TY - JOUR
T1 - The Effect of Tobacco Use on the Expression of Placental Transporters in Alaska Native Women
AU - McColl, Eliza R.
AU - Kwok, Jacinda
AU - Benowitz, Neal L.
AU - Patten, Christi A.
AU - Hughes, Christine A.
AU - Koller, Kathryn R.
AU - Flanagan, Christie A.
AU - Thomas, Timothy K.
AU - Hiratsuka, Vanessa Y.
AU - Tyndale, Rachel F.
AU - Piquette-Miller, Micheline
N1 - Funding Information:
This work was supported by the Canadian Institutes of Health Research (PJT‐169195, GSD‐164238, FDN‐154294), the National Cancer Institute (U54CA153605) the National Institute on Drug Abuse (P30DA012393). R.F.T. also received funding from the Canada Research Chairs Program and the Centre for Addiction and Mental Health.
Funding Information:
This work was supported by the Canadian Institutes of Health Research (PJT-169195, GSD-164238, FDN-154294), the National Cancer Institute (U54CA153605) the National Institute on Drug Abuse (P30DA012393). R.F.T. also received funding from the Canada Research Chairs Program and the Centre for Addiction and Mental Health. The authors wish to acknowledge the contributions of Dr. Meghan Chenoweth and Qian Zhao from University of Toronto and Dr. Judith Kaur from Mayo Clinic. We would also like to thank the Alaska Native women who donated their placentas to be used in this study and the ANTHC and SCF tribal and executive review boards for their participation in its preparation for publication. Lastly, we acknowledge that Toronto is the unceded territory of many nations, including the Huron-Wendat, the Seneca, and the Mississaugas of the Credit River. We are grateful to have had the opportunity to conduct our research on this land.
Publisher Copyright:
© 2022 The Authors. Clinical Pharmacology & Therapeutics © 2022 American Society for Clinical Pharmacology and Therapeutics.
PY - 2023/3
Y1 - 2023/3
N2 - Prenatal tobacco use among Alaska Native (AN) women has decreased substantially over the past two decades. Previous research suggests that providing AN women with feedback regarding fetal exposure to tobacco may further promote cessation. Transporters in the placenta regulate fetal exposure to nutrients and xenobiotics, including compounds associated with tobacco use. We examined whether prenatal tobacco use impacts transporter expression in the placenta, and whether this is influenced by fetal sex, degree of tobacco exposure, or transporter genotype. At delivery, we obtained placental samples from AN research participants who smoked cigarettes, used commercial chew or iqmik (oral tobacco), or did not use tobacco during pregnancy. Transporter expression was evaluated using qRT-PCR and Western blotting and tested for correlations between transcript levels and urinary biomarkers of tobacco use. The impact of BCRP/ABCG2 and OATP2B1/SLCO2B1 genotypes on protein expression was also examined. Oral tobacco use was associated with decreased P-gp and increased MRP1, MRP3, LAT1, and PMAT mRNA expression. Transcript levels of multiple transporters significantly correlated with tobacco biomarkers in maternal and fetal urine. In women carrying male fetuses, both smoking and oral tobacco were associated with decreased P-gp. Oral tobacco was also associated with decreased LAT1 in women carrying female fetuses. BCRP and OATP2B1 genotypes did not appear to impact protein expression. In conclusion, prenatal tobacco use is associated with altered expression of multiple placental transporters which differs by fetal sex. As transcript levels of multiple transporters were significantly correlated with tobacco use biomarkers, eliminating prenatal tobacco use should alleviate these changes.
AB - Prenatal tobacco use among Alaska Native (AN) women has decreased substantially over the past two decades. Previous research suggests that providing AN women with feedback regarding fetal exposure to tobacco may further promote cessation. Transporters in the placenta regulate fetal exposure to nutrients and xenobiotics, including compounds associated with tobacco use. We examined whether prenatal tobacco use impacts transporter expression in the placenta, and whether this is influenced by fetal sex, degree of tobacco exposure, or transporter genotype. At delivery, we obtained placental samples from AN research participants who smoked cigarettes, used commercial chew or iqmik (oral tobacco), or did not use tobacco during pregnancy. Transporter expression was evaluated using qRT-PCR and Western blotting and tested for correlations between transcript levels and urinary biomarkers of tobacco use. The impact of BCRP/ABCG2 and OATP2B1/SLCO2B1 genotypes on protein expression was also examined. Oral tobacco use was associated with decreased P-gp and increased MRP1, MRP3, LAT1, and PMAT mRNA expression. Transcript levels of multiple transporters significantly correlated with tobacco biomarkers in maternal and fetal urine. In women carrying male fetuses, both smoking and oral tobacco were associated with decreased P-gp. Oral tobacco was also associated with decreased LAT1 in women carrying female fetuses. BCRP and OATP2B1 genotypes did not appear to impact protein expression. In conclusion, prenatal tobacco use is associated with altered expression of multiple placental transporters which differs by fetal sex. As transcript levels of multiple transporters were significantly correlated with tobacco use biomarkers, eliminating prenatal tobacco use should alleviate these changes.
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U2 - 10.1002/cpt.2737
DO - 10.1002/cpt.2737
M3 - Article
C2 - 36053152
AN - SCOPUS:85138953721
SN - 0009-9236
VL - 113
SP - 634
EP - 642
JO - Clinical pharmacology and therapeutics
JF - Clinical pharmacology and therapeutics
IS - 3
ER -