Comparative influence of nootropic preparations on the emetic effect of morphine

The effect of electroshock (ECS) and piracetam, oxiracetam or N-acetylglycinamide on the passive avoidance conditioned response in rats was studied. The antiemetic effect of the compounds was examined in cats as well. The results obtained allowed us to distinct the nootropic and antiemetic action of the drugs. The substances possessed a similar ability to prevent ECS-induced amnesia. On the contrary, oxiracetam completely prevented the emetic response to morphine at doses 100 times lower and piracetam at doses 10 times higher then those of the opioid. N-Acetylglycinamide had no antiemetic activity. The results obtained show that oxiracetam is 100 times more active in antiemetic test than piracetam. These data comprise the novel properties of nootropic drugs.     

Morphine-like activity of the enkephalin analog Tyr-D-Ala-Gly-Phe-NH2

The analgetic activity of the tetrapeptide enkephalin analog, its influence on the interneuronal transmission of excitation in various areas of the central nervous system and on opiate receptors of vas deferens were studied. The tetrapeptide was found to have a marked analgetic effect during intravenous injection to mice but to be less active than morphine. The tetrapeptide as well as morphine inhibited the impulse summation in rabbits and both spontaneous and bradykinin-induced neuronal activity in the rat sensory motor cortex. The tetrapeptide inhibited the contractions of isolated vas deferens in mice. The opiate antagonist naloxone eliminated both analgetic effect of the tetrapeptide and its inhibitory effect on the impulse summation, neuronal activity and contractions of vas deferens.     

Participation of dihydropyridine-sensitive calcium channels in psychotropic effects of nootropic drugs

Administration of Ca-entry blockers with different chemical structure before the braining sessions produced the reduction of memory retention in mice and rats in the one-trial passive avoidance tests. This effect was absent in animals treated immediately after training test. Nootropic drugs piracetam and oxiracetam corrected the retention of memory when injected just after training test. Chronic treatment of rats with increasing doses of the nootropic drugs produced about two-fold tissue-specific elevation in the density of DHP-receptors, associated with L-type Ca-channels in synaptosomal membranes of rat cerebral cortex. Maximal effect was observed in a dose of 10 mg/kg. Diltiazem, administrated in a dose of 10 mg/kg, produced about two-fold decrease in the receptors density measured 24 hrs after the first injection. Oxiracetam (10 mg/kg) completely antagonized the effect of Ca-entry blocker. These data imply that nootropic action of piracetam and oxiracetam is mediated by L-type Ca-channels.     

Reflexogenic changes in the spontaneous and evoked activity of the parafascicular neurons in the rat thalamus during electroacupuncture stimulation

Acute experiments on cats were made to study the electroacupuncture (EAP) effect on neuronal impulse activity in the parafascicular complex (PFC) of the thalamus in response to solitary peripheral nociceptive and non-nociceptive stimuli. EAP stimulation affects the pattern of spontaneous and evoked activity of PFC neurons and forms their new functional status. It is suggested that the analgetic effect is brought about by the changes in neuronal activity in subcortical structures of the brain including the thalamic nuclei which transmit the ascending nociceptive input.     

Effect of morphine on the sensitivity of cerebral cortical neurons to acetylcholine

Sensitivity of sensorimotor cortical neurons to microiontophoretically applied morphine and acetylcholine has been studied in the experiments on unanesthetized rabbits. The predominant reaction to morphine and acetylcholine was decrease and increase in the rate of neuronal impulse activity, respectively. There was no correlation in the responses to morphine and acetylcholine. Atropine failed to influence the morphine effect. When both drugs are simultaneously applied to neurons, morphine decreases both excitatory and inhibitory responses to acetylcholine. This effect of morphine may occur in the case when the drug is applied in doses which do not change spontaneous neuronal activity. On the contrary, excitatory effect of glutamic acid decreased only when morphine was applied in doses causing local anesthetic effect and decreasing background neuronal activity. It is suggested that morphine can exercise a modulating influence on choline receptors of cortical neurons.     

Influence of vibration on the spontaneous neuronal activity of the neurons of the superior vestibular nucleus

The results of vibration action (5, 10 and 15 daily) on spontaneous neuronal activity of superior vestibular nucleus were studied using software for biological signals. Average histograms and autocorrelograms were drawn up after computerized interspike interval analysis. The results have demonstated that neurons of superior vestibular nucleus have mean frequency 14.0 +/- 1.4 Hz. The results obtained suggest significant reconstruction of spontaneous impulse activity in neurons of the superior vestibular nucleus within postvibration period.     

Effect of electroacupuncture on the nature of changes in the activity of neurons in the 2d somatosensory region of the cerebral cortex

Effects of electroacupuncture (EAP) on the character of spontaneous and evoked neuronal impulse activity changes in the second somatosensory area (S2) of the brain cortex by nociceptive and non-nociceptive stimulation were studied in acute experiments on cats. It was demonstrated that EAP changed the character of S2 neurons activity and formed their new functional state. After EAP activity of non-nociceptive neurons were not changed, evoked activity of nociceptive neurons were inhibited. It is suggested, that EAP preferential blocking the protopathic components of the acute pain.     

Effects of nootropic drugs on brain cholinergic and dopaminergic transmission

High affinity choline uptake (HACU) in the hippocampus and striatal concentration of dopamine (DA) and homovanillic acid (HVA) as measures of the in vivo acetylcholine and DA turnover, respectively, were estimated in male rats, Long-Evans, following 6-day administration of various nootropics in clinically relevant doses: piracetam and its derivatives pramiracetam and oxiracetam (100 mg/kg/day), pyritinol (50 mg/kg/day). Piracetam treatment was without effect on HACU, but induced significant increase of HVA in the striatum leaving striatal DA concentration unchanged. On the contrary, pyritinol, pramiracetam and oxiracetam increased HACU, but did not change striatal DA and HVA levels.     

The Role of Calcium Ions in Modulation of Impulse Activity of the Isolated Muscle Spindle of the Frog Rana temporaria

The effect of various concentrations of Ca⁺² and Mg⁺² as well as of calcium channel blockers verapamil and nifedipin on impulse activity of frog isolated muscle spindles was studied. Removal of Ca ions from the external Ringer solution was established to increase spontaneous and evoked activity of the muscle spindle. A 4- and 8-fold increase of Ca⁺² concentration produces inhibition and complete cessation of the spontaneous and evoked activity in the muscle spindle. Replacement of Ca⁺² by Mg⁺² is observed to cause no statistically significant change of the spontaneous activity of the isolated muscle spindle; at the same time, at the dynamic spindle extension, the impulse activity rate at the dynamic and static phases of the response rises. Nifedipin and verapamil, blockers of Ca⁺² channels, suppress impulse activity both in norm and on the background of increased impulse activity evoked by removal of Ca⁺² from the external solution. An increase of muscle spindle impulse activity after the removal of Ca⁺² from the external solution is accounted for by transformation of calcium channels of the muscle spindle sensory endings into selective sodium channels.     

N-methyl-D-aspartate effect on spontaneous activity of 16–20-day-old chick embryo spinal cord

The effects of N-methyl-D-aspartate (NMDA) and the NMDA receptor antagonist, 2-amino-5-phosphonovaleric acid (2-APV), on spontaneous activity of dorsal and ventral roots (DR and VR, respectively) generated by isolated spinal cord from 16–20-day-old chick embryo were studied. This activity was synchronous oscillations of electrotonic potentials in DR and VR. There was no impulse activity in the VR. When NMDA was applied at 2–25 µM, the amplitudes of the oscillations increased, the impulse activities in VR and DR developed, and the tonic component of electrotonic potentials appeared. At 20 µM, 2-APV decreased both, the spontaneous and NMDA induced activity. After sectioning of the spinal cord, the neuronal network of the isolated dorsal arm conserved the capacity to generate spontaneous activity in the DR which increased after NMDA application. There was no rhythm in the ventral part of the spinal cord. The localization of the NMDA-sensitive neuronal network, generator of the rhythmic (motor) activity, in the spinal cord is discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 23, No. 2, pp. 205–213, March–April, 1991.     

Nootropic Drugs Positively Modulate α-Amino-3-Hydroxy-5-Methyl-4-Isoxazolepropionic Acid-Sensitive Glutamate Receptors in Neuronal Cultures

Micromolar concentrations of piracetam, aniracetam, and oxiracetam enhanced alpha-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-stimulated 45Ca2+ influx in primary cultures of cerebellar granule cells. Nootropic drugs increased the efficacy but not the potency of AMPA and their action persisted in the presence of the voltage-sensitive calcium channel blocker nifedipine. Potentiation by oxiracetam was specific for AMPA receptor-mediated signal transduction, as the drug changed neither the stimulation of 45Ca2+ influx by kainate or N-methyl-D-aspartate nor the activation of inositol phospholipid hydrolysis elicited by quisqualate or (+-)-1-aminocyclopentane-trans-1,3-dicarboxylic acid. Piracetam, aniracetam, and oxiracetam increased the maximal density of the specific binding sites for [3H]AMPA in synaptic membranes from rat cerebral cortex. Taken collectively, these results support the view that nootropic drugs act as positive modulators of AMPA-sensitive glutamate receptors in neurons.     

Spike activity of mesencephalic neurons during nociceptive stimulation of the alert cat

Rate of reorganizations of neuronal impulse activity in the ventromedial parts of the midbrain of alert rats in conditions of nociceptive and non-nociceptive actions is determined by biological value of used stimuli and closely correlates with spontaneous and evoked changes of the motor activity and oscillations of vegetative parameters. The character of reorganizations of discharge activity (activation, inhibition) significantly differs in cells of various types, singled out on the basis of differences of electrophysiological properties and predominantly localized in different parts of the studied brain areas. The revealed characteristics of the functional properties of the neurones are discussed in connection with supposed differences of their neurotransmitter specificity and their role in providing for different chains of adaptive activity of the organism.     

Effects of ibogaine,and cocaine and morphine after ibogaine,on ventral tegmental dopamine neurons

Ibogaine, an indole containing alkaloid, has been shown to reduce the rate of injection of morphine and cocaine in self-administration protocols. Since morphine- and cocaine-induced modulation of dopamine release is impulse dependent and essential for their reinforcing effects, disruption of dopamine neuronal activity by ibogaine could explain its purported ‘antiaddictive’ properties. Therefore, the present study was designed to determine: (1) the acute effects of ibogaine on the activity of VTA dopamine neurons, and (2) whether ibogaine pretreatment causes a persistent modification of the dopamine neuronal response to morphine and cocaine. Extracellular recordings in anesthetized animals found that intravenous ibogaine markedly excited VTA dopamine neuronal firing. However, ibogaine pretreatment (6–8 hr and 19 hr before) failed to alter either the spontaneous activity of VTA neurons, or the response of these dopamine neurons to morphine or cocaine. Thus, ibogaine's excitatory effect on VTA neurons is not longlasting nor does it persistently alter cocaine- or morphine-induced changes in dopamine neuron impulse activity. Therefore, other mechanisms must be explored to account for the proposed antiaddictive properties of ibogaine.     

Effect of piracetam on the habituation of the neuronal cholinoreceptor membrane of the edible snail

Piracetam is shown to modulate the habituation pattern of cholinoreceptor neuronal membrane in Helix lucorum. Piracetam (10(-2) M) intensified the reversible decrease of depolarization and spike discharge induced by the local microionophoretic rhythmical application of acetylcholine to the neuron soma. The ability of piracetam to intensify the habituation of neuronal cholinoreceptor membrane may serve as a model of its facilitating effect on the development of habituation of behavioural reactions. Piracetam (5.10(-2) M) was shown to induce a shift in the membrane potential towards depolarization in the majority of identified neurons studied.     

Spike activity of neurons of the ventromedial hypothalamus of the rat during stress

In fixed Wistar line rats, neuronal activity of the ventromedial hypothalamus was studied in conditions of acute emotional stress elicited by electric stimulation of the ventromedial hypothalamus stochastically alternating with electrocutaneous stimuli. Distinctions were revealed in neuronal activity of the animals with different stress resistance. The pattern of neuronal impulse activity proved to be the most informative one.     

Combinations of active striatal neurons connected selectively with certain behavioral actions of the monkey Macaca mulatta

At present there is widely spread concept of populational coding of information by brain neurons; it is based first of all on results of comparison of neuronal activity with parameters of the used stimulus. Relation between the neuronal activity coding and the observed behavioral actions has been practically not studied. In the present work, neuronal impulse activity has been studied in groups of 6 neurons recorded in parallel. Distribution of frequencies of the presence of cases of excitation of one or several cells has been established to differ statistically significantly form the theoretical distribution of the same values; this indicates that under real conditions, the appearance of individual combinations of active neurons is not random, but is connected to a certain degree with conditions of experiment. The selective combinations of neuronal activity have revealed to be different at stages of program. This indicates that organization of different behavioral actions is associated with activities of certain combinations of neurons.     

Combinations of active striatal neurons connected selectively with certain behavioral actions of the monkey <Emphasis Type="Italic">Macaca mulatta</Emphasis>

At present there is widely spread concept of populational coding of information by brain neurons; it is based first of all on results of comparison of neuronal activity with parameters of the used stimulus. Relation between the neuronal activity coding and the observed behavioral actions has been practically not studied. In the present work, neuronal impulse activity has been studied in groups of 6 neurons recorded in parallel. Distribution of frequencies of the presence of cases of excitation of one or several cells has been established to differ statistically significantly from the theoretical distribution of the same values; this indicates that under real conditions, the appearance of individual combinations of active neurons is not random, but is connected to a certain degree with conditions of experiment. The selective combinations of neuronal activity have been revealed to be different at stages of program. This indicates that organization of different behavioral actions is associated with activities of certain combinations of neurons.     

The effect of cyclic nucleotides on the rhythmogenicity of the lymphatic center in the frog Rana temporaria]

Studies have been made of the effect of cAMP on the spontaneous impulse activity of lymphatic pacemaker neurons in the frog. It was shown that inhibition of phosphodiesterases by papaverine and 3-isobutyl-1-methylxanthin resulted in the increase in rhythm of bursting impulse activity of the lymphatic centre turning it into a continuous one. The same effect was produced by dibutyryl-cAMP, and to a lower extent--by cAMP. CGMP blocked rhythmic activity of the centre. Possible role of cyclic nucleotides in rhythmic activity of pacemaker cells in the spinal centre of the lymphatic hearts in the frog is discussed.     

Effect of a derivative of GABA, phenibut, on behavior and the activity of visual cortex neurons of the rabbit during elaboration of a defensive reflex and internal inhibition

In experiments on alert non-immobilized rabbits the effect of subcutaneous administration of the GABA-derivate--phenibut on behaviour, slow potentials and impulse activity of neurones of the visual cortex was studied during elaboration of a defensive reflex to light flashes and of conditioned inhibition. During the action of phenibut late negative-positive components of the evoked potentials to flashes, corresponding inhibitory pauses and postinhibitory activation gradually increased; then stable predominance of slow high-amplitude potential oscillations and corresponding neuronal group bursts appeared, separated by inhibitory pauses and in intersignal periods. Reinforcing stimulus, as before phenibut administration, lowered the amplitudes of slow potential oscillations and weakened inhibitory pauses in neuronal impulse activity. Dynamics of movements in response to the stimuli was of a phasic character. 3 hours after phenibut administration the discrimination of reinforced and inhibitory light flashes has distinctly improved. The obtained results confirm the initial concept of the significant role of the GABA-ergic inhibitory system in the process of elaboration of internal inhibition.     

Metabolic features of the adaptive effect of delta-sleep inducing peptide and piracetam under hyperoxic conditions.

Adaptive effects of delta-sleep inducing peptide (DSIP, 12 microgram/100 g body weight, single intraperitoneal injection) and piracetam (3 mg/100 g body weight, daily intraperitoneal injection for 3 days) are manifested via differential changes in neurotransmitter amino acids (GABA, glutamate, aspartate), modulation of transport ATPase activity, and decreased accumulation of lipid peroxidation products (conjugated dienes, malonic dialdehyde, Schiff bases) in various fractions of neuronal membranes (myelin, synaptic and mitochondrial membranes) in the sensomotor cortex of rat brain. Under hyperbaric oxygenation (0.3 MPa for 2 h), the combination of DSIP and piracetam enhanced the protective effect of each compound.