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Query: UMLS:C0432222 (SEM)
 47,337 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Prolactin and alpha-1,4-glucosidase levels in seminal plasma were measured in poorly coagulated (I), deficiently coagulated (II) and normally coagulated (III and IV) human ejaculates having 0-20%, 21-50% and 51-100% coagulum respectively 4 min after emission. The prolactin concentration (ng ml-1, mean +/- SEM) in poorly coagulated (5.2 +/- 0.48) and deficiently coagulated (7.6 +/- 0.72) samples was significantly lower than in the normally coagulated groups III (51-75% coagulum, 8.2 +/- 0.43) and IV (76-100% coagulum, 9.9 +/- 0.59) as well as the presumably fertile samples (9.2 +/- 0.74). A highly significant positive correlation was observed between the prolactin level and the percentage coagulum of the ejaculates (r = 0.686, n = 58, P less than 0.001). In contrast, the epididymal marker, alpha-glucosidase showed no relationship to seminal coagulation.
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PMID:Prolactin and alpha-1,4-glucosidase activity in normal and poorly coagulated human semen. 206 61

To study the effects of clonidine on growth and plasma somatomedin C (SmC) levels, 42 male Wistar rats aged 28 days and weighing 75 to 105 g were given clonidine (1.5 micrograms/ml in drinking water), or filtered water alone and were weighed weekly. After 0, 4 and 8 weeks, the animals were sacrificed under ether anesthesia, their length was measured and blood was collected by cardiac puncture for measurement of SmC concentration. Growth and the weight/length ratio were lower, and plasma SmC levels (mean +/- SEM) were greater in the treated groups after 4 (616 +/- 44.7 vs 433.2 +/- 39.38 ng/ml, P less than 0.01) and 8 (595.2 +/- 28.3 vs 412.66 +/- 39.01 ng/ml, P less than 0.01) weeks of treatment, suggesting that clonidine treatment increased growth hormone secretion. In other experiments, treated animals showed increased food intake only during the first week of treatment and decreased epididymal fat weight after 3 weeks (1.412 +/- 0.0536 vs 1.6 +/- 0.1336 mg/100 g body weight, P less than 0.01). The results suggest that clonidine acts at the level of the central nervous system involving transitory modulation of food intake, as well as on the regulation of energy metabolism.
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PMID:Effect of clonidine on growth and plasma somatomedin C levels of young rats. 210 Oct 52

The purpose of this study was to investigate the effects of voluntary running on the glucose metabolism in isolated adipocytes. Male rats of the Wistar strain, 5 weeks old were separately fed on usual rat food in cages equipped with a rotating wheel. The control rats were kept in small cages without wheels for 8 weeks in both experiments. The exercised rats ran approximately 2 km/day during this period. There were significant differences in the body weights and the weights of the epididymal fat pads between the exercised rats (373.5 +/- 10.3 g SEM and 4.2 +/- 0.3 g SEM) and the sedentary rats (437.8 +/- 17.6 g SEM and 7.9 +/- 0.3 g SEM) (p less than 0.05 in both cases). The rate of [U-14C]-glucose oxidation measured by 14CO2 production in adipocyte cultures showed a tendency toward greater stimulation in the exercised rats than in the sedentary ones, both when no insulin was added to the incubating medium (0.42 +/- 0.18% SEM vs. 0.11 +/- 0.02% SEM, p less than 0.10) and when insulin was added (0.81 +/- 0.36% SEM vs. 0.15 +/- 0.02% SEM, p less than 0.05). Hexokinase activity in the cells also seemed to be more stimulated in the exercised rats than in the sedentary ones. Conversion of [U-14C]-glucose to triglyceride was not affected significantly in the above experiment either with respect of the exercised rats vs. sedentary rats or with respect of the presence of insulin in the incubating medium.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:[Glucose metabolism in epididymal adipocytes of rats taking voluntary exercise]. 268 11

A new method was developed which is suitable for the preparation of mammalian sperm for scanning electron microscopy under either laboratory or field conditions. Samples of ejaculates from humans, two ferret species, and epididymal sperm from the African elephant were diluted in Millonig phosphate buffer and then fixed in glutaraldehyde solution. A small sample of the fixed sperm suspension was diluted in the same buffer, withdrawn with a syringe, and injected very slowly onto either a cellulose acetate or a polycarbonate membrane filter. This step was essential to concentrate the dilute sperm samples. During the various dilution steps most of the granular prostatic secretions were lost. However, a protein-like sheath, which remained attached to most sperm, obscured the surface features and had to be removed for SEM studies. It was removed by prolonged fixation/etching in 1% osmium tetroxide. Membrane filters containing sperm on their surfaces then were dehydrated, dried by the critical point drying method, and sputter coated with gold. Polycarbonate filters were superior to cellulose acetate filters in producing a flat and homogeneous background.
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PMID:Use of membrane filters and osmium tetroxide etching in the preparation of sperm for scanning electron microscopy. 275 3

Chylomicrons obtained from the thoracic duct of rats fed [3H]7,12-dimethylbenz(a)anthracene (DMBA), a polycyclic aromatic hydrocarbon, were infused intravenously into rats with bile fistulas. Over 17 hr, 55.9 +/- 3.2% (mean +/- SEM) of the radioactivity was recovered in bile and 6.7 +/- 0.5% in urine. Minor amounts were deposited in liver, kidneys and epididymal fat pads. Injection of DMBA in ethanolic solution gave a similar pattern, while biliary DMBA metabolites resulted in higher recovery in urine and lower recovery in fat. In conclusion, the major part of chylomicron DMBA is rapidly excreted via the biliary route, while a fraction is probably retained in adipose tissue.
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PMID:Fate of 7,12-dimethylbenz(a)anthracene absorbed from the rat intestine and transported in chylomicrons. 311 May 31

We have studied the acute effect of hOG and testosterone administration to immature rats, on testicular (particulate fraction and cytosol) and epididymal (cytosol) ABP levels. One and four hours after a single dose of 10 IU hCG/rat, ABP concentration decreased slightly in testicular membranes and cytosol, but increased markedly in epididymal cytosol (169 +/- 5 and 182 +/- 5 at 1 and 4 h respectively, compared to 113 +/- 13 fmoles/mg protein in control animals, mean +/- SEM). Since testicular and epididymal concentrations of testosterone increased after hCG, as expected, the effect might have been mediated by gonadotrophin stimulated testosterone production in Leydig cells. To test this hypothesis, the hCG effect was studied in rats that previously had received aminoglutethimide to block steroidogenesis. Under these conditions, hCG failed to increase epididymal ABP. Finally, administration of testosterone propionate was also able to stimulate epididymal ABP, but with delayed response: the increase was observed 4 h after injection (212 +/- 18 compared to 127 +/- 28 fmoles/mg protein in control animals, mean +/- SEM). It is concluded that the hCG-induced increase of intratesticular androgen levels results in rapid passage of ABP from testis to epididymis.
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PMID:Acute effect of hCG on testicular and epididymal levels of androgen binding protein (ABP) in the immature rat. 360

The annual reproductive cycle of the male little brown bat, in contrast to seasonal reproductive patterns of other mammals, is differentiated by an asynchronous recrudescence of the testis and the accessory reproductive glands. Spermatogenesis occurs during the summer, whereas fully stimulated accessory organs, stored epididymal spermatozoa, and sexual behavior are expressed later during a mating period that extends, albeit interrupted by hibernation, from late summer until early spring. To investigate whether changes in high affinity androgen-binding activity in the circulation are related to the delayed renewal of the accessory organs, plasma sex steroid-binding protein (SBP) and total testosterone (T) levels were measured throughout the year. From these data and determinations of association constants for T binding to SBP and albumin at both hibernating (4 degrees C) and active (40 degrees C) temperatures, estimates of the unbound ("free") and albumin-bound T fractions were made and correlated with changes in the accessory reproductive organs. Plasma SBP concentrations (mean +/- SEM) exhibited wide seasonal fluctuations: they were baseline in May (10 +/- 2 nM) following spring arousal, increased dramatically in June (184 +/- 24 nM), and reached peak levels in early July (262 +/- 29 nM), where they remained until August. In late August they began to fall (104 +/- 23 nM) and then returned to baseline during the hibernation period (October-April). Although total T levels were also elevated in June, it appeared that the unbound ("free") and the unbound plus albumin-bound T fractions did not increase until late July. Since the accessory gland weights did not begin to increase until late July as well, it was concluded that increases in the unbound and albumin-bound T fractions may be an important factor in the recrudescence of the accessories and that increased SBP activity in early summer may play a role in the regression and delayed renewal of these organs. However, what factor(s) maintain the accessory glands, epididymal spermatozoa, and sexual behavior during the breeding and hibernation periods when all T fractions were low are, as yet, undetermined.
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PMID:Annual variations in plasma sex steroid-binding protein and testosterone concentrations in the adult male little brown bat: relation to the asynchronous recrudescence of the testis and accessory reproductive organs. 407 6

The concentration of glucose in the plasma of alloxan-diabetic rats was 23.4 +/- 0.86 mM (mean +/- SEM; n = 18), and the concentration of insulin was 11.4 +/- 1.67 microU/ml (mean +/- SEM; n = 17). The weights of the ventral prostate (0.45 +/- 0.03 vs. 0.72 +/- 0.04 g) and seminal vesicles (1.23 +/- 0.06 vs. 1.84 +/- 0.08 g) were decreased compared to control values and the rats lost body weight, but the weights of the testes were not significantly different from control values (3.14 +/- 0.08 vs. 3.23 +/- 0.14 g/pair). Similar changes were seen in streptozotocin-diabetic rats. The concentration of fructose (micromoles per g fresh wt) was greater in the coagulating gland of alloxan-diabetic (19.6 +/- 1.3; n = 17) than control rats (9.1 +/- 0.7; n = 18). The production of 14CO2 from D-[U-14C]glucose by spermatozoa or seminiferous tubules from diabetic rats was decreased compared to that in controls [28 +/- 3 vs. 53 +/- 6 nmol glucose converted/10(8) spermatozoa X 30 min (n = 8) and 0.81 +/- 0.03 vs. 1.08 +/- 0.03 mumol glucose converted/g fresh wt X 30 min (n = 7)]. There was no change in the production of lactate or 3HOH from D-[2-3H] glucose, and the presence of insulin (10 mU/ml) in the incubation had little effect. Rat epididymal spermatozoa took up 2-deoxy-D-glucose by a facilitated diffusion mechanism; the Km was about 0.2 mM, with a maximum velocity of about 0.10 nmol/10(6) spermatozoa X 10 sec. Neither alloxan-diabetes nor the presence of insulin (10 mU/ml) had an appreciable effect on these parameters.
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PMID:The effect of experimentally induced diabetes on the metabolism of glucose by seminiferous tubules and epididymal spermatozoa from the rat. 623 7

Uncontrolled diabetes in rats is associated with reduced levels of both serum somatomedins and hepatic somatomedins. Hepatic somatomedins are recognized after extraction with 5 mol/L acetic acid, have a higher molecular weight (about 30,000) than serum somatomedins (about 8,000), despite acid conditions that dissociate somatomedins from circulating carrier proteins, and stimulate cartilage when given in vivo. To determine if hepatic somatomedins--as potential prohormones--have insulin-like activity comparable with serum somatomedins, their effects on rat epididymal adipose tissue were examined. Somatomedins were prepared from serum and liver extracts by gel filtration on Sephadex G-75, pH 2.4. In initial studies with fat pad segments, extracted hepatic somatomedins increased glucose oxidation only 64 +/- 11% above buffer (mean +/- SEM), while stimulation of 372 +/- 48% was provided by extracted serum somatomedins of comparable cartilage-stimulating potency (P less than 0.01, liver v serum). Further examination was performed with isolated adipocytes in a system sensitive to insulin at a concentration of 10 microU/mL (stimulation 100% above buffer). In dose-response studies measuring glucose oxidation, hepatic somatomedins had insulin-like activity of 16 microU/mL versus 55 microU/mL for serum somatomedins equipotent on cartilage (P less than 0.05); measuring glucose incorporation into total lipids, hepatic somatomedins had undetectable activity while serum somatomedins had activity of 28 microU/mL. It is concluded that hepatic somatomedins with potent cartilage-stimulating activity have greatly reduced insulin-like activity. The apparent dissociation in biologic activity of hepatic somatomedins suggests that while they may be prohormones, they may also represent a class of growth factors separate from the circulating somatomedins.
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PMID:Nutrition and somatomedin. X. Comparison of insulin-like activity of somatomedins extracted from liver and serum. 641 11

Using a propagating cell culture system of adipocyte precursors from 70-400-g rats, we explored the possibility that regional variations in properties of adipose tissue may reflect site-specific characteristics intrinsic to the cells, rather than extracellular influences. Initially, studies were made of the nature of the fibroblastlike cells from perirenal adipose tissue stroma. Using colony-forming techniques, it was shown that these cells were adipocyte precursors; each confluent colony that was derived from a single cell displayed differentiated adipocytes. This characteristic was evident in cells from rats of all ages and persisted during secondary culture. At all ages of rats studied, perirenal cells replicated more rapidly than epididymal precursors, e.g., for 179-g rats the population-doubling times were 19.3 +/- 0.7 vs. 25.5 +/- 1.2 h (means +/- SEM, P less than 0.03). With aging of the rats, the replication rate of their perirenal cells decreased progressively. Under clonal conditions, the colony size distribution of both perirenal and epididymal precursors revealed heterogeneity in their capacity for replication, perirenal cells showing greater proliferation. These also differentiated more extensively by morphologic and enzymatic criteria. Age and site had effects that persisted through many cell generations; however, high-fat feeding had no perpetuating influence. The dissimilar properties of perirenal as compared with epididymal precursors may reflect differences in regulation of gene expression. The data are also compatible with a later development in embryological life of perirenal tissue. We suggest that the composition of the adipocyte precursor pool is an important determinant of the growth of adipose tissue that occurs in response to a nutrient load. Interregional or interindividual variation in composition may explain regional and individual differences in fat accumulation.
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PMID:Influence of anatomic site and age on the replication and differentiation of rat adipocyte precursors in culture. 663 May 8


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