Biomedical subjects

I Parker

Publications and source records attributed to I Parker.

At least 91 records · Page 5Linked to original sources

PubMed1987

Cocaine-sensitive O-methylation of noradrenaline in dental pulp of the rabbit: comparison with the rabbit ear artery.

Incisor pulp from the rabbit metabolises exogenous noradrenaline in concentrations between 0.12 and 1.2 mumol/l mainly to NMN. Effects of chronic sympathetic denervation indicated that in incisor pulp the NMN is extraneuronal in origin, and that DOPEG and DOMA formation, as well as a major part of the noradrenaline which accumulates in the tissue, are associated with the sympathetic nerves. NMN formation was unaffected by hydrocortisone 210 mumol/l, but was strongly inhibited by cocaine 30 mumol/l. These effects contrasted with those in the rabbit ear artery, where NMN formation was increased by cocaine 30 mumol/l and decreased by hydrocortisone 210 mumol/l. In COMT-inhibited denervated pulp, cocaine inhibited the accumulation of noradrenaline. Monoamine fluorescence histochemistry of pulp exposed to noradrenaline 50 mumol/l indicated that cocaine-sensitive uptake occurred in fibroblasts. It is concluded that O-methylation of noradrenaline in dental pulp involves prior uptake of the amine by a process resembling uptake1 but which is distinguished from uptake1 by its extraneuronal location.

Animals↗

PubMed1987

Oscillatory chloride current evoked by temperature jumps during muscarinic and serotonergic activation in Xenopus oocyte.

1. Membrane currents were recorded from voltage-clamped oocytes of Xenopus laevis, during temperature jumps imposed by a heating light. Resting oocytes usually showed little response, but large oscillatory membrane currents developed in response to cooling steps applied during activation of 'native' muscarinic receptors. 2. Similar temperature jump (Tjump) currents were seen during activation of oscillatory chloride currents mediated by muscarinic acetylcholine (ACh), serotonin, glutamate and noradrenaline receptors, expressed in the oocyte following injection with messenger ribonucleic acid (mRNA) from rat brain. The Tjump response during muscarinic activation was selectively blocked by atropine, and that during serotonergic activation by methysergide. In contrast, the 'smooth' membrane currents elicited by nicotinic ACh, kainate and gamma-aminobutyric acid (GABA) were not accompanied by Tjump responses. 3. Rapid cooling of the oocyte gave larger Tjump currents than a gradual cooling over a few seconds. The size of the Tjump current elicited by a fixed cooling step increased linearly with the preceding time of warming, becoming maximal at intervals greater than about 100 s. 4. The Tjump current was inward at a clamp potential of -60 mV and reversed direction at about -22 mV, which corresponds to the chloride equilibrium potential in the oocyte. In low-chloride solution the reversal potential was shifted to more positive potentials, but it was almost unchanged by changes in potassium and sodium concentration. The size of the Tjump current decreased as the membrane potential was made more negative than about -40 mV. 5. The period of oscillation of the Tjump current increased with decreasing temperature, following a Q10 of 3.15. Depolarization also caused a small increase in period. 6. The Tjump current was not abolished in calcium-free solution, or by addition of manganese or lanthanum to the bathing solution. However, it was abolished by intracellular injection of the calcium-chelating agent EGTA. 7. Intracellular injection of inositol 1,4,5-trisphosphate evoked an oscillatory membrane current, during which Tjump responses developed similar to those after muscarinic activation. Intracellular injection of calcium evoked a chloride current, but this was not accompanied by Tjump responses. 8. We conclude that the oscillatory currents evoked by temperature jumps arise from chloride channels activated by intracellular calcium. This calcium is probably mobilized from intracellular stores by inositol trisphosphate which is liberated as a result of activation of muscarinic receptors, and also receptors for serotonin and glutamate.(ABSTRACT TRUNCATED AT 400 WORDS)

Acetylcholine↗

PubMed1987

Effects of hypertonic solutions on calcium transients in frog twitch muscle fibres.

1. The effects of hypertonic solutions on excitation-contraction (e.-c.) coupling in frog skeletal muscle fibres were investigated using Arsenazo III to monitor intracellular calcium transients in voltage-clamped fibres. 2. In solutions made hypertonic with sucrose or sodium chloride, the size of the Arsenazo signal evoked by a 5 ms depolarization to 0 mV was little altered by increases in tonicity up to about twice normal, but declined in higher tonicities, and was almost completely suppressed at 4 times normal tonicity. 3. The latency to onset of the Arsenazo signal was increased in hypertonic solutions (2.3 and 3.1 times normal tonicity), but the decay time constant of the signal was little changed with tonicities up to 2.3 times normal. 4. The rheobase potential for a just-detectable Arsenazo signal was shifted about 4 mV more negative by increases in tonicity up to 2.3 times normal, but further increases reversed the direction of the shift, and in 3.95 times normal tonicity the rheobase was 10 mV more positive than in normal Ringer solution. 5. With short (less than 10 ms) pulse durations the depolarization needed to elicit a threshold Arsenazo signal increased steeply with increasing tonicity. Changes in the strength-duration curve could be accounted for by an increase in the time constant for build-up of a hypothetical coupler in the e.-c. coupling process. 6. Solutions of about twice normal tonicity are commonly used to suppress muscle contraction. Since the size of the Arsenazo signal was only slightly reduced by this tonicity, the main effect is presumably on the contractile proteins.

Animals↗

PubMed1986

Neurotensin and substance P receptors expressed in Xenopus oocytes by messenger RNA from rat brain.

Xenopus oocytes were induced to acquire sensitivity to neurotensin and substance P, by injecting them with a fraction of poly(A)+ mRNA from rat brain. Non-injected oocytes, and oocytes injected with other brain mRNAs, failed to show responses, suggesting that receptors to these peptides were expressed by specific brain mRNAs. Responses to substance P and neurotensin comprised an oscillatory chloride current, and a smooth current having different ionic basis. These currents resembled those seen during activation of muscarinic and serotonergic receptors, but were not blocked by the corresponding antagonists atropine and methysergide. The responses to substance P, and to a lesser extent to neurotensin, showed a long-lasting desensitization. Similarities between the oscillatory currents evoked by the peptides acetylcholine and serotonin suggest that all these receptors may 'link in' to a common intracellular messenger pathway.

Animals↗

PubMed1986

Minimal latency of calcium release in frog twitch muscle fibres.

Intracellular release of calcium in frog skeletal muscle fibres was monitored by the use of arsenazo III, in response to voltage clamped depolarizing pulses. A latency of a few milliseconds was evident between the onset of depolarization and the first detectable rise in the arsenazo-calcium signal, and this decreased logarithmically as the depolarization was increased. The minimal latency with strong depolarization (to +20 to +100 mV) was about 2 ms at 5 degrees C. This delay appears to be sufficiently long to be compatible with a chemically mediated coupling mechanism between depolarization and calcium release from the sarcoplasmic reticulum.

Animals↗

PubMed1986

Changes in intracellular calcium and in membrane currents evoked by injection of inositol trisphosphate into Xenopus oocytes.

Intracellular calcium was monitored by the use of aequorin in voltage-clamped oocytes of Xenopus laevis. Injection of inositol trisphosphate (IP3) into oocytes elicited slowly rising and decaying aequorin/calcium signals and produced oscillatory chloride membrane currents. These responses did not depend upon extracellular calcium, since they could be elicited in calcium-free solution and after addition of cobalt or lanthanum to block calcium channels in the surface membrane. We conclude that IP3 causes the release of calcium from intracellular stores in the oocyte. Injections of calcium gave aequorin and membrane current responses that were more transient than those seen with IP3.

Aequorin↗

PubMed1986

Catecholamine contents of rabbit gingiva and dental pulp.

The contents of endogenous noradrenaline (NA) in rabbit gingiva and dental pulp were approximately 15-fold greater than either adrenaline (A) or dopamine (DA). Whereas catecholamine contents of maxillary incisor pulps were similar to those in mandibular incisor pulps, variations existed between gingiva excised from different regions. Both reserpine pretreatment and chronic sympathetic denervation greatly decreased the NA contents. These findings support the view that NA is the sympathetic neurotransmitter in dental pulp and gingiva.

Animals↗

PubMed1986

Role of sympathetic nerves in the metabolism of exogenous noradrenaline in rabbit gingival tissue and ear artery.

Uptake and metabolism of 3H-noradrenaline 0.18 mumol/l was examined in rabbit gingival slices and ear artery segments. The tissues were incubated with the 3H-amine for 30 min. The artery accumulated approximately ten times more of the 3H-amine and generated four times more 3H-metabolites than the gingiva. In both tissues, chronic sympathetic denervation resulted in marked decreases in 3H-noradrenaline accumulation and deamination. An inhibitor of sympathetic neuronal uptake, cocaine 30 mumol/l, strongly inhibited the firmly-bound component of 3H-noradrenaline accumulation by the tissues and strongly decreased the accumulation of deaminated metabolites in the incubating medium. It is concluded that the sympathetic nerve terminals play an important role in the accumulation and deamination of noradrenaline in the gingiva and in the artery. Chronic sympathetic denervation resulted in increased 3H-normetanephrine (NMN) formation by the gingiva and the artery, indicating that in both tissues the noradrenaline was O-methylated at sites extraneuronal to the sympathetic nerves. Differences between the effects of cocaine in the gingiva and artery, with respect to 3H-NMN accumulation in the incubating medium, are interpreted as evidence that in the gingiva, but not in the artery, cocaine inhibits extraneuronal O-methylation, as well as neuronal uptake, of noradrenaline.

Animals↗

PubMed1986

A general approach to the optimization of the conformation of ring molecules with an application to valinomycin.

A general and efficient methodology is presented which allows molecules containing one or many rings of any size to be manipulated within energy minimization procedures. Variables describing the conformation of the molecules concerned are limited to dihedral and ring valence angles and the ring closure conditions are treated as equality constraints. An application is made to the ion transporter valinomycin and its complexes with K+ and Na+ which illustrates the possibilities of the approach and leads to results which allow a better understanding of the conformational mechanics of this important ionophore.

Mathematics↗

PubMed1986

Actions of pentobarbital on rat brain receptors expressed in Xenopus oocytes.

Functional receptor channels activated by GABA and other neurotransmitters were "transplanted" from rat brain to Xenopus oocytes by injecting the oocytes with total poly(A)+ mRNA isolated from rat or chick brain. Membrane currents elicited in the oocyte by GABA inverted polarity at about the chloride equilibrium potential (ca. -25 mV). Pentobarbital potentiated the GABA-activated currents, without appreciably changing the reversal potential or form of the current-voltage relationship. At low (less than 10(-5) M) concentrations of GABA, pentobarbital (100 microM) potentiated the responses by a factor of 10 or more, but responses to high (ca. 1 mM) concentrations of GABA were almost unchanged. Half-maximal activation of the response was obtained with about 3 X 10(-5) M GABA when applied alone and with about 4 X 10(-6) M GABA when applied together with 100 microM pentobarbital. At low doses of GABA, the size of the current increased as the 1.4th power of GABA concentration, but this relationship became nearly linear in the presence of pentobarbital. The potentiation of the GABA response increased linearly with concentrations of pentobarbital up to about 300 microM, reaching a maximum of about 50-fold. At higher concentrations of pentobarbital, the response to GABA declined. Relaxations of GABA-activated currents following voltage steps became slower in the presence of pentobarbital, suggesting that the open life-time of the channels was prolonged. In addition to actions on GABA-activated currents, pentobarbital itself elicited a small membrane current that inverted polarity at a potential (-10 mV) more positive than the GABA-activated current.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗

PubMed1985

On the orientation of foreign neurotransmitter receptors in Xenopus oocytes.

Xenopus oocytes can be made to incorporate into their membrane foreign neurotransmitter receptors and voltage-activated sodium channels. In their original location the receptors are normally activated by the extracellular action of transmitter substances. Tests were made to see if some of the newly synthesized foreign receptors were inserted in the oocyte membrane with their active site facing inwards. Since intracellular injections of acetylcholine, gamma-aminobutyric acid, serotonin and kainic acid and tetrodotoxin into the oocyte failed to elicit a response, we conclude that very few, or none, of the receptor molecules expressed in the oocyte by the exogenous mRNA are inserted with the wrong orientation in the membrane.

Animals↗

PubMed1985

Messenger RNA from bovine retina induces kainate and glycine receptors in Xenopus oocytes.

The retina contains several types of nerve cells that communicate through chemical synapses. The transmitter and receptor molecules that mediate signal transmission across these synapses need further characterization. For this purpose, poly (A)+ mRNA was isolated from bovine retinas and injected into Xenopus laevis oocytes. Translation of the foreign mRNA induced the oocyte membrane to acquire functional receptors to kainate and, to a lesser extent, also receptors to glycine, gamma-aminobutryic acid (GABA), aspartate and glutamate. Thus, the cells in the retina must contain different messengers coding for these neurotransmitter receptors. Activation of the kainate receptors opens membrane channels, generating an ionic current which has an equilibrium potential close to 0 mv. The current is well maintained during prolonged application of kainate, and hence these receptors may be involved in the neurotoxic effects produced by kainate in the retina.

Animals↗

PubMed1985

A transient inward current elicited by hyperpolarization during serotonin activation in Xenopus oocytes.

Activation of serotonin, glutamate or muscarinic receptors, incorporated into the membrane of Xenopus oocytes following injection of messenger RNA from rat brain, caused the development of a transient inward (Tin) current when the membrane was hyperpolarized. A detailed study was made of the Tin current induced during serotonin activation. The current is due principally to efflux of chloride ions, and is presumably activated by an influx of calcium ions, because it was blocked by removal of calcium from the bathing medium, by addition of manganese, cobalt or lanthanum, or by intracellular injection of EGTA. During application of serotonin, the amplitude of the Tin current increased slowly, and after washing it persisted for longer than the direct serotonin-induced current. The amplitude of the Tin current was sensitive to temperature and pH, and was abolished at pH 6.5 or by cooling to 12 degrees C. The Tin current may be of importance in regulating the excitability of neurons in the central nervous system.

Animals↗

PubMed1985

Intracellular Ca2+-dependent and Ca2+-independent responses of rat brain serotonin receptors transplanted to Xenopus oocytes.

Xenopus oocytes injected with messenger RNA extracted from rat brain are induced to acquire a variety of neurotransmitter receptors and voltage-operated membrane channels. Activation of the receptors to serotonin, acetylcholine (muscarinic) and glutamate elicits oscillatory membrane currents carried by chloride ions. These currents are not abolished by removing external calcium, but are completely abolished after EGTA is injected into the oocytes to chelate intracellular calcium. A smooth current response to serotonin remained in EGTA-loaded oocytes, indicating that this response does not require intracellular calcium. In contrast to the oscillatory chloride currents, the chloride currents activated by GABA or glycine are not abolished by intracellular injection of EGTA. Thus, there appear to be two classes of chloride channels one of which requires intracellular calcium to open.

Animals↗

PubMed1985

Post-synaptic calcium influx at the giant synapse of the squid during activation by glutamate.

Changes in free calcium were monitored in the post-synaptic axon of the giant synapse of the squid, using the calcium indicators aequorin and Arsenazo III. The peak size of the calcium-dependent optical signals recorded from aequorin and Arsenazo III both showed a linear relation with the amount of calcium injected ionophoretically into the axon, but the Arsenazo signal had a slower time course than the aequorin. Ionophoretic application of glutamate to the post-synaptic axon depolarized the axon and caused a rise in intracellular free calcium. Aequorin signals were detected in natural sea water, and their size increased when the calcium concentration in the sea water was raised. Arsenazo signals could be detected only in high-calcium (55 mM) sea water. Intracellular calcium signals were detected also during bath application of several glutamate analogues, including kainate, ibotenate, and aspartate. The peak amplitude of the intracellular calcium signal, monitored with both indicators, increased with increasing ionophoretic glutamate dose, and varied linearly with the integral of the glutamate-induced membrane depolarization. No calcium signals were detected when depolarizations, similar to those produced by glutamate, were induced by current injection in the absence of glutamate. We conclude that glutamate increases the calcium permeability of the post-synaptic membrane, independently of the glutamate-induced depolarization. The glutamate-induced depolarization and the rise in intracellular free calcium increased roughly linearly as the membrane potential was made more negative. Extrapolation of these data indicated that the glutamate depolarization would reduce to zero at about -30 mV, while the calcium signals would be suppressed at about +50 mV.

Aequorin↗

PubMed1985

Effect of prazosin on the efflux of 3H-norepinephrine and metabolites from the intima and adventitia of the rabbit ear artery.

The spontaneous and stimulation-induced (SI) effluxes of 3H-norepinephrine (3H-NE) and its metabolites from the intimal and adventitial surfaces of perfused segments of rabbit ear arteries were determined; vessels were previously incubated with 3H-NE (0.6 microM). The total SI adventitial efflux of 3H was approximately 10-fold greater than the intimal efflux, contained a higher percentage of unchanged 3H-NE (48 vs. 12%) and a lower percentage of O-methylated metabolites (17 vs. 55%); there was little difference between the percentages of deaminated catechols (35 vs. 31%). Prazosin, at a concentration (0.24 microM) which prevented the arteries constricting during stimulation, had little effect on the composition of the SI effluxes; however, it caused 2- to 3-fold increases in the effluxes of 3H-NE and its metabolites into the lumen during the period of stimulation. This effect is attributed to the failure of the vessel wall to thicken during stimulation, thus facilitating diffusion of 3H-NE and its intraneuronally formed metabolites across the media. Prazosin decreased the percentage of unchanged 3H-NE and increased that of the deaminated catechols in the spontaneous efflux; these effects are attributed to a direct effect of prazosin on the intra-neuronal metabolism of 3H-NE.

Animals↗

PubMed1984

Messenger RNA from rat brain induces noradrenaline and dopamine receptors in Xenopus oocytes.

Xenopus oocytes were induced to acquire sensitivity to noradrenaline and dopamine, by injecting them with poly(A)+ mRNA isolated from rat brain. In mRNA-injected oocytes, both neurotransmitters elicited a smooth inward membrane current on which was superimposed an oscillatory inward current, which was carried mainly by chloride ions. This contrasts with the native responses that are sometimes seen in non-injected oocytes, where noradrenaline and dopamine both elicit smooth outward currents that are carried mainly by potassium ions. The serotonin antagonist methysergide blocked the induced responses to both noradrenaline and dopamine, and the noradrenaline response was blocked by propranolol.

Animals↗

PubMed1984

Glutamate and kainate receptors induced by rat brain messenger RNA in Xenopus oocytes.

Xenopus laevis oocytes injected with poly(A)+ mRNA extracted from rat brain became sensitive to serotonin, glutamate, kainate, acetylcholine and gamma-aminobutyrate. Application of these substances to mRNA-injected oocytes elicited membrane currents. The glutamate- and acetylcholine-induced currents usually showed oscillations, while the kainate current was smooth. The current oscillations during glutamate application reversed direction at about the chloride equilibrium potential (-24 mV), but the reversal potential for the kainate current was close to 0 mV. The current-voltage relation for the glutamate-induced current oscillations showed strong rectification at hyperpolarized potentials, while that for the kainate current was nearly linear. In some oocytes, glutamate elicited smooth membrane currents, with oscillations either absent, or appearing after a delay. The reversal potential of this component was close to 0 mV, and was clearly different from that of the oscillatory component. The appearance of glutamate and kainate sensitivity in the oocyte membrane is due to the translation of the foreign messenger RNA, and not to activation of the oocytes' own genome, because oocytes still become sensitive when transcription is prevented by enucleation or by treatment with actinomycin D. It appears that mRNA from rat brain contains translationally active messengers which code for various neurotransmitter receptors. When this mRNA is injected into Xenopus oocytes, the messengers are translated and receptors are inserted into the oocyte membrane, where they form functionally active receptor-channel complexes.

Animals↗