Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P56851 (epididymal)
 11,273 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

The biosynthesis and secretion of epididymal proteins were studied in an in vitro system using explants from rabbit epididymis cultured in a defined medium. Epididymal explants actively incorporated [35S]methionine into cellular proteins, about 7% of them being secreted into the medium. SDS-PAGE of the labeled proteins secreted to the medium showed regional differences in their synthesis and secretion along the epididymal tract. Castration resulted in the inhibition of the synthesis and secretion of at least two polypeptides of Mr 150,000 and 21,000, but at the same time induced the appearance of other polypeptides. Immunoprecipitations with a specific antibody indicated that the variations in the amounts of the secreted 21 kDa component were associated with differences in its rate of synthesis. Epididymis from immature rabbits synthesized some polypeptides that are repressed in the adult state. The results suggest a dual effect of testosterone on rabbit epididymal secretory proteins.
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PMID:In vitro biosynthesis and secretion of rabbit epididymal secretory proteins: regulation by androgens. 273 56

Morphological and histological features of rete testis, vas efferens, epididymis and vas deferens were studied in the langur monkey. Tubular extensions of rete were located towards lateral side of the testis. Its epithelium comprises mostly of cuboidal cells with hyaline cytoplasm. Three to nine bundles of vas efferens, emerging below the cranial pole of the testis, were observed. Vas efferens epithelium comprises of ciliated and nonciliated cells. Epididymis could be divided into six zones on the basis of cytological features. Principal cells, basal cells, apical cells and intraepithelial lymphocytes were observed in the epididymal epithelium, but their number, shape, size and location of nuclei varied in different zones. Vas deferens epithelium comprises of principal cells, basal cells, apical cells and few intraepithelial lymphocytes. Epithelium is surrounded by lamina propria, longitudinal, circular and longitudinal muscle layers.
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PMID:Structure of rete testis, vas efferens, epididymis and vas deferens of langur monkey (Presbytis entellus entellus Dufresne). 322 54

A synthetic substrate (p-nitrophenyl-alpha-D-glucopyranoside) was used to measure the acid and neutral alpha-glucosidase activity in bull seminal plasma, spermatozoa and in homogenates of bull reproductive organs. Marked differences were observed in the activities of these enzymes in the various tissues studied. Epididymis and particularly its caput region contained the highest specific activity of acid alpha-glucosidase. The activity of neutral alpha-glucosidase was highest in testis and in different parts of the epididymis. Seminal plasma, spermatozoa and seminal vesicle secretion contained only the acid enzyme activity. After fractionation with anion exchange chromatography in HPLC (Mono Q) and chromatofocussing, acid alpha-glucosidase activity of seminal plasma was recovered in two fractions with different pI values. The corresponding activities were found in the secretion of seminal vesicles, which thus form the major secretory source of seminal plasma acid alpha-glucosidase. In the fractionation with gel filtration on Sepharose 6B, the acid alpha-glucosidase had a smaller molecular weight than did the neutral enzyme. In anion exchange chromatography and chromatofocussing the testicular and epididymal homogenates each contained two acid and two neutral isoenzymes. In both fractionations the elution pattern of acid alpha-glucosidase was clearly different from that of the enzymes in seminal plasma. The pH optimum of acid alpha-glucosidase ranged from 3.75 to 4.5 and that of the neutral enzyme from 6.5 to 7.0. The neutral activity was more sensitive to many divalent metal ions and differences were also observed in the response of the enzymes to different concentrations of turanose and KCl.
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PMID:Acid and neutral alpha-glucosidase in the reproductive organs and seminal plasma of the bull. 390 Mar 85

Alteration of epididymal function and its relation to maturation of spermatozoa was studied in 54 adult male albino rats. Levels of free and bound sialic acid in the spermatozoa and luminal contents of the epididymis and vas deferens were determined. A group of 10 received rabbit antiserum to ovine luteinizing hormone (LHAS) sc .2 ml/day for 5 days. 2 groups of 8 animals each received 2.5 mg cyproterone acetate twice daily for either 15 or 30 days. 16 animals served as intact controls and 12 animals served as castrate controls. Epididymis and vas deferens sperm counts were not affected by LHAS for 5 days or by cyproterone acetate for 15 days; however, sperm counts were decreased in the corpus (p less than .02), cauda (p less than .05), epididymidis and vas deferens (p less than .01) when rats were treated with cyproterone acetate for 30 days. Castration resulted in a marked reduction in all regions within 5 days. In the intact rats spermatozoa sialic acid decreased in the cauda epididymidis (p less than .01) and increased in the vas deferens (p less than .001). Sialic acid concentration was similar in those treated with either LHAS or cyproterone acetate for 30 days. Bound sialic acid in the epididymal fluid increased (p less than .02) to a maximum in the corpus and cauda and decreased in the vas deferens (p less than .05). LHAS or cyproterone acetate caused a reduction in bound sialic acid in the fluid of the epididymis and vas deferens.
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PMID:Alteration of epididymal function and its relation to maturation of spermatozoa. 421 24

Epididymis were collected from cyproterone acetate-treated Black Bengal goats. Treatment for 70 days reduced the epididymal weight. Caput epididymidis showed drastic decrease in the height of the epithelium, loss of stereocilia, the number of narrow cells and apical cells. Though the corpus showed dramatic changes after treatment, cauda epididymidis showed moderate changes.
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PMID:Epididymal histoarchitecture of goats under chronic cyproterone acetate. 622 77

The effects of oral administration of clomiphene citrate (50 mg/kg body weight) on the testis, epididymis and accessory sex glands of the musk shrew were investigated. The drug induced duration-dependent alterations in the weight and histology of these organs. The drug produced significant reduction in testicular weight with severe degenerative changes in seminiferous tubules; Leydig cells were also atrophied. However, no significant change was found in the levels of protein, RNA and DNA in the testes of drug-treated animals as compared with controls. Epididymis in drug-treated shrews exhibited significant decrease in weight and regressive histological changes. Spermatozoa collected from the cauda epididymidis of drug-treated shrews were immotile and often fragmented. Clomiphene treatment also induced regressive histological changes in the prostate and ampullary gland accompanied by significant decrease in the weight. The treatment also caused significant decrease in the level of fructose in the ampullary glands. Following withdrawal of the drug, the reproductive organs returned to their normal state. Full recovery was noticed in the accessory sex glands 28 days after drug withdrawal. However, full spermatogenic activity and normal epididymal histology were achieved only after 56 days The mechanism of action of clomiphene on the male reproductive organs is briefly discussed.
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PMID:Effect of clomiphene citrate on the testis, epididymis and accessory sex glands of the musk shrew (Suncus murinus L.). 661 57

Incremental levels of trilinoelaidate (tt18:2) were fed to rats for 11 weeks and changes in lung and epididymal lipid fatty acid composition were determined, and concentrations of prostanoids in serum, lung and stomach fundus were measured. Platelet aggregation to various agonists was tested. In the lung there was a concomitant increase of linoelaidate corresponding to incremental dietary levels in all lipid classes (phosphatidylcholine, phosphatidylethanolamine, phosphatidylserine-phosphatidylinositol and neutral lipids). Arachidonic acid in lung phosphatidylcholine was markedly decreased. Epididymis accumulated linoelaidate in only the neutral lipid fraction; no tt18:2 was found in any of the phospholipid classes. Serum prostanoid levels (thromboxane B2 and prostaglandins PGF2 alpha and PGE) were significantly decreased in rats fed high levels of tt18:2, but were not altered at lower levels of consumption; the concentrations of 6-keto-PGF1 alpha were not significantly altered at any level of tt18:2. Platelet responsiveness to various agonists was not significantly altered by incremental dietary trilinoelaidate, i.e., ADP, thrombin, collagen and calcium elicited similar aggregation responses. In conclusion, dietary trilinoelaidate at low levels of consumption, while being incorporated into various lipid classes, did not alter serum and tissue prostanoid levels or markedly affect platelet aggregation.
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PMID:Dietary trilinoelaidate: effects on organ fatty acid composition, prostanoid biosynthesis and platelet function in rats. 669 85

Epididymis-secreted proteins D and E have been purified to homogeneity and partially characterized, and it is shown that monoclonal antibody (MAb) 4E9 (raised against a detergent extract of rat caudal epididymal sperm [Moore et al., 1994: Mol Reprod Dev 37(2):181-194]) recognizes protein E, but not protein D. The molecular weight of protein D (approximately 30 kD) is approximately 2 kD lower than protein E (approximately 32 kD). The NH2-terminus of each protein is blocked; however, microsequencing of internal peptides confirms earlier reports of significant sequence identity between the two proteins. High performance liquid chromatography tryptic peptide mapping showed peak differences between the two proteins, but it was not possible to obtain amino acid sequence in the peaks that were different. The epitope for MAb 4E9 was localized in the blocked NH2-terminus-CNBr peptide derived from protein E. The epitope was destroyed by protease treatment of protein E. Removal of N-linked oligosaccharides did not destroy the epitope for MAb 4E9 and did not affect the molecular weight difference between the proteins.
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PMID:Identification of the rat epididymis-secreted 4E9 antigen as protein E: further biochemical characterization of the highly homologous epididymal secretory proteins D and E. 886 48

Epididymis is a site of sperm maturation and storage. Limited and directed-proteolysis regulated by plasminogen activator (PA), plasminogen activator inhibitor type-1 (PAI-1) and other related factors may play an essential role in these processes. Our previous studies have demonstrated that rat epididymis expressed luteinizing hormone receptor (LHR), tissue type (t) and urokinase type (u)PA, mRNAs, and tPA activity was stimulated in vitro by human chorionic gonoadotrophin (HCG). In the present study we further examined localization of mRNAs for tPA, uPA, LHR, androgen receptor (AR), as well as inhibin subunits alpha, betaA and betaB in rhesus monkey epididymis. Using in-situ hybridization with digoxygenin-labelled cRNA probes, we have demonstrated that tPA and PAI-1 mRNAs were localized in epithelial cells of adult monkey epididymis. uPA mRNA was localized in the same areas, but to a much smaller extent. tPA, uPA and PAI-1 mRNAs were greatly expressed in the caput and corpus of adult epididymis than in other regions. In-vitro experiments showed that both tPA and uPA activities in epididymal cells were dramatically stimulated by HCG, but not by follicle stimulating hormone (FSH). LHR (but not FSH receptor) and AR mRNAs were localized in the epithelial cells of the epididymis. However, LHR mRNA was detected in both adult and immature infant monkeys, whereas AR was found only in the adult. Inhibin alpha, betaA and betaB mRNAs were also detected in this organ, betaA mRNA being more strongly expressed in the caput than in other regions of the epididymis. We suggest that LH and androgen may be the key hormones in coordination with the PA-PAI-1 system in regulating epididymal differentiation and sperm maturation.
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PMID:Localization of plasminogen activator and inhibitor, LH and androgen receptors and inhibin subunits in monkey epididymis. 943 19

Adult male albino rats were treated with 0.4 mg nicotine/100 g body weight either orally or intraperitoneally for 30 days. All animals were autopsied on the 31st day. Epididymis and vas deferens were dissected out, weighed and processed for biochemical estimations. Nicotine caused a reduction in the weight of epididymis and vas deferens in both drug treated groups. The total cholesterol content is increased while protein, DNA and RNA contents and the epididymal sperm count were decreased. The acid phosphatase content is also decreased, whereas alkaline phosphatase is increased. The surface epithelial cell height of these ducts is decreased and secretory activity is reduced with the disruption of epithelial cell projections. These changes may be due to non-availability of androgens in nicotine treated rats.
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PMID:Nicotine induced inhibition of the activities of accessory reproductive ducts in male rats. 961 35


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