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1.
  • 1.1. The effects of various biogenic amines on contractions of the ABRM of M. edulis in response to repetitive electrical stimulation, ACh and high K+ concentration were examined.
  • 2.2. Octopamine, serotonin, dopamine, noradrenaline, tyramine and phenylethanolamine potentiated the contractions of ABRM. Octopamine was found to be the most potent. Histamine did not potentiate.
  • 3.3. Phentolamine blocked the potentiating action of octopamine and noradrenaline and partially blocked dopamine, but it did not block serotonin. Phentolamine also blocked the potentiating after-effect of repetitive electrical stimulation on subsequent contractions. It is suggested that octopamine is a neurotransmitter or a local neurohormone which potentiates contraction of the ABRM.
  • 4.4. Under certain conditions, high concentrations of dopamine and serotonin inhibited contractions in response to ACh and high K+ concentration. Thus, these amines have not only potentiating but also inhibitory action on contraction of the ABRM, in addition to relaxing catch.
  • 5.5. It is suggested that a wide spectrum of substances participates in the physiological control of contractility in the ABRM.
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2.
  • 1.1. Lateral ciliary activity and DOPA decarboxylase were measured in the ctenidium of Crassostrea virginica (Gmelin).
  • 2.2. Activity of the lateral cilia is dependent upon branchial nerve (Paparo, 1985a,b) and on intracellular calcium homostasis (Baker, 1963; Rassmussen, 1970, 1971; Romero and Wittman, 1971; Blanstein et al., 1978).
  • 3.3. PTZ induced lamella morphogenesis in eytosomes with subsequent release of calcium into the cytosol. This cilio-inhibition was enhanced in the presence of additional calcium in the perfusate.
  • 4.4. Prolonged exposure to light also induces fully converted membranous eytosomes with subsequent production of a gradual lateral cilio-inhibition. Darkness produces the opposite effect, in that secondary membranous conversions of cytosomes are inhibited.
  • 5.5. In the presence of A-23187 (a calcium releasing agent), inhibition of lateral activity is produced, independent of cytosomal conversion.
  • 6.6. It is postulated that photic electrical and chemical stimulation of neuronal chromoproteins can lead to release of calcium from sequestered cytosomal stores which triggers a neuro-exocytosis of a neuroinhibitory transmitter, dopamine.
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3.
  • 1.1. Subcellular distribution of (NA+, K+-ATPase and ouabain-insensitive ATPase (Mg2+-ATPase) are compared in branchial tissues of the euryhaline crab, Eriocheir sinensis, acclimated to fresh water.
  • 2.2. Both the anterior and posterior gills contain cAMP-dependent protein kinase and endogenous protein substrate for phosphorylation.
  • 3.3. Phosphorylation occurs in both “particulate” and “soluble” subcellular fractions but its stimulation by cAMP is restricted to the “soluble” fraction.
  • 4.4. serotonin (5-HT) and dopamine receptors are present only in the “light particulate” fraction isolated from the posterior gills.
  • 1.(a) Serotonin and dopamine have no effect on the phosphorylation observed in a subcellular fraction alone.
  • 2.(b) Activation of the phosphorylation by serotonin and dopamine is found when the soluble fraction (source of cAMP-dependent protein kinase) is added to the fraction P3 from the posterior gills.
  • 3.(c) No activation occurs with the fractions P3 as well as P1 or P2 (not shown) from anterior gills of fresh water crab.
  • 4.(d) Cyproheptadine, a serotonin receptor antagonist, inhibits the 5-HT dependent increase in phosphorylation.
  • 5.(e) The dopamine receptor antagonist, chlorpromazine, inhibits dopamine-stimulated phosphorylation.
  • 6.5. Ouabain mimics the effect of cyproheptadine on the serotonin-stimulated phosphorylation found in the posterior gills.
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4.
  • 1.1. The intestinal nerve of the fowl was studied in vitro.
  • 2.2. A significantly larger amplitude spike discharge was recorded in side branches of the nerve which innervate the gut when the aboral end of the main nerve trunk was stimulated than when the oral end was stimulated.
  • 3.3. Postganglionic autonomic neurones innervating the smooth muscle of the ileum are not located in the intestinal nerve. Evidence is presented, however, supporting the idea that such neurones innervating the rectum are located in the rectal position of the nerve.
  • 4.4. The increase in intraluminal pressure and circular muscle tension in the ileum was greater following aboral nerve stimulation than following oral nerve stimulation.
  • 5.5. It is suggested that excitatory efferent nerve fibres ascend the intestinal nerve to innervate the ileum.
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5.
  • 1.1. A granular or vesicular fraction was isolated from the muscles of the locust, Locust migratoria, and allowed to react with isolated myofibrils in order to examine whether or not this fraction could act as a relaxing factor as in the case of mammalian muscle.
  • 2.2. The granules obtained from the muscle of this insect were very effective in inhibiting myofibrillar ATPase, whether the myofibrils were prepared from the same muscles or from the rabbit muscles.
  • 3.3. Superprecipitation of a puridied actomyosin preparation was greatly retarded by the addition of these granules.
  • 4.4. Evidence was put forward that the granules are acting, in the presence of ATP, by removing calcium from myofibrils because of their strong calcium-binding capacity.
  • 5.5. These observations seem to suggest that the insect granules are also capable of acting as relaxing factor and that all muscles, whether in the vertebrates or in the invertebrates, can be considered as identical systems in so far as the chemical mechanism of contraction-relaxation is concerned.
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6.
  • 1.1. Dopamine levels and DOPA-decarboxylase activity were measured in cerebral ganglia and haemolymph of female Periplaneta americana.
  • 2.2. Measurements were made at four points in the oothecal cycle of cockroaches known to drop oothecae at regular three day intervals.
  • 3.3. Dopamine levels and DOPA-decarboxylase activity in haemocytes and plasma cycle in phase with ootheca formation; their levels in haemolymph are maximal when a half visible, untanned ootheca is present.
  • 4.4. In the cerebral ganglia dopamine levels and DOPA-decarboxylase also cycle in phase with ootheca formation suggesting that cerebral ganglion dopamine metabolism is under the same controls as dopamine metabolism associated with oothecal tanning.
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7.
  • 1.1. Submandibular secretion during parasympathetic stimulation (5 Hz) was examined in streptozotocin-diabetic and age-matched control rats.
  • 2.2. At 3 weeks, but not 3 and 6 months, flow rate was initially greater than in controls, but it declined rapidly after 30 min.
  • 3.3. The reduction in flow rate was associated with oedema of the gLond.
  • 4.4. At 3 months, graded stimulation revealed a tendency to oedema at frequencies of 10 Hz and above.
  • 5.5. Morphologically, submandibular capillary density was increased in diabetic rats.
  • 6.6. Thus, in diabetes the submandibular gland appears less able to withstand continuous parasympathetic stimulation, due in part to an increase in tissue capillary area.
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8.
  • 1.1. Kidneys of Lophius were perfused from the renal portal vein with a Ringer's solution.
  • 2.2. Mammalian and piscine neurohypophysial hormones (in doses of 20–500 ng/kg body wt) did not affect the rate of urine production or the urinary concentration of inorganic ions.
  • 3.3. The rate of urine production and the urinary concentration of magnesium and sodium ions varied with the concentration of magnesium in the perfusate.
  • 4.4. The rate of urine production was positively correlated with urine magnesium concentration (r = 0.83 ± 0.04) and negatively correlated with that of sodium (r = −0.40).
  • 5.5. The urinary concentration of sodium ions varied inversely with that of magnesium ions (r = −0.89).
  • 6.6. Ouabain treatment (0.1–0.8 mM/l) reduced the rate of urine production by over 60% and altered, to varying extents, the pattern of electrolyte excretion. A simple model for the mode of formation of urine by the aglomerular kidney, based on the present results and other observations is suggested.
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9.
  • 1.1. Adenylate cyclase activity was assayed in the optic lobe of Octopus vulgaris.
  • 2.2. Both octopamine and dopamine stimulate the octopus adenylate cyclase, apparently by competing with the same receptor site.
  • 3.3. (±)-2-Amino-6,7-dihydroxy-1,2,3,4-tetrahydronaphthalene-HBr (6,7-ADTN) and a number of phenylethanolamine derivatives stimulate the octopus adenylate cyclase activity.
  • 4.4. The dopamine D-1 antagonists R(+)-7-chloro-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-HCl (SCH-23390) and (±)-7-bromo-8-hydroxy-3-methyl-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-HCl (SKF-83566) are unable to antagonize the effects of dopamine and octopamine, and similarly ineffective is the agonist (±)-1-phenyl-2,3,4,5-tetrahydro-1H-3-benzazepine-7,8-diol-HCl (SKF-38393).
  • 5.5. No detectable binding of labelled SCH-23390 occurs on membrane preparations from octopus optic lobe.
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10.
  • 1.1. The medial (MGF), lateral (LGF) and motor (RMS-2) giant neurons were confirmed as neural components in the earthworm Amynthas hawayanus polysynaptic reflex circuit by simultaneous potential recording and dye injection.
  • 2.2. The reflex was initiated from the mechanoreceptors when evoked by mechanical stimulation but electrical stimulation also evoked an antidromic response in the motoneuron.
  • 3.3. The primary reflex response propagates decrementally along both giant axons but directly evoked action potentials conduct in an all-or-none fashion.
  • 4.4. The secondary reflex response continues to propagate after the primary response disappears.
  • 5.5. A rhythmically discharging neuron of uncertain function was also identified.
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11.
  • 1.1. We evaluated the effect of electric shock on swimming leeches by measuring changes in high-energy phosphate metabolism using in vivo31P-NMR.
  • 2.2. Leeches electrically stimulated during swimming showed anodal galvanotaxis, and stopped swimming with stimulation at strong current.
  • 3.3. Comparison of the concentrations of high-energy phosphate metabolites before and after electric shock using 31P-NMR revealed a marked decrease in β-ATP and an increase in that of Pi.
  • 4.4. Electric shock apparently induces excessive muscle fatigue in leeches, resulting in transient paralysis.
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12.
  • 1.1. Pondwater acclimated Carunculina texasensis and Ligumia subrostrata experienced a 230% increase in Na influx when injected with dibutyryl cyclic AMP (0.4mM/l blood).
  • 2.2. Theophylline, a phosphodiesterase inhibitor, or indomethacin, an inhibitor of prostaglandin (PG) synthetase, caused a dose dependent stimulation of Na transport.
  • 3.3. Prostaglandin E2 injected into mussels caused an inhibition of Na influx. Arachidonic acid, the precursor of PGE2, inhibited Na influx or stimulated Na efflux depending on the animal's acclimation conditions.
  • 4.4. Chloride transport was unaffected by the drugs used in this study.
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13.
  • 1.1. As reflected by increasing plasma concentrations of cortisol, norepinephrine, epinephrine and dopamine, a marked stimulation of the adrenal cortex and of the sympathetic nervous system occurred in Syrian hamsters during moderate hypothermia induced by helium-oxygen atmosphere and cold.
  • 2.2. A profound hyperglycemia was observed during hypothermia.
  • 3.3. All effects due to the helium-oxygen atmosphere and cold exposure (helox-cold) disappeared almost completely after rewarming.
  • 4.4. The results corroborate the hypothesis of an involvement of the adrenal cortex combined with the sympathetic nervous system in the control of acute induced heat production.
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14.
  • 1.1. The electric organ discharge (EOD) frequency modulations evoked by brief water vibration were analysed in the pulse-type fish Gymnotus carapo.
  • 2.2. The response consisted of a transient increase of the EOD frequency at short latency (30 msec). Response profiles were characteristic of the specimen and relatively independent on stimulus intensity.
  • 3.3. Conversely, they were dependent on stimulation sequence, showing a rapid decrement along successive stimuli and high temporal discrimination.
  • 4.4. The brief latencies indicate a relatively simple neural circuit.
  • 5.5. The response may be an electrolocation enhancement strategy for the detection of moving objects based on “sampling” the periphery at a higher frequency.
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15.
  • 1.1. Bending tests were performed on intact arms of two starfishes of different orders to obtain stiffness of the arm.
  • 2.2. Linckia laevigata without stimulation showed a wide variety of arm stiffness of 2.24–51.3 MPa (average: 8.0 MPa). Mechanical stimulation increased the stiffness by 2.5 times.
  • 3.3. In Asterias forbesii, isolated arms were 23 times stiffer than intact ones. Anesthesia with 0.1% MS-222 or menthol-saturated sea water increased the stiffness by 7–170 times.
  • 4.4. Ion dependence of stiffness suggests that the catch connective tissue was involved in the stiffness change.
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16.
  • 1.1. Role of NADP-glutamate dehydrogenase in the depletion of citrate was analyzed using permeabilized yeast cells.
  • 2.2. Citrate was converted to 2-oxoglutarate, which was then metabolized to glutamate by NADP-glutamate dehydrogenase in the presence of ammonium ion.
  • 3.3. Formation of 2-oxoglutarate plus glutamate was in good agreement with the concentration of citrate decreased. Glutamate formation can be a good indicator of the depletion of citrate, because 70% of the citrate decreased was converted to glutamate.
  • 4.4. Glycolytic activity was closely correlated with the decrease in citrate under the in situ conditions.
  • 5.5. NADP-glutamate dehydrogenase increased in anaerobically grown yeast cells.
  • 6.6. An effective depletion of citrate by increased synthesis of NADP-glutamate dehydrogenase can explain the lowered mechanism of citrate causing glycolytic stimulation under the anaerobic growth conditions of yeast.
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17.
  • 1.1. Optimum in vitro conditions, and kinetics of the enzyme catechol-O-methyltransferase from the brain of the male African catfish were studied.
  • 2.2. A saturated level for S-adenosylmethionine, as methyldonor, and magnesium as cofactor was reached at 5 μM and 10 mM, respectively.
  • 3.3. The addition of ascorbic acid, as an antioxidant, and tranylcypromine, as a MAO inhibitor, was not necessary, during incubations with fore-brain homogenates.
  • 4.4. Kinetic analysis of the methylation of catecholestrone, catecholestradiol and dopamine showed Km values of 1.2, 0.6 and 0.5 μM, respectively.
  • 5.5. The affinity of the catecholsubstrates for the enzyme catechol-O-methyltransferase is much higher in the brain of the African catfish than in tissues of mammals.
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18.
  • 1.1. This study examined the effect of the monoamines dopamine and octopamine, as well as tyrosine on the oxygen affinity and cooperativity of oxygen binding by the hemocyanin of the marine gastropod Busycon canaliculatum. The effect of temperature on hemocyanin oxygen affinity was also examined.
  • 2.2. Freezing Busycon hemocyanin did not affect the binding of oxygen.
  • 3.3. Dopamine, octopamine and tyrosine had no significant effect on the oxygen affinity or cooperativity of oxygen binding by the hemocyanin of B. canaliculatum.
  • 4.4. It was concluded that Busycon hemocyanin either has no binding sites for the two monoamines or for tyrosine, or that binding of the molecules has no functional significance.
  • 5.5. Both temperature sensitivity and affinity of hemocyanin-oxygen binding were similar to values previously reported for hemocyanin of Busycon from other localities.
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19.
  • 1.1. The phenoloxidase activity, protein and carbohydrate levels were studied for 24 hr in the hemolymph of the migratory grasshopper, Melanoplus sanguinipes after artificial wounding of the insect cuticle or the injection of Beauveria bassiana conidia.
  • 2.2. Injection or wounding induced a primary response and phenoloxidase activity was found to increase within 10–60 min. The values for phenoloxidase activity in viable B. bassiana-injected insects exhibited a secondary response, i.e., an increase 24 hr after injection.
  • 3.3. In wounded insects and those injected with inactivated conidia, the phenoloxidase activity receded after the initial increase and remained at low levels.
  • 4.4. Protein concentrations in the hemolymph increased immediately after infection and wounding and returned to basal levels during the course of the experiment.
  • 5.5. Injection of viable B. bassiana resulted in a gradual increase in the protein concentrations between 12 and 24 hr.
  • 6.6. There was no apparent change in the carbohydrate levels in either B. bassiana-infected or wounded insects.
  • 7.7. These results are discussed in relation to their possible role(s) and interrelationships in the immune response to infection or wounding. Furthermore, we suggest that a “factor” is released after mechanical injury of the integument.
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20.
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