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a progestin compound (trade name Provera) used to treat menstrual disorders (同)Provera
a salt or ester of acetic acid (同)ethanoate

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酢酸(さくさん)塩;アセテート(酢酸人造絹糸)

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出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2013/09/29 19:01:02」(JST)

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This article is about the progestin drug. For the less active metabolite, see medroxyprogesterone.

Medroxyprogesterone acetate (INN, USAN, BAN), also known as 17α-hydroxy-6α-methylprogesterone acetate, and commonly abbreviated as MPA, is a steroidal progestin, a synthetic variant of the human hormone progesterone.^[2]^[3] It is used as a contraceptive, in hormone replacement therapy and for the treatment of endometriosis as well as several other indications.

MPA is a more potent derivative of its parent compound medroxyprogesterone (MP). While medroxyprogesterone is sometimes used as a synonym for medroxyprogesterone acetate,^[3] what is normally being administered is MPA and not MP.^[4]

History[edit]

MPA was independently discovered in 1956^[5] by Syntex^[6] and the Upjohn Company.^[7]

Indications[edit]

In females, the most common use of MPA is as an oral or depot-injected contraceptive and also as the progestin component of menopausal hormone replacement therapy to prevent endometrial hyperplasia and cancer. MPA is also used as a treatment for endometriosis, dysmenorrhea, and amenorrhea.^[8] MPA, along with other progestins were developed to allow the hormones to be taken orally, as progesterone (the hormone made by the human body) could not be taken orally before the process of micronization was developed.^[9]

In males, MPA has been used to control inappropriate sexual behavior to chemically castrate convicted sex offenders.^[10]

MPA is an extremely effective contraceptive when used with relatively high doses to prevent ovulation. It has also been used to treat benign prostatic hyperplasia, as a palliative appetite stimulant for cancer patients, and at high doses (800 mg per day) to treat hormone-dependent cancers of primarily the breast, but also other types.^[11]

Though not used as a treatment for epilepsy, MPA reduces the frequency of seizures and does not interact with anti-epileptic medications. MPA does not interfere with blood clotting and appears to improve blood parameters for women with sickle cell anemia. Similarly, MPA does not appear to affect liver metabolism, and may improve primary biliary cirrhosis and chronic active hepatitis. Women taking MPA may experience spotting shortly after starting the medication but is not usually serious enough to require medical intervention. With longer use amenorrhoea can occur as can irregular menstruation which is a major source of dissatisfaction, though both can result in improvements with iron deficiency and risk of pelvic inflammatory disease and often do not result in discontinuing the medication.^[11] MPA is also prescribed in combination with an estrogen to prevent endometrial hyperplasia in post-menopausal women who are undergoing hormone replacement therapy.^[12]

MPA has also been prescribed in hormone replacement therapy for male-to-female transsexuals due to its antiandrogen and progestogen effects.

Pharmacodynamics[edit]

Activity profile[edit]

MPA acts as an agonist of the progesterone, androgen, and glucocorticoid receptors (PR, AR, and GR, respectively),^[1] activating these receptors with EC₅₀ values of approximately 0.01 nM, 1 nM, and 10 nM, respectively.^[13] It has very low and likely completely insignificant affinity for the estrogen and mineralocorticoid receptors (ER and MR, respectively).^[1] Although the EC50 values of MPA at the PR and the AR and GR are separated by several orders of magnitude, because it is so potent, and because it is used at relatively high doses in humans, it is likely that the overall activation of each of the three receptors is fairly similar.^{[citation needed]} The intrinsic activities of MPA in activating the PR and the AR have been reported to be at least equivalent to those of progesterone and dihydrotestosterone (DHT), respectively, indicating that it is a full agonist of these receptors.^[14]^[15]

In addition to its direct effects on steroid receptors, MPA, at sufficient doses, inhibits the hypothalamic-pituitary-adrenal (HPA) and hypothalamic-pituitary-gonadal (HPG) axes, resulting in a marked suppression of gonadotropin, androgen, estrogen, adrenocorticotropic hormone (ACTH), and cortisol levels as well as concentrations of sex hormone-binding globulin (SHBG).^[16] There is evidence that the downregulatory effects of MPA on the HPG axis are mediated by activation of both PRs and ARs in the pituitary gland.^[17]^[18] Due to its effects on androgen levels, MPA has strong functional antiandrogen properties, and it is used in androgen-sensitive conditions such as precocious puberty in prepubescent boys and hypersexuality in men.^[19] In addition, since it affects estrogen levels similarly, unlike many other antiandrogens such as spironolactone and cyproterone acetate which have a high propensity for causing gynecomastia via indirect stimulation of estrogen, MPA is not thought to possess any estrogenic effects. Indeed, due to its inhibitory effects on estrogen levels, it has potent antiestrogenic effects, and has been used to treat precocious puberty in prepubescent girls. Accordingly, MPA should not be used in high doses without an estrogen in women due to the risk of osteoporosis and other symptoms associated with hypoestrogenism.^[20]

As mentioned above, MPA is a potent full agonist of the AR. Its activation of the AR has been shown to play an important and major role in its antigonadotropic effects and in its beneficial effects against breast cancer.^[17]^[21]^[22] However, although MPA does have the capacity to cause androgenic side effects such as acne and hirsutism in some patients (especially women),^[23]^[24] it seldom actually does so, and when it does, the effects tend to be only mild, regardless of the dosage used.^[17] In fact, likely due to its suppressive actions on androgen levels, it has been reported that MPA is generally highly effective in improving pre-existing symptoms of hirsutism in women with the condition.^[25]^[26] Moreover, MPA rarely causes any androgenic effects in children with precocious puberty, even at very high doses.^[27] The reason for the general lack of virilizing effects with MPA, despite it binding to and activating the AR with a high affinity and this action playing an importoant role in many of its physiological and therapeutic effects, is not entirely clear. However, MPA has been found to interact with the AR in a fundamentally different way than other agonists of the receptor such as dihydrotestosterone (DHT).^[14] The result of this difference appears to be that MPA binds to the AR with a similar affinity and intrinsic activity to that of DHT, but requires about 100-fold higher concentrations for a comparable induction of gene transcription, while at the same time not antagonizing the transcriptional activity of normal androgens like DHT at any concentration.^[14] Thus, this may explain the low propensity of MPA for producing androgenic side effects.

As an agonist of the GR, MPA has glucocorticoid properties, and as a result can cause symptoms of Cushing's syndrome, steroid diabetes, and adrenal insufficiency at sufficiently high doses.^{[citation needed]}

Although MPA and the related drug megestrol acetate (which is a close analogue) have been extensively used as appetite stimulants, the mechanism of action of their beneficial effects on appetite is not entirely clear. However, glucocorticoid, cytokine, and possibly anabolic-related mechanisms are all thought to possibly be involved, and a number of downstream changes have been implicated, including stimulation of the release of neuropeptide Y in the hypothalamus, modulation of calcium channels in the ventromedial hypothalamus, and inhibition of the secretion of proinflammatory cytokines including IL-1α, IL-1β, IL-6, and TNF-α, actions that have all been linked to an increased appetite.^[28]

Comparison to medroxyprogesterone[edit]

MP, the parent drug of MPA, is a metabolite of MPA.^[29] While both the parent medroxyprogesterone (MP) and its acylated derivative medroxyprogesterone acetate (MPA) bind to the progesterone receptor (PR) and both act as agonists, MPA has approximately 100 fold higher binding affinity and transactivation potency compared to MP.^[30] As such, MP is not used clinically, though it has seen some use in veterinary medicine.^[31]

Ligand	PR K_i (nM)	Coactivator recruitment EC₅₀ (nM)	Reporter cell line EC₅₀ (nM)
Progesterone	4.3 ± 1.0	0.9 ± 0.2	25 ± 11
Medroxyprogesterone acetate	1.2 ± 0.3	0.6 ± 0.08	0.15 ± 0.03
Medroxyprogesterone	241 ± 96	47 ± 14	32 ± 1

Pharmacokinetics[edit]

MPA is well-absorbed orally and through intramuscular injection, peaking at 2–4 hours for the former. The half life is 12 to 17 hours for an oral dose, and 40 to 50 days (!) for an intramuscular injection. MPA binds to albumin in the blood, and is metabolized primarily through the liver via hydroxylation and conjugation.^[3] Intramuscular MPA is released slowly; a 150 mg dose is first detectable in the blood 30 minutes after injection, plateauing at 1.0 ng/mL for three months, followed by a gradual, tapering decline that lasts up to nine months in some women. The high levels of MPA in the blood inhibits luteinizing hormone and ovulation for several months, with an accompanying decrease in serum progesterone to below 0.4 ng/mL. Ovulation resumes when once blood levels of MPA fall below 0.1 ng/ml. Serum estradiol remains at approximately 50 pg/nl for approximately four months post-injection (with a range of 10-92 pg/nL after several years of use), rising once MPA levels fall below 0.5 ng/ml.^[32]

Hot flashes are rare while MPA is found at significant blood levels in the body, and the vaginal lining remains moist and creased. The endometrium undergoes atrophy, with small, straight glands and a stroma that is decidualized. Cervical mucus remains viscous. Because of its steady blood levels over the long term and multiple effects that prevent fertilisation, MPA is a very effective means of birth control.^[32]

Adverse effects[edit]

In females, the most common adverse effects are acne, changes in menstrual flow, drowsiness, and can cause birth defects if taken by pregnant women. Other common side effects include breast tenderness, increased facial hair, decreased scalp hair, difficulty falling or remaining asleep, stomach pain, and weight loss or gain.^[8]

The Women's Health Initiative investigated the use of MPA and conjugated equine estrogens compared to placebo. The study was prematurely terminated when previously-unexpected risks were discovered, specifically the finding that though the all-cause mortality was not affected by the hormone therapy, the benefits of the hormone replacement therapy (reduced risk of hip fracture, colorectal and endometrial cancer and all other causes of death) were offset by increased risk of coronary heart disease, breast cancer, strokes and pulmonary embolism.^[33]

At high doses for the treatment of breast cancer, MPA can cause weight gain, worsen diabetes mellitus and edema (particularly of the face). Adverse effects peak at five weeks, and are reduced with lower doses. Less frequent effects may include thrombosis (though it is not clear if this is truly a risk, it can not be ruled out), painful urination, anxiety, headache, nausea and vomiting. When used to treat benign prostatic hyperplasia, more frequent complaints include reduced libido, impotence, reduced ejaculate volume, and within three days, chemical castration. MPA may cause reduced bone density though this appears to be reversible to a normal level even after years of use. At extremely high doses (used to treat cancer, not for contraception) MPA may cause adrenal suppression and interfere with carbohydrate metabolism but does not cause diabetes.^[11]

Fetuses exposed to progesterones have demonstrated higher rates of genital abnormalities, low birth weight, and increased ectopic pregnancy particularly when MPA is used as an injected form of long-term birth control. When used as a form of injected birth control, MPA can reduce fertility for as long as 10 months, taking longer for overweight or obese women. When combined with conjugated equine estrogens (Premarin), MPA has been associated with an increased risk of breast cancer, dementia and thrombus in the eye. In combination with estrogens in general, MPA may increase the risk of cardiovascular disease, with a stronger association when used by post-menopausal women also taking CEE. MPA is not recommended for use prior to menarche or before or during recovery from surgery.^[3] It was because of these unexpected interactions that the Women's Health Initiative study was ended early due the extra risks of hormone replacement therapy,^[34] producing a dramatic decrease in both new and renewal prescriptions for hormone therapy.^[35]

Interactions[edit]

MPA increases the risk of breast cancer, dementia and thrombus when used in combination with conjugated equine estrogens to treat the symptoms of menopause.^[3] When used as a contraceptive, MPA does not generally interact with other drugs. When combined with aminoglutethimide to treat metastases from breast cancer, MPA is associated with an increase in depression.^[11] St John's wort may decrease its effectiveness as a contraceptive.^[3]

Comparison with progesterone[edit]

Proponents of bioidentical hormone replacement therapy believe progesterone offers fewer side effects and improved quality of life compared to MPA.^[36] The evidence for this view has been questioned; MPA is better absorbed when taken orally, with a much longer half life leading to more stable blood levels^[37] though it may lead to greater breast tenderness and more sporadic vaginal bleeding.^[36] The two compounds do not differentiate in their ability to suppress endometrial hyperplasia,^[36] nor does either increase the risk of pulmonary embolism.^[38] The two compounds have not been adequately compared in direct tests to clear conclusions about safety and superiority.^[9]

Chemical synthesis[edit]

MPA can be prepared in 12 reaction steps using the following sequence:^[39]

Synthesis of medroxyprogesterone acetate

References[edit]

^ ^a ^b ^c ^d Schindler AE, Campagnoli C, Druckmann R, Huber J, Pasqualini JR, Schweppe KW, Thijssen JH (2008). "Classification and pharmacology of progestins". Maturitas 61 (1-2): 171–80. doi:10.1016/j.maturitas.2003.09.014. PMID 19434889.
^ Hall JA, Morton I (1999). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer. p. 173. ISBN 978-0-7514-0499-9. Retrieved 28 May 2012.
^ ^a ^b ^c ^d ^e ^f "MedroxyPROGESTERone: Drug Information Provided by Lexi-Comp". Merck Manual. 2009-12-01. Retrieved 2010-07-08.
^ Lenco W, Mcknight M, Macdonald AS (January 1975). "Effects of cortisone acetate, methylprednisolone and medroxyprogesterone on wound contracture and epithelization in rabbits". Ann. Surg. 181 (1): 67–73. doi:10.1097/00000658-197501000-00015. PMC 1343717. PMID 1119869.
^ Sneader, Walter (2005). "Chapter 18: Hormone analogs". Drug discovery: a history. New York: Wiley. p. 204. ISBN 0-471-89980-1.
^ FR 1295307, "Procédé de préparation de dérivés cyclopentano-phénanthréniques", published 1962-06-08, assigned to Syntex SA
^ US granted 3377364, Spero G, "6-methyl-17alpha-hydroxyprogesterone, the lower fatty acid 17-acylates and methods for producing the same", published 1968-04-09, assigned to Upjohn Company
^ ^a ^b "Medroxyprogesterone". MedlinePlus. 2008-01-09. Retrieved 2010-07-02.
^ ^a ^b Panay N, Fenton A (2010). "Bioidentical hormones: what is all the hype about?". Climacteric : the journal of the International Menopause Society 13 (1): 1–3. doi:10.3109/13697130903550250. PMID 20067429. edit
^ Light SA, Holroyd S (March 2006). "The use of medroxyprogesterone acetate for the treatment of sexually inappropriate behaviour in patients with dementia". J Psychiatry Neurosci 31 (2): 132–4. PMC 1413960. PMID 16575429.
^ ^a ^b ^c ^d Meyler L (2009). Meyler's side effects of endocrine and metabolic drugs. Amsterdam: Elsevier Science. pp. 281–284. ISBN 0-444-53271-4.
^ Furness S, Roberts H, Marjoribanks J, Lethaby A, Hickey M, Farquhar C (2009). "Hormone therapy in postmenopausal women and risk of endometrial hyperplasia". Cochrane Database of Systematic Reviews (2): CD000402. doi:10.1002/14651858.CD000402.pub3. PMID 19370558. edit
^ World Health Organization (2004). Residues of Some Veterinary Drugs in Animals and Food: Monographs Prepared by the Sixty-second Meeting of the Joint FAO/WHO Expert Committee on Food Additives, Rome, 4-12 February 2004. Food & Agriculture Org. p. 49. ISBN 978-92-5-105195-5. Retrieved 28 May 2012.
^ ^a ^b ^c Kemppainen JA, Langley E, Wong CI, Bobseine K, Kelce WR, Wilson EM (March 1999). "Distinguishing androgen receptor agonists and antagonists: distinct mechanisms of activation by medroxyprogesterone acetate and dihydrotestosterone". Molecular Endocrinology (Baltimore, Md.) 13 (3): 440–54. PMID 10077001.
^ Bentel JM, Birrell SN, Pickering MA, Holds DJ, Horsfall DJ, Tilley WD (August 1999). "Androgen receptor agonist activity of the synthetic progestin, medroxyprogesterone acetate, in human breast cancer cells". Molecular and Cellular Endocrinology 154 (1-2): 11–20. doi:10.1016/S0303-7207(99)00109-4. PMID 10509795.
^ Genazzani AR (15 January 1993). Frontiers in Gynecologic and Obstetric Investigation. Taylor & Francis. p. 320. ISBN 978-1-85070-486-7. Retrieved 28 May 2012.
^ ^a ^b ^c Poulin R, Baker D, Poirier D, Labrie F (March 1989). "Androgen and glucocorticoid receptor-mediated inhibition of cell proliferation by medroxyprogesterone acetate in ZR-75-1 human breast cancer cells". Breast Cancer Research and Treatment 13 (2): 161–72. PMID 2525057.
^ Brady BM, Anderson RA, Kinniburgh D, Baird DT (April 2003). "Demonstration of progesterone receptor-mediated gonadotrophin suppression in the human male". Clinical Endocrinology 58 (4): 506–12. PMID 12641635.
^ Saleh FM, Grudzinskas AJ, Bradford JM (11 February 2009). Sex Offenders: Identification, Risk Assessment, Treatment, and Legal Issues. Oxford University Press. p. 44. ISBN 978-0-19-517704-6. Retrieved 28 May 2012.
^ Stuart MC, Kouimtzi M, Hill SR (2009). Who Model Formulary 2008. World Health Organization. p. 368. ISBN 978-92-4-154765-9. Retrieved 28 May 2012.
^ Birrell SN, Hall RE, Tilley WD (January 1998). "Role of the androgen receptor in human breast cancer". Journal of Mammary Gland Biology and Neoplasia 3 (1): 95–103. PMID 10819508.
^ Buchanan G, Birrell SN, Peters AA, Bianco-Miotto T, Ramsay K, Cops EJ, Yang M, Harris JM, Simila HA, Moore NL, Bentel JM, Ricciardelli C, Horsfall DJ, Butler LM, Tilley WD (September 2005). "Decreased androgen receptor levels and receptor function in breast cancer contribute to the failure of response to medroxyprogesterone acetate". Cancer Research 65 (18): 8487–96. doi:10.1158/0008-5472.CAN-04-3077. PMID 16166329.
^ Rees MCP, Hope S, Ravnikar V (12 August 2005). The Abnormal Menstrual Cycle. Taylor & Francis. p. 213. ISBN 978-1-84214-212-7. Retrieved 2 June 2012.
^ Aronson JK (20 January 2009). Meyler's Side Effects of Endocrine and Metabolic Drugs. Elsevier. p. 283. ISBN 978-0-444-53271-8. Retrieved 2 June 2012.
^ Ettinger B, Golditch IM (December 1977). "Medroxyprogesterone acetate for the evaluation of hypertestosteronism in hirsute women". Fertility and Sterility 28 (12): 1285–8. PMID 590535.
^ Correa de Oliveira RF, Novaes LP, Lima MB, Rodrigues J, Franco S, Khenaifes AI, Francalanci CP (December 1975). "A new treatment for hirsutism". Annals of Internal Medicine 83 (6): 817–9. PMID 1200527.
^ Richman RA, Underwood LE, French FS, Van Wyk JJ (December 1971). "Adverse effects of large doses of medroxyprogesterone (MPA) in idiopathic isosexual precocity". The Journal of Pediatrics 79 (6): 963–71. PMID 4332067.
^ Doyle D, Hanks G, Cherny NI (3 February 2005). Oxford Textbook Of Palliative Medicine. Oxford University Press. p. 553. ISBN 978-0-19-856698-4. Retrieved 28 May 2012.
^ Ishihara M, Kirdani Y, Osawa Y, Sandberg AA (January 1976). "The metabolic fate of medroxyprogesterone acetate in the baboon". J. Steroid Biochem. 7 (1): 65–70. doi:10.1016/0022-4731(76)90167-9. PMID 1271819.
^ Pullen MA, Laping N, Edwards R, Bray J (September 2006). "Determination of conformational changes in the progesterone receptor using ELISA-like assays". Steroids 71 (9): 792–8. doi:10.1016/j.steroids.2006.05.009. PMID 16784762.
^ Index Nominum 2000: International Drug Directory. Taylor & Francis US. 2000. p. 638. ISBN 978-3-88763-075-1. Retrieved 28 May 2012.
^ ^a ^b Mishell DR Jr (1996). "Pharmacokinetics of depot medroxyprogesterone acetate contraception". The Journal of reproductive medicine 41 (5 Suppl): 381–390. PMID 8725700. edit
^ Rossouw JE, Anderson GL, Prentice RL, LaCroix AZ, Kooperberg C, Stefanick ML, Jackson RD, Beresford SA, Howard BV, Johnson KC, Kotchen JM, Ockene J; Writing Group for the Women's Health Initiative Investigators (2002). "Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women's Health Initiative randomized controlled trial". JAMA: the Journal of the American Medical Association 288 (3): 321–333. doi:10.1001/jama.288.3.321. PMID 12117397. edit
^ Prentice RL, Anderson GL (2008). "The women's health initiative: lessons learned". Annual review of public health 29: 131–150. doi:10.1146/annurev.publhealth.29.020907.090947. PMID 18348708. edit
^ Buist DS, Newton KM, Miglioretti DL, Beverly K, Connelly MT, Andrade S, Hartsfield CL, Wei F, Chan KA, Kessler L (2004). "Hormone therapy prescribing patterns in the United States". Obstetrics and gynecology 104 (5 Pt 1): 1042–1050. doi:10.1097/01.AOG.0000143826.38439.af. PMID 15516400. edit
^ ^a ^b ^c Holtorf K (January 2009). "The bioidentical hormone debate: are bioidentical hormones (estradiol, estriol, and progesterone) safer or more efficacious than commonly used synthetic versions in hormone replacement therapy?" (pdf). Postgrad Med 121 (1): 73–85. doi:10.3810/pgm.2009.01.1949. PMID 19179815.
^ Cirigliano M (2007). "Bioidentical hormone therapy: a review of the evidence" (pdf). Journal of Womens Health 16 (5): 600–31. doi:10.1089/jwh.2006.0311. PMID 17627398.
^ Boothby LA, Doering PL (August 2008). "Bioidentical hormone therapy: a panacea that lacks supportive evidence". Curr. Opin. Obstet. Gynecol. 20 (4): 400–7. doi:10.1097/GCO.0b013e3283081ae9. PMID 18660693.
^ Babcock JC, Gutsell ES, Herr ME, Hogg JA, Stucki JC, Barnes LE, Dulin WE (1958). J. Amer. Chem. Soc. 80 (11): 2904. doi:10.1021/ja01544a079. . See also hydroxyprogesterone caproate for the preparation of the reactant used in this sequence:

UpToDate Contents

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1. 避妊のための酢酸メドロキシプロゲステロンデポ剤 depot medroxyprogesterone acetate for contraception
2. 子宮内膜増殖症の管理 management of endometrial hyperplasia
3. 避妊している女性におけるホルモン剤内服中の出血の管理 management of unscheduled bleeding in women using contraception
4. 重度または持続性子宮出血の管理 managing an episode of severe or prolonged uterine bleeding
5. 閉経後のホルモン療法で用いる製剤 preparations for postmenopausal hormone therapy

English Journal

Impact of Reminder Systems in Clinical Settings to Improve Family Planning Outcomes: A Systematic Review.

Zapata LB1, Tregear SJ2, Tiller M2, Pazol K3, Mautone-Smith N4, Gavin LE4.
American journal of preventive medicine.Am J Prev Med.2015 Aug;49(2S1):S57-S64. doi: 10.1016/j.amepre.2015.03.018.
CONTEXT: This systematic review evaluated the evidence on the impact of family planning reminder systems-interventions intended to remind patients of behaviors to achieve reproductive health goals (e.g., daily text messages reminding oral contraceptive [OC] users to take a pill)-to provide informati
PMID 26190847

Effects of estradiol, progestogens, and of tibolone on breast proliferation and apoptosis.

Pompei LM1, Cunha EP, Steiner ML, Theodoro TR, Mader AM, Petri G, Pinhal MA, Fernandes CE.
Climacteric : the journal of the International Menopause Society.Climacteric.2015 Aug;18(4):518-22. doi: 10.3109/13697137.2015.1020482. Epub 2015 Apr 1.
Aim To study the effects of estrogen therapy, alone or combined with progestogens, and of tibolone on the expression of proliferation and apoptosis markers in normal breast tissue. Methods Thirty 250-day-old Wistar rats were castrated and 3 weeks later received one of the following treatments by gav
PMID 25830529

Is expression of rat breast matrix components influenced by estrogen, progestins and tibolone?

Cunha EP1, Pompei LM, Theodoro TR, Steiner ML, Silva VF, Silveira ER, Mader AM, Pinhal MA, Fernandes CE.
Climacteric : the journal of the International Menopause Society.Climacteric.2015 Aug;18(4):523-7. doi: 10.3109/13697137.2015.1007122. Epub 2015 Mar 2.
Aim To study the effects of estrogen therapy, alone or combined with progestogens, and of tibolone on the expression of heparanase (HSPE), extracellular matrix metalloproteinases 2 and 9 (MMP-2 and MMP-9), perlecan and proliferating cell nuclear antigen (PCNA) in normal breast tissue. Methods Thirty
PMID 25603456

Japanese Journal

症例高用量酢酸メドロキシプロゲステロンによる妊孕性温存療法を2度施行するも再発し,手術療法を施行した若年性子宮体癌の1例

山下美智子,辻江智子,久保田哲他
産科と婦人科 79(4), 513-516, 2012-04-00
NAID 40019249211

症例子宮体癌術後の多発肺転移に対しmedroxyprogesterone acetateが奏効し,長期生存が得られている1例

土田達,折坂俊介,堀芳秋他
産婦人科の実際 61(3), 523-527, 2012-03-00
NAID 40019232218

症例報告酢酸メドロキシプロゲステロンが奏効したアロマターゼ阻害剤抵抗性転移性乳癌の一例

平井慶充,尾浦正二,吉増達也他
和歌山医学 62(4), 115-117, 2011-12-00
NAID 40019180120

Related Pictures

★リンクテーブル★

リンク元	「メドロキシプロゲステロン」「MPA」「DMPA」
関連記事	「medroxyprogesterone」

「メドロキシプロゲステロン」

Medroxyprogesterone acetate
Systematic (IUPAC) name
	17α-hydroxy-6α-methylpregn-4-ene-3,20-dione acetate
Clinical data
Trade names	Depo-Provera (injection), Provera (oral)
AHFS/Drugs.com	FDA Professional Drug Information
MedlinePlus	a604039
Pregnancy cat.	X (US)
Legal status	℞ Prescription only
Routes	Oral, IM
Pharmacokinetic data
Bioavailability	99%
Protein binding	88% (to albumin)
Half-life	40-60 hours
Identifiers
CAS number	71-58-9
ATC code	G03AC06 G03DA02, L02AB02
PubChem	CID 6279
IUPHAR ligand	2879
DrugBank	DB00603
ChemSpider	6043
UNII	C2QI4IOI2G
KEGG	C08150
ChEBI	CHEBI:6716
ChEMBL	CHEMBL717
Chemical data
Formula	C24H34O4
Mol. mass	386.52 g/mol
(what is this?) (verify);

　　[★]

英: medroxyprogesterone
化: 酢酸メドロキシプロゲステロン medroxyprogesterone acetate MPA、medroxyprogesterone 17-acetate、メドロキシプロゲステロン酢酸エステル
商: ヒスロン、プロベラ、ヒスロンH、Provera, Depo-Provera, DMPA, Provera

合成プロゲストーゲン;抗悪性腫瘍薬

適応

子宮体癌、乳癌

黄体ホルモン療法は，類内膜腺癌G1あるいはプロゲステロン受容体陽性の進行・再発症例に用いられる（グレードB）。(参考1)

参考

1. 子宮体癌治療ガイドライン(2006年)

http://www.jsgo.gr.jp/guideline/taigan.html

「MPA」

　　[★]

「DMPA」

　　[★] メドロキシプロゲステロン。medroxyprogesterone acetate Provera, Depo-Provera

「medroxyprogesterone」

　　[★]

メドロキシプロゲステロン

関: medroxyprogesterone 17-acetate、medroxyprogesterone acetate

[pmid19434889-1] Schindler AE, Campagnoli C, Druckmann R, Huber J, Pasqualini JR, Schweppe KW, Thijssen JH (2008). "Classification and pharmacology of progestins". Maturitas 61 (1-2): 171–80. doi:10.1016/j.maturitas.2003.09.014. PMID 19434889.

[MortonMorton1999-2] Hall JA, Morton I (1999). Concise Dictionary of Pharmacological Agents: Properties and Synonyms. Springer. p. 173. ISBN 978-0-7514-0499-9. Retrieved 28 May 2012.

[Merck-3] ^ ^a ^b ^c ^d ^e ^f "MedroxyPROGESTERone: Drug Information Provided by Lexi-Comp". Merck Manual. 2009-12-01. Retrieved 2010-07-08.

[pmid1119869-4] Lenco W, Mcknight M, Macdonald AS (January 1975). "Effects of cortisone acetate, methylprednisolone and medroxyprogesterone on wound contracture and epithelization in rabbits". Ann. Surg. 181 (1): 67–73. doi:10.1097/00000658-197501000-00015. PMC 1343717. PMID 1119869.

[isbn0-471-89980-1-5] Sneader, Walter (2005). "Chapter 18: Hormone analogs". Drug discovery: a history. New York: Wiley. p. 204. ISBN 0-471-89980-1.

[FR1295307-6] FR 1295307, "Procédé de préparation de dérivés cyclopentano-phénanthréniques", published 1962-06-08, assigned to Syntex SA

[US3377364-7] US granted 3377364, Spero G, "6-methyl-17alpha-hydroxyprogesterone, the lower fatty acid 17-acylates and methods for producing the same", published 1968-04-09, assigned to Upjohn Company

[Medline-8] "Medroxyprogesterone". MedlinePlus. 2008-01-09. Retrieved 2010-07-02.

[Panay2010-9] Panay N, Fenton A (2010). "Bioidentical hormones: what is all the hype about?". Climacteric : the journal of the International Menopause Society 13 (1): 1–3. doi:10.3109/13697130903550250. PMID 20067429. edit

[pmid16575429-10] Light SA, Holroyd S (March 2006). "The use of medroxyprogesterone acetate for the treatment of sexually inappropriate behaviour in patients with dementia". J Psychiatry Neurosci 31 (2): 132–4. PMC 1413960. PMID 16575429.

[Meyler-11] Meyler L (2009). Meyler's side effects of endocrine and metabolic drugs. Amsterdam: Elsevier Science. pp. 281–284. ISBN 0-444-53271-4.

[12] Furness S, Roberts H, Marjoribanks J, Lethaby A, Hickey M, Farquhar C (2009). "Hormone therapy in postmenopausal women and risk of endometrial hyperplasia". Cochrane Database of Systematic Reviews (2): CD000402. doi:10.1002/14651858.CD000402.pub3. PMID 19370558. edit

[Organization2004-13] World Health Organization (2004). Residues of Some Veterinary Drugs in Animals and Food: Monographs Prepared by the Sixty-second Meeting of the Joint FAO/WHO Expert Committee on Food Additives, Rome, 4-12 February 2004. Food & Agriculture Org. p. 49. ISBN 978-92-5-105195-5. Retrieved 28 May 2012.

[pmid10077001-14] Kemppainen JA, Langley E, Wong CI, Bobseine K, Kelce WR, Wilson EM (March 1999). "Distinguishing androgen receptor agonists and antagonists: distinct mechanisms of activation by medroxyprogesterone acetate and dihydrotestosterone". Molecular Endocrinology (Baltimore, Md.) 13 (3): 440–54. PMID 10077001.

[pmid10509795-15] Bentel JM, Birrell SN, Pickering MA, Holds DJ, Horsfall DJ, Tilley WD (August 1999). "Androgen receptor agonist activity of the synthetic progestin, medroxyprogesterone acetate, in human breast cancer cells". Molecular and Cellular Endocrinology 154 (1-2): 11–20. doi:10.1016/S0303-7207(99)00109-4. PMID 10509795.

[Genazzani1993-16] Genazzani AR (15 January 1993). Frontiers in Gynecologic and Obstetric Investigation. Taylor & Francis. p. 320. ISBN 978-1-85070-486-7. Retrieved 28 May 2012.

[pmid2525057-17] Poulin R, Baker D, Poirier D, Labrie F (March 1989). "Androgen and glucocorticoid receptor-mediated inhibition of cell proliferation by medroxyprogesterone acetate in ZR-75-1 human breast cancer cells". Breast Cancer Research and Treatment 13 (2): 161–72. PMID 2525057.

[pmid12641635-18] Brady BM, Anderson RA, Kinniburgh D, Baird DT (April 2003). "Demonstration of progesterone receptor-mediated gonadotrophin suppression in the human male". Clinical Endocrinology 58 (4): 506–12. PMID 12641635.

[SalehGrudzinskas2009-19] Saleh FM, Grudzinskas AJ, Bradford JM (11 February 2009). Sex Offenders: Identification, Risk Assessment, Treatment, and Legal Issues. Oxford University Press. p. 44. ISBN 978-0-19-517704-6. Retrieved 28 May 2012.

[StuartKouimtzi2009-20] Stuart MC, Kouimtzi M, Hill SR (2009). Who Model Formulary 2008. World Health Organization. p. 368. ISBN 978-92-4-154765-9. Retrieved 28 May 2012.

[pmid10819508-21] Birrell SN, Hall RE, Tilley WD (January 1998). "Role of the androgen receptor in human breast cancer". Journal of Mammary Gland Biology and Neoplasia 3 (1): 95–103. PMID 10819508.

[pmid16166329-22] Buchanan G, Birrell SN, Peters AA, Bianco-Miotto T, Ramsay K, Cops EJ, Yang M, Harris JM, Simila HA, Moore NL, Bentel JM, Ricciardelli C, Horsfall DJ, Butler LM, Tilley WD (September 2005). "Decreased androgen receptor levels and receptor function in breast cancer contribute to the failure of response to medroxyprogesterone acetate". Cancer Research 65 (18): 8487–96. doi:10.1158/0008-5472.CAN-04-3077. PMID 16166329.

[ReesHope2005-23] Rees MCP, Hope S, Ravnikar V (12 August 2005). The Abnormal Menstrual Cycle. Taylor & Francis. p. 213. ISBN 978-1-84214-212-7. Retrieved 2 June 2012.

[Aronson2009-24] Aronson JK (20 January 2009). Meyler's Side Effects of Endocrine and Metabolic Drugs. Elsevier. p. 283. ISBN 978-0-444-53271-8. Retrieved 2 June 2012.

[pmid590535-25] Ettinger B, Golditch IM (December 1977). "Medroxyprogesterone acetate for the evaluation of hypertestosteronism in hirsute women". Fertility and Sterility 28 (12): 1285–8. PMID 590535.

[pmid1200527-26] Correa de Oliveira RF, Novaes LP, Lima MB, Rodrigues J, Franco S, Khenaifes AI, Francalanci CP (December 1975). "A new treatment for hirsutism". Annals of Internal Medicine 83 (6): 817–9. PMID 1200527.

[pmid4332067-27] Richman RA, Underwood LE, French FS, Van Wyk JJ (December 1971). "Adverse effects of large doses of medroxyprogesterone (MPA) in idiopathic isosexual precocity". The Journal of Pediatrics 79 (6): 963–71. PMID 4332067.

[DoyleHanks2005-28] Doyle D, Hanks G, Cherny NI (3 February 2005). Oxford Textbook Of Palliative Medicine. Oxford University Press. p. 553. ISBN 978-0-19-856698-4. Retrieved 28 May 2012.

[pmid1271819-29] Ishihara M, Kirdani Y, Osawa Y, Sandberg AA (January 1976). "The metabolic fate of medroxyprogesterone acetate in the baboon". J. Steroid Biochem. 7 (1): 65–70. doi:10.1016/0022-4731(76)90167-9. PMID 1271819.

[pmid16784762-30] Pullen MA, Laping N, Edwards R, Bray J (September 2006). "Determination of conformational changes in the progesterone receptor using ELISA-like assays". Steroids 71 (9): 792–8. doi:10.1016/j.steroids.2006.05.009. PMID 16784762.

[Index_Nominum_2000:_International_Drug_Directory-31] Index Nominum 2000: International Drug Directory. Taylor & Francis US. 2000. p. 638. ISBN 978-3-88763-075-1. Retrieved 28 May 2012.

[Mishell-32] Mishell DR Jr (1996). "Pharmacokinetics of depot medroxyprogesterone acetate contraception". The Journal of reproductive medicine 41 (5 Suppl): 381–390. PMID 8725700. edit

[33] Rossouw JE, Anderson GL, Prentice RL, LaCroix AZ, Kooperberg C, Stefanick ML, Jackson RD, Beresford SA, Howard BV, Johnson KC, Kotchen JM, Ockene J; Writing Group for the Women's Health Initiative Investigators (2002). "Risks and benefits of estrogen plus progestin in healthy postmenopausal women: principal results from the Women's Health Initiative randomized controlled trial". JAMA: the Journal of the American Medical Association 288 (3): 321–333. doi:10.1001/jama.288.3.321. PMID 12117397. edit

[34] Prentice RL, Anderson GL (2008). "The women's health initiative: lessons learned". Annual review of public health 29: 131–150. doi:10.1146/annurev.publhealth.29.020907.090947. PMID 18348708. edit

[35] Buist DS, Newton KM, Miglioretti DL, Beverly K, Connelly MT, Andrade S, Hartsfield CL, Wei F, Chan KA, Kessler L (2004). "Hormone therapy prescribing patterns in the United States". Obstetrics and gynecology 104 (5 Pt 1): 1042–1050. doi:10.1097/01.AOG.0000143826.38439.af. PMID 15516400. edit

[Holtorf2009-36] Holtorf K (January 2009). "The bioidentical hormone debate: are bioidentical hormones (estradiol, estriol, and progesterone) safer or more efficacious than commonly used synthetic versions in hormone replacement therapy?" (pdf). Postgrad Med 121 (1): 73–85. doi:10.3810/pgm.2009.01.1949. PMID 19179815.

[Cirigliano-37] Cirigliano M (2007). "Bioidentical hormone therapy: a review of the evidence" (pdf). Journal of Womens Health 16 (5): 600–31. doi:10.1089/jwh.2006.0311. PMID 17627398.

[38] Boothby LA, Doering PL (August 2008). "Bioidentical hormone therapy: a panacea that lacks supportive evidence". Curr. Opin. Obstet. Gynecol. 20 (4): 400–7. doi:10.1097/GCO.0b013e3283081ae9. PMID 18660693.

[39] Babcock JC, Gutsell ES, Herr ME, Hogg JA, Stucki JC, Barnes LE, Dulin WE (1958). J. Amer. Chem. Soc. 80 (11): 2904. doi:10.1021/ja01544a079. . See also hydroxyprogesterone caproate for the preparation of the reactant used in this sequence:

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medroxyprogesterone acetate