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)

Oral administration of di(2-ethylhexyl)phthalate (DEHP) in doses of 250, 500, 1000 and 2000 mg/kg to adult rats for 15 days caused a significant dose dependent decrease in the sperm count of the epididymal spermatozoa. The activity of gamma-glutamyl transpeptidase (gamma GT) and lactate dehydrogenase (LDH) was significantly increased in the animals of the treated groups. An increase in the activity of beta-glucuronidase and decrease in the activity of acid phosphatase was also observed at the highest dose of DEHP. The activity of sorbitol dehydrogenase (SDH) was found to be decreased in the animals exposed to 1000 and 2000 mg/kg of DEHP. These results suggest that DEHP can affect spermatogenesis by altering the activities of the enzymes responsible for the maturation of sperms. The reduced number of sperms may be responsible for the antifertilic effects of DEHP.
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PMID:Effect of di(2-ethylhexyl)phthalate (DEHP) on spermatogenesis in adult rats. 287 65

Sperm maturation and storage occur in a unique milieu created in large part by the epididymal epithelium. To learn more about the interaction of the epididymal epithelial cell with both luminal and systemic environments, we now report on the preparation and characterization of epididymal epithelial cell plasma membranes. A preparation enriched for epididymal epithelial cell plasma membranes was isolated from collagenase-digested epididymal tubule fragments by hand-Dounce homogenization, differential centrifugation, and sucrose gradient centrifugation. The final membrane fraction was enriched 11-fold for the plasma membrane marker 5'-nucleotidase; 2.6-fold for the lysosomal marker acid phosphatase, and 3-fold for the Golgi marker thiamine pyrophosphatase. No enrichment was observed for mitochondrial or endoplasmic reticulum enzyme markers. Specific and saturable transferrin-binding activity was also detected in the final preparation. Electron microscopy revealed the presence of vesicles and sheets of membranes as well as an occasional Golgi apparatus. The plasma membrane fraction was used to generate monoclonal antibodies. Of 102 wells exhibiting growth, 12 were positive by immunofluorescent staining of frozen sections. Ten of these recognized determinants in epithelial cells, and 2 stained peritubular smooth muscle cells. Most of the epithelial cell-specific antibodies stained brush border alone or in combination with the basolateral plasma membrane. Three antibodies stained the Golgi apparatus. Most antibodies were specific for particular epididymal regions, 3 also recognized determinants in the kidney, and 1 stained residual bodies in the testis.
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PMID:Isolation and characterization of epididymal epithelial cell plasma membranes. 336 69

The anticancer and immunosuppressive drug cyclophosphamide is extensively used in clinical practice and is known to alter fertility in man. We showed previously that treatment of male rats with low daily doses of cyclophosphamide over a 9-week period caused fetal malformations, a high rate of postimplantation loss and affected epididymal and sperm histology. In the present study, five biochemical measures of epididymal function were used to characterize further the effects of cyclophosphamide on the epididymis. For 1, 3, 6, or 9 weeks, adult Sprague-Dawley rats were gavage-fed daily with saline (control), 5.1 (low dose), or 6.8 (high dose) mg/kg of cyclophosphamide. The specific activities of the two glycolytic enzymes aldolase and lactate dehydrogenase (LDH), the mitochondrial enzyme succinate dehydrogenase, the cytosolic enzyme carnitine acetyltransferase and the lysosomal enzyme acid phosphatase were determined in cytosolic and mitochondrial subcellular fractions from four segments of the epididymis. Cyclophosphamide caused decreases in protein concentrations in all segments of the epididymis only after 6 weeks of treatment with the high dose. The specific activities of aldolase, LDH and succinate dehydrogenase did not differ from control with respect to dose or duration of treatment. In contrast, there were significant effects of cyclophosphamide on carnitine acetyltransferase and acid phosphatase specific activity. After 1 week of treatment, there was a transient dose-related decrease in the specific activity of carnitine acetyltransferase, which was most striking for the corpus epididymidis (76% of control), but which did not differ from control after 3, 6, and 9 weeks. After 6 weeks of treatment with the high dose of cyclophosphamide, carnitine acetyltransferase specific activity in the initial segment and the corpus epididymidis was elevated to 165 and 140%, respectively, as compared with the 1-week high dose values. The specific activity of acid phosphatase did not differ from control after 1 and 9 weeks of treatment. At 3 and 6 weeks, however, there was a dose-related increase in acid phosphatase specific activity for all regions of the epididymis that was most marked in the cauda after the 6-week treatment (140% of control). Therefore, low dose, daily treatment of male rats with cyclophosphamide not only alters specific enzymes in specific segments of the epididymis, but acts in a dose- and time-dependent manner. It is possible that these changes could be mediated by direct, toxic effects of the drug on the epithelium or be secondary to alterations in the spermatozoa as a result of the treatment.
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PMID:Effects of cyclophosphamide on selected cytosolic and mitochondrial enzymes in the epididymis of the rat. 338 43

Daily oral administration of acrylonitrile (10 mg/kg body weight) to mice for a period of 60 days caused a significant decrease in the activity of testicular sorbitol dehydrogenase and acid phosphatase, and an increase in that of lactate dehydrogenase and beta-glucuronidase. Histopathological studies revealed degeneration of the seminiferous tubules. A decrease in the sperm counts of the epididymal spermatozoa was also observed in the animals of the acrylonitrile-exposed group. These observations suggest that acrylonitrile may affect the male reproductive function by causing testicular injury.
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PMID:Testicular effects of acrylonitrile in mice. 338 48

Relative activities of acid and alkaline phosphatases in rat reproductive tissue were studied in young adult (10-12 months) and aged (30-34 months) rats. Prostatic alkaline phosphatase alone increased in aged animals. Moreover, prostate preparations contain two isoenzymes of alkaline phosphatase whereas only one was found in epididymal tissues. Age-associated changes in the prostatic alkaline phosphatase isoenzyme ratios were observed. No significant age-related changes in acid phosphatase tartrate sensitivity were found. Techniques for the preparation of prostate and epididymis tissue extracts are reported.
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PMID:Prostate gland and epididymis phosphatase isoenzymes: comparisons of young adult and aged rats. 341 51

The measurement of biochemical markers in human seminal plasma is important in the evaluation of male infertility. We recommend the measurement of one representative substance for each organ involved in seminal fluid production as a routine diagnostic tool: The initial fructose level for seminal vesicular function, citrate or acid phosphatase for the prostate gland and free carnitine as an index of epididymal function. A biochemical analysis of seminal fluid enables us to detect disturbances of the male adnexal organs and may lead to more exact therapy.
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PMID:Recommended biochemical parameters for routine semen analysis. 379 10

Dehydrogenase and hydrolase activities were assessed histochemically during postnatal development of the mouse epididymis. At birth the activities of various enzymes were demonstrable along the epithelium at the same intensity. Variations occurred in the intensity of enzyme activities in principal cells, leading to regional differentiation which progressed according to an ascending pattern from the distal part (2nd week) to the medial and proximal parts (3rd week). The proximal part reached its definitive differentiation at the 4th week when the 5 segments characteristic of the adult state were distinguishable. At the same time, 3 types of "apical cells" (narrow, prominent and mitochondria-goblet cells) in the proximal part and "clear cells" in the medial and distal parts showed higher activity of several enzymes (dehydrogenases, acid phosphatase, Ca2+-ATPase) than did adjacent principal cells. This histochemical data has led us to propose a model for epididymal cell differentiation in the mouse. The role of androgens in the development of those regional differences is discussed.
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PMID:Postnatal differentiation of the enzymatic activity of the mouse epididymis. 383 61

The biochemical analysis of human semen is based on assays of certain compounds in the ejaculate, which are secreted by the prostate (acid phosphatase, citrate, zinc), the seminal vesicles (fructose), and the epididymis (free carnitine). The information provided by seminal biochemistry is relevant not only for the investigation of male sterility, but also to endocrinology, urology and pharmacology. In the case of excretory azoospermia, the carnitine level is lower than 300 nmoles, which allows a differentiation between secretory and excretory azoospermia. Occlusions can be located by measuring prostatic and vesicular markers: they are normal if the occlusion is deferential or epididymal; if the fructose level is zero and the level of prostatic markers is high, there is an occlusion in the ejaculatory ducts or a bilateral deferential agenesia. The information provided by seminal biochemistry in the investigation of male sterility remains limited. It will probably be enhanced when spermatozoon biochemistry is better understood.
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PMID:[Azoospermia, asthenozoospermia and seminal biochemistry]. 400 66

Changes in the biochemical composition of semen, which reflect the accessory sex organ functions, following danazol (100 mg/day; orally) plus testosterone enanthate (50 mg/month; i.m.) administration have been investigated in langur monkey. The levels of acid phosphatase, lactic dehydrogenase and glycerylphosphorylcholine in the semen decreased significantly; whereas fructose, citric acid, magnesium and semen volume did not show any significant changes. A gradual decrease in the motility and count of spermatozoa was observed. At 60 days of treatment all animals became azoospermic. No drug related hematological changes were observed. The combination therapy impaired the epididymal and prostatic functions along with suppression of spermatogenesis.
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PMID:Changes in the biochemical composition of semen following danazol plus testosterone enanthate administration to the langur monkey. 400 68

The activity of N-acetyl-beta-D-glucosaminidase (NAG, 60.1 units/mg protein) and of acid phosphatase (57.7 units/mg protein) in fluid from the cauda epididymidis formed without any contribution from the testis (fluid obtained from a perfused and isolated cauda epididymidis or from an epididymis whose corresponding efferent ducts had been ligated for 40 days) was significantly higher than the activity of these enzymes in normal fluid (39.6 and 41.2 units/mg protein, respectively). Arylsulphatase activity of the locally formed fluid (11.2 units/mg protein) was lower than that of normal fluid (74.1 units/mg protein). The rete testis fluid was relatively rich in arylsulphatase since the ratio of arylsulphatase to acid phosphatase activity was 17 times higher in this fluid than in locally formed fluid. It is concluded that the activities of NAG and acid phosphatase in normal fluid from the epididymis originate in the epididymal tissue, while most of the arylsulphatase activity comes from the testis.
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PMID:The origin of some acid hydrolases of the fluid of the rat cauda epididymidis. 403 Apr 97


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