Specificity of induction of cancer protective enzymes by analogues of tert-butyl-4-hydroxyanisole (BHA)

Hans J. Prochaska, Howard S. Bregman, Mary J. De Long, Paul Talalay

Research output: Contribution to journalArticle

Abstract

Protection by 2(3)-tert-butyl-4-hydroxyanisole (BHA) and related phenols against chemical carcinogens, mutagens and other toxins has been attributed to the elevation of tissue levels of non-oxygenative detoxification enzymes. To analyze the mechanisms and specificity of these enzyme inductions, we synthesized a series of mono- and dialkyl ethers of tert-butylhydroquinone (R1O-[(CH3)3C-C6H3]-OR2) and its dimer. The abilities of these compounds to elevate the cytosolic specific activities of glutathione S-transferases (measured with 1-chloro-2,4-dinitrobenzene and l,2-dichloro-4-nitrobenzene) and of NAD(P)H: quinone reductase in liver, upper small intestine and forestomach of female CD-1 mice were evaluated. The animals were fed five daily doses of 50 gmmoles of each monomer (or 25 μmoles of each dimer). The structures of the monomers examined were: R1 = H and R2 = CH3 (I), R2 = C2 H5 (VI), R2 = (CH2)2CH3 (VIII), R2 = CH1(CH3)2 (X); R1 = CH3 and R2 = C2H5 (VII), R2 = (CH2) 2CH3 (IX), R2 = CH(CH3)2 (XI); R2 = CH3 and R1 = C2H5 (III), R1 = (CH2)2 CH3 (IV) and R1 = CH(CH3)2 (V). In addition, the monomethyl (XIII), monoethyl (XIV) and mono-n-propyl (XV) ethers of BHA dimer (XII; 2,2'-dihydroxy-3,3'-di-tert-butyl-5,5'-dimethoxybiphenyl) were also prepared. Under the conditions tested, all compounds were ineffective as enzyme inducers in the forestomach but produced coordinate induction of enzymes (generally 2- to 6-fold) in the cytosols of liver and mucosa of proximal small intestine. Increases in bulk of R1 and R2 beyond methyl groups tended to decrease the inductive potency of both monomers and dimers. The lack of strict structural specificity suggests that the induction depends on metabolic conversion of the analogues to common types of metabolites.

Original languageEnglish (US)
Pages (from-to)3909-3914
Number of pages6
JournalBiochemical Pharmacology
Volume34
Issue number21
DOIs
StatePublished - Nov 1 1985

ASJC Scopus subject areas

  • Biochemistry
  • Pharmacology

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