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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
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  • Προβολή τεκμηρίου
  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
Όλο το DSpace
  • Κοινότητες & Συλλογές
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Altered activity of xenobiotic detoxifying enzymes at menopause – A cross-sectional study

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Συγγραφέας
Tsiokou V., Kilindris T., Begas E., Kouvaras E., Kouretas D., Asprodini E.K.
Ημερομηνία
2020
Γλώσσα
en
DOI
10.1016/j.envres.2019.109074
Λέξη-κλειδί
arylamine acetyltransferase
caffeine
cytochrome P450 1A2
cytochrome P450 2A6
xanthine oxidase
xenobiotic agent
arylamine acetyltransferase
cytochrome P450 1A2
NAT2 protein, human
detoxification
drug
enzyme activity
metabolism
metabolite
xenobiotics
adult
aged
aging
Article
controlled study
cross-sectional study
enzyme activity
female
human
major clinical study
male
menopause
non-smoker
postmenopause
premenopause
priority journal
urine sampling
metabolism
Arylamine N-Acetyltransferase
Caffeine
Cross-Sectional Studies
Cytochrome P-450 CYP1A2
Female
Humans
Male
Menopause
Xenobiotics
Academic Press Inc.
Εμφάνιση Μεταδεδομένων
Επιτομή
Xenobiotic metabolism at menopause is an under-investigated topic, albeit women spend one-third of their life in the postmenopausal period. The present study examined the effect of menopause on the in vivo activities of CYP1A2, CYP2A6, xanthine oxidase (XO) and N-acetyltransferase-2 (NAT2) xenobiotic metabolizing enzymes. Enzyme activity was determined in 152 non-smoking volunteers following oral intake of a single dose of 200 mg caffeine and subsequent determination of caffeine metabolite ratios (CMRs) in a 6-h urine sample as follows: CYP1A2: (AFMU+1U+1X)/17U, CYP2A6: 17U/(17U + 17X), XO: 1U/(1U+1X) and NAT2: AFMU/(AFMU+1U+1X). CMRs among groups were analyzed using one-way ANOVA. Significantly lower CYP1A2 and higher CYP2A6 CMRs were observed in postmenopausal compared to premenopausal women and age-matched men. These changes could be attributed to menopause rather than chronological aging since an age-related effect was not observed in premenopausal women or men of any age group. XO CMRs were higher in postmenopausal women and men>50 compared to premenopausal women and men<50, respectively, suggesting an age-related increase in XO activity. No significant alterations were discerned in NAT2 CMRs, in either slow- or rapid-acetylators, indicating that menopause exerts minimal modulation of xenobiotics metabolized by this enzyme. This study provides evidence that the transition to menopause induces significant alterations in xenobiotic-metabolizing enzymes independent of chronological aging suggesting altered metabolism of pharmaceutical and environmental agents. © 2020 Elsevier Inc.
URI
http://hdl.handle.net/11615/79990
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19735]

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