Physiotherapy Department, Federal University of Alfenas (UNIFAL), Alfenas, Brazil.
State University of Midwest Paraná - Unicentro, Guarapuava, PR, Brazil.
Lasers Med Sci. 2022 Mar;37(2):821-829. doi: 10.1007/s10103-021-03318-w. Epub 2021 Apr 22.
This study aimed to investigate the central involvement of 5-HT1A receptors in the nociceptive behavior of mice submitted to the chronic constriction injury (CCI) of sciatic nerve and the subsequent application of photobiomodulation (PBM). Male mice (Swiss-albino) were submitted to CCI and subsequently received an infusion of WAY100635 (5-HT1A receptor antagonist) or intracerebroventricular saline (ICV), followed by infrared laser irradiation (808 nm), in continuous mode, with the power of 100 mW and a dose of 0 J/cm (control group) or 50 J/cm. The thermal hyperalgesia was evaluated by hot plate test, while mechanical allodynia was evaluated by von Frey filaments. After CCI, animals showed a reduction in the nociceptive threshold (p<0.001) when compared to the sham group. In von Frey test, the CCI + saline + PBM 50 J/cm group showed an increase in nociceptive threshold (p<0.001) in all measurement moments in comparison with groups CCI + SALINE + PBM 0 J/cm, CCI + WAY100635 + PBM 50 J/cm, and CCI + WAY100635 + PBM 0 J/cm. Similarly, in hot plate test, CCI + SALINE + PBM 50 J/cm group showed an increase in nociceptive threshold after application of PBM at 120 and 180 min. Because of the results found, it can be suggested the involvement of 5-HT1A receptors in the central nervous system, since WAY100635 was able to reverse the antinociceptive effect provided by PBM in animals submitted to CCI.
本研究旨在探讨 5-HT1A 受体在慢性坐骨神经缩窄损伤(CCI)后小鼠痛觉行为中的中枢作用,以及随后的光生物调节(PBM)应用。雄性小鼠(瑞士白化病)接受 CCI 后,随后接受 WAY100635(5-HT1A 受体拮抗剂)或脑室生理盐水(ICV)输注,随后进行红外激光照射(808nm),连续模式,功率为 100mW,剂量为 0J/cm(对照组)或 50J/cm。热痛觉过敏通过热板试验评估,机械性痛觉过敏通过 von Frey 纤维评估。CCI 后,与假手术组相比,动物的痛觉阈值降低(p<0.001)。在 von Frey 试验中,与 CCI + SALINE + PBM 0J/cm 组、CCI + WAY100635 + PBM 50J/cm 组和 CCI + WAY100635 + PBM 0J/cm 组相比,CCI + SALINE + PBM 50J/cm 组在所有测量时刻的痛觉阈值均增加(p<0.001)。同样,在热板试验中,CCI + SALINE + PBM 50J/cm 组在应用 PBM 后 120 和 180 分钟时痛觉阈值增加。由于发现的结果,可以认为 5-HT1A 受体参与了中枢神经系统,因为 WAY100635 能够逆转 CCI 后动物的 PBM 提供的抗伤害作用。