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)

Lactate dehydrogenase isozyme X (LDH X), malate dehydrogenase (MDH) and total soluble protein have been determined in lysates of spermatozoa isolated from caput, corpus and cauda of rat epididymis. Transit of spermatozoa through epididymis is accompanied by a reduction of LDH X, MDH and total protein per cell in sexually rested animals. The profiles of reduction along epididymal segments are different for the three variables studied. Mating with receptive females during the 5 days prior to determinations increases significantly the levels of MDH in spermatozoa from all sections of epididymis and produces increase of total soluble protein in the cells contained in cauda.
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PMID:Lactate dehydrogenase X, malate dehydrogenase and total protein in rat spermatozoa during epididymal transit. 395 58

The effects of the four major components of dietary fiber--cellulose, hemicellulose, pectin and lignin--on lipid metabolism were studied in meal-fed Wistar rats maintained on a cholesterol-free semipurified diet for 21 days. Transit time was decreased and fecal weight increased compared to rats fed a fiber-free diet. Rats fed cellulose or lignin gained significantly less weight than rats fed hemicellulose or pectin. The fibers had no effect on serum cholesterol levels, but serum triacylglycerol levels were significantly higher in rats fed cellulose. Liver cholesterol levels were higher in cellulose-fed rats but liver triacylglycerol levels were highest in rats fed hemicellulose or pectin. Hepatic cholesterol 7 alpha-hydroxylase and HMG-CoA reductase activities were highest in rats fed cellulose and pectin, respectively. Epididymal fat cell size was similar in all groups but fat cell number was highest in pectin-fed rats. Perirenal fat cell size was greatest in rats fed cellulose or lignin and fat cell number in rats fed cellulose or hemicellulose. Lipoprotein lipase activity (per 10(6) cells) was elevated in epididymal fat of rats fed pectin and in perirenal fat of rats fed hemicellulose. Carcass lipid accumulation was highest in rats fed cellulose or lignin. Rats fed cellulose accumulated significantly higher levels of carcass cholesterol and triacylglycerol. Of the fibers fed, cellulose led to an accumulation of serum, liver and carcass lipid. The four fibers fed represent purified and altered forms of cellular components and the observed effects cannot be extrapolated to diets containing foods rich in one or another of these components.
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PMID:Influence of dietary fiber on lipid metabolism in meal-fed rats. 631 82

The transit of spermatozoa in the genital tract of the male mouse was investigated by quantitative light microscopic autoradiography after intraperitoneal injection of tritiated thymidine. Transit duration in the caput and the corpus of the epididymis was shown to be 3 days; the total duration of transit in the genital tract was 5 days. These findings indicate that the time required for the transit of spermatozoa in the epididymal caput and corpus was comparable to that calculated in other mammals studied. However, the duration of sperm storage in the epididymal cauda appeared to be shorter than that previously reported for rodents.
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PMID:Autoradiographic investigation of sperm transit through the male mouse genital tract after tritiated thymidine incorporation. 652 16

Testicular and epididymal spermatozoal reserves were determined for 11 healthy men, 1 vasectomized man, and 12 others. For healthy men, testis weight (19 testes) averages 16.9 + or - 1.2 gm and daily spermatozoal production was 4.25 times 10(6)9m (range = 1.4-6.3 times 10(6)/9m). Based on our total sample of 23 patients, 67% of the men 20-50 years old probably produce between 45 times 10(6) and 207 times 10(6) spermatozoa/day. Daily spermatozoal production was normal in 1 vasectomized man. Epididymal reserves of healthy men totaled 182 times 10(6) spermatozoa/epididymis, of whch 26% were in the caput, 23% in the corpus, and 52% in the cauda. The enterval between any previous ejaculation and death was unknown but we assumed that these values are typical for men copulating or masturbating every 1-7 days. Extragonadal spermatozoal reserves totaled approximately 440 times 10(6) of which less than 225 times 10(6) would be available for ejaculation in the ductuli deferentia and caudae epididymides. Transit time of spermatozoa through the caput, corpus, and cauda epididymidis was estimated at 0.72, 0.71, and 1.76 days. In a vasectomized man extragonadal reserves totaled 7 times 10(6) spermatozoa or about 75 days of production by the testes. Thus, spermatozoal production in man is much less efficient than in other mammals, the extragonadal reserves of spermatozoa are small and maturation of spermatozoa in the caput plus corpus epididymidis occurs in less than 2 days. In terms of these quantitative characterisitics, the reproductive capacity of man is cosiderably less than that of the rhesus monkey.
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PMID:Daily spermatozoal production and epididymal spermatozoal reserves of the human male. 677 1

1. Isolated cells from primary cultures of rat epididymal epithelial cells were employed for the study of adrenaline-stimulated Cl- transport using a Cl-(-)sensitive fluorophore 6-methoxy-N-(3-sulphopropyl) quinolinium (SPQ). SPQ was loaded into the cells by the hypotonic shock method. 2. The resting intracellular Cl- concentration, estimated in the presence of nigericin and tributyltin in high-K+ solution, was 62.3 +/- 0.2 mM. This value was not altered in the presence of 1 microM adrenaline. When extracellular Cl- was replaced by NO3-, an increase in fluorescence corresponding to a decrease in intracellular Cl- was observed. The initial outward Cl- movement was estimated to be 0.54 +/- 0.08 mM s-1. This value was increased by incubating the cells with adrenaline. The stimulatory effect of adrenaline was reduced by 1 mM DPC. 3. Addition of Cl- to cells previously depleted of Cl- caused an instantaneous decrease in fluorescence due to the entry of Cl-. The initial rate of Cl- entry was -0.62 +/- 0.13 mM s-1. Adrenaline increased the rate of entry to -2.13 +/- 0.08 mM s-1. The adrenaline-stimulated rate of entry was reduced by DPC or frusemide (0.5 mM) and was completely blocked in the presence of both agents. 4. In Na(+)-free solution, the adrenaline-stimulated rise of rate of Cl- entry was reduced in the presence of DPC. Frusemide had no effect on the entry rate. 5. The stimulatory effect of adrenaline were abolished by propranolol (5 microM) but not by phentolamine (5 microM). Conversely, isoprenaline (1 microM) and forskolin (1 microM) mimicked the effects of adrenaline.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Adrenaline-regulated Cl- transport in cultured single rat epididymal cells measured by an entrapped Cl-(-)sensitive fluorophore. 800 8