Naloxone-dependent depression by morphine of responses of snail neurons to serotonin

Morphine, added to the extracellular solution in a concentration of 1·10^–5 M, quickly and reversibly weakens the depolarizing and hyperpolarizing responses of neurons of the snailHelix lucorum evoked by 1·10^–6 M serotonin. The inhibitory effect of morphine is completely abolished by the addition of naloxone (1·10^–5 M), suggesting that opiate receptors are involved in the process. Interaction between morphine and serotonin is noncompetitive in type, as is shown by the character of the dose-effect curves recorded during the action of serotonin before and after morphine application.Institute of Psychiatry, Academy of Medical Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 13, No. 6, pp. 589–593, November–December, 1981.     

Inhibitory and activatory effects of dopamine on neurons in slices of the compact zone of theSubstantia nigra of rats

Effects of dopamine on the background spike activity of functionally (according to their electrophysiological characteristics) identified dopaminergic (DA) or non-dopaminergic (non-DA) neurons of the compact zone of thesubstantia nigra were studied on slices of the midbrain of adult rats. In the majority of DA neurons, dopamine suppressed the background activity in a dose-dependent manner. Sensitivity of these cells to dopamine varied within a wide range: IC₅₀, the concentration providing the 50% maximum effect, equalled from 3 to 3,000 µM in different units. A part of DA neurons responded to dopamine with an increase in their activity. Mixed responses, in which an initial suppression of impulsation was replaced by a slow-developing activation, was observed in some neurons. Non-DA neurons usually responded to dopamine by an enhancement of impulsation; yet, the cells with inhibitory or mixed responses similar to those of DA neurons could be found in this population as well. Sensitivity of non-DA neurons to dopamine was about the same as that of DA-cells, without the dependence on the direction of responses. S(–)-suipiride, a blocker of D₂ receptors, decreased the inhibitory component of all tested responses to dopamine both in DA and non-DA neurons and evoked no changes in the excitatory component. At the same time, R(+)-SCH 23390 HC1, a blocker of D₁ receptors, suppressed the activatory component of responses with no effect on the inhibitory component. We conclude that both types of DA receptors, D₂ and D₁ receptors, can be present on the DA and non-DA neurons. Dopamine, influencing these receptors, suppresses or facilitates, respectively, the spike activity of these cells. The relative amount of such receptors is the main factor determining the pattern and dynamics of the integral response to dopamine application. The possible functional role of the presence of both D₁ and D₂ receptors on the membrane of a single neuron is discussed.Neirofiziologiya/Neurophysiology, Vol. 27, No. 4, pp. 268–277, July–August, 1995.     

Ionic mechanisms underlying modulating effects of serotonin on acetylcholine-induced responses in Helix pomatia neurons

The ionic mechanisms underlying modulatory effects of serotonin on acetylcholine-response in identified and nonidentifiedHelix pomatia neurons were investigated using voltage-clamping techniques at the neuronal membrane. External application of 10^–5–10^–4 M serotonin to the membrane of neurons responding to application of acetylcholine depending on Na⁺ depolarization (D_Na response) reduced membrane conductivity during response to acetylcholine without changing reversal potential of acetylcholine-induced current. Acetylcholine (10^–6–10^–4 M) administration took place 1–3 min later. Neurons with response to acetylcholine application dependent on Cl⁺ depolarization (D_Cl response) or hyperpolarization (H_Cl response) behaved similarly. Analogous effects could be produced by external application of theophylline which, together with the latency and residual effect characteristic of serotonin action points to the participation of intracellular processes associated with the cellular cyclase system in the changes produced by serotonin in acetylcholineinduced response. Serotonin brought about a shift in reversal potential and an increase in the acetylcholine-induced current in those neurons where this response was associated with changed permeability at the membrane to certain types of ions. During two-stage acetylcholine-induced response of the D_Na-H_K type, serotonin inhibited the inward current stage. Mechanisms underlying modulatory serotonin action on acetylcholine-induced response in test neurons are discussed in the light of our findings.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 20, No. 1, pp. 57–64, January–February, 1988.     

Responses of rat spinal ganglion neurons mediated by activation of serotonin receptors of the third type

Application of serotonin (5-hydroxytryptamine; 5-HT) to rat dorsal root ganglion neurons under conditions in which potassium conductance was blocked by cesium ions elicited depolarizing responses followed by an increase in membrane conductance. The responses did not exhibit desensitization and were due to activation of 5-HT receptors of the third type (5-HT₃Rs), since they were insensitive to methysergide, the 5-HT₂R antagonist, but were inhibited by tropicetrone (ISC 205–930) and metoclopramide, the 5-HT₃R antagonists. The reversal potential of the 5-HT-induced depolarizing responses was –11.9 mV; their amplitude decreased following a decrease in extracellular Na⁺ concentration but remained constant after intracellular injection of GTP. The amplitude of the responses increased following elevation of intracellular cAMP concentration caused by theophylline or sodium fluoride whose potentiating effect was reduced by butamide, a protein kinase A inhibitor. Potentiation of the 5-HT-induced responses was also produced by increased intracellular Ca²⁺ concentration following either direct intracellular injections or a burst of action potentials. The potentiation could be prevented by trifluoroperazine, the calmodulin inhibitor. The 5-HT effects were also potentiated by methylfurmetide, an activator of muscarinic acetylcholine receptors. The effect of methylfurmetide was slightly decreased by trifluoroperazine and was markedly decreased by polymixin B, a protein kinase C inhibitor. The effects of 5-HT were also enhanced by ethanol.Neirofiziologiya/Neurophysiology, Vol. 25, pp. 258–263, July–August, 1993.     

Effect of monoamines on motoneurons of the isolated rat spinal cord

Superfusion of isolated hemisected spinal cords of 9-13-day old rats with noradrenalin (NA) solution depolarized or hyperpolarized the motoneurons depending on the NA concentration. Both effects were the result of the direct action of NA on the motoneurons, for they were given in medium containing an excess of Mg and deficiency of Ca ions.a-Adrenoblockers depressed both the depolarizing and hyperpolarizing effects of NA. The depolarizing effect of dopamine on motoneurons was abolished in medium containing excess of Mg ions. Its direct hyperpolarizing action of motoneurons was suppressed by haloperidol but unchanged by phentolamine. The depolarizing effect of serotonin and its metabolites — mexamine, kynurenine, and 3-hydroxy-anthranilic acid — persisted in the presence of an excess of Mg and deficiency of Ca ions, but it was suppressed by deseryl (methysergide) and the benzyl analog of serotonin. The hyperpolarizing effect of serotonin at high concentrations (10^–4–10^–3 M), revealed in some experiments, was abolished in medium containing excess of magnesium ions in the presence of morphine.A. M. Gorkii Donetsk State Medical Institute. Translated from Neirofiziologiya, Vol. 12, No. 4, pp. 391–396, July–August, 1980.     

Effect of noradrenalin and serotonin on synaptic transmission in the rat spinal cord

Experiments on superfused isolated spinal cord preparations from rats aged 8–13 days showed that noradrenal in and serotonin have only a weak effect on monosynaptic reflex discharges but a substantial effect on polysynaptic motoneuronal discharges: noradrenalin potentiates whereas serotonin inhibits them. Both amines inhibit dorsal root potentials evoked by stimulation of high-threshold afferents. Potentiation of polysynaptic motoneuronal discharges induced by noradrenalin is connected with hyperpolarization of high-threshold afferents due to inhibition of the function of neurons in the substantia gelatinosa, and with increased excitability of interneurons participating in the generation of motoneuronal discharges. Serotonin inhibits polysynaptic motoneuronal discharges through its direct depolarizing effect on terminals of high-threshold afferents and depression of interneuron activity responsible for these discharges. Adrenergic and serotonin receptors, mediating these effects of noradrenalin and serotonin, were subjected to pharmacologic analysis.A. M. Gor'kii Donetsk Medical Institute. Translated from Neirofiziologiya, Vol. 14, No. 3, pp. 241–247, May–June, 1982.     

Dopamine and serotonin effects on neurons of dorsal root ganglion isolated from rats

The effects of 1×10^–8–1×10^–5 M dopamine (DA) and serotonin (HT) on membrane potential, input resistance (R_M), and action potential (AP) when added to the superfusing fluid for 0.5 min were investigated in perfused dorsal root ganglia (DRG) neurons isolated from 30–36-day old rats during experiments using intracellular recording techniques. Application of DA induced reversible changes in membrane potential in 48 out of 52 test cells as compared with 38 out of 44 for HT. Distribution of different patterns of response to DA and HT was similar: depolarization was recorded in 64.6 and 73.7% and hyperpolarization in 16.7 and 15.8%; two-stage response occurred in 18.7 and 10.5% of responding cells, respectively. Both monoamines induced reversible change in the AP and R_M pattern in a number of cells. Depolarization was accompanied by a decline and hyperpolarization by a rise in R_M. Both substances were found to affect mainly those neurons with electrophysiological properties characteristic of small cells. The possibility of afferent spike train modulation at the level of primary sensory neurons is suggested.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian USSR, Kiev. Translated from Neirofiziologiya, Vol. 21, No. 5, pp. 644–651, September–October, 1989.     

Postsynaptic metabolic monoamine modulation of effects mediated by NMDA-glutamate receptors in frog spinal motoneurons

We investigated the effect of monoamines and their agonists and antagonists upon responses of motoneurons medicated by NMDA-glutamate receptors. It was found that adrenalin strengthens the responses studied through activation of -and -adrenoreceptors. This effect of adrenalin is suppressed by an -adrenoblocker (phentolamine) and a -adrenoblocker (propranolol); it is restored by an -adrenomimetic (phenylephrine hydrochloride) and a -adrenomimetic (neoepinephrine). In 66% of the cases, dopamine inhibited motoneurons responses; in 34% of the cases, it strengthened such responses. In the presence of a selective blocker of D₂-dopamine receptors (sulpiride), it only strengthened motoneuron responses. Serotonin strengthens responses of motoneurons; its action is suppressed by a blocker of type-II serotonin receptors (dezeril). A selective agonist of subtype-1A serotonin receptors, campirone, suppresses motoneuron responses. The effect of campirone is weakened by propranolol. The strengthening of NMDA-responses of motoneurons evoked by neoepinephrine and dopamine in the presence of sulpiride is weakened by a blocker of cAMP-dependent protein kinase, tolbutamide, and the strengthening of responses by phenylephrine hydrochloride and serotonin is weakened by an inhibitor of calmodulin, trifluoroperazine.M. Gorky Medical Institute, Ukrainian Ministry of Public Health, Donetsk. Translated from Neurofiziologiya, Vol. 23, No. 6, pp. 683–690, November–December, 1991.     

Glial uptake of monoamines in primary cultures of rat median raphe nucleus and cerebellum

Summary Glial uptake of serotonin and dopamine was studied in primary cultures of the median raphe nucleus and cerebellum by using consecutive demonstration of monoamine fluorescence and glial fibrillary acidic protein immunofluorescence. Most of the glial cells taking up monoamines were glial fibrillary acidic protein positive. Astrocytes with a strong immunoreactivity exhibited monoamine fluorescence only occasionally, although such cells did take up L-dopa readily. Glial fibrillary acidic protein negative cells — morphologically identified as astrocytes — were seen to exhibit monoamine fluorescence after exposure. Glial uptake of serotonin at a concentration of 10^–4 M was detected in cerebellar cultures but not in cultures from the median raphe nucleus. When the concentration was 10^–3 M uptake of serotonin took place in both the areas but was weaker in cultures from the median raphe nucleus. At concentrations greater than 10^–5 M glial uptake of dopamine was detected in cultures from both the regions studied. No region dependent differences in glial uptake of dopamine was demonstrated, however. Based on these observations astrocytes and astrocyte-like glial cells take up dopamine and serotonin. Also glial cells with a remarkably high content of the glial fibrillary acidic protein are more resistant to monoamine uptake than cells exhibiting less intense or no glial fibrillary acidic protein immunofluorescence. The existence of regional differences in uptake of serotonin between the median raphe nucleus and cerebellum suggests that glial uptake of monoamines is not an entirely passive mechanism but may be actively controlled by glial cells in a region dependent manner.     

Effects of dopamine on background and evoked activity in interneurons of a spinal cord segment isolated from infant rats

The effects of 1·10^–5–1·10^–3 M dopamine on background and evoked interneuronal-activity was investigated during experiments on a spinal cord segment isolated from 11–18-day old infnat rats. Dopamine induced an increase in background firing activity rate in 52.5% and a reduced rate in 42.5% of the total sample of responding cells. Dopamine exerted a primarily inhibitory effect on interneuronal activity invoked by dorsal root stimulation, as witnessed by the reduced amplitude of the postsynaptic component of field potentials in the dorsal horn together with the fact that invoked activity was depressed in 66.7% of total interneurons responding to dopamine and facilitated in only 33.3% of these cells. All dopamine-induced effects were reversible and dose-dependent. Dopamine-induced effects disappeared after superfusing the brain with a solution containing 0–0.1 mM Ca²⁺ and 2 mM Mn²⁺, suggesting that this response is of transsynaptic origin. In other cells the excitatory or inhibitory action of dopamine also persisted in a medium blocking synaptic transmission; this would indicate the possibility of dopamine exerting depolarizing and hyperpolarizing effects on the interneuron membrane directly. Contrasting responses to dopamine in interneurons may be attributed to the presence of different types of dopamine receptors in the spinal cord.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 21, No. 1, pp. 7–16, January–February, 1989.     

Ionic mechanisms of the effect of phenibut and gaba not associated with a change in the function of the chloride channels

In experiments on isolated spinal cord of young rats 7–14 days old under conditions of takeoff of the electrical activity of the spinal roots with a sugar bridge, it was established that the GABA-mimetic phenibut induces direct depolarization of the motoneurons. In the same concentration range (10^–5-10^–4 M), GABA has a dual effect. The depolarizing component of the action of GABA in part of the experiments and the depolarizing effect of phenibut in all the experiments are preserved in the presence of picrotoxin (10^–5 M) and under conditions of superfusion of the brain with a solution with a reduced chloride concentration. This depolarizing effect of phenibut, not associated with the activation of GABA_A receptors and chloride channels coupled with them, is unchanged in a medium with Na⁺ deficiency, is enhanced during depolarization of the motoneurons due to an increased concentration of K⁺ (10 mM) and in the presence of imidazole, but is entirely eliminated in a medium with Ca²⁺ deficiency, containing 2 mM Mn²⁺, or in the presence of theophylline (10^–4 M). It is suggested that phenibut, and to some degree, GABA lower the intracellular concentration of cAMP by means of activation of the GABA_B receptors, which leads to blocking of the functional activity of the potential-dependent calcium channels and a decrease in the calcium-activated outflowing potassium currents. The ability to weaken the inflowing calcium currents may also be the basis of the presynaptic inhibiting effect of GABA and GABA-mimetics (phenibut, baclofen, etc.) on the pulsed release of mediators by the axon terminals of catecholaminergic, glutamatergic, and GABA-ergic neurons.A. M. Gor'kii Donetsk Medical Institute. Translated from Neirofiziologiya, Vol. 17, No. 4, pp. 481–489, July–August, 1985.     

Dopamine Preferentially Inhibits NMDA Receptor-Mediated EPSCs by Acting on Presynaptic D1 Receptors in Nucleus Accumbens during Postnatal Development

Nucleus accumbens (nAcb), a major site of action of drugs of abuse and dopamine (DA) signalling in MSNs (medium spiny neurons), is critically involved in mediating behavioural responses of drug addiction. Most studies have evaluated the effects of DA on MSN firing properties but thus far, the effects of DA on a cellular circuit involving glutamatergic afferents to the nAcb have remained rather elusive. In this study we attempted to characterize the effects of dopamine (DA) on evoked glutamatergic excitatory postsynaptic currents (EPSCs) in nAcb medium spiny (MS) neurons in 1 to 21 day-old rat pups. The EPSCs evoked by local nAcb stimuli displayed both AMPA/KA and NMDA receptor-mediated components. The addition of DA to the superfusing medium produced a marked decrease of both components of the EPSCs that did not change during the postnatal period studied. Pharmacologically isolated AMPA/KA receptor-mediated response was inhibited on average by 40% whereas the isolated NMDA receptor-mediated EPSC was decreased by 90%. The effect of DA on evoked EPSCs were mimicked by the D₁-like receptor agonist SKF 38393 and antagonized by the D₁-like receptor antagonist SCH 23390 whereas D₂-like receptor agonist or antagonist respectively failed to mimic or to block the action of DA. DA did not change the membrane input conductance of MS neurons or the characteristics of EPSCs produced by the local administration of glutamate in the presence of tetrodotoxin. In contrast, DA altered the paired-pulse ratio of evoked EPSCs. The present results show that the activation D₁-like dopaminergic receptors modulate glutamatergic neurotransmission by preferentially inhibiting NMDA receptor-mediated EPSC through presynaptic mechanisms.     

Possible Participation of Serotonin in the Peripheral Link of the Defensive Reflex in the Mollusc Lymnaea stagnalis

The contractions of the dorsal longitudinal muscle of the mollusc Lymnaea stagnalis L., which are evoked by electric stimulation of n. cervicalis inferior were studied. It has been shown that an increase of magnesium ion concentration in saline to 10–15 mM decreases reversibly amplitude of the evoked contractions. Application of serotonin produced a dual effect: at concentrations of 2 × 10^–5–10^–6 M, it enhanced muscle contractions, whereas at concentrations above 10-5 M, on the contrary, decreased them. The inhibitory effect of the serotonin antagonist mianserin on the evoked contraction amplitude increased with elevation of its concentrations in the studied range (from 10^–5 to 10^–3 M). The enhancing effect of serotonin on muscle contractions was blocked either by previous mianserin application or its application on the background of the already acting serotonin. A participation of serotoninergic mechanisms in the control of the contractile function of the studied muscle is suggested.     

Cocaine Inhibits Dopamine D2 Receptor Signaling via Sigma-1-D2 Receptor Heteromers

Under normal conditions the brain maintains a delicate balance between inputs of reward seeking controlled by neurons containing the D₁-like family of dopamine receptors and inputs of aversion coming from neurons containing the D₂-like family of dopamine receptors. Cocaine is able to subvert these balanced inputs by altering the cell signaling of these two pathways such that D₁ reward seeking pathway dominates. Here, we provide an explanation at the cellular and biochemical level how cocaine may achieve this. Exploring the effect of cocaine on dopamine D₂ receptors function, we present evidence of σ₁ receptor molecular and functional interaction with dopamine D₂ receptors. Using biophysical, biochemical, and cell biology approaches, we discovered that D₂ receptors (the long isoform of the D₂ receptor) can complex with σ₁ receptors, a result that is specific to D₂ receptors, as D₃ and D₄ receptors did not form heteromers. We demonstrate that the σ₁-D₂ receptor heteromers consist of higher order oligomers, are found in mouse striatum and that cocaine, by binding to σ₁ -D₂ receptor heteromers, inhibits downstream signaling in both cultured cells and in mouse striatum. In contrast, in striatum from σ₁ knockout animals these complexes are not found and this inhibition is not seen. Taken together, these data illuminate the mechanism by which the initial exposure to cocaine can inhibit signaling via D₂ receptor containing neurons, destabilizing the delicate signaling balance influencing drug seeking that emanates from the D₁ and D₂ receptor containing neurons in the brain.     

Effects of vasopressin on the somatic membrane of spinal ganglia neurons

Intracellular recording from the soma of 68 sensory neurons was performed during experiments on perfused cerebrospinal ganglia (CSG) isolated from 22- to 36-day-old rats. Application of vasopressin (VP) to the CSG produced a response in 59 cells (or 87.76%). Depolarization was noted in 67.8% of those responding, two-stage response in 16.95%, and hyperpolarization in 15.25%. All responses were dose-dependent and reversible. Membrane resistance (R_m) following depolarization declined but increased following hyperpolarization. Application of VP produced a lengthening of action potentials (AP) and a decline both in AP amplitude and after-hyperpolarization. A correlation was revealed between the biophysical properties of CSG neurons and the pattern of their response to VP. Neurons with a slow velocity of axonal conductance, protracted AP, and high R_m (small cells) had the lowest sensitivity threshold to VP at a concentration of 1·10^–11 M and responded with prolonged high-amplitude depolarizing potentials. Cells with a high velocity of axonal conductance, short-lasting AP, and low R_m responded to VP at a concentration of 1·10^–8 M, although response was occasionally lacking even at a concentration of 1·10^–6 M. Depolarization was more short-lived in these neurons and characterized by lower amplitude; cases of hyperpolarization were sometimes observed. Findings from our study would indicate that VP exerts an effect on the soma or primary sensory neurons, acting preferentially on small CSG cells.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 20, No. 6, pp. 801–808, November–December, 1988.     

Metabolic and ionic dependence of serotonin-induced neuronal response in rat sensory ganglia

Intracellular recording techniques were used to investigate the effects of neuronal serotonin application, either by micropipet under pressure or by addition to the superfusing fluid, on membrane potential and conductance during experiments on spinal ganglia cells from adult rats. Serotonin action on spinal ganglia neurons induced depolarization with reduced conductance, hyperpolarization, and increased membrane conductance, as well as mixed response. Only one response pattern was examined. Depolarization response in spinal ganglia neurons sensitive to methysergide were potentiated by activating type 2 serotonin receptors (5HT₂): e- and hyperpolarizing response insensitive to methysergide, propranolol, and cocaine action was produced via type 1 serotonin receptor (5HT_1A). Neuronal response produced by serotonin (5HT₂ mediation) did not depend on change in intraneuronal concentration of cAMP and the action of pertussis toxin. The second pattern of response was inhibited in the presence of pertussis toxin and modulated considerably by change in intraneuronal cAMP concentration and tryptazine action. Findings from research on ionic dependence showed that response mediated by 5HT₂ resulted from blockade of M-current potassium channels and that brought about by 5HT_1A is associated with disturbed function of cAMP-dependent potassium ionic channels.A. M. Gorkii Medical Institute, Donetsk. Translated from Neirofiziologiya, Vol. 21, No. 1, pp. 86–93, January–February, 1989.     

Serotonin-induced changes in the excitability of cultured antennal-lobe neurons of the sphinx moth Manduca sexta

The modulatory actions of 5-hydroxy-tryptamine (5HT or serotonin) on a morphologically identifiable class of neurons dissociated from antennal lobes of Manduca sexta at stages 9–15 of the 18 stages of metamorphic adult development were examined in vitro with whole-cell patch-clamp recording techniques. Action potentials could be elicited from approximately 20% of the cells. These cells were used to examine effects of 5HT (5 × 10^–6 to 5 × 10^–4 M) on cell excitability and action-potential waveform. 5HT increased the number of spikes elicited by a constant depolarizing current pulse and reduced the latency of responses. 5HT also led to broadening of action potentials in these neurons and increased cell input resistance. Modulation of potassium channels by 5HT is likely to contribute to these responses. 5HT causes reversible reduction of at least 3 distinct potassium currents, one of which is described for the first time in this study. Because effects of 5HT on antennal-lobe neurons in culture mimic those observed in situ in the brain of the adult moth, in vitro analysis should contribute to elucidation of the cellular mechanisms that underlie the modulatory effects of 5HT on central olfactory neurons in the moth.     

Effects of indomethacin and PGE1 on the vasoconstrictor responses of the rabbit ear artery to nerve stimulation

Actions of PGE₁ and indomethacin on electrically induced vasoconstriction in isolated ear arteries of rabbits were studied. PGE₁ (8.5 × 10⁻⁹ M) reduced the vasoconstriction; this inhibition was inversely related to the rate of stimulation. Indomethacin (1.5 × 10⁻⁶ M) potentiated the constrictor responses to nerve stimulation. The degree of this potentiation was also frequency-dependent being greater at low (1 – 2 Hz) than at high (8 – 16 Hz) rate of stimulation. These findings support the view that prostaglandins, in addition to their action on vascular smooth muscle cells, play a functional role in the regulation of tone of the rabbit ear artery by a negative feed-back control of adrenergic neurotransmission.     

Synthesis and structure-activity relationship of 1H-indole-3-carboxylic acid pyridine-3-ylamides: a novel series of 5-HT2C receptor antagonists

A novel series of 1H-indole-3-carboxylic acid pyridine-3-ylamides were synthesized and identified to show high affinity and selectivity for 5-HT_2C receptor. Among them, 1H-indole-3-carboxylic acid[6-(2-chloro-pyridin-3-yloxy)-pyridin-3-yl]-amide (15k) exhibits the highest affinity (IC₅₀ = 0.5 nM) with an excellent selectivity (>2000 times) over other serotonin (5-HT_1A, 5-HT_2A, and 5-HT₆) and dopamine (D₂–D₄) receptors.     

Comparison of direct influences of the perforant path on hippocampal CA1 and CA3 neurons in vitro

The efficiency of synapses of the perforant path located on terminals of apical dendrites of CA₁ and CA₃ neurons was investigated in sections of the guinea pig hippocampus in vitro. Neurons of both areas were shown to respond to stimulation of the perforant path by action potential generation. Responses of most CA₁ neurons appeared to repetitive stimulation with a frequency of up to 30–80/sec. Neurons in area CA₃ respond only to low-frequency stimulation (under 5/sec). Posttetanic potentiation of responses to stimulation of the perforant path was found in both areas of the hippocampus.Institute of Biophysics, Academy of Sciences of the USSR, Pushchino-on-Oka. Translated from Neirofiziologiya, Vol. 11, No. 4, pp. 303–310, July–August, 1979.