Publication: Ventrolateral periaqueductal gray lesion attenuates nociception but does not change anxiety-like indices or fear-induced antinociception in mice
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Undergraduate course
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Publisher
Elsevier B.V.
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Article
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Abstract
The exposure of rodents to an open elevated plus-maze (oEPM: four open arms raised from the floor) elicits naloxone-insensitive antinociception. Midazolam infusion into the dorsal portion of the periaque-ductal gray (dPAG), a structure of the descending inhibitory system of pain, failed to alter oEPM-induced antinociception. Chemical lesion of dorsomedial and dorsolateral PAG attenuated defensive behavior in the standard EPM (sEPM), an animal model of anxiety, but failed to change oEPM-induced antinociception. The present study investigated the effects of bilateral lesion, with the injection of NMDA (N-methyl-D-aspartic acid), of the ventrolateral column of PAG (vIPAG) (i) on nociceptive response induced by 2.5% formalin injected into the right hind paw (nociception test) in mice exposed to the enclosed EPM (eEPM: four enclosed arms - a non-aversive situation) or to the oEPM and (ii) on anxiety indices in mice exposed to the sEPM without prior formalin injection. Results showed that oEPM-induced antinociception was not altered by lesion of vIPAG. Nevertheless, the lesion reduced the nociceptive response in mice exposed to the eEPM and increased general locomotor activity during the eEPM and oEPM exposure. Furthermore, vIPAG lesion did not alter anxiety-like indices in mice exposed to the sEPM. The results suggest that vIPAG does not play a role in oEPM-induced antinociception or in defensive reactions assessed in the sEPM. Moreover, vIPAG inactivation induces pain inhibition in mice not exposed to an aversive situation and seems to increase general activity. (C) 2011 Elsevier B.V. All rights reserved.
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Keywords
Anxiety, Fear, Different types of EPM, Antinociception, Formalin test, NMDA lesion, Ventrolateral periaqueductal gray, Mice
Language
English
Citation
Behavioural Brain Research. Amsterdam: Elsevier B.V., v. 219, n. 2, p. 248-253, 2011.
