Progesterone hormone synthesis

Pregnenolone is transported from the mitochondria to the ER, where a hydroxyl oxidation and migration of the double bond yield progesterone. Pregnenolone synthesis in the adrenal cortex is activated by adrenocorticotropic hormone (ACTH), a peptide of 39 amino acid residues secreted by the anterior pituitary gland. 

Congenital defects in the biosynthesis of steroid hormones can lead to severe developmental disturbances, in the adrenogenital syndrome (AGS), which is relatively common, there is usually a defect in 21-hydroxylase, which is needed for synthesis of cortisol and aldosterone from progesterone. Reduced synthesis of this hormone leads to increased formation of testosterone, resulting in masculin-ization of female fetuses. With early diagnosis, this condition can be avoided by providing the mother with hormone treatment before birth. 

If implantation occurs, human chorionic gonadotropin, produced initially by the trophoblast and later by the placenta, maintains steroid hormone synthesis by the corpus luteum during the early stages of pregnancy. Thereafter, the placenta itself becomes the major site of estrogen and progesterone synthesis. 

In a recent review, Thompson and Bannigan [373] noted that Cd accumulates in the ovary with age and is associated with decrements in oocyte development. Whereas several animal studies noticed decreased ovarial steroid hormone synthesis and release in rats following CLCE [374,375], in vitro studies have demonstrated increased progesterone production (reviewed in [376]). The reasons for these differences are unclear. 

Like steroid hormones, thyroid hormones interact with receptors to alter genomic activity and affect the synthesis of specific proteins during development [25-28], As with testosterone and progesterone, metabolic transformation of thyroxine (T4) is critical to its action [25-28]. Moreover, as with steroid hormones, thyroid hormones alter brain functions in adult life in ways that both resemble and differ from their action during development [25-28]. 

The Wharton-Grob fragmentation and the cationic cyclisation of polyolefins. Synthesis o/Cecropia juvenile hormone and d, -progesterone. 

Figure 19.8 A brief summary of the pathways for formation and secretion of oestradiol and progesterone within the cells of the follicle. Cholesterol is taken up by thecal cells in a complex with low density lipoprotein. In the thecal cells, cholesterol is converted to testosterone which is released to be taken up by granulosa cells where it is converted into oestradiol. For synthesis of progesterone in the granulosa cells, cholesterol is synthesised de novo within the cells from acetyl-CoA. In the follicle the enzyme aromatase, which produces the aromab c ring in the female sex hormones, is restricted to the granulosa cells. The reacrions that are stimulated by LH and FSH increase synthesis and, therefore, secretion of testosterone and increased synthesis of oestrogens and progesterone.

Figure 19.11 Hormones secreted by the hypothalamus, anterior pituitary, ovary and testis and feedback regulation. GnRH is gonadotrophin-releasing hormone the gonadotrophins are follicle-stimulating hormone (FSH) and luteinising hormone (LH). The effect of these hormones on activities in the ovary and testes is shown. FSH stimulates synthesis and secretion of oestradiol from follicle, and spermatogenesis in testis. LH stimulates synthesis and secretion of progesterone from corpus luteum and synthesis and secretion of testosterone by the Leydig cells.

Many steroid hormones are regulated by this type of axis—e.g., thyroxin, cortisol, estradiol, progesterone, and testosterone. In the case of the glucocorticoids, the hypothalamus releases corticotropin-releasing hormone (CRH or corticoliberin, a peptide consisting of 41 amino acids), which in turn releases corticotropin (ACTFl, 39 AAs) in the pituitary gland. Corticotropin stimulates synthesis and release of the glandular steroid hormone cortisol in the adrenal cortex. 

It stimulates placental progesterone synthesis and increases the secretion of placental hormones. 

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