TY - JOUR
T1 - Role of the NLRP3 inflammasome in a model of acute burn-induced pain
AU - Deuis, Jennifer R.
AU - Yin, Kathleen
AU - Cooper, Matthew A.
AU - Schroder, Kate
AU - Vetter, Irina
PY - 2017/3/1
Y1 - 2017/3/1
N2 - The NLRP3 inflammasome is a multi-protein complex that assembles in response to tissue damage or infection, triggering activation of caspase-1, an enzyme that converts interleukin (IL)-1β into its active form. A role for the NLRP3 inflammasome is emerging in inflammatory pain, but its influence in other pain types is largely unexamined. Therefore the aim of this study was to assess the role of the NLRP3 inflammasome and its downstream product caspase-1 in a model of acute burn-induced pain in male mice. A superficial burn was induced on the plantar surface of the left hind paw using a hot plate set at 52.5 °C for 25 s. Development of burn-induced mechanical allodynia, thermal allodynia, edema and weight bearing changes was assessed in Nlrp3−/− and caspase-1-deficient (Ice−/−) mice, and in mice administered the selective NLRP3 inflammasome inhibitor MCC950. Burn-induced mechanical and thermal allodynia developed normally in Nlrp3−/− and Ice−/− mice and mice administered MCC950. Burn-induced edema was significantly reduced in Ice−/− mice only. Burn-induced weight bearing changes were attenuated in Nlrp3−/− mice and mice administered MCC950 72 h after burn only. This study suggests that NLRP3 and its downstream product caspase-1 have a limited role in the development of burn-induced pain.
AB - The NLRP3 inflammasome is a multi-protein complex that assembles in response to tissue damage or infection, triggering activation of caspase-1, an enzyme that converts interleukin (IL)-1β into its active form. A role for the NLRP3 inflammasome is emerging in inflammatory pain, but its influence in other pain types is largely unexamined. Therefore the aim of this study was to assess the role of the NLRP3 inflammasome and its downstream product caspase-1 in a model of acute burn-induced pain in male mice. A superficial burn was induced on the plantar surface of the left hind paw using a hot plate set at 52.5 °C for 25 s. Development of burn-induced mechanical allodynia, thermal allodynia, edema and weight bearing changes was assessed in Nlrp3−/− and caspase-1-deficient (Ice−/−) mice, and in mice administered the selective NLRP3 inflammasome inhibitor MCC950. Burn-induced mechanical and thermal allodynia developed normally in Nlrp3−/− and Ice−/− mice and mice administered MCC950. Burn-induced edema was significantly reduced in Ice−/− mice only. Burn-induced weight bearing changes were attenuated in Nlrp3−/− mice and mice administered MCC950 72 h after burn only. This study suggests that NLRP3 and its downstream product caspase-1 have a limited role in the development of burn-induced pain.
KW - NLRP3 inflammasome
KW - caspase-1
KW - interleukin-1β
KW - burns
KW - mouse model
KW - pain
UR - http://www.scopus.com/inward/record.url?scp=85009266866&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/arc/FT130101215
UR - http://purl.org/au-research/grants/arc/FT130100361
UR - http://purl.org/au-research/grants/nhmrc/1059354
U2 - 10.1016/j.burns.2016.09.001
DO - 10.1016/j.burns.2016.09.001
M3 - Article
C2 - 28040362
AN - SCOPUS:85009266866
SN - 0305-4179
VL - 43
SP - 304
EP - 309
JO - Burns
JF - Burns
IS - 2
ER -