HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Induction of aryl hydrocarbon hydroxylase and forestomach tumors ben benzo(a)pyrene.

Abstract
While papillomatous tumors developed in the forestomach of female Ha/ICR mice after a 12-week chronic feeding period of benzo(a)pyrene (BP), no tumors developed in the glandular portion of stomach or in the lung or liver. Among all tissues examined, the forestomach showed the greatest increase of aryl hydrocarbon hydroxylase (AHH) activity following acute or chronic administration of BP. Single acute doses of BP induced AHH activity in forestomach, glandular stomach, lung, and small intestine, but not in the kidney and liver of these animals. Similarly, after chronic administration of BP, AHH activity was inducible in the forestomach, glandular stomach, and lung, but again not in the liver. Although the formation of tumors is associated with greater inducibility of AHH activity in the forestomach after BP administration, the relationship between tissue inducibility of AHH activity and susceptibility to BP carcinogenesis is still not clear. Further studies regarding the formation of specific carcinogenic epoxides of BP in itssues both susceptible (e.g., forestomach) and resistant to BP carcinogenesis would more clearly define the relationship between AHH inducibility and BP carcinogenesis.
AuthorsA J Triolo, G E Aponte, D L Herr
JournalCancer research (Cancer Res) Vol. 37 Issue 9 Pg. 3018-21 (Sep 1977) ISSN: 0008-5472 [Print] United States
PMID884659 (Publication Type: Journal Article, Research Support, U.S. Gov't, Non-P.H.S.)
Chemical References
  • Benzopyrenes
  • Aryl Hydrocarbon Hydroxylases
Topics
  • Animals
  • Aryl Hydrocarbon Hydroxylases (biosynthesis)
  • Benzopyrenes (metabolism, pharmacology)
  • Enzyme Induction (drug effects)
  • Female
  • Intestine, Small (enzymology)
  • Kidney (enzymology)
  • Liver (enzymology)
  • Lung (enzymology)
  • Mice
  • Mice, Inbred ICR
  • Neoplasms, Experimental (chemically induced, enzymology)
  • Organ Specificity
  • Species Specificity
  • Stomach (enzymology)
  • Stomach Neoplasms (chemically induced, enzymology)

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: