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

The spontaneous contractility of rat epididymis was recorded in vivo and the effects of various autonomic drugs were studied. Norepinephrine, epinephrine, and orciprenaline produced a sudden increase in tonus and in the size and frequency of epididymal contractions. Phentolamine (an alpha-blocker agent) inhibited the effects of norepinephrine. On the other hand, alprenolol (a beta-blocker agent) inhibited the effects of orciprenaline but did not block the effects of norepinephrine. In addition, phentolamine and alprenolol decreased the spontaneous activity of the epididymis. Acetylcholine produced effects similar to those of norepinephrine. These effects were blocked by atropine. The results described would indicate the presence of the two receptors, alpha and beta, and that both are mediators of stimulatory effects.
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PMID:Effects of autonomic drugs on epididymal contractions. 0 41

The influence of dietary fat on prostaglandin production and lipolysis was tested in basal and norepinephrine stimulated adipocytes isolated from the epididymal fat pads of fasted rats. Seven diets varying in fat calories and polyunsaturation were utilized. No basal differences were noted for prostaglandin E2 production or lipolysis. Norepinephrine stimulated prostaglandin E2 and F2alpha production was significantly (P less than 0.01) increased with greater polyunsaturation of fat, but not by increased fat calories. Norepinephrine stimulated lipolysis was depressed by an increase in fat calories but was unaffected by the degree of polyunsaturation of fat. This is in vitro evidence against the concept that prostaglandins play a feedback regulator role in fat cell lipolysis since no correlation could be made between the two parameters.
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PMID:Prostaglandin production and lipolysis in isolated rat adipocytes as affected by dietary fat. 74 82

The effects of norepinephrine, phentalamine, oxytocin, vasopressin, several prostaglandins, and indomethacin on the spontaneous motility of isolated guinea pig cauda epididymidis were explored. Phentolamine and indomethacin reduced the isometric peak tension of spontaneous epididymal contractions. Phentolamine also depressed the frequency. Both findings suggest that catecholamines and endogenous prostaglandins are in some way regulators of the spontaneous motility of the cauda epididymidis. Norepinephrine resulted in the development of a distinct, sustained, tonic contraction without phasic activity, whereas prostaglandins E1, E2, and F2 alpha elicited a tonic increase accompanied by frequent, superimposed, phasic contractions. Both oxytocin and vasopressin comparably enhanced epididymal motility, producing contractile responses similar to those observed with prostaglandins. Since the epididymal contractions can influence the time spent by spermatozoa in passing through the ductus epididymidis, the above-mentioned compounds could play an important role in spermatozoal transport via modulation of epididymal contractile activity. In addition, such naturally occurring substances might regulate the release of sperm from the last portion of the epididymis into the ductus deferens.
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PMID:Physiologic and pharmacologic studies on the motility of isolated guinea pig cauda epididymidis. 80 41

Isolated adipocytes were prepared from epididymal adipose tissues removed from rats which had been fed or starved for 48 h (fed adipocytes or fasted adipocytes). These cells were incubated at 37 degrees C for 90 min in media containing 0, 3, or 30 mM glucose, with or without norepinephrine (1.0 mug/ml). Then the concentrations of free fatty acids (FFA) and free glycerol (FG) in the total mixture (medium plus cells) and in the medium alone were measured. Addition of glucose to the medium increased the total PG, presumably by increasing the basal lipolysis, and it decreased the intracellular retention ratio of FG (the ratio of intracellular FG to total FG). Addition of glucose did not change the total FFA, but decreased the FFA/FG ratio, presumably by increasing reesterification. The increase in FG and decrease in the FFA/FG ratio on addition of glucose were greater in fed than in fasted adipocytes. The intracellular retention ratio of FFA also decreased on addition of glucose. Glucose enhanced norepinephrine-induced lipolysis (release of free glycerol), and this effect of glucose was greater in fasted adipocytes. However, the increase in FFA in fasted adipocytes induced by norepinephrine was not altered by addition of glucose. In fed adipocytes norepinephrine decreased the total FFA in the presence of glucose. Reesterification of FFA following norepinephrine was increased by addition of glucose. Norepinephrine decreased the intracellular retention ratios of FG and FFA in the presence of glucose. These results suggest that the passage of the lipolytic products, FFA and FG, through the cell membranes may not occur by simple diffusion, but may require energy.
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PMID:Effect of glucose on lipolysis and on release of lipolytic products in isolated adipocytes. 114 32

1. Electrical and mechanical responses of epididymal and prostatic regions of rat, rabbit and guinea-pig vas deferens have been examined to investigate regional variation in purinergic and adrenergic mechanisms. 2. Noradrenaline was significantly more potent in producing contraction in epididymal segments of the muscle than in prostatic segments. 3. ATP and alpha,beta,methylene ATP were significantly more potent in producing contraction of prostatic segments than epididymal segments. 4. In guinea-pig vas deferens the resting membrane potential was greater in smooth muscle cells in the prostatic region than in the epididymal. Excitatory junction potentials (EJPs) in both the epididymal and prostatic regions were of similar magnitude and were almost abolished by the P2x-purinoceptor antagonist suramin. 5. The alpha-adrenoceptor antagonist phentolamine had no inhibitory action on EJPs in either region of the guinea-pig vas deferens.
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PMID:Regional variation in purinergic and adrenergic responses in isolated vas deferens of rat, rabbit and guinea-pig. 147 7

Brown adipose tissue (BAT) is a major site of nonshivering thermogenesis (NST) during cold acclimation for most mammals. Repetitive nonthermal stress such as immobilization has been shown to enhance the capacity of NST as cold acclimation. In the present study, the effects of running training, another type of nonthermal stress, were investigated on in vitro thermogenesis and the cellularity of interscapular BAT in rats. The rats were subjected to treadmill running for 30 min daily at 30m/min under 8 degrees inclination for 4-5 weeks. In vitro thermogenesis was then measured in minced tissue blocks incubated in a Krebs-Ringer phosphate buffer containing glucose and albumin at 37 degrees C, using a Clark type oxygen electrode. The trained rats showed less body weight gain during the experiment. The weights of BAT and epididymal white adipose tissue were smaller in the trained rats. Noradrenaline- and glucagon-stimulated oxygen consumption were also significantly smaller in the trained rats. The tissue DNA level was greater in the trained rats, but the DNA content per tissue pad did not significantly differ. The results indicate that running training reduces BAT thermogenesis, possibly as an adaptation to conserve energy substrates for physical work.
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PMID:Effects of running training on in vitro brown adipose tissue thermogenesis in rats. 163 84

Male Sprague-Dawley rats displayed significantly higher rates of triglyceride/fatty acid (TG/FFA) substrate cycling in subcutaneous, perigenital, and mesenteric white adipose tissue, compared to females. To investigate possible regulation via androgens and estrogens, male rats were treated with the androgen antagonist, cyproterone acetate (10 mg daily in subcutaneous injections), or estradiol polyphosphate (0.3 mg intramuscularly, given as a single dose). Estradiol treatment did not affect TG/FFA cycling. Treatment with cyproterone acetate significantly decreased TG/FFA cycling in perigenital (epididymal) tissue. This effect could however largely be ascribed to concomitant inhibition of food intake by cyproterone acetate. The effects of cyproterone acetate on the two axes of TG/FFA cycling (lipolysis and re-esterification) were further studied in vitro. Norepinephrine-stimulated glycerol release from perigenital adipocytes was inhibited, whereas activities of esterification enzymes (GPAT and PPH) was essentially unaffected. We conclude that androgens seem to affect TG/FFA cycling indirectly via the lipolytic axis.
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PMID:Sex difference in triglyceride/fatty acid substrate cycling of rat adipose tissue: indirect regulation by androgens. 183 7

The inhibitory effect of alpha-agonists noradrenaline and phenylephrine on the maximal alpha 1-adrenergic contractile response was studied in the rat isolated vas deferens and its epididymal and prostatic sections. The degree of noradrenaline (2.10(-5) M) inhibition of the maximal response was directly related to the magnitude of response to noradrenaline in the same concentration. The response of the epididymal section to phenylephrine reached its maximum and terminated faster than the response to noradrenaline. Both the activation and the desensitization seem to proceed faster in alpha 1-adrenoreceptors. The inhibition of the maximal response under the effect of phenylephrine (2.10(-5) M) was more obvious than the response to it in the same concentration. Noradrenaline seem to produce desensitization of alpha 1-adrenoreceptors involved in the response whereas phenylepinephrine produces desensitization in uninvolved ones, too.
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PMID:[Regularities of the alpha-agonists inhibitory effect on the magnitude of maximum adrenergic response of the rat vas deferens]. 253 71

Electrical field stimulation of ring preparations of the epididymal (Ve) and prostatic (Vp) parts of the human isolated vas deferens produced contractions with similar frequency-dependence and appearance. The contractions of Ve, but not of Vp preparations were abolished by tetrodotoxin (10(-6)M). Noradrenaline (NA), phenylephrine, and methoxamine, but not clonidine induced repetitive, phasic contractions in both Ve and Vp preparations, and increased the amplitude of electrically induced responses. Clonidine concentration-dependently decreased electrically induced contractions in Ve preparations, but had no significant effects in Vp preparations. Phentolamine and prazosin abolished electrically induced contractions in Ve but not in Vp preparations. In Ve rings the contractions were increased by rauwolscine; no such effect was observed in Vp preparations. Isoprenaline, propranolol, acetylcholine and carbachol had no effects in the Ve or Vp preparations. Scopolamine and atropine reduced electrically induced responses. Clonidine decreased and rauwolscine increased the electrically induced release of 3H in both Ve and Vp preparations pre-loaded with 3H-NA. Phenylephrine, prazosin, isoprenaline, propranolol, carbachol and scopolamine had minor or no effects on the 3H release. Radioligand receptor binding experiments using 3H-prazosin and 3H-rauwolscine as ligands revealed similar densities of alpha 1- and alpha 2-adrenoreceptors in the human vas deferens. There seemed to be no differences in their distribution between the epididymal, middle and prostatic part of the organ. It is concluded that the neurotransmission in the human vas deferens is noradrenergic and mediated via alpha 1-adrenoreceptors. The prazosin and tetrodotoxin resistant part of the electrically induced contraction in Vp preparations may be caused by direct smooth muscle stimulation.
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PMID:Effect of drugs interacting with adrenoreceptors and muscarinic receptors in the epididymal and prostatic parts of the human isolated vas deferens. 299 31

In this paper, estimates of the selectivities of a series of twelve sympathomimetic agents acting at postjunctional alpha 1- and prejunctional alpha 2-adrenoreceptors were investigated, using epididymal and prostatic segments of the rat vas deferens. The relative order of potency for the twelve agonists at prejunctional alpha 2-adrenoreceptors mediating inhibition of field-stimulation-induced contractions in the prostatic segment of the vas deferens was: clonidine greater than (-)-adrenaline greater than xylazine greater than or equal to (-)-noradrenaline greater than (+)-adrenaline greater than dopamine greater than or equal to phenylephrine greater than or equal to metaraminol greater than or equal to (+)-noradrenaline greater than (-)-isoprenaline greater than methoxamine greater than (+)-isoprenaline. The relative order of potency for the agonists at postjunctional alpha 1-adrenoreceptors mediating contraction of smooth muscle in epididymal segments of the vas deferens was: (-)-adrenaline greater than or equal to (-)-noradrenaline greater than phenylephrine greater than clonidine greater than or equal to (+)-adrenaline greater than or equal to methoxamine greater than or equal to (+)-noradrenaline greater than or equal to metaraminol greater than or equal to dopamine greater than or equal to (-)-isoprenaline greater than or equal to xylazine; (+)-isoprenaline was inactive. (+)-Noradrenaline, the stereoisomers of adrenaline and isoprenaline, dopamine, clonidine, xylazine and metaraminol displayed alpha 2-selectivity whereas phenylephrine and methoxamine displayed alpha 1-adrenoreceptor selectivity. (-)-Noradrenaline possessed a similar potency at both alpha 1- and alpha 2-adrenoreceptors thus making it non-selective by the criteria used in this study.(ABSTRACT TRUNCATED AT 250 WORDS)
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PMID:Selectivities of some agonists acting at alpha 1- and alpha 2-adrenoreceptors in the rat vas deferens. 300 22


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