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Biomedical subjects

W G Wiest

Publications and source records attributed to W G Wiest.

At least 19 recordsLinked to original sources

Augmentation of the response of mouse uterine epithelial cells to estradiol by uterine stroma.

The effect of estrogen on the in vitro growth of mouse uterine epithelial cells was assessed. Epithelial cells from the immature mouse uterus were successfully cultivated in a 1:1 mixture of Dulbecco's Modified Eagle's Medium and Ham's F-12 supplemented with insulin (5 micrograms/ml), transferrin (10 micrograms/ml), hydrocortisone (10(-7) M), BSA (2 mg/ml), and fetuin (1 mg/ml). Addition of 17 beta-estradiol in the range of 1-100 nM did not significantly change the total DNA content of the epithelial cells. A binding component of [3H]estradiol by cultured uterine cells was shown to be specific, saturable, and of high affinity. Kd values for specific binding by epithelial and stromal cells were 1.0-1.7 x 10(-10) M. Maximal specific binding was 0.74 and 2.3 fmol/micrograms DNA for epithelial and stromal cells, respectively. Treatment of epithelial and stromal cells for 4 days with 10 nM estradiol led to a 2- to 6-fold increase in progesterone receptor concentration. Treatment of epithelial and stromal cells in mixed culture for 4 days with 10 nM estradiol resulted in a significant increase in total DNA. That epithelial-stromal contact was critical for estradiol stimulation was shown by the fact that if the cell types were separated into two compartments which still allowed free media mixing, total DNA was not enhanced by estradiol. These observations are organized into a model for mitogenic action of estradiol that seems to reconcile observed disparities in the action of the hormone in vivo and in vitro.

Animals↗

Protein kinase stimulation of steroidogenesis in rat luteal cell mitochondria.

The regulatory role of cAMP-dependent protein kinase in steroidogenesis was examined in luteal cell mitochondria prepared from heavily luteinized prepubertal rat ovaries. The cAMP-dependent protein kinase, localized in luteal mitochondria, comprised 5.5% of the total cellular protein kinase activity (cAMP-dependent). Intact mitochondria supported by a suitable electron-donor substrate and inhibited by isoxazole converted cholesterol to a single steroid product, pregnenolone. Neither (Bu)2 cAMP nor a crude preparation of cytosolic protein kinase stimulated pregnenolone production from cholesterol when added to intact luteal cell mitochondria; however, mitochondria treated with 10 mM CaCl2 became responsive to both (Bu)2 cAMP and protein kinase by showing increased pregnenolone production. Likewise, the addition of cytosol protein kinase to incubations of cholesterol and crude cholesterol sidechain cleavage enzyme (cytochrome P-450cscc) isolated from luteal mitochondria, also stimulated pregnenolone production. Cholesterol-poor mitochondria, depleted of endogenous sterol by prolonged preincubation, when subsequently incubated with Ca+2 plus (Bu)2 cAMP and protein kinase showed significantly increased pregnenolone production. Conversely, mitochondria with greatly increased intramitochondrial cholesterol after preincubation with 200 microM cholesterol and a cytochrome P-450cscc inhibitor (aminoglutethimide) synthesized pregnenolone in significantly higher amounts than either normal or cholesterol-poor mitochondria after removal of the aminoglutethimide block. However, addition of (Bu)2cAMP or protein kinase to Ca+2-treated cholesterol-rich mitochondria failed to additionally stimulate pregnenolone synthesis. We conclude from these observations that the mitochondrial membrane normally excludes protein kinase and (Bu)2cAMP from any stimulatory action on cholesterol side-chain cleavage. Disruption of the mitochondrial membrane by high Ca+2 concentrations eliminates this barrier and permits (Bu)2cAMP and protein kinase stimulation of the CSCC enzyme system. The mechanism of stimulation is not clear. It could involve direct action on the CSCC enzyme. Alternatively, an increase in either intramitochondrial transport or binding of cholesterol substrate to the CSCC enzyme could be facilitated by protein kinase action. Direct stimulation of the enzyme by protein kinase seems less likely, since increased enzyme activity was not observed in the presence of high concentrations of intramitochondrial cholesterol substrate.

Animals↗

High-density-lipoprotein cholesterol in bodybuilders v powerlifters. Negative effects of androgen use.

To determine the relationship between lipid profiles and the type of weight training and to assess the effects of anabolic-androgenic steroids on lipids, bodybuilders and powerlifters of similar age, body fat, and testosterone levels were studied before and after androgen use. Before androgen administration powerlifters had lower levels of plasma high-density-lipoprotein cholesterol (HDL-C) and HDL2-C (38 +/- 2; 6 +/- 1 mg/dL; means +/- SE, n = 8) than bodybuilders (55 +/- 2; 12 +/- 1 mg/dL; n = 8) and runners of comparable age and body fat (47 +/- 2; 14 +/- 2 mg/dL; n = 8), while levels of low-density-lipoprotein cholesterol (LDL-C) were higher in powerlifters (138 +/- 10 mg/dL) than in bodybuilders (104 +/- 7 mg/dL) and runners (110 +/- 6 mg/dL). Therefore, powerlifters had higher LDL-C/HDL-C ratios (3.7 +/- 0.3) than bodybuilders (2.0 +/- 0.2) and runners (2.4 +/- 0.2). Androgen use by eight bodybuilders and four powerlifters lowered values of both HDL-C and HDL2-C by 55% and raised values of LDL-C (61% +/- 10%) and LDL-C/HDL-C ratios (280% +/- 40%). Therefore, the training regimen of bodybuilders is associated with a more favorable lipid profile than the training used by powerlifters. Androgen use by strength-trained athletes may increase their risk for coronary heart disease.

Adult↗

Uterotropic action of indomethacin on the rat uterus.

Administration of indomethacin (10 mg/kg body weight, twice daily for 6 days) resulted in a significant (P less than 0.01) increase in the weight, and cross-sectional area of uteri of ovariectomized rats, whereas no such effects were observed following indomethacin administration to normal cycling rats. Prostaglandin F2 alpha (PGF2 alpha) content (ng/uterus) and concentration (ng/g wet weight) in the uterus of indomethacin-treated animals were reduced 40.4% and 60.8%. Simultaneous administration of either estradiol-17 beta (E2), progesterone testosterone with indomethacin to ovariectomized rats failed to reduce the uterine weight increase. On the contrary, concomitant administration of E2 (25 or 100 ng/day) and indomethacin resulted in uterine weight increases which were greater than those associated with indomethacin alone. Uterine E2 content was significantly higher in animals treated with indomethacin plus E2 as compared to those given estradiol alone. Uterine uptake of 2,4,6,7-[3H]E2 following i.v. administration was greater in animals pretreated with indomethacin (5 mg/kg, twice daily) for 3 days than in ovariectomized controls. These results suggest that prostaglandins may be involved in the regulation of uterine growth.

Animals↗

Gonadotropin and lipoprotein receptor levels in rat luteal cells of early pregnancy.

Dispersed cells from rat corpora lutea isolated on pregnancy days, 5, 7, 10 and 13, yielded three distinct sub-populations of luteal cells when centrifuged in a continuous, 0-40%, Metrizamide density gradient. Bands I and II (refract. ind. 1.340-1.346) constituted highly enriched, functional, luteal cell fractions. The more dense fraction (Band III, refract. ind. 1.348-1.355), while contaminated with non-luteal cells, also contained cells capable of progesterone production. Progesterone synthesis by all three sub-populations was stimulated by LH, and each sub-population bound [125I]-labeled hCG and [125I]-labeled HDL with high affinity. However, the concentrations of LH/hCG and lipoprotein binding sites were greater in Band I + II than in Band III. Progesterone secretion during the selected days of pregnancy, being high on days 5 and 13 with a nadir on day 10, was shown to correlate with the concentration of LH/hCG-binding sites present on Band I + II cells. This correlation was not seen when comparing Band III cells. The concentration of HDL-binding sites did not vary significantly with the sub-populations of luteal cells isolated on the selected days of pregnancy.

Animals↗

Effect of low density and high density lipoproteins on progesterone secretion by dispersed corpora luteal cells from rats treated with aminopyrazolo-(3,4-d)pyrimidine.

Immature female rats, superovulated and treated daily for 3 days with 4-aminopyrazolo-(3,4-d)pyrimidine (APP), showed a marked reduction in plasma cholesterol levels, which is reflected by reduced levels of very low density, low density (LDL), and high density (HDL) lipoproteins. Luteal cells from non-APP-treated rats released 2444 +/- 212 ng progesterone/mg protein in 4 h, which slowly increased to 2806 +/- 327 after 20 h. Luteal cells from APP-treated animals showed a similar pattern at about half the level of progesterone production. In the presence of 100 ng LH/ml, progesterone levels were stimulated 2-fold in both APP-treated and nontreated controls. The addition of either human HDL or LDL to any of the preparations markedly increased the progesterone level. These results support the hypothesis that APP treatment reduces the ability of dispersed luteal cells to secret progesterone. This effect is partially overcome by the addition of either HDL or LDL to the incubation media in vitro, suggesting that rat luteal tissue can use either human HDL or LDL as a source of cholesterol. However, about 5 times as much human LDL-derived cholesterol was required to stimulate equivalent increases in progesterone compared to human HDL cholesterol.

Adenine↗

Daily and circadian variations in serum free testosterone levels are not clinically significant.

Serum free testosterone levels were measured daily during an ovulatory, endocrinologically normal cycle in five women and at 6-hour intervals on six consecutive days near midcycle in four of these women. During ovulatory cycles, serum free and total testosterone, unlike the gonadotropins, estradiol, and progesterone, did not fluctuate in a cyclic pattern. The 6-hour assays demonstrated close parallelism of free and total testosterone levels and no circadian pattern similar to the diurnal variation seen in serum cortisol values. During both study intervals, the serum free testosterone levels rarely exceeded the upper limit of the normal range defined for our laboratory. Thus, serum free testosterone values measured in blood samples obtained at any day are equally reliable for clinical use.

Circadian Rhythm↗

Metabolism of progesterone by placentas from several mammalian species in vitro.

20-alpha-Hydroxysteroid oxidoreductase (20-alpha-HSDH) activity and 20-alpha-dihydroprogesterone concentration (20-alpha-DHP) reach peak values in the human placenta after vaginal delivery. To determine if these findings are unique to the human, we measured 20-alpha-HSDH activity as well as endogenous progesterone (P) and 20-alpha-DHP concentration in the soluble supernatant fraction of placental tissues obtained from rodents (rat, rabbit, guinea pig), ungulates (horse, zebra, giraffe, cow), and primates (squirrel monkey, orangutan, man). P concentration was very low in rodents (mean 0.60 ng/mg protein), increased slightly in ungulates (mean 2.89 ng/mg protein), and reached a maximum value in the human (34.43 ng/mg protein). 20-alpha-DHP concentration had a strong positive correlation (r = 0.93) with P tissue content; it was low in rodents (mean 0.21 ng/mg protein), increased slightly in ungulates (mean 0.79 ng/mg protein), and reached a maximum value in the human (39.53 ng/mg protein). 20-alpha-HSDH activity, however, had a poor correlation with 20-alpha-DHP tissue concentrations: Its lowest value was in the guinea pig (9.34 pmole/mg protein/hour) and the highest was in the horse (3.19 nmole/mg protein/hour). These results indicate that a high level of activity of the P to 20-alpha-DHP pathway with significant tissue accumulation of 20-alpha-DHP is unique to the human placenta and reinforce the possibility of its causing in situ P withdrawal as a part of the overall mechanism of human parturition.

20-alpha-Dihydroprogesterone↗

20 alpha-Hydroxysteroid oxidoreductase activity and 20 alpha-dihydroprogesterone concentration in human placenta before and after parturition.

The objective of this investigation was to determine if decreased biosynthesis or increased catabolism of progesterone (P) during labor was responsible for the decreased concentration of hormone observed in the human placenta after labor and vaginal delivery. No significant difference was found in P biosynthesis by placental tissues examined before and after labor as evidenced by a similar activity of 3 beta-hydroxysteroid dehydrogenase: delta 5-isomerase. In contrast, there was a marked increase in P catabolism during labor, as shown by a significant (p less than 0.05) change in placental 20 alpha-hydroxysteroid oxidoreductase activity which increased from 835.5 +/- 103 (mean +/- SEM) pmoles of 20 alpha-dihydroprogesterone (20 alpha-DHP) generated per milligram of protein per hour before labor to 1,160.4 +/- 101 pmoles/mg/hr after labor. A similar significant (p less than 0.02) increase in enzyme activity was noticed in parallel assays of the reverse (20 alpha-DHP leads to P) reaction. As a consequence of increased P catabolism, placentas after labor had a 20 alpha-DHP concentration of 63.7 +/- 9.5 (mean +/- SEM) ng/mg protein, a value which was significantly (p less than 0.05) larger than that found before labor (37.8 +/- 8.3 ng/mg protein). These changes resulted in a modification of the placental tissue P/20 alpha-DHP ratio which decreased from 2/1 before to 1/1 after labor. The results indicate that the catabolism of P to 20 alpha-DHP increases significantly during human parturition. This phenomenon may be of importance in the mechanism of initiation and continuation of labor.

20-Hydroxysteroid Dehydrogenases↗

Radioimmunoassay of serum and ovarian pregnenolone in immature rats.

Antiserum was generated in a rabbit against pregnenolone-16 alpha-carboxyethyl thioether conjugated to bovine serum albumin. The antibody, used for the assay of pregnenolone in extracts of serum and tissue homogenates, proved sufficiently specific to allow direct assay of extracts without chromatography. Sensitivity, defined as that point on the standard inhibition curve equal to the lower value 2 SD from the mean radioactivity bound to antibody in the buffer control (zero hormone) tubes, was 0.02 ng. The accuracy was confirmed by the recovery of known amounts of pregnenolone added to serum and aqueous buffer medium. The inter- and intra-assay coefficients of variation were respectively 10.6% and 9.1%. Specificity was confirmed by checking cross reactivity of various steroids and by finding comparable pregnenolone levels in samples before and after chromatography. The administration of aminoglutethimide to rats resulted in the reduction of ovarian and serum pregnenolone levels. Administration of isoxazole, on the other hand, caused an increase in both serum and tissue pregnenolone levels. These findings are in agreement with accepted views of the action of these two metabolic blocking agents.

Animals↗

Pseudocorpus luteum insufficiency: a local defect of progesterone action on endometrial stroma.

A 23-yr-old woman whose initial complaint was infertility demonstrated glandular stromal dissociation with failure of the endometrial stroma to undergo pseudodecidualization in repeated endometrial biopsies taken late in the luteal phase. As the clinical presentation was consistent with the inadequate corpus luteum syndrome, hormone measurements were performed. The endometrial biopsy was abnormal during cycles in which the serum pattern of progesterone, estradiol, FSH, and LH was normal. Exogenous progesterone did not correct the abnormality. The patient, by in vitro studies, has approximately one half the number of high affinity progesterone-binding sites in the cytosol fraction of her endometrium compared to preparations from two normal control subjects. Since her cytosol-binding protein was qualitatively identical to two control subjects, the incomplete maturation of her endometrial stroma may represent an absence or reduced number of stromal cytosol receptors and/or a resistance to specific hormone action in an individual target tissue.

Adult↗

Elevated free testosterone in an obese, hirsute premenarchial girl: effects of norethynodrel and mestranol.

An 11-year-old premenarchial girl who demonstrated the clinical and biochemical abnormalities of the Stein-Leventhal syndrome is reported. Although the concentration of total circulating testosterone was within normal limits, levels of free testosterone and testosterone-estradiol-binding globulin (12.9 to 22.7 pg/ml and 7.9 to 11 X 10(-9) moles/liter, respectively) were markedly different from those of prepubertal girls (1.1 +/- 0.9 pg/ml and 102 +/- 27 X 10%-9) moles/liter, mean +/- 1 SD) and normal women (4.3 +/- 1.2 pg/ml and 82 +/- 30 X 10(-9) moles/liter). Luteinizing hormone but not follicle-stimulating hormone concentrations were increased. In the absence of abnormal adrenal steroid excretion or response to dexamethasone suppression and with a clear biochemical response to oral contraceptives (decreased levels of luteinizing hormone and free testosterone and increased concentrations of testosterone-estradiol-binding globulin), this patient closely resembles older individuals with the Stein-Leventhal syndrome. Therefore, the measurement of testosterone-estradiol-binding globulin and free testosterone may be useful in the laboratory evaluation of any adolescent girl in whom no other cause for hirsutism can be identified.

Adolescent↗

Free testosterone concentration in serum: a method for determination.

Two procedures for quantifying serum levels of testosterone-estradiol-binding globulin (TeBG) have been evaluated. Both procedures utilize indirect methods for assessing the extent of protein-steroid interaction for the purpose of devising a clinically feasible procedure for estimating serum free testosterone. In the first method serum protein concentration was varied by dilution until 50 per cent of steroid binding was obtained at a given concentration of steroid. Dextran-coated charcoal was used for separating TeBG-bound steroid from the unbound fraction. In the second procedure DEAE-cellulose filtration was used to isolate the TeBG-steroid complex for quantitation. Having a sufficiently accurate measure of TeBG levels together with a knowledge of the total endogenous testosterone permitted the estimation of serum free testosterone based on the binding affinities of serum proteins. The preferred DEAE-cellulose filtration method has proved useful for routine clinical evaluation of physiologically effective androgen levels.

Charcoal↗