Epidemiological and laboratory studies suggest that dietary broccoli may pre
vent or delay a
varietyof cancers. Broccoli and other crucifers contain a relati
vely unique family of secondary metabolitescalled glucosinolates. Glucoraphanin, the major glucosinolate in broccoli, is hydrolyzed by anendogenous plant myrosinase to form either the potent anticarcinogen sulforaphane (SF) orsulforaphane nitrile (SF nitrile). The bioacti
vities of SF and SF nitrile were compared in rats andin mouse hepatoma cells. Male, 4-week-old, Fischer 344 rats were administered SF or SF nitrile(200, 500, or 1000
![](/images/entities/mgr.gif)
mol/kg) by ga
vage daily for 5 days. Hepatic, colonic mucosal, and pancreaticquinone reductase and glutathione
S-transferase acti
vities were induced by high doses of SF, butnot by SF nitrile. When Hepa 1c1c7 cells were exposed to increasing le
vels of each compound for 24h, quinone reductase showed a 3-fold maximal induction o
ver control at 2.5
![](/images/entities/mgr.gif)
M SF and a 3.5-foldmaximal induction o
ver control at 2000
![](/images/entities/mgr.gif)
M SF nitrile, the highest concentration tested. These resultsdemonstrate that SF nitrile is substantially less potent than SF as an inducing agent of phase IIdetoxification enzymes. Therefore, glucoraphanin hydrolysis directed toward the production of SFrather than SF nitrile could increase the potential chemoprotecti
ve effects of broccoli.Keywords: Broccoli; glucosinolates; sulforaphane; sulforaphane nitrile; isothiocyanate; quinonereductase; glutathione S-transferase; Brassica oleracea