Effect of Ethisterone, Β-Œstradiol and Progesterone on the Phagocytic

Total Page:16

File Type:pdf, Size:1020Kb

Effect of Ethisterone, Β-Œstradiol and Progesterone on the Phagocytic No. 4553 February 2, 1957 NATURE 261 Effect of Ethisterone, [3-<Estradiol and two weeks, four showed vital staining appearances Activity similar to the controls, while the remaining two Progesterone on the Phagocytic es. Reticulo-Endothelial System animals showed reduced activity of the macrophag of the The results, therefore, suggest that, in the male THE reticulo-endothelial cells are known to form guinea pig, ethisterone, [3-restradiol and progesterone an important part of the defence mechanism of the have little or no effect on the activity of the reticulo­ body against infection. At the site of a cute infections, endothelial system and in this respect differ greatly neutrophil leucocytes attack the invading organisms from the cestrogens. while the reticulo-endothelial macrophages phago­ The substances used in these investigations were cytose the dead bacteria and dead tissue cells. provided by Dr. Tindall, of Organon Laboratories, In chronic infections such as tuberculosis, the Ltd., to whom we offer our grateful thanks. phagocytic activity of the macrophages forms the T. NICOL main line of defence against the invading organisms. R. s. SNELL Further, there is much circumstantial evidence in Department of Anatomy, both acute and chronic infections to show that the King's College, 1·eticulo-endothelial cells raise the humoral resistance London, W.C.2. Nov. 9. patient by the production of antibodies. It of the 1 Nicol, T., Helmy, I. D., and Abou-Z1kry, A., Brit. J. Sura., 40, 166 has already been demonstra ted that the phagocytic (1952). activity of the reticulo-endotholial system is stimu­ • Nicol, T., and Snell, R. S., Nature, 174, 554 (1954): 177, 430 (1956). 2 [178, 1405 (1956) J. lated by restrogens1 ; that cortisone , testosterone, ' Snell, R. S., and Nicol, T., Nature androstene-3[3-l 71X-diol3 depress the phagocytio • Nicol, T., and Snell, R. S., Nature, 175, 995 (1965). activity ; and that deoxyoortioosterone• has no appreciablo effect. The present communication deals with the e ffects Isolation of Nigerose from Floridean of ethisterone, [3 -restradiol and progesterone. Forty­ Starch three male guinea pigs were used. The reticulo­ IT is generally agreed that the iodine-staining by giving all endothelial macrophages were studied polysaccharide isolated from many red algae is a blue the animals one daily injection of trypan glucan of the amylopectin type in which the cha.in­ being subcutaneously for the last six days prior to forming links are IX-1 : 4 and the branch links, was killed by chloroform. The dosage of the dye 01:-l : 6-glucosidic. The floridean starch from Dilsea per calculated on the basis of O ·8 ml. of a 1 edulis appears to differ, in finer details of structure, body­ cent solution in distilled water per 100 gm. from one sample to another. This difference turns only weight. Seven of the animals were given dye m ainly on the presence or the absence of a third type as controls. The hormone treatment 1 and were used of link, namely, the 1: 3-glucosidic linkage • The shown given to the remaining thirty-six animals is m ajority of investigations favour the view that in Table 1. 1 : 3-glucosidic linkages are in fact not present in Dilsea starch•. We therefore think it desirable to Table 1. HORMONE TREATMENT GIVEN TO THmTY•SIX ANIMALS record some observations made in the course of a Dally dose Duration comprehensive linkage analysis of £1.oridean starch No.of Hormone used intra- of which establish that a small proportion of 1 : 3-links animals muscularly treatment is an integral part of the starch structure and, more­ ---6 Ethisterone (Organon) dis- 0 ·5 mgm. 2 weeks over, that these links have the IX-configuration. solved in ethyl oleate Floridean starch was extracted from Dilsea edulis 6 Ethisterone (Organon) dis- 0·5 mgm. 4 weeks by the method of Barry et al. 1 and was purified by solved in ethyl oleate precipitation with iodine• and by use of cetyl tri­ 6 /1-CE•tradl ol (Organon) dis- 0·5mgm. 2 weeks methyl ammonium bromide ('Cetavlon') to precipitate solved In ethyl oleate a galactan sulphate impurity•. The starch (92·5 per 6 /1-CEstradlol ~rganon) dis- 0 ·5 mgm. 4 weeks cent polyglucose) had [1X]~ + 187° (water) and blue in et yl oleate solved value, 0·065. The starch (12·5 gm.) was hydrolysed 6 Progesterone (Organon) dis- 6·0 mgm. 2 weeks by 0·33N sulphuric acid (1·25 litres) at 100° In ethyl oleate solved to the stage of an apparent conversion into glucose 6 Progesterone (Organon) dis- 3 ·0mgm. 3 weeks of 53·4 per cent (2·15 hr.). After being cooled, ethyl oleate solved In neutralized and concentrated, the hydrolysate was chromatographed on a column of charcoal-'Celite'•. but Specimens were taken from the splean, liver and Glucose was the only monosaccharide obtained, into two lymph nodes and fixed in Heidenhain's Susa fluid. the disaccharides were readily separated entirely of Sections were cut at 10µ thick and stained with weak fractions, the first consisting almost as its [3-octa­ eosin, dilute carbol fuchsin or alum carmine. The isomaltose (289 mgm.), characterized [1XJt 96 ·9° in activity of the reticulo-endothelial system in the acetate (melting point 142 ·3° ; + organs studied was assessed by the number of dye­ chloroform). The second disaccharide fraction was bearing cells and the intensity of the vital staining. mainly maltose but contained a small amount of In the animals which received ethisterone and another disaccharide, which was separated from the [3-restradiol, a moderate number of dye granules was maltose by taking advantage of its greater electro­ present in the macrophages of the spleen, liver and phoretic mobility in borate buffer•. The amorphous lymph nodes and the vital staining appearances solid obtained (34·6 mgm.) migrated as a single closely resembled those in the control animals. In substance during both paper chromatography and the six animals which received 3 mgm. of progesterone electrophoresis and had mobilities in each system daily for three weeks the vital staining appearances identical with those of authentic nigerose. It showed were similar to those of the controls. In the group [1Xn + 136·9° (water) and its f,-octa-acetate had which received 5 mgm. of progesterone daily for melting point and mixed melting point 147-48° and © 1957 Nature Publishing Group.
Recommended publications
  • Pp375-430-Annex 1.Qxd
    ANNEX 1 CHEMICAL AND PHYSICAL DATA ON COMPOUNDS USED IN COMBINED ESTROGEN–PROGESTOGEN CONTRACEPTIVES AND HORMONAL MENOPAUSAL THERAPY Annex 1 describes the chemical and physical data, technical products, trends in produc- tion by region and uses of estrogens and progestogens in combined estrogen–progestogen contraceptives and hormonal menopausal therapy. Estrogens and progestogens are listed separately in alphabetical order. Trade names for these compounds alone and in combination are given in Annexes 2–4. Sales are listed according to the regions designated by WHO. These are: Africa: Algeria, Angola, Benin, Botswana, Burkina Faso, Burundi, Cameroon, Cape Verde, Central African Republic, Chad, Comoros, Congo, Côte d'Ivoire, Democratic Republic of the Congo, Equatorial Guinea, Eritrea, Ethiopia, Gabon, Gambia, Ghana, Guinea, Guinea-Bissau, Kenya, Lesotho, Liberia, Madagascar, Malawi, Mali, Mauritania, Mauritius, Mozambique, Namibia, Niger, Nigeria, Rwanda, Sao Tome and Principe, Senegal, Seychelles, Sierra Leone, South Africa, Swaziland, Togo, Uganda, United Republic of Tanzania, Zambia and Zimbabwe America (North): Canada, Central America (Antigua and Barbuda, Bahamas, Barbados, Belize, Costa Rica, Cuba, Dominica, El Salvador, Grenada, Guatemala, Haiti, Honduras, Jamaica, Mexico, Nicaragua, Panama, Puerto Rico, Saint Kitts and Nevis, Saint Lucia, Saint Vincent and the Grenadines, Suriname, Trinidad and Tobago), United States of America America (South): Argentina, Bolivia, Brazil, Chile, Colombia, Dominican Republic, Ecuador, Guyana, Paraguay,
    [Show full text]
  • Exposure to Female Hormone Drugs During Pregnancy
    British Journal of Cancer (1999) 80(7), 1092–1097 © 1999 Cancer Research Campaign Article no. bjoc.1998.0469 Exposure to female hormone drugs during pregnancy: effect on malformations and cancer E Hemminki, M Gissler and H Toukomaa National Research and Development Centre for Welfare and Health, Health Services Research Unit, PO Box 220, 00531 Helsinki, Finland Summary This study aimed to investigate whether the use of female sex hormone drugs during pregnancy is a risk factor for subsequent breast and other oestrogen-dependent cancers among mothers and their children and for genital malformations in the children. A retrospective cohort of 2052 hormone-drug exposed mothers, 2038 control mothers and their 4130 infants was collected from maternity centres in Helsinki from 1954 to 1963. Cancer cases were searched for in national registers through record linkage. Exposures were examined by the type of the drug (oestrogen, progestin only) and by timing (early in pregnancy, only late in pregnancy). There were no statistically significant differences between the groups with regard to mothers’ cancer, either in total or in specified hormone-dependent cancers. The total number of malformations recorded, as well as malformations of the genitals in male infants, were higher among exposed children. The number of cancers among the offspring was small and none of the differences between groups were statistically significant. The study supports the hypothesis that oestrogen or progestin drug therapy during pregnancy causes malformations among children who were exposed in utero but does not support the hypothesis that it causes cancer later in life in the mother; the power to study cancers in offspring, however, was very low.
    [Show full text]
  • State of the Science Report | 19Th Annual PCF Scientific Retreat 2 Session 9 the Good, the Bad and the Ugly of Preclinical and Observational Research
    STATE OF Highlights from the 19th Annual PCF THE SCIENCE Scientific Retreat REPORT October 2012 Provided with the compliments of the Prostate Cancer Foundation Table of Contents Introduction ......................................................................................................................... 4 Special lecture Tumor Heterogeneity: Clonality and Consequences ..................................................................... 5 Session 1 Field Cancerization & the Tumor Microenvironment ..................................................................... 7 Special Lecture Cancer Interception & Metabolic Transformation ........................................................................ 10 Session 2 Role of Growth Factor and Signal Transduction Alterations in Prostate Cancer Initiation, Progression and Therapy Resistance .......................................................................................................... 12 Session 3 Advances in Molecular Imaging of Prostate Cancer .................................................................... 17 Breakthrough Lecture Organoids: A Profound New Prostate Cancer Model System ........................................................ 23 PCF-StandUpToCancer Dream Team Overview 1 ............................................................... 25 PCF-StandUpToCancer Dream Team Overview 2 ............................................................... 28 Exceptional Progress Report – PCF Young Investigator Integrated Molecular Analysis of Circulating Tumor Cells:
    [Show full text]
  • Pharmacology on Your Palms CLASSIFICATION of the DRUGS
    Pharmacology on your palms CLASSIFICATION OF THE DRUGS DRUGS FROM DRUGS AFFECTING THE ORGANS CHEMOTHERAPEUTIC DIFFERENT DRUGS AFFECTING THE NERVOUS SYSTEM AND TISSUES DRUGS PHARMACOLOGICAL GROUPS Drugs affecting peripheral Antitumor drugs Drugs affecting the cardiovascular Antimicrobial, antiviral, Drugs affecting the nervous system Antiallergic drugs system antiparasitic drugs central nervous system Drugs affecting the sensory Antidotes nerve endings Cardiac glycosides Antibiotics CNS DEPRESSANTS (AFFECTING THE Antihypertensive drugs Sulfonamides Analgesics (opioid, AFFERENT INNERVATION) Antianginal drugs Antituberculous drugs analgesics-antipyretics, Antiarrhythmic drugs Antihelminthic drugs NSAIDs) Local anaesthetics Antihyperlipidemic drugs Antifungal drugs Sedative and hypnotic Coating drugs Spasmolytics Antiviral drugs drugs Adsorbents Drugs affecting the excretory system Antimalarial drugs Tranquilizers Astringents Diuretics Antisyphilitic drugs Neuroleptics Expectorants Drugs affecting the hemopoietic system Antiseptics Anticonvulsants Irritant drugs Drugs affecting blood coagulation Disinfectants Antiparkinsonian drugs Drugs affecting peripheral Drugs affecting erythro- and leukopoiesis General anaesthetics neurotransmitter processes Drugs affecting the digestive system CNS STIMULANTS (AFFECTING THE Anorectic drugs Psychomotor stimulants EFFERENT PART OF THE Bitter stuffs. Drugs for replacement therapy Analeptics NERVOUS SYSTEM) Antiacid drugs Antidepressants Direct-acting-cholinomimetics Antiulcer drugs Nootropics (Cognitive
    [Show full text]
  • Progestin - Wikipedia, the Free Encyclopedia
    Progestin - Wikipedia, the free encyclopedia http://en.wikipedia.org/wiki/Progestin From Wikipedia, the free encyclopedia A progestin is a synthetic[1] progestogen that has progestinic effects similar to progesterone. [2] The two most common uses of progestins are for hormonal contraception (either alone or with an estrogen), and to prevent endometrial hyperplasia from unopposed estrogen in hormone replacement therapy. Progestins are also used to treat secondary amenorrhea, dysfunctional uterine bleeding and endometriosis, and as palliative treatment of endometrial cancer, renal cell carcinoma, breast cancer, and prostate cancer. High-dose megestrol acetate is used to treat anorexia, cachexia, and AIDS-related wasting. Progesterone (or sometimes the progestin dydrogesterone or 17α-hydroxyprogesterone caproate) is used for luteal support in IVF protocols, questionably for treatment of recurrent pregnancy loss, and for prevention of preterm birth in pregnant women with a history of at least one spontaneous preterm birth.[3] They are also used in judicial chemical castration of sex offenders as well as a treatment options for those suffering from paraphilia. Co-inventor Luis E. Miramontes's signed laboratory notebook. October 15, 1951 1 History 2 Examples 3 Methods of progestin-based contraception 4 See also 5 References The recognition of progesterone's ability to suppress ovulation during pregnancy spawned a search for a similar hormone that could bypass the problems associated with administering progesterone (low bioavailability when administered
    [Show full text]
  • Treatment of Acne with Oral Contraceptives: Criteria for Pill Selection George T
    Treatment of Acne With Oral Contraceptives: Criteria for Pill Selection George T. Koulianos, MD, Mobile, Alabama Combination oral contraceptives (OCs) (those that actively promoted to the specialty. Thus, under- contain estrogen and progestin) are widely used in standing of these preparations may be limited and the treatment of acne because they modify an somewhat skewed. Marketing based on outdated excessively androgenic hormonal environment and animal bioassays has distorted clinicians’ apprecia- can decrease lesions. Dermatologists’ knowledge tion of OC options. Direct-to-consumer advertising of the most appropriate OC may be hampered by an has been another misleading factor; prominent incomplete understanding of these agents, mislead- claims about acne, which drive patients to request ing promotion, and confusion surrounding the new “the pill,” often overshadow more important health generation of OCs. Despite reports attributing sig- concerns and benefits. Finally, the recent develop- nificance to the degree of androgenicity of the prog- ment of a new generation of OCs containing prog- estin components of OCs, in vitro and animal estins, intended to be less androgenic than their bioassays of androgenicity have little clinical rele- earlier counterparts, may have further confused the vance. Because all of today’s low-dose combination issue. Although these progestins have proven no OCs are estrogen dominant, they are equally bene- better than the older ones, recent discussions of ficial in women with androgenic conditions such as their use in acne therapy have left many physicians acne. Use of the OC containing the lowest dose of and patients with the mistaken impression that only each hormone, consistent with the patient’s needs, certain OC formulations are appropriate to this can enhance compliance by preventing or limiting indication.
    [Show full text]
  • IIHHHHHHHHHHHHH US005094.857A United States Patent (19) 11) Patent Number: 5,094,857 Luderschmidt (45) Date of Patent: Mar
    IIHHHHHHHHHHHHH US005094.857A United States Patent (19) 11) Patent Number: 5,094,857 Luderschmidt (45) Date of Patent: Mar. 10, 1992 54 TREATMENT OF ACNE OR AND 163490 12/1985 European Pat. Off. ROGENETICALOPECA BY TOPICAL 285563 10/1988 European Pat. Off. 316780 5/1989 European Pat. Off. ADMINISTRATION OF ETHISTERONE 356382 2/1990 European Pat. Off. 76 Inventor: Christoph Luderschmidt, Orthstrasse 3338339 4/1984 Fed. Rep. of Germany . 22, D-8000 Munchen, Fed. Rep. of 3738620 5/1989 Fed. Rep. of Germany . Germany 3836862 5/1990 Fed. Rep. of Germany . 2131292A 6/1984 United Kingdom . (21) Appl. No.: 606,949 2131292B 3/1987 United Kingdom. (22 Filed: Oct. 31, 1990 OTHER PUBLICATIONS Luder Schmidt CA.112:133196w (1989). Related U.S. Application Data Schmidt CA106:149804e (1987). 63 Continuation of Ser. No. 268,153, Nov. 7, 1988, aban Mortimer CA.104:136092e(1985). doned. Mortimer GA. 104:136094c (1985). 30 Foreign Application Priority Data Luderschmidt GA.104:6216ic (1985). Luderschmidt GA. 102:143355e (1984). Nov. 13, 1987 (DEl Fed. Rep. of Germany ....... 3738620 Mortimer GA.101:1370455(1984). 51) Int. Cl.......................... A61K 7/06; A61K 7/48; Mortimer GA. 101:116766n(1984). A61K 31/565; A61L 15/03 Schmidt, J. B. et al., Med. Welt. 36:1 122 (1985). 52 U.S. C. .................................... 424/449; 514/859; Schmidt, J. B. et al., Hautarzt 38(3):470-473 Aug. 514/947; 514/169 (1987). 58) Field of Search ................................ 514/169-182, Toth, F et al., Z. Arztl. Fortbild (Jena) 64(3):122-131 514/859, 947; 424/449 Feb. 1, 1990.
    [Show full text]
  • Progress in Antiandrogen Design Targeting Hormone Binding Pocket to Circumvent Mutation Based Resistance
    REVIEW published: 24 March 2015 doi: 10.3389/fphar.2015.00057 Progress in antiandrogen design targeting hormone binding pocket to circumvent mutation based resistance Xiaohong Tian 1, Yang He 2 and Jinming Zhou 2* 1 Lady Davis Institute, Jewish General Hospital, Mcgill University, Montreal, QC, Canada, 2 Immunology, Institute of Medicinal Biotechnology Chinese Academy of Medical Science, Beijing, China Androgen receptor (AR) plays a critical role in the development and progression of prostate cancer (PCa). Current clinically used antiandrogens such as flutamide, bicalutamide, and newly approved enzalutamide mainly target the hormone binding Edited by: pocket (HBP) of AR. However, over time, drug resistance invariably develops and Rongtuan Lin, switches these antiandrogens from antagonist to agonist of the AR. Accumulated McGill University, Canada evidence indicates that AR mutation is an important cause for the drug resistance. This Reviewed by: review will give an overview of the mutation based resistance of the current clinically Vincenzo Arena, Università Cattolica del Sacro Cuore, used antiandrogens and the rational drug design to overcome the resistance, provides a Italy promising strategy for the development of the new generation of antiandrogens targeting Mohamed Diwan M. AbdulHameed, Department of Defense Biotechnology HBP. High Performance Computing Keywords: androgen receptor, antiandrogen, drug resistance, mutation, rational drug design Software Applications Institute, USA *Correspondence: Jinming Zhou, Introduction Immunology, Institute of Medicinal Biotechnology Chinese Academy of Prostate cancer (PCa) is one of the most common cancer and the second leading cause of can- Medical Science, Tian Tan Xi Li 1, cer death in men in the western countries (Jemal et al., 2011). AR, a member of nuclear receptor Beijing 100050, China [email protected] family that is activated by binding of androgens (Roy et al., 1999), plays an important role in pro- moting the development of PCa (Dong et al., 2005).
    [Show full text]
  • Progesterone in Peri- and Postmenopause: a Review Progesteron in Der Peri-Und Postmenopause – Ein Überblick
    Review 995 Progesterone in Peri- and Postmenopause: A Review Progesteron in der Peri-und Postmenopause – ein Überblick Author P.-A. Regidor1,2 Affiliations 1 Praxis für Frauenheilkunde, München 2 Velvian GmbH, Ismaning Key words Abstract Zusammenfassung l" hormone therapy ! ! l" progesterone Around 14.5 million peri- and postmenopausal Aktuell leben 14,5 Millionen peri- und post- l" menopause women currently live in Germany. Moreover, ap- menopausale Frauen in Deutschland. Gleichzeitig l" menopausal symptoms proximately 450 000 women, each with a life ex- gibt es ungefähr 450 000 neue menopausale Frau- Schlüsselwörter pectancy of around 85 years, reach menopause en pro Jahr, die eine Lebenserwartung von bis zu l" Hormontherapie every year in Germany. The challenge is therefore 85 Jahren haben. Die Herausforderung besteht l" Progesteron to find a therapy with few side effects which daher in einer möglichst nebenwirkungsarmen l" Menopause could improve the quality of life of women with Therapie bei den Frauen mit menopausalen Be- l" Wechseljahresbeschwerden menopausal symptoms. The aim of hormone schwerden, um einer Verschlechterung ihrer Le- therapy (HT) is to remedy hormone deficiencies bensqualität entgegenzuwirken. Ziel einer Hor- using substances that offer the best trade-off montherapie (HT) sollte die Behebung des Hor- between benefits and risks. This is where proges- monmangels sein, wobei Substanzen mit dem terone has a new and important role to play. Pro- besten Nutzen-Risiko-Profil eingesetzt werden Deutschsprachige gesterone is one of the most important gestagens. sollten. Hier spielt Progesteron eine neue und Zusatzinformationen Biologically effective progesterone formulations wichtige Rolle. Beim Progesteron handelt es sich online abrufbar unter: created with micronization techniques have been um den wichtigsten Vertreter der Gestagene.
    [Show full text]
  • RR-17: Scoping Review of Prenatal
    NTP RESEARCH REPOrt ON THE SCOPING REVIEW OF PRENATAL EXPOSURE TO PROGESTOGENS AND ADVERSE HEALTH OUTCOMES NTP RR 17 SEPTEMBER 2020 NTP Research Report on the Scoping Review of Prenatal Exposure to Progestogens and Adverse Health Outcomes Research Report 17 September 2020 National Toxicology Program Public Health Service U.S. Department of Health and Human Services ISSN: 2473-4756 Research Triangle Park, North Carolina, USA Scoping Review of Prenatal Exposure to Progestogens and Adverse Health Outcomes Foreword The National Toxicology Program (NTP), established in 1978, is an interagency program within the Public Health Service of the U.S. Department of Health and Human Services. Its activities are executed through a partnership of the National Institute for Occupational Safety and Health (part of the Centers for Disease Control and Prevention), the Food and Drug Administration (primarily at the National Center for Toxicological Research), and the National Institute of Environmental Health Sciences (part of the National Institutes of Health), where the program is administratively located. NTP offers a unique venue for the testing, research, and analysis of agents of concern to identify toxic and biological effects, provide information that strengthens the science base, and inform decisions by health regulatory and research agencies to safeguard public health. NTP also works to develop and apply new and improved methods and approaches that advance toxicology and better assess health effects from environmental exposures. NTP reports the findings from many of its studies in the NTP Technical Report and Monograph series. NTP uses the Research Report series, which began in 2016, to report on work that does not fit readily into one of those two series, such as pilot studies, assay development or optimization studies, literature surveys or scoping reviews, and handbooks on NTP procedures or study specifications.
    [Show full text]
  • Recent Advances in the Analysis of Steroid Hormones and Related Drugs
    ANALYTICAL SCIENCES MAY 2004, VOL. 20 767 2004 © The Japan Society for Analytical Chemistry Reviews Recent Advances in the Analysis of Steroid Hormones and Related Drugs Sándor GÖRÖG Gedeon Richter Ltd., P.O.B. 27, H-1475 Budapest, Hungary The development during the last 15 years and the state-of-the-art in the analysis of bulk steroid hormone drugs and hormone-like structures and pharmaceutical formulations made thereof are summarized. Other steroids (sterols, bile acids, cardiac glycosides, vitamins D) as well as biological-clinical aspects and pharmacokinetic and metabolic studies are excluded from this review. The state-of-the-art is summarized based on comparisons of monographs in the latest editions of the European Pharmacopoeia, United States Pharmacopoeia and the Japanese Pharmacopoeia. This is followed by sections dealing with new developments in the methodology for the fields of spectroscopic and spectrophotometric, chromatographic, electrophoretic and hyphenated techniques as well electroanalytical methods. The review is terminated by two problem-oriented sections: examples on impurity and degradation profiling as well as enantiomeric analysis. (Received January 14, 2004; Accepted February 2, 2004) 1 Introduction 767 4·3 Supercritical fluid chromatography (SFC) 2 Steroid Hormone Drugs in Pharmacopoeias 768 4·4 High-performance liquid chromatography 2·1 Assay of bulk drug materials (HPLC) and HPLC-MS 2·2 Related impurities test of bulk drug materials 5 Electrophoretic and Related Methods 776 2·3 Assay of steroid hormone formulations
    [Show full text]
  • Downloaded from Bioscientifica.Com at 10/01/2021 06:44:53AM Via Free Access
    57 1 S GIATTI and others Progestins in the brain 57: 2 R109–R126 Review The other side of progestins: effects in the brain Correspondence Silvia Giatti, Roberto Cosimo Melcangi and Marzia Pesaresi should be addressed Department of Pharmacological and Biomolecular Sciences, Center of Excellence on Neurodegenerative to R C Melcangi Diseases, Università degli Studi di Milano, Milan, Italy Email [email protected] Abstract Progestins are a broad class of progestational agents widely differing in their Key Words chemical structures and pharmacological properties. Despite emerging data f progesterone suggest that progestins, besides their action as endometrial protection, can also have f testosterone multiple nonreproductive functions, much remains to be discovered regarding the f combined oral actions exerted by these molecules in the nervous system. Here, we report the role contraceptive exerted by different progestins, currently used for contraception or in postmenopausal f hormone replacement therapy hormone replacement therapies, in regulating cognitive functions as well as social f neuroprotection behavior and mood. We provide evidence that the effects and mechanisms underlying their actions are still confusing due to the use of different estrogens and progestins as well as different doses, duration of exposure, route of administration, baseline hormonal status and age of treated women. We also discuss the emerging issue concerning the relevant increase of these substances in the environment, able to deeply affect aquatic wildlife as well as to exert a possible influence in humans, which may be exposed to these compounds via contaminated drinking water and seafood. Journal of Molecular Endocrinology Finally, we report literature data showing the neurobiological action of progestins and in particular their importance during neurodegenerative events.
    [Show full text]