Brain research
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Considering the importance of a deeper understanding of the effect throughout life of opioid analgesia at birth, our objective was to determine whether morphine administration in early life, once a day for 7 days in 8-day-old rats, alters the nociceptive response over the short (P16), medium (P30), and long term (P60) and to evaluate which system is involved in the altered nociceptive response. The nociceptive responses were assessed by the formalin test, and the behavior analyzed was the total time spent in biting and flicking of the formalin-injected hindpaw, recorded during the first 5 min (phase I) and from 15-30 min (phase II). The morphine group showed no change in nociceptive response at P16, but at P30 and P60, the nociceptive response was increased in phase I, and in both phases, respectively. ⋯ These results indicate that early morphine exposure causes an increase in the nociceptive response in adult life. It is possible that this lower nociception threshold is due to neuroadaptations in nociceptive circuits, such as the glutamatergic system. Thus, this work demonstrates the importance of evaluating clinical consequences related to early opioid administration and suggests a need for a novel design of agents that may counteract opiate-induced neuroplastic changes.
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Endoplasmic reticulum (ER) stress has been implicated in the pathology of cerebral ischemia. During prolonged period of stress or when the adaptive response fails, apoptotic cell death ensues. Cerebral ischemic postconditioning (Postcond) has been shown to reduce cerebral ischemia/reperfusion (I/R) injury in both focal and global cerebral ischemia model. ⋯ LY294002, a phosphoinositide 3-kinase inhibitor, increased the number of TUNEL-positive cells suppressed by Postcond in penumbra. In addition, LY294002 diminished the effect of Postcond on the activation of CHOP, caspase-12 and GRP78. These results suggest that Postcond protects brain from I/R injury by suppressing ER stress-induced apoptosis and PI3K/Akt pathway is involved.
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We used rapid event-related fMRI to explore factors modulating the activation of orthographic and phonological representations of print during a visual lexical decision task. Stimuli included homophonous word and nonword stimuli (MAID, BRANE), which have been shown behaviorally to produce longer response times due to phonological mediation effects. We also manipulated participants' reliance on orthography by varying the extent to which nonword foils were orthographically typical (wordlike context) or atypical (non-wordlike context) of real words. ⋯ Homophonous effects in the non-wordlike context were primarily isolated to medial extrastriate regions, hypothesized to be involved in low level visual processing and not reading-related processing per se. These findings demonstrate that the degree to which phonological and orthographic representations of print are activated depends not only on homophony, but also on the word-likeness of nonword stimuli. Implications for models of visual word recognition are discussed.