Pereira · Journal of agricultural and food chemistry 2002 · laboratory experimental study · n=?

Influence of temperature and ontogeny on the levels of glucosinolates in broccoli (Brassica oleracea Var. italica) sprouts and their effect on the induction of mammalian phase 2 enzymes.

Cited 172 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

Bench laboratory study evaluating plant biochemistry and in vitro enzyme induction with no human subjects.

PubMed 12358509 · doi:10.1021/jf020309x · record verified 2026-08-30

What was done

The authors investigated how growing temperature and developmental stage (ontogeny over an 11-day period) affect glucosinolate levels (specifically glucoraphanin) in broccoli (Brassica oleracea Var. italica) sprouts, and evaluated their capacity to induce mammalian phase 2 detoxification enzymes. Seedlings were cultivated across day/night temperature regimes (30/15 degrees C, 22/15 degrees C, and 18/12 degrees C) and constant temperatures (11.3 degrees C and 33.1 degrees C), and anatomical distribution between cotyledons and roots was measured.

What was found

Sprouts grown under a 30/15 degrees C day/night regime had significantly higher glucosinolate levels across six consecutive days postemergence compared to 22/15 degrees C and 18/12 degrees C regimes (p < 0.001). Both higher (33.1 degrees C) and lower (11.3 degrees C) constant temperatures induced higher glucosinolate levels in sprouts grown to uniform size. Glucosinolates were highest in cotyledons and lowest in roots. Nongerminated seeds had the highest glucosinolate content and concordantly greater induction of mammalian phase 2 detoxication enzymes, with levels declining as sprouts matured. Specific numerical concentrations and fold-induction values were not reported in the abstract.

Why it matters

This study identifies temperature stress and early developmental timing as key factors maximizing glucoraphanin content in broccoli sprouts. It highlights nongerminated seeds and younger sprouts as having the highest potency for phase 2 enzyme induction.

Limits

This was an in vitro plant cultivation and bench biochemical study without animal or human in vivo feeding trials. The abstract omits sample sizes, experimental replicate numbers, quantitative concentration metrics, and the specific mammalian enzyme assay model used.

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