity)
  • Humans
  • Imides (chemistry, toxicity)
  • Inhibitory Concentration 50
  • Phthalimides (pharmacology)
  • Pregnancy
  • Protoporphyrinogen Oxidase (antagonists & inhibitors, metabolism)
  • Rabbits
  • Rats, Sprague-Dawley
  • Ribs (abnormalities, embryology)
  • Species Specificity

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: