AA · Adrenal Androgens
7РП — „Хора“ (Действия „Мария Кюри“)
- Период
- 2008-02-18 → 2010-02-17
- Финансиране от ЕС
- 169 391 €
- Участници
- 1
- Схема
- MC-IEF
Линиите свързват координатора с партньорите.
Накратко на български
Генетичният дефицит на ензима P450 оксидоредуктаза влияе върху производството на хормони, което води до необичайно развитие на половите органи при новородени. Разбирането на тези мутации помага да се обясни защо при някои деца се наблюдава недостиг или излишък на андрогени по време на бременността.
Кратко обяснение, генерирано от езиков модел по текста на CORDIS. Оригиналът е по-долу.
Резултати накратко
Adrenal Androgens
Recently, important insights into human sexual differentiation have been gained from P450 oxidoreductase deficiency (ORD), a novel congenital adrenal hyperplasia (CAH) variant with apparent combined 17-hydroxylase and 21-hydroxylase deficiency. POR transfers electrons from NADPH to all microsomally located cytochrome P450 (CYP) enzymes, including 17-hydroxylase and 21-hydroxylase and therefore exerts crucial, albeit indirect effects on steroidogenesis. We have recently shown that specific mutations within the POR molecule might have differential effects on the enzymatic activity of P450 enzymes requiring electron transfer from POR. Whilst all other CAH variants manifest with either 46,XX DSD or 46,XY disordered sex development (DSD), ORD can manifest with both. Affected boys may present with 46,XY DSD, i.e. undervirilization of their external genitalia, which appears logic as the POR mutations lead to a partial loss of 17-hydroxylase deficiency and thus to sex steroid deficiency. However, whilst circulating androgens are invariably low in both males and females, affected girls often present with virilised genitalia at birth, i.e. 46,XX DSD, indicating prenatal androgen excess.
Текст от CORDIS, на английски · Данни: CORDIS, © Европейски съюз
Цел на проекта
The differentiation of male and female phenotype is established at 7-12 weeks post conceptionem. During this period, maintaining the appropiate intrauterine hormone environment is essential. In contrast to other species, the regulation of human sexual differentiation is linked with the development of the adrenal cortex, as can be concluded from the disorders (virilization and adrenal insufficiency in the newborn) observed in patients suffering from congenital adrenal hyperplasia (CAH), one of the most common known autosomal recessive disorders. Until now, the explanation for the corrupted sexual differentiation in CAH is mainly hypothetical and relies heavily upon extrapolation from the adult adrenocortical function. The so far widely accepted explanation upon regulation of steroidogenesis during development is based on the description of the so called classical pathway of steroidogenesis. In this pathway the conversion of 17-hydroxyprogesterone to dehydroepiandrosterone (DHEA) plays a pivotal role. Recent data of the host lab, however, indicate the existance of an alternative, previously unrecognized pathway in human androgen synthesis present in fetal and early neonatal life only, not involving DHEA. As the structure and function of the human fetal adrenal gland is unique and different from the adult human adrenal gland and rodents do not synthesize adrenal androgens at all, the studies require the analysis of human fetal tissue.The main goal of this project is to determine the expression and activity of the proposed alternative androgen pathway during normal human fetal development and its significance for sexual differentiation and disordered sex development. The proposed alternative androgen pathway may play a crucial role in the prenatal virilization of females suffering from CAH due to 21-hydroxylase deficiency and it is very likely that it plays an important role in normal human sexual differentiation and maintenace of pregnancy.
Оригинален текст от CORDIS (на английски).
Участници
- THE UNIVERSITY OF BIRMINGHAM · BirminghamКоординаторОбединеното кралство
Връзки
Данни: CORDIS, © Европейски съюз