Progesterone attenuates cocaine-induced responses

In this review, we summarize literature focused on how progesterone alters cocaine-induced psychomotor, reinforcement, and physiological responses. Clinical studies suggest that progesterone attenuates the subjective effects of cocaine. Similarly, preclinical studies have demonstrated that cocaine-induced reward and psychomotor responses are attenuated after progesterone administration. In rats progesterone also reduces the reinforcement effects of cocaine attenuates acquisition, escalation, reinstatement of cocaine self-administration, and cocaine-seeking behaviors. Progesterone also counteracts the facilitatory effects of estrogen on cocaine self-administration and psychomotor activation. These findings suggest that progesterone has a potential in clinical applications as a treatment for cocaine addiction. Constantly changing progesterone serum levels in female humans and rats affect the female's reinforcement responses to cocaine and may in part contribute to the known sex differences in cocaine responses.     

Progesterone Deficiency and Premature Labour

Plasma oestradiol 17β and progesterone levels in 11 patients admitted to hospital for threatened premature labour of unknown aetiology were compared with those of women at similar stages of gestation whose pregnancy was normal. Oestradiol levels in the study group were slightly higher than in the normal controls but their progesterone levels were significantly lower. This progesterone deficiency increased the oestradiol/progesterone ratio in the study group patients, and it increased still more as the progesterone withdrawal continued during premature labour.Since uterine activity during pregnancy is regulated by a balanced action of several factors a deficiency in progesterone, an opponent of uterine activity, creates a regulatory imbalance which, if uncorrected, provokes premature labour. An increase in uterine volume stimulates uterine activity, and the present study reinforced our previous conclusion that the uterine-volume/plasma-progesterone ratio is a more accurate measure of the state of regulatory balance than the progesterone level alone.The cause of the progesterone deficiency in these cases remains unexplained, but we suggest that placental growth and function are contributory factors. We are investigating ways of correcting the resulting imbalance in the regulatory mechanism.     

Transformations of Progesterone by Basidiomycetes

A total of 254 basidiomycete cultures have been examined for their action on progesterone. Of these, 54 showed transformation products by thin-film and gas-liquid chromatography. The major product formed by eight of these organisms acting on progesterone has been isolated and identified.     

Progesterone receptors on human spermatozoa

Progesterone, primarily recognized as a female steroid hormone, is reported to affect several sperm functions especially capacitation, motility and acrosome reaction. These effects of progesterone on the spermatozoa are mediated via the progesterone binding sites/progesterone receptor (PR) on the acrosomal membrane. These receptors in response to progesterone increase the intercellular Ca2+ levels and stimulate Ca2+ influx in the mature human spermatozoa via non-genomic mode of actions. Characterization of this receptor reveals that the sperm PR is masked protein and is exposed to the surface by some non-ionic detergents. Localized on to the acrosome region of the spermatozoa, these receptors are recognized by most antibodies directed towards the C-terminal region of the conventional PR. The estimated molecular weight of PR on spermatozoa varies from 27 kDa to 85 kDa. At the molecular level, sequences encoding for the entire DNA and hormone binding domains of the conventional PR are detected in the mRNA derived from spermatozoa. No insertions, deletions or mutations are detected in this region. These results are suggestive of the fact that at least the C terminal region of the conventional PR is conserved in the sperm. It is hypothesized that post-translational modifications or peptide splicing of the conventional PR in spermatozoa may possibly lead to the variant of the steroid hormone receptor. Detailed characterization of the sperm PR will be important in understanding the alternate non-genomic mode of action of steroid hormone receptors.     

Source of Ovarian Preovulatory Progesterone

AN increase in plasma progesterone has been detected before ovulation in several species. There is, however, no definitive information as to which ovarian compartments produce this progesterone. Previous results with the golden hamster have demonstrated a preovulatory progesterone surge after the critical period for gonadotrophin release on the afternoon of pro-oestrus (day 4)^1,2. This is paralleled by the development of 3β-hydroxysteroid dehydrogenase (3βHSD) activity in the theca interna and granulosa of pre-ovulatory follicles³, suggesting they could be a source of preovulatory progesterone. As the interstitium also contains 3βHSD activity, it could be an additional source of progesterone³. Hamster corpora lutea, however, have negligible 3βHSD activity during pro-oestrus³ and are not capable of producing progesterone when isolated and incubated in vitro (Leavitt et al., unpublished work).     

Progesterone fate in rabbit cornea

Excised cornea from adult New Zealand rabbits were incubated with progesterone-4-14C in Eagle's media for 96 hr. Samples were inactivated at intervals of 24 hr incubation periods. The following metabolites of progesterone were isolated: 20 alpha-Hydroxy-4-pregnen-3-one, 20-hydroxy-4-pregnen-3-one, 5 alpha-pregnane-3,20-dione; 5 beta-pregnane-3,20-dione and 6 beta-hydroxy-4-pregnen-3,20-dione. 20 alpha-Hydroxy-pregnen-3-one was the predominant metabolite of progesterone-4-14C. A linear increase was observed throughout 96 hr. The opposite was found for 5 alpha and 5 beta pregnane-3,20-dione. Compounds remaining at the origin of the paper chromatograms contained 6 beta-hydroxy-4-pregnen-3,20-dione and other still unidentified metabolites of progesterone-4-14C. Presence of 20 alpha and 20 beta-reductase; 5 alpha and 5 beta-reductase and 6 beta-hydroxylase enzyme systems are involved in corneal progesterone metabolism. No fungal neither bacterial enzymatic biotransformation occurred in the culture media.     

Progesterone in bovine milk fat

The progesterone (P(4)) concentration (ng/5 mul) in the fat portion of cow's milk was measured on days 0, 12, 20, 24, and 30 after insemination in an effort to assess the ability of this analysis to judge the reproductive status of dairy cows. Pregnancy was determined by rectal palpation at approximately 40 days after insemination. The mean P(4) concentration (ng/5 mul) +/- SD in the pregnant cows (n=17) was 0.14+/-.07, 1.31+/-.36, 1.41+/-.52, 1.22+/-.21, and 1.30+/-.43 on post-insemination days 0, 12, 20, 24, and 30 respectively. At these same intervals the P(4) concentration in the non-pregnant (NP) cows (n=18) was 0.14+/-.06, 1.26+/-.37, 0.56+/-.52, 0.57+/-.42, and 1.08+/-.59. On days 20 and 24 after insemination, mean P(4) levels were significantly (P<.001) elevated in the pregnant cows. It was concluded that an accurate assessment of the reproductive status of a cow, milk samples from days 0, 20, and 24 post-insemination would have to be analyzed for milkfat P(4) concentrations. In order to determine the percentage of cows inseminated out of the periestrual period, milkfat P(4) concentrations were ascertained in milk collected from 165 cows at the time of insemination. Cows that conceived (n=38) had a mean milkfat P(4) concentration at the time of insemination of 0.16+/-.09. The upper limit for P(4) in the milkfat at the time of insemination in cows that conceived was calculated to be 0.43 ng/5 mul milkfat. Subsequently, it was found that of the 14 cows that had P(4) levels above this upper limit at time of insemination, nine were inseminated at a period other than in the periestrual period and five were inseminated while already pregnant.