Urinary cysteinyl progestogens: Occurrence and origin

[Display omitted] •16-Cysteinyl-progesterone and 16-cysteinyl-pregnenolone are excreted in human urine.•Chemically synthesized materials and LC–MS/MS allowed unequivocal identification.•Different experiments point toward an adrenal origin for both novel progestogens.•16-Cysteinyl-progesterone is als...

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Published inThe Journal of steroid biochemistry and molecular biology Vol. 152; pp. 53 - 61
Main Authors Marcos, Josep, Pol, Marta, Fabregat, Andreu, Ventura, Rosa, Renau, Nuria, Hanzu, Felicia A., Casals, Gregori, Marfà, Santi, Barceló, Bernardí, Barceló, Antonia, Robles, Juan, Segura, Jordi, Pozo, Oscar J.
Format Journal Article
LanguageEnglish
Published England Elsevier Ltd 01.08.2015
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Abstract [Display omitted] •16-Cysteinyl-progesterone and 16-cysteinyl-pregnenolone are excreted in human urine.•Chemically synthesized materials and LC–MS/MS allowed unequivocal identification.•Different experiments point toward an adrenal origin for both novel progestogens.•16-Cysteinyl-progesterone is also produced by the ovaries but not by the placenta.•Human hepatocytes do not convert progesterone to 16-dehydroprogesterone. The presence of two cysteinyl progestogens, 16-cysteinyl-progesterone (16-Cys-Prog) and 16-cysteinyl-pregnenolone (16-Cys-Preg), in human urine is described for the first time. Their occurrence was unequivocally confirmed by comparison with synthesized material by using mass spectrometric detectors. Several experiments were performed in order to clarify their origin. The adrenal origin of both 16-Cys-Prog and 16-Cys-Preg can be inferred from the increase in their concentrations after ACTH stimulatory test, together with their circadian variation similar to the one observed for cortisol. Moreover, the notable increase in excretions of 16-Cys-Prog during the luteal phase of the menstrual cycle points towards an ovarian production for this progestogen. However, the analysis of samples during the course of two pregnancies revealed that, in spite of the large amounts of progesterone produced during gestation, the human placenta lacks the capacity to make 16-Cys-Prog. The adrenal and ovarian origin has been further indicated by the absence of both metabolites in samples collected from a subject with bilateral adrenalectomy and hypogonadotrophyic hypogonadism. Regarding liver action, in vitro studies with hepatocytes and progesterone indicate that, although the liver is able to metabolize progesterone to 6-dehydroprogesterone, it has not the enzymatic machinery for the generation of 16-dehydroprogesterone. Taken together, these results open the possibility for a noninvasive test for the simultaneous evaluation of progesterone biosynthesis in different organs.
AbstractList [Display omitted] •16-Cysteinyl-progesterone and 16-cysteinyl-pregnenolone are excreted in human urine.•Chemically synthesized materials and LC–MS/MS allowed unequivocal identification.•Different experiments point toward an adrenal origin for both novel progestogens.•16-Cysteinyl-progesterone is also produced by the ovaries but not by the placenta.•Human hepatocytes do not convert progesterone to 16-dehydroprogesterone. The presence of two cysteinyl progestogens, 16-cysteinyl-progesterone (16-Cys-Prog) and 16-cysteinyl-pregnenolone (16-Cys-Preg), in human urine is described for the first time. Their occurrence was unequivocally confirmed by comparison with synthesized material by using mass spectrometric detectors. Several experiments were performed in order to clarify their origin. The adrenal origin of both 16-Cys-Prog and 16-Cys-Preg can be inferred from the increase in their concentrations after ACTH stimulatory test, together with their circadian variation similar to the one observed for cortisol. Moreover, the notable increase in excretions of 16-Cys-Prog during the luteal phase of the menstrual cycle points towards an ovarian production for this progestogen. However, the analysis of samples during the course of two pregnancies revealed that, in spite of the large amounts of progesterone produced during gestation, the human placenta lacks the capacity to make 16-Cys-Prog. The adrenal and ovarian origin has been further indicated by the absence of both metabolites in samples collected from a subject with bilateral adrenalectomy and hypogonadotrophyic hypogonadism. Regarding liver action, in vitro studies with hepatocytes and progesterone indicate that, although the liver is able to metabolize progesterone to 6-dehydroprogesterone, it has not the enzymatic machinery for the generation of 16-dehydroprogesterone. Taken together, these results open the possibility for a noninvasive test for the simultaneous evaluation of progesterone biosynthesis in different organs.
The presence of two cysteinyl progestogens, 16-cysteinyl-progesterone (16-Cys-Prog) and 16-cysteinyl-pregnenolone (16-Cys-Preg), in human urine is described for the first time. Their occurrence was unequivocally confirmed by comparison with synthesized material by using mass spectrometric detectors. Several experiments were performed in order to clarify their origin. The adrenal origin of both 16-Cys-Prog and 16-Cys-Preg can be inferred from the increase in their concentrations after ACTH stimulatory test, together with their circadian variation similar to the one observed for cortisol. Moreover, the notable increase in excretions of 16-Cys-Prog during the luteal phase of the menstrual cycle points towards an ovarian production for this progestogen. However, the analysis of samples during the course of two pregnancies revealed that, in spite of the large amounts of progesterone produced during gestation, the human placenta lacks the capacity to make 16-Cys-Prog. The adrenal and ovarian origin has been further indicated by the absence of both metabolites in samples collected from a subject with bilateral adrenalectomy and hypogonadotrophyic hypogonadism. Regarding liver action, in vitro studies with hepatocytes and progesterone indicate that, although the liver is able to metabolize progesterone to 6-dehydroprogesterone, it has not the enzymatic machinery for the generation of 16-dehydroprogesterone. Taken together, these results open the possibility for a noninvasive test for the simultaneous evaluation of progesterone biosynthesis in different organs.
The presence of two cysteinyl progestogens, 16-cysteinyl-progesterone (16-Cys-Prog) and 16-cysteinyl-pregnenolone (16-Cys-Preg), in human urine is described for the first time. Their occurrence was unequivocally confirmed by comparison with synthesized material by using mass spectrometric detectors. Several experiments were performed in order to clarify their origin. The adrenal origin of both 16-Cys-Prog and 16-Cys-Preg can be inferred from the increase in their concentrations after ACTH stimulatory test, together with their circadian variation similar to the one observed for cortisol. Moreover, the notable increase in excretions of 16-Cys-Prog during the luteal phase of the menstrual cycle points towards an ovarian production for this progestogen. However, the analysis of samples during the course of two pregnancies revealed that, in spite of the large amounts of progesterone produced during gestation, the human placenta lacks the capacity to make 16-Cys-Prog. The adrenal and ovarian origin has been further indicated by the absence of both metabolites in samples collected from a subject with bilateral adrenalectomy and hypogonadotrophyic hypogonadism. Regarding liver action, in vitro studies with hepatocytes and progesterone indicate that, although the liver is able to metabolize progesterone to 6-dehydroprogesterone, it has not the enzymatic machinery for the generation of 16-dehydroprogesterone. Taken together, these results open the possibility for a noninvasive test for the simultaneous evaluation of progesterone biosynthesis in different organs.The presence of two cysteinyl progestogens, 16-cysteinyl-progesterone (16-Cys-Prog) and 16-cysteinyl-pregnenolone (16-Cys-Preg), in human urine is described for the first time. Their occurrence was unequivocally confirmed by comparison with synthesized material by using mass spectrometric detectors. Several experiments were performed in order to clarify their origin. The adrenal origin of both 16-Cys-Prog and 16-Cys-Preg can be inferred from the increase in their concentrations after ACTH stimulatory test, together with their circadian variation similar to the one observed for cortisol. Moreover, the notable increase in excretions of 16-Cys-Prog during the luteal phase of the menstrual cycle points towards an ovarian production for this progestogen. However, the analysis of samples during the course of two pregnancies revealed that, in spite of the large amounts of progesterone produced during gestation, the human placenta lacks the capacity to make 16-Cys-Prog. The adrenal and ovarian origin has been further indicated by the absence of both metabolites in samples collected from a subject with bilateral adrenalectomy and hypogonadotrophyic hypogonadism. Regarding liver action, in vitro studies with hepatocytes and progesterone indicate that, although the liver is able to metabolize progesterone to 6-dehydroprogesterone, it has not the enzymatic machinery for the generation of 16-dehydroprogesterone. Taken together, these results open the possibility for a noninvasive test for the simultaneous evaluation of progesterone biosynthesis in different organs.
Author Ventura, Rosa
Marcos, Josep
Fabregat, Andreu
Robles, Juan
Segura, Jordi
Marfà, Santi
Barceló, Bernardí
Barceló, Antonia
Casals, Gregori
Renau, Nuria
Hanzu, Felicia A.
Pol, Marta
Pozo, Oscar J.
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Keywords Cysteinyl
Placenta
Adrenal glands
Gonads
Mass spectrometry
Progestogen
Language English
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Snippet [Display omitted] •16-Cysteinyl-progesterone and 16-cysteinyl-pregnenolone are excreted in human urine.•Chemically synthesized materials and LC–MS/MS allowed...
The presence of two cysteinyl progestogens, 16-cysteinyl-progesterone (16-Cys-Prog) and 16-cysteinyl-pregnenolone (16-Cys-Preg), in human urine is described...
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SubjectTerms Adrenal glands
Adrenocorticotropic Hormone - pharmacology
Adult
Cell Line, Tumor
Child
Cysteine - analogs & derivatives
Cysteine - urine
Cysteinyl
Female
Gonads
Hep G2 Cells
Hepatocytes - metabolism
Humans
Hydrocortisone - pharmacology
Liver - metabolism
Luteal Phase
Male
Mass spectrometry
Ovary - metabolism
Placenta
Placenta - metabolism
Pregnancy
Pregnenolone - analogs & derivatives
Pregnenolone - urine
Progesterone - analogs & derivatives
Progesterone - urine
Progestins - urine
Progestogen
Title Urinary cysteinyl progestogens: Occurrence and origin
URI https://dx.doi.org/10.1016/j.jsbmb.2015.04.015
https://www.ncbi.nlm.nih.gov/pubmed/25913395
https://www.proquest.com/docview/1696188930
Volume 152
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