Neural Mechanisms of Play

Author(s): Pellis, S.M., Iwaniuk, A.N.
NIFP Rating: 7

Recent studies have shown that contrary to expectation, larger-brained species within mammalian orders are not more likely to engage in play. This is true for juvenile rodents, juvenile marsupials and adult primates. Neither does the relative size of the neocortex predict the prevalence of play in species of marsupials and primates. Two methodological limitations may […]

Author(s): Kisko, T.M., Braun, M.D., Michels, S., Witt, S.H., Rietschel, M., Culmsee, C., Schwarting, R.K.W., Wˆhr, M.
NIFP Rating: 6

As cross-disorder risk gene, CACNA1C is implicated in the etiology of all major neuropsychiatric disorders characterized by deficits in social behavior and communication and there is evidence for sex-dependent influences of single-nucleotide polymorphisms within CACNA1C on diagnosis, course, and recovery in humans. In this study, we aimed, therefore, at further exploring the role of Cacna1c […]

Author(s): Kamitakahara, H., Monfils, M.-H., Forgie, M.L., Kolb, B., Pellis, S.M.
NIFP Rating: 6

The cortex is not necessary for rats to engage in play fighting, but it is necessary for them to modify their pattern of play fighting in different contexts. Two experiments were conducted to determine the role of the motor cortex (MC). Rats with bilateral ablations of the MC performed on Postnatal Day 10 failed to […]

Author(s): Field, E.F., Whishaw, I.Q., Pellis, S.M., Watson, N.V.
NIFP Rating: 6

The frequency of playful attack and the style of playful defense, are modifiable by gonadal steroids and change after puberty in male and female rats. The present study examined the play behavior exhibited by testicular feminized mutation (tfm)-affected males, who are insensitive to androgens but can bind estrogens aromatized from androgens, to determine the relative […]

Author(s): Daftary, S.S., J. Panksepp, Dong, Y., Saal, D.B.
NIFP Rating: 4

Stress facilitates development of addictive behaviors in part by stress-induced increase in the strength of glutamatergic synapses at dopamine (DA) neurons within the ventral tegmental area (VTA). Here, we further demonstrate that this stress-induced synaptic adaptation is glucocorticoid-dependent and is progressively developed. Activation of glucocorticoid receptors (GRs) either by in vivo injection of dexamethasone (Dex) […]

Author(s): J. Burgdorf, J. Panksepp, M.C. Beinfeld, R.A. Kroes, J.R. Moskal
NIFP Rating: 4

Brain cholecystokinin (CCK) levels have been shown to be elevated in animals defeated during adult social aggression. The present experiment evaluated whether similar effects are evident in prolonged bouts of juvenile social-play fighting, which tend to switch from largely positive to some negative affect after approximately 15 min into a half-hour play session, as indexed […]

Author(s): Himmler, B.T., Kisko, T.M., Euston, D.R., Kolb, B., Pellis, S.M.
NIFP Rating: 4

During playful interactions, rats emit increased levels of 50-kHz vocalizations. It is possible that these vocalizations are used as play signals that promote and maintain playful contact. The study investigated this possibility. It was predicted that if these vocalizations are used as play signals, they should be more prevalent (1) before an attack, (2) in […]

Author(s): Gartstein, M.A., Bridgett, D.J., Young, B.N., J. Panksepp, Power, T.
NIFP Rating: 3

Effortful control (EC) refers to the ability to inhibit a dominant response to perform a subdominant one and has been shown as protective against a myriad of difficulties. Research examining precursors of EC has been limited to date, and in this study, infancy contributors to toddler EC were examined. Specifically, parent/family background variables (e.g., education, […]

Author(s): Dyck, A.C.F., Ivanco, T.L.
NIFP Rating: 3

Purpose: Young children have a high risk of concussion or mild traumatic brain injury (mTBI). Children often appear healthy soon after mTBI, but some have pervasive cognitive and/or motor impairments. Understanding underlying mechanisms recruited after concussion may help for return to play protocols and mitigating what might be lifelong impairments. Methods: We investigated molecular and […]

Author(s): Pellis, S.M., Hastings, E., Shimizu, T., Kamitakahara, H., Komorowska, J., Forgie, M.L., Kolb, B.
NIFP Rating: 3

In a series of 3 experiments on rats, 2 hypotheses were tested: (a) that damage to the orbital frontal cortex (OFC) would alter the socially relevant context for executing defensive responses but not their performance and (b) that damage done to the OFC in early infancy would produce more deficits in social behavior than similar […]

Author(s): Farinelli, M., J. Panksepp, Gestieri, L., Maffei, M., Agati, R., Cevolani, D., Pedone, V., Northoff, G.
NIFP Rating: 2

The aim of the current study was to investigate basic emotions and attachment in a sample of 86 stroke patients. We included a control group of 115 orthopedic patients (matched for age and cognitive status) without brain lesions to control for unspecific general illness effects of a traumatic recent event on basic emotions and attachment. […]

Author(s): Pellis, S.M., de laCruz, F., Pellis, V.C., Teitelbaum, P.
NIFP Rating: 2

Although cataleptic rats do not spontaneously orient, scan, or walk, they will cling, stand, right themselves in the air, and resist being displaced from a stable position (Schallert, Whishaw, De Ryck, & Teitelbaum, 1978). Morphine produces a state of immobility in which all reflexes used for stable static support (e.g., standing, righting, clinging, and bracing) […]

Author(s): Palagi, E., Norscia, I., Pressi, S., Cordoni, G.
NIFP Rating: 7

play fighting, a common form of mammalian play, can escalate into aggression if playful motivation is misinterpreted and not shared by players. In primates, playful facial expressions and mimicry can be performed to signal and share playful motivation. Here we compare play facial expressions (play face [PF]: lower teeth exposed; full play face [FPF]: upper […]

Author(s): Smith, L.K., Field, E.F., Forgie, M.L., Pellis, S.M.
NIFP Rating: 2

The play fighting behaviour of male rats (Rattus norvegicus) castrated at weaning was compared to that of intact controls during the juvenile and post-pubertal phases of development. Following puberty, both the castrated and intact animals exhibited an age-related change in their play fighting; the frequency of initiating play fighting decreased and juvenile patterns of playful […]

Author(s): Pellis, Sergio, Pellis, Vivien
NIFP Rating: 9

Rough-and-tumble play, also called play fighting, is a form of play in which partners compete with one another to gain some advantage (e.g., strike, bite, push onto ground), but do so without the severity or consequences of serious fighting, which it resembles (Aldis, 1975). Play fighting is one of the most commonly reported forms of […]

Author(s): J. Panksepp
NIFP Rating: 8

Free play, in which children develop their own activities, including rough-and-tumble activities that, as the term play implies, involves physical activity such as running, jumping, play fighting, and wrestling, are increasingly recognized as essential components of a child’s development. Both human and animal studies have provided evidence that periods of play improve social skills, impulse […]

Author(s): Iwaniuk, A.N., Pellis, S.M., Whishaw, I.Q.
NIFP Rating: 2

Using a data set of 69 different mammalian species, Heffner and Masterton propose that the longer and deeper the fibres of the corticospinal tract, the greater an animal’s digital dexterity. Because of the effects that phylogeny may have upon the extant phenotype of a given species, however, data from a wide range of species can […]

Author(s): Deak, T., J. Panksepp
NIFP Rating: 1

Play behavior was assessed in juvenile rat pups following chronic administration of scopolamine (0.5 or 1.0 mg/kg, i.p.) to one partner in each dyad of rats. Scopolamine administration significantly reduced the number of pins and mean pin duration of both playmates in pairs where only one rat was injected with scopolamine (irrespective of dose). However, […]

Author(s): Groeneweg, F.L., Trattnig, C., Kuhse, J., Nawrotzki, R.A., Kirsch, J.
NIFP Rating: 1

Scaffolding proteins underlying postsynaptic membrane specializations are important structural and functional components of both excitatory and inhibitory synapses. At inhibitory synapses, gephyrin was identified as anchoring protein. Gephyrin self-assembles into a complex flat submembranous lattice that slows the lateral mobility of glycine and GABAA receptors, thus allowing for their clustering at postsynaptic sites. The structure […]

Author(s): Pellis, S.M., Pellis, V.C., Iwaniuk, A.N.
NIFP Rating: 2

Even though behavior tends to occur as a continuous stream of action in most situations, there are discernible regularities that lead observers to label and measure discrete “behavior patterns. ” Yet such discrete actions may not be how the nervous system organizes motor output. Sometimes, the perceived regularities are emergent properties of the interaction among […]

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