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 in | The Journal of steroid biochemistry and molecular biology Vol. 152; pp. 53 - 61 |
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Main Authors | , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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. |
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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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CitedBy_id | crossref_primary_10_1016_j_jsbmb_2015_12_012 crossref_primary_10_4155_bio_2017_0285 crossref_primary_10_1016_j_jsbmb_2018_02_013 crossref_primary_10_1016_j_jsbmb_2019_105439 crossref_primary_10_1016_j_envint_2021_106750 crossref_primary_10_1016_j_talanta_2017_03_032 crossref_primary_10_4155_bio_15_176 |
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Keywords | Cysteinyl Placenta Adrenal glands Gonads Mass spectrometry Progestogen |
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•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 |
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