2007
DOI: 10.1002/bdrb.20102
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Differential metabolism of benzo[α]pyrene in vitro by human placental tissues exposed to active maternal cigarette smoke

Abstract: The metabolic characteristic of human placenta for xenobiotic exposure substrates is based on the expression and function of diverse enzymes, and such metabolism exhibited inter-individual variation for toxic metabolite production or detoxification of the substrates in response to maternal smoke exposure.

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Cited by 26 publications
(13 citation statements)
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“…In some studies, placental microsomes from smokers and nonsmokers have been compared. Interindividual variation in response to benzo-[a]-pyrene or in the ability to detoxify have been found to be high (Sanyal and Li, 2007).…”
Section: Placentamentioning
confidence: 99%
“…In some studies, placental microsomes from smokers and nonsmokers have been compared. Interindividual variation in response to benzo-[a]-pyrene or in the ability to detoxify have been found to be high (Sanyal and Li, 2007).…”
Section: Placentamentioning
confidence: 99%
“…We observed small positive associations with some CHD phenotypic subtypes, although effect measure estimates were generally imprecise. Future investigations could be improved by working with larger sample sizes in populations with higher potential for PAH exposure and by incorporating information on maternal and fetal genotypes related to PAH metabolism, because ongoing research suggests that genetic susceptibility in combination with environmental exposures predisposes individuals to the greatest risk (Whyatt et al, 1998; Wassenberg and Di Giulio, 2004; Wassenberg et al, 2005; Shimada, 2006; Sanyal and Li, 2007). …”
Section: Discussionmentioning
confidence: 99%
“…The placenta expresses markedly augmented PAHs metabolism capabilities in response to cigarette smoke exposure during pregnancy, indicating that placental metabolism may be an important mediator of adverse effects induced by exposure to tobacco smoke, 27 resulting in a lower production of PAH-DNA adducts in the fetus. However, PAHs, such as B[a]P, readily cross the placenta, and PAH-DNA adducts are easily detectable in fetuses and neonates because they are particularly prone to form and maintain adducts because detoxification and DNA repair capabilities are reduced during fetal development.…”
Section: Discussionmentioning
confidence: 99%