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Query: UNIPROT:P56851 (epididymal)
 11,273 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

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 response of peripheral tissues to insulin is reduced in fasting and diabetes mellitus. The experiments described herein were designed to determine whether insulin-stimulated glucose oxidation is affected by the free-fatty acid-derived plasma metabolites acetone, acetol, and propylene glycol (1,2-propanediol [1,2-PD]), concentrations of which are elevated in both starvation and diabetic ketosis. In epididymal adipose tissue from fed and 48-h--fasted rats given 3% acetone drinking water for 7 days, insulin-stimulated glucose oxidation was reduced by approximately 30-40%. After ingestion of 2% acetol for 7 days, basal and insulin-stimulated glucose oxidation was lowered approximately 30%, whereas the consumption of 1,2-PD had no influence on either basal or insulin-stimulated glucose oxidation. Similar effects on glucose oxidation were observed in isolated adipocytes from fed rats after ingestion of 3% acetone and 2% acetol for 7 days. The reduction in insulin-stimulated glucose oxidation in adipose tissue in vitro required the consumption of 3% acetone water for greater than 3 days. In 48-h--fasted rats that ingested 3% acetone for 5 days, insulin-stimulated glucose oxidation remained depressed 4 days after withdrawal of acetone from the drinking water. These studies imply that at least part of the insulin resistance indigenous to fasting and diabetic ketosis may be attributed to the metabolic influence of acetone and/or acetol in body fluids.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Acetone and acetol inhibition of insulin-stimulated glucose oxidation in adipose tissue and isolated adipocytes. 218 Jul 56

It has been known for more than a decade that in many mammalian species including man, spermatozoa once shed from the testis are immature, immotile and incapable of fertilizing the ovum. During their transit through the epididymis, they undergo various morphological and functional changes that confer on them the ability to ascend the female tract, to undergo an acrosome reaction, to penetrate the zona pellucida and to effect a successful fertilization. By the time spermatozoa have reached the cauda epididymidis, they are held in a quiescent state by factors in the epididymal fluid. The epididymis plays a vital role by creating a favourable fluid environment for sperm maturation and storage. The exact mechanisms underlying sperm maturation and storage are unclear and it appears that no single epididymal factor is held entirely responsible. In contrast, spermatozoa are directly bathed in the epididymal fluid; the fluidity of the microenvironmental has a direct effect on epididymal spermatozoa. The epididymal epithelium has been shown to transport electrolytes and water by processes involving ion pumps, ion carriers and ion channels. These components are under nervous, hormonal and paracrine control and are susceptible to interference by pharmacological agents. This paper reviews the physiology of electrolytes and fluid transport in the epididymis and describes how abnormal fluid transport across the epididymal duct could predispose towards epididymal obstruction, a condition that may occur in cystic fibrosis, Young's syndrome or other unexplained cases of male infertility.
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PMID:Abnormal fluid transport by the epididymis as a cause of obstructive azoospermia. 219 16

We analyzed retrospectively data from 148 chow-fed male Wistar rats killed between the age of 6 wk and 2 yr while varying in body weight from 136 to 917 g. The purpose of this study was to clarify the relationship of body weight and body lipid content with the composition and cellularity of the epididymal and retroperitoneal fat depots. A positive linear association was found between body weight and body water or fat-free dry residue, whereas total body lipid exhibited a curvilinear relationship with body weight. The weight of the epididymal pads was linearly related to body weight but not to body lipid. In contrast, retroperitoneal pad weight was exponentially related to body weight and paralleled total body lipid. A strong linear correlation was found between total body lipid and weight (r = 0.959) or depot lipid content (r = 0.967) of the retroperitoneal fat pads. In this rat model of aging and spontaneous obesity, significant regional differences exist in adipose depot composition and cellularity. A practical outcome of this study is a simple and accurate prediction of body lipid content from the gravimetric determination of the retroperitoneal fat depots.
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PMID:Model of spontaneous obesity in aging male Wistar rats. 226 Jul 22

Correlated responses in whole-body composition were determined in 12-wk-old male mice from replicate lines selected for 12 generations for high (HF) or low (LF) epididymal fat pad weight as a percentage of body weight (EPID) and high (HL) or low (LL) hind carcass weight as a percentage of body weight. The HF and LF lines diverged (P less than .01) in body fat percentage (FAT) and subcutaneous depot fat by 93 and 71%, respectively, of the control line (RC) mean. EPID increased (P less than .01) proportionately more than FAT in the HF line; EPID decreased (P less than .01) proportionately less than FAT in LF. Protein, fat and water as a percentage of empty body weight showed negative correlated responses (P less than .01) due to selection for EPID, but lean body mass, body weight and body length had positive correlated responses (P less than .01). Correlated responses of fat-free protein and ash percentage were minor. Correlated responses in HL and LL were the mirror images of those in HF and LF, but they generally were of smaller magnitude. The results indicate that, although there are high positive genetic correlations between fat depots in mice, local control of lipogenesis and(or) lipolysis exists at different sites of fat deposition. Further, the lack of correlated responses in fat-free percentage of protein (and percentage of ash) suggests that additive genetic variances are low for these traits and(or) the genetic correlations of these traits with the selection criteria are low.
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PMID:Correlated responses in body composition based on selection for different indicator traits in mice. 226 8

Diethylene glycol (DEG) and diethylene glycol monoethyl ether (DEGEE) were evaluated for reproductive toxicity in CD-1 mice using a continuous breeding protocol. Compounds were administered in the drinking water at 0, 0.35, 1.75, and 3.5% w/v (DEG) or 0, 0.25 1.25, and 2.5% w/v (DEGEE). Exposure of the breeding pairs to 3.5% DEG for 14 weeks produced statistically significant decreases in the number of litters per pair, live pups per litter, proportion of pups born alive, and live pup weight. There was also a significant increase in the cumulative days to litter and a significant decrease in the number of pairs producing the third, fourth, and fifth litters for the 3.5% DEG-exposed mice. A crossover mating trial of the F0 mice to determine the affected sex was inconclusive, but suggested that offspring development was compromised in females exposed to 3.5% DEG. Slight maternal (F0) toxicity was noted for the 3.5 DEG group (7% decrease in body weight). The F1 generation, at 3.5% DEG, had decreased body weights at birth and exhibited poor postnatal survival. At the intermediate dose of DEG, body weights of both sexes were depressed at weaning, at onset of mating, and at necropsy. However, no adverse effects on reproduction were observed. DEGEE had no effect on reproduction in the F0 or F1 generation mice despite a 34% decrease in cauda epididymal sperm motility in the F1 males at 2.5% DEGEE. Other signs of toxicity observed in these F1 mice included increased relative liver weights. These data indicate that DEG is a reproductive toxicant in Swiss mice affecting fertility and reproductive performance, albeit at high doses (equivalent to 6.1 g/kg/day). However, its monoethyl derivative, DEGEE, is without adverse effects on fertility and reproductive performance.
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PMID:Reproductive effects of diethylene glycol and diethylene glycol monoethyl ether in Swiss CD-1 mice assessed by a continuous breeding protocol. 234 Sep 88

The effects of 11 weeks of severe dietary restriction alone or in combination with either high- or low-intensity exercise on conservation of protein were studied in 32 male Sprague-Dawley rats. The rats were assigned to one of four groups: sedentary control (C), diet restriction alone (DO) or diet restriction in combination with either high-intensity (HI) or low-intensity (LO) exercise. The groups trained at either 75 percent (HI) or 37.5 percent (LO) of maximal running speed for up to 45 or 90 min/day, 5 days/week, respectively. Total (g) proteins, fat, water and ash content did not differ between the DO, HI and LO groups and were all reduced significantly in comparison to C. Similarly, heart, gastrocnemius muscle and epididymal fat pad masses were significantly reduced for the DO, HI and LO groups in comparison to C. However, the absolute decrease in heart mass was reduced for the HI group (heart mass = 0.31 percent of body mass) in comparison to the DO group (heart mass = 0.28 percent of body mass). Thus, in lean rats undergoing severe dietary restrictions, neither high- nor low-intensity exercise appears to affect total protein conservation in comparison to diet alone. However, high-intensity exercise training appears to attenuate cardiac but not skeletal muscle mass loss in the face of severe dietary restriction.
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PMID:Neither high- nor low-intensity exercise promotes whole-body conservation of protein during severe dietary restrictions. 234 Dec 32

Replicate differences were studied in lines of mice selected at 12 weeks of age for high (HF1, HF2) or low (LF1, LF2) right epididymal fat pad weight as a percentage of body weight (%EFP); for high (HL1, HL2) or low (LL1, LL2) hind carcass weight as a percentage of body weight (%HC); and randomly (RC1, RC2). Correlated traits were subcutaneous fat pad weight as a percentage of body weight (%SFP), water weight in hind carcass as a percentage of hind carcass weight (%WAT), body weights at 3, 6, and 12 weeks of age, and 3- to 6-week weight gain. Individual and maternal effects contributed to significant genetic drift for selected and correlated traits. No evidence indicated that drift was greater in selection treatments than in controls. Significant heterosis in replicate crosses within selection treatments was found for %HC in HL, LL, and LF and for %EFP in HF. Heterosis was insignificant in crosses of control replicates. Divergence in parental lines and replicate crosses was similar, indicating that differences in heterosis between high and low lines were small relative to divergence. Asymmetry tended to be greater between replicate crosses and parental lines, because selected replicates have greater average heterosis than control replicates. Multivariate discriminant function and Mahalanobis distance analysis of selected traits showed that divergence between replicates within selection treatments was much less than among selection treatments.
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PMID:Replicate differences in lines of mice selected for body composition. 235 89

1. Endothelin, a novel potent vasoconstrictor peptide produced by vascular endothelial cells stimulated anion secretion by a cultured secretory epithelium derived from the rat epididymis as measured by changes in short-circuit current (SCC). 2. Stimulation of the SCC was observed when endothelin was added to the basolateral or the apical side of the epithelium. The response to basolateral application was greater than that to apical application. The EC50 values were found to be 1.3 nM and 3.0 nM for basolateral and apical application, respectively. These values were about half an order to one order of magnitude higher than that required for its vasoconstrictor action. 3. The stimulation of SCC by endothelin was accompanied by a rise in the intracellular adenosine 3':5'-cyclic monophosphate (cyclic AMP) content in epididymal monolayers. 4. The effect of endothelin on SCC was mediated through an increase in prostaglandin synthesis by the tissues and was not blocked by an antagonist of angiotensin II (Sar1 Ile8 angiotensin II) or of adrenaline (propranolol). 5. It is speculated that endogenous endothelin plays an important role in the control of water and electrolyte transport in the epididymis.
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PMID:Endothelin stimulates short circuit current in a cultured epithelium. 248

We have used the tritiated water method to quantitate the effects of thyroid hormone on lipogenesis in the rat and then determined the contribution of this process to thyroid hormone-induced thermogenesis. After thyroid hormone administration to hypothyroid animals, fatty acid synthesis rose after a lag time of 12-16 h and reached a plateau after 4-5 days. This is consistent with the kinetics of an increase in oxygen consumption measured by others in similar animals. A diurnal variation was maintained in all thyroid states, with the peak value in the middle of the dark period being 3-fold higher than the nadir. Fatty acid synthesis in the livers of hyperthyroid animals was 3- to 4-fold higher than that in euthyroid rats, which, in turn, was 3- to 5-fold higher than the rate observed in hypothyroid rats. Slightly smaller but similar fold increases were measured in epididymal fat. A stimulation of fatty acid synthesis by thyroid hormone was also measured in the rest of the carcass, with hyperthyroid rates being twice those in hypothyroid animals. The contribution of the liver was much greater in hyperthyroid rats (34% of total fatty acid synthesis) than in hypothyroid animals (5%). The energy costs of this synthesis were calculated and compared to published values for total oxygen consumption in different thyroid states. Thus, 6-10% of the total increment in oxygen consumption between hyperthyroid and hypothyroid animals could be attributed to lipogenesis, depending on which published figures were used. About 3% of this increment was due to the liver alone.
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PMID:The regulation of lipogenesis by thyroid hormone and its contribution to thermogenesis. 258 43


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