Further developments in neurobiological research, including lesion and brain imaging studies, have established a clearer view of the functional neuroanatomy of REM sleep and dreaming. To what degree, and in what way, implications can be drawn from these findings for the psychology of dreaming is controversial. Human regional cerebral blood flow during rapid eye movement sleep. Simes CA, Valle AC, Timo-Iaria C. Correlation between concomitant theta waves in nucleus reticularis pontis oralis and in the hippocampus, thalamus and neocortex during dreaming in rats. Ergebn. In rats, heart rate is clearly accelerated during the periods of oniric activity, expressed as rostrum+vibrissae, eye, head, ear and limb movements. Electroencephal Clin Neurophysiol 1987;66:383-90. Dreaming has been a subject of cogitation since remote Antiquity. Roffwarg HP, Herman J, Lamstein S. The middle ear muscles: predictability of their phasic action in REM sleep from dream recall. Baldissera F, Broggi G. An analysis of potential changes in the spinal cord during desynchronized sleep. Miyauchi S, Takino R, Fukuda H, Torii S. Electrophysiological evidence for dreaming. News Physiol Sci 1998;13:91-7. Moruzzi G. The sleep-wakefulness cycle. It seems that not only humans but also dogs, cows, sheep and goats and the entire family of four-legged viviparous animals do dream. Clipboard, Search History, and several other advanced features are temporarily unavailable. Electrophysiological manifestations of wakefulness and desynchronized sleep in the rat. Foulkes D. Children's dreams. WebDreams are still taken by a majority of the human kind as premonitory, ascribing them the function of telling us that something important will happen. Stimulus response theory of dream: The stimulus response theory which existed prior to Freud is based upon the associationistic stimulus response view. This theory stresses the relationship between brain changes during sleep and changes in perceptual efficiency. Some disturbing stimuli force activity into one portion of the cerebral cortex. 54. These patients are not able to produce visual reminiscences, which may be explained by the fact that visual information is permanently kept in the visual cortex. 98. Hernndez-Pen R. A neurophysiologic model of dreams and hallucinations. This author "thus proposes a psychoanalytical model of dreaming, in which dreams constitute a way of representing the individual's inner world with internal objects related with one another and with the self" (135). The atonia of myoclonia of active (REM) sleep. Brain Res 1967;6:706-15. However, reflex penile erection is facilitated after spinal transection whereas mesencephalic transections significantly increase the latency to its reflex induction, without affecting the percentage of tests eliciting an erectile event. 25. In cats, cortical electro-oscillograms are also desynchronized but in the hippocampus theta waves (that will be later described) predominate. No wonder that most dreams in humans have a visual component, explaining the reason why eye movements occur in any kind of dream, alone or as part of non-visual dreams. Brain Develop 1994;16:81-91. Brainstem mechanisms of slow-wave sleep and REM sleep. Activity of the red nucleus during deep, desynchronized sleep in the unrestrained cat. Schmidek WR, Hoshino K, Schmidek M, Timo-Iaria C. Influence of environmental temperature on the sleep-wakefulness cycle in the rat. It is most likely an elementary brain activity in homeotherms and thus, if dreaming has a function, it probably plays a similar role in the human brain and in nonhuman brains as well. Oswald I. Brainstem control of the events of REM sleep. There are two kinds of vegetative components: 1. Such a recovery means that other mechanisms are put into action that are able to generate not only wakefulness but desynchronized sleep as well. Springer Verlag, Frankfurt 1953. Narcolepsy. 42. Weed & Halam listed in 1896 (4,7) the proportion of several kinds of dreams as related to their sensory content. 104. Later, school and work dominate the mental field and the main features in dreams also change accordingly, supporting this hypothesis. 14. Rapid increase of an immediate early gene messenger RNA in hippocampal neurons by synaptic NMDA receptor activation. C R S Soc Biol 1978;172:9-21. Brainstem Control of Wakefulness and Sleep. Doneshka P, Kehaiyov A. Desynchronization is the rule, during this phase, in all cortical electro-oscillograms in humans and other primates. 4. J Neurophysiol 1938;1:413-30. & Ajmone-Marsan, C. 12. (eds. Such patterns mimic oniric eye movements, which may occur in functional coincidence or not with the visual scenes that are dreamed of. Decety J, Jeannerod M, Durozard DR, Baveal J. This may be related to the presence of pet animals in most families in the Western countries and consequently this "subject" probably becomes the main thought of children. government site. Two major theories have been proposed regarding the neural circuits involved in dreaming. Accordingly, they are known as PGO (pontine, occipital cortex and lateral geniculate nucleus) potentials. 82. Mol Brain Sci 1995;32:211-20. 99. Those that are common to all behaviors (increase in heart rate, blood pressure, blood flow to the nervous system and muscles, ventilation, pupil diameter and palmar and plantar electrical conductance) and are intended to increase the supply of blood, oxygen, glucose etc. 128. In humans, Hansotia and colleagues (34) found in humans, in accordance with our own observations in rats and cats, that oniric eye movements may be directed to one side or the other, not exclusively to one side, as stated by Vanni-Mercier and co-workers (29). Predicting Intention to Participate in Community Physical Activities for Adults with Physical Disabilities. During a visual dream the eyes move (Figure 3) whereas during an auditory dream the middle ear ossicles (stapedius and tensor tympani) are activated (Figure 4). The result of such conscious identification is a dream. official website and that any information you provide is encrypted Exp Brain Res 1989;74:11-23. In fact, all the phases of wakefulness and sleep, including desynchronized sleep, occur in the cerebellar cortex. Those that are specific to certain behaviors. Arch Ital Biol 1965;103:369-96. Curr Opin Neurobiol 1992;2:759-63. 52. In 1937, Fenn & Bursh, recording the eye movements while their subjects closed and opened the eyes, found that the voltage (V) of the potentials that expressed the movements were proportional to the angle of rotation [V=k.2.sen] in which V is the voltage of the recorded potentials, k is a factor of proportionality and is the angle of rotation (28). Often eye movements are preceded in the electroencephalogram by small sawthoot-waves that superimpose on desynchronized potentials (figure 3). Considering that desynchronization is predominant all over the cortex in humans and in the frontal cortex of both cats and rats, we consider it to be a phylogenetically more recent functional acquisition. Recently a more acceptable evidence in favor of the consolidation hypothesis arises from the study of a gene involved in neuronal activation This gene protein, zif-268 (98), binds to a specific DNA molecule present in the promoters of a variety of genes expressed in the nervous system (99) and its up-regulation is thought to initiate a program of gene regulation leading to neuronal plasticity (100). 89. Differentiating Oneiric Stupor in Agrypnia Excitata From Dreaming Disorders. By visually examining the amplitude of theta waves in these examples it seems they vary at random but when the instant variation of voltage is plotted as a function of time, a regular variation appears during the phasic movements (figure 10). (ed. As shown in figure 11, comparison of the instant voltage of theta waves among several regions of the brain shows that the correlation coefficient (r) may be very high. Dreams during REM sleep tend to be longer, more vivid, more story-like, and more bizarre than those during NREM sleep. yet, it is well known since Kohlschtter and Michelson (4,8) that the threshold to awaken a human being during desynchronized sleep is much lower than the one to produce wakefulness during synchronized sleep. Braz J Med Biol Res 1996;29:1645-50. J Neurosci 1995;15:3500-8. Steriade M, McCarley RW. Vanni-Mercier and co-workers (1994) believe, however, that in cats eye movements during desynchronized sleep are in general asymmetric, that is, the eyes tend to move preferentially to one side of the visual field, what, according to these authors, disprove the hypothesis of the scanning character of eye movements during dreams (29). It is thus not surprising that during dreaming activity in rats both rostrum and vibrissae move preponderantly, probably because most of their dreams contain olfactory and snout tactile components. Perspective of Motor Behavior and its Neural Basis. Webikea satsumas plant stand; how do i pair my schwinn bluetooth; meter reading crossword clue; May 14 2022; Uncategorized; what is the physiological function theory of dreams WebHe says the function of dreams is that by reproducing difficult or unsolved life situations or experiences, the dream aids towards a solving or resolution of the problems. activation-synthesis. In rats we have recorded ear movements in paradoxical sleep, which we attribute to the occurrence of auditory dreams (see Figure 9). Arch Ital Biol 1969;107:175-216. Marini G. Motor phenomena during sleep. Gottesman C, Gandolfo G, Zernicki B. Kuboyama T, Hori A, Sato T, Mikami T, yamaki T, Ueda S. Changes in cerebral blood flow velocity in healthy young men during overnight sleep and while awake.Electroencephalogr Clin Neurophysiol 1997;102:125-31. (eds.) Gardner Jr R, Grossman WI, Roffwarg HP, Weiner H. The relationship of small limb movements during REM sleep to dreamed limb action. Such movements may take the sleeper to fall off the bed. Selective deactivation of the dorsolateral prefrontal cortex has been found in desynchronized sleep. Energy conservation theory posits that the main function of sleep is to reduce a person's energy demand during part of the day and night when it is least efficient to hunt for food. Physiol Rev 1967;47:117-77. Gassel MM, Marchiafava PL, Pompeiano O. General Learning Press, 1970. Studi Psicologici e Clinici di un Alienista. In: Klemm, W. R. & Vertes, R. P. When a dream is a nightmare, both motor and vegetative events may be very intense. Our experience with eye movements in rats (30-32) and cats (33) shows, however, that eye movements are sometimes asymmetric but in other occasions they tend to be of the scanning kind. C R Soc Biol (Paris) 1938;128:533-9. Behav Brain Sci 2000;23:1008-9. Changes in hippocampal gene expression associated with the induction of long-term potentiation. 30. In 1867, Michelson, a physiologist who was a relative to Kohlschtter, replicated his study and obtained the curve shown in figure 1 (4,8). Figure 6 shows an increase in heart rate from 150 bpm to 180 bpm (the latter is the normal heart rate during resting wakefulness in this species), coinciding with the peak of eye movements. Hansotia P, Broste S, Ruggles K, Wall R, Friske M. Eye movement patterns in REM sleep. Maquet P, Peters JM, Aerts J, Delfiore G, Degueldre C, Luxen A, et al. During this bright period of the Middle Ages some physicians also reasoned about dreams. WebEssentially, during sleep the mind integrates new information acquired during the previous day into memory and processes it by making necessary connections. Phenomenal dream content, however, is not as disorganized as such views imply. Advances in Sleep Research, vol. Science 1994;265:676-9. The authors suggest that such a disturbance of reproduction occurs because desynchronized sleep (and consequently dreaming) was prevented to occur normally in infancy but the functional meaning of this interesting phenomenon. ), Brainstem Mechanisms of Behavior. Kohyama J, Shimomira M, Iwakawa y. Brainstem control of phasic mucsle activity during REM sleep: a review and hypothesis. Animal experimentation, by making it possible to implant electrodes in any part of the nervous system and to lesion and stimulate (electrically or chemically) also any nucleus or pathway, has been of the utmost relevance for the understanding of the mechanisms causing not only sleep but also the manifestations of dreaming. Absence of ponto-geniculo-occipital (PGO) spikes in rats. 133. (eds.) In cats, tympanic muscles sometimes contract during desynchronized sleep (38), as shown in Figure 4. Instead, they thought that dreams were not provoked by spirits, ghosts or gods, which took over the mind to express themselves through dreaming. Later, theta waves were also found in rats during both attentive wakefulness and desynchronized sleep (19,30,31,74-76). These findings point to a decreased activation of executive and association cortex during desynchronized sleep, what is suggestive that the processes involved in building up wakeful thought and dreaming may be distinct. To discuss this issue we will concentrate only on a few hypotheses. In rats subjected to early desynchronized sleep deprivation, ejaculation was deeply reduced in adulthood (114,115), what is a profound impairment of a very important instinctive behavior. The very essence of dreams is, certainly, memorized information. Spreng LF, Johnson LC, Lubin A. Autonomic correlates of eye movement bursts during state REM sleep. Experientia 1964;20:1-3. 65. 2009 Nov;10(11):803-13. doi: 10.1038/nrn2716. Experimental methodologies permitted investigation of the responsiveness of dreams to external stimulation and the effects of deprivation of REM sleep. The data reported in table 1 reflect a close distribution of the dream content as related to their sensory content. We spend a lot of time sleeping. It is likely that even strong stimuli may be ineffective in producing an arousal during sleep if they are trivial, whereas light stimulation containing relevant information may be highly efficient. In 1896 Weed & Halam (4) published the first quantification of dreams content. 51. Movements of the eyes when the lids are closed. Cien Cult 1995;47:221-34. It would appear that the intense activation of desynchronized sleep must overcome this demodulation and persist into subsequent waking, in order for very vivid dreams to be remembered. Considering that most dreams in rats (31,32) are related to olfaction, not to vision, potentials that resemble PGOs in the amygdala of this animal species should also be taken as signs of dreaming rather than PGOs. 24. Electroencephal Clin Neurophysiol 1955:673-690. By lesioning the alphacoeruleus nuclei such an inhibitory effect is prevented and during oniric activity the movements generated by the dream itself can be expressed, as was clearly demonstrated in Jouvet's Laboratory (50,51) in cats; the animal suddenly gets up, walks, miews and strikes with the paws, as if the animal were awake. However, we still do not know why most motor units are inactivated while a few ones are mobilized, causing real but incoherent and non-efficient movements. Kohyama T, Hori A, Sato T, Nikami T, yamaki T, Veda S. Changes in cerebral blood flow velocity in healthy young men during overnight sleep and while awake. Shiromani PJ, Lai yy, Siegel JM. The PGO potentials are correlates of dreams. 92. In 1986 Vertes advanced the hypothesis that random endogenous activation of the brain stem (dreaming?) 69. Theta waves, discovered by Jung and Kornmller in 1938 (72), were extensively studied by Green & Arduini (73), who proved they are related to arousal. Aristotle. A direct pathway arising in the region of the coeruleus complex that projects to the bulbar medial reticular formation was described by Magoun & Rhines (1946) and does heavily inhibit motoneurons (49). One is that dreams are generated by the activation of neural activity in the brainstem and its signal transmission to the cortex. World Fed Sleep Res Soc Newsletter 1997;5:22-3. Temporal patterns of discharges of pyramidal tract neurons during sleep and waking in the monkey. Karger, Basel, 1997:65-76. C R Soc Biol (Paris) 1959;153:1024-8. This hyperpolarization is due to an increased motoneuronal membrane permeability to chloride ions, which suggests that glycine or -GABA are released on the motoneuronal membrane during desynchronized sleep (44). In 1944 Obhlmeyer, Brilmayer & Uhlstrung (10) observed that in humans penile erection occurs during sleep at intervals of 85 minutes, which is the average duration of a sleep cycle. Researchers working on dream usually do not believe that dreaming may occur in non-human animals, probably due to religious and philosophical reasons but also to a great mistake, i.e., that dreaming is a high level mental activity, such as doing mathematics, but it is not. Different effects of several brain areas may affect dreaming in different ways. Inasmuch as rats do not tell us their dreams, we inferred the kinds of dreams by considering the patterns of movements the animals performed. Longitudinal studies. "Dreams are not ghosts (phantasmata), since they are closely related to the events of the previous day". Science 1987;238:797-9. No PGO potentials have been found in rats (70). Brain activity during this time keeps us functioning and ready to process information when we wake up the next morning! Erlbaum, 1992. Visual dreams provoke eye movements. However, psychoanalysts take into account only a few dreams that are occasionally recalled, despite the fact that we dream four or five episodes every night, what means that the fraction of dreams we can recall is a small portion of what we in fact do experience as dreams. Valle AC, Timo-Iaria C, Sameshima K, yamashita R. Theta waves and behavioral manifestations of alertness and dreaming activity in the rat. What is the Braz J Med Biol Res 1990;23:617-20. We found that, in the average, during attentive wakefulness heart rate is nearly 320 bpm; in synchronized sleep it decreases to 244 bpm and during phasic movements that unveil oniric activity it increases again. C R Soc Biol (Paris) 1969;163:181-6. Such electrophysiological studies demonstrate that the abovementioned sites in the central nervous system are involved in the oniric movements but they do not prove that such structures generate them. Deprivation of desynchronized sleep during early development not only retards brain maturation but also inhibits the growth response to the brain environmental stimulation later in life (113). The narrower is the angle of rotation, the lower is the recorded potential, which happens when attention is being directed to a very small part of the object or when the object is very near. As pointed Roberts LA, Higgins MJ, O'Shaughnessy CT, Stone TW, Morris BJ. Hodes R, Dement WC. Revonsuo A. Baldissera F, Cesa-Bianchi MG, Mancia M. Spinal reflexes in normal and unrestrained cats during sleep and wakefulness. The first oscillation lasts around two hours, when sleep attains its deepest level; the ensuing cycles last less and their depth tends to decrease until arousal finally occurs, a sequence that recent research has fully confirmed. 49. Cravo SLD, Lopes OU, Fraga CAB, Timo-Iaria C. Cardiovascular adjustments to noxious stimulation in decerebrate cats. When a dream has a verbal content the tongue, lips and other facial muscles do contract and if the dream is deambulatory several lower limb muscles do contract, expressing the behavior triggered by the imagined walking. Physiology and Psychology. Exptl Neurol 1963;8:93-111. The tonic inhibition of motoneurons by circuits in the alphacoeruleus nucleus during desynchronized sleep is mediated by hyperpolarization of their membrane (41-43). Heart rate decreases down to nearly 150 bpm 1 or 2 seconds following the cessation of eye movements. Brooks DC, Bizzi E. Brain stem electrical activity during deep sleep. 114. As stated above, any behavior is expressed as a combination of motor components and vegetative components. According to this impossible hypothesis, during desynchronized sleep, in which the brain is rather isolated from its normal input/output, a non-specific endogenous activation in the brain stem is probably responsible for the reverse learning. WebDream theories developed by Freud suggest that dreams are psychological, revealing hidden urges, for example. 74. J Sleep Res 1993;2:63-9. World Fed Sleep Res Soc Newsletter 1997;5:20-1. New findings on the neurological organization of dreaming: implications for psychoanalysis. Neurosc Biobehav Rev 1992;16:372-97. 135. Forebrain activation in REM sleep: an FDG, PET study. Mancia M. One possible function of sleep: to produce dreams. Vogel GW, Foulkes D, Trosman H. Ego functions and dreaming during sleep onset. A dream is a conscious experience that occurs during sleep. It has been proposed (120,123,124) that presleep mentation is infrequently incorporated in top dreams and that "naturalistic" day time events rarely enter dream content, but several authors correlated dream content to the previous day events, starting with Aristotle 2,400 years ago and with Calkins in 1893. Regional cerebral blood flow throughout the sleep-cyle an (H2O)-O-15 PET study. In humans, equivalent potentials can be recorded from the occipital cortex. Possible role for the transcription factor zif268/egr-1, polyoma enhancer activator 3, and AP2. Eye movements in humans predominate because vision is our main sensory channel and our visual memory is overwhelmingly predominant, resulting in preponderance of visual dreams. Such hypothesis is grounded on the following steps. Neuroscience 1997;78:13-38. It may be more appropriate to explain the latter authors' results by reasoning that dreams are originated in memorized information and are, accordingly, closely related to events occurring before sleep. During oniric activity, however, phasic increases in heart rate, blood pressure and ventilation do occur that are closely related to the dream that is going on. On Sleep and Dreams. Sigmund Freuds theory of dreams suggests that dreams represent unconscious desires, thoughts, wish fulfillment, and motivations. During normal walking the tibialis anterior and the gastrocnemius muscles are mobilized in opposition but when they contract as part of a dream their contraction may be in opposition (in some periods), what happens in normal deambulatory movements, or simultaneous (in subsequent or preceding periods), which does not occur in normal deambulation. 10. Such high values of r may mean that theta waves arrive in such areas almost synchronously, coming from some other sites in the central nervous system. For instance, during desynchronized sleep theta waves, in rats, are highly coherent in nucleus reticularis pontis oralis and in the fronto-parietal cortex, as well as with the hippocampus (78). Unable to load your collection due to an error, Unable to load your delegates due to an error. Hypotheses attributing a function to dreams tend to invoke reasons not well founded and in some cases they are rather fancy or even mystic. 102. If, as an advantage, in humans such manifestations of dreams can be related to their reported content, in non-human animals it is possible to record with a high degree of accuracy not only the motor and the vegetative manifestations of dremaing but the electro-oscillograms of many central structures as well. Figure 9 illustrates an episode of olfactory and vibrissal movements. If we dream we are walking, the electromyographic recordings from muscles involved in such behavior show quite clearly that they are not able to produce normal movements. Santos LM, Valle AC, Sameshima K, Silva MTP, Timo-Iaria C. A linear relationship between theta waves frequency and the speed of learning in rats. WebPhysiological function Theory regular brain stimulation from REM sleep may help develop and preserve neural pathways. 93. Accessibility Hobson JA, Pace-Schott EF, Stickgold R. Dreaming and the brain: toward a cognitive neuroscience of conscious states. Functional neuroanatomy of human rapid-eye-movement sleep and dreaming. Wallace CS, Withers GS, George VM, Clayton OF, Greenough WT. Unless we agree that such movements in human and in non-human animals are manifestations of dreaming activity, it is impossible to explain the electro-oscillograms and the movements that both classes of animals exhibit during desynchronized sleep. Timo-Iaria C. Early research on dreaming. Axons from neurons of the nucleus reticularis gigantocellularis descend along the ventral and ventrolateral funiculi and connect with inhibitory interneurons in the spinal cord (55,56). Foulkes D. A cognitive-psychological model of REM dream production. Therefore, theta waves undergo both AM and FM changes that certainly carry some kind of information that may prove in the future to be crucial for understanding dreams. 1996 Sep 12;383(6596):163-6. doi: 10.1038/383163a0. Psychophysiology 1968;4:311-23. According to this author, in children at the age of two, when the hippocampus, which is still in the process of development at birth, becomes functional, REM sleep takes on its interpretive memory function (134). 68. Descending projections from the dorsolateral pontine tegmentum to the paramedian reticular nucleus of the caudal medulla in the cat. Functional neuroanatomy of human rapid-eye-movement sleep and dreaming. Moruzzi G. Action inhibitrice du palocervelet sur les reflexes circulatoires et respiratoires d'origine sino-carotidinne. Physiol Behav 1972;8:363-71. Moruzzi G. Active processes in the brain stem during sleep. 115. Expt Neurol 1976;53:328-38. Unauthorized use of these marks is strictly prohibited. 66. J Neurophysiol 1964;27:152-71. Aserinsky E, Kleitman N. Regularly occurring periods of eye motility and concomitant phenomena during sleep. They also argue that even "expensive and cumbersome evoked potential and computer averaging approaches have not helped us to analyze and compare desynchronized sleep physiology with that of waking in an effective way". (eds.) 13 Loomis AL, Harvey DN, Hobart GA. Distribution of disturbance patterns in the human electroencephalogram, with special reference to sleep. Petersohn D, Schoch S, Brinkmann DR, Thiel G. The human synapsin II gene promoter. Harvey Lect 1963;58:233-97. The Neuropsychology of Sleep and Dreaming. 127. 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