期刊
NEUROSCIENCE
卷 235, 期 -, 页码 10-15出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2013.01.005
关键词
A-fibers; cerebral ischemia; LPA(1) receptor; neuropathic pain
资金
- Ministry of Education, Culture, Sports, Science and Technology (MEXT)
- Health and Labor Sciences Research Grants on Research from the Ministry of Health, Labor and Welfare
We demonstrated previously that the lysophosphatidic acid-1 (LPA(1)) receptor plays a crucial role in the. initiation of peripheral nerve injury-induced neuropathic pain through the alternation of pain-related genes/proteins expression and demyelination. The present study revealed that mild cerebral ischemia by left transient middle cerebral artery occlusion (tMCAO) for 15 min causes the hypersensitive responses (paw withdrawal) to the nociception by electrical stimuli to the paw by the use of Neurometer Current Perception Threshold/C (CPT/C). The hypersensitivity or neuropathic pain was only observed by the stimulation with 250 and 2000, but not 5 Hz, which are the characterized sine-wave frequencies of A delta-, A beta- or C-fibers, respectively. The significant neuropathic pain was observed from day 2 through week 2 on the right paw after tMCAO, while there was slight but significant pain sensitivity on the left paw at day 7. The neuropathic pain on the contralateral side at week 2 after tMCAO was completely abolished in LPA(1)(-/-) mice. These results suggest that LPA(1) receptor signaling plays key roles in the development of central neuropathic pain following cerebral ischemia as well as the peripheral neuropathic pain following partial sciatic nerve injury. (C) 2013 IBRO. Published by Elsevier Ltd. All rights reserved.
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