1964
DOI: 10.1530/acta.0.0450321
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Purification of Gonadotrophin From Human Menopausal Urine

Abstract: Gonadotrophins were prepared from human postmenopausal urine with the kaolin-acetone method and purified by adsorption of impurities on diethylamine ethyl cellulose (DEAE-C). The last step, namely chromatography on the column of permutit, resulted in a significantly improved specific activity. The immunoelectrophoresis showed that the purified HMG is not homogeneous and that the constituents are glycoproteins which migrate into the region α1, α2 and β globulins.

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Cited by 38 publications
(17 citation statements)
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“…The Donini et al. (10), and Canfield et al (11) were tested in radioimmunoassays: (1) second international reference preparation of human postmenopausal gonadotropin (2IRPHMG) with biological activity of 40 international units (IU) per ampoule or 1 IU = 0.2295 mg for both hLH and human follicle-stimulating hormone (hFSH, follitropin); (2) (14). Cleavage from resin and removal of protecting groups were accomplished by treatment with liquid hydrogen fluoride.…”
mentioning
confidence: 99%
“…The Donini et al. (10), and Canfield et al (11) were tested in radioimmunoassays: (1) second international reference preparation of human postmenopausal gonadotropin (2IRPHMG) with biological activity of 40 international units (IU) per ampoule or 1 IU = 0.2295 mg for both hLH and human follicle-stimulating hormone (hFSH, follitropin); (2) (14). Cleavage from resin and removal of protecting groups were accomplished by treatment with liquid hydrogen fluoride.…”
mentioning
confidence: 99%
“…Esterification of the hydroxyl group of 17/3-hydroxyandrostano-[2,3-d]-isoxazole with 3-cyclohexylpropionic acid affords a potent anabolic agent with long duration of action and minimal androgenicity. A good myotrophic to androgenic ratio appears also to be present in 17/3-hydroxy-l7a-methylandrostano-[3,2-c]-isoxazole (Arnold & others, 1963b ;Donini & Montezemolo, 1961) where the side of the isoxazole ring involved in the ring fusion has been changed. This compound would seem to show negligible progestational activity and to have a low inhibitory effect on pituitary gonadotrophin production.…”
Section: Anabolic Agentsmentioning
confidence: 99%
“…However, and contrary to the old and simple conception derived from animal experiments that FSH acts on the tubules and LH on Leydig cells [11], it was not until recent years that the availability of highly purified preparations of human pituitary (HPG) [10] and urinary preparations (HMG) [9] containing both FSH and LH activities, has made possible some progress of our knowledge in the regulation of human spermatogenesis. Although several earlier reports [2] have emphasized the usefulness of high and long-term administration of human chorionic gonadotropin (HCG) alone in stimulating germinal epithelium in prepuberal hypogonadotropic patients (eunuchoids) and, more recently, the necessity of adding prepara tions with FSH activity (HMG) for the completion of spermatogenesis [14, 28], no one was able to prove that the beneficial eifect of HCG could be replaced by testosterone, as it seems to occur in hypophysectomized rats [6].…”
Section: Introductionmentioning
confidence: 96%