P 2 Y 2 Receptors Mediate Masseter Muscle Mechanical Hypersensitivity in Rats
P Y receptors (P Y Rs) are among the various receptors that play an important role in nociception. The goal of this research was to investigate possible P Y R expression changes in the trigeminal ganglion (TRG) in bilateral masseter muscle (MM) hypersensitivity following unilateral MM inflammation....
Saved in:
Published in | Journal of pain research Vol. 13; pp. 1323 - 1333 |
---|---|
Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
New Zealand
01.06.2020
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | P
Y
receptors (P
Y
Rs) are among the various receptors that play an important role in nociception. The goal of this research was to investigate possible P
Y
R expression changes in the trigeminal ganglion (TRG) in bilateral masseter muscle (MM) hypersensitivity following unilateral MM inflammation. The impact of unilateral intramasseteric administration of P
Y
R antagonist on bilateral MM hypersensitivity was also explored.
Bilateral MM hypersensitivity was provoked by unilateral intramasseteric injection of complete Freund's adjuvant (CFA). The head withdrawal threshold (HWT) was assessed bilaterally 4 days later. Bilateral TRG and MM isolation were followed, and quantitative real-time polymerase chain reaction (qRT-PCR) and histopathological analysis were carried out on these tissues, respectively. The involvement of P
Y
Rs in nocifensive behavior was evaluated by administering two doses of P
Y
R antagonist AR-C118925 (0.2 or 1 mg/100 μL) in inflamed MM 4 days post-CFA administration. Bilateral HWT was assessed at different time points following antagonist injection.
qRT-PCR analysis demonstrated P
Y
R up-regulation in TRG ipsilateral to the site of CFA administration. Compared to the controls, both doses of AR-C118925 injected ipsilateral to the TRG increased the bilateral HWT at 30, 60, 90, and 120 minutes after antagonist administration.
The findings suggest that P
Y
Rs may affect MM inflammatory hypersensitivity owing to its up-regulation in the TRG in MM inflammatory pain states. |
---|---|
ISSN: | 1178-7090 1178-7090 |
DOI: | 10.2147/JPR.S239831 |