Ingestion motor programs of Aplysia are modulated by short-term synaptic enhancement in cerebral-buccal interneuron pathways

In the sea slug Aplysia, buccal synapses of cerebral-buccal interneurons (CBIs) CBI-2 and CBI-12 exhibit short-term synaptic enhancement (STE), including frequency-dependant facilitation and augmentation/post-tetanic potentiation (AUG/PTP). The STE that results from driving CBI-2 or CBI-12 is associated with significantly decreased latency to burst onset in buccal premotor neurons and motor neurons, increased cycle frequency of ingestion buccal motor programs (iBMPs) and increased intraburst firing frequency of buccal neurons during iBMPs. Tests of paired-pulse facilitation during AUG/PTP suggest that the locus for this plasticity is presynaptic. The AUG/PTP is not elicited by heterosynaptic pathways, indicating that its origin is homosynaptic. At low CBI-2 and CBI-12 firing frequencies, STE is likely to contribute to iBMP initiation, while at higher firing frequencies, STE is correlated with increased cycle frequency of iBMPs. Thus, STE is an important component of the mechanisms whereby cerebral neurons regulate cyclic feeding programs and likely contributes to observed variations in behavioral responses, including feeding arousal. Electronic Publication     

Dynamics of post-denervational modifications of spinal reflex activity in albino rats

In experiments on rats, we studied the characteristics of reflex discharges in the ventral root (VR) L ₅; the discharges were evoked by stimulation of segmental (peripheral nerve or dorsal root, DR) and suprasegmental vestibular (stimulation of the round window of the labyrinth) inputs. Potentials were recorded within different time intervals (from 1 to 150 days) after transection of the sciatic nerve (SN); measures preventing regeneration of its fibers were used. Modifications of the segmental responses related to post-denervational changes included four phases: (i) latent period, (ii) post-denervational spinal hyperreflexia (PDSH), (iii) partial suppression of monosynaptic discharges (MDs) in the VR, and (iv) complete disappearance of VR MDs resulting from late post-denervational changes. The latency of post-denervational modifications was about 18–48 h after the moment of transection of the SN. Within the PDSH phase, modifications were the greatest 3 to 5 days after transection; these changes could be more adequately estimated in the case of stimulation of the DR on the side of transection and not under conditions of stimulation of the central segment of the transected SN per se. Within this phase, the amplitudes of VR MDs and responses to vestibular stimulation were augmented two to three and four to five times, as compared with the respective indices in intact animals. From the 7th to 10th day after the nerve transection, the amplitude of VR MDs progressively dropped, and on about the 20th day these discharges practically disappeared, while polysynaptic components of segmental responses were preserved. Vestibular responses within this period were, as earlier, considerably facilitated. On the 60th and 150th days (within the phase of late post-denervational modifications) there were no VR MDs after stimulation of segmental inputs, and polysynaptic responses were exclusively observed. The amplitude of discharges evoked by vestibular stimulation became lower than in the PDSH state but remained significantly higher than the control values of this parameter. Probable mechanisms of post-denervational modifications of the evoked spinal activity within different time intervals after transection of the SN are discussed. Neirofiziologiya/Neurophysiology, Vol. 39, No. 1, pp. 37–46, January–February, 2007.     

Changes in Electrogenesis in the Motor Nerve Terminal with Long-Lasting High-Frequency Activation as a Factor of the Control of Transmitter Release

Using the technique of extracellular recording from the region of the neuromuscular junction in the cutaneous-sternal muscle in the frog under conditions of a reduced concentration of Ca²⁺ in the surrounding milieu, we demonstrated that long-lasting (10 min) rhythmic stimulation of the motor nerve with a frequency of 10 sec^{− 1} leads to a gradual increase in the evoked transmitter release. These changes are accompanied by a decrease in the amplitude of electrical responses of the nerve terminal (NT) and by a retardation of its second phase, as well as by a diminution of the third phase. Under conditions of long-lasting (5 min) stimulation with a frequency of 50 sec⁻¹, we observed a two-phase change in the intensity of transmitter release: on the 2nd min, the initial rise was replaced by inhibition. Modifications of the response of the NT with different stimulation frequencies were qualitatively similar, but with a frequency of 10 sec⁻¹ they were clearly expressed. Mathematical simulation of ion currents in the NT demonstrated that voltage-dependent potassium and sodium channels are inactivated in the course of long-lasting high-frequency excitation; the shape of the action potential is modified with changes in the rate of such inactivation. This leads to either an increase or a decrease of the inward calcium current. We conclude that the change in electrogenesis in the NT with long-lasting high-frequency activation of neuromuscular junctions exerts a significant influence on the dynamics of transmitter release. Neirofiziologiya/Neurophysiology, Vol. 37, No. 2, pp. 108–115, March–April, 2005.     

Facilitation and Depression of Neuromuscular Transmission under Conditions of Blockade of Ryanodine Receptors

In our experiments on mice, end-plate currents (EPC) evoked by stimulation of the phrenic nerve were intracellularly recorded in neuromuscular synaptic junctions of the phrenic muscle. We studied the effects of a specific blocker of ryanodine receptors, ryanodine (10 to 20 M), on the amplitude and time parameters of EPC under conditions of tetanic facilitation and depression of synaptic transmission at frequencies of stimulation of 4 to 200 sec^-1. Ryanodine inhibited facilitation at stimulation frequencies of 7 to 70 sec^-1 (with maximum effect at 20 sec^-1) and accelerated depression. In the presence of ryanodine, an initial rundown of the EPC amplitude in the course of depression of transmission increased at high frequencies of stimulation (50 to 100 sec^-1), whereas the EPC amplitude at the plateau level decreased already at low frequencies (4 to 7 sec^-1). We concluded that the changes in facilitation and depression resulted from blocking of the presynaptic ryanodine receptors by ryanodine. It seems probable that calcium release from the calcium stores in murine motor terminals is a factor involved in the control of processes of transmitter secretion during short-term rhythmic activation of the junction.     

Mechanisms of Long-Lasting Depression of Synaptic Transmission in the CA1 Region of the Rat Hippocampus

Low-frequency tetanic stimulation (2 sec^-1, 5 min) of Schaffer collaterals (SchC) in superfused slices of the dorsal hippocampus of 12- to 15-day-old rats was demonstrated to evoke homosynaptic long-lasting depression (LLD) of synaptic transmission. The same procedure applied to hippocampal slices of mature (8-week-old or older) rats failed to elicit LLD. Low-frequency tetanic stimulation of the alveus in hippocampal slices, applied under conditions of intensified NMDA glutamate receptor functioning, led to the development of heterosynaptic LLD of synaptic transmission in the SchC–dendrites of the CA1 pyramidal neurons system. Both LLD cases were either absent or weakened when hippocampal slices were treated with a competitive blocker of the NMDA glutamate receptors, D-2-amino-5-phosphonovalerate (50 M). Morphine hydrochloride (10 M), as well as inhibitors of calmodulin and calcineurin (trifluoroperasine and cyclosporin A in concentrations of 1 and 50 M, respectively), interfered with induction of LLD or decreased its intensity. A blocker of the L-type voltage-dependent Ca²⁺ channels, nifedipine (10 M), did not influence homosynaptic LLD, but decreased heterosynaptic depression. Both types of depression of synaptic transmission were facilitated upon application of substances possessing a nootropic activity, 1 mM pyracetam or 5 M carbacetam. A blocker of NO synthase, N-nitro-L-arginine (10 M) did not alter either type of LLD. When hippocampal slices were influenced with a blocker of the A1 adenosine receptors, 1,3-dipropyl-8-phenylxanthine (1 M, 15 min), both LLD forms were intensified, and the development of homosynaptic LLD of synaptic transmission became possible in hippocampal slices of mature rats. When hippocampal slices were treated with an inhibitor of protein kinase C, polymyxin B (50 M, 15 min), intensification of LLD and, in particular, the development of homosynaptic LLD of synaptic transmission were observed. When an inhibitor of phospholipase A2, mepacrine (25 M, 15 min), was applied to hippocampal slices, both forms of LLD of synaptic transmission were significantly suppressed.     

The base-catalyzed isomerization of trans-RCo(H2O)L (L=5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene)

The sec, rac-CH₃Co(H₂O)L²⁺ (L=5,7,7,12,14,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-4,11-diene) was prepared successfully via meso-CH₃Co(H₂O)L²⁺ in aqueous solution. The isomerizations from meso-RCo(H₂O)L²⁺ (R=CH₃, C₂H₅ and C₃H₇) and sec, rac-CH₃Co(H₂O)L²⁺ to pri, rac-RCo(H₂O)L²⁺ were both base catalyzed in aqueous solution. The kinetic results showed the reaction to be first order in both organocobalt complex and hydroxide ion with the reactivity order for the alkyl group being C₃H₇ ∼ C₂H₅ ? CH₃. However, the conversion from the most steric hindered isomer form of sec, rac- was slow. The ratio of the isomerization rate constants between meso-CH₃Co(H₂O)L²⁺ and sec, rac-CH₃Co(H₂O)L²⁺ to pri, rac-CH₃Co(H₂O)L²⁺ is almost a factor of 100. The thermodynamic activation parameters for these isomerization reactions were investigated.     

Effect of peripheral heating and cooling on spinal reflex activity

The effects of heating and cooling the skin of the thigh and leg on the character of changes in monosynaptic and polysynaptic reflexes and of the first negative wave (N_`) of the dorsal cord potential was studied in acute experiments on lightly anesthetized cats. During cooling of the skin the amplitude of the monosynaptic reflex and N₁-wave was increased while the polysynaptic reflex was inhibited; during heating the amplitude of the monosynaptic reflex and N₁-wave was reduced while the polysynaptic reflex was increased. After de-efferentation the cooling effect was reduced, and after division of the spinal cord responses to cooling of the skin were considerably inhibited. The mechanism of the selective action of cooling and heating of the skin on monosynaptic and polysynaptic reflexes are discussed.Institute of Physiology, Academy of Sciences of the Kazakh SSR, Alma-Ata. Translated from Neirofiziologiya, Vol. 5, No. 2, pp. 181–185, March–April, 1973.     

Laryngeal motor control in frogs: Role of vagal and laryngeal feedback

Using decerebrate frogs (Rana catesbeiana), we investigated the role of vagal and laryngeal sensory feedback in controlling motor activation of the larynx. Vagal and laryngeal nerve afferents were activated by electrical stimulation of the intact vagal and laryngeal nerves. Pulmonary afferents were activated by lung inflation. Reflex responses were recorded by measuring efferent activity in the laryngeal branch of the vagus (Xℓ) and changes in glottal aperture. Two glottic closure reflexes were identified, one evoked by lung inflation or electrical stimulation of the main branch of the vagus (Xm), and the other by electrical stimulation of Xℓ. Lung inflation evoked a decrementing burst of Xℓ efferent activity and electrical stimulation of Xm resulted in a brief burst of Xℓ action potentials. Electrical stimulation of Xℓ evoked a triphasic mechanical response, an abrupt glottal constriction followed by glottal dilatation followed by a long-lasting glottal constriction. The first phase was inferred to be a direct (nonreflex) response to the stimulus, whereas the second and third represent reflex responses to the activation of laryngeal afferents. Intracellular recordings of membrane potential of vagal motoneurons of lung and nonlung types revealed EPSPs in both types of neurons evoked by stimulation of Xm or Xℓ, indicating activation of glottal dilator and constrictor motoneurons. In summary, we have identified two novel reflexes producing glottic closure, one stimulated by activation of pulmonary receptors and the other by laryngeal receptors. The former may be part of an inspiratory terminating reflex and the latter may represent an airway protective reflex. © 1997 John Wiley & Sons, Inc. J Neurobiol 33: 213–222, 1997     

Effects of hypoxia on the respiratory activity generated by semi-isolated medullo-spinal preparations of early postnatal rats

The effects of short- and long-lasting (2-min-long and up to 30-min-long) hypoxia episodes on the inspiratory activity (IA) recorded from then. phrenicus were tested in experiments on superfusedin situ semi-isolated medullo-spinal preparations (SIMSP) of newborn (the lst day of life) and 4- to 5-day-old rats. Hypoxia was provided by superfusion of the preparations with low-O₂ solution. Short-lasting hypoxia evoked no significant modulation of the IA in preparations of newborn animals, while two-phase responses (an initial, up to 30 sec, increase in the frequency of inspiratory discharges, followed by their longer, up to 4 min, suppression) were observed in 4- to 5-day-old preparations. Long-lasting hypoxia suppressed activity in then. phrenicus of 1-day-old preparations, and this effect was replaced in five cases by the development of sporadic low-amplitude and short-lasting inspiratory discharges. These shortened discharges were qualified as gasps. The responses of 4- to 5-day-old SIMSP to long-lasting hypoxia episodes were more complex. An initial increase in the IA frequency lasted up to 30 sec, and in 4–6 min it was followed by complete suppression of the activity. In some of the SIMSP, permanent tonic activity appeared in then. phrenicus within the period of total absence of inspiratory discharges, which could be followed by generation of short low-amplitude gasping discharges. Against the background of gasping pattern, eupnoe-like discharges appeared in four preparations. Under control conditions, transerve section of the ventrolateral medullary regions (VLMR) at a middle level of then. hypoglossus root abolished respiratory activity in all studied SIMSP. Yet, in some of the SIMSP of both newborn and 4- to 5-day-old animals long-lasting hypoxia testing evoked weak tonic activity in then. phrenicus followed by the appearance of gasping discharges. After the transection of the VLMR at the caudal edge of then. hypoglossus root, long-lasting hypoxia evoked only weak tonic responses in some SIMSP of both age groups, and there were no phasic discharges in this case. The results of our experiments, first, show that the respiratory activity in newborn animals is more resistant to hypoxia than that in 4-to 5-day-old rats, and, second, they allow us to suppose that the gasp-generating medullary structures are localized in more caudal medullary regions. We discuss the questions of how the eupnoe-generating and gasp-generating medullary structures are formed in rats during their initial four to five postnatal days, and what specific features are typical of hypoxia-related respiratory responses in these animals.Neirofiziologiya/Neurophysiology, Vol. 28, No. 2/3, pp. 121–131, March–June, 1996.     

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.     

Post-tetanic potentiation of polysynaptic reflexes of the spinal cord

The phenomenon of post-tetanic potentiation has been studied in the cat spinal cord with particular reference to polysynaptic responses. Following tetanization of dorsal roots, these reflexes show an increased response, as measured in terms of their voltage-time area, with a predominant change in the earlier reflex pathways. Both of these changes in the reflex discharge have a time course of 15 to 25 seconds. Post-tetanic potentiation is also observed in response to stimulation of a dorsal rootlet following tetanization of another rootlet in the same or in a neighboring segment. This effect can be explained by post-tetanic changes in the terminals of secondary, and possibly higher order, internuncial cells, essentially similar to those changes in the primary afferent terminals which give rise to potentiation of the monosynaptic reflex.     

Transfer of habituation in Aplysia: contribution of heterosynaptic pathways in habituation of the gill-withdrawal reflex

Habituation of the Aplysia gill-withdrawal reflex (and siphon-withdrawal reflex) has been attributed to low-frequency homosynaptic depression at central sensory-motor synapses. The recent demonstration that transfer of habituation between stimulation sites occurs in this model system has prompted the hypothesis that heterosynaptic inhibitory pathways also play a role in the mediation of habituation behavior. To test this hypothesis, the sites and mechanisms of neural plasticity which underlie transfer of habituation in Aplysia were examined. Transfer of habituation is a reduction in the reflex evoked at one stimulation site (siphon) due to repeated presentation of a stimulus to a second site (gill). Centrally mediated transfer of habituation, measured in a preparation lacking the siphon-gill peripheral nervous system (PNS), was associated with a reduced excitatory response in central motor neurons. Repeated tactile stimulation of the gill did not attenuate the gill response evoked by electrical stimulation of the branchial nerve nor the mechanoreceptor response recorded in LE sensory neurons. In contrast, repeated stimulation of siphon or gill at a site which was "off" the sensory field of a specific mechanoreceptor led to a diminution in synaptic transmission between that sensory neuron and its followers (motor neurons and inter-neurons). These data demonstrate that centrally mediated transfer of habituation results from heterosynaptic modulation of synaptic transmission at the sensory-motor (and sensory-interneuron) synapses. Therefore, habituation behavior in Aplysia is mediated through the conjoint action of homosynaptic and heterosynaptic inhibitory processes.     

Control of gill reflex habituation and the rate of EPSP decrement of L7 by a common source in the CNS of Aplysia

It was found in older Aplysia that the rate of decrement of the EPSP evoked in L₇ by repeated tactile stimulation of the gill was dependent on the strength of the applied stimulus and that the rate of decrement paralleled the rate of gill reflex habituation. As the stimulus intensity was increased both rates slowed. In contrast, it was found in young Aplysia that the rate of EPSP decrement and the rate of gill reflex habituation were independent of the strength of the stimulus applied to the gill. Neither rate changed as the stimulus intensity was changed. Moreover, L₇'s of young animals are more responsive to tactile stimuli applied to the gill than are L₇'s of older animals and the difference in excitability is not due to any differences in passive membrane properties between the L₇'s in young and older Aplysia. These findings are fully consistent with and supportive of the proposal that a common neuronal source in the parieto-visceral ganglion of Aplysia controls the rate of gill reflex habituation, the synaptic input to L₇, and the rate of decrement of this input, evoked by repeated tactile stimulation of the gill. Additinally, it was proposed that this common source is developed in completely in the young. As a consequence of this incomplete development, young Aplysia exhibit less adaptability to changing stimulus conditions and, in general, less ability to suppress their behavior. It may thus be possible to study directly developmental changes in the nervous system which act to transform juvenile behavior to adult behavior.     

Functional characteristics of Schaffer's collaterals studied in vivo and in vitro

A comparative analysis was made of the functional characteristics of connections between hippocampal areas CA₃ and CA₁ (Schaffer's collaterals) in experiments in vivo on unanesthetized rabbits and in vitro on surviving slices of guinea pig hippocampus, with extracellular recording in area CA₁. In the case of electrical stimulation of the collaterals in vitro, post-activational inhibition was weak, responses of inhibition of spontaneous discharges were absent, and low frequencies of stimulation were more effective than in vivo. Posttetanic changes were found more frequently in experiments in vitro and they lasted longer than in vivo. The predominant effect of tetanization under normal conditions was depression, but during incubation it was facilitation of responses. The possible causes of these differences are discussed.Institute of Biophysics, Academy of Sciences of the USSR, Puschino-on-Oka. Translated from Neirofiziologiya, Vol. 11, No. 3, pp. 208–217, May–June, 1979.     

Reorganization of segmental responses to peripheral stimulation during fictitious scratching in cats

Segmental reflex responses of the lumbosacral region of the spinal cord to stimulation of peripheral afferents were studied in immobilized decerebrate cats before and after application of D-tubocurarine or bicuculline to the superior cervical segments, potentiating the scratch reflex, and also during fictitious scratching evoked by mechanical stimulation of the ear. Application of these substances led to inhibition of the N₁-component of the dorsal cord potential, the dorsal root potential, and polysynaptic responses in efferent nerves. The appearance of fictitious scratching was accompanied by additional tonic inhibition of these responses, against the background of which modulation of the amplitudes of the responses was observed depending on the phase of fictitious scratching. Modulation of amplitudes of monosynaptic reflexes also developed during fictitious scratching. Against the background of these results the mechanisms and physiological role of reorganization of segmental responses during activation of the spinal scratching generator are discussed.A. A. Bogomolets Institute of Physiology, Academy of Sciences of the Ukrainian SSR, Kiev. Translated from Neirofiziologiya, Vol. 13, No. 2, pp. 196–203, March–April, 1981.     

Study on the relationship between calcium-induced calcium release from mitochondria and PTP opening

The permeability transition pore (PTP) is central for mitochondria function. PTP either open in low-conductance state to carry out mCICR (Ca²⁺-induced Ca²⁺ release from mitochondria) and play roles in cell phsyiological activities or open in high-conductance conformation to release harmful substances and play important roles in cell pathological responses and apoptosis. The results of study on the relationship between mCICR and PTP opening show Ca²⁺ concentrations but not the Ca²⁺ delivery mode determined the occurrence of mCICR or PTP opening. Ca²⁺-induced PTP opening began with and depended on mCICR. mCICR was a prerequisite for H₂O₂ and As₂O₃-induced PTP opening. The results indicated that the PTP opening was determined by Ca²⁺ stimulation intensity but not mode. PTP could switch from low- to high-conductance conformation and the PTP open by high-conductance began with low-conductance state. mCICR is necessary for Ca²⁺-dependent PTP opening. Our data suggested also that it would be possible to control cellular responses first by modulating mCICR, then by regulating PTP opening.     

Investigation of heterosynaptic interactions in hippocampal areas CA1, and CA3 in vitro

Heterosynaptic interactions between synapses located at a considerable distance from the cell body (perforant path) and lying close to the body of the neuron (synapses of Schaffer's collaterals and axons of the dentate fascia) on guinea pig hippocampal neurons were investigatedin vitro. It was shown by the paired stimulus method that, using stimulation of subthreshold intensity for action potential generation, spatiotemporal summation takes place in both pairs of synaptic systems. If above-threshold stimulation was used, afferents lying close to the cell body suppressed responses evoked by stimulation of distant afferents for a longer time (up to 20 msec in area CA₁ and up to 300 msec in area CA₃) than during the opposite combination of stimuli (up to 3–8 msec). After tetanization of the dentate fascia depression of responses of area CA₃ neurons to stimulation of the perforant path was observed for 2–30 min. In the remaining cases, no significant prolonged heterosynaptic posttetanic changes were observed. The possible mechanisms of these interactions are discussed.Institute of Biophysics, Academy of Sciences of the USSR, Pushchino-on-Oka. Translated from Neirofiziologiya, Vol. 11, No. 6, pp. 524–532, November–December, 1979.     

Induction of heterosynaptic and homosynaptic LTD in hippocampal sub-regions in vivo

Establishing the conditions under which long-term depression (LTD) can be induced in vitro remains an important empirical issue. While heterosynaptic LTD is readily elicited in the hippocampus in vivo, the induction of homosynaptic LTD has been more problematic, both in CA1 and in the dentate gyrus. Our work has demonstrated, however, that 900 pulses at 1 Hz will reliably induce LTD in both area CA1 and the dentate gyrus of pentobarbital-anesthetized animals, when the stimulating and recording electrodes are in close proximity to each other.     

Effects of Local and Remote Muscle Pain on Stretch ReflexActivities in the Elbow Joint Flexors and Extensors of Unanesthetized Cats

In experiments on unanesthetized cats, we compared the effects of experimentally induced pain in the m. biceps brachii or in the neck muscles on EMG activity of the flexors and extensors of the elbow joint (mm. biceps et triceps brachii, respectively) evoked by a passive extension-flexion of the above joint. Muscle pain was induced by injections of 0.5 ml of a hypertonic (7%) NaCl solution into the above-mentioned muscles. In the case of pain in the biceps, i.e., in the muscle directly involved in realization of the reflex, we observed an increase in the amplitude and significant shortening of the latency of EMG responses of this muscle. The amplitude of a short-latency (supposedly monosynaptic) component of the biceps reflex (М1 response) increased by 65%, while an increment of the latter (supposedly polysynaptic) М2 component was 117%. When pain was induced in anatomically remote neck muscles, the stretch reflex in the biceps was considerably suppressed. The maximum amplitudes of the М1 and М2 components decreased by 25 and 30%, respectively, but the latencies of these components decreased significantly, similarly to what was observed in the case of induction of experimental pain in the biceps. Under both conditions of experimental pain, changes in the parameters of EMG responses of the forearm extensor (m. triceps brachii) demonstrated similarity with those of the biceps responses. The maximum effect of pain induction was observed within the first 5 min after injections of the hypertonic solution; full recovery of the stretch reflex parameters was observed on the 20th to 30th min. We conclude that the effects of pain induction on the reflex under study are not generalized. They depend on the site of such induction with respect to the muscle where the stretch reflex is elicited. Unidirectional effects of both types of pain on the antagonist muscles allow us to suppose that modulation of the reflex reactions upon pain induction is mediated by influences from the supraspinal CNS structures. Induction of pain in the biceps increased the amplitude of EMG manifestations of the stretch reflex, while such induction in the neck muscles decreased such responses; nonetheless, in both cases the latency of the reflexes decreased. This fact allows us to believe that the sensitivity of muscle spindles increased under both conditions of the pain influence.     

Conformational change of the triple-helical structure. IV. Kinetics of the helix-folding of (Pro-Pro-Gly)n (n = 10, 12, and 15)

The kinetic curves of the helix-refolding of (PPG)_n (n = 10, 12, and 15) were analyzed with an all-or-none model. The Arrhenius plot of the overall rate constant of the helixfolding k_F showed a negative activation energy at high temperature. With the aid of a sequential model, it was concluded that the reason for the anomaly was the instability of short helices (shorter than seven helical units in a trimeric molecule), and/or the more rapid rates of helix-folding and helix-opening for shorter helices. The rate constant of the formation of one helical unit composed of three tripeptides at an end of a long helix was calculated to be 10^2–4 sec^?1. It was much smaller than that for other kinds of helices, such as an α helix (10¹⁰ sec^?1) or a double helix of nucleic acids (10^7–9sec^?1).