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Progesterone chemical structure
Progesterone

pregn-4-ene-3,20-dione
IUPAC name
CAS number
57-83-0
ATC code

G03DA04

PubChem
5994
DrugBank
APRD00700
Chemical formula C21H30O2
Molecular weight 314.47
Bioavailability prolonged absorption, half-life approx 25-50 hours
Metabolism hepatic to pregnanediols and pregnanolones
Elimination half-life 34.8-55.13 hours
Excretion renal
Pregnancy category B (USA)
Legal status
Routes of administration oral, implant

Progesterone is a C-21 steroid hormone involved in the female menstrual cycle, pregnancy (supports gestation) and embryogenesis of humans and other species. Progesterone belongs to a class of hormones called progestogens, and is the major naturally occurring human progestogen.

Progesterone should not be confused with progestins, which are synthetically produced progestogens.


Chemistry[]

Like other steroids, progesterone consists of four interconnected cyclic hydrocarbons. Progesterone contains ketone and oxygenated functional groups, as well as two methyl branches. Like all steroid hormones, it is hydrophobic. This is mostly due to its lack of very polar functional groups.

Synthesis[]

Progesterone, like all other steroid hormones, is synthesized from pregnenolone, a derivative of cholesterol. This conversion takes place in two steps. The 3-hydroxyl group is converted to a keto group and the double bond is moved to C-4, from C-5.

Reaction-Pregnenolone-Progesterone

Conversion of Pregnenolone to Progesterone

Progesterone is the precursor of the mineralocorticoid aldosterone, and after conversion to 17-hydroxyprogesterone (another natural progestogen) of cortisol and androstenedione. Androstenedione can be converted to testosterone, estrone and estradiol.

DHEA1

Progesterone is important for aldosterone (mineralocorticoid) synthesis, as 17-hydroxyprogesterone is for cortisol (glucocorticoid), and androstenedione for sex steroids.

Sources[]

Progesterone is produced in the adrenal glands, the gonads (specifically after ovulation in the corpus luteum), the brain, and, during pregnancy, in the placenta. In humans, increasing amounts of progesterone are produced during pregnancy, initially the source is the corpus luteum that has been "rescued" by the presence of human chorionic gonadotropins (hCG) from the conceptus, but after the 8th week production of progesterone shifts over to the placenta. The placenta utilizes maternal cholesterol as the initial substrate, and most of the produced progesterone enters the maternal circulation, but some is picked up by the fetal circulation and is used as substrate for fetal corticosteroids. At term the placenta produces about 250 mg progesterone per day.

Levels[]

Estradiol

Progesterone levels (black line) during the menstrual cycle

In women, progesterone levels are relatively low during the preovulatory phase of the menstrual cycle, rise after ovulation, and are elevated during the luteal phase. In women progesterone levels tend to be < 2 ng/ml prior to ovulation, and > 5 ng/ml after ovulation. If pregnancy occurs, progesterone levels are maintained at luteal levels initially. With the onset of the luteal-placental shift in progesterone support of the pregnancy levels start to rise further and may reach 100-200 ng/ml at term. Whether a decrease in progesterone levels is critical for the initiation of labor has been argued and may be species-specific. After delivery of the placenta and during lactation, progesterone levels are very low.

Progesterone levels are relatively low in children and postmenopausal women[1]. Adult males have levels similar to those in women during the follicular phase of the menstrual cycle.

Effects[]

Progesterone exerts its action primarily through the intracellular progesterone receptor though a distinct, membrane bound progesterone receptor has recently been discovered.[How to reference and link to summary or text] It has a number of physiological effects, often regulatory, not least of the effects of estrogen. Estrogen often induces a multiplication of progesterone receptors.

Reproduction[]

Progesterone converts the endometrium to its secretory stage to prepare the uterus for implantation. At the same time progesterone affects the vaginal epithelium and cervical mucus. If pregnancy does not occur, progesterone levels will decrease, leading, in the human, to menstruation. Normal menstrual bleeding is progesterone withdrawal bleeding.

During implantation and gestation, progesterone appears to decrease the maternal immune response to allow for the acceptance of the pregnancy. Progesterone decreases contractility of the uterine smooth muscle. The fetus metabolizes placental progesterone in the production of adrenal mineralo- and glucosteroids. A drop in progesterone levels is possibly one step that facilitates the onset of labor. In addition progesterone inhibits lactation during pregnancy. The fall in progesterone levels following delivery is one of the triggers for milk production .

Neurosteroid[]

Progesterone, like pregnenolone and dehydroepiandrosterone, belongs to the group of neurosteroids that are found in high concentrations in certain areas in the brain and are synthesized there. Neurosteroids affect synaptic functioning, are neuroprotective, and affect myelinization.[1] They are investigated for their potential to improve memory and cognitive ability. Progesterone as a neuroprotectant affects regulation of apoptotic genes. Its effect as a neurosteroid works predominantly through the GSK-3 beta pathway, as an inhibitor. Other GSK-3 beta inhibitors include bipolar mood stabilizers, lithium and valproic acid. It also raises epidermal growth factor-1 levels, a factor often used to induce proliferation, and used to sustain cultures of stem cells.

Other systems[]

Progesterone has multiple effects outside of the reproductive system. Progesterone is thermogenic, raising the core temperature. It reduces spasm and relaxes smooth muscle. Bronchi are widened and mucus regulated. Progesterone receptors are widely present in submucosal tissue. Progesterone acts as an antiinflammatory agent and regulates the immune response. Gall-bladder activity is reduced. Other effects include normalizing blood clotting and vascular tone, zinc and copper levels, cell oxygen levels, and use of fat stores for energy. Progesterone also assists in thyroid function, in bone building by osteoblasts, in bone, teeth, gums, joint, tendon, ligament and skin resilience and in some cases healing by regulating various types of collagen, and in nerve function and healing by regulating myelin. Progesterone appears to prevent endometrial cancer (involving the uterine lining) by regulating the effects of estrogen.

Medical Applications[]

Progesterone is poorly absorbed by oral ingestion unless micronised and in oil, or with fatty foods; it does not dissolve in water. Products such as Prometrium, Utrogestan and Microgest are therefore capsules containing micronised progesterone in oil - in all three mentioned that is peanut oil, which may cause serious allergic reactions in some people, but compounding pharmacies, which have the facilities and licenses to make their own products, can use alternatives. Vaginal and rectal application is also effective, with products such as Cyclogest, which is progesterone in cocoa butter in the form of pessaries. Progesterone can be given by injection, but because it has a short half-life they need to be daily. Implants, for a longer period, are also available. Marketing of progesterone phamaceutical products, country to country, varies considerably, with many countries having no oral progesterone products marketed, but they can usually be specially imported by pharmacies through international wholesalers.

"Natural progesterone" products derived from yams, do not require a prescription. Wild yams contain a plant steroid called diosgenin, which the human body cannot metabolize into progesterone. Diogenin can only be chemically processed into progesterone in labs.

Progesterone is used to control anovulatory bleeding. It is also used to prepare uterine lining in infertility therapy and to support early pregnancy. Patients with recurrent pregnancy loss due to inadequate progesterone production may receive progesterone.

Progesterone is being investigated as potentially beneficial in Multiple Sclerosis, since the characteristic deterioration of the Myelin insulation of nerves halts during pregnancy, when progesterone levels are raised, but commences again when the levels drop.

Since most progesterone in males is produced in the process of testicular production of testosterone, and most in females by the ovaries, the shutting down (whether by natural or chemical means), or removal, of those inevitably causes a considerable reduction in progesterone levels. Previous concentration upon the role of progestagens in female reproduction, when progesterone was simply considered a "female hormone" obscured the significance of progesterone elsewhere in both sexes.

The tendency for progesterone to have a regulatory effect, and the presence of progesterone receptors in many types of body tissue, and the pattern of deterioration (or tumour formation) in many of those increasing in later years when progesterone levels have dropped, is prompting widespread research into the potential value of maintaining progesterone levels in both males and females.

Progesterone is used in hormone therapy for transsexual women, and some Intersex women - especially when synthetic progestins have been ineffective or caused side-effects - since normal breast tissue cannot develop except in the presence of both progestogen and estrogen. Mammary glandular tissue is otherwise fibrotic, the breast shape conical and the areola immature, Progesterone can correct those even after years of inadequate hormonal treatment. Research usually cited against such value was conducted using Provera, a synthetic progestin. Progesterone also has a role in skin elasticity and bone strength, in respiration, in nerve tissue and in female sexuality, and the presence of progesterone receptors in certain muscle and fat tissue may hint at a role in sexually-dimorphic proportions of those.

These roles of progesterone may not be fulfilled by synthetic progestins which were designed solely to mimic progesterone's uterine effects.

Progesterone receptor antagonists, or selective progesterone receptor modulators (SPRM)s, such as RU-486 (Mifepristone), can be used to prevent conception or induce medical abortions.

Oral birth control pills do not contain progesterone but a progestin.

See also[]

  • Bioidentical hormone replacement therapy

References[]

  1. Schumacher M, Guennoun R, Robert F, et al. Local synthesis and dual actions of progesterone in the nervous system: neuroprotection and myelination. Growth Horm IGF Res. 2004 Jun;14 Suppl A:S18-33. PMID 15135772

External links[]


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Target-derived NGF, BDNF, NT-3

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